Name: rs5803286
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.

rs5803286

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:45165807-45165830 (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(T)₁₇ / del(T)₁₅ / del(T)₁₄ / d…
del(T)₁₇ / del(T)₁₅ / del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₂ / dup(T)₁₄ / dup(T)₁₇ / dup(T)₁₈ / ins(T)₄₇
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₄=0.04113 (475/11548, ALFA)
del(T)₅=0.2680 (1342/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GTF2F2 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	11548	TTTTTTTTTTTTTTTTTTTTTTTT=0.91782	TTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00017, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.04113, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00433, TTTTTTTTTTTTTTTTTTTTTTTTT=0.02338, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00918, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00139, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00260	0.92418	0.003912	0.071908	11
European	Sub	10392	TTTTTTTTTTTTTTTTTTTTTTTT=0.90906	TTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00019, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.04561, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00481, TTTTTTTTTTTTTTTTTTTTTTTTT=0.02589, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.01001, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00154, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00289	0.915084	0.004381	0.080534	9
African	Sub	336	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	328	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	96	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	76	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	46	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	380	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	62	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	236	TTTTTTTTTTTTTTTTTTTTTTTT=0.983	TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.008, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	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
Allele Frequency Aggregator	Total	Global	11548	(T)₂₄=0.91782	del(T)₁₇=0.00000, del(T)₁₅=0.00000, del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00017, del(T)₁₀=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.04113, delTTT=0.00000, delTT=0.00000, delT=0.00433, dupT=0.02338, dupTT=0.00918, dupTTT=0.00139, dup(T)₄=0.00260
Allele Frequency Aggregator	European	Sub	10392	(T)₂₄=0.90906	del(T)₁₇=0.00000, del(T)₁₅=0.00000, del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00019, del(T)₁₀=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.04561, delTTT=0.00000, delTT=0.00000, delT=0.00481, dupT=0.02589, dupTT=0.01001, dupTTT=0.00154, dup(T)₄=0.00289
Allele Frequency Aggregator	Latin American 2	Sub	380	(T)₂₄=1.000	del(T)₁₇=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	African	Sub	336	(T)₂₄=1.000	del(T)₁₇=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	236	(T)₂₄=0.983	del(T)₁₇=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.004, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.004, dupTT=0.008, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Asian	Sub	96	(T)₂₄=1.00	del(T)₁₇=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	62	(T)₂₄=1.00	del(T)₁₇=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	46	(T)₂₄=1.00	del(T)₁₇=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
1000Genomes	Global	Study-wide	5008	(T)₂₄=0.7320	del(T)₅=0.2680
1000Genomes	African	Sub	1322	(T)₂₄=0.4985	del(T)₅=0.5015
1000Genomes	East Asian	Sub	1008	(T)₂₄=0.8740	del(T)₅=0.1260
1000Genomes	Europe	Sub	1006	(T)₂₄=0.7704	del(T)₅=0.2296
1000Genomes	South Asian	Sub	978	(T)₂₄=0.809	del(T)₅=0.191
1000Genomes	American	Sub	694	(T)₂₄=0.807	del(T)₅=0.193

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 13	NC_000013.11:g.45165814_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165816_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165817_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165818_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165819_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165820_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165821_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165823_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165824_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165825_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165826_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165827_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165828_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165829_45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165830del
GRCh38.p14 chr 13	NC_000013.11:g.45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165829_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165828_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165827_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165826_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165825_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165824_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165823_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165822_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165819_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165817_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165814_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165813_45165830dup
GRCh38.p14 chr 13	NC_000013.11:g.45165830_45165831insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 13	NC_000013.10:g.45739949_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739951_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739952_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739953_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739954_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739955_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739956_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739958_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739959_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739960_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739961_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739962_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739963_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739964_45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739965del
GRCh37.p13 chr 13	NC_000013.10:g.45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739964_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739963_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739962_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739961_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739960_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739959_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739958_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739957_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739954_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739952_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739949_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739948_45739965dup
GRCh37.p13 chr 13	NC_000013.10:g.45739965_45739966insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: GTF2F2, general transcription factor IIF subunit 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GTF2F2 transcript	NM_004128.3:c.304+13983_3… NM_004128.3:c.304+13983_304+13999del	N/A	Intron Variant
GTF2F2 transcript variant X1	XM_011535052.4:c.304+1398… XM_011535052.4:c.304+13983_304+13999del	N/A	Intron Variant
GTF2F2 transcript variant X3	XM_011535053.4:c.304+1398… XM_011535053.4:c.304+13983_304+13999del	N/A	Intron Variant
GTF2F2 transcript variant X2	XM_017020551.2:c.	N/A	Genic Upstream Transcript 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	(T)₂₄=	del(T)₁₇	del(T)₁₅	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₂	dup(T)₁₄	dup(T)₁₇	dup(T)₁₈	ins(T)₄₇
GRCh38.p14 chr 13	NC_000013.11:g.45165807_45165830=	NC_000013.11:g.45165814_45165830del	NC_000013.11:g.45165816_45165830del	NC_000013.11:g.45165817_45165830del	NC_000013.11:g.45165818_45165830del	NC_000013.11:g.45165819_45165830del	NC_000013.11:g.45165820_45165830del	NC_000013.11:g.45165821_45165830del	NC_000013.11:g.45165823_45165830del	NC_000013.11:g.45165824_45165830del	NC_000013.11:g.45165825_45165830del	NC_000013.11:g.45165826_45165830del	NC_000013.11:g.45165827_45165830del	NC_000013.11:g.45165828_45165830del	NC_000013.11:g.45165829_45165830del	NC_000013.11:g.45165830del	NC_000013.11:g.45165830dup	NC_000013.11:g.45165829_45165830dup	NC_000013.11:g.45165828_45165830dup	NC_000013.11:g.45165827_45165830dup	NC_000013.11:g.45165826_45165830dup	NC_000013.11:g.45165825_45165830dup	NC_000013.11:g.45165824_45165830dup	NC_000013.11:g.45165823_45165830dup	NC_000013.11:g.45165822_45165830dup	NC_000013.11:g.45165819_45165830dup	NC_000013.11:g.45165817_45165830dup	NC_000013.11:g.45165814_45165830dup	NC_000013.11:g.45165813_45165830dup	NC_000013.11:g.45165830_45165831insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 13	NC_000013.10:g.45739942_45739965=	NC_000013.10:g.45739949_45739965del	NC_000013.10:g.45739951_45739965del	NC_000013.10:g.45739952_45739965del	NC_000013.10:g.45739953_45739965del	NC_000013.10:g.45739954_45739965del	NC_000013.10:g.45739955_45739965del	NC_000013.10:g.45739956_45739965del	NC_000013.10:g.45739958_45739965del	NC_000013.10:g.45739959_45739965del	NC_000013.10:g.45739960_45739965del	NC_000013.10:g.45739961_45739965del	NC_000013.10:g.45739962_45739965del	NC_000013.10:g.45739963_45739965del	NC_000013.10:g.45739964_45739965del	NC_000013.10:g.45739965del	NC_000013.10:g.45739965dup	NC_000013.10:g.45739964_45739965dup	NC_000013.10:g.45739963_45739965dup	NC_000013.10:g.45739962_45739965dup	NC_000013.10:g.45739961_45739965dup	NC_000013.10:g.45739960_45739965dup	NC_000013.10:g.45739959_45739965dup	NC_000013.10:g.45739958_45739965dup	NC_000013.10:g.45739957_45739965dup	NC_000013.10:g.45739954_45739965dup	NC_000013.10:g.45739952_45739965dup	NC_000013.10:g.45739949_45739965dup	NC_000013.10:g.45739948_45739965dup	NC_000013.10:g.45739965_45739966insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GTF2F2 transcript	NM_004128.2:c.304+13976=	NM_004128.2:c.304+13983_304+13999del	NM_004128.2:c.304+13985_304+13999del	NM_004128.2:c.304+13986_304+13999del	NM_004128.2:c.304+13987_304+13999del	NM_004128.2:c.304+13988_304+13999del	NM_004128.2:c.304+13989_304+13999del	NM_004128.2:c.304+13990_304+13999del	NM_004128.2:c.304+13992_304+13999del	NM_004128.2:c.304+13993_304+13999del	NM_004128.2:c.304+13994_304+13999del	NM_004128.2:c.304+13995_304+13999del	NM_004128.2:c.304+13996_304+13999del	NM_004128.2:c.304+13997_304+13999del	NM_004128.2:c.304+13998_304+13999del	NM_004128.2:c.304+13999del	NM_004128.2:c.304+13999dup	NM_004128.2:c.304+13998_304+13999dup	NM_004128.2:c.304+13997_304+13999dup	NM_004128.2:c.304+13996_304+13999dup	NM_004128.2:c.304+13995_304+13999dup	NM_004128.2:c.304+13994_304+13999dup	NM_004128.2:c.304+13993_304+13999dup	NM_004128.2:c.304+13992_304+13999dup	NM_004128.2:c.304+13991_304+13999dup	NM_004128.2:c.304+13988_304+13999dup	NM_004128.2:c.304+13986_304+13999dup	NM_004128.2:c.304+13983_304+13999dup	NM_004128.2:c.304+13982_304+13999dup	NM_004128.2:c.304+13999_304+14000insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GTF2F2 transcript	NM_004128.3:c.304+13976=	NM_004128.3:c.304+13983_304+13999del	NM_004128.3:c.304+13985_304+13999del	NM_004128.3:c.304+13986_304+13999del	NM_004128.3:c.304+13987_304+13999del	NM_004128.3:c.304+13988_304+13999del	NM_004128.3:c.304+13989_304+13999del	NM_004128.3:c.304+13990_304+13999del	NM_004128.3:c.304+13992_304+13999del	NM_004128.3:c.304+13993_304+13999del	NM_004128.3:c.304+13994_304+13999del	NM_004128.3:c.304+13995_304+13999del	NM_004128.3:c.304+13996_304+13999del	NM_004128.3:c.304+13997_304+13999del	NM_004128.3:c.304+13998_304+13999del	NM_004128.3:c.304+13999del	NM_004128.3:c.304+13999dup	NM_004128.3:c.304+13998_304+13999dup	NM_004128.3:c.304+13997_304+13999dup	NM_004128.3:c.304+13996_304+13999dup	NM_004128.3:c.304+13995_304+13999dup	NM_004128.3:c.304+13994_304+13999dup	NM_004128.3:c.304+13993_304+13999dup	NM_004128.3:c.304+13992_304+13999dup	NM_004128.3:c.304+13991_304+13999dup	NM_004128.3:c.304+13988_304+13999dup	NM_004128.3:c.304+13986_304+13999dup	NM_004128.3:c.304+13983_304+13999dup	NM_004128.3:c.304+13982_304+13999dup	NM_004128.3:c.304+13999_304+14000insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GTF2F2 transcript variant X1	XM_011535052.4:c.304+13976=	XM_011535052.4:c.304+13983_304+13999del	XM_011535052.4:c.304+13985_304+13999del	XM_011535052.4:c.304+13986_304+13999del	XM_011535052.4:c.304+13987_304+13999del	XM_011535052.4:c.304+13988_304+13999del	XM_011535052.4:c.304+13989_304+13999del	XM_011535052.4:c.304+13990_304+13999del	XM_011535052.4:c.304+13992_304+13999del	XM_011535052.4:c.304+13993_304+13999del	XM_011535052.4:c.304+13994_304+13999del	XM_011535052.4:c.304+13995_304+13999del	XM_011535052.4:c.304+13996_304+13999del	XM_011535052.4:c.304+13997_304+13999del	XM_011535052.4:c.304+13998_304+13999del	XM_011535052.4:c.304+13999del	XM_011535052.4:c.304+13999dup	XM_011535052.4:c.304+13998_304+13999dup	XM_011535052.4:c.304+13997_304+13999dup	XM_011535052.4:c.304+13996_304+13999dup	XM_011535052.4:c.304+13995_304+13999dup	XM_011535052.4:c.304+13994_304+13999dup	XM_011535052.4:c.304+13993_304+13999dup	XM_011535052.4:c.304+13992_304+13999dup	XM_011535052.4:c.304+13991_304+13999dup	XM_011535052.4:c.304+13988_304+13999dup	XM_011535052.4:c.304+13986_304+13999dup	XM_011535052.4:c.304+13983_304+13999dup	XM_011535052.4:c.304+13982_304+13999dup	XM_011535052.4:c.304+13999_304+14000insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GTF2F2 transcript variant X3	XM_011535053.4:c.304+13976=	XM_011535053.4:c.304+13983_304+13999del	XM_011535053.4:c.304+13985_304+13999del	XM_011535053.4:c.304+13986_304+13999del	XM_011535053.4:c.304+13987_304+13999del	XM_011535053.4:c.304+13988_304+13999del	XM_011535053.4:c.304+13989_304+13999del	XM_011535053.4:c.304+13990_304+13999del	XM_011535053.4:c.304+13992_304+13999del	XM_011535053.4:c.304+13993_304+13999del	XM_011535053.4:c.304+13994_304+13999del	XM_011535053.4:c.304+13995_304+13999del	XM_011535053.4:c.304+13996_304+13999del	XM_011535053.4:c.304+13997_304+13999del	XM_011535053.4:c.304+13998_304+13999del	XM_011535053.4:c.304+13999del	XM_011535053.4:c.304+13999dup	XM_011535053.4:c.304+13998_304+13999dup	XM_011535053.4:c.304+13997_304+13999dup	XM_011535053.4:c.304+13996_304+13999dup	XM_011535053.4:c.304+13995_304+13999dup	XM_011535053.4:c.304+13994_304+13999dup	XM_011535053.4:c.304+13993_304+13999dup	XM_011535053.4:c.304+13992_304+13999dup	XM_011535053.4:c.304+13991_304+13999dup	XM_011535053.4:c.304+13988_304+13999dup	XM_011535053.4:c.304+13986_304+13999dup	XM_011535053.4:c.304+13983_304+13999dup	XM_011535053.4:c.304+13982_304+13999dup	XM_011535053.4:c.304+13999_304+14000insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

74 SubSNP, 49 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83190564	Dec 15, 2007 (137)
2	BCMHGSC_JDW	ss103545874	Mar 15, 2016 (147)
3	BCMHGSC_JDW	ss103545876	Mar 15, 2016 (147)
4	1000GENOMES	ss1373114406	Aug 21, 2014 (142)
5	SWEGEN	ss3010962761	Nov 08, 2017 (151)
6	EVA_DECODE	ss3695220862	Jul 13, 2019 (153)
7	EVA_DECODE	ss3695220863	Jul 13, 2019 (153)
8	EVA_DECODE	ss3695220864	Jul 13, 2019 (153)
9	EVA_DECODE	ss3695220865	Jul 13, 2019 (153)
10	EVA_DECODE	ss3695220866	Jul 13, 2019 (153)
11	EVA_DECODE	ss3695220867	Jul 13, 2019 (153)
12	KHV_HUMAN_GENOMES	ss3816751797	Jul 13, 2019 (153)
13	EVA	ss3833528740	Apr 27, 2020 (154)
14	KOGIC	ss3973494409	Apr 27, 2020 (154)
15	KOGIC	ss3973494410	Apr 27, 2020 (154)
16	KOGIC	ss3973494411	Apr 27, 2020 (154)
17	KOGIC	ss3973494412	Apr 27, 2020 (154)
18	KOGIC	ss3973494413	Apr 27, 2020 (154)
19	KOGIC	ss3973494414	Apr 27, 2020 (154)
20	GNOMAD	ss4265239192	Apr 26, 2021 (155)
21	GNOMAD	ss4265239193	Apr 26, 2021 (155)
22	GNOMAD	ss4265239194	Apr 26, 2021 (155)
23	GNOMAD	ss4265239195	Apr 26, 2021 (155)
24	GNOMAD	ss4265239196	Apr 26, 2021 (155)
25	GNOMAD	ss4265239197	Apr 26, 2021 (155)
26	GNOMAD	ss4265239198	Apr 26, 2021 (155)
27	GNOMAD	ss4265239199	Apr 26, 2021 (155)
28	GNOMAD	ss4265239200	Apr 26, 2021 (155)
29	GNOMAD	ss4265239201	Apr 26, 2021 (155)
30	GNOMAD	ss4265239202	Apr 26, 2021 (155)
31	GNOMAD	ss4265239203	Apr 26, 2021 (155)
32	GNOMAD	ss4265239204	Apr 26, 2021 (155)
33	GNOMAD	ss4265239205	Apr 26, 2021 (155)
34	GNOMAD	ss4265239206	Apr 26, 2021 (155)
35	GNOMAD	ss4265239207	Apr 26, 2021 (155)
36	GNOMAD	ss4265239208	Apr 26, 2021 (155)
37	GNOMAD	ss4265239209	Apr 26, 2021 (155)
38	GNOMAD	ss4265239210	Apr 26, 2021 (155)
39	GNOMAD	ss4265239211	Apr 26, 2021 (155)
40	GNOMAD	ss4265239212	Apr 26, 2021 (155)
41	GNOMAD	ss4265239213	Apr 26, 2021 (155)
42	GNOMAD	ss4265239214	Apr 26, 2021 (155)
43	GNOMAD	ss4265239215	Apr 26, 2021 (155)
44	GNOMAD	ss4265239216	Apr 26, 2021 (155)
45	GNOMAD	ss4265239217	Apr 26, 2021 (155)
46	GNOMAD	ss4265239218	Apr 26, 2021 (155)
47	TOPMED	ss4945057360	Apr 26, 2021 (155)
48	TOPMED	ss4945057361	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5209836788	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5209836789	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5209836790	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5209836791	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5209836792	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5209836793	Apr 26, 2021 (155)
55	1000G_HIGH_COVERAGE	ss5293611852	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5293611853	Oct 16, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5293611854	Oct 16, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5293611855	Oct 16, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5293611856	Oct 16, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5293611857	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5487987625	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5487987626	Oct 16, 2022 (156)
63	HUGCELL_USP	ss5487987627	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5487987628	Oct 16, 2022 (156)
65	HUGCELL_USP	ss5487987629	Oct 16, 2022 (156)
66	HUGCELL_USP	ss5487987630	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5761665828	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5761665829	Oct 16, 2022 (156)
69	TOMMO_GENOMICS	ss5761665830	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5761665831	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5761665832	Oct 16, 2022 (156)
72	TOMMO_GENOMICS	ss5761665833	Oct 16, 2022 (156)
73	EVA	ss5839426924	Oct 16, 2022 (156)
74	EVA	ss5839426925	Oct 16, 2022 (156)
75	1000Genomes	NC_000013.10 - 45739942	Oct 12, 2018 (152)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429709229 (NC_000013.11:45165806::T 4840/82248) Row 429709230 (NC_000013.11:45165806::TT 1802/82208) Row 429709231 (NC_000013.11:45165806::TTT 306/82294)...	-	Apr 26, 2021 (155)
103	Korean Genome Project Submission ignored due to conflicting rows: Row 29872410 (NC_000013.11:45165811:T: 209/1828) Row 29872411 (NC_000013.11:45165812::T 197/1828) Row 29872412 (NC_000013.11:45165806:TTTTTT: 5/1828)...	-	Apr 27, 2020 (154)
104	Korean Genome Project Submission ignored due to conflicting rows: Row 29872410 (NC_000013.11:45165811:T: 209/1828) Row 29872411 (NC_000013.11:45165812::T 197/1828) Row 29872412 (NC_000013.11:45165806:TTTTTT: 5/1828)...	-	Apr 27, 2020 (154)
105	Korean Genome Project Submission ignored due to conflicting rows: Row 29872410 (NC_000013.11:45165811:T: 209/1828) Row 29872411 (NC_000013.11:45165812::T 197/1828) Row 29872412 (NC_000013.11:45165806:TTTTTT: 5/1828)...	-	Apr 27, 2020 (154)
106	Korean Genome Project Submission ignored due to conflicting rows: Row 29872410 (NC_000013.11:45165811:T: 209/1828) Row 29872411 (NC_000013.11:45165812::T 197/1828) Row 29872412 (NC_000013.11:45165806:TTTTTT: 5/1828)...	-	Apr 27, 2020 (154)
107	Korean Genome Project Submission ignored due to conflicting rows: Row 29872410 (NC_000013.11:45165811:T: 209/1828) Row 29872411 (NC_000013.11:45165812::T 197/1828) Row 29872412 (NC_000013.11:45165806:TTTTTT: 5/1828)...	-	Apr 27, 2020 (154)
108	Korean Genome Project Submission ignored due to conflicting rows: Row 29872410 (NC_000013.11:45165811:T: 209/1828) Row 29872411 (NC_000013.11:45165812::T 197/1828) Row 29872412 (NC_000013.11:45165806:TTTTTT: 5/1828)...	-	Apr 27, 2020 (154)
109	8.3KJPN Submission ignored due to conflicting rows: Row 67806095 (NC_000013.10:45739941:TTTTT: 385/16686) Row 67806096 (NC_000013.10:45739941::T 213/16686) Row 67806097 (NC_000013.10:45739941:TTTTTTT: 7/16686)...	-	Apr 26, 2021 (155)
110	8.3KJPN Submission ignored due to conflicting rows: Row 67806095 (NC_000013.10:45739941:TTTTT: 385/16686) Row 67806096 (NC_000013.10:45739941::T 213/16686) Row 67806097 (NC_000013.10:45739941:TTTTTTT: 7/16686)...	-	Apr 26, 2021 (155)
111	8.3KJPN Submission ignored due to conflicting rows: Row 67806095 (NC_000013.10:45739941:TTTTT: 385/16686) Row 67806096 (NC_000013.10:45739941::T 213/16686) Row 67806097 (NC_000013.10:45739941:TTTTTTT: 7/16686)...	-	Apr 26, 2021 (155)
112	8.3KJPN Submission ignored due to conflicting rows: Row 67806095 (NC_000013.10:45739941:TTTTT: 385/16686) Row 67806096 (NC_000013.10:45739941::T 213/16686) Row 67806097 (NC_000013.10:45739941:TTTTTTT: 7/16686)...	-	Apr 26, 2021 (155)
113	8.3KJPN Submission ignored due to conflicting rows: Row 67806095 (NC_000013.10:45739941:TTTTT: 385/16686) Row 67806096 (NC_000013.10:45739941::T 213/16686) Row 67806097 (NC_000013.10:45739941:TTTTTTT: 7/16686)...	-	Apr 26, 2021 (155)
114	8.3KJPN Submission ignored due to conflicting rows: Row 67806095 (NC_000013.10:45739941:TTTTT: 385/16686) Row 67806096 (NC_000013.10:45739941::T 213/16686) Row 67806097 (NC_000013.10:45739941:TTTTTTT: 7/16686)...	-	Apr 26, 2021 (155)
115	14KJPN Submission ignored due to conflicting rows: Row 95502932 (NC_000013.11:45165806:TTTTT: 757/28152) Row 95502933 (NC_000013.11:45165806:TTTTTTT: 13/28152) Row 95502934 (NC_000013.11:45165806::T 251/28152)...	-	Oct 16, 2022 (156)
116	14KJPN Submission ignored due to conflicting rows: Row 95502932 (NC_000013.11:45165806:TTTTT: 757/28152) Row 95502933 (NC_000013.11:45165806:TTTTTTT: 13/28152) Row 95502934 (NC_000013.11:45165806::T 251/28152)...	-	Oct 16, 2022 (156)
117	14KJPN Submission ignored due to conflicting rows: Row 95502932 (NC_000013.11:45165806:TTTTT: 757/28152) Row 95502933 (NC_000013.11:45165806:TTTTTTT: 13/28152) Row 95502934 (NC_000013.11:45165806::T 251/28152)...	-	Oct 16, 2022 (156)
118	14KJPN Submission ignored due to conflicting rows: Row 95502932 (NC_000013.11:45165806:TTTTT: 757/28152) Row 95502933 (NC_000013.11:45165806:TTTTTTT: 13/28152) Row 95502934 (NC_000013.11:45165806::T 251/28152)...	-	Oct 16, 2022 (156)
119	14KJPN Submission ignored due to conflicting rows: Row 95502932 (NC_000013.11:45165806:TTTTT: 757/28152) Row 95502933 (NC_000013.11:45165806:TTTTTTT: 13/28152) Row 95502934 (NC_000013.11:45165806::T 251/28152)...	-	Oct 16, 2022 (156)
120	14KJPN Submission ignored due to conflicting rows: Row 95502932 (NC_000013.11:45165806:TTTTT: 757/28152) Row 95502933 (NC_000013.11:45165806:TTTTTTT: 13/28152) Row 95502934 (NC_000013.11:45165806::T 251/28152)...	-	Oct 16, 2022 (156)
121	TopMed Submission ignored due to conflicting rows: Row 160603018 (NC_000013.11:45165806:TTTTTTTTTTTTTTT: 3/264690) Row 160603019 (NC_000013.11:45165806:TTTTTTTTTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
122	TopMed Submission ignored due to conflicting rows: Row 160603018 (NC_000013.11:45165806:TTTTTTTTTTTTTTT: 3/264690) Row 160603019 (NC_000013.11:45165806:TTTTTTTTTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
123	ALFA	NC_000013.11 - 45165807	Apr 26, 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)
rs35574661	May 23, 2006 (127)
rs59341566	May 11, 2012 (137)
rs77650506	Apr 25, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4945057361	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTT	(self)
ss4945057360	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4265239218	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4265239217	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4265239216	NC_000013.11:45165806:TTTTTTTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3695220862, ss4265239215	NC_000013.11:45165806:TTTTTTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4265239214	NC_000013.11:45165806:TTTTTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4265239213	NC_000013.11:45165806:TTTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5209836790	NC_000013.10:45739941:TTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4265239212, ss5761665829	NC_000013.11:45165806:TTTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3973494411, ss4265239211	NC_000013.11:45165806:TTTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
60949906, ss1373114406, ss5209836788, ss5839426925	NC_000013.10:45739941:TTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3816751797, ss4265239210, ss5293611856, ss5487987625, ss5761665828	NC_000013.11:45165806:TTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3973494412	NC_000013.11:45165807:TTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3695220863	NC_000013.11:45165812:TTTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3010962761, ss3833528740, ss5209836792, ss5839426924	NC_000013.10:45739941:TTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4265239209, ss5293611857, ss5487987627, ss5761665833	NC_000013.11:45165806:TTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3973494413	NC_000013.11:45165808:TTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3695220864	NC_000013.11:45165813:TTTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5209836793	NC_000013.10:45739941:TTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239208, ss5293611853, ss5487987630, ss5761665832	NC_000013.11:45165806:TTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3973494414	NC_000013.11:45165809:TTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3695220865	NC_000013.11:45165814:TTT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239207, ss5293611854, ss5487987629	NC_000013.11:45165806:TT:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss83190564	NC_000013.9:44637964:T:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5209836791	NC_000013.10:45739941:T:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239206, ss5293611855, ss5487987628, ss5761665831	NC_000013.11:45165806:T:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3973494409	NC_000013.11:45165811:T:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3695220866	NC_000013.11:45165816:T:	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5209836789	NC_000013.10:45739941::T	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239192, ss5293611852, ss5487987626, ss5761665830	NC_000013.11:45165806::T	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3973494410	NC_000013.11:45165812::T	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3695220867	NC_000013.11:45165817::T	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239193	NC_000013.11:45165806::TT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239194	NC_000013.11:45165806::TTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239195	NC_000013.11:45165806::TTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7297661963	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss103545876	NT_024524.14:26719965:G:TTTTG	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239196	NC_000013.11:45165806::TTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239197	NC_000013.11:45165806::TTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss103545874	NT_024524.14:26719965:G:TTTTTTG	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239198	NC_000013.11:45165806::TTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239199	NC_000013.11:45165806::TTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239200	NC_000013.11:45165806::TTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239201	NC_000013.11:45165806::TTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239202	NC_000013.11:45165806::TTTTTTTTTTT… NC_000013.11:45165806::TTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239203	NC_000013.11:45165806::TTTTTTTTTTT… NC_000013.11:45165806::TTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239204	NC_000013.11:45165806::TTTTTTTTTTT… NC_000013.11:45165806::TTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4265239205	NC_000013.11:45165806::TTTTTTTTTTT… NC_000013.11:45165806::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:45165806:TTTTTTTTTTTT… NC_000013.11:45165806:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs5803286

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

rs5803286