Name: rs35952853
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs35952853

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:10949827-10949848 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₁ / del(A)₉ / del(A)₈ / del…
del(A)₁₁ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₁₀ / dup(A)₁₁ / ins(A)₂₆ / ins(A)₃₀
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.3984 (1995/5008, 1000G)
del(A)₁₁=0.0000 (0/4418, ALFA)
del(A)₉=0.0000 (0/4418, ALFA) (+ 14 more)
del(A)₈=0.0000 (0/4418, ALFA)
del(A)₇=0.0000 (0/4418, ALFA)
del(A)₆=0.0000 (0/4418, ALFA)
del(A)₅=0.0000 (0/4418, ALFA)
del(A)₄=0.0000 (0/4418, ALFA)
delAAA=0.0000 (0/4418, ALFA)
delAA=0.0000 (0/4418, ALFA)
delA=0.0000 (0/4418, ALFA)
dupA=0.0000 (0/4418, ALFA)
dupAA=0.0000 (0/4418, ALFA)
dupAAA=0.0000 (0/4418, ALFA)
dup(A)₄=0.0000 (0/4418, ALFA)
dup(A)₅=0.0000 (0/4418, ALFA)
dup(A)₆=0.0000 (0/4418, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CELF2 : Intron Variant
LINC00710 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	4418	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	3730	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	270	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	268	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
East Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	30	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	216	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	14	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	148	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₂₂=0.6016	delA=0.3984
1000Genomes	African	Sub	1322	(A)₂₂=0.7239	delA=0.2761
1000Genomes	East Asian	Sub	1008	(A)₂₂=0.4147	delA=0.5853
1000Genomes	Europe	Sub	1006	(A)₂₂=0.6590	delA=0.3410
1000Genomes	South Asian	Sub	978	(A)₂₂=0.536	delA=0.464
1000Genomes	American	Sub	694	(A)₂₂=0.650	delA=0.350
Allele Frequency Aggregator	Total	Global	4418	(A)₂₂=1.0000	del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	European	Sub	3730	(A)₂₂=1.0000	del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	African	Sub	270	(A)₂₂=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	216	(A)₂₂=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Other	Sub	148	(A)₂₂=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	30	(A)₂₂=1.00	del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(A)₂₂=1.00	del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Asian	Sub	10	(A)₂₂=1.0	del(A)₁₁=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0, dup(A)₆=0.0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 10	NC_000010.11:g.10949838_10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949840_10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949841_10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949842_10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949843_10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949844_10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949845_10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949846_10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949847_10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949848del
GRCh38.p14 chr 10	NC_000010.11:g.10949848dup
GRCh38.p14 chr 10	NC_000010.11:g.10949847_10949848dup
GRCh38.p14 chr 10	NC_000010.11:g.10949846_10949848dup
GRCh38.p14 chr 10	NC_000010.11:g.10949845_10949848dup
GRCh38.p14 chr 10	NC_000010.11:g.10949844_10949848dup
GRCh38.p14 chr 10	NC_000010.11:g.10949843_10949848dup
GRCh38.p14 chr 10	NC_000010.11:g.10949842_10949848dup
GRCh38.p14 chr 10	NC_000010.11:g.10949839_10949848dup
GRCh38.p14 chr 10	NC_000010.11:g.10949838_10949848dup
GRCh38.p14 chr 10	NC_000010.11:g.10949848_10949849insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 10	NC_000010.11:g.10949848_10949849insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.10991801_10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991803_10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991804_10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991805_10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991806_10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991807_10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991808_10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991809_10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991810_10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991811del
GRCh37.p13 chr 10	NC_000010.10:g.10991811dup
GRCh37.p13 chr 10	NC_000010.10:g.10991810_10991811dup
GRCh37.p13 chr 10	NC_000010.10:g.10991809_10991811dup
GRCh37.p13 chr 10	NC_000010.10:g.10991808_10991811dup
GRCh37.p13 chr 10	NC_000010.10:g.10991807_10991811dup
GRCh37.p13 chr 10	NC_000010.10:g.10991806_10991811dup
GRCh37.p13 chr 10	NC_000010.10:g.10991805_10991811dup
GRCh37.p13 chr 10	NC_000010.10:g.10991802_10991811dup
GRCh37.p13 chr 10	NC_000010.10:g.10991801_10991811dup
GRCh37.p13 chr 10	NC_000010.10:g.10991811_10991812insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.10991811_10991812insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: CELF2, CUGBP Elav-like family member 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CELF2 transcript variant 5	NM_001326317.2:c.-20+2983… NM_001326317.2:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant 6	NM_001326318.2:c.-20+2983… NM_001326318.2:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant 7	NM_001326319.2:c.-20+9384… NM_001326319.2:c.-20+9384_-20+9394del	N/A	Intron Variant
CELF2 transcript variant 8	NM_001326320.2:c.-20+2983… NM_001326320.2:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant 9	NM_001326321.2:c.-20+2983… NM_001326321.2:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant 10	NM_001326323.2:c.-20+2983… NM_001326323.2:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant 11	NM_001326324.2:c.-20+2983… NM_001326324.2:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant 12	NM_001326325.2:c.146+2983… NM_001326325.2:c.146+29839_146+29849del	N/A	Intron Variant
CELF2 transcript variant 13	NM_001326326.2:c.89+29839… NM_001326326.2:c.89+29839_89+29849del	N/A	Intron Variant
CELF2 transcript variant 14	NM_001326327.2:c.89+29839… NM_001326327.2:c.89+29839_89+29849del	N/A	Intron Variant
CELF2 transcript variant 15	NM_001326328.2:c.-20+2983… NM_001326328.2:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant 1	NM_001025076.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 3	NM_001025077.3:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 4	NM_001083591.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 16	NM_001326329.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 17	NM_001326330.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 18	NM_001326331.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 19	NM_001326332.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 20	NM_001326333.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 21	NM_001326334.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 22	NM_001326335.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 23	NM_001326336.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 24	NM_001326337.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 25	NM_001326338.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 26	NM_001326339.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 27	NM_001326340.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 28	NM_001326341.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 29	NM_001326342.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 30	NM_001326343.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 31	NM_001326344.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 32	NM_001326345.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 33	NM_001326346.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 34	NM_001326347.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 35	NM_001326348.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 36	NM_001326349.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 37	NM_001394502.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 38	NM_001394513.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 39	NM_001394517.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 40	NM_001394518.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 41	NM_001394519.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant 2	NM_006561.4:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X1	XM_047424482.1:c.146+2983… XM_047424482.1:c.146+29839_146+29849del	N/A	Intron Variant
CELF2 transcript variant X2	XM_047424483.1:c.146+2983… XM_047424483.1:c.146+29839_146+29849del	N/A	Intron Variant
CELF2 transcript variant X4	XM_047424484.1:c.89+29839… XM_047424484.1:c.89+29839_89+29849del	N/A	Intron Variant
CELF2 transcript variant X5	XM_047424485.1:c.89+29839… XM_047424485.1:c.89+29839_89+29849del	N/A	Intron Variant
CELF2 transcript variant X7	XM_047424487.1:c.89+29839… XM_047424487.1:c.89+29839_89+29849del	N/A	Intron Variant
CELF2 transcript variant X8	XM_047424488.1:c.-20+2983… XM_047424488.1:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant X10	XM_047424490.1:c.-20+2983… XM_047424490.1:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant X11	XM_047424491.1:c.-20+2983… XM_047424491.1:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant X12	XM_047424492.1:c.-20+9384… XM_047424492.1:c.-20+9384_-20+9394del	N/A	Intron Variant
CELF2 transcript variant X14	XM_047424494.1:c.-20+9384… XM_047424494.1:c.-20+9384_-20+9394del	N/A	Intron Variant
CELF2 transcript variant X16	XM_047424496.1:c.-20+9384… XM_047424496.1:c.-20+9384_-20+9394del	N/A	Intron Variant
CELF2 transcript variant X18	XM_047424499.1:c.-20+9384… XM_047424499.1:c.-20+9384_-20+9394del	N/A	Intron Variant
CELF2 transcript variant X29	XM_047424501.1:c.-20+2983… XM_047424501.1:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant X23	XM_047424506.1:c.89+29839… XM_047424506.1:c.89+29839_89+29849del	N/A	Intron Variant
CELF2 transcript variant X25	XM_047424508.1:c.-20+2983… XM_047424508.1:c.-20+29839_-20+29849del	N/A	Intron Variant
CELF2 transcript variant X3	XM_024447776.2:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X6	XM_047424486.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X9	XM_047424489.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X13	XM_047424493.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X15	XM_047424495.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X17	XM_047424498.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X28	XM_047424500.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X19	XM_047424502.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X20	XM_047424503.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X21	XM_047424504.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X22	XM_047424505.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X24	XM_047424507.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X26	XM_047424509.1:c.	N/A	Genic Upstream Transcript Variant
CELF2 transcript variant X27	XM_047424510.1:c.	N/A	Genic Upstream Transcript Variant

Gene: LINC00710, long intergenic non-protein coding RNA 710 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00710 transcript variant 1	NR_015413.1:n.	N/A	Intron Variant
LINC00710 transcript variant 2	NR_024410.1:n.	N/A	Intron Variant
LINC00710 transcript variant 3	NR_024411.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₂₂=	del(A)₁₁	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₁₀	dup(A)₁₁	ins(A)₂₆	ins(A)₃₀
GRCh38.p14 chr 10	NC_000010.11:g.10949827_10949848=	NC_000010.11:g.10949838_10949848del	NC_000010.11:g.10949840_10949848del	NC_000010.11:g.10949841_10949848del	NC_000010.11:g.10949842_10949848del	NC_000010.11:g.10949843_10949848del	NC_000010.11:g.10949844_10949848del	NC_000010.11:g.10949845_10949848del	NC_000010.11:g.10949846_10949848del	NC_000010.11:g.10949847_10949848del	NC_000010.11:g.10949848del	NC_000010.11:g.10949848dup	NC_000010.11:g.10949847_10949848dup	NC_000010.11:g.10949846_10949848dup	NC_000010.11:g.10949845_10949848dup	NC_000010.11:g.10949844_10949848dup	NC_000010.11:g.10949843_10949848dup	NC_000010.11:g.10949842_10949848dup	NC_000010.11:g.10949839_10949848dup	NC_000010.11:g.10949838_10949848dup	NC_000010.11:g.10949848_10949849insAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:g.10949848_10949849insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.10991790_10991811=	NC_000010.10:g.10991801_10991811del	NC_000010.10:g.10991803_10991811del	NC_000010.10:g.10991804_10991811del	NC_000010.10:g.10991805_10991811del	NC_000010.10:g.10991806_10991811del	NC_000010.10:g.10991807_10991811del	NC_000010.10:g.10991808_10991811del	NC_000010.10:g.10991809_10991811del	NC_000010.10:g.10991810_10991811del	NC_000010.10:g.10991811del	NC_000010.10:g.10991811dup	NC_000010.10:g.10991810_10991811dup	NC_000010.10:g.10991809_10991811dup	NC_000010.10:g.10991808_10991811dup	NC_000010.10:g.10991807_10991811dup	NC_000010.10:g.10991806_10991811dup	NC_000010.10:g.10991805_10991811dup	NC_000010.10:g.10991802_10991811dup	NC_000010.10:g.10991801_10991811dup	NC_000010.10:g.10991811_10991812insAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.10:g.10991811_10991812insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 5	NM_001326317.2:c.-20+29828=	NM_001326317.2:c.-20+29839_-20+29849del	NM_001326317.2:c.-20+29841_-20+29849del	NM_001326317.2:c.-20+29842_-20+29849del	NM_001326317.2:c.-20+29843_-20+29849del	NM_001326317.2:c.-20+29844_-20+29849del	NM_001326317.2:c.-20+29845_-20+29849del	NM_001326317.2:c.-20+29846_-20+29849del	NM_001326317.2:c.-20+29847_-20+29849del	NM_001326317.2:c.-20+29848_-20+29849del	NM_001326317.2:c.-20+29849del	NM_001326317.2:c.-20+29849dup	NM_001326317.2:c.-20+29848_-20+29849dup	NM_001326317.2:c.-20+29847_-20+29849dup	NM_001326317.2:c.-20+29846_-20+29849dup	NM_001326317.2:c.-20+29845_-20+29849dup	NM_001326317.2:c.-20+29844_-20+29849dup	NM_001326317.2:c.-20+29843_-20+29849dup	NM_001326317.2:c.-20+29840_-20+29849dup	NM_001326317.2:c.-20+29839_-20+29849dup	NM_001326317.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326317.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 6	NM_001326318.2:c.-20+29828=	NM_001326318.2:c.-20+29839_-20+29849del	NM_001326318.2:c.-20+29841_-20+29849del	NM_001326318.2:c.-20+29842_-20+29849del	NM_001326318.2:c.-20+29843_-20+29849del	NM_001326318.2:c.-20+29844_-20+29849del	NM_001326318.2:c.-20+29845_-20+29849del	NM_001326318.2:c.-20+29846_-20+29849del	NM_001326318.2:c.-20+29847_-20+29849del	NM_001326318.2:c.-20+29848_-20+29849del	NM_001326318.2:c.-20+29849del	NM_001326318.2:c.-20+29849dup	NM_001326318.2:c.-20+29848_-20+29849dup	NM_001326318.2:c.-20+29847_-20+29849dup	NM_001326318.2:c.-20+29846_-20+29849dup	NM_001326318.2:c.-20+29845_-20+29849dup	NM_001326318.2:c.-20+29844_-20+29849dup	NM_001326318.2:c.-20+29843_-20+29849dup	NM_001326318.2:c.-20+29840_-20+29849dup	NM_001326318.2:c.-20+29839_-20+29849dup	NM_001326318.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326318.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 7	NM_001326319.2:c.-20+9373=	NM_001326319.2:c.-20+9384_-20+9394del	NM_001326319.2:c.-20+9386_-20+9394del	NM_001326319.2:c.-20+9387_-20+9394del	NM_001326319.2:c.-20+9388_-20+9394del	NM_001326319.2:c.-20+9389_-20+9394del	NM_001326319.2:c.-20+9390_-20+9394del	NM_001326319.2:c.-20+9391_-20+9394del	NM_001326319.2:c.-20+9392_-20+9394del	NM_001326319.2:c.-20+9393_-20+9394del	NM_001326319.2:c.-20+9394del	NM_001326319.2:c.-20+9394dup	NM_001326319.2:c.-20+9393_-20+9394dup	NM_001326319.2:c.-20+9392_-20+9394dup	NM_001326319.2:c.-20+9391_-20+9394dup	NM_001326319.2:c.-20+9390_-20+9394dup	NM_001326319.2:c.-20+9389_-20+9394dup	NM_001326319.2:c.-20+9388_-20+9394dup	NM_001326319.2:c.-20+9385_-20+9394dup	NM_001326319.2:c.-20+9384_-20+9394dup	NM_001326319.2:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326319.2:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 8	NM_001326320.2:c.-20+29828=	NM_001326320.2:c.-20+29839_-20+29849del	NM_001326320.2:c.-20+29841_-20+29849del	NM_001326320.2:c.-20+29842_-20+29849del	NM_001326320.2:c.-20+29843_-20+29849del	NM_001326320.2:c.-20+29844_-20+29849del	NM_001326320.2:c.-20+29845_-20+29849del	NM_001326320.2:c.-20+29846_-20+29849del	NM_001326320.2:c.-20+29847_-20+29849del	NM_001326320.2:c.-20+29848_-20+29849del	NM_001326320.2:c.-20+29849del	NM_001326320.2:c.-20+29849dup	NM_001326320.2:c.-20+29848_-20+29849dup	NM_001326320.2:c.-20+29847_-20+29849dup	NM_001326320.2:c.-20+29846_-20+29849dup	NM_001326320.2:c.-20+29845_-20+29849dup	NM_001326320.2:c.-20+29844_-20+29849dup	NM_001326320.2:c.-20+29843_-20+29849dup	NM_001326320.2:c.-20+29840_-20+29849dup	NM_001326320.2:c.-20+29839_-20+29849dup	NM_001326320.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326320.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 9	NM_001326321.2:c.-20+29828=	NM_001326321.2:c.-20+29839_-20+29849del	NM_001326321.2:c.-20+29841_-20+29849del	NM_001326321.2:c.-20+29842_-20+29849del	NM_001326321.2:c.-20+29843_-20+29849del	NM_001326321.2:c.-20+29844_-20+29849del	NM_001326321.2:c.-20+29845_-20+29849del	NM_001326321.2:c.-20+29846_-20+29849del	NM_001326321.2:c.-20+29847_-20+29849del	NM_001326321.2:c.-20+29848_-20+29849del	NM_001326321.2:c.-20+29849del	NM_001326321.2:c.-20+29849dup	NM_001326321.2:c.-20+29848_-20+29849dup	NM_001326321.2:c.-20+29847_-20+29849dup	NM_001326321.2:c.-20+29846_-20+29849dup	NM_001326321.2:c.-20+29845_-20+29849dup	NM_001326321.2:c.-20+29844_-20+29849dup	NM_001326321.2:c.-20+29843_-20+29849dup	NM_001326321.2:c.-20+29840_-20+29849dup	NM_001326321.2:c.-20+29839_-20+29849dup	NM_001326321.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326321.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 10	NM_001326323.2:c.-20+29828=	NM_001326323.2:c.-20+29839_-20+29849del	NM_001326323.2:c.-20+29841_-20+29849del	NM_001326323.2:c.-20+29842_-20+29849del	NM_001326323.2:c.-20+29843_-20+29849del	NM_001326323.2:c.-20+29844_-20+29849del	NM_001326323.2:c.-20+29845_-20+29849del	NM_001326323.2:c.-20+29846_-20+29849del	NM_001326323.2:c.-20+29847_-20+29849del	NM_001326323.2:c.-20+29848_-20+29849del	NM_001326323.2:c.-20+29849del	NM_001326323.2:c.-20+29849dup	NM_001326323.2:c.-20+29848_-20+29849dup	NM_001326323.2:c.-20+29847_-20+29849dup	NM_001326323.2:c.-20+29846_-20+29849dup	NM_001326323.2:c.-20+29845_-20+29849dup	NM_001326323.2:c.-20+29844_-20+29849dup	NM_001326323.2:c.-20+29843_-20+29849dup	NM_001326323.2:c.-20+29840_-20+29849dup	NM_001326323.2:c.-20+29839_-20+29849dup	NM_001326323.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326323.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 11	NM_001326324.2:c.-20+29828=	NM_001326324.2:c.-20+29839_-20+29849del	NM_001326324.2:c.-20+29841_-20+29849del	NM_001326324.2:c.-20+29842_-20+29849del	NM_001326324.2:c.-20+29843_-20+29849del	NM_001326324.2:c.-20+29844_-20+29849del	NM_001326324.2:c.-20+29845_-20+29849del	NM_001326324.2:c.-20+29846_-20+29849del	NM_001326324.2:c.-20+29847_-20+29849del	NM_001326324.2:c.-20+29848_-20+29849del	NM_001326324.2:c.-20+29849del	NM_001326324.2:c.-20+29849dup	NM_001326324.2:c.-20+29848_-20+29849dup	NM_001326324.2:c.-20+29847_-20+29849dup	NM_001326324.2:c.-20+29846_-20+29849dup	NM_001326324.2:c.-20+29845_-20+29849dup	NM_001326324.2:c.-20+29844_-20+29849dup	NM_001326324.2:c.-20+29843_-20+29849dup	NM_001326324.2:c.-20+29840_-20+29849dup	NM_001326324.2:c.-20+29839_-20+29849dup	NM_001326324.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326324.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 12	NM_001326325.2:c.146+29828=	NM_001326325.2:c.146+29839_146+29849del	NM_001326325.2:c.146+29841_146+29849del	NM_001326325.2:c.146+29842_146+29849del	NM_001326325.2:c.146+29843_146+29849del	NM_001326325.2:c.146+29844_146+29849del	NM_001326325.2:c.146+29845_146+29849del	NM_001326325.2:c.146+29846_146+29849del	NM_001326325.2:c.146+29847_146+29849del	NM_001326325.2:c.146+29848_146+29849del	NM_001326325.2:c.146+29849del	NM_001326325.2:c.146+29849dup	NM_001326325.2:c.146+29848_146+29849dup	NM_001326325.2:c.146+29847_146+29849dup	NM_001326325.2:c.146+29846_146+29849dup	NM_001326325.2:c.146+29845_146+29849dup	NM_001326325.2:c.146+29844_146+29849dup	NM_001326325.2:c.146+29843_146+29849dup	NM_001326325.2:c.146+29840_146+29849dup	NM_001326325.2:c.146+29839_146+29849dup	NM_001326325.2:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326325.2:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 13	NM_001326326.2:c.89+29828=	NM_001326326.2:c.89+29839_89+29849del	NM_001326326.2:c.89+29841_89+29849del	NM_001326326.2:c.89+29842_89+29849del	NM_001326326.2:c.89+29843_89+29849del	NM_001326326.2:c.89+29844_89+29849del	NM_001326326.2:c.89+29845_89+29849del	NM_001326326.2:c.89+29846_89+29849del	NM_001326326.2:c.89+29847_89+29849del	NM_001326326.2:c.89+29848_89+29849del	NM_001326326.2:c.89+29849del	NM_001326326.2:c.89+29849dup	NM_001326326.2:c.89+29848_89+29849dup	NM_001326326.2:c.89+29847_89+29849dup	NM_001326326.2:c.89+29846_89+29849dup	NM_001326326.2:c.89+29845_89+29849dup	NM_001326326.2:c.89+29844_89+29849dup	NM_001326326.2:c.89+29843_89+29849dup	NM_001326326.2:c.89+29840_89+29849dup	NM_001326326.2:c.89+29839_89+29849dup	NM_001326326.2:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326326.2:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 14	NM_001326327.2:c.89+29828=	NM_001326327.2:c.89+29839_89+29849del	NM_001326327.2:c.89+29841_89+29849del	NM_001326327.2:c.89+29842_89+29849del	NM_001326327.2:c.89+29843_89+29849del	NM_001326327.2:c.89+29844_89+29849del	NM_001326327.2:c.89+29845_89+29849del	NM_001326327.2:c.89+29846_89+29849del	NM_001326327.2:c.89+29847_89+29849del	NM_001326327.2:c.89+29848_89+29849del	NM_001326327.2:c.89+29849del	NM_001326327.2:c.89+29849dup	NM_001326327.2:c.89+29848_89+29849dup	NM_001326327.2:c.89+29847_89+29849dup	NM_001326327.2:c.89+29846_89+29849dup	NM_001326327.2:c.89+29845_89+29849dup	NM_001326327.2:c.89+29844_89+29849dup	NM_001326327.2:c.89+29843_89+29849dup	NM_001326327.2:c.89+29840_89+29849dup	NM_001326327.2:c.89+29839_89+29849dup	NM_001326327.2:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326327.2:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant 15	NM_001326328.2:c.-20+29828=	NM_001326328.2:c.-20+29839_-20+29849del	NM_001326328.2:c.-20+29841_-20+29849del	NM_001326328.2:c.-20+29842_-20+29849del	NM_001326328.2:c.-20+29843_-20+29849del	NM_001326328.2:c.-20+29844_-20+29849del	NM_001326328.2:c.-20+29845_-20+29849del	NM_001326328.2:c.-20+29846_-20+29849del	NM_001326328.2:c.-20+29847_-20+29849del	NM_001326328.2:c.-20+29848_-20+29849del	NM_001326328.2:c.-20+29849del	NM_001326328.2:c.-20+29849dup	NM_001326328.2:c.-20+29848_-20+29849dup	NM_001326328.2:c.-20+29847_-20+29849dup	NM_001326328.2:c.-20+29846_-20+29849dup	NM_001326328.2:c.-20+29845_-20+29849dup	NM_001326328.2:c.-20+29844_-20+29849dup	NM_001326328.2:c.-20+29843_-20+29849dup	NM_001326328.2:c.-20+29840_-20+29849dup	NM_001326328.2:c.-20+29839_-20+29849dup	NM_001326328.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001326328.2:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X1	XM_005252346.1:c.146+29828=	XM_005252346.1:c.146+29839_146+29849del	XM_005252346.1:c.146+29841_146+29849del	XM_005252346.1:c.146+29842_146+29849del	XM_005252346.1:c.146+29843_146+29849del	XM_005252346.1:c.146+29844_146+29849del	XM_005252346.1:c.146+29845_146+29849del	XM_005252346.1:c.146+29846_146+29849del	XM_005252346.1:c.146+29847_146+29849del	XM_005252346.1:c.146+29848_146+29849del	XM_005252346.1:c.146+29849del	XM_005252346.1:c.146+29849dup	XM_005252346.1:c.146+29848_146+29849dup	XM_005252346.1:c.146+29847_146+29849dup	XM_005252346.1:c.146+29846_146+29849dup	XM_005252346.1:c.146+29845_146+29849dup	XM_005252346.1:c.146+29844_146+29849dup	XM_005252346.1:c.146+29843_146+29849dup	XM_005252346.1:c.146+29840_146+29849dup	XM_005252346.1:c.146+29839_146+29849dup	XM_005252346.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252346.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X2	XM_005252347.1:c.146+29828=	XM_005252347.1:c.146+29839_146+29849del	XM_005252347.1:c.146+29841_146+29849del	XM_005252347.1:c.146+29842_146+29849del	XM_005252347.1:c.146+29843_146+29849del	XM_005252347.1:c.146+29844_146+29849del	XM_005252347.1:c.146+29845_146+29849del	XM_005252347.1:c.146+29846_146+29849del	XM_005252347.1:c.146+29847_146+29849del	XM_005252347.1:c.146+29848_146+29849del	XM_005252347.1:c.146+29849del	XM_005252347.1:c.146+29849dup	XM_005252347.1:c.146+29848_146+29849dup	XM_005252347.1:c.146+29847_146+29849dup	XM_005252347.1:c.146+29846_146+29849dup	XM_005252347.1:c.146+29845_146+29849dup	XM_005252347.1:c.146+29844_146+29849dup	XM_005252347.1:c.146+29843_146+29849dup	XM_005252347.1:c.146+29840_146+29849dup	XM_005252347.1:c.146+29839_146+29849dup	XM_005252347.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252347.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X3	XM_005252348.1:c.146+29828=	XM_005252348.1:c.146+29839_146+29849del	XM_005252348.1:c.146+29841_146+29849del	XM_005252348.1:c.146+29842_146+29849del	XM_005252348.1:c.146+29843_146+29849del	XM_005252348.1:c.146+29844_146+29849del	XM_005252348.1:c.146+29845_146+29849del	XM_005252348.1:c.146+29846_146+29849del	XM_005252348.1:c.146+29847_146+29849del	XM_005252348.1:c.146+29848_146+29849del	XM_005252348.1:c.146+29849del	XM_005252348.1:c.146+29849dup	XM_005252348.1:c.146+29848_146+29849dup	XM_005252348.1:c.146+29847_146+29849dup	XM_005252348.1:c.146+29846_146+29849dup	XM_005252348.1:c.146+29845_146+29849dup	XM_005252348.1:c.146+29844_146+29849dup	XM_005252348.1:c.146+29843_146+29849dup	XM_005252348.1:c.146+29840_146+29849dup	XM_005252348.1:c.146+29839_146+29849dup	XM_005252348.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252348.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X4	XM_005252349.1:c.146+29828=	XM_005252349.1:c.146+29839_146+29849del	XM_005252349.1:c.146+29841_146+29849del	XM_005252349.1:c.146+29842_146+29849del	XM_005252349.1:c.146+29843_146+29849del	XM_005252349.1:c.146+29844_146+29849del	XM_005252349.1:c.146+29845_146+29849del	XM_005252349.1:c.146+29846_146+29849del	XM_005252349.1:c.146+29847_146+29849del	XM_005252349.1:c.146+29848_146+29849del	XM_005252349.1:c.146+29849del	XM_005252349.1:c.146+29849dup	XM_005252349.1:c.146+29848_146+29849dup	XM_005252349.1:c.146+29847_146+29849dup	XM_005252349.1:c.146+29846_146+29849dup	XM_005252349.1:c.146+29845_146+29849dup	XM_005252349.1:c.146+29844_146+29849dup	XM_005252349.1:c.146+29843_146+29849dup	XM_005252349.1:c.146+29840_146+29849dup	XM_005252349.1:c.146+29839_146+29849dup	XM_005252349.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252349.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X5	XM_005252350.1:c.146+29828=	XM_005252350.1:c.146+29839_146+29849del	XM_005252350.1:c.146+29841_146+29849del	XM_005252350.1:c.146+29842_146+29849del	XM_005252350.1:c.146+29843_146+29849del	XM_005252350.1:c.146+29844_146+29849del	XM_005252350.1:c.146+29845_146+29849del	XM_005252350.1:c.146+29846_146+29849del	XM_005252350.1:c.146+29847_146+29849del	XM_005252350.1:c.146+29848_146+29849del	XM_005252350.1:c.146+29849del	XM_005252350.1:c.146+29849dup	XM_005252350.1:c.146+29848_146+29849dup	XM_005252350.1:c.146+29847_146+29849dup	XM_005252350.1:c.146+29846_146+29849dup	XM_005252350.1:c.146+29845_146+29849dup	XM_005252350.1:c.146+29844_146+29849dup	XM_005252350.1:c.146+29843_146+29849dup	XM_005252350.1:c.146+29840_146+29849dup	XM_005252350.1:c.146+29839_146+29849dup	XM_005252350.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252350.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X6	XM_005252351.1:c.146+29828=	XM_005252351.1:c.146+29839_146+29849del	XM_005252351.1:c.146+29841_146+29849del	XM_005252351.1:c.146+29842_146+29849del	XM_005252351.1:c.146+29843_146+29849del	XM_005252351.1:c.146+29844_146+29849del	XM_005252351.1:c.146+29845_146+29849del	XM_005252351.1:c.146+29846_146+29849del	XM_005252351.1:c.146+29847_146+29849del	XM_005252351.1:c.146+29848_146+29849del	XM_005252351.1:c.146+29849del	XM_005252351.1:c.146+29849dup	XM_005252351.1:c.146+29848_146+29849dup	XM_005252351.1:c.146+29847_146+29849dup	XM_005252351.1:c.146+29846_146+29849dup	XM_005252351.1:c.146+29845_146+29849dup	XM_005252351.1:c.146+29844_146+29849dup	XM_005252351.1:c.146+29843_146+29849dup	XM_005252351.1:c.146+29840_146+29849dup	XM_005252351.1:c.146+29839_146+29849dup	XM_005252351.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252351.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X1	XM_047424482.1:c.146+29828=	XM_047424482.1:c.146+29839_146+29849del	XM_047424482.1:c.146+29841_146+29849del	XM_047424482.1:c.146+29842_146+29849del	XM_047424482.1:c.146+29843_146+29849del	XM_047424482.1:c.146+29844_146+29849del	XM_047424482.1:c.146+29845_146+29849del	XM_047424482.1:c.146+29846_146+29849del	XM_047424482.1:c.146+29847_146+29849del	XM_047424482.1:c.146+29848_146+29849del	XM_047424482.1:c.146+29849del	XM_047424482.1:c.146+29849dup	XM_047424482.1:c.146+29848_146+29849dup	XM_047424482.1:c.146+29847_146+29849dup	XM_047424482.1:c.146+29846_146+29849dup	XM_047424482.1:c.146+29845_146+29849dup	XM_047424482.1:c.146+29844_146+29849dup	XM_047424482.1:c.146+29843_146+29849dup	XM_047424482.1:c.146+29840_146+29849dup	XM_047424482.1:c.146+29839_146+29849dup	XM_047424482.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424482.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X2	XM_047424483.1:c.146+29828=	XM_047424483.1:c.146+29839_146+29849del	XM_047424483.1:c.146+29841_146+29849del	XM_047424483.1:c.146+29842_146+29849del	XM_047424483.1:c.146+29843_146+29849del	XM_047424483.1:c.146+29844_146+29849del	XM_047424483.1:c.146+29845_146+29849del	XM_047424483.1:c.146+29846_146+29849del	XM_047424483.1:c.146+29847_146+29849del	XM_047424483.1:c.146+29848_146+29849del	XM_047424483.1:c.146+29849del	XM_047424483.1:c.146+29849dup	XM_047424483.1:c.146+29848_146+29849dup	XM_047424483.1:c.146+29847_146+29849dup	XM_047424483.1:c.146+29846_146+29849dup	XM_047424483.1:c.146+29845_146+29849dup	XM_047424483.1:c.146+29844_146+29849dup	XM_047424483.1:c.146+29843_146+29849dup	XM_047424483.1:c.146+29840_146+29849dup	XM_047424483.1:c.146+29839_146+29849dup	XM_047424483.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424483.1:c.146+29849_146+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X4	XM_047424484.1:c.89+29828=	XM_047424484.1:c.89+29839_89+29849del	XM_047424484.1:c.89+29841_89+29849del	XM_047424484.1:c.89+29842_89+29849del	XM_047424484.1:c.89+29843_89+29849del	XM_047424484.1:c.89+29844_89+29849del	XM_047424484.1:c.89+29845_89+29849del	XM_047424484.1:c.89+29846_89+29849del	XM_047424484.1:c.89+29847_89+29849del	XM_047424484.1:c.89+29848_89+29849del	XM_047424484.1:c.89+29849del	XM_047424484.1:c.89+29849dup	XM_047424484.1:c.89+29848_89+29849dup	XM_047424484.1:c.89+29847_89+29849dup	XM_047424484.1:c.89+29846_89+29849dup	XM_047424484.1:c.89+29845_89+29849dup	XM_047424484.1:c.89+29844_89+29849dup	XM_047424484.1:c.89+29843_89+29849dup	XM_047424484.1:c.89+29840_89+29849dup	XM_047424484.1:c.89+29839_89+29849dup	XM_047424484.1:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424484.1:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X5	XM_047424485.1:c.89+29828=	XM_047424485.1:c.89+29839_89+29849del	XM_047424485.1:c.89+29841_89+29849del	XM_047424485.1:c.89+29842_89+29849del	XM_047424485.1:c.89+29843_89+29849del	XM_047424485.1:c.89+29844_89+29849del	XM_047424485.1:c.89+29845_89+29849del	XM_047424485.1:c.89+29846_89+29849del	XM_047424485.1:c.89+29847_89+29849del	XM_047424485.1:c.89+29848_89+29849del	XM_047424485.1:c.89+29849del	XM_047424485.1:c.89+29849dup	XM_047424485.1:c.89+29848_89+29849dup	XM_047424485.1:c.89+29847_89+29849dup	XM_047424485.1:c.89+29846_89+29849dup	XM_047424485.1:c.89+29845_89+29849dup	XM_047424485.1:c.89+29844_89+29849dup	XM_047424485.1:c.89+29843_89+29849dup	XM_047424485.1:c.89+29840_89+29849dup	XM_047424485.1:c.89+29839_89+29849dup	XM_047424485.1:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424485.1:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X7	XM_047424487.1:c.89+29828=	XM_047424487.1:c.89+29839_89+29849del	XM_047424487.1:c.89+29841_89+29849del	XM_047424487.1:c.89+29842_89+29849del	XM_047424487.1:c.89+29843_89+29849del	XM_047424487.1:c.89+29844_89+29849del	XM_047424487.1:c.89+29845_89+29849del	XM_047424487.1:c.89+29846_89+29849del	XM_047424487.1:c.89+29847_89+29849del	XM_047424487.1:c.89+29848_89+29849del	XM_047424487.1:c.89+29849del	XM_047424487.1:c.89+29849dup	XM_047424487.1:c.89+29848_89+29849dup	XM_047424487.1:c.89+29847_89+29849dup	XM_047424487.1:c.89+29846_89+29849dup	XM_047424487.1:c.89+29845_89+29849dup	XM_047424487.1:c.89+29844_89+29849dup	XM_047424487.1:c.89+29843_89+29849dup	XM_047424487.1:c.89+29840_89+29849dup	XM_047424487.1:c.89+29839_89+29849dup	XM_047424487.1:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424487.1:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X8	XM_047424488.1:c.-20+29828=	XM_047424488.1:c.-20+29839_-20+29849del	XM_047424488.1:c.-20+29841_-20+29849del	XM_047424488.1:c.-20+29842_-20+29849del	XM_047424488.1:c.-20+29843_-20+29849del	XM_047424488.1:c.-20+29844_-20+29849del	XM_047424488.1:c.-20+29845_-20+29849del	XM_047424488.1:c.-20+29846_-20+29849del	XM_047424488.1:c.-20+29847_-20+29849del	XM_047424488.1:c.-20+29848_-20+29849del	XM_047424488.1:c.-20+29849del	XM_047424488.1:c.-20+29849dup	XM_047424488.1:c.-20+29848_-20+29849dup	XM_047424488.1:c.-20+29847_-20+29849dup	XM_047424488.1:c.-20+29846_-20+29849dup	XM_047424488.1:c.-20+29845_-20+29849dup	XM_047424488.1:c.-20+29844_-20+29849dup	XM_047424488.1:c.-20+29843_-20+29849dup	XM_047424488.1:c.-20+29840_-20+29849dup	XM_047424488.1:c.-20+29839_-20+29849dup	XM_047424488.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424488.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X10	XM_047424490.1:c.-20+29828=	XM_047424490.1:c.-20+29839_-20+29849del	XM_047424490.1:c.-20+29841_-20+29849del	XM_047424490.1:c.-20+29842_-20+29849del	XM_047424490.1:c.-20+29843_-20+29849del	XM_047424490.1:c.-20+29844_-20+29849del	XM_047424490.1:c.-20+29845_-20+29849del	XM_047424490.1:c.-20+29846_-20+29849del	XM_047424490.1:c.-20+29847_-20+29849del	XM_047424490.1:c.-20+29848_-20+29849del	XM_047424490.1:c.-20+29849del	XM_047424490.1:c.-20+29849dup	XM_047424490.1:c.-20+29848_-20+29849dup	XM_047424490.1:c.-20+29847_-20+29849dup	XM_047424490.1:c.-20+29846_-20+29849dup	XM_047424490.1:c.-20+29845_-20+29849dup	XM_047424490.1:c.-20+29844_-20+29849dup	XM_047424490.1:c.-20+29843_-20+29849dup	XM_047424490.1:c.-20+29840_-20+29849dup	XM_047424490.1:c.-20+29839_-20+29849dup	XM_047424490.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424490.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X11	XM_047424491.1:c.-20+29828=	XM_047424491.1:c.-20+29839_-20+29849del	XM_047424491.1:c.-20+29841_-20+29849del	XM_047424491.1:c.-20+29842_-20+29849del	XM_047424491.1:c.-20+29843_-20+29849del	XM_047424491.1:c.-20+29844_-20+29849del	XM_047424491.1:c.-20+29845_-20+29849del	XM_047424491.1:c.-20+29846_-20+29849del	XM_047424491.1:c.-20+29847_-20+29849del	XM_047424491.1:c.-20+29848_-20+29849del	XM_047424491.1:c.-20+29849del	XM_047424491.1:c.-20+29849dup	XM_047424491.1:c.-20+29848_-20+29849dup	XM_047424491.1:c.-20+29847_-20+29849dup	XM_047424491.1:c.-20+29846_-20+29849dup	XM_047424491.1:c.-20+29845_-20+29849dup	XM_047424491.1:c.-20+29844_-20+29849dup	XM_047424491.1:c.-20+29843_-20+29849dup	XM_047424491.1:c.-20+29840_-20+29849dup	XM_047424491.1:c.-20+29839_-20+29849dup	XM_047424491.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424491.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X12	XM_047424492.1:c.-20+9373=	XM_047424492.1:c.-20+9384_-20+9394del	XM_047424492.1:c.-20+9386_-20+9394del	XM_047424492.1:c.-20+9387_-20+9394del	XM_047424492.1:c.-20+9388_-20+9394del	XM_047424492.1:c.-20+9389_-20+9394del	XM_047424492.1:c.-20+9390_-20+9394del	XM_047424492.1:c.-20+9391_-20+9394del	XM_047424492.1:c.-20+9392_-20+9394del	XM_047424492.1:c.-20+9393_-20+9394del	XM_047424492.1:c.-20+9394del	XM_047424492.1:c.-20+9394dup	XM_047424492.1:c.-20+9393_-20+9394dup	XM_047424492.1:c.-20+9392_-20+9394dup	XM_047424492.1:c.-20+9391_-20+9394dup	XM_047424492.1:c.-20+9390_-20+9394dup	XM_047424492.1:c.-20+9389_-20+9394dup	XM_047424492.1:c.-20+9388_-20+9394dup	XM_047424492.1:c.-20+9385_-20+9394dup	XM_047424492.1:c.-20+9384_-20+9394dup	XM_047424492.1:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424492.1:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X14	XM_047424494.1:c.-20+9373=	XM_047424494.1:c.-20+9384_-20+9394del	XM_047424494.1:c.-20+9386_-20+9394del	XM_047424494.1:c.-20+9387_-20+9394del	XM_047424494.1:c.-20+9388_-20+9394del	XM_047424494.1:c.-20+9389_-20+9394del	XM_047424494.1:c.-20+9390_-20+9394del	XM_047424494.1:c.-20+9391_-20+9394del	XM_047424494.1:c.-20+9392_-20+9394del	XM_047424494.1:c.-20+9393_-20+9394del	XM_047424494.1:c.-20+9394del	XM_047424494.1:c.-20+9394dup	XM_047424494.1:c.-20+9393_-20+9394dup	XM_047424494.1:c.-20+9392_-20+9394dup	XM_047424494.1:c.-20+9391_-20+9394dup	XM_047424494.1:c.-20+9390_-20+9394dup	XM_047424494.1:c.-20+9389_-20+9394dup	XM_047424494.1:c.-20+9388_-20+9394dup	XM_047424494.1:c.-20+9385_-20+9394dup	XM_047424494.1:c.-20+9384_-20+9394dup	XM_047424494.1:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424494.1:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X16	XM_047424496.1:c.-20+9373=	XM_047424496.1:c.-20+9384_-20+9394del	XM_047424496.1:c.-20+9386_-20+9394del	XM_047424496.1:c.-20+9387_-20+9394del	XM_047424496.1:c.-20+9388_-20+9394del	XM_047424496.1:c.-20+9389_-20+9394del	XM_047424496.1:c.-20+9390_-20+9394del	XM_047424496.1:c.-20+9391_-20+9394del	XM_047424496.1:c.-20+9392_-20+9394del	XM_047424496.1:c.-20+9393_-20+9394del	XM_047424496.1:c.-20+9394del	XM_047424496.1:c.-20+9394dup	XM_047424496.1:c.-20+9393_-20+9394dup	XM_047424496.1:c.-20+9392_-20+9394dup	XM_047424496.1:c.-20+9391_-20+9394dup	XM_047424496.1:c.-20+9390_-20+9394dup	XM_047424496.1:c.-20+9389_-20+9394dup	XM_047424496.1:c.-20+9388_-20+9394dup	XM_047424496.1:c.-20+9385_-20+9394dup	XM_047424496.1:c.-20+9384_-20+9394dup	XM_047424496.1:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424496.1:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X18	XM_047424499.1:c.-20+9373=	XM_047424499.1:c.-20+9384_-20+9394del	XM_047424499.1:c.-20+9386_-20+9394del	XM_047424499.1:c.-20+9387_-20+9394del	XM_047424499.1:c.-20+9388_-20+9394del	XM_047424499.1:c.-20+9389_-20+9394del	XM_047424499.1:c.-20+9390_-20+9394del	XM_047424499.1:c.-20+9391_-20+9394del	XM_047424499.1:c.-20+9392_-20+9394del	XM_047424499.1:c.-20+9393_-20+9394del	XM_047424499.1:c.-20+9394del	XM_047424499.1:c.-20+9394dup	XM_047424499.1:c.-20+9393_-20+9394dup	XM_047424499.1:c.-20+9392_-20+9394dup	XM_047424499.1:c.-20+9391_-20+9394dup	XM_047424499.1:c.-20+9390_-20+9394dup	XM_047424499.1:c.-20+9389_-20+9394dup	XM_047424499.1:c.-20+9388_-20+9394dup	XM_047424499.1:c.-20+9385_-20+9394dup	XM_047424499.1:c.-20+9384_-20+9394dup	XM_047424499.1:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424499.1:c.-20+9394_-20+9395insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X29	XM_047424501.1:c.-20+29828=	XM_047424501.1:c.-20+29839_-20+29849del	XM_047424501.1:c.-20+29841_-20+29849del	XM_047424501.1:c.-20+29842_-20+29849del	XM_047424501.1:c.-20+29843_-20+29849del	XM_047424501.1:c.-20+29844_-20+29849del	XM_047424501.1:c.-20+29845_-20+29849del	XM_047424501.1:c.-20+29846_-20+29849del	XM_047424501.1:c.-20+29847_-20+29849del	XM_047424501.1:c.-20+29848_-20+29849del	XM_047424501.1:c.-20+29849del	XM_047424501.1:c.-20+29849dup	XM_047424501.1:c.-20+29848_-20+29849dup	XM_047424501.1:c.-20+29847_-20+29849dup	XM_047424501.1:c.-20+29846_-20+29849dup	XM_047424501.1:c.-20+29845_-20+29849dup	XM_047424501.1:c.-20+29844_-20+29849dup	XM_047424501.1:c.-20+29843_-20+29849dup	XM_047424501.1:c.-20+29840_-20+29849dup	XM_047424501.1:c.-20+29839_-20+29849dup	XM_047424501.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424501.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X23	XM_047424506.1:c.89+29828=	XM_047424506.1:c.89+29839_89+29849del	XM_047424506.1:c.89+29841_89+29849del	XM_047424506.1:c.89+29842_89+29849del	XM_047424506.1:c.89+29843_89+29849del	XM_047424506.1:c.89+29844_89+29849del	XM_047424506.1:c.89+29845_89+29849del	XM_047424506.1:c.89+29846_89+29849del	XM_047424506.1:c.89+29847_89+29849del	XM_047424506.1:c.89+29848_89+29849del	XM_047424506.1:c.89+29849del	XM_047424506.1:c.89+29849dup	XM_047424506.1:c.89+29848_89+29849dup	XM_047424506.1:c.89+29847_89+29849dup	XM_047424506.1:c.89+29846_89+29849dup	XM_047424506.1:c.89+29845_89+29849dup	XM_047424506.1:c.89+29844_89+29849dup	XM_047424506.1:c.89+29843_89+29849dup	XM_047424506.1:c.89+29840_89+29849dup	XM_047424506.1:c.89+29839_89+29849dup	XM_047424506.1:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424506.1:c.89+29849_89+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CELF2 transcript variant X25	XM_047424508.1:c.-20+29828=	XM_047424508.1:c.-20+29839_-20+29849del	XM_047424508.1:c.-20+29841_-20+29849del	XM_047424508.1:c.-20+29842_-20+29849del	XM_047424508.1:c.-20+29843_-20+29849del	XM_047424508.1:c.-20+29844_-20+29849del	XM_047424508.1:c.-20+29845_-20+29849del	XM_047424508.1:c.-20+29846_-20+29849del	XM_047424508.1:c.-20+29847_-20+29849del	XM_047424508.1:c.-20+29848_-20+29849del	XM_047424508.1:c.-20+29849del	XM_047424508.1:c.-20+29849dup	XM_047424508.1:c.-20+29848_-20+29849dup	XM_047424508.1:c.-20+29847_-20+29849dup	XM_047424508.1:c.-20+29846_-20+29849dup	XM_047424508.1:c.-20+29845_-20+29849dup	XM_047424508.1:c.-20+29844_-20+29849dup	XM_047424508.1:c.-20+29843_-20+29849dup	XM_047424508.1:c.-20+29840_-20+29849dup	XM_047424508.1:c.-20+29839_-20+29849dup	XM_047424508.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047424508.1:c.-20+29849_-20+29850insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

56 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39732884	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95532909	Feb 05, 2009 (130)
3	PJP	ss294642103	May 09, 2011 (134)
4	PJP	ss294642104	May 09, 2011 (134)
5	1000GENOMES	ss1369113184	Aug 21, 2014 (142)
6	SWEGEN	ss3005937094	Nov 08, 2017 (151)
7	EVA_DECODE	ss3689281603	Jul 13, 2019 (153)
8	EVA_DECODE	ss3689281604	Jul 13, 2019 (153)
9	EVA_DECODE	ss3689281605	Jul 13, 2019 (153)
10	EVA_DECODE	ss3689281606	Jul 13, 2019 (153)
11	EVA_DECODE	ss3689281607	Jul 13, 2019 (153)
12	ACPOP	ss3737062068	Jul 13, 2019 (153)
13	ACPOP	ss3737062069	Jul 13, 2019 (153)
14	ACPOP	ss3737062070	Jul 13, 2019 (153)
15	ACPOP	ss3737062071	Jul 13, 2019 (153)
16	KHV_HUMAN_GENOMES	ss3813108556	Jul 13, 2019 (153)
17	GNOMAD	ss4212929146	Apr 27, 2021 (155)
18	GNOMAD	ss4212929147	Apr 27, 2021 (155)
19	GNOMAD	ss4212929148	Apr 27, 2021 (155)
20	GNOMAD	ss4212929149	Apr 27, 2021 (155)
21	GNOMAD	ss4212929150	Apr 27, 2021 (155)
22	GNOMAD	ss4212929151	Apr 27, 2021 (155)
23	GNOMAD	ss4212929152	Apr 27, 2021 (155)
24	GNOMAD	ss4212929153	Apr 27, 2021 (155)
25	GNOMAD	ss4212929154	Apr 27, 2021 (155)
26	GNOMAD	ss4212929155	Apr 27, 2021 (155)
27	GNOMAD	ss4212929156	Apr 27, 2021 (155)
28	GNOMAD	ss4212929157	Apr 27, 2021 (155)
29	GNOMAD	ss4212929158	Apr 27, 2021 (155)
30	GNOMAD	ss4212929159	Apr 27, 2021 (155)
31	GNOMAD	ss4212929160	Apr 27, 2021 (155)
32	GNOMAD	ss4212929161	Apr 27, 2021 (155)
33	GNOMAD	ss4212929162	Apr 27, 2021 (155)
34	GNOMAD	ss4212929163	Apr 27, 2021 (155)
35	GNOMAD	ss4212929164	Apr 27, 2021 (155)
36	GNOMAD	ss4212929165	Apr 27, 2021 (155)
37	TOPMED	ss4842447642	Apr 27, 2021 (155)
38	TOPMED	ss4842447643	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5196262030	Apr 27, 2021 (155)
40	TOMMO_GENOMICS	ss5196262031	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5196262032	Apr 27, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5282918974	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5282918975	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5282918976	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5282918977	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5282918978	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5478697003	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5478697004	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5478697005	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5478697006	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5741108752	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5741108753	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5741108755	Oct 16, 2022 (156)
54	EVA	ss5823976654	Oct 16, 2022 (156)
55	EVA	ss5823976655	Oct 16, 2022 (156)
56	EVA	ss5849437487	Oct 16, 2022 (156)
57	1000Genomes	NC_000010.10 - 10991790	Oct 12, 2018 (152)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343443791 (NC_000010.11:10949826::A 1582/75226) Row 343443792 (NC_000010.11:10949826::AA 325/75436) Row 343443793 (NC_000010.11:10949826::AAA 21/75468)...	-	Apr 27, 2021 (155)
78	Northern Sweden Submission ignored due to conflicting rows: Row 10346933 (NC_000010.10:10991789:A: 60/556) Row 10346934 (NC_000010.10:10991789:AA: 26/556) Row 10346935 (NC_000010.10:10991789::AAAA 12/556)...	-	Jul 13, 2019 (153)
79	Northern Sweden Submission ignored due to conflicting rows: Row 10346933 (NC_000010.10:10991789:A: 60/556) Row 10346934 (NC_000010.10:10991789:AA: 26/556) Row 10346935 (NC_000010.10:10991789::AAAA 12/556)...	-	Jul 13, 2019 (153)
80	Northern Sweden Submission ignored due to conflicting rows: Row 10346933 (NC_000010.10:10991789:A: 60/556) Row 10346934 (NC_000010.10:10991789:AA: 26/556) Row 10346935 (NC_000010.10:10991789::AAAA 12/556)...	-	Jul 13, 2019 (153)
81	Northern Sweden Submission ignored due to conflicting rows: Row 10346933 (NC_000010.10:10991789:A: 60/556) Row 10346934 (NC_000010.10:10991789:AA: 26/556) Row 10346935 (NC_000010.10:10991789::AAAA 12/556)...	-	Jul 13, 2019 (153)
82	8.3KJPN Submission ignored due to conflicting rows: Row 54231337 (NC_000010.10:10991789:A: 9867/16248) Row 54231338 (NC_000010.10:10991789:AA: 34/16248) Row 54231339 (NC_000010.10:10991789::A 9/16248)	-	Apr 27, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 54231337 (NC_000010.10:10991789:A: 9867/16248) Row 54231338 (NC_000010.10:10991789:AA: 34/16248) Row 54231339 (NC_000010.10:10991789::A 9/16248)	-	Apr 27, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 54231337 (NC_000010.10:10991789:A: 9867/16248) Row 54231338 (NC_000010.10:10991789:AA: 34/16248) Row 54231339 (NC_000010.10:10991789::A 9/16248)	-	Apr 27, 2021 (155)
85	14KJPN Submission ignored due to conflicting rows: Row 74945856 (NC_000010.11:10949826:A: 16712/27592) Row 74945857 (NC_000010.11:10949826:AA: 57/27592) Row 74945859 (NC_000010.11:10949826::A 20/27592)	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 74945856 (NC_000010.11:10949826:A: 16712/27592) Row 74945857 (NC_000010.11:10949826:AA: 57/27592) Row 74945859 (NC_000010.11:10949826::A 20/27592)	-	Oct 16, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 74945856 (NC_000010.11:10949826:A: 16712/27592) Row 74945857 (NC_000010.11:10949826:AA: 57/27592) Row 74945859 (NC_000010.11:10949826::A 20/27592)	-	Oct 16, 2022 (156)
88	TopMed Submission ignored due to conflicting rows: Row 57993297 (NC_000010.11:10949826:AAAAAAAA: 10/264690) Row 57993298 (NC_000010.11:10949826:AAAAAAAAAAA: 1/264690)	-	Apr 27, 2021 (155)
89	TopMed Submission ignored due to conflicting rows: Row 57993297 (NC_000010.11:10949826:AAAAAAAA: 10/264690) Row 57993298 (NC_000010.11:10949826:AAAAAAAAAAA: 1/264690)	-	Apr 27, 2021 (155)
90	ALFA	NC_000010.11 - 10949827	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs67010134	Feb 26, 2009 (130)
rs67010135	Feb 26, 2009 (130)
rs77232024	Oct 13, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4212929165, ss4842447643	NC_000010.11:10949826:AAAAAAAAAAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4212929164	NC_000010.11:10949826:AAAAAAAAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4212929163, ss4842447642	NC_000010.11:10949826:AAAAAAAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4212929162	NC_000010.11:10949826:AAAAAAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4212929161	NC_000010.11:10949826:AAAAAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4212929160	NC_000010.11:10949826:AAAAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3689281607, ss4212929159	NC_000010.11:10949826:AAAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5823976655	NC_000010.10:10991789:AAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
ss4212929158, ss5282918978	NC_000010.11:10949826:AAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3689281606	NC_000010.11:10949827:AAA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3005937094, ss3737062069, ss5196262031, ss5823976654	NC_000010.10:10991789:AA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4212929157, ss5282918975, ss5478697004, ss5741108753, ss5849437487	NC_000010.11:10949826:AA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3689281605	NC_000010.11:10949828:AA:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss294642103	NC_000010.9:11031795:A:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss294642104	NC_000010.9:11031816:A:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
48621082, ss1369113184, ss3737062068, ss5196262030	NC_000010.10:10991789:A:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3813108556, ss4212929156, ss5282918974, ss5478697005, ss5741108752	NC_000010.11:10949826:A:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3689281604	NC_000010.11:10949829:A:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss39732884, ss95532909	NT_008705.16:10931810:A:	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5196262032	NC_000010.10:10991789::A	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929146, ss5282918976, ss5478697003, ss5741108755	NC_000010.11:10949826::A	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3689281603	NC_000010.11:10949830::A	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929147, ss5282918977, ss5478697006	NC_000010.11:10949826::AA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929148	NC_000010.11:10949826::AAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3737062070	NC_000010.10:10991789::AAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929149	NC_000010.11:10949826::AAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929150	NC_000010.11:10949826::AAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929151	NC_000010.11:10949826::AAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9358541660	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929152	NC_000010.11:10949826::AAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929153	NC_000010.11:10949826::AAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929154	NC_000010.11:10949826::AAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212929155	NC_000010.11:10949826::AAAAAAAAAAA… NC_000010.11:10949826::AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3737062071	NC_000010.10:10991789::AAAAAAAAAAA… NC_000010.10:10991789::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:10949826:AAAAAAAAAAAA… NC_000010.11:10949826:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs35952853

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs35952853