Name: rs534798966
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.

rs534798966

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:73063319-73063340 (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)₁₃ / del(A)₁₁ / del(A)₁₀ / d…
del(A)₁₃ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₇ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.00000 (0/12910, ALFA)
del(A)₁₁=0.00000 (0/12910, ALFA)
del(A)₁₀=0.00000 (0/12910, ALFA) (+ 13 more)
del(A)₉=0.00000 (0/12910, ALFA)
del(A)₈=0.00000 (0/12910, ALFA)
del(A)₇=0.00000 (0/12910, ALFA)
del(A)₆=0.00000 (0/12910, ALFA)
del(A)₅=0.00000 (0/12910, ALFA)
del(A)₄=0.00000 (0/12910, ALFA)
delAAA=0.00000 (0/12910, ALFA)
delAA=0.00000 (0/12910, ALFA)
delA=0.00000 (0/12910, ALFA)
dupA=0.00000 (0/12910, ALFA)
dupAA=0.00000 (0/12910, ALFA)
dupAAA=0.00000 (0/12910, ALFA)
dup(A)₄=0.00000 (0/12910, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PPP4R2 : Intron Variant
EBLN2 : 3 Prime UTR Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	12910	AAAAAAAAAAAAAAAAAAAAAA=1.00000	AAAAAAAAA=0.00000, AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000	1.0	N/A
European	Sub	9412	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	2154	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	82	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	2072	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	104	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
East Asian	Sub	80	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	134	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	574	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	94	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	438	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	12910	(A)₂₂=1.00000	del(A)₁₃=0.00000, del(A)₁₁=0.00000, del(A)₁₀=0.00000, del(A)₉=0.00000, del(A)₈=0.00000, del(A)₇=0.00000, del(A)₆=0.00000, del(A)₅=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00000, dupAA=0.00000, dupAAA=0.00000, dup(A)₄=0.00000
Allele Frequency Aggregator	European	Sub	9412	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	2154	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	574	(A)₂₂=1.000	del(A)₁₃=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)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	438	(A)₂₂=1.000	del(A)₁₃=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)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	134	(A)₂₂=1.000	del(A)₁₃=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)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Asian	Sub	104	(A)₂₂=1.000	del(A)₁₃=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)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	94	(A)₂₂=1.00	del(A)₁₃=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)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00

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 3	NC_000003.12:g.73063328_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063330_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063331_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063332_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063333_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063334_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063335_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063336_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063337_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063338_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063339_73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063340del
GRCh38.p14 chr 3	NC_000003.12:g.73063340dup
GRCh38.p14 chr 3	NC_000003.12:g.73063339_73063340dup
GRCh38.p14 chr 3	NC_000003.12:g.73063338_73063340dup
GRCh38.p14 chr 3	NC_000003.12:g.73063337_73063340dup
GRCh38.p14 chr 3	NC_000003.12:g.73063336_73063340dup
GRCh38.p14 chr 3	NC_000003.12:g.73063334_73063340dup
GRCh38.p14 chr 3	NC_000003.12:g.73063333_73063340dup
GRCh37.p13 chr 3	NC_000003.11:g.73112479_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112481_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112482_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112483_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112484_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112485_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112486_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112487_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112488_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112489_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112490_73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112491del
GRCh37.p13 chr 3	NC_000003.11:g.73112491dup
GRCh37.p13 chr 3	NC_000003.11:g.73112490_73112491dup
GRCh37.p13 chr 3	NC_000003.11:g.73112489_73112491dup
GRCh37.p13 chr 3	NC_000003.11:g.73112488_73112491dup
GRCh37.p13 chr 3	NC_000003.11:g.73112487_73112491dup
GRCh37.p13 chr 3	NC_000003.11:g.73112485_73112491dup
GRCh37.p13 chr 3	NC_000003.11:g.73112484_73112491dup

Gene: PPP4R2, protein phosphatase 4 regulatory subunit 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PPP4R2 transcript variant 2	NM_001318025.2:c.249-345_… NM_001318025.2:c.249-345_249-333del	N/A	Intron Variant
PPP4R2 transcript variant 3	NM_001318026.2:c.306-345_… NM_001318026.2:c.306-345_306-333del	N/A	Intron Variant
PPP4R2 transcript variant 4	NM_001318027.2:c.-32-345_… NM_001318027.2:c.-32-345_-32-333del	N/A	Intron Variant
PPP4R2 transcript variant 1	NM_174907.4:c.420-345_420… NM_174907.4:c.420-345_420-333del	N/A	Intron Variant
PPP4R2 transcript variant 5	NM_001318028.2:c.	N/A	Genic Downstream Transcript Variant

Gene: EBLN2, endogenous Bornavirus like nucleoprotein 2 (plus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
EBLN2 transcript	NM_018029.4:c.	N/A	3 Prime UTR 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)₁₃	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₇	dup(A)₈
GRCh38.p14 chr 3	NC_000003.12:g.73063319_73063340=	NC_000003.12:g.73063328_73063340del	NC_000003.12:g.73063330_73063340del	NC_000003.12:g.73063331_73063340del	NC_000003.12:g.73063332_73063340del	NC_000003.12:g.73063333_73063340del	NC_000003.12:g.73063334_73063340del	NC_000003.12:g.73063335_73063340del	NC_000003.12:g.73063336_73063340del	NC_000003.12:g.73063337_73063340del	NC_000003.12:g.73063338_73063340del	NC_000003.12:g.73063339_73063340del	NC_000003.12:g.73063340del	NC_000003.12:g.73063340dup	NC_000003.12:g.73063339_73063340dup	NC_000003.12:g.73063338_73063340dup	NC_000003.12:g.73063337_73063340dup	NC_000003.12:g.73063336_73063340dup	NC_000003.12:g.73063334_73063340dup	NC_000003.12:g.73063333_73063340dup
GRCh37.p13 chr 3	NC_000003.11:g.73112470_73112491=	NC_000003.11:g.73112479_73112491del	NC_000003.11:g.73112481_73112491del	NC_000003.11:g.73112482_73112491del	NC_000003.11:g.73112483_73112491del	NC_000003.11:g.73112484_73112491del	NC_000003.11:g.73112485_73112491del	NC_000003.11:g.73112486_73112491del	NC_000003.11:g.73112487_73112491del	NC_000003.11:g.73112488_73112491del	NC_000003.11:g.73112489_73112491del	NC_000003.11:g.73112490_73112491del	NC_000003.11:g.73112491del	NC_000003.11:g.73112491dup	NC_000003.11:g.73112490_73112491dup	NC_000003.11:g.73112489_73112491dup	NC_000003.11:g.73112488_73112491dup	NC_000003.11:g.73112487_73112491dup	NC_000003.11:g.73112485_73112491dup	NC_000003.11:g.73112484_73112491dup
PPP4R2 transcript variant 2	NM_001318025.2:c.249-354=	NM_001318025.2:c.249-345_249-333del	NM_001318025.2:c.249-343_249-333del	NM_001318025.2:c.249-342_249-333del	NM_001318025.2:c.249-341_249-333del	NM_001318025.2:c.249-340_249-333del	NM_001318025.2:c.249-339_249-333del	NM_001318025.2:c.249-338_249-333del	NM_001318025.2:c.249-337_249-333del	NM_001318025.2:c.249-336_249-333del	NM_001318025.2:c.249-335_249-333del	NM_001318025.2:c.249-334_249-333del	NM_001318025.2:c.249-333del	NM_001318025.2:c.249-333dup	NM_001318025.2:c.249-334_249-333dup	NM_001318025.2:c.249-335_249-333dup	NM_001318025.2:c.249-336_249-333dup	NM_001318025.2:c.249-337_249-333dup	NM_001318025.2:c.249-339_249-333dup	NM_001318025.2:c.249-340_249-333dup
PPP4R2 transcript variant 3	NM_001318026.2:c.306-354=	NM_001318026.2:c.306-345_306-333del	NM_001318026.2:c.306-343_306-333del	NM_001318026.2:c.306-342_306-333del	NM_001318026.2:c.306-341_306-333del	NM_001318026.2:c.306-340_306-333del	NM_001318026.2:c.306-339_306-333del	NM_001318026.2:c.306-338_306-333del	NM_001318026.2:c.306-337_306-333del	NM_001318026.2:c.306-336_306-333del	NM_001318026.2:c.306-335_306-333del	NM_001318026.2:c.306-334_306-333del	NM_001318026.2:c.306-333del	NM_001318026.2:c.306-333dup	NM_001318026.2:c.306-334_306-333dup	NM_001318026.2:c.306-335_306-333dup	NM_001318026.2:c.306-336_306-333dup	NM_001318026.2:c.306-337_306-333dup	NM_001318026.2:c.306-339_306-333dup	NM_001318026.2:c.306-340_306-333dup
PPP4R2 transcript variant 4	NM_001318027.2:c.-32-354=	NM_001318027.2:c.-32-345_-32-333del	NM_001318027.2:c.-32-343_-32-333del	NM_001318027.2:c.-32-342_-32-333del	NM_001318027.2:c.-32-341_-32-333del	NM_001318027.2:c.-32-340_-32-333del	NM_001318027.2:c.-32-339_-32-333del	NM_001318027.2:c.-32-338_-32-333del	NM_001318027.2:c.-32-337_-32-333del	NM_001318027.2:c.-32-336_-32-333del	NM_001318027.2:c.-32-335_-32-333del	NM_001318027.2:c.-32-334_-32-333del	NM_001318027.2:c.-32-333del	NM_001318027.2:c.-32-333dup	NM_001318027.2:c.-32-334_-32-333dup	NM_001318027.2:c.-32-335_-32-333dup	NM_001318027.2:c.-32-336_-32-333dup	NM_001318027.2:c.-32-337_-32-333dup	NM_001318027.2:c.-32-339_-32-333dup	NM_001318027.2:c.-32-340_-32-333dup
PPP4R2 transcript	NM_174907.2:c.420-354=	NM_174907.2:c.420-345_420-333del	NM_174907.2:c.420-343_420-333del	NM_174907.2:c.420-342_420-333del	NM_174907.2:c.420-341_420-333del	NM_174907.2:c.420-340_420-333del	NM_174907.2:c.420-339_420-333del	NM_174907.2:c.420-338_420-333del	NM_174907.2:c.420-337_420-333del	NM_174907.2:c.420-336_420-333del	NM_174907.2:c.420-335_420-333del	NM_174907.2:c.420-334_420-333del	NM_174907.2:c.420-333del	NM_174907.2:c.420-333dup	NM_174907.2:c.420-334_420-333dup	NM_174907.2:c.420-335_420-333dup	NM_174907.2:c.420-336_420-333dup	NM_174907.2:c.420-337_420-333dup	NM_174907.2:c.420-339_420-333dup	NM_174907.2:c.420-340_420-333dup
PPP4R2 transcript variant 1	NM_174907.4:c.420-354=	NM_174907.4:c.420-345_420-333del	NM_174907.4:c.420-343_420-333del	NM_174907.4:c.420-342_420-333del	NM_174907.4:c.420-341_420-333del	NM_174907.4:c.420-340_420-333del	NM_174907.4:c.420-339_420-333del	NM_174907.4:c.420-338_420-333del	NM_174907.4:c.420-337_420-333del	NM_174907.4:c.420-336_420-333del	NM_174907.4:c.420-335_420-333del	NM_174907.4:c.420-334_420-333del	NM_174907.4:c.420-333del	NM_174907.4:c.420-333dup	NM_174907.4:c.420-334_420-333dup	NM_174907.4:c.420-335_420-333dup	NM_174907.4:c.420-336_420-333dup	NM_174907.4:c.420-337_420-333dup	NM_174907.4:c.420-339_420-333dup	NM_174907.4:c.420-340_420-333dup
PPP4R2 transcript variant X1	XM_005264714.1:c.249-354=	XM_005264714.1:c.249-345_249-333del	XM_005264714.1:c.249-343_249-333del	XM_005264714.1:c.249-342_249-333del	XM_005264714.1:c.249-341_249-333del	XM_005264714.1:c.249-340_249-333del	XM_005264714.1:c.249-339_249-333del	XM_005264714.1:c.249-338_249-333del	XM_005264714.1:c.249-337_249-333del	XM_005264714.1:c.249-336_249-333del	XM_005264714.1:c.249-335_249-333del	XM_005264714.1:c.249-334_249-333del	XM_005264714.1:c.249-333del	XM_005264714.1:c.249-333dup	XM_005264714.1:c.249-334_249-333dup	XM_005264714.1:c.249-335_249-333dup	XM_005264714.1:c.249-336_249-333dup	XM_005264714.1:c.249-337_249-333dup	XM_005264714.1:c.249-339_249-333dup	XM_005264714.1:c.249-340_249-333dup

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#.

50 SubSNP, 38 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss2992548157	Nov 08, 2017 (151)
2	MCHAISSO	ss3065886791	Nov 08, 2017 (151)
3	KOGIC	ss3951556845	Apr 25, 2020 (154)
4	KOGIC	ss3951556846	Apr 25, 2020 (154)
5	KOGIC	ss3951556847	Apr 25, 2020 (154)
6	KOGIC	ss3951556848	Apr 25, 2020 (154)
7	KOGIC	ss3951556849	Apr 25, 2020 (154)
8	GNOMAD	ss4073747079	Apr 26, 2021 (155)
9	GNOMAD	ss4073747080	Apr 26, 2021 (155)
10	GNOMAD	ss4073747081	Apr 26, 2021 (155)
11	GNOMAD	ss4073747082	Apr 26, 2021 (155)
12	GNOMAD	ss4073747083	Apr 26, 2021 (155)
13	GNOMAD	ss4073747084	Apr 26, 2021 (155)
14	GNOMAD	ss4073747085	Apr 26, 2021 (155)
15	GNOMAD	ss4073747087	Apr 26, 2021 (155)
16	GNOMAD	ss4073747088	Apr 26, 2021 (155)
17	GNOMAD	ss4073747089	Apr 26, 2021 (155)
18	GNOMAD	ss4073747090	Apr 26, 2021 (155)
19	GNOMAD	ss4073747091	Apr 26, 2021 (155)
20	GNOMAD	ss4073747092	Apr 26, 2021 (155)
21	GNOMAD	ss4073747093	Apr 26, 2021 (155)
22	GNOMAD	ss4073747094	Apr 26, 2021 (155)
23	GNOMAD	ss4073747095	Apr 26, 2021 (155)
24	GNOMAD	ss4073747096	Apr 26, 2021 (155)
25	TOPMED	ss4569830242	Apr 26, 2021 (155)
26	TOPMED	ss4569830243	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5159819917	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5159819918	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5159819919	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5159819920	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5159819921	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5159819922	Apr 26, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5254596073	Oct 12, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5254596074	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5254596075	Oct 12, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5254596076	Oct 12, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5254596077	Oct 12, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5254596078	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5453935352	Oct 12, 2022 (156)
40	HUGCELL_USP	ss5453935353	Oct 12, 2022 (156)
41	HUGCELL_USP	ss5453935354	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5453935355	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5453935356	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5453935357	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5691675966	Oct 12, 2022 (156)
46	TOMMO_GENOMICS	ss5691675967	Oct 12, 2022 (156)
47	TOMMO_GENOMICS	ss5691675968	Oct 12, 2022 (156)
48	TOMMO_GENOMICS	ss5691675969	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5691675970	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5691675971	Oct 12, 2022 (156)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112118816 (NC_000003.12:73063318::A 3649/66614) Row 112118817 (NC_000003.12:73063318::AA 1224/66610) Row 112118818 (NC_000003.12:73063318::AAA 43/66606)...	-	Apr 26, 2021 (155)
69	Korean Genome Project Submission ignored due to conflicting rows: Row 7934846 (NC_000003.12:73063322::A 125/1820) Row 7934847 (NC_000003.12:73063321:A: 112/1820) Row 7934848 (NC_000003.12:73063320:AA: 55/1820)...	-	Apr 25, 2020 (154)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 7934846 (NC_000003.12:73063322::A 125/1820) Row 7934847 (NC_000003.12:73063321:A: 112/1820) Row 7934848 (NC_000003.12:73063320:AA: 55/1820)...	-	Apr 25, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 7934846 (NC_000003.12:73063322::A 125/1820) Row 7934847 (NC_000003.12:73063321:A: 112/1820) Row 7934848 (NC_000003.12:73063320:AA: 55/1820)...	-	Apr 25, 2020 (154)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 7934846 (NC_000003.12:73063322::A 125/1820) Row 7934847 (NC_000003.12:73063321:A: 112/1820) Row 7934848 (NC_000003.12:73063320:AA: 55/1820)...	-	Apr 25, 2020 (154)
73	Korean Genome Project Submission ignored due to conflicting rows: Row 7934846 (NC_000003.12:73063322::A 125/1820) Row 7934847 (NC_000003.12:73063321:A: 112/1820) Row 7934848 (NC_000003.12:73063320:AA: 55/1820)...	-	Apr 25, 2020 (154)
74	8.3KJPN Submission ignored due to conflicting rows: Row 17789224 (NC_000003.11:73112469:AA: 183/16660) Row 17789225 (NC_000003.11:73112469:A: 48/16660) Row 17789226 (NC_000003.11:73112469::A 90/16660)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 17789224 (NC_000003.11:73112469:AA: 183/16660) Row 17789225 (NC_000003.11:73112469:A: 48/16660) Row 17789226 (NC_000003.11:73112469::A 90/16660)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 17789224 (NC_000003.11:73112469:AA: 183/16660) Row 17789225 (NC_000003.11:73112469:A: 48/16660) Row 17789226 (NC_000003.11:73112469::A 90/16660)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 17789224 (NC_000003.11:73112469:AA: 183/16660) Row 17789225 (NC_000003.11:73112469:A: 48/16660) Row 17789226 (NC_000003.11:73112469::A 90/16660)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 17789224 (NC_000003.11:73112469:AA: 183/16660) Row 17789225 (NC_000003.11:73112469:A: 48/16660) Row 17789226 (NC_000003.11:73112469::A 90/16660)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 17789224 (NC_000003.11:73112469:AA: 183/16660) Row 17789225 (NC_000003.11:73112469:A: 48/16660) Row 17789226 (NC_000003.11:73112469::A 90/16660)...	-	Apr 26, 2021 (155)
80	14KJPN Submission ignored due to conflicting rows: Row 25513070 (NC_000003.12:73063318:AA: 315/28250) Row 25513071 (NC_000003.12:73063318:A: 65/28250) Row 25513072 (NC_000003.12:73063318::A 173/28250)...	-	Oct 12, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 25513070 (NC_000003.12:73063318:AA: 315/28250) Row 25513071 (NC_000003.12:73063318:A: 65/28250) Row 25513072 (NC_000003.12:73063318::A 173/28250)...	-	Oct 12, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 25513070 (NC_000003.12:73063318:AA: 315/28250) Row 25513071 (NC_000003.12:73063318:A: 65/28250) Row 25513072 (NC_000003.12:73063318::A 173/28250)...	-	Oct 12, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 25513070 (NC_000003.12:73063318:AA: 315/28250) Row 25513071 (NC_000003.12:73063318:A: 65/28250) Row 25513072 (NC_000003.12:73063318::A 173/28250)...	-	Oct 12, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 25513070 (NC_000003.12:73063318:AA: 315/28250) Row 25513071 (NC_000003.12:73063318:A: 65/28250) Row 25513072 (NC_000003.12:73063318::A 173/28250)...	-	Oct 12, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 25513070 (NC_000003.12:73063318:AA: 315/28250) Row 25513071 (NC_000003.12:73063318:A: 65/28250) Row 25513072 (NC_000003.12:73063318::A 173/28250)...	-	Oct 12, 2022 (156)
86	TopMed Submission ignored due to conflicting rows: Row 407207797 (NC_000003.12:73063318:AAAAAAA: 9/264690) Row 407207798 (NC_000003.12:73063318:AAAAAAAAAA: 3/264690)	-	Apr 26, 2021 (155)
87	TopMed Submission ignored due to conflicting rows: Row 407207797 (NC_000003.12:73063318:AAAAAAA: 9/264690) Row 407207798 (NC_000003.12:73063318:AAAAAAAAAA: 3/264690)	-	Apr 26, 2021 (155)
88	ALFA	NC_000003.12 - 73063319	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4073747096	NC_000003.12:73063318:AAAAAAAAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss5159819921	NC_000003.11:73112469:AAAAAAAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4073747095, ss4569830243, ss5453935357, ss5691675970	NC_000003.12:73063318:AAAAAAAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4073747094	NC_000003.12:73063318:AAAAAAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4073747093	NC_000003.12:73063318:AAAAAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4073747092, ss4569830242	NC_000003.12:73063318:AAAAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4073747091	NC_000003.12:73063318:AAAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss2992548157	NC_000003.11:73112469:AAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4073747090	NC_000003.12:73063318:AAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5159819920	NC_000003.11:73112469:AAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3951556848, ss4073747089, ss5254596078, ss5453935355, ss5691675969	NC_000003.12:73063318:AAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4073747088, ss5453935356	NC_000003.12:73063318:AAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5159819917	NC_000003.11:73112469:AA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4073747087, ss5254596077, ss5691675966	NC_000003.12:73063318:AA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3951556847	NC_000003.12:73063320:AA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5159819918	NC_000003.11:73112469:A:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5254596076, ss5453935352, ss5691675967	NC_000003.12:73063318:A:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3951556846	NC_000003.12:73063321:A:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5159819919	NC_000003.11:73112469::A	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073747079, ss5254596073, ss5453935353, ss5691675968	NC_000003.12:73063318::A	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3951556845	NC_000003.12:73063322::A	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3065886791, ss4073747080, ss5254596074, ss5453935354	NC_000003.12:73063318::AA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5159819922	NC_000003.11:73112469::AAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073747081, ss5254596075, ss5691675971	NC_000003.12:73063318::AAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3951556849	NC_000003.12:73063322::AAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073747082	NC_000003.12:73063318::AAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12582813838	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073747083	NC_000003.12:73063318::AAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073747084	NC_000003.12:73063318::AAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073747085	NC_000003.12:73063318::AAAAAAAA	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2419889260	NC_000003.11:73112469:AAAAAAAAA:	NC_000003.12:73063318:AAAAAAAAAAAA… NC_000003.12:73063318:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

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

No publications for rs534798966

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

rs534798966