Name: rs34759526
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.

rs34759526

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:3689243-3689262 (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)₇ / del(T)₆ / del(…
del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.00661 (111/16804, ALFA)
delT=0.3261 (1633/5008, 1000G)
delT=0.035 (21/598, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TRAP1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	16804	TTTTTTTTTTTTTTTTTTTT=0.99054	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00661, TTTTTTTTTTTTTTTTTTTTT=0.00214, TTTTTTTTTTTTTTTTTTTTTTT=0.00036, TTTTTTTTTTTTTTTTTTTTTT=0.00036	0.986952	0.00012	0.012928	1
European	Sub	13484	TTTTTTTTTTTTTTTTTTTT=0.98828	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00816, TTTTTTTTTTTTTTTTTTTTT=0.00267, TTTTTTTTTTTTTTTTTTTTTTT=0.00044, TTTTTTTTTTTTTTTTTTTTTT=0.00044	0.983866	0.000149	0.015984	0
African	Sub	2014	TTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	70	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1944	TTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	96	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	74	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	22	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	128	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	574	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	78	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	430	TTTTTTTTTTTTTTTTTTTT=0.998	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.002, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	0.995349	0.0	0.004651	0

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

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	16804	(T)₂₀=0.99054	del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00661, dupT=0.00214, dupTT=0.00036, dupTTT=0.00036
Allele Frequency Aggregator	European	Sub	13484	(T)₂₀=0.98828	del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00816, dupT=0.00267, dupTT=0.00044, dupTTT=0.00044
Allele Frequency Aggregator	African	Sub	2014	(T)₂₀=1.0000	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	574	(T)₂₀=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=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	430	(T)₂₀=0.998	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.002, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	128	(T)₂₀=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=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	96	(T)₂₀=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=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	78	(T)₂₀=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
1000Genomes	Global	Study-wide	5008	(T)₂₀=0.6739	delT=0.3261
1000Genomes	African	Sub	1322	(T)₂₀=0.6800	delT=0.3200
1000Genomes	East Asian	Sub	1008	(T)₂₀=0.6657	delT=0.3343
1000Genomes	Europe	Sub	1006	(T)₂₀=0.6938	delT=0.3062
1000Genomes	South Asian	Sub	978	(T)₂₀=0.647	delT=0.353
1000Genomes	American	Sub	694	(T)₂₀=0.683	delT=0.317
Northern Sweden	ACPOP	Study-wide	598	(T)₂₀=0.965	delT=0.035

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 16	NC_000016.10:g.3689255_3689262del
GRCh38.p14 chr 16	NC_000016.10:g.3689256_3689262del
GRCh38.p14 chr 16	NC_000016.10:g.3689257_3689262del
GRCh38.p14 chr 16	NC_000016.10:g.3689258_3689262del
GRCh38.p14 chr 16	NC_000016.10:g.3689259_3689262del
GRCh38.p14 chr 16	NC_000016.10:g.3689260_3689262del
GRCh38.p14 chr 16	NC_000016.10:g.3689261_3689262del
GRCh38.p14 chr 16	NC_000016.10:g.3689262del
GRCh38.p14 chr 16	NC_000016.10:g.3689262dup
GRCh38.p14 chr 16	NC_000016.10:g.3689261_3689262dup
GRCh38.p14 chr 16	NC_000016.10:g.3689260_3689262dup
GRCh38.p14 chr 16	NC_000016.10:g.3689259_3689262dup
GRCh38.p14 chr 16	NC_000016.10:g.3689258_3689262dup
GRCh37.p13 chr 16	NC_000016.9:g.3739256_3739263del
GRCh37.p13 chr 16	NC_000016.9:g.3739257_3739263del
GRCh37.p13 chr 16	NC_000016.9:g.3739258_3739263del
GRCh37.p13 chr 16	NC_000016.9:g.3739259_3739263del
GRCh37.p13 chr 16	NC_000016.9:g.3739260_3739263del
GRCh37.p13 chr 16	NC_000016.9:g.3739261_3739263del
GRCh37.p13 chr 16	NC_000016.9:g.3739262_3739263del
GRCh37.p13 chr 16	NC_000016.9:g.3739263del
GRCh37.p13 chr 16	NC_000016.9:g.3739263dup
GRCh37.p13 chr 16	NC_000016.9:g.3739262_3739263dup
GRCh37.p13 chr 16	NC_000016.9:g.3739261_3739263dup
GRCh37.p13 chr 16	NC_000016.9:g.3739260_3739263dup
GRCh37.p13 chr 16	NC_000016.9:g.3739259_3739263dup
TRAP1 RefSeqGene	NG_033088.1:g.33348_33355del
TRAP1 RefSeqGene	NG_033088.1:g.33349_33355del
TRAP1 RefSeqGene	NG_033088.1:g.33350_33355del
TRAP1 RefSeqGene	NG_033088.1:g.33351_33355del
TRAP1 RefSeqGene	NG_033088.1:g.33352_33355del
TRAP1 RefSeqGene	NG_033088.1:g.33353_33355del
TRAP1 RefSeqGene	NG_033088.1:g.33354_33355del
TRAP1 RefSeqGene	NG_033088.1:g.33355del
TRAP1 RefSeqGene	NG_033088.1:g.33355dup
TRAP1 RefSeqGene	NG_033088.1:g.33354_33355dup
TRAP1 RefSeqGene	NG_033088.1:g.33353_33355dup
TRAP1 RefSeqGene	NG_033088.1:g.33352_33355dup
TRAP1 RefSeqGene	NG_033088.1:g.33351_33355dup

Gene: TRAP1, TNF receptor associated protein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TRAP1 transcript variant 2	NM_001272049.2:c.89-113_8… NM_001272049.2:c.89-113_89-106del	N/A	Intron Variant
TRAP1 transcript variant 1	NM_016292.3:c.248-113_248… NM_016292.3:c.248-113_248-106del	N/A	Intron Variant
TRAP1 transcript variant X1	XM_011522345.3:c.-173-113… XM_011522345.3:c.-173-113_-173-106del	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)₂₀=	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅
GRCh38.p14 chr 16	NC_000016.10:g.3689243_3689262=	NC_000016.10:g.3689255_3689262del	NC_000016.10:g.3689256_3689262del	NC_000016.10:g.3689257_3689262del	NC_000016.10:g.3689258_3689262del	NC_000016.10:g.3689259_3689262del	NC_000016.10:g.3689260_3689262del	NC_000016.10:g.3689261_3689262del	NC_000016.10:g.3689262del	NC_000016.10:g.3689262dup	NC_000016.10:g.3689261_3689262dup	NC_000016.10:g.3689260_3689262dup	NC_000016.10:g.3689259_3689262dup	NC_000016.10:g.3689258_3689262dup
GRCh37.p13 chr 16	NC_000016.9:g.3739244_3739263=	NC_000016.9:g.3739256_3739263del	NC_000016.9:g.3739257_3739263del	NC_000016.9:g.3739258_3739263del	NC_000016.9:g.3739259_3739263del	NC_000016.9:g.3739260_3739263del	NC_000016.9:g.3739261_3739263del	NC_000016.9:g.3739262_3739263del	NC_000016.9:g.3739263del	NC_000016.9:g.3739263dup	NC_000016.9:g.3739262_3739263dup	NC_000016.9:g.3739261_3739263dup	NC_000016.9:g.3739260_3739263dup	NC_000016.9:g.3739259_3739263dup
TRAP1 RefSeqGene	NG_033088.1:g.33336_33355=	NG_033088.1:g.33348_33355del	NG_033088.1:g.33349_33355del	NG_033088.1:g.33350_33355del	NG_033088.1:g.33351_33355del	NG_033088.1:g.33352_33355del	NG_033088.1:g.33353_33355del	NG_033088.1:g.33354_33355del	NG_033088.1:g.33355del	NG_033088.1:g.33355dup	NG_033088.1:g.33354_33355dup	NG_033088.1:g.33353_33355dup	NG_033088.1:g.33352_33355dup	NG_033088.1:g.33351_33355dup
TRAP1 transcript variant 2	NM_001272049.1:c.89-106=	NM_001272049.1:c.89-113_89-106del	NM_001272049.1:c.89-112_89-106del	NM_001272049.1:c.89-111_89-106del	NM_001272049.1:c.89-110_89-106del	NM_001272049.1:c.89-109_89-106del	NM_001272049.1:c.89-108_89-106del	NM_001272049.1:c.89-107_89-106del	NM_001272049.1:c.89-106del	NM_001272049.1:c.89-106dup	NM_001272049.1:c.89-107_89-106dup	NM_001272049.1:c.89-108_89-106dup	NM_001272049.1:c.89-109_89-106dup	NM_001272049.1:c.89-110_89-106dup
TRAP1 transcript variant 2	NM_001272049.2:c.89-106=	NM_001272049.2:c.89-113_89-106del	NM_001272049.2:c.89-112_89-106del	NM_001272049.2:c.89-111_89-106del	NM_001272049.2:c.89-110_89-106del	NM_001272049.2:c.89-109_89-106del	NM_001272049.2:c.89-108_89-106del	NM_001272049.2:c.89-107_89-106del	NM_001272049.2:c.89-106del	NM_001272049.2:c.89-106dup	NM_001272049.2:c.89-107_89-106dup	NM_001272049.2:c.89-108_89-106dup	NM_001272049.2:c.89-109_89-106dup	NM_001272049.2:c.89-110_89-106dup
TRAP1 transcript variant 1	NM_016292.2:c.248-106=	NM_016292.2:c.248-113_248-106del	NM_016292.2:c.248-112_248-106del	NM_016292.2:c.248-111_248-106del	NM_016292.2:c.248-110_248-106del	NM_016292.2:c.248-109_248-106del	NM_016292.2:c.248-108_248-106del	NM_016292.2:c.248-107_248-106del	NM_016292.2:c.248-106del	NM_016292.2:c.248-106dup	NM_016292.2:c.248-107_248-106dup	NM_016292.2:c.248-108_248-106dup	NM_016292.2:c.248-109_248-106dup	NM_016292.2:c.248-110_248-106dup
TRAP1 transcript variant 1	NM_016292.3:c.248-106=	NM_016292.3:c.248-113_248-106del	NM_016292.3:c.248-112_248-106del	NM_016292.3:c.248-111_248-106del	NM_016292.3:c.248-110_248-106del	NM_016292.3:c.248-109_248-106del	NM_016292.3:c.248-108_248-106del	NM_016292.3:c.248-107_248-106del	NM_016292.3:c.248-106del	NM_016292.3:c.248-106dup	NM_016292.3:c.248-107_248-106dup	NM_016292.3:c.248-108_248-106dup	NM_016292.3:c.248-109_248-106dup	NM_016292.3:c.248-110_248-106dup
TRAP1 transcript variant X1	XM_011522345.3:c.-173-106=	XM_011522345.3:c.-173-113_-173-106del	XM_011522345.3:c.-173-112_-173-106del	XM_011522345.3:c.-173-111_-173-106del	XM_011522345.3:c.-173-110_-173-106del	XM_011522345.3:c.-173-109_-173-106del	XM_011522345.3:c.-173-108_-173-106del	XM_011522345.3:c.-173-107_-173-106del	XM_011522345.3:c.-173-106del	XM_011522345.3:c.-173-106dup	XM_011522345.3:c.-173-107_-173-106dup	XM_011522345.3:c.-173-108_-173-106dup	XM_011522345.3:c.-173-109_-173-106dup	XM_011522345.3:c.-173-110_-173-106dup

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#.

39 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40708689	Mar 14, 2006 (126)
2	SSMP	ss664313645	Apr 01, 2015 (144)
3	SSIP	ss947350833	Aug 21, 2014 (142)
4	1000GENOMES	ss1375477901	Aug 21, 2014 (142)
5	SWEGEN	ss3013951281	Nov 08, 2017 (151)
6	ACPOP	ss3741274181	Jul 13, 2019 (153)
7	KHV_HUMAN_GENOMES	ss3818894107	Jul 13, 2019 (153)
8	EVA	ss3834437342	Apr 27, 2020 (154)
9	FSA-LAB	ss3984086303	Apr 27, 2021 (155)
10	EVA	ss3986673623	Apr 27, 2021 (155)
11	GNOMAD	ss4295751602	Apr 27, 2021 (155)
12	GNOMAD	ss4295751603	Apr 27, 2021 (155)
13	GNOMAD	ss4295751604	Apr 27, 2021 (155)
14	GNOMAD	ss4295751605	Apr 27, 2021 (155)
15	GNOMAD	ss4295751606	Apr 27, 2021 (155)
16	GNOMAD	ss4295751607	Apr 27, 2021 (155)
17	GNOMAD	ss4295751608	Apr 27, 2021 (155)
18	GNOMAD	ss4295751609	Apr 27, 2021 (155)
19	GNOMAD	ss4295751610	Apr 27, 2021 (155)
20	GNOMAD	ss4295751611	Apr 27, 2021 (155)
21	GNOMAD	ss4295751612	Apr 27, 2021 (155)
22	GNOMAD	ss4295751613	Apr 27, 2021 (155)
23	TOPMED	ss5005389513	Apr 27, 2021 (155)
24	TOPMED	ss5005389514	Apr 27, 2021 (155)
25	TOPMED	ss5005389515	Apr 27, 2021 (155)
26	EVA	ss5141990019	Apr 27, 2021 (155)
27	TOMMO_GENOMICS	ss5218101926	Apr 27, 2021 (155)
28	TOMMO_GENOMICS	ss5218101927	Apr 27, 2021 (155)
29	1000G_HIGH_COVERAGE	ss5299882456	Oct 17, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5299882457	Oct 17, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5299882458	Oct 17, 2022 (156)
32	HUGCELL_USP	ss5493435636	Oct 17, 2022 (156)
33	HUGCELL_USP	ss5493435637	Oct 17, 2022 (156)
34	HUGCELL_USP	ss5493435638	Oct 17, 2022 (156)
35	TOMMO_GENOMICS	ss5772486927	Oct 17, 2022 (156)
36	TOMMO_GENOMICS	ss5772486928	Oct 17, 2022 (156)
37	TOMMO_GENOMICS	ss5772486929	Oct 17, 2022 (156)
38	TOMMO_GENOMICS	ss5772486930	Oct 17, 2022 (156)
39	EVA	ss5980899198	Oct 17, 2022 (156)
40	1000Genomes	NC_000016.9 - 3739244	Oct 12, 2018 (152)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480821613 (NC_000016.10:3689242::T 5083/121938) Row 480821614 (NC_000016.10:3689242::TT 105/121930) Row 480821615 (NC_000016.10:3689242::TTT 41/121946)...	-	Apr 27, 2021 (155)
53	Northern Sweden	NC_000016.9 - 3739244	Jul 13, 2019 (153)
54	8.3KJPN Submission ignored due to conflicting rows: Row 76071233 (NC_000016.9:3739243:T: 822/16754) Row 76071234 (NC_000016.9:3739243::T 28/16754)	-	Apr 27, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 76071233 (NC_000016.9:3739243:T: 822/16754) Row 76071234 (NC_000016.9:3739243::T 28/16754)	-	Apr 27, 2021 (155)
56	14KJPN Submission ignored due to conflicting rows: Row 106324031 (NC_000016.10:3689242:T: 1433/28256) Row 106324032 (NC_000016.10:3689242::T 42/28256) Row 106324033 (NC_000016.10:3689242:TT: 2/28256)...	-	Oct 17, 2022 (156)
57	14KJPN Submission ignored due to conflicting rows: Row 106324031 (NC_000016.10:3689242:T: 1433/28256) Row 106324032 (NC_000016.10:3689242::T 42/28256) Row 106324033 (NC_000016.10:3689242:TT: 2/28256)...	-	Oct 17, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 106324031 (NC_000016.10:3689242:T: 1433/28256) Row 106324032 (NC_000016.10:3689242::T 42/28256) Row 106324033 (NC_000016.10:3689242:TT: 2/28256)...	-	Oct 17, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 106324031 (NC_000016.10:3689242:T: 1433/28256) Row 106324032 (NC_000016.10:3689242::T 42/28256) Row 106324033 (NC_000016.10:3689242:TT: 2/28256)...	-	Oct 17, 2022 (156)
60	TopMed Submission ignored due to conflicting rows: Row 220935174 (NC_000016.10:3689242:TTTTTT: 1/264690) Row 220935175 (NC_000016.10:3689242:TTTTTTT: 8/264690) Row 220935176 (NC_000016.10:3689242:TTTTTTTT: 6/264690)	-	Apr 27, 2021 (155)
61	TopMed Submission ignored due to conflicting rows: Row 220935174 (NC_000016.10:3689242:TTTTTT: 1/264690) Row 220935175 (NC_000016.10:3689242:TTTTTTT: 8/264690) Row 220935176 (NC_000016.10:3689242:TTTTTTTT: 6/264690)	-	Apr 27, 2021 (155)
62	TopMed Submission ignored due to conflicting rows: Row 220935174 (NC_000016.10:3689242:TTTTTT: 1/264690) Row 220935175 (NC_000016.10:3689242:TTTTTTT: 8/264690) Row 220935176 (NC_000016.10:3689242:TTTTTTTT: 6/264690)	-	Apr 27, 2021 (155)
63	ALFA	NC_000016.10 - 3689243	Apr 27, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4295751613, ss5005389515	NC_000016.10:3689242:TTTTTTTT:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4295751612, ss5005389514	NC_000016.10:3689242:TTTTTTT:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5005389513	NC_000016.10:3689242:TTTTTT:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4295751611	NC_000016.10:3689242:TTTTT:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4295751610, ss5772486930	NC_000016.10:3689242:TTTT:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4295751609	NC_000016.10:3689242:TTT:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3984086303	NC_000016.9:3739243:TT:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4295751608, ss5493435638, ss5772486929	NC_000016.10:3689242:TT:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
68220623, 14559046, ss1375477901, ss3013951281, ss3741274181, ss3986673623, ss5218101926, ss5980899198	NC_000016.9:3739243:T:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3818894107, ss4295751607, ss5299882456, ss5493435637, ss5772486927	NC_000016.10:3689242:T:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss40708689	NT_010393.16:3679262:T:	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss664313645, ss3834437342, ss5218101927	NC_000016.9:3739243::T	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss947350833	NC_000016.9:3739244::T	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4295751602, ss5299882457, ss5493435636, ss5772486928	NC_000016.10:3689242::T	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4295751603, ss5141990019, ss5299882458	NC_000016.10:3689242::TT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4295751604	NC_000016.10:3689242::TTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
1022334346	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4295751605	NC_000016.10:3689242::TTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4295751606	NC_000016.10:3689242::TTTTT	NC_000016.10:3689242:TTTTTTTTTTTTT… NC_000016.10:3689242:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34759526

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

rs34759526