Name: rs3058398
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.

rs3058398

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:35111236-35111257 (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)₁₂ / del(A)₁₁ / del(A)₁₀ / d…
del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₇ / dup(A)₈ / dup(A)₁₀ / dup(A)₁₂ / dup(A)₁₃ / dup(A)₁₄ / dup(A)₂₁ / ins(A)₂₅ / ins(A)₂₇
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.2993 (1499/5008, 1000G)
del(A)₁₂=0.000 (0/864, ALFA)
del(A)₁₁=0.000 (0/864, ALFA) (+ 11 more)
del(A)₁₀=0.000 (0/864, ALFA)
del(A)₉=0.000 (0/864, ALFA)
del(A)₈=0.000 (0/864, ALFA)
del(A)₇=0.000 (0/864, ALFA)
del(A)₅=0.000 (0/864, ALFA)
delAAA=0.000 (0/864, ALFA)
delAA=0.000 (0/864, ALFA)
delA=0.000 (0/864, ALFA)
dupA=0.000 (0/864, ALFA)
dupAA=0.000 (0/864, ALFA)
dup(A)₄=0.000 (0/864, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PPP2R3C : Intron Variant
LOC101927178 : 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	864	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	538	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	272	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	16	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	256	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	2	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	12	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	30	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	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
1000Genomes	Global	Study-wide	5008	(A)₂₂=0.7007	delAA=0.2993
1000Genomes	African	Sub	1322	(A)₂₂=0.7216	delAA=0.2784
1000Genomes	East Asian	Sub	1008	(A)₂₂=0.6369	delAA=0.3631
1000Genomes	Europe	Sub	1006	(A)₂₂=0.7594	delAA=0.2406
1000Genomes	South Asian	Sub	978	(A)₂₂=0.649	delAA=0.351
1000Genomes	American	Sub	694	(A)₂₂=0.741	delAA=0.259
Allele Frequency Aggregator	Total	Global	864	(A)₂₂=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	European	Sub	538	(A)₂₂=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	African	Sub	272	(A)₂₂=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	30	(A)₂₂=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	12	(A)₂₂=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	6	(A)₂₂=1.0	del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₅=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)₄=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(A)₂₂=1.0	del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₅=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)₄=0.0
Allele Frequency Aggregator	Latin American 1	Sub	2	(A)₂₂=1.0	del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₅=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)₄=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 14	NC_000014.9:g.35111246_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111247_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111248_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111249_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111250_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111251_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111253_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111254_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111255_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111256_35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111257del
GRCh38.p14 chr 14	NC_000014.9:g.35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111256_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111255_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111254_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111253_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111251_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111250_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111248_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111246_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111245_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111244_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111237_35111257dup
GRCh38.p14 chr 14	NC_000014.9:g.35111257_35111258insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 14	NC_000014.9:g.35111257_35111258insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 14	NC_000014.8:g.35580452_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580453_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580454_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580455_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580456_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580457_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580459_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580460_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580461_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580462_35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580463del
GRCh37.p13 chr 14	NC_000014.8:g.35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580462_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580461_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580460_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580459_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580457_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580456_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580454_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580452_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580451_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580450_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580443_35580463dup
GRCh37.p13 chr 14	NC_000014.8:g.35580463_35580464insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 14	NC_000014.8:g.35580463_35580464insAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: PPP2R3C, protein phosphatase 2 regulatory subunit B''gamma (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PPP2R3C transcript variant 2	NM_001305155.2:c.-144-618… NM_001305155.2:c.-144-618_-144-607del	N/A	Intron Variant
PPP2R3C transcript variant 3	NM_001305156.2:c.-144-618… NM_001305156.2:c.-144-618_-144-607del	N/A	Intron Variant
PPP2R3C transcript variant 1	NM_017917.4:c.187-618_187… NM_017917.4:c.187-618_187-607del	N/A	Intron Variant
PPP2R3C transcript variant 4	NR_130972.2:n.	N/A	Intron Variant
PPP2R3C transcript variant X1	XM_005267782.5:c.187-618_… XM_005267782.5:c.187-618_187-607del	N/A	Intron Variant
PPP2R3C transcript variant X2	XM_024449638.2:c.94-618_9… XM_024449638.2:c.94-618_94-607del	N/A	Intron Variant
PPP2R3C transcript variant X3	XM_024449639.2:c.31-618_3… XM_024449639.2:c.31-618_31-607del	N/A	Intron Variant
PPP2R3C transcript variant X4	XM_047431517.1:c.187-618_… XM_047431517.1:c.187-618_187-607del	N/A	Intron Variant

Gene: LOC101927178, uncharacterized LOC101927178 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC101927178 transcript	NR_110415.1: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)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₇	dup(A)₈	dup(A)₁₀	dup(A)₁₂	dup(A)₁₃	dup(A)₁₄	dup(A)₂₁	ins(A)₂₅	ins(A)₂₇
GRCh38.p14 chr 14	NC_000014.9:g.35111236_35111257=	NC_000014.9:g.35111246_35111257del	NC_000014.9:g.35111247_35111257del	NC_000014.9:g.35111248_35111257del	NC_000014.9:g.35111249_35111257del	NC_000014.9:g.35111250_35111257del	NC_000014.9:g.35111251_35111257del	NC_000014.9:g.35111253_35111257del	NC_000014.9:g.35111254_35111257del	NC_000014.9:g.35111255_35111257del	NC_000014.9:g.35111256_35111257del	NC_000014.9:g.35111257del	NC_000014.9:g.35111257dup	NC_000014.9:g.35111256_35111257dup	NC_000014.9:g.35111255_35111257dup	NC_000014.9:g.35111254_35111257dup	NC_000014.9:g.35111253_35111257dup	NC_000014.9:g.35111251_35111257dup	NC_000014.9:g.35111250_35111257dup	NC_000014.9:g.35111248_35111257dup	NC_000014.9:g.35111246_35111257dup	NC_000014.9:g.35111245_35111257dup	NC_000014.9:g.35111244_35111257dup	NC_000014.9:g.35111237_35111257dup	NC_000014.9:g.35111257_35111258insAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:g.35111257_35111258insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 14	NC_000014.8:g.35580442_35580463=	NC_000014.8:g.35580452_35580463del	NC_000014.8:g.35580453_35580463del	NC_000014.8:g.35580454_35580463del	NC_000014.8:g.35580455_35580463del	NC_000014.8:g.35580456_35580463del	NC_000014.8:g.35580457_35580463del	NC_000014.8:g.35580459_35580463del	NC_000014.8:g.35580460_35580463del	NC_000014.8:g.35580461_35580463del	NC_000014.8:g.35580462_35580463del	NC_000014.8:g.35580463del	NC_000014.8:g.35580463dup	NC_000014.8:g.35580462_35580463dup	NC_000014.8:g.35580461_35580463dup	NC_000014.8:g.35580460_35580463dup	NC_000014.8:g.35580459_35580463dup	NC_000014.8:g.35580457_35580463dup	NC_000014.8:g.35580456_35580463dup	NC_000014.8:g.35580454_35580463dup	NC_000014.8:g.35580452_35580463dup	NC_000014.8:g.35580451_35580463dup	NC_000014.8:g.35580450_35580463dup	NC_000014.8:g.35580443_35580463dup	NC_000014.8:g.35580463_35580464insAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000014.8:g.35580463_35580464insAAAAAAAAAAAAAAAAAAAAAAAAAAA
PPP2R3C transcript variant 2	NM_001305155.2:c.-144-607=	NM_001305155.2:c.-144-618_-144-607del	NM_001305155.2:c.-144-617_-144-607del	NM_001305155.2:c.-144-616_-144-607del	NM_001305155.2:c.-144-615_-144-607del	NM_001305155.2:c.-144-614_-144-607del	NM_001305155.2:c.-144-613_-144-607del	NM_001305155.2:c.-144-611_-144-607del	NM_001305155.2:c.-144-610_-144-607del	NM_001305155.2:c.-144-609_-144-607del	NM_001305155.2:c.-144-608_-144-607del	NM_001305155.2:c.-144-607del	NM_001305155.2:c.-144-607dup	NM_001305155.2:c.-144-608_-144-607dup	NM_001305155.2:c.-144-609_-144-607dup	NM_001305155.2:c.-144-610_-144-607dup	NM_001305155.2:c.-144-611_-144-607dup	NM_001305155.2:c.-144-613_-144-607dup	NM_001305155.2:c.-144-614_-144-607dup	NM_001305155.2:c.-144-616_-144-607dup	NM_001305155.2:c.-144-618_-144-607dup	NM_001305155.2:c.-144-619_-144-607dup	NM_001305155.2:c.-144-620_-144-607dup	NM_001305155.2:c.-144-627_-144-607dup	NM_001305155.2:c.-144-607_-144-606insTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001305155.2:c.-144-607_-144-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant 3	NM_001305156.2:c.-144-607=	NM_001305156.2:c.-144-618_-144-607del	NM_001305156.2:c.-144-617_-144-607del	NM_001305156.2:c.-144-616_-144-607del	NM_001305156.2:c.-144-615_-144-607del	NM_001305156.2:c.-144-614_-144-607del	NM_001305156.2:c.-144-613_-144-607del	NM_001305156.2:c.-144-611_-144-607del	NM_001305156.2:c.-144-610_-144-607del	NM_001305156.2:c.-144-609_-144-607del	NM_001305156.2:c.-144-608_-144-607del	NM_001305156.2:c.-144-607del	NM_001305156.2:c.-144-607dup	NM_001305156.2:c.-144-608_-144-607dup	NM_001305156.2:c.-144-609_-144-607dup	NM_001305156.2:c.-144-610_-144-607dup	NM_001305156.2:c.-144-611_-144-607dup	NM_001305156.2:c.-144-613_-144-607dup	NM_001305156.2:c.-144-614_-144-607dup	NM_001305156.2:c.-144-616_-144-607dup	NM_001305156.2:c.-144-618_-144-607dup	NM_001305156.2:c.-144-619_-144-607dup	NM_001305156.2:c.-144-620_-144-607dup	NM_001305156.2:c.-144-627_-144-607dup	NM_001305156.2:c.-144-607_-144-606insTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001305156.2:c.-144-607_-144-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript	NM_017917.2:c.187-607=	NM_017917.2:c.187-618_187-607del	NM_017917.2:c.187-617_187-607del	NM_017917.2:c.187-616_187-607del	NM_017917.2:c.187-615_187-607del	NM_017917.2:c.187-614_187-607del	NM_017917.2:c.187-613_187-607del	NM_017917.2:c.187-611_187-607del	NM_017917.2:c.187-610_187-607del	NM_017917.2:c.187-609_187-607del	NM_017917.2:c.187-608_187-607del	NM_017917.2:c.187-607del	NM_017917.2:c.187-607dup	NM_017917.2:c.187-608_187-607dup	NM_017917.2:c.187-609_187-607dup	NM_017917.2:c.187-610_187-607dup	NM_017917.2:c.187-611_187-607dup	NM_017917.2:c.187-613_187-607dup	NM_017917.2:c.187-614_187-607dup	NM_017917.2:c.187-616_187-607dup	NM_017917.2:c.187-618_187-607dup	NM_017917.2:c.187-619_187-607dup	NM_017917.2:c.187-620_187-607dup	NM_017917.2:c.187-627_187-607dup	NM_017917.2:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTT	NM_017917.2:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant 1	NM_017917.4:c.187-607=	NM_017917.4:c.187-618_187-607del	NM_017917.4:c.187-617_187-607del	NM_017917.4:c.187-616_187-607del	NM_017917.4:c.187-615_187-607del	NM_017917.4:c.187-614_187-607del	NM_017917.4:c.187-613_187-607del	NM_017917.4:c.187-611_187-607del	NM_017917.4:c.187-610_187-607del	NM_017917.4:c.187-609_187-607del	NM_017917.4:c.187-608_187-607del	NM_017917.4:c.187-607del	NM_017917.4:c.187-607dup	NM_017917.4:c.187-608_187-607dup	NM_017917.4:c.187-609_187-607dup	NM_017917.4:c.187-610_187-607dup	NM_017917.4:c.187-611_187-607dup	NM_017917.4:c.187-613_187-607dup	NM_017917.4:c.187-614_187-607dup	NM_017917.4:c.187-616_187-607dup	NM_017917.4:c.187-618_187-607dup	NM_017917.4:c.187-619_187-607dup	NM_017917.4:c.187-620_187-607dup	NM_017917.4:c.187-627_187-607dup	NM_017917.4:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTT	NM_017917.4:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant X1	XM_005267782.1:c.187-607=	XM_005267782.1:c.187-618_187-607del	XM_005267782.1:c.187-617_187-607del	XM_005267782.1:c.187-616_187-607del	XM_005267782.1:c.187-615_187-607del	XM_005267782.1:c.187-614_187-607del	XM_005267782.1:c.187-613_187-607del	XM_005267782.1:c.187-611_187-607del	XM_005267782.1:c.187-610_187-607del	XM_005267782.1:c.187-609_187-607del	XM_005267782.1:c.187-608_187-607del	XM_005267782.1:c.187-607del	XM_005267782.1:c.187-607dup	XM_005267782.1:c.187-608_187-607dup	XM_005267782.1:c.187-609_187-607dup	XM_005267782.1:c.187-610_187-607dup	XM_005267782.1:c.187-611_187-607dup	XM_005267782.1:c.187-613_187-607dup	XM_005267782.1:c.187-614_187-607dup	XM_005267782.1:c.187-616_187-607dup	XM_005267782.1:c.187-618_187-607dup	XM_005267782.1:c.187-619_187-607dup	XM_005267782.1:c.187-620_187-607dup	XM_005267782.1:c.187-627_187-607dup	XM_005267782.1:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267782.1:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant X1	XM_005267782.5:c.187-607=	XM_005267782.5:c.187-618_187-607del	XM_005267782.5:c.187-617_187-607del	XM_005267782.5:c.187-616_187-607del	XM_005267782.5:c.187-615_187-607del	XM_005267782.5:c.187-614_187-607del	XM_005267782.5:c.187-613_187-607del	XM_005267782.5:c.187-611_187-607del	XM_005267782.5:c.187-610_187-607del	XM_005267782.5:c.187-609_187-607del	XM_005267782.5:c.187-608_187-607del	XM_005267782.5:c.187-607del	XM_005267782.5:c.187-607dup	XM_005267782.5:c.187-608_187-607dup	XM_005267782.5:c.187-609_187-607dup	XM_005267782.5:c.187-610_187-607dup	XM_005267782.5:c.187-611_187-607dup	XM_005267782.5:c.187-613_187-607dup	XM_005267782.5:c.187-614_187-607dup	XM_005267782.5:c.187-616_187-607dup	XM_005267782.5:c.187-618_187-607dup	XM_005267782.5:c.187-619_187-607dup	XM_005267782.5:c.187-620_187-607dup	XM_005267782.5:c.187-627_187-607dup	XM_005267782.5:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267782.5:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant X2	XM_005267783.1:c.187-607=	XM_005267783.1:c.187-618_187-607del	XM_005267783.1:c.187-617_187-607del	XM_005267783.1:c.187-616_187-607del	XM_005267783.1:c.187-615_187-607del	XM_005267783.1:c.187-614_187-607del	XM_005267783.1:c.187-613_187-607del	XM_005267783.1:c.187-611_187-607del	XM_005267783.1:c.187-610_187-607del	XM_005267783.1:c.187-609_187-607del	XM_005267783.1:c.187-608_187-607del	XM_005267783.1:c.187-607del	XM_005267783.1:c.187-607dup	XM_005267783.1:c.187-608_187-607dup	XM_005267783.1:c.187-609_187-607dup	XM_005267783.1:c.187-610_187-607dup	XM_005267783.1:c.187-611_187-607dup	XM_005267783.1:c.187-613_187-607dup	XM_005267783.1:c.187-614_187-607dup	XM_005267783.1:c.187-616_187-607dup	XM_005267783.1:c.187-618_187-607dup	XM_005267783.1:c.187-619_187-607dup	XM_005267783.1:c.187-620_187-607dup	XM_005267783.1:c.187-627_187-607dup	XM_005267783.1:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267783.1:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant X3	XM_005267784.1:c.-144-607=	XM_005267784.1:c.-144-618_-144-607del	XM_005267784.1:c.-144-617_-144-607del	XM_005267784.1:c.-144-616_-144-607del	XM_005267784.1:c.-144-615_-144-607del	XM_005267784.1:c.-144-614_-144-607del	XM_005267784.1:c.-144-613_-144-607del	XM_005267784.1:c.-144-611_-144-607del	XM_005267784.1:c.-144-610_-144-607del	XM_005267784.1:c.-144-609_-144-607del	XM_005267784.1:c.-144-608_-144-607del	XM_005267784.1:c.-144-607del	XM_005267784.1:c.-144-607dup	XM_005267784.1:c.-144-608_-144-607dup	XM_005267784.1:c.-144-609_-144-607dup	XM_005267784.1:c.-144-610_-144-607dup	XM_005267784.1:c.-144-611_-144-607dup	XM_005267784.1:c.-144-613_-144-607dup	XM_005267784.1:c.-144-614_-144-607dup	XM_005267784.1:c.-144-616_-144-607dup	XM_005267784.1:c.-144-618_-144-607dup	XM_005267784.1:c.-144-619_-144-607dup	XM_005267784.1:c.-144-620_-144-607dup	XM_005267784.1:c.-144-627_-144-607dup	XM_005267784.1:c.-144-607_-144-606insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267784.1:c.-144-607_-144-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant X4	XM_005267785.1:c.187-607=	XM_005267785.1:c.187-618_187-607del	XM_005267785.1:c.187-617_187-607del	XM_005267785.1:c.187-616_187-607del	XM_005267785.1:c.187-615_187-607del	XM_005267785.1:c.187-614_187-607del	XM_005267785.1:c.187-613_187-607del	XM_005267785.1:c.187-611_187-607del	XM_005267785.1:c.187-610_187-607del	XM_005267785.1:c.187-609_187-607del	XM_005267785.1:c.187-608_187-607del	XM_005267785.1:c.187-607del	XM_005267785.1:c.187-607dup	XM_005267785.1:c.187-608_187-607dup	XM_005267785.1:c.187-609_187-607dup	XM_005267785.1:c.187-610_187-607dup	XM_005267785.1:c.187-611_187-607dup	XM_005267785.1:c.187-613_187-607dup	XM_005267785.1:c.187-614_187-607dup	XM_005267785.1:c.187-616_187-607dup	XM_005267785.1:c.187-618_187-607dup	XM_005267785.1:c.187-619_187-607dup	XM_005267785.1:c.187-620_187-607dup	XM_005267785.1:c.187-627_187-607dup	XM_005267785.1:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005267785.1:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant X2	XM_024449638.2:c.94-607=	XM_024449638.2:c.94-618_94-607del	XM_024449638.2:c.94-617_94-607del	XM_024449638.2:c.94-616_94-607del	XM_024449638.2:c.94-615_94-607del	XM_024449638.2:c.94-614_94-607del	XM_024449638.2:c.94-613_94-607del	XM_024449638.2:c.94-611_94-607del	XM_024449638.2:c.94-610_94-607del	XM_024449638.2:c.94-609_94-607del	XM_024449638.2:c.94-608_94-607del	XM_024449638.2:c.94-607del	XM_024449638.2:c.94-607dup	XM_024449638.2:c.94-608_94-607dup	XM_024449638.2:c.94-609_94-607dup	XM_024449638.2:c.94-610_94-607dup	XM_024449638.2:c.94-611_94-607dup	XM_024449638.2:c.94-613_94-607dup	XM_024449638.2:c.94-614_94-607dup	XM_024449638.2:c.94-616_94-607dup	XM_024449638.2:c.94-618_94-607dup	XM_024449638.2:c.94-619_94-607dup	XM_024449638.2:c.94-620_94-607dup	XM_024449638.2:c.94-627_94-607dup	XM_024449638.2:c.94-607_94-606insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024449638.2:c.94-607_94-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant X3	XM_024449639.2:c.31-607=	XM_024449639.2:c.31-618_31-607del	XM_024449639.2:c.31-617_31-607del	XM_024449639.2:c.31-616_31-607del	XM_024449639.2:c.31-615_31-607del	XM_024449639.2:c.31-614_31-607del	XM_024449639.2:c.31-613_31-607del	XM_024449639.2:c.31-611_31-607del	XM_024449639.2:c.31-610_31-607del	XM_024449639.2:c.31-609_31-607del	XM_024449639.2:c.31-608_31-607del	XM_024449639.2:c.31-607del	XM_024449639.2:c.31-607dup	XM_024449639.2:c.31-608_31-607dup	XM_024449639.2:c.31-609_31-607dup	XM_024449639.2:c.31-610_31-607dup	XM_024449639.2:c.31-611_31-607dup	XM_024449639.2:c.31-613_31-607dup	XM_024449639.2:c.31-614_31-607dup	XM_024449639.2:c.31-616_31-607dup	XM_024449639.2:c.31-618_31-607dup	XM_024449639.2:c.31-619_31-607dup	XM_024449639.2:c.31-620_31-607dup	XM_024449639.2:c.31-627_31-607dup	XM_024449639.2:c.31-607_31-606insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024449639.2:c.31-607_31-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT
PPP2R3C transcript variant X4	XM_047431517.1:c.187-607=	XM_047431517.1:c.187-618_187-607del	XM_047431517.1:c.187-617_187-607del	XM_047431517.1:c.187-616_187-607del	XM_047431517.1:c.187-615_187-607del	XM_047431517.1:c.187-614_187-607del	XM_047431517.1:c.187-613_187-607del	XM_047431517.1:c.187-611_187-607del	XM_047431517.1:c.187-610_187-607del	XM_047431517.1:c.187-609_187-607del	XM_047431517.1:c.187-608_187-607del	XM_047431517.1:c.187-607del	XM_047431517.1:c.187-607dup	XM_047431517.1:c.187-608_187-607dup	XM_047431517.1:c.187-609_187-607dup	XM_047431517.1:c.187-610_187-607dup	XM_047431517.1:c.187-611_187-607dup	XM_047431517.1:c.187-613_187-607dup	XM_047431517.1:c.187-614_187-607dup	XM_047431517.1:c.187-616_187-607dup	XM_047431517.1:c.187-618_187-607dup	XM_047431517.1:c.187-619_187-607dup	XM_047431517.1:c.187-620_187-607dup	XM_047431517.1:c.187-627_187-607dup	XM_047431517.1:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047431517.1:c.187-607_187-606insTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

61 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4289688	Mar 15, 2016 (147)
2	ABI	ss40450192	Mar 15, 2006 (137)
3	HUMANGENOME_JCVI	ss96889628	Feb 13, 2009 (137)
4	PJP	ss294826942	May 09, 2011 (137)
5	1000GENOMES	ss1373927692	Aug 21, 2014 (142)
6	SWEGEN	ss3012004433	Nov 08, 2017 (151)
7	MCHAISSO	ss3064623371	Nov 08, 2017 (151)
8	EVA_DECODE	ss3696442414	Jul 13, 2019 (153)
9	EVA_DECODE	ss3696442415	Jul 13, 2019 (153)
10	EVA_DECODE	ss3696442416	Jul 13, 2019 (153)
11	EVA_DECODE	ss3696442417	Jul 13, 2019 (153)
12	EVA_DECODE	ss3696442418	Jul 13, 2019 (153)
13	PACBIO	ss3787632028	Jul 13, 2019 (153)
14	PACBIO	ss3792675948	Jul 13, 2019 (153)
15	PACBIO	ss3792675949	Jul 13, 2019 (153)
16	PACBIO	ss3792675950	Jul 13, 2019 (153)
17	PACBIO	ss3797560050	Jul 13, 2019 (153)
18	PACBIO	ss3797560051	Jul 13, 2019 (153)
19	KHV_HUMAN_GENOMES	ss3817507271	Jul 13, 2019 (153)
20	EVA	ss3833855169	Apr 27, 2020 (154)
21	GNOMAD	ss4275944585	Apr 27, 2021 (155)
22	GNOMAD	ss4275944586	Apr 27, 2021 (155)
23	GNOMAD	ss4275944587	Apr 27, 2021 (155)
24	GNOMAD	ss4275944588	Apr 27, 2021 (155)
25	GNOMAD	ss4275944589	Apr 27, 2021 (155)
26	GNOMAD	ss4275944590	Apr 27, 2021 (155)
27	GNOMAD	ss4275944591	Apr 27, 2021 (155)
28	GNOMAD	ss4275944592	Apr 27, 2021 (155)
29	GNOMAD	ss4275944593	Apr 27, 2021 (155)
30	GNOMAD	ss4275944594	Apr 27, 2021 (155)
31	GNOMAD	ss4275944595	Apr 27, 2021 (155)
32	GNOMAD	ss4275944596	Apr 27, 2021 (155)
33	GNOMAD	ss4275944597	Apr 27, 2021 (155)
34	GNOMAD	ss4275944598	Apr 27, 2021 (155)
35	GNOMAD	ss4275944599	Apr 27, 2021 (155)
36	GNOMAD	ss4275944600	Apr 27, 2021 (155)
37	GNOMAD	ss4275944601	Apr 27, 2021 (155)
38	GNOMAD	ss4275944602	Apr 27, 2021 (155)
39	GNOMAD	ss4275944603	Apr 27, 2021 (155)
40	GNOMAD	ss4275944604	Apr 27, 2021 (155)
41	GNOMAD	ss4275944605	Apr 27, 2021 (155)
42	GNOMAD	ss4275944606	Apr 27, 2021 (155)
43	GNOMAD	ss4275944607	Apr 27, 2021 (155)
44	TOMMO_GENOMICS	ss5212688705	Apr 27, 2021 (155)
45	TOMMO_GENOMICS	ss5212688706	Apr 27, 2021 (155)
46	TOMMO_GENOMICS	ss5212688707	Apr 27, 2021 (155)
47	TOMMO_GENOMICS	ss5212688708	Apr 27, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5295797122	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5295797123	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5295797124	Oct 16, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5295797125	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5489895649	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5489895650	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5489895651	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5489895652	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5765336692	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5765336693	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5765336694	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5765336695	Oct 16, 2022 (156)
60	EVA	ss5840940094	Oct 16, 2022 (156)
61	EVA	ss5840940095	Oct 16, 2022 (156)
62	1000Genomes	NC_000014.8 - 35580442	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447658082 (NC_000014.9:35111235::A 1542/81892) Row 447658083 (NC_000014.9:35111235::AA 78/81840) Row 447658084 (NC_000014.9:35111235::AAA 182/81682)...	-	Apr 27, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 70658012 (NC_000014.8:35580441:AA: 4903/16576) Row 70658013 (NC_000014.8:35580441:AAA: 34/16576) Row 70658014 (NC_000014.8:35580441:A: 1814/16576)...	-	Apr 27, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 70658012 (NC_000014.8:35580441:AA: 4903/16576) Row 70658013 (NC_000014.8:35580441:AAA: 34/16576) Row 70658014 (NC_000014.8:35580441:A: 1814/16576)...	-	Apr 27, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 70658012 (NC_000014.8:35580441:AA: 4903/16576) Row 70658013 (NC_000014.8:35580441:AAA: 34/16576) Row 70658014 (NC_000014.8:35580441:A: 1814/16576)...	-	Apr 27, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 70658012 (NC_000014.8:35580441:AA: 4903/16576) Row 70658013 (NC_000014.8:35580441:AAA: 34/16576) Row 70658014 (NC_000014.8:35580441:A: 1814/16576)...	-	Apr 27, 2021 (155)
90	14KJPN Submission ignored due to conflicting rows: Row 99173796 (NC_000014.9:35111235:AA: 9364/27504) Row 99173797 (NC_000014.9:35111235:A: 3283/27504) Row 99173798 (NC_000014.9:35111235::A 110/27504)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 99173796 (NC_000014.9:35111235:AA: 9364/27504) Row 99173797 (NC_000014.9:35111235:A: 3283/27504) Row 99173798 (NC_000014.9:35111235::A 110/27504)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 99173796 (NC_000014.9:35111235:AA: 9364/27504) Row 99173797 (NC_000014.9:35111235:A: 3283/27504) Row 99173798 (NC_000014.9:35111235::A 110/27504)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 99173796 (NC_000014.9:35111235:AA: 9364/27504) Row 99173797 (NC_000014.9:35111235:A: 3283/27504) Row 99173798 (NC_000014.9:35111235::A 110/27504)...	-	Oct 16, 2022 (156)
94	ALFA	NC_000014.9 - 35111236	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)
rs35883184	May 11, 2012 (137)
rs71435857	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4275944607	NC_000014.9:35111235:AAAAAAAAAAAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4275944606	NC_000014.9:35111235:AAAAAAAAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4275944605	NC_000014.9:35111235:AAAAAAAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4275944604	NC_000014.9:35111235:AAAAAAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3696442418, ss4275944603	NC_000014.9:35111235:AAAAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4275944602	NC_000014.9:35111235:AAAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3787632028, ss3792675948, ss5212688706, ss5840940095	NC_000014.8:35580441:AAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3064623371, ss4275944601, ss5295797125, ss5489895650, ss5765336695	NC_000014.9:35111235:AAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3696442417	NC_000014.9:35111237:AAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
63483110, ss1373927692, ss3012004433, ss3792675949, ss3797560050, ss3833855169, ss5212688705, ss5840940094	NC_000014.8:35580441:AA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3817507271, ss4275944600, ss5295797123, ss5489895651, ss5765336692	NC_000014.9:35111235:AA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3696442416	NC_000014.9:35111238:AA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4289688	NT_026437.12:16580460:AA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss294826942	NC_000014.7:34650192:A:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3792675950, ss3797560051, ss5212688707	NC_000014.8:35580441:A:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944599, ss5295797122, ss5489895649, ss5765336693	NC_000014.9:35111235:A:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3696442415	NC_000014.9:35111239:A:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss96889628	NT_026437.12:16580441:A:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss40450192	NT_026437.12:16580462:A:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5212688708	NC_000014.8:35580441::A	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944585, ss5295797124, ss5489895652, ss5765336694	NC_000014.9:35111235::A	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3696442414	NC_000014.9:35111240::A	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944586	NC_000014.9:35111235::AA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944587	NC_000014.9:35111235::AAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944588	NC_000014.9:35111235::AAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4707789643	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944589	NC_000014.9:35111235::AAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944590	NC_000014.9:35111235::AAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944591	NC_000014.9:35111235::AAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944592	NC_000014.9:35111235::AAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944593	NC_000014.9:35111235::AAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944594	NC_000014.9:35111235::AAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944595	NC_000014.9:35111235::AAAAAAAAAAAA… NC_000014.9:35111235::AAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944596	NC_000014.9:35111235::AAAAAAAAAAAA… NC_000014.9:35111235::AAAAAAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944597	NC_000014.9:35111235::AAAAAAAAAAAA… NC_000014.9:35111235::AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4275944598	NC_000014.9:35111235::AAAAAAAAAAAA… NC_000014.9:35111235::AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3208014726	NC_000014.9:35111235:AAAAAAAAAA:	NC_000014.9:35111235:AAAAAAAAAAAAA… NC_000014.9:35111235:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA

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

No publications for rs3058398

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

rs3058398