Name: rs61176259
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.

rs61176259

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:2968989-2969009 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₈ / del(T)₆ / del(T)₅ / delT…
del(T)₈ / del(T)₆ / del(T)₅ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₈
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₈=0.0000 (0/3388, ALFA)
del(T)₆=0.0000 (0/3388, ALFA)
del(T)₅=0.0000 (0/3388, ALFA) (+ 7 more)
delTTT=0.0000 (0/3388, ALFA)
delTT=0.0000 (0/3388, ALFA)
delT=0.0000 (0/3388, ALFA)
dupT=0.0000 (0/3388, ALFA)
dupTT=0.0000 (0/3388, ALFA)
dupTTT=0.0000 (0/3388, ALFA)
delT=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NAP1L4 : 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	3388	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	2508	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	338	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
African Others	Sub	12	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	326	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Asian	Sub	64	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	46	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	48	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	264	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	144	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=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	3388	(T)₂₁=1.0000	del(T)₈=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	2508	(T)₂₁=1.0000	del(T)₈=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	338	(T)₂₁=1.000	del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	264	(T)₂₁=1.000	del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	144	(T)₂₁=1.000	del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	64	(T)₂₁=1.00	del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	48	(T)₂₁=1.00	del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(T)₂₁=1.00	del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
The Danish reference pan genome	Danish	Study-wide	40	(T)₂₁=0.62	delT=0.38

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 11	NC_000011.10:g.2969002_2969009del
GRCh38.p14 chr 11	NC_000011.10:g.2969004_2969009del
GRCh38.p14 chr 11	NC_000011.10:g.2969005_2969009del
GRCh38.p14 chr 11	NC_000011.10:g.2969007_2969009del
GRCh38.p14 chr 11	NC_000011.10:g.2969008_2969009del
GRCh38.p14 chr 11	NC_000011.10:g.2969009del
GRCh38.p14 chr 11	NC_000011.10:g.2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2969008_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2969007_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2969006_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2969005_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2969004_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2969003_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2969002_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2969000_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2968999_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2968995_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2968994_2969009dup
GRCh38.p14 chr 11	NC_000011.10:g.2968992_2969009dup
GRCh37.p13 chr 11	NC_000011.9:g.2990232_2990239del
GRCh37.p13 chr 11	NC_000011.9:g.2990234_2990239del
GRCh37.p13 chr 11	NC_000011.9:g.2990235_2990239del
GRCh37.p13 chr 11	NC_000011.9:g.2990237_2990239del
GRCh37.p13 chr 11	NC_000011.9:g.2990238_2990239del
GRCh37.p13 chr 11	NC_000011.9:g.2990239del
GRCh37.p13 chr 11	NC_000011.9:g.2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990238_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990237_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990236_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990235_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990234_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990233_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990232_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990230_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990229_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990225_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990224_2990239dup
GRCh37.p13 chr 11	NC_000011.9:g.2990222_2990239dup

Gene: NAP1L4, nucleosome assembly protein 1 like 4 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NAP1L4 transcript variant 2	NM_001369375.1:c.534+807_… NM_001369375.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 3	NM_001369376.1:c.534+807_… NM_001369376.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 4	NM_001369377.1:c.534+807_… NM_001369377.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 5	NM_001369378.1:c.534+807_… NM_001369378.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 6	NM_001369379.1:c.534+807_… NM_001369379.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 7	NM_001369380.1:c.534+807_… NM_001369380.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 8	NM_001369381.1:c.534+807_… NM_001369381.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 9	NM_001369382.1:c.534+807_… NM_001369382.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 10	NM_001369383.1:c.534+807_… NM_001369383.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 11	NM_001369384.1:c.534+807_… NM_001369384.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 12	NM_001369385.1:c.534+807_… NM_001369385.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 13	NM_001369386.1:c.534+807_… NM_001369386.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 14	NM_001369388.1:c.534+807_… NM_001369388.1:c.534+807_534+814del	N/A	Intron Variant
NAP1L4 transcript variant 1	NM_005969.4:c.534+807_534… NM_005969.4:c.534+807_534+814del	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	(T)₂₁=	del(T)₈	del(T)₆	del(T)₅	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₁₀	dup(T)₁₁	dup(T)₁₅	dup(T)₁₆	dup(T)₁₈
GRCh38.p14 chr 11	NC_000011.10:g.2968989_2969009=	NC_000011.10:g.2969002_2969009del	NC_000011.10:g.2969004_2969009del	NC_000011.10:g.2969005_2969009del	NC_000011.10:g.2969007_2969009del	NC_000011.10:g.2969008_2969009del	NC_000011.10:g.2969009del	NC_000011.10:g.2969009dup	NC_000011.10:g.2969008_2969009dup	NC_000011.10:g.2969007_2969009dup	NC_000011.10:g.2969006_2969009dup	NC_000011.10:g.2969005_2969009dup	NC_000011.10:g.2969004_2969009dup	NC_000011.10:g.2969003_2969009dup	NC_000011.10:g.2969002_2969009dup	NC_000011.10:g.2969000_2969009dup	NC_000011.10:g.2968999_2969009dup	NC_000011.10:g.2968995_2969009dup	NC_000011.10:g.2968994_2969009dup	NC_000011.10:g.2968992_2969009dup
GRCh37.p13 chr 11	NC_000011.9:g.2990219_2990239=	NC_000011.9:g.2990232_2990239del	NC_000011.9:g.2990234_2990239del	NC_000011.9:g.2990235_2990239del	NC_000011.9:g.2990237_2990239del	NC_000011.9:g.2990238_2990239del	NC_000011.9:g.2990239del	NC_000011.9:g.2990239dup	NC_000011.9:g.2990238_2990239dup	NC_000011.9:g.2990237_2990239dup	NC_000011.9:g.2990236_2990239dup	NC_000011.9:g.2990235_2990239dup	NC_000011.9:g.2990234_2990239dup	NC_000011.9:g.2990233_2990239dup	NC_000011.9:g.2990232_2990239dup	NC_000011.9:g.2990230_2990239dup	NC_000011.9:g.2990229_2990239dup	NC_000011.9:g.2990225_2990239dup	NC_000011.9:g.2990224_2990239dup	NC_000011.9:g.2990222_2990239dup
NAP1L4 transcript variant 2	NM_001369375.1:c.534+814=	NM_001369375.1:c.534+807_534+814del	NM_001369375.1:c.534+809_534+814del	NM_001369375.1:c.534+810_534+814del	NM_001369375.1:c.534+812_534+814del	NM_001369375.1:c.534+813_534+814del	NM_001369375.1:c.534+814del	NM_001369375.1:c.534+814dup	NM_001369375.1:c.534+813_534+814dup	NM_001369375.1:c.534+812_534+814dup	NM_001369375.1:c.534+811_534+814dup	NM_001369375.1:c.534+810_534+814dup	NM_001369375.1:c.534+809_534+814dup	NM_001369375.1:c.534+808_534+814dup	NM_001369375.1:c.534+807_534+814dup	NM_001369375.1:c.534+805_534+814dup	NM_001369375.1:c.534+804_534+814dup	NM_001369375.1:c.534+800_534+814dup	NM_001369375.1:c.534+799_534+814dup	NM_001369375.1:c.534+797_534+814dup
NAP1L4 transcript variant 3	NM_001369376.1:c.534+814=	NM_001369376.1:c.534+807_534+814del	NM_001369376.1:c.534+809_534+814del	NM_001369376.1:c.534+810_534+814del	NM_001369376.1:c.534+812_534+814del	NM_001369376.1:c.534+813_534+814del	NM_001369376.1:c.534+814del	NM_001369376.1:c.534+814dup	NM_001369376.1:c.534+813_534+814dup	NM_001369376.1:c.534+812_534+814dup	NM_001369376.1:c.534+811_534+814dup	NM_001369376.1:c.534+810_534+814dup	NM_001369376.1:c.534+809_534+814dup	NM_001369376.1:c.534+808_534+814dup	NM_001369376.1:c.534+807_534+814dup	NM_001369376.1:c.534+805_534+814dup	NM_001369376.1:c.534+804_534+814dup	NM_001369376.1:c.534+800_534+814dup	NM_001369376.1:c.534+799_534+814dup	NM_001369376.1:c.534+797_534+814dup
NAP1L4 transcript variant 4	NM_001369377.1:c.534+814=	NM_001369377.1:c.534+807_534+814del	NM_001369377.1:c.534+809_534+814del	NM_001369377.1:c.534+810_534+814del	NM_001369377.1:c.534+812_534+814del	NM_001369377.1:c.534+813_534+814del	NM_001369377.1:c.534+814del	NM_001369377.1:c.534+814dup	NM_001369377.1:c.534+813_534+814dup	NM_001369377.1:c.534+812_534+814dup	NM_001369377.1:c.534+811_534+814dup	NM_001369377.1:c.534+810_534+814dup	NM_001369377.1:c.534+809_534+814dup	NM_001369377.1:c.534+808_534+814dup	NM_001369377.1:c.534+807_534+814dup	NM_001369377.1:c.534+805_534+814dup	NM_001369377.1:c.534+804_534+814dup	NM_001369377.1:c.534+800_534+814dup	NM_001369377.1:c.534+799_534+814dup	NM_001369377.1:c.534+797_534+814dup
NAP1L4 transcript variant 5	NM_001369378.1:c.534+814=	NM_001369378.1:c.534+807_534+814del	NM_001369378.1:c.534+809_534+814del	NM_001369378.1:c.534+810_534+814del	NM_001369378.1:c.534+812_534+814del	NM_001369378.1:c.534+813_534+814del	NM_001369378.1:c.534+814del	NM_001369378.1:c.534+814dup	NM_001369378.1:c.534+813_534+814dup	NM_001369378.1:c.534+812_534+814dup	NM_001369378.1:c.534+811_534+814dup	NM_001369378.1:c.534+810_534+814dup	NM_001369378.1:c.534+809_534+814dup	NM_001369378.1:c.534+808_534+814dup	NM_001369378.1:c.534+807_534+814dup	NM_001369378.1:c.534+805_534+814dup	NM_001369378.1:c.534+804_534+814dup	NM_001369378.1:c.534+800_534+814dup	NM_001369378.1:c.534+799_534+814dup	NM_001369378.1:c.534+797_534+814dup
NAP1L4 transcript variant 6	NM_001369379.1:c.534+814=	NM_001369379.1:c.534+807_534+814del	NM_001369379.1:c.534+809_534+814del	NM_001369379.1:c.534+810_534+814del	NM_001369379.1:c.534+812_534+814del	NM_001369379.1:c.534+813_534+814del	NM_001369379.1:c.534+814del	NM_001369379.1:c.534+814dup	NM_001369379.1:c.534+813_534+814dup	NM_001369379.1:c.534+812_534+814dup	NM_001369379.1:c.534+811_534+814dup	NM_001369379.1:c.534+810_534+814dup	NM_001369379.1:c.534+809_534+814dup	NM_001369379.1:c.534+808_534+814dup	NM_001369379.1:c.534+807_534+814dup	NM_001369379.1:c.534+805_534+814dup	NM_001369379.1:c.534+804_534+814dup	NM_001369379.1:c.534+800_534+814dup	NM_001369379.1:c.534+799_534+814dup	NM_001369379.1:c.534+797_534+814dup
NAP1L4 transcript variant 7	NM_001369380.1:c.534+814=	NM_001369380.1:c.534+807_534+814del	NM_001369380.1:c.534+809_534+814del	NM_001369380.1:c.534+810_534+814del	NM_001369380.1:c.534+812_534+814del	NM_001369380.1:c.534+813_534+814del	NM_001369380.1:c.534+814del	NM_001369380.1:c.534+814dup	NM_001369380.1:c.534+813_534+814dup	NM_001369380.1:c.534+812_534+814dup	NM_001369380.1:c.534+811_534+814dup	NM_001369380.1:c.534+810_534+814dup	NM_001369380.1:c.534+809_534+814dup	NM_001369380.1:c.534+808_534+814dup	NM_001369380.1:c.534+807_534+814dup	NM_001369380.1:c.534+805_534+814dup	NM_001369380.1:c.534+804_534+814dup	NM_001369380.1:c.534+800_534+814dup	NM_001369380.1:c.534+799_534+814dup	NM_001369380.1:c.534+797_534+814dup
NAP1L4 transcript variant 8	NM_001369381.1:c.534+814=	NM_001369381.1:c.534+807_534+814del	NM_001369381.1:c.534+809_534+814del	NM_001369381.1:c.534+810_534+814del	NM_001369381.1:c.534+812_534+814del	NM_001369381.1:c.534+813_534+814del	NM_001369381.1:c.534+814del	NM_001369381.1:c.534+814dup	NM_001369381.1:c.534+813_534+814dup	NM_001369381.1:c.534+812_534+814dup	NM_001369381.1:c.534+811_534+814dup	NM_001369381.1:c.534+810_534+814dup	NM_001369381.1:c.534+809_534+814dup	NM_001369381.1:c.534+808_534+814dup	NM_001369381.1:c.534+807_534+814dup	NM_001369381.1:c.534+805_534+814dup	NM_001369381.1:c.534+804_534+814dup	NM_001369381.1:c.534+800_534+814dup	NM_001369381.1:c.534+799_534+814dup	NM_001369381.1:c.534+797_534+814dup
NAP1L4 transcript variant 9	NM_001369382.1:c.534+814=	NM_001369382.1:c.534+807_534+814del	NM_001369382.1:c.534+809_534+814del	NM_001369382.1:c.534+810_534+814del	NM_001369382.1:c.534+812_534+814del	NM_001369382.1:c.534+813_534+814del	NM_001369382.1:c.534+814del	NM_001369382.1:c.534+814dup	NM_001369382.1:c.534+813_534+814dup	NM_001369382.1:c.534+812_534+814dup	NM_001369382.1:c.534+811_534+814dup	NM_001369382.1:c.534+810_534+814dup	NM_001369382.1:c.534+809_534+814dup	NM_001369382.1:c.534+808_534+814dup	NM_001369382.1:c.534+807_534+814dup	NM_001369382.1:c.534+805_534+814dup	NM_001369382.1:c.534+804_534+814dup	NM_001369382.1:c.534+800_534+814dup	NM_001369382.1:c.534+799_534+814dup	NM_001369382.1:c.534+797_534+814dup
NAP1L4 transcript variant 10	NM_001369383.1:c.534+814=	NM_001369383.1:c.534+807_534+814del	NM_001369383.1:c.534+809_534+814del	NM_001369383.1:c.534+810_534+814del	NM_001369383.1:c.534+812_534+814del	NM_001369383.1:c.534+813_534+814del	NM_001369383.1:c.534+814del	NM_001369383.1:c.534+814dup	NM_001369383.1:c.534+813_534+814dup	NM_001369383.1:c.534+812_534+814dup	NM_001369383.1:c.534+811_534+814dup	NM_001369383.1:c.534+810_534+814dup	NM_001369383.1:c.534+809_534+814dup	NM_001369383.1:c.534+808_534+814dup	NM_001369383.1:c.534+807_534+814dup	NM_001369383.1:c.534+805_534+814dup	NM_001369383.1:c.534+804_534+814dup	NM_001369383.1:c.534+800_534+814dup	NM_001369383.1:c.534+799_534+814dup	NM_001369383.1:c.534+797_534+814dup
NAP1L4 transcript variant 11	NM_001369384.1:c.534+814=	NM_001369384.1:c.534+807_534+814del	NM_001369384.1:c.534+809_534+814del	NM_001369384.1:c.534+810_534+814del	NM_001369384.1:c.534+812_534+814del	NM_001369384.1:c.534+813_534+814del	NM_001369384.1:c.534+814del	NM_001369384.1:c.534+814dup	NM_001369384.1:c.534+813_534+814dup	NM_001369384.1:c.534+812_534+814dup	NM_001369384.1:c.534+811_534+814dup	NM_001369384.1:c.534+810_534+814dup	NM_001369384.1:c.534+809_534+814dup	NM_001369384.1:c.534+808_534+814dup	NM_001369384.1:c.534+807_534+814dup	NM_001369384.1:c.534+805_534+814dup	NM_001369384.1:c.534+804_534+814dup	NM_001369384.1:c.534+800_534+814dup	NM_001369384.1:c.534+799_534+814dup	NM_001369384.1:c.534+797_534+814dup
NAP1L4 transcript variant 12	NM_001369385.1:c.534+814=	NM_001369385.1:c.534+807_534+814del	NM_001369385.1:c.534+809_534+814del	NM_001369385.1:c.534+810_534+814del	NM_001369385.1:c.534+812_534+814del	NM_001369385.1:c.534+813_534+814del	NM_001369385.1:c.534+814del	NM_001369385.1:c.534+814dup	NM_001369385.1:c.534+813_534+814dup	NM_001369385.1:c.534+812_534+814dup	NM_001369385.1:c.534+811_534+814dup	NM_001369385.1:c.534+810_534+814dup	NM_001369385.1:c.534+809_534+814dup	NM_001369385.1:c.534+808_534+814dup	NM_001369385.1:c.534+807_534+814dup	NM_001369385.1:c.534+805_534+814dup	NM_001369385.1:c.534+804_534+814dup	NM_001369385.1:c.534+800_534+814dup	NM_001369385.1:c.534+799_534+814dup	NM_001369385.1:c.534+797_534+814dup
NAP1L4 transcript variant 13	NM_001369386.1:c.534+814=	NM_001369386.1:c.534+807_534+814del	NM_001369386.1:c.534+809_534+814del	NM_001369386.1:c.534+810_534+814del	NM_001369386.1:c.534+812_534+814del	NM_001369386.1:c.534+813_534+814del	NM_001369386.1:c.534+814del	NM_001369386.1:c.534+814dup	NM_001369386.1:c.534+813_534+814dup	NM_001369386.1:c.534+812_534+814dup	NM_001369386.1:c.534+811_534+814dup	NM_001369386.1:c.534+810_534+814dup	NM_001369386.1:c.534+809_534+814dup	NM_001369386.1:c.534+808_534+814dup	NM_001369386.1:c.534+807_534+814dup	NM_001369386.1:c.534+805_534+814dup	NM_001369386.1:c.534+804_534+814dup	NM_001369386.1:c.534+800_534+814dup	NM_001369386.1:c.534+799_534+814dup	NM_001369386.1:c.534+797_534+814dup
NAP1L4 transcript variant 14	NM_001369388.1:c.534+814=	NM_001369388.1:c.534+807_534+814del	NM_001369388.1:c.534+809_534+814del	NM_001369388.1:c.534+810_534+814del	NM_001369388.1:c.534+812_534+814del	NM_001369388.1:c.534+813_534+814del	NM_001369388.1:c.534+814del	NM_001369388.1:c.534+814dup	NM_001369388.1:c.534+813_534+814dup	NM_001369388.1:c.534+812_534+814dup	NM_001369388.1:c.534+811_534+814dup	NM_001369388.1:c.534+810_534+814dup	NM_001369388.1:c.534+809_534+814dup	NM_001369388.1:c.534+808_534+814dup	NM_001369388.1:c.534+807_534+814dup	NM_001369388.1:c.534+805_534+814dup	NM_001369388.1:c.534+804_534+814dup	NM_001369388.1:c.534+800_534+814dup	NM_001369388.1:c.534+799_534+814dup	NM_001369388.1:c.534+797_534+814dup
NAP1L4 transcript	NM_005969.3:c.534+814=	NM_005969.3:c.534+807_534+814del	NM_005969.3:c.534+809_534+814del	NM_005969.3:c.534+810_534+814del	NM_005969.3:c.534+812_534+814del	NM_005969.3:c.534+813_534+814del	NM_005969.3:c.534+814del	NM_005969.3:c.534+814dup	NM_005969.3:c.534+813_534+814dup	NM_005969.3:c.534+812_534+814dup	NM_005969.3:c.534+811_534+814dup	NM_005969.3:c.534+810_534+814dup	NM_005969.3:c.534+809_534+814dup	NM_005969.3:c.534+808_534+814dup	NM_005969.3:c.534+807_534+814dup	NM_005969.3:c.534+805_534+814dup	NM_005969.3:c.534+804_534+814dup	NM_005969.3:c.534+800_534+814dup	NM_005969.3:c.534+799_534+814dup	NM_005969.3:c.534+797_534+814dup
NAP1L4 transcript variant 1	NM_005969.4:c.534+814=	NM_005969.4:c.534+807_534+814del	NM_005969.4:c.534+809_534+814del	NM_005969.4:c.534+810_534+814del	NM_005969.4:c.534+812_534+814del	NM_005969.4:c.534+813_534+814del	NM_005969.4:c.534+814del	NM_005969.4:c.534+814dup	NM_005969.4:c.534+813_534+814dup	NM_005969.4:c.534+812_534+814dup	NM_005969.4:c.534+811_534+814dup	NM_005969.4:c.534+810_534+814dup	NM_005969.4:c.534+809_534+814dup	NM_005969.4:c.534+808_534+814dup	NM_005969.4:c.534+807_534+814dup	NM_005969.4:c.534+805_534+814dup	NM_005969.4:c.534+804_534+814dup	NM_005969.4:c.534+800_534+814dup	NM_005969.4:c.534+799_534+814dup	NM_005969.4:c.534+797_534+814dup
NAP1L4 transcript variant X1	XM_005252935.1:c.534+814=	XM_005252935.1:c.534+807_534+814del	XM_005252935.1:c.534+809_534+814del	XM_005252935.1:c.534+810_534+814del	XM_005252935.1:c.534+812_534+814del	XM_005252935.1:c.534+813_534+814del	XM_005252935.1:c.534+814del	XM_005252935.1:c.534+814dup	XM_005252935.1:c.534+813_534+814dup	XM_005252935.1:c.534+812_534+814dup	XM_005252935.1:c.534+811_534+814dup	XM_005252935.1:c.534+810_534+814dup	XM_005252935.1:c.534+809_534+814dup	XM_005252935.1:c.534+808_534+814dup	XM_005252935.1:c.534+807_534+814dup	XM_005252935.1:c.534+805_534+814dup	XM_005252935.1:c.534+804_534+814dup	XM_005252935.1:c.534+800_534+814dup	XM_005252935.1:c.534+799_534+814dup	XM_005252935.1:c.534+797_534+814dup
NAP1L4 transcript variant X2	XM_005252936.1:c.534+814=	XM_005252936.1:c.534+807_534+814del	XM_005252936.1:c.534+809_534+814del	XM_005252936.1:c.534+810_534+814del	XM_005252936.1:c.534+812_534+814del	XM_005252936.1:c.534+813_534+814del	XM_005252936.1:c.534+814del	XM_005252936.1:c.534+814dup	XM_005252936.1:c.534+813_534+814dup	XM_005252936.1:c.534+812_534+814dup	XM_005252936.1:c.534+811_534+814dup	XM_005252936.1:c.534+810_534+814dup	XM_005252936.1:c.534+809_534+814dup	XM_005252936.1:c.534+808_534+814dup	XM_005252936.1:c.534+807_534+814dup	XM_005252936.1:c.534+805_534+814dup	XM_005252936.1:c.534+804_534+814dup	XM_005252936.1:c.534+800_534+814dup	XM_005252936.1:c.534+799_534+814dup	XM_005252936.1:c.534+797_534+814dup
NAP1L4 transcript variant X3	XM_005252937.1:c.534+814=	XM_005252937.1:c.534+807_534+814del	XM_005252937.1:c.534+809_534+814del	XM_005252937.1:c.534+810_534+814del	XM_005252937.1:c.534+812_534+814del	XM_005252937.1:c.534+813_534+814del	XM_005252937.1:c.534+814del	XM_005252937.1:c.534+814dup	XM_005252937.1:c.534+813_534+814dup	XM_005252937.1:c.534+812_534+814dup	XM_005252937.1:c.534+811_534+814dup	XM_005252937.1:c.534+810_534+814dup	XM_005252937.1:c.534+809_534+814dup	XM_005252937.1:c.534+808_534+814dup	XM_005252937.1:c.534+807_534+814dup	XM_005252937.1:c.534+805_534+814dup	XM_005252937.1:c.534+804_534+814dup	XM_005252937.1:c.534+800_534+814dup	XM_005252937.1:c.534+799_534+814dup	XM_005252937.1:c.534+797_534+814dup
NAP1L4 transcript variant X4	XM_005252938.1:c.534+814=	XM_005252938.1:c.534+807_534+814del	XM_005252938.1:c.534+809_534+814del	XM_005252938.1:c.534+810_534+814del	XM_005252938.1:c.534+812_534+814del	XM_005252938.1:c.534+813_534+814del	XM_005252938.1:c.534+814del	XM_005252938.1:c.534+814dup	XM_005252938.1:c.534+813_534+814dup	XM_005252938.1:c.534+812_534+814dup	XM_005252938.1:c.534+811_534+814dup	XM_005252938.1:c.534+810_534+814dup	XM_005252938.1:c.534+809_534+814dup	XM_005252938.1:c.534+808_534+814dup	XM_005252938.1:c.534+807_534+814dup	XM_005252938.1:c.534+805_534+814dup	XM_005252938.1:c.534+804_534+814dup	XM_005252938.1:c.534+800_534+814dup	XM_005252938.1:c.534+799_534+814dup	XM_005252938.1:c.534+797_534+814dup

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#.

53 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81034387	Dec 16, 2007 (129)
2	HUMANGENOME_JCVI	ss95558599	Feb 06, 2009 (130)
3	BCMHGSC_JDW	ss103519115	Mar 15, 2016 (147)
4	EVA_GENOME_DK	ss1574294753	Apr 01, 2015 (144)
5	SWEGEN	ss3007486192	Nov 08, 2017 (151)
6	MCHAISSO	ss3064500999	Nov 08, 2017 (151)
7	MCHAISSO	ss3065412601	Nov 08, 2017 (151)
8	EVA_DECODE	ss3691090079	Jul 13, 2019 (153)
9	EVA_DECODE	ss3691090080	Jul 13, 2019 (153)
10	EVA_DECODE	ss3691090081	Jul 13, 2019 (153)
11	EVA_DECODE	ss3691090082	Jul 13, 2019 (153)
12	EVA_DECODE	ss3691090083	Jul 13, 2019 (153)
13	EVA_DECODE	ss3691090088	Jul 13, 2019 (153)
14	EVA	ss3832440833	Apr 26, 2020 (154)
15	EVA	ss3839762855	Apr 26, 2020 (154)
16	KOGIC	ss3969079857	Apr 26, 2020 (154)
17	KOGIC	ss3969079858	Apr 26, 2020 (154)
18	KOGIC	ss3969079859	Apr 26, 2020 (154)
19	VINODS	ss4029433260	Apr 26, 2021 (155)
20	GNOMAD	ss4229003819	Apr 26, 2021 (155)
21	GNOMAD	ss4229003820	Apr 26, 2021 (155)
22	GNOMAD	ss4229003821	Apr 26, 2021 (155)
23	GNOMAD	ss4229003822	Apr 26, 2021 (155)
24	GNOMAD	ss4229003823	Apr 26, 2021 (155)
25	GNOMAD	ss4229003824	Apr 26, 2021 (155)
26	GNOMAD	ss4229003825	Apr 26, 2021 (155)
27	GNOMAD	ss4229003826	Apr 26, 2021 (155)
28	GNOMAD	ss4229003827	Apr 26, 2021 (155)
29	GNOMAD	ss4229003828	Apr 26, 2021 (155)
30	GNOMAD	ss4229003829	Apr 26, 2021 (155)
31	GNOMAD	ss4229003830	Apr 26, 2021 (155)
32	GNOMAD	ss4229003831	Apr 26, 2021 (155)
33	GNOMAD	ss4229003833	Apr 26, 2021 (155)
34	GNOMAD	ss4229003834	Apr 26, 2021 (155)
35	GNOMAD	ss4229003835	Apr 26, 2021 (155)
36	GNOMAD	ss4229003836	Apr 26, 2021 (155)
37	GNOMAD	ss4229003837	Apr 26, 2021 (155)
38	GNOMAD	ss4229003838	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5200397999	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5200398000	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5200398001	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5200398002	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5200398003	Apr 26, 2021 (155)
44	HUGCELL_USP	ss5481515783	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5481515784	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5481515785	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5747072425	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5747072426	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5747072427	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5747072428	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5747072429	Oct 16, 2022 (156)
52	EVA	ss5849830477	Oct 16, 2022 (156)
53	EVA	ss5980654668	Oct 16, 2022 (156)
54	The Danish reference pan genome	NC_000011.9 - 2990219	Apr 26, 2020 (154)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369585784 (NC_000011.10:2968988::T 3965/105104) Row 369585785 (NC_000011.10:2968988::TT 172/105376) Row 369585786 (NC_000011.10:2968988::TTT 14/105424)...	-	Apr 26, 2021 (155)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 25457858 (NC_000011.10:2968989::T 61/352) Row 25457859 (NC_000011.10:2968988:T: 13/352) Row 25457860 (NC_000011.10:2968989::TT 26/352)	-	Apr 26, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 25457858 (NC_000011.10:2968989::T 61/352) Row 25457859 (NC_000011.10:2968988:T: 13/352) Row 25457860 (NC_000011.10:2968989::TT 26/352)	-	Apr 26, 2020 (154)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 25457858 (NC_000011.10:2968989::T 61/352) Row 25457859 (NC_000011.10:2968988:T: 13/352) Row 25457860 (NC_000011.10:2968989::TT 26/352)	-	Apr 26, 2020 (154)
77	8.3KJPN Submission ignored due to conflicting rows: Row 58367306 (NC_000011.9:2990218:T: 4094/10718) Row 58367307 (NC_000011.9:2990218::T 435/10718) Row 58367308 (NC_000011.9:2990218:TT: 10/10718)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 58367306 (NC_000011.9:2990218:T: 4094/10718) Row 58367307 (NC_000011.9:2990218::T 435/10718) Row 58367308 (NC_000011.9:2990218:TT: 10/10718)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 58367306 (NC_000011.9:2990218:T: 4094/10718) Row 58367307 (NC_000011.9:2990218::T 435/10718) Row 58367308 (NC_000011.9:2990218:TT: 10/10718)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 58367306 (NC_000011.9:2990218:T: 4094/10718) Row 58367307 (NC_000011.9:2990218::T 435/10718) Row 58367308 (NC_000011.9:2990218:TT: 10/10718)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 58367306 (NC_000011.9:2990218:T: 4094/10718) Row 58367307 (NC_000011.9:2990218::T 435/10718) Row 58367308 (NC_000011.9:2990218:TT: 10/10718)...	-	Apr 26, 2021 (155)
82	14KJPN Submission ignored due to conflicting rows: Row 80909529 (NC_000011.10:2968988:T: 6784/28250) Row 80909530 (NC_000011.10:2968988::T 877/28250) Row 80909531 (NC_000011.10:2968988:TT: 15/28250)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 80909529 (NC_000011.10:2968988:T: 6784/28250) Row 80909530 (NC_000011.10:2968988::T 877/28250) Row 80909531 (NC_000011.10:2968988:TT: 15/28250)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 80909529 (NC_000011.10:2968988:T: 6784/28250) Row 80909530 (NC_000011.10:2968988::T 877/28250) Row 80909531 (NC_000011.10:2968988:TT: 15/28250)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 80909529 (NC_000011.10:2968988:T: 6784/28250) Row 80909530 (NC_000011.10:2968988::T 877/28250) Row 80909531 (NC_000011.10:2968988:TT: 15/28250)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 80909529 (NC_000011.10:2968988:T: 6784/28250) Row 80909530 (NC_000011.10:2968988::T 877/28250) Row 80909531 (NC_000011.10:2968988:TT: 15/28250)...	-	Oct 16, 2022 (156)
87	ALFA	NC_000011.10 - 2968989	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)
rs796177565	Nov 08, 2017 (151)
rs79557289	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4229003838	NC_000011.10:2968988:TTTTTTTT:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1267108562	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4229003837	NC_000011.10:2968988:TTTTTT:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1267108562	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4229003836	NC_000011.10:2968988:TTTTT:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
1267108562	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3691090079, ss4229003835	NC_000011.10:2968988:TTT:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
1267108562	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5200398001	NC_000011.9:2990218:TT:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4229003834, ss5747072427	NC_000011.10:2968988:TT:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
1267108562	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3691090080	NC_000011.10:2968989:TT:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4029433260	NT_187585.1:200059:TT:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss81034387	NC_000011.8:2946814:T:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
275372, ss1574294753, ss3007486192, ss3832440833, ss3839762855, ss5200397999, ss5980654668	NC_000011.9:2990218:T:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3064500999, ss3065412601, ss3969079858, ss4229003833, ss5481515784, ss5747072425, ss5849830477	NC_000011.10:2968988:T:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
1267108562	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3691090081	NC_000011.10:2968990:T:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss103519115	NT_009237.18:2930237:T:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss95558599	NT_009237.18:2930238:T:	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5200398000	NC_000011.9:2990218::T	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003819, ss5481515783, ss5747072426	NC_000011.10:2968988::T	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
1267108562	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3969079857	NC_000011.10:2968989::T	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3691090082	NC_000011.10:2968991::T	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3691090088	NC_000011.10:2968994::T	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss103519115	NT_009237.18:2930237:T:TT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5200398002	NC_000011.9:2990218::TT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003820, ss5481515785, ss5747072428	NC_000011.10:2968988::TT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
1267108562	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3969079859	NC_000011.10:2968989::TT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3691090083	NC_000011.10:2968991::TT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5200398003	NC_000011.9:2990218::TTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003821, ss5747072429	NC_000011.10:2968988::TTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
1267108562	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003822	NC_000011.10:2968988::TTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003823	NC_000011.10:2968988::TTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003824	NC_000011.10:2968988::TTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003825	NC_000011.10:2968988::TTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003826	NC_000011.10:2968988::TTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003827	NC_000011.10:2968988::TTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003828	NC_000011.10:2968988::TTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003829	NC_000011.10:2968988::TTTTTTTTTTTT… NC_000011.10:2968988::TTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003830	NC_000011.10:2968988::TTTTTTTTTTTT… NC_000011.10:2968988::TTTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229003831	NC_000011.10:2968988::TTTTTTTTTTTT… NC_000011.10:2968988::TTTTTTTTTTTTTTTTTT	NC_000011.10:2968988:TTTTTTTTTTTTT… NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs61176259

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

rs61176259