Name: rs1211486616
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.

rs1211486616

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:53315535-53315557 (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)₁₅ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₅ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₉
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₅=0.0000 (0/3576, ALFA)
del(A)₁₃=0.0000 (0/3576, ALFA)
del(A)₁₂=0.0000 (0/3576, ALFA) (+ 12 more)
del(A)₁₁=0.0000 (0/3576, ALFA)
del(A)₉=0.0000 (0/3576, ALFA)
del(A)₈=0.0000 (0/3576, ALFA)
del(A)₇=0.0000 (0/3576, ALFA)
del(A)₆=0.0000 (0/3576, ALFA)
delAAA=0.0000 (0/3576, ALFA)
delAA=0.0000 (0/3576, ALFA)
delA=0.0000 (0/3576, ALFA)
dupA=0.0000 (0/3576, ALFA)
dupAA=0.0000 (0/3576, ALFA)
dupAAA=0.0000 (0/3576, ALFA)
dup(A)₅=0.0000 (0/3576, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DCP1A : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	3576	AAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1796	AAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1416	AAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	62	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1354	AAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	34	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	28	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	44	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	112	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	40	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	134	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	3576	(A)₂₃=1.0000	del(A)₁₅=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	1796	(A)₂₃=1.0000	del(A)₁₅=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	1416	(A)₂₃=1.0000	del(A)₁₅=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	Other	Sub	134	(A)₂₃=1.000	del(A)₁₅=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	112	(A)₂₃=1.000	del(A)₁₅=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	44	(A)₂₃=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	40	(A)₂₃=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	34	(A)₂₃=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=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.53315543_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315545_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315546_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315547_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315549_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315550_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315551_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315552_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315553_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315554_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315555_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315556_53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315557del
GRCh38.p14 chr 3	NC_000003.12:g.53315557dup
GRCh38.p14 chr 3	NC_000003.12:g.53315556_53315557dup
GRCh38.p14 chr 3	NC_000003.12:g.53315555_53315557dup
GRCh38.p14 chr 3	NC_000003.12:g.53315554_53315557dup
GRCh38.p14 chr 3	NC_000003.12:g.53315553_53315557dup
GRCh38.p14 chr 3	NC_000003.12:g.53315552_53315557dup
GRCh38.p14 chr 3	NC_000003.12:g.53315551_53315557dup
GRCh38.p14 chr 3	NC_000003.12:g.53315549_53315557dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164498_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164500_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164501_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164502_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164504_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164505_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164506_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164507_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164508_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164509_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164510_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164511_164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164512del
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164512dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164511_164512dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164510_164512dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164509_164512dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164508_164512dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164507_164512dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164506_164512dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164504_164512dup
GRCh37.p13 chr 3	NC_000003.11:g.53349572_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349574_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349575_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349576_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349578_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349579_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349580_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349581_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349582_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349583_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349584_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349585_53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349586del
GRCh37.p13 chr 3	NC_000003.11:g.53349586dup
GRCh37.p13 chr 3	NC_000003.11:g.53349585_53349586dup
GRCh37.p13 chr 3	NC_000003.11:g.53349584_53349586dup
GRCh37.p13 chr 3	NC_000003.11:g.53349583_53349586dup
GRCh37.p13 chr 3	NC_000003.11:g.53349582_53349586dup
GRCh37.p13 chr 3	NC_000003.11:g.53349581_53349586dup
GRCh37.p13 chr 3	NC_000003.11:g.53349580_53349586dup
GRCh37.p13 chr 3	NC_000003.11:g.53349578_53349586dup

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

Molecule type	Change	Amino acid[Codon]	SO Term
DCP1A transcript variant 2	NM_001290204.2:c.372-3170… NM_001290204.2:c.372-3170_372-3156del	N/A	Intron Variant
DCP1A transcript variant 3	NM_001290205.2:c.156-3170… NM_001290205.2:c.156-3170_156-3156del	N/A	Intron Variant
DCP1A transcript variant 4	NM_001290206.2:c.9-3170_9… NM_001290206.2:c.9-3170_9-3156del	N/A	Intron Variant
DCP1A transcript variant 5	NM_001290207.2:c.9-3170_9… NM_001290207.2:c.9-3170_9-3156del	N/A	Intron Variant
DCP1A transcript variant 1	NM_018403.7:c.372-3170_37… NM_018403.7:c.372-3170_372-3156del	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)₂₃=	del(A)₁₅	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₉
GRCh38.p14 chr 3	NC_000003.12:g.53315535_53315557=	NC_000003.12:g.53315543_53315557del	NC_000003.12:g.53315545_53315557del	NC_000003.12:g.53315546_53315557del	NC_000003.12:g.53315547_53315557del	NC_000003.12:g.53315549_53315557del	NC_000003.12:g.53315550_53315557del	NC_000003.12:g.53315551_53315557del	NC_000003.12:g.53315552_53315557del	NC_000003.12:g.53315553_53315557del	NC_000003.12:g.53315554_53315557del	NC_000003.12:g.53315555_53315557del	NC_000003.12:g.53315556_53315557del	NC_000003.12:g.53315557del	NC_000003.12:g.53315557dup	NC_000003.12:g.53315556_53315557dup	NC_000003.12:g.53315555_53315557dup	NC_000003.12:g.53315554_53315557dup	NC_000003.12:g.53315553_53315557dup	NC_000003.12:g.53315552_53315557dup	NC_000003.12:g.53315551_53315557dup	NC_000003.12:g.53315549_53315557dup
GRCh37.p13 chr 3 fix patch HG957_PATCH	NW_004775426.1:g.164490_164512=	NW_004775426.1:g.164498_164512del	NW_004775426.1:g.164500_164512del	NW_004775426.1:g.164501_164512del	NW_004775426.1:g.164502_164512del	NW_004775426.1:g.164504_164512del	NW_004775426.1:g.164505_164512del	NW_004775426.1:g.164506_164512del	NW_004775426.1:g.164507_164512del	NW_004775426.1:g.164508_164512del	NW_004775426.1:g.164509_164512del	NW_004775426.1:g.164510_164512del	NW_004775426.1:g.164511_164512del	NW_004775426.1:g.164512del	NW_004775426.1:g.164512dup	NW_004775426.1:g.164511_164512dup	NW_004775426.1:g.164510_164512dup	NW_004775426.1:g.164509_164512dup	NW_004775426.1:g.164508_164512dup	NW_004775426.1:g.164507_164512dup	NW_004775426.1:g.164506_164512dup	NW_004775426.1:g.164504_164512dup
GRCh37.p13 chr 3	NC_000003.11:g.53349564_53349586=	NC_000003.11:g.53349572_53349586del	NC_000003.11:g.53349574_53349586del	NC_000003.11:g.53349575_53349586del	NC_000003.11:g.53349576_53349586del	NC_000003.11:g.53349578_53349586del	NC_000003.11:g.53349579_53349586del	NC_000003.11:g.53349580_53349586del	NC_000003.11:g.53349581_53349586del	NC_000003.11:g.53349582_53349586del	NC_000003.11:g.53349583_53349586del	NC_000003.11:g.53349584_53349586del	NC_000003.11:g.53349585_53349586del	NC_000003.11:g.53349586del	NC_000003.11:g.53349586dup	NC_000003.11:g.53349585_53349586dup	NC_000003.11:g.53349584_53349586dup	NC_000003.11:g.53349583_53349586dup	NC_000003.11:g.53349582_53349586dup	NC_000003.11:g.53349581_53349586dup	NC_000003.11:g.53349580_53349586dup	NC_000003.11:g.53349578_53349586dup
DCP1A transcript variant 2	NM_001290204.2:c.372-3156=	NM_001290204.2:c.372-3170_372-3156del	NM_001290204.2:c.372-3168_372-3156del	NM_001290204.2:c.372-3167_372-3156del	NM_001290204.2:c.372-3166_372-3156del	NM_001290204.2:c.372-3164_372-3156del	NM_001290204.2:c.372-3163_372-3156del	NM_001290204.2:c.372-3162_372-3156del	NM_001290204.2:c.372-3161_372-3156del	NM_001290204.2:c.372-3160_372-3156del	NM_001290204.2:c.372-3159_372-3156del	NM_001290204.2:c.372-3158_372-3156del	NM_001290204.2:c.372-3157_372-3156del	NM_001290204.2:c.372-3156del	NM_001290204.2:c.372-3156dup	NM_001290204.2:c.372-3157_372-3156dup	NM_001290204.2:c.372-3158_372-3156dup	NM_001290204.2:c.372-3159_372-3156dup	NM_001290204.2:c.372-3160_372-3156dup	NM_001290204.2:c.372-3161_372-3156dup	NM_001290204.2:c.372-3162_372-3156dup	NM_001290204.2:c.372-3164_372-3156dup
DCP1A transcript variant 3	NM_001290205.2:c.156-3156=	NM_001290205.2:c.156-3170_156-3156del	NM_001290205.2:c.156-3168_156-3156del	NM_001290205.2:c.156-3167_156-3156del	NM_001290205.2:c.156-3166_156-3156del	NM_001290205.2:c.156-3164_156-3156del	NM_001290205.2:c.156-3163_156-3156del	NM_001290205.2:c.156-3162_156-3156del	NM_001290205.2:c.156-3161_156-3156del	NM_001290205.2:c.156-3160_156-3156del	NM_001290205.2:c.156-3159_156-3156del	NM_001290205.2:c.156-3158_156-3156del	NM_001290205.2:c.156-3157_156-3156del	NM_001290205.2:c.156-3156del	NM_001290205.2:c.156-3156dup	NM_001290205.2:c.156-3157_156-3156dup	NM_001290205.2:c.156-3158_156-3156dup	NM_001290205.2:c.156-3159_156-3156dup	NM_001290205.2:c.156-3160_156-3156dup	NM_001290205.2:c.156-3161_156-3156dup	NM_001290205.2:c.156-3162_156-3156dup	NM_001290205.2:c.156-3164_156-3156dup
DCP1A transcript variant 4	NM_001290206.2:c.9-3156=	NM_001290206.2:c.9-3170_9-3156del	NM_001290206.2:c.9-3168_9-3156del	NM_001290206.2:c.9-3167_9-3156del	NM_001290206.2:c.9-3166_9-3156del	NM_001290206.2:c.9-3164_9-3156del	NM_001290206.2:c.9-3163_9-3156del	NM_001290206.2:c.9-3162_9-3156del	NM_001290206.2:c.9-3161_9-3156del	NM_001290206.2:c.9-3160_9-3156del	NM_001290206.2:c.9-3159_9-3156del	NM_001290206.2:c.9-3158_9-3156del	NM_001290206.2:c.9-3157_9-3156del	NM_001290206.2:c.9-3156del	NM_001290206.2:c.9-3156dup	NM_001290206.2:c.9-3157_9-3156dup	NM_001290206.2:c.9-3158_9-3156dup	NM_001290206.2:c.9-3159_9-3156dup	NM_001290206.2:c.9-3160_9-3156dup	NM_001290206.2:c.9-3161_9-3156dup	NM_001290206.2:c.9-3162_9-3156dup	NM_001290206.2:c.9-3164_9-3156dup
DCP1A transcript variant 5	NM_001290207.2:c.9-3156=	NM_001290207.2:c.9-3170_9-3156del	NM_001290207.2:c.9-3168_9-3156del	NM_001290207.2:c.9-3167_9-3156del	NM_001290207.2:c.9-3166_9-3156del	NM_001290207.2:c.9-3164_9-3156del	NM_001290207.2:c.9-3163_9-3156del	NM_001290207.2:c.9-3162_9-3156del	NM_001290207.2:c.9-3161_9-3156del	NM_001290207.2:c.9-3160_9-3156del	NM_001290207.2:c.9-3159_9-3156del	NM_001290207.2:c.9-3158_9-3156del	NM_001290207.2:c.9-3157_9-3156del	NM_001290207.2:c.9-3156del	NM_001290207.2:c.9-3156dup	NM_001290207.2:c.9-3157_9-3156dup	NM_001290207.2:c.9-3158_9-3156dup	NM_001290207.2:c.9-3159_9-3156dup	NM_001290207.2:c.9-3160_9-3156dup	NM_001290207.2:c.9-3161_9-3156dup	NM_001290207.2:c.9-3162_9-3156dup	NM_001290207.2:c.9-3164_9-3156dup
DCP1A transcript	NM_018403.5:c.372-3155=	NM_018403.5:c.372-3169_372-3155del	NM_018403.5:c.372-3167_372-3155del	NM_018403.5:c.372-3166_372-3155del	NM_018403.5:c.372-3165_372-3155del	NM_018403.5:c.372-3163_372-3155del	NM_018403.5:c.372-3162_372-3155del	NM_018403.5:c.372-3161_372-3155del	NM_018403.5:c.372-3160_372-3155del	NM_018403.5:c.372-3159_372-3155del	NM_018403.5:c.372-3158_372-3155del	NM_018403.5:c.372-3157_372-3155del	NM_018403.5:c.372-3156_372-3155del	NM_018403.5:c.372-3155del	NM_018403.5:c.372-3155dup	NM_018403.5:c.372-3156_372-3155dup	NM_018403.5:c.372-3157_372-3155dup	NM_018403.5:c.372-3158_372-3155dup	NM_018403.5:c.372-3159_372-3155dup	NM_018403.5:c.372-3160_372-3155dup	NM_018403.5:c.372-3161_372-3155dup	NM_018403.5:c.372-3163_372-3155dup
DCP1A transcript variant 1	NM_018403.7:c.372-3156=	NM_018403.7:c.372-3170_372-3156del	NM_018403.7:c.372-3168_372-3156del	NM_018403.7:c.372-3167_372-3156del	NM_018403.7:c.372-3166_372-3156del	NM_018403.7:c.372-3164_372-3156del	NM_018403.7:c.372-3163_372-3156del	NM_018403.7:c.372-3162_372-3156del	NM_018403.7:c.372-3161_372-3156del	NM_018403.7:c.372-3160_372-3156del	NM_018403.7:c.372-3159_372-3156del	NM_018403.7:c.372-3158_372-3156del	NM_018403.7:c.372-3157_372-3156del	NM_018403.7:c.372-3156del	NM_018403.7:c.372-3156dup	NM_018403.7:c.372-3157_372-3156dup	NM_018403.7:c.372-3158_372-3156dup	NM_018403.7:c.372-3159_372-3156dup	NM_018403.7:c.372-3160_372-3156dup	NM_018403.7:c.372-3161_372-3156dup	NM_018403.7:c.372-3162_372-3156dup	NM_018403.7:c.372-3164_372-3156dup
DCP1A transcript variant X1	XM_005265320.1:c.372-3155=	XM_005265320.1:c.372-3169_372-3155del	XM_005265320.1:c.372-3167_372-3155del	XM_005265320.1:c.372-3166_372-3155del	XM_005265320.1:c.372-3165_372-3155del	XM_005265320.1:c.372-3163_372-3155del	XM_005265320.1:c.372-3162_372-3155del	XM_005265320.1:c.372-3161_372-3155del	XM_005265320.1:c.372-3160_372-3155del	XM_005265320.1:c.372-3159_372-3155del	XM_005265320.1:c.372-3158_372-3155del	XM_005265320.1:c.372-3157_372-3155del	XM_005265320.1:c.372-3156_372-3155del	XM_005265320.1:c.372-3155del	XM_005265320.1:c.372-3155dup	XM_005265320.1:c.372-3156_372-3155dup	XM_005265320.1:c.372-3157_372-3155dup	XM_005265320.1:c.372-3158_372-3155dup	XM_005265320.1:c.372-3159_372-3155dup	XM_005265320.1:c.372-3160_372-3155dup	XM_005265320.1:c.372-3161_372-3155dup	XM_005265320.1:c.372-3163_372-3155dup
DCP1A transcript variant X1	XM_005278358.1:c.372-3156=	XM_005278358.1:c.372-3170_372-3156del	XM_005278358.1:c.372-3168_372-3156del	XM_005278358.1:c.372-3167_372-3156del	XM_005278358.1:c.372-3166_372-3156del	XM_005278358.1:c.372-3164_372-3156del	XM_005278358.1:c.372-3163_372-3156del	XM_005278358.1:c.372-3162_372-3156del	XM_005278358.1:c.372-3161_372-3156del	XM_005278358.1:c.372-3160_372-3156del	XM_005278358.1:c.372-3159_372-3156del	XM_005278358.1:c.372-3158_372-3156del	XM_005278358.1:c.372-3157_372-3156del	XM_005278358.1:c.372-3156del	XM_005278358.1:c.372-3156dup	XM_005278358.1:c.372-3157_372-3156dup	XM_005278358.1:c.372-3158_372-3156dup	XM_005278358.1:c.372-3159_372-3156dup	XM_005278358.1:c.372-3160_372-3156dup	XM_005278358.1:c.372-3161_372-3156dup	XM_005278358.1:c.372-3162_372-3156dup	XM_005278358.1:c.372-3164_372-3156dup
DCP1A transcript variant X2	XM_005278359.1:c.9-3156=	XM_005278359.1:c.9-3170_9-3156del	XM_005278359.1:c.9-3168_9-3156del	XM_005278359.1:c.9-3167_9-3156del	XM_005278359.1:c.9-3166_9-3156del	XM_005278359.1:c.9-3164_9-3156del	XM_005278359.1:c.9-3163_9-3156del	XM_005278359.1:c.9-3162_9-3156del	XM_005278359.1:c.9-3161_9-3156del	XM_005278359.1:c.9-3160_9-3156del	XM_005278359.1:c.9-3159_9-3156del	XM_005278359.1:c.9-3158_9-3156del	XM_005278359.1:c.9-3157_9-3156del	XM_005278359.1:c.9-3156del	XM_005278359.1:c.9-3156dup	XM_005278359.1:c.9-3157_9-3156dup	XM_005278359.1:c.9-3158_9-3156dup	XM_005278359.1:c.9-3159_9-3156dup	XM_005278359.1:c.9-3160_9-3156dup	XM_005278359.1:c.9-3161_9-3156dup	XM_005278359.1:c.9-3162_9-3156dup	XM_005278359.1:c.9-3164_9-3156dup
DCP1A transcript variant X3	XM_005278360.1:c.9-3156=	XM_005278360.1:c.9-3170_9-3156del	XM_005278360.1:c.9-3168_9-3156del	XM_005278360.1:c.9-3167_9-3156del	XM_005278360.1:c.9-3166_9-3156del	XM_005278360.1:c.9-3164_9-3156del	XM_005278360.1:c.9-3163_9-3156del	XM_005278360.1:c.9-3162_9-3156del	XM_005278360.1:c.9-3161_9-3156del	XM_005278360.1:c.9-3160_9-3156del	XM_005278360.1:c.9-3159_9-3156del	XM_005278360.1:c.9-3158_9-3156del	XM_005278360.1:c.9-3157_9-3156del	XM_005278360.1:c.9-3156del	XM_005278360.1:c.9-3156dup	XM_005278360.1:c.9-3157_9-3156dup	XM_005278360.1:c.9-3158_9-3156dup	XM_005278360.1:c.9-3159_9-3156dup	XM_005278360.1:c.9-3160_9-3156dup	XM_005278360.1:c.9-3161_9-3156dup	XM_005278360.1:c.9-3162_9-3156dup	XM_005278360.1:c.9-3164_9-3156dup

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#.

44 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3709227022	Jul 13, 2019 (153)
2	EVA_DECODE	ss3709227023	Jul 13, 2019 (153)
3	EVA_DECODE	ss3709227024	Jul 13, 2019 (153)
4	EVA_DECODE	ss3709227025	Jul 13, 2019 (153)
5	EVA_DECODE	ss3709227026	Jul 13, 2019 (153)
6	EVA_DECODE	ss3709227027	Jul 13, 2019 (153)
7	EVA	ss3827807129	Apr 25, 2020 (154)
8	GNOMAD	ss4071116446	Apr 26, 2021 (155)
9	GNOMAD	ss4071116447	Apr 26, 2021 (155)
10	GNOMAD	ss4071116448	Apr 26, 2021 (155)
11	GNOMAD	ss4071116449	Apr 26, 2021 (155)
12	GNOMAD	ss4071116450	Apr 26, 2021 (155)
13	GNOMAD	ss4071116451	Apr 26, 2021 (155)
14	GNOMAD	ss4071116452	Apr 26, 2021 (155)
15	GNOMAD	ss4071116453	Apr 26, 2021 (155)
16	GNOMAD	ss4071116454	Apr 26, 2021 (155)
17	GNOMAD	ss4071116455	Apr 26, 2021 (155)
18	GNOMAD	ss4071116456	Apr 26, 2021 (155)
19	GNOMAD	ss4071116457	Apr 26, 2021 (155)
20	GNOMAD	ss4071116458	Apr 26, 2021 (155)
21	GNOMAD	ss4071116459	Apr 26, 2021 (155)
22	GNOMAD	ss4071116460	Apr 26, 2021 (155)
23	GNOMAD	ss4071116461	Apr 26, 2021 (155)
24	GNOMAD	ss4071116462	Apr 26, 2021 (155)
25	GNOMAD	ss4071116463	Apr 26, 2021 (155)
26	GNOMAD	ss4071116464	Apr 26, 2021 (155)
27	GNOMAD	ss4071116465	Apr 26, 2021 (155)
28	GNOMAD	ss4071116466	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5159157469	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5159157470	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5159157471	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5159157472	Apr 26, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5254078746	Oct 12, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5254078747	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5254078748	Oct 12, 2022 (156)
36	HUGCELL_USP	ss5453469633	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5453469634	Oct 12, 2022 (156)
38	HUGCELL_USP	ss5453469635	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5453469636	Oct 12, 2022 (156)
40	HUGCELL_USP	ss5453469637	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5690823007	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5690823008	Oct 12, 2022 (156)
43	TOMMO_GENOMICS	ss5690823009	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5690823010	Oct 12, 2022 (156)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107785979 (NC_000003.12:53315534::A 11129/60746) Row 107785980 (NC_000003.12:53315534::AA 1316/59942) Row 107785981 (NC_000003.12:53315534::AAA 183/60880)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 17126776 (NC_000003.11:53349563:A: 3278/16482) Row 17126777 (NC_000003.11:53349563::A 1040/16482) Row 17126778 (NC_000003.11:53349563::AA 64/16482)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 17126776 (NC_000003.11:53349563:A: 3278/16482) Row 17126777 (NC_000003.11:53349563::A 1040/16482) Row 17126778 (NC_000003.11:53349563::AA 64/16482)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 17126776 (NC_000003.11:53349563:A: 3278/16482) Row 17126777 (NC_000003.11:53349563::A 1040/16482) Row 17126778 (NC_000003.11:53349563::AA 64/16482)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 17126776 (NC_000003.11:53349563:A: 3278/16482) Row 17126777 (NC_000003.11:53349563::A 1040/16482) Row 17126778 (NC_000003.11:53349563::AA 64/16482)...	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 24660111 (NC_000003.12:53315534:A: 6498/28112) Row 24660112 (NC_000003.12:53315534::A 1767/28112) Row 24660113 (NC_000003.12:53315534::AA 96/28112)...	-	Oct 12, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 24660111 (NC_000003.12:53315534:A: 6498/28112) Row 24660112 (NC_000003.12:53315534::A 1767/28112) Row 24660113 (NC_000003.12:53315534::AA 96/28112)...	-	Oct 12, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 24660111 (NC_000003.12:53315534:A: 6498/28112) Row 24660112 (NC_000003.12:53315534::A 1767/28112) Row 24660113 (NC_000003.12:53315534::AA 96/28112)...	-	Oct 12, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 24660111 (NC_000003.12:53315534:A: 6498/28112) Row 24660112 (NC_000003.12:53315534::A 1767/28112) Row 24660113 (NC_000003.12:53315534::AA 96/28112)...	-	Oct 12, 2022 (156)
74	ALFA	NC_000003.12 - 53315535	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
ss4071116466	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4071116465	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4071116464	NC_000003.12:53315534:AAAAAAAAAAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4071116463	NC_000003.12:53315534:AAAAAAAAAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4071116462	NC_000003.12:53315534:AAAAAAAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4071116461	NC_000003.12:53315534:AAAAAAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3709227027, ss4071116460, ss5254078748, ss5453469637	NC_000003.12:53315534:AAAAAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4071116459	NC_000003.12:53315534:AAAAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4071116458	NC_000003.12:53315534:AAAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4071116457	NC_000003.12:53315534:AAAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4071116456	NC_000003.12:53315534:AAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3709227026	NC_000003.12:53315538:AAA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5159157472	NC_000003.11:53349563:AA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116455, ss5254078747, ss5453469635, ss5690823010	NC_000003.12:53315534:AA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3709227025	NC_000003.12:53315539:AA:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5159157469	NC_000003.11:53349563:A:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116454, ss5453469636, ss5690823007	NC_000003.12:53315534:A:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709227024	NC_000003.12:53315540:A:	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5159157470	NC_000003.11:53349563::A	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116446, ss5453469634, ss5690823008	NC_000003.12:53315534::A	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709227023	NC_000003.12:53315541::A	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3827807129, ss5159157471	NC_000003.11:53349563::AA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116447, ss5254078746, ss5453469633, ss5690823009	NC_000003.12:53315534::AA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709227022	NC_000003.12:53315541::AA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116448	NC_000003.12:53315534::AAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116449	NC_000003.12:53315534::AAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116450	NC_000003.12:53315534::AAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
1744786372	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116451	NC_000003.12:53315534::AAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116452	NC_000003.12:53315534::AAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4071116453	NC_000003.12:53315534::AAAAAAAAA	NC_000003.12:53315534:AAAAAAAAAAAA… NC_000003.12:53315534:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs1211486616

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

rs1211486616