Name: rs35055326
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.

rs35055326

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:35265454-35265466 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₅
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.20642 (2172/10522, ALFA)
delT=0.0525 (161/3065, 1000G)
dupT=0.348 (208/598, NorthernSweden) (+ 1 more)
dupT=0.25 (10/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC1A2 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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	10522	(T)₁₃=0.77856	delTT=0.00000, delT=0.00580, dupT=0.20642, dupTT=0.00865, dupTTT=0.00057
Allele Frequency Aggregator	European	Sub	8204	(T)₁₃=0.7432	delTT=0.0000, delT=0.0055, dupT=0.2426, dupTT=0.0082, dupTTT=0.0006
Allele Frequency Aggregator	African	Sub	1328	(T)₁₃=0.9759	delTT=0.0000, delT=0.0038, dupT=0.0188, dupTT=0.0015, dupTTT=0.0000
Allele Frequency Aggregator	Other	Sub	592	(T)₁₃=0.696	delTT=0.000, delT=0.019, dupT=0.248, dupTT=0.035, dupTTT=0.002
Allele Frequency Aggregator	Latin American 2	Sub	278	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	50	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	50	(T)₁₃=0.78	delTT=0.00, delT=0.00, dupT=0.20, dupTT=0.02, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
1000Genomes	Global	Study-wide	3065	(T)₁₃=0.9475	delT=0.0525
1000Genomes	African	Sub	988	(T)₁₃=0.841	delT=0.159
1000Genomes	Europe	Sub	604	(T)₁₃=0.998	delT=0.002
1000Genomes	East Asian	Sub	534	(T)₁₃=1.000	delT=0.000
1000Genomes	South Asian	Sub	508	(T)₁₃=1.000	delT=0.000
1000Genomes	American	Sub	431	(T)₁₃=0.993	delT=0.007
Northern Sweden	ACPOP	Study-wide	598	- No frequency provided	dupT=0.348
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.25

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.35265464_35265466del
GRCh38.p14 chr 11	NC_000011.10:g.35265465_35265466del
GRCh38.p14 chr 11	NC_000011.10:g.35265466del
GRCh38.p14 chr 11	NC_000011.10:g.35265466dup
GRCh38.p14 chr 11	NC_000011.10:g.35265465_35265466dup
GRCh38.p14 chr 11	NC_000011.10:g.35265464_35265466dup
GRCh38.p14 chr 11	NC_000011.10:g.35265462_35265466dup
GRCh37.p13 chr 11	NC_000011.9:g.35287011_35287013del
GRCh37.p13 chr 11	NC_000011.9:g.35287012_35287013del
GRCh37.p13 chr 11	NC_000011.9:g.35287013del
GRCh37.p13 chr 11	NC_000011.9:g.35287013dup
GRCh37.p13 chr 11	NC_000011.9:g.35287012_35287013dup
GRCh37.p13 chr 11	NC_000011.9:g.35287011_35287013dup
GRCh37.p13 chr 11	NC_000011.9:g.35287009_35287013dup
SLC1A2 RefSeqGene	NG_008727.2:g.159103_159105del
SLC1A2 RefSeqGene	NG_008727.2:g.159104_159105del
SLC1A2 RefSeqGene	NG_008727.2:g.159105del
SLC1A2 RefSeqGene	NG_008727.2:g.159105dup
SLC1A2 RefSeqGene	NG_008727.2:g.159104_159105dup
SLC1A2 RefSeqGene	NG_008727.2:g.159103_159105dup
SLC1A2 RefSeqGene	NG_008727.2:g.159101_159105dup

Gene: SLC1A2, solute carrier family 1 member 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC1A2 transcript variant 2	NM_001195728.3:c.1626+71_… NM_001195728.3:c.1626+71_1626+73del	N/A	Intron Variant
SLC1A2 transcript variant 3	NM_001252652.2:c.1626+71_… NM_001252652.2:c.1626+71_1626+73del	N/A	Intron Variant
SLC1A2 transcript variant 1	NM_004171.4:c.1653+71_165… NM_004171.4:c.1653+71_1653+73del	N/A	Intron Variant
SLC1A2 transcript variant X4	XM_011520285.2:c.1641+71_… XM_011520285.2:c.1641+71_1641+73del	N/A	Intron Variant
SLC1A2 transcript variant X3	XM_017018136.1:c.1668+71_… XM_017018136.1:c.1668+71_1668+73del	N/A	Intron Variant
SLC1A2 transcript variant X6	XM_017018137.2:c.1626+71_… XM_017018137.2:c.1626+71_1626+73del	N/A	Intron Variant
SLC1A2 transcript variant X7	XM_017018138.2:c.1626+71_… XM_017018138.2:c.1626+71_1626+73del	N/A	Intron Variant
SLC1A2 transcript variant X9	XM_017018139.2:c.1419+71_… XM_017018139.2:c.1419+71_1419+73del	N/A	Intron Variant
SLC1A2 transcript variant X1	XM_047427436.1:c.1737+71_… XM_047427436.1:c.1737+71_1737+73del	N/A	Intron Variant
SLC1A2 transcript variant X2	XM_047427437.1:c.1647+71_… XM_047427437.1:c.1647+71_1647+73del	N/A	Intron Variant
SLC1A2 transcript variant X5	XM_047427438.1:c.1626+71_… XM_047427438.1:c.1626+71_1626+73del	N/A	Intron Variant
SLC1A2 transcript variant X8	XM_047427440.1:c.1626+71_… XM_047427440.1:c.1626+71_1626+73del	N/A	Intron Variant
SLC1A2 transcript variant X12	XM_047427441.1:c.1503+71_… XM_047427441.1:c.1503+71_1503+73del	N/A	Intron Variant
SLC1A2 transcript variant X10	XM_047427442.1:c.1626+71_… XM_047427442.1:c.1626+71_1626+73del	N/A	Intron Variant
SLC1A2 transcript variant X11	XM_047427443.1:c.1626+71_… XM_047427443.1:c.1626+71_1626+73del	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)₁₃=	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₅
GRCh38.p14 chr 11	NC_000011.10:g.35265454_35265466=	NC_000011.10:g.35265464_35265466del	NC_000011.10:g.35265465_35265466del	NC_000011.10:g.35265466del	NC_000011.10:g.35265466dup	NC_000011.10:g.35265465_35265466dup	NC_000011.10:g.35265464_35265466dup	NC_000011.10:g.35265462_35265466dup
GRCh37.p13 chr 11	NC_000011.9:g.35287001_35287013=	NC_000011.9:g.35287011_35287013del	NC_000011.9:g.35287012_35287013del	NC_000011.9:g.35287013del	NC_000011.9:g.35287013dup	NC_000011.9:g.35287012_35287013dup	NC_000011.9:g.35287011_35287013dup	NC_000011.9:g.35287009_35287013dup
SLC1A2 RefSeqGene	NG_008727.2:g.159093_159105=	NG_008727.2:g.159103_159105del	NG_008727.2:g.159104_159105del	NG_008727.2:g.159105del	NG_008727.2:g.159105dup	NG_008727.2:g.159104_159105dup	NG_008727.2:g.159103_159105dup	NG_008727.2:g.159101_159105dup
SLC1A2 transcript variant 2	NM_001195728.2:c.1626+73=	NM_001195728.2:c.1626+71_1626+73del	NM_001195728.2:c.1626+72_1626+73del	NM_001195728.2:c.1626+73del	NM_001195728.2:c.1626+73dup	NM_001195728.2:c.1626+72_1626+73dup	NM_001195728.2:c.1626+71_1626+73dup	NM_001195728.2:c.1626+69_1626+73dup
SLC1A2 transcript variant 2	NM_001195728.3:c.1626+73=	NM_001195728.3:c.1626+71_1626+73del	NM_001195728.3:c.1626+72_1626+73del	NM_001195728.3:c.1626+73del	NM_001195728.3:c.1626+73dup	NM_001195728.3:c.1626+72_1626+73dup	NM_001195728.3:c.1626+71_1626+73dup	NM_001195728.3:c.1626+69_1626+73dup
SLC1A2 transcript variant 3	NM_001252652.1:c.1626+73=	NM_001252652.1:c.1626+71_1626+73del	NM_001252652.1:c.1626+72_1626+73del	NM_001252652.1:c.1626+73del	NM_001252652.1:c.1626+73dup	NM_001252652.1:c.1626+72_1626+73dup	NM_001252652.1:c.1626+71_1626+73dup	NM_001252652.1:c.1626+69_1626+73dup
SLC1A2 transcript variant 3	NM_001252652.2:c.1626+73=	NM_001252652.2:c.1626+71_1626+73del	NM_001252652.2:c.1626+72_1626+73del	NM_001252652.2:c.1626+73del	NM_001252652.2:c.1626+73dup	NM_001252652.2:c.1626+72_1626+73dup	NM_001252652.2:c.1626+71_1626+73dup	NM_001252652.2:c.1626+69_1626+73dup
SLC1A2 transcript variant 1	NM_004171.3:c.1653+73=	NM_004171.3:c.1653+71_1653+73del	NM_004171.3:c.1653+72_1653+73del	NM_004171.3:c.1653+73del	NM_004171.3:c.1653+73dup	NM_004171.3:c.1653+72_1653+73dup	NM_004171.3:c.1653+71_1653+73dup	NM_004171.3:c.1653+69_1653+73dup
SLC1A2 transcript variant 1	NM_004171.4:c.1653+73=	NM_004171.4:c.1653+71_1653+73del	NM_004171.4:c.1653+72_1653+73del	NM_004171.4:c.1653+73del	NM_004171.4:c.1653+73dup	NM_004171.4:c.1653+72_1653+73dup	NM_004171.4:c.1653+71_1653+73dup	NM_004171.4:c.1653+69_1653+73dup
SLC1A2 transcript variant X1	XM_005253066.1:c.1701+73=	XM_005253066.1:c.1701+71_1701+73del	XM_005253066.1:c.1701+72_1701+73del	XM_005253066.1:c.1701+73del	XM_005253066.1:c.1701+73dup	XM_005253066.1:c.1701+72_1701+73dup	XM_005253066.1:c.1701+71_1701+73dup	XM_005253066.1:c.1701+69_1701+73dup
SLC1A2 transcript variant X2	XM_005253067.1:c.1644+73=	XM_005253067.1:c.1644+71_1644+73del	XM_005253067.1:c.1644+72_1644+73del	XM_005253067.1:c.1644+73del	XM_005253067.1:c.1644+73dup	XM_005253067.1:c.1644+72_1644+73dup	XM_005253067.1:c.1644+71_1644+73dup	XM_005253067.1:c.1644+69_1644+73dup
SLC1A2 transcript variant X4	XM_011520285.2:c.1641+73=	XM_011520285.2:c.1641+71_1641+73del	XM_011520285.2:c.1641+72_1641+73del	XM_011520285.2:c.1641+73del	XM_011520285.2:c.1641+73dup	XM_011520285.2:c.1641+72_1641+73dup	XM_011520285.2:c.1641+71_1641+73dup	XM_011520285.2:c.1641+69_1641+73dup
SLC1A2 transcript variant X3	XM_017018136.1:c.1668+73=	XM_017018136.1:c.1668+71_1668+73del	XM_017018136.1:c.1668+72_1668+73del	XM_017018136.1:c.1668+73del	XM_017018136.1:c.1668+73dup	XM_017018136.1:c.1668+72_1668+73dup	XM_017018136.1:c.1668+71_1668+73dup	XM_017018136.1:c.1668+69_1668+73dup
SLC1A2 transcript variant X6	XM_017018137.2:c.1626+73=	XM_017018137.2:c.1626+71_1626+73del	XM_017018137.2:c.1626+72_1626+73del	XM_017018137.2:c.1626+73del	XM_017018137.2:c.1626+73dup	XM_017018137.2:c.1626+72_1626+73dup	XM_017018137.2:c.1626+71_1626+73dup	XM_017018137.2:c.1626+69_1626+73dup
SLC1A2 transcript variant X7	XM_017018138.2:c.1626+73=	XM_017018138.2:c.1626+71_1626+73del	XM_017018138.2:c.1626+72_1626+73del	XM_017018138.2:c.1626+73del	XM_017018138.2:c.1626+73dup	XM_017018138.2:c.1626+72_1626+73dup	XM_017018138.2:c.1626+71_1626+73dup	XM_017018138.2:c.1626+69_1626+73dup
SLC1A2 transcript variant X9	XM_017018139.2:c.1419+73=	XM_017018139.2:c.1419+71_1419+73del	XM_017018139.2:c.1419+72_1419+73del	XM_017018139.2:c.1419+73del	XM_017018139.2:c.1419+73dup	XM_017018139.2:c.1419+72_1419+73dup	XM_017018139.2:c.1419+71_1419+73dup	XM_017018139.2:c.1419+69_1419+73dup
SLC1A2 transcript variant X1	XM_047427436.1:c.1737+73=	XM_047427436.1:c.1737+71_1737+73del	XM_047427436.1:c.1737+72_1737+73del	XM_047427436.1:c.1737+73del	XM_047427436.1:c.1737+73dup	XM_047427436.1:c.1737+72_1737+73dup	XM_047427436.1:c.1737+71_1737+73dup	XM_047427436.1:c.1737+69_1737+73dup
SLC1A2 transcript variant X2	XM_047427437.1:c.1647+73=	XM_047427437.1:c.1647+71_1647+73del	XM_047427437.1:c.1647+72_1647+73del	XM_047427437.1:c.1647+73del	XM_047427437.1:c.1647+73dup	XM_047427437.1:c.1647+72_1647+73dup	XM_047427437.1:c.1647+71_1647+73dup	XM_047427437.1:c.1647+69_1647+73dup
SLC1A2 transcript variant X5	XM_047427438.1:c.1626+73=	XM_047427438.1:c.1626+71_1626+73del	XM_047427438.1:c.1626+72_1626+73del	XM_047427438.1:c.1626+73del	XM_047427438.1:c.1626+73dup	XM_047427438.1:c.1626+72_1626+73dup	XM_047427438.1:c.1626+71_1626+73dup	XM_047427438.1:c.1626+69_1626+73dup
SLC1A2 transcript variant X8	XM_047427440.1:c.1626+73=	XM_047427440.1:c.1626+71_1626+73del	XM_047427440.1:c.1626+72_1626+73del	XM_047427440.1:c.1626+73del	XM_047427440.1:c.1626+73dup	XM_047427440.1:c.1626+72_1626+73dup	XM_047427440.1:c.1626+71_1626+73dup	XM_047427440.1:c.1626+69_1626+73dup
SLC1A2 transcript variant X12	XM_047427441.1:c.1503+73=	XM_047427441.1:c.1503+71_1503+73del	XM_047427441.1:c.1503+72_1503+73del	XM_047427441.1:c.1503+73del	XM_047427441.1:c.1503+73dup	XM_047427441.1:c.1503+72_1503+73dup	XM_047427441.1:c.1503+71_1503+73dup	XM_047427441.1:c.1503+69_1503+73dup
SLC1A2 transcript variant X10	XM_047427442.1:c.1626+73=	XM_047427442.1:c.1626+71_1626+73del	XM_047427442.1:c.1626+72_1626+73del	XM_047427442.1:c.1626+73del	XM_047427442.1:c.1626+73dup	XM_047427442.1:c.1626+72_1626+73dup	XM_047427442.1:c.1626+71_1626+73dup	XM_047427442.1:c.1626+69_1626+73dup
SLC1A2 transcript variant X11	XM_047427443.1:c.1626+73=	XM_047427443.1:c.1626+71_1626+73del	XM_047427443.1:c.1626+72_1626+73del	XM_047427443.1:c.1626+73del	XM_047427443.1:c.1626+73dup	XM_047427443.1:c.1626+72_1626+73dup	XM_047427443.1:c.1626+71_1626+73dup	XM_047427443.1:c.1626+69_1626+73dup

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#.

66 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39913123	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss97433683	Oct 12, 2018 (152)
3	BL	ss256112208	May 09, 2011 (138)
4	GMI	ss289063354	May 04, 2012 (137)
5	PJP	ss294698127	May 09, 2011 (137)
6	SSMP	ss664048359	Apr 01, 2015 (144)
7	BILGI_BIOE	ss666531303	Apr 25, 2013 (138)
8	1000GENOMES	ss1370770034	Aug 21, 2014 (142)
9	1000GENOMES	ss1370770037	Aug 21, 2014 (142)
10	EVA_GENOME_DK	ss1574335639	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1707064458	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1707064459	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1707064480	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1707064483	Apr 01, 2015 (144)
15	EVA_EXAC	ss1711967436	Apr 01, 2015 (144)
16	EVA_EXAC	ss1711967437	Apr 01, 2015 (144)
17	EVA_EXAC	ss1711967438	Apr 01, 2015 (144)
18	EVA_EXAC	ss1711967439	Jan 10, 2018 (151)
19	EVA_EXAC	ss1711967440	Apr 01, 2015 (144)
20	EVA_EXAC	ss1711967441	Apr 01, 2015 (144)
21	SYSTEMSBIOZJU	ss2627787495	Nov 08, 2017 (151)
22	SWEGEN	ss3007882069	Nov 08, 2017 (151)
23	MCHAISSO	ss3063687757	Nov 08, 2017 (151)
24	MCHAISSO	ss3064512307	Nov 08, 2017 (151)
25	URBANLAB	ss3649579978	Oct 12, 2018 (152)
26	EVA_DECODE	ss3691561264	Jul 13, 2019 (153)
27	EVA_DECODE	ss3691561265	Jul 13, 2019 (153)
28	EVA_DECODE	ss3691561266	Jul 13, 2019 (153)
29	ACPOP	ss3738080079	Jul 13, 2019 (153)
30	PACBIO	ss3786922431	Jul 13, 2019 (153)
31	PACBIO	ss3792069041	Jul 13, 2019 (153)
32	PACBIO	ss3796951194	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3814507034	Jul 13, 2019 (153)
34	KHV_HUMAN_GENOMES	ss3814507035	Jul 13, 2019 (153)
35	EVA	ss3832573481	Apr 26, 2020 (154)
36	EVA	ss3839837929	Apr 26, 2020 (154)
37	EVA	ss3845315620	Apr 26, 2020 (154)
38	KOGIC	ss3969546218	Apr 26, 2020 (154)
39	KOGIC	ss3969546219	Apr 26, 2020 (154)
40	KOGIC	ss3969546220	Apr 26, 2020 (154)
41	FSA-LAB	ss3984000045	Apr 26, 2021 (155)
42	FSA-LAB	ss3984000046	Apr 26, 2021 (155)
43	GNOMAD	ss4233095734	Apr 26, 2021 (155)
44	GNOMAD	ss4233095735	Apr 26, 2021 (155)
45	GNOMAD	ss4233095736	Apr 26, 2021 (155)
46	GNOMAD	ss4233095737	Apr 26, 2021 (155)
47	GNOMAD	ss4233095739	Apr 26, 2021 (155)
48	GNOMAD	ss4233095740	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5201463637	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5201463638	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5201463639	Apr 26, 2021 (155)
52	1000G_HIGH_COVERAGE	ss5287009876	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5287009877	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5287009878	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5482250430	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5482250431	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5482250432	Oct 16, 2022 (156)
58	EVA	ss5624019387	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5748439127	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5748439128	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5748439129	Oct 16, 2022 (156)
62	EVA	ss5800167466	Oct 16, 2022 (156)
63	YY_MCH	ss5812282738	Oct 16, 2022 (156)
64	EVA	ss5836503006	Oct 16, 2022 (156)
65	EVA	ss5849936284	Oct 16, 2022 (156)
66	EVA	ss5919530033	Oct 16, 2022 (156)
67	1000Genomes	NC_000011.9 - 35287001	Oct 12, 2018 (152)
68	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29624434 (NC_000011.9:35287000::T 1473/3854) Row 29624435 (NC_000011.9:35287000::TT 64/3854)	-	Oct 12, 2018 (152)
69	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29624434 (NC_000011.9:35287000::T 1473/3854) Row 29624435 (NC_000011.9:35287000::TT 64/3854)	-	Oct 12, 2018 (152)
70	ExAC Submission ignored due to conflicting rows: Row 574501 (NC_000011.9:35287000:TTT: 8/85582) Row 574502 (NC_000011.9:35287000:TT: 268/85582) Row 574503 (NC_000011.9:35287000:T: 9612/85582) Row 574504 (NC_000011.9:35287000::T 31976/85582) Row 574505 (NC_000011.9:35287000::TT 1685/85582) Row 574506 (NC_000011.9:35287000::TTT 20/85582)	-	Oct 12, 2018 (152)
71	ExAC Submission ignored due to conflicting rows: Row 574501 (NC_000011.9:35287000:TTT: 8/85582) Row 574502 (NC_000011.9:35287000:TT: 268/85582) Row 574503 (NC_000011.9:35287000:T: 9612/85582) Row 574504 (NC_000011.9:35287000::T 31976/85582) Row 574505 (NC_000011.9:35287000::TT 1685/85582) Row 574506 (NC_000011.9:35287000::TTT 20/85582)	-	Oct 12, 2018 (152)
72	ExAC Submission ignored due to conflicting rows: Row 574501 (NC_000011.9:35287000:TTT: 8/85582) Row 574502 (NC_000011.9:35287000:TT: 268/85582) Row 574503 (NC_000011.9:35287000:T: 9612/85582) Row 574504 (NC_000011.9:35287000::T 31976/85582) Row 574505 (NC_000011.9:35287000::TT 1685/85582) Row 574506 (NC_000011.9:35287000::TTT 20/85582)	-	Oct 12, 2018 (152)
73	ExAC Submission ignored due to conflicting rows: Row 574501 (NC_000011.9:35287000:TTT: 8/85582) Row 574502 (NC_000011.9:35287000:TT: 268/85582) Row 574503 (NC_000011.9:35287000:T: 9612/85582) Row 574504 (NC_000011.9:35287000::T 31976/85582) Row 574505 (NC_000011.9:35287000::TT 1685/85582) Row 574506 (NC_000011.9:35287000::TTT 20/85582)	-	Oct 12, 2018 (152)
74	ExAC Submission ignored due to conflicting rows: Row 574501 (NC_000011.9:35287000:TTT: 8/85582) Row 574502 (NC_000011.9:35287000:TT: 268/85582) Row 574503 (NC_000011.9:35287000:T: 9612/85582) Row 574504 (NC_000011.9:35287000::T 31976/85582) Row 574505 (NC_000011.9:35287000::TT 1685/85582) Row 574506 (NC_000011.9:35287000::TTT 20/85582)	-	Oct 12, 2018 (152)
75	ExAC Submission ignored due to conflicting rows: Row 574501 (NC_000011.9:35287000:TTT: 8/85582) Row 574502 (NC_000011.9:35287000:TT: 268/85582) Row 574503 (NC_000011.9:35287000:T: 9612/85582) Row 574504 (NC_000011.9:35287000::T 31976/85582) Row 574505 (NC_000011.9:35287000::TT 1685/85582) Row 574506 (NC_000011.9:35287000::TTT 20/85582)	-	Oct 12, 2018 (152)
76	The Danish reference pan genome	NC_000011.9 - 35287001	Apr 26, 2020 (154)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376396806 (NC_000011.10:35265453::T 45688/135098) Row 376396807 (NC_000011.10:35265453::TT 1494/135242) Row 376396808 (NC_000011.10:35265453::TTT 35/135290)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376396806 (NC_000011.10:35265453::T 45688/135098) Row 376396807 (NC_000011.10:35265453::TT 1494/135242) Row 376396808 (NC_000011.10:35265453::TTT 35/135290)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376396806 (NC_000011.10:35265453::T 45688/135098) Row 376396807 (NC_000011.10:35265453::TT 1494/135242) Row 376396808 (NC_000011.10:35265453::TTT 35/135290)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376396806 (NC_000011.10:35265453::T 45688/135098) Row 376396807 (NC_000011.10:35265453::TT 1494/135242) Row 376396808 (NC_000011.10:35265453::TTT 35/135290)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376396806 (NC_000011.10:35265453::T 45688/135098) Row 376396807 (NC_000011.10:35265453::TT 1494/135242) Row 376396808 (NC_000011.10:35265453::TTT 35/135290)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376396806 (NC_000011.10:35265453::T 45688/135098) Row 376396807 (NC_000011.10:35265453::TT 1494/135242) Row 376396808 (NC_000011.10:35265453::TTT 35/135290)...	-	Apr 26, 2021 (155)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 25924219 (NC_000011.10:35265453:T: 28/1832) Row 25924220 (NC_000011.10:35265454::T 746/1832) Row 25924221 (NC_000011.10:35265454::TT 18/1832)	-	Apr 26, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 25924219 (NC_000011.10:35265453:T: 28/1832) Row 25924220 (NC_000011.10:35265454::T 746/1832) Row 25924221 (NC_000011.10:35265454::TT 18/1832)	-	Apr 26, 2020 (154)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 25924219 (NC_000011.10:35265453:T: 28/1832) Row 25924220 (NC_000011.10:35265454::T 746/1832) Row 25924221 (NC_000011.10:35265454::TT 18/1832)	-	Apr 26, 2020 (154)
86	Northern Sweden	NC_000011.9 - 35287001	Jul 13, 2019 (153)
87	8.3KJPN Submission ignored due to conflicting rows: Row 59432944 (NC_000011.9:35287000::T 6717/16756) Row 59432945 (NC_000011.9:35287000:T: 14/16756) Row 59432946 (NC_000011.9:35287000::TT 9/16756)	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 59432944 (NC_000011.9:35287000::T 6717/16756) Row 59432945 (NC_000011.9:35287000:T: 14/16756) Row 59432946 (NC_000011.9:35287000::TT 9/16756)	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 59432944 (NC_000011.9:35287000::T 6717/16756) Row 59432945 (NC_000011.9:35287000:T: 14/16756) Row 59432946 (NC_000011.9:35287000::TT 9/16756)	-	Apr 26, 2021 (155)
90	14KJPN Submission ignored due to conflicting rows: Row 82276231 (NC_000011.10:35265453::T 11363/28258) Row 82276232 (NC_000011.10:35265453:T: 18/28258) Row 82276233 (NC_000011.10:35265453::TT 12/28258)	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 82276231 (NC_000011.10:35265453::T 11363/28258) Row 82276232 (NC_000011.10:35265453:T: 18/28258) Row 82276233 (NC_000011.10:35265453::TT 12/28258)	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 82276231 (NC_000011.10:35265453::T 11363/28258) Row 82276232 (NC_000011.10:35265453:T: 18/28258) Row 82276233 (NC_000011.10:35265453::TT 12/28258)	-	Oct 16, 2022 (156)
93	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29624434 (NC_000011.9:35287000::T 1389/3708) Row 29624435 (NC_000011.9:35287000::TT 66/3708)	-	Oct 12, 2018 (152)
94	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29624434 (NC_000011.9:35287000::T 1389/3708) Row 29624435 (NC_000011.9:35287000::TT 66/3708)	-	Oct 12, 2018 (152)
95	ALFA	NC_000011.10 - 35265454	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)
rs796340682	Nov 08, 2017 (151)
rs72401312	May 11, 2012 (137)
rs148063589	May 11, 2012 (137)
rs148942352	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1711967441	NC_000011.9:35287000:TTT:	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss1711967439	NC_000011.9:35287000:TT:	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4233095740	NC_000011.10:35265453:TT:	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
12971961195	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
53323986, ss1370770034, ss1711967438, ss3007882069, ss5201463638	NC_000011.9:35287000:T:	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3691561264, ss3814507035, ss3969546218, ss4233095739, ss5287009877, ss5482250432, ss5748439128	NC_000011.10:35265453:T:	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
12971961195	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss256112208	NC_000011.8:35243576::T	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss294698127	NC_000011.8:35243583::T	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss289063354	NC_000011.8:35243589::T	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
290369, 11364944, ss664048359, ss666531303, ss1574335639, ss1707064458, ss1707064480, ss1711967436, ss2627787495, ss3738080079, ss3786922431, ss3792069041, ss3796951194, ss3832573481, ss3839837929, ss3984000045, ss5201463637, ss5624019387, ss5800167466, ss5836503006	NC_000011.9:35287000::T	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1370770037	NC_000011.9:35287001::T	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3063687757, ss3064512307, ss3649579978, ss3845315620, ss4233095734, ss5287009876, ss5482250430, ss5748439127, ss5812282738, ss5849936284, ss5919530033	NC_000011.10:35265453::T	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
12971961195	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3691561265, ss3814507034, ss3969546219	NC_000011.10:35265454::T	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss39913123, ss97433683	NT_009237.18:35227013::T	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1707064459, ss1707064483, ss1711967437, ss5201463639	NC_000011.9:35287000::TT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3984000046	NC_000011.9:35287013::TT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4233095735, ss5287009878, ss5482250431, ss5748439129	NC_000011.10:35265453::TT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12971961195	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3691561266, ss3969546220	NC_000011.10:35265454::TT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1711967440	NC_000011.9:35287000::TTT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4233095736	NC_000011.10:35265453::TTT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12971961195	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4233095737	NC_000011.10:35265453::TTTTT	NC_000011.10:35265453:TTTTTTTTTTTT… NC_000011.10:35265453:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(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 rs35055326

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

rs35055326