Name: rs11451581
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.

rs11451581

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:53323862-53323882 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₁ / del(A)₆ / del(A)₅ / del…
del(A)₁₁ / 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)₁₁=0.000004 (1/264690, TOPMED)
dupAA=0.06165 (824/13365, ALFA)
dupA=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DCP1A : Intron Variant
LOC124909380 : 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	13365	AAAAAAAAAAAAAAAAAAAAA=0.92974	AAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAA=0.00584, AAAAAAAAAAAAAAAAAAAAAAA=0.06165, AAAAAAAAAAAAAAAAAAAAAAAA=0.00187, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00030, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00060, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000	0.897557	0.020916	0.081527	32
European	Sub	10953	AAAAAAAAAAAAAAAAAAAAA=0.91454	AAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAA=0.00703, AAAAAAAAAAAAAAAAAAAAAAA=0.07505, AAAAAAAAAAAAAAAAAAAAAAAA=0.00228, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00037, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00073, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000	0.874836	0.025631	0.099532	32
African	Sub	1516	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	56	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1460	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	94	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	72	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	22	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	78	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	354	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	66	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	304	AAAAAAAAAAAAAAAAAAAAA=0.990	AAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.003, AAAAAAAAAAAAAAAAAAAAAAA=0.007, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	0.986755	0.0	0.013245	0

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
TopMed	Global	Study-wide	264690	(A)₂₁=0.999996	del(A)₁₁=0.000004
Allele Frequency Aggregator	Total	Global	13365	(A)₂₁=0.92974	del(A)₁₁=0.00000, del(A)₆=0.00000, del(A)₄=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00584, dupAA=0.06165, dupAAA=0.00187, dup(A)₄=0.00060, dup(A)₅=0.00000, dup(A)₈=0.00030
Allele Frequency Aggregator	European	Sub	10953	(A)₂₁=0.91454	del(A)₁₁=0.00000, del(A)₆=0.00000, del(A)₄=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00703, dupAA=0.07505, dupAAA=0.00228, dup(A)₄=0.00073, dup(A)₅=0.00000, dup(A)₈=0.00037
Allele Frequency Aggregator	African	Sub	1516	(A)₂₁=1.0000	del(A)₁₁=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₈=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	354	(A)₂₁=1.000	del(A)₁₁=0.000, del(A)₆=0.000, del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₈=0.000
Allele Frequency Aggregator	Other	Sub	304	(A)₂₁=0.990	del(A)₁₁=0.000, del(A)₆=0.000, del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.003, dupAA=0.007, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₈=0.000
Allele Frequency Aggregator	Asian	Sub	94	(A)₂₁=1.00	del(A)₁₁=0.00, del(A)₆=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₈=0.00
Allele Frequency Aggregator	Latin American 1	Sub	78	(A)₂₁=1.00	del(A)₁₁=0.00, del(A)₆=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	66	(A)₂₁=1.00	del(A)₁₁=0.00, del(A)₆=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₈=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.47

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.53323872_53323882del
GRCh38.p14 chr 3	NC_000003.12:g.53323877_53323882del
GRCh38.p14 chr 3	NC_000003.12:g.53323878_53323882del
GRCh38.p14 chr 3	NC_000003.12:g.53323879_53323882del
GRCh38.p14 chr 3	NC_000003.12:g.53323880_53323882del
GRCh38.p14 chr 3	NC_000003.12:g.53323881_53323882del
GRCh38.p14 chr 3	NC_000003.12:g.53323882del
GRCh38.p14 chr 3	NC_000003.12:g.53323882dup
GRCh38.p14 chr 3	NC_000003.12:g.53323881_53323882dup
GRCh38.p14 chr 3	NC_000003.12:g.53323880_53323882dup
GRCh38.p14 chr 3	NC_000003.12:g.53323879_53323882dup
GRCh38.p14 chr 3	NC_000003.12:g.53323878_53323882dup
GRCh38.p14 chr 3	NC_000003.12:g.53323876_53323882dup
GRCh38.p14 chr 3	NC_000003.12:g.53323875_53323882dup
GRCh37.p13 chr 3	NC_000003.11:g.53357899_53357909del
GRCh37.p13 chr 3	NC_000003.11:g.53357904_53357909del
GRCh37.p13 chr 3	NC_000003.11:g.53357905_53357909del
GRCh37.p13 chr 3	NC_000003.11:g.53357906_53357909del
GRCh37.p13 chr 3	NC_000003.11:g.53357907_53357909del
GRCh37.p13 chr 3	NC_000003.11:g.53357908_53357909del
GRCh37.p13 chr 3	NC_000003.11:g.53357909del
GRCh37.p13 chr 3	NC_000003.11:g.53357909dup
GRCh37.p13 chr 3	NC_000003.11:g.53357908_53357909dup
GRCh37.p13 chr 3	NC_000003.11:g.53357907_53357909dup
GRCh37.p13 chr 3	NC_000003.11:g.53357906_53357909dup
GRCh37.p13 chr 3	NC_000003.11:g.53357905_53357909dup
GRCh37.p13 chr 3	NC_000003.11:g.53357903_53357909dup
GRCh37.p13 chr 3	NC_000003.11:g.53357902_53357909dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172827_172837del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172832_172837del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172833_172837del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172834_172837del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172835_172837del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172836_172837del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172837del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172837dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172836_172837dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172835_172837dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172834_172837dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172833_172837dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172831_172837dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172830_172837dup

Gene: DCP1A, decapping mRNA 1A (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DCP1A transcript variant 2	NM_001290204.2:c.305-4399… NM_001290204.2:c.305-4399_305-4389del	N/A	Intron Variant
DCP1A transcript variant 3	NM_001290205.2:c.89-4399_… NM_001290205.2:c.89-4399_89-4389del	N/A	Intron Variant
DCP1A transcript variant 4	NM_001290206.2:c.-59-4399… NM_001290206.2:c.-59-4399_-59-4389del	N/A	Intron Variant
DCP1A transcript variant 5	NM_001290207.2:c.-59-4399… NM_001290207.2:c.-59-4399_-59-4389del	N/A	Intron Variant
DCP1A transcript variant 1	NM_018403.7:c.305-4399_30… NM_018403.7:c.305-4399_305-4389del	N/A	Intron Variant

Gene: LOC124909380, uncharacterized LOC124909380 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124909380 transcript	XR_007095912.1: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)₂₁=	del(A)₁₁	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.53323862_53323882=	NC_000003.12:g.53323872_53323882del	NC_000003.12:g.53323877_53323882del	NC_000003.12:g.53323878_53323882del	NC_000003.12:g.53323879_53323882del	NC_000003.12:g.53323880_53323882del	NC_000003.12:g.53323881_53323882del	NC_000003.12:g.53323882del	NC_000003.12:g.53323882dup	NC_000003.12:g.53323881_53323882dup	NC_000003.12:g.53323880_53323882dup	NC_000003.12:g.53323879_53323882dup	NC_000003.12:g.53323878_53323882dup	NC_000003.12:g.53323876_53323882dup	NC_000003.12:g.53323875_53323882dup
GRCh37.p13 chr 3	NC_000003.11:g.53357889_53357909=	NC_000003.11:g.53357899_53357909del	NC_000003.11:g.53357904_53357909del	NC_000003.11:g.53357905_53357909del	NC_000003.11:g.53357906_53357909del	NC_000003.11:g.53357907_53357909del	NC_000003.11:g.53357908_53357909del	NC_000003.11:g.53357909del	NC_000003.11:g.53357909dup	NC_000003.11:g.53357908_53357909dup	NC_000003.11:g.53357907_53357909dup	NC_000003.11:g.53357906_53357909dup	NC_000003.11:g.53357905_53357909dup	NC_000003.11:g.53357903_53357909dup	NC_000003.11:g.53357902_53357909dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.172817_172837=	NW_004775426.1:g.172827_172837del	NW_004775426.1:g.172832_172837del	NW_004775426.1:g.172833_172837del	NW_004775426.1:g.172834_172837del	NW_004775426.1:g.172835_172837del	NW_004775426.1:g.172836_172837del	NW_004775426.1:g.172837del	NW_004775426.1:g.172837dup	NW_004775426.1:g.172836_172837dup	NW_004775426.1:g.172835_172837dup	NW_004775426.1:g.172834_172837dup	NW_004775426.1:g.172833_172837dup	NW_004775426.1:g.172831_172837dup	NW_004775426.1:g.172830_172837dup
DCP1A transcript variant 2	NM_001290204.2:c.305-4389=	NM_001290204.2:c.305-4399_305-4389del	NM_001290204.2:c.305-4394_305-4389del	NM_001290204.2:c.305-4393_305-4389del	NM_001290204.2:c.305-4392_305-4389del	NM_001290204.2:c.305-4391_305-4389del	NM_001290204.2:c.305-4390_305-4389del	NM_001290204.2:c.305-4389del	NM_001290204.2:c.305-4389dup	NM_001290204.2:c.305-4390_305-4389dup	NM_001290204.2:c.305-4391_305-4389dup	NM_001290204.2:c.305-4392_305-4389dup	NM_001290204.2:c.305-4393_305-4389dup	NM_001290204.2:c.305-4395_305-4389dup	NM_001290204.2:c.305-4396_305-4389dup
DCP1A transcript variant 3	NM_001290205.2:c.89-4389=	NM_001290205.2:c.89-4399_89-4389del	NM_001290205.2:c.89-4394_89-4389del	NM_001290205.2:c.89-4393_89-4389del	NM_001290205.2:c.89-4392_89-4389del	NM_001290205.2:c.89-4391_89-4389del	NM_001290205.2:c.89-4390_89-4389del	NM_001290205.2:c.89-4389del	NM_001290205.2:c.89-4389dup	NM_001290205.2:c.89-4390_89-4389dup	NM_001290205.2:c.89-4391_89-4389dup	NM_001290205.2:c.89-4392_89-4389dup	NM_001290205.2:c.89-4393_89-4389dup	NM_001290205.2:c.89-4395_89-4389dup	NM_001290205.2:c.89-4396_89-4389dup
DCP1A transcript variant 4	NM_001290206.2:c.-59-4389=	NM_001290206.2:c.-59-4399_-59-4389del	NM_001290206.2:c.-59-4394_-59-4389del	NM_001290206.2:c.-59-4393_-59-4389del	NM_001290206.2:c.-59-4392_-59-4389del	NM_001290206.2:c.-59-4391_-59-4389del	NM_001290206.2:c.-59-4390_-59-4389del	NM_001290206.2:c.-59-4389del	NM_001290206.2:c.-59-4389dup	NM_001290206.2:c.-59-4390_-59-4389dup	NM_001290206.2:c.-59-4391_-59-4389dup	NM_001290206.2:c.-59-4392_-59-4389dup	NM_001290206.2:c.-59-4393_-59-4389dup	NM_001290206.2:c.-59-4395_-59-4389dup	NM_001290206.2:c.-59-4396_-59-4389dup
DCP1A transcript variant 5	NM_001290207.2:c.-59-4389=	NM_001290207.2:c.-59-4399_-59-4389del	NM_001290207.2:c.-59-4394_-59-4389del	NM_001290207.2:c.-59-4393_-59-4389del	NM_001290207.2:c.-59-4392_-59-4389del	NM_001290207.2:c.-59-4391_-59-4389del	NM_001290207.2:c.-59-4390_-59-4389del	NM_001290207.2:c.-59-4389del	NM_001290207.2:c.-59-4389dup	NM_001290207.2:c.-59-4390_-59-4389dup	NM_001290207.2:c.-59-4391_-59-4389dup	NM_001290207.2:c.-59-4392_-59-4389dup	NM_001290207.2:c.-59-4393_-59-4389dup	NM_001290207.2:c.-59-4395_-59-4389dup	NM_001290207.2:c.-59-4396_-59-4389dup
DCP1A transcript	NM_018403.5:c.305-4389=	NM_018403.5:c.305-4399_305-4389del	NM_018403.5:c.305-4394_305-4389del	NM_018403.5:c.305-4393_305-4389del	NM_018403.5:c.305-4392_305-4389del	NM_018403.5:c.305-4391_305-4389del	NM_018403.5:c.305-4390_305-4389del	NM_018403.5:c.305-4389del	NM_018403.5:c.305-4389dup	NM_018403.5:c.305-4390_305-4389dup	NM_018403.5:c.305-4391_305-4389dup	NM_018403.5:c.305-4392_305-4389dup	NM_018403.5:c.305-4393_305-4389dup	NM_018403.5:c.305-4395_305-4389dup	NM_018403.5:c.305-4396_305-4389dup
DCP1A transcript variant 1	NM_018403.7:c.305-4389=	NM_018403.7:c.305-4399_305-4389del	NM_018403.7:c.305-4394_305-4389del	NM_018403.7:c.305-4393_305-4389del	NM_018403.7:c.305-4392_305-4389del	NM_018403.7:c.305-4391_305-4389del	NM_018403.7:c.305-4390_305-4389del	NM_018403.7:c.305-4389del	NM_018403.7:c.305-4389dup	NM_018403.7:c.305-4390_305-4389dup	NM_018403.7:c.305-4391_305-4389dup	NM_018403.7:c.305-4392_305-4389dup	NM_018403.7:c.305-4393_305-4389dup	NM_018403.7:c.305-4395_305-4389dup	NM_018403.7:c.305-4396_305-4389dup
DCP1A transcript variant X1	XM_005265320.1:c.305-4389=	XM_005265320.1:c.305-4399_305-4389del	XM_005265320.1:c.305-4394_305-4389del	XM_005265320.1:c.305-4393_305-4389del	XM_005265320.1:c.305-4392_305-4389del	XM_005265320.1:c.305-4391_305-4389del	XM_005265320.1:c.305-4390_305-4389del	XM_005265320.1:c.305-4389del	XM_005265320.1:c.305-4389dup	XM_005265320.1:c.305-4390_305-4389dup	XM_005265320.1:c.305-4391_305-4389dup	XM_005265320.1:c.305-4392_305-4389dup	XM_005265320.1:c.305-4393_305-4389dup	XM_005265320.1:c.305-4395_305-4389dup	XM_005265320.1:c.305-4396_305-4389dup
DCP1A transcript variant X1	XM_005278358.1:c.305-4389=	XM_005278358.1:c.305-4399_305-4389del	XM_005278358.1:c.305-4394_305-4389del	XM_005278358.1:c.305-4393_305-4389del	XM_005278358.1:c.305-4392_305-4389del	XM_005278358.1:c.305-4391_305-4389del	XM_005278358.1:c.305-4390_305-4389del	XM_005278358.1:c.305-4389del	XM_005278358.1:c.305-4389dup	XM_005278358.1:c.305-4390_305-4389dup	XM_005278358.1:c.305-4391_305-4389dup	XM_005278358.1:c.305-4392_305-4389dup	XM_005278358.1:c.305-4393_305-4389dup	XM_005278358.1:c.305-4395_305-4389dup	XM_005278358.1:c.305-4396_305-4389dup
DCP1A transcript variant X2	XM_005278359.1:c.-59-4389=	XM_005278359.1:c.-59-4399_-59-4389del	XM_005278359.1:c.-59-4394_-59-4389del	XM_005278359.1:c.-59-4393_-59-4389del	XM_005278359.1:c.-59-4392_-59-4389del	XM_005278359.1:c.-59-4391_-59-4389del	XM_005278359.1:c.-59-4390_-59-4389del	XM_005278359.1:c.-59-4389del	XM_005278359.1:c.-59-4389dup	XM_005278359.1:c.-59-4390_-59-4389dup	XM_005278359.1:c.-59-4391_-59-4389dup	XM_005278359.1:c.-59-4392_-59-4389dup	XM_005278359.1:c.-59-4393_-59-4389dup	XM_005278359.1:c.-59-4395_-59-4389dup	XM_005278359.1:c.-59-4396_-59-4389dup
DCP1A transcript variant X3	XM_005278360.1:c.-59-4389=	XM_005278360.1:c.-59-4399_-59-4389del	XM_005278360.1:c.-59-4394_-59-4389del	XM_005278360.1:c.-59-4393_-59-4389del	XM_005278360.1:c.-59-4392_-59-4389del	XM_005278360.1:c.-59-4391_-59-4389del	XM_005278360.1:c.-59-4390_-59-4389del	XM_005278360.1:c.-59-4389del	XM_005278360.1:c.-59-4389dup	XM_005278360.1:c.-59-4390_-59-4389dup	XM_005278360.1:c.-59-4391_-59-4389dup	XM_005278360.1:c.-59-4392_-59-4389dup	XM_005278360.1:c.-59-4393_-59-4389dup	XM_005278360.1:c.-59-4395_-59-4389dup	XM_005278360.1:c.-59-4396_-59-4389dup

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#.

57 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42031006	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95946874	Dec 05, 2013 (142)
3	PJP	ss295100479	May 09, 2011 (135)
4	PJP	ss295100480	May 09, 2011 (134)
5	BILGI_BIOE	ss666206576	Apr 25, 2013 (138)
6	SSIP	ss947086961	Aug 21, 2014 (142)
7	EVA_GENOME_DK	ss1575939726	Apr 09, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1703626746	Apr 09, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1703626747	Apr 09, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1703626868	Apr 09, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1703626871	Apr 09, 2015 (144)
12	SWEGEN	ss2992311445	Oct 12, 2018 (152)
13	SWEGEN	ss2992311446	Oct 12, 2018 (152)
14	URBANLAB	ss3647402832	Oct 12, 2018 (152)
15	EVA_DECODE	ss3709227139	Jul 13, 2019 (153)
16	EVA_DECODE	ss3709227140	Jul 13, 2019 (153)
17	EVA_DECODE	ss3709227141	Jul 13, 2019 (153)
18	EVA_DECODE	ss3709227142	Jul 13, 2019 (153)
19	EVA_DECODE	ss3709227143	Jul 13, 2019 (153)
20	EVA_DECODE	ss3709227144	Jul 13, 2019 (153)
21	EVA	ss3827807147	Apr 25, 2020 (154)
22	EVA	ss3842751084	Apr 25, 2020 (154)
23	GNOMAD	ss4071118323	Apr 26, 2021 (155)
24	GNOMAD	ss4071118324	Apr 26, 2021 (155)
25	GNOMAD	ss4071118325	Apr 26, 2021 (155)
26	GNOMAD	ss4071118326	Apr 26, 2021 (155)
27	GNOMAD	ss4071118327	Apr 26, 2021 (155)
28	GNOMAD	ss4071118328	Apr 26, 2021 (155)
29	GNOMAD	ss4071118330	Apr 26, 2021 (155)
30	GNOMAD	ss4071118331	Apr 26, 2021 (155)
31	GNOMAD	ss4071118332	Apr 26, 2021 (155)
32	GNOMAD	ss4071118333	Apr 26, 2021 (155)
33	GNOMAD	ss4071118334	Apr 26, 2021 (155)
34	GNOMAD	ss4071118335	Apr 26, 2021 (155)
35	GNOMAD	ss4071118336	Apr 26, 2021 (155)
36	TOPMED	ss4564650322	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5159157749	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5159157750	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5159157751	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5159157752	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5159157753	Apr 26, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5254078952	Oct 12, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5254078953	Oct 12, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5254078954	Oct 12, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5254078955	Oct 12, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5254078956	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5453469824	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5453469825	Oct 12, 2022 (156)
49	HUGCELL_USP	ss5453469826	Oct 12, 2022 (156)
50	HUGCELL_USP	ss5453469827	Oct 12, 2022 (156)
51	TOMMO_GENOMICS	ss5690823378	Oct 12, 2022 (156)
52	TOMMO_GENOMICS	ss5690823379	Oct 12, 2022 (156)
53	TOMMO_GENOMICS	ss5690823380	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5690823381	Oct 12, 2022 (156)
55	TOMMO_GENOMICS	ss5690823383	Oct 12, 2022 (156)
56	EVA	ss5825751660	Oct 12, 2022 (156)
57	EVA	ss5825751661	Oct 12, 2022 (156)
58	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 8443367 (NC_000003.11:53357888::AA 812/3854) Row 8443368 (NC_000003.11:53357888::A 999/3854)	-	Oct 12, 2018 (152)
59	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 8443367 (NC_000003.11:53357888::AA 812/3854) Row 8443368 (NC_000003.11:53357888::A 999/3854)	-	Oct 12, 2018 (152)
60	The Danish reference pan genome	NC_000003.11 - 53357889	Apr 25, 2020 (154)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107787857 (NC_000003.12:53323861::A 6491/66198) Row 107787858 (NC_000003.12:53323861::AA 15881/66512) Row 107787859 (NC_000003.12:53323861::AAA 352/66686)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 17127056 (NC_000003.11:53357888::AA 616/16720) Row 17127057 (NC_000003.11:53357888:A: 40/16720) Row 17127058 (NC_000003.11:53357888::A 428/16720)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 17127056 (NC_000003.11:53357888::AA 616/16720) Row 17127057 (NC_000003.11:53357888:A: 40/16720) Row 17127058 (NC_000003.11:53357888::A 428/16720)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 17127056 (NC_000003.11:53357888::AA 616/16720) Row 17127057 (NC_000003.11:53357888:A: 40/16720) Row 17127058 (NC_000003.11:53357888::A 428/16720)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 17127056 (NC_000003.11:53357888::AA 616/16720) Row 17127057 (NC_000003.11:53357888:A: 40/16720) Row 17127058 (NC_000003.11:53357888::A 428/16720)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 17127056 (NC_000003.11:53357888::AA 616/16720) Row 17127057 (NC_000003.11:53357888:A: 40/16720) Row 17127058 (NC_000003.11:53357888::A 428/16720)...	-	Apr 26, 2021 (155)
79	14KJPN Submission ignored due to conflicting rows: Row 24660482 (NC_000003.12:53323861::A 637/28240) Row 24660483 (NC_000003.12:53323861::AA 1038/28240) Row 24660484 (NC_000003.12:53323861:A: 54/28240)...	-	Oct 12, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 24660482 (NC_000003.12:53323861::A 637/28240) Row 24660483 (NC_000003.12:53323861::AA 1038/28240) Row 24660484 (NC_000003.12:53323861:A: 54/28240)...	-	Oct 12, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 24660482 (NC_000003.12:53323861::A 637/28240) Row 24660483 (NC_000003.12:53323861::AA 1038/28240) Row 24660484 (NC_000003.12:53323861:A: 54/28240)...	-	Oct 12, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 24660482 (NC_000003.12:53323861::A 637/28240) Row 24660483 (NC_000003.12:53323861::AA 1038/28240) Row 24660484 (NC_000003.12:53323861:A: 54/28240)...	-	Oct 12, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 24660482 (NC_000003.12:53323861::A 637/28240) Row 24660483 (NC_000003.12:53323861::AA 1038/28240) Row 24660484 (NC_000003.12:53323861:A: 54/28240)...	-	Oct 12, 2022 (156)
84	TopMed	NC_000003.12 - 53323862	Apr 26, 2021 (155)
85	UK 10K study - Twins Submission ignored due to conflicting rows: Row 8443367 (NC_000003.11:53357888::AA 669/3708) Row 8443368 (NC_000003.11:53357888::A 999/3708)	-	Oct 12, 2018 (152)
86	UK 10K study - Twins Submission ignored due to conflicting rows: Row 8443367 (NC_000003.11:53357888::AA 669/3708) Row 8443368 (NC_000003.11:53357888::A 999/3708)	-	Oct 12, 2018 (152)
87	ALFA	NC_000003.12 - 53323862	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs398038701	Aug 21, 2014 (142)
rs67030736	May 11, 2012 (137)
rs67030737	Feb 26, 2009 (130)
rs67030738	Feb 26, 2009 (130)
rs71278603	May 11, 2012 (137)
rs148097516	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
402027877, ss4071118336, ss4564650322	NC_000003.12:53323861:AAAAAAAAAAA:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4071118335	NC_000003.12:53323861:AAAAAA:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4071118334	NC_000003.12:53323861:AAAAA:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5159157753	NC_000003.11:53357888:AAAA:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4071118333, ss5690823383	NC_000003.12:53323861:AAAA:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3709227144, ss4071118332	NC_000003.12:53323861:AAA:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4071118331	NC_000003.12:53323861:AA:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3709227143	NC_000003.12:53323862:AA:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5159157750	NC_000003.11:53357888:A:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4071118330, ss5254078956, ss5453469824, ss5690823380	NC_000003.12:53323861:A:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3709227142	NC_000003.12:53323863:A:	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss295100479	NC_000003.10:53332929::A	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss295100480	NC_000003.10:53332949::A	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
825113, ss1575939726, ss1703626747, ss1703626871, ss2992311446, ss3827807147, ss5159157751	NC_000003.11:53357888::A	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3647402832, ss3842751084, ss4071118323, ss5254078952, ss5453469825, ss5690823378	NC_000003.12:53323861::A	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709227141	NC_000003.12:53323864::A	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss42031006	NT_022517.18:53297888::A	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss95946874	NT_022517.18:53297909::A	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss666206576, ss947086961, ss1703626746, ss1703626868, ss2992311445, ss5159157749, ss5825751660	NC_000003.11:53357888::AA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071118324, ss5254078953, ss5453469826, ss5690823379	NC_000003.12:53323861::AA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709227140	NC_000003.12:53323864::AA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5159157752, ss5825751661	NC_000003.11:53357888::AAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071118325, ss5254078955, ss5453469827, ss5690823381	NC_000003.12:53323861::AAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709227139	NC_000003.12:53323864::AAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071118326, ss5254078954	NC_000003.12:53323861::AAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071118327	NC_000003.12:53323861::AAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071118328	NC_000003.12:53323861::AAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12203376003	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53323861:AAAAAAAAAAAA… NC_000003.12:53323861:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

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

No publications for rs11451581

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

rs11451581