Name: rs370068876
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.

rs370068876

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:94239197-94239208 (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: delTT / delT / dupT / dupTT / dupT…
delTT / delT / dupT / dupTT / dupTTT / dup(T)₆ / ins(T)₁₅
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.01972 (252/12782, ALFA)
delT=0.0622 (269/4322, 1000G)
dupT=0.12 (5/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PPP4R4 : 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	12782	TTTTTTTTTTTT=0.97802	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00219, TTTTTTTTTTTTT=0.01972, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00008, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000	0.962748	0.001886	0.035366	21
European	Sub	10540	TTTTTTTTTTTT=0.97343	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00266, TTTTTTTTTTTTT=0.02381, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00009, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000	0.95497	0.00229	0.04274	16
African	Sub	1172	TTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	36	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1136	TTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	104	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	80	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	86	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	508	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	62	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	310	TTTTTTTTTTTT=0.997	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	0.993548	0.0	0.006452	0

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	12782	(T)₁₂=0.97802	delTT=0.00000, delT=0.00219, dupT=0.01972, dupTT=0.00000, dupTTT=0.00000, ins(T)₁₅=0.00008
Allele Frequency Aggregator	European	Sub	10540	(T)₁₂=0.97343	delTT=0.00000, delT=0.00266, dupT=0.02381, dupTT=0.00000, dupTTT=0.00000, ins(T)₁₅=0.00009
Allele Frequency Aggregator	African	Sub	1172	(T)₁₂=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, ins(T)₁₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	508	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, ins(T)₁₅=0.000
Allele Frequency Aggregator	Other	Sub	310	(T)₁₂=0.997	delTT=0.000, delT=0.000, dupT=0.003, dupTT=0.000, dupTTT=0.000, ins(T)₁₅=0.000
Allele Frequency Aggregator	Asian	Sub	104	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, ins(T)₁₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	86	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, ins(T)₁₅=0.00
Allele Frequency Aggregator	South Asian	Sub	62	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, ins(T)₁₅=0.00
1000Genomes	Global	Study-wide	4322	(T)₁₂=0.9378	delT=0.0622
1000Genomes	East Asian	Sub	973	(T)₁₂=0.979	delT=0.021
1000Genomes	African	Sub	953	(T)₁₂=0.816	delT=0.184
1000Genomes	Europe	Sub	927	(T)₁₂=0.978	delT=0.022
1000Genomes	South Asian	Sub	826	(T)₁₂=0.959	delT=0.041
1000Genomes	American	Sub	643	(T)₁₂=0.969	delT=0.031
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.12

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 14	NC_000014.9:g.94239207_94239208del
GRCh38.p14 chr 14	NC_000014.9:g.94239208del
GRCh38.p14 chr 14	NC_000014.9:g.94239208dup
GRCh38.p14 chr 14	NC_000014.9:g.94239207_94239208dup
GRCh38.p14 chr 14	NC_000014.9:g.94239206_94239208dup
GRCh38.p14 chr 14	NC_000014.9:g.94239203_94239208dup
GRCh38.p14 chr 14	NC_000014.9:g.94239208_94239209insTTTTTTTTTTTTTTT
GRCh38.p14 chr 14 alt locus HSCHR14_7_CTG1	NT_187601.1:g.1353769_1353770del
GRCh38.p14 chr 14 alt locus HSCHR14_7_CTG1	NT_187601.1:g.1353770del
GRCh38.p14 chr 14 alt locus HSCHR14_7_CTG1	NT_187601.1:g.1353770dup
GRCh38.p14 chr 14 alt locus HSCHR14_7_CTG1	NT_187601.1:g.1353769_1353770dup
GRCh38.p14 chr 14 alt locus HSCHR14_7_CTG1	NT_187601.1:g.1353768_1353770dup
GRCh38.p14 chr 14 alt locus HSCHR14_7_CTG1	NT_187601.1:g.1353765_1353770dup
GRCh38.p14 chr 14 alt locus HSCHR14_7_CTG1	NT_187601.1:g.1353770_1353771insTTTTTTTTTTTTTTT
GRCh37.p13 chr 14	NC_000014.8:g.94705544_94705545del
GRCh37.p13 chr 14	NC_000014.8:g.94705545del
GRCh37.p13 chr 14	NC_000014.8:g.94705545dup
GRCh37.p13 chr 14	NC_000014.8:g.94705544_94705545dup
GRCh37.p13 chr 14	NC_000014.8:g.94705543_94705545dup
GRCh37.p13 chr 14	NC_000014.8:g.94705540_94705545dup
GRCh37.p13 chr 14	NC_000014.8:g.94705545_94705546insTTTTTTTTTTTTTTT

Gene: PPP4R4, protein phosphatase 4 regulatory subunit 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PPP4R4 transcript variant 3	NM_001348142.2:c.611-1466… NM_001348142.2:c.611-1466_611-1465del	N/A	Intron Variant
PPP4R4 transcript variant 4	NM_001348143.2:c.533-1466… NM_001348143.2:c.533-1466_533-1465del	N/A	Intron Variant
PPP4R4 transcript variant 5	NM_001348144.2:c.533-1466… NM_001348144.2:c.533-1466_533-1465del	N/A	Intron Variant
PPP4R4 transcript variant 1	NM_058237.2:c.854-1466_85… NM_058237.2:c.854-1466_854-1465del	N/A	Intron Variant
PPP4R4 transcript variant 6	NM_001348145.2:c.	N/A	Genic Downstream Transcript Variant
PPP4R4 transcript variant 2	NM_020958.3:c.	N/A	Genic Downstream Transcript Variant
PPP4R4 transcript variant 7	NR_145441.2:n.	N/A	Intron Variant
PPP4R4 transcript variant X3	XM_011537039.3:c.533-1466… XM_011537039.3:c.533-1466_533-1465del	N/A	Intron Variant
PPP4R4 transcript variant X5	XM_011537040.3:c.533-1466… XM_011537040.3:c.533-1466_533-1465del	N/A	Intron Variant
PPP4R4 transcript variant X2	XM_017021528.3:c.593-1466… XM_017021528.3:c.593-1466_593-1465del	N/A	Intron Variant
PPP4R4 transcript variant X1	XM_024449672.2:c.611-1466… XM_024449672.2:c.611-1466_611-1465del	N/A	Intron Variant
PPP4R4 transcript variant X4	XM_024449673.2:c.533-1466… XM_024449673.2:c.533-1466_533-1465del	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)₁₂=	delTT	delT	dupT	dupTT	dupTTT	dup(T)₆	ins(T)₁₅
GRCh38.p14 chr 14	NC_000014.9:g.94239197_94239208=	NC_000014.9:g.94239207_94239208del	NC_000014.9:g.94239208del	NC_000014.9:g.94239208dup	NC_000014.9:g.94239207_94239208dup	NC_000014.9:g.94239206_94239208dup	NC_000014.9:g.94239203_94239208dup	NC_000014.9:g.94239208_94239209insTTTTTTTTTTTTTTT
GRCh38.p14 chr 14 alt locus HSCHR14_7_CTG1	NT_187601.1:g.1353759_1353770=	NT_187601.1:g.1353769_1353770del	NT_187601.1:g.1353770del	NT_187601.1:g.1353770dup	NT_187601.1:g.1353769_1353770dup	NT_187601.1:g.1353768_1353770dup	NT_187601.1:g.1353765_1353770dup	NT_187601.1:g.1353770_1353771insTTTTTTTTTTTTTTT
GRCh37.p13 chr 14	NC_000014.8:g.94705534_94705545=	NC_000014.8:g.94705544_94705545del	NC_000014.8:g.94705545del	NC_000014.8:g.94705545dup	NC_000014.8:g.94705544_94705545dup	NC_000014.8:g.94705543_94705545dup	NC_000014.8:g.94705540_94705545dup	NC_000014.8:g.94705545_94705546insTTTTTTTTTTTTTTT
PPP4R4 transcript variant 3	NM_001348142.2:c.611-1476=	NM_001348142.2:c.611-1466_611-1465del	NM_001348142.2:c.611-1465del	NM_001348142.2:c.611-1465dup	NM_001348142.2:c.611-1466_611-1465dup	NM_001348142.2:c.611-1467_611-1465dup	NM_001348142.2:c.611-1470_611-1465dup	NM_001348142.2:c.611-1465_611-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant 4	NM_001348143.2:c.533-1476=	NM_001348143.2:c.533-1466_533-1465del	NM_001348143.2:c.533-1465del	NM_001348143.2:c.533-1465dup	NM_001348143.2:c.533-1466_533-1465dup	NM_001348143.2:c.533-1467_533-1465dup	NM_001348143.2:c.533-1470_533-1465dup	NM_001348143.2:c.533-1465_533-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant 5	NM_001348144.2:c.533-1476=	NM_001348144.2:c.533-1466_533-1465del	NM_001348144.2:c.533-1465del	NM_001348144.2:c.533-1465dup	NM_001348144.2:c.533-1466_533-1465dup	NM_001348144.2:c.533-1467_533-1465dup	NM_001348144.2:c.533-1470_533-1465dup	NM_001348144.2:c.533-1465_533-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant 1	NM_058237.1:c.854-1476=	NM_058237.1:c.854-1466_854-1465del	NM_058237.1:c.854-1465del	NM_058237.1:c.854-1465dup	NM_058237.1:c.854-1466_854-1465dup	NM_058237.1:c.854-1467_854-1465dup	NM_058237.1:c.854-1470_854-1465dup	NM_058237.1:c.854-1465_854-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant 1	NM_058237.2:c.854-1476=	NM_058237.2:c.854-1466_854-1465del	NM_058237.2:c.854-1465del	NM_058237.2:c.854-1465dup	NM_058237.2:c.854-1466_854-1465dup	NM_058237.2:c.854-1467_854-1465dup	NM_058237.2:c.854-1470_854-1465dup	NM_058237.2:c.854-1465_854-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant X2	XM_005267930.1:c.533-1476=	XM_005267930.1:c.533-1466_533-1465del	XM_005267930.1:c.533-1465del	XM_005267930.1:c.533-1465dup	XM_005267930.1:c.533-1466_533-1465dup	XM_005267930.1:c.533-1467_533-1465dup	XM_005267930.1:c.533-1470_533-1465dup	XM_005267930.1:c.533-1465_533-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant X5	XM_005267931.1:c.533-1476=	XM_005267931.1:c.533-1466_533-1465del	XM_005267931.1:c.533-1465del	XM_005267931.1:c.533-1465dup	XM_005267931.1:c.533-1466_533-1465dup	XM_005267931.1:c.533-1467_533-1465dup	XM_005267931.1:c.533-1470_533-1465dup	XM_005267931.1:c.533-1465_533-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant X3	XM_011537039.3:c.533-1476=	XM_011537039.3:c.533-1466_533-1465del	XM_011537039.3:c.533-1465del	XM_011537039.3:c.533-1465dup	XM_011537039.3:c.533-1466_533-1465dup	XM_011537039.3:c.533-1467_533-1465dup	XM_011537039.3:c.533-1470_533-1465dup	XM_011537039.3:c.533-1465_533-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant X5	XM_011537040.3:c.533-1476=	XM_011537040.3:c.533-1466_533-1465del	XM_011537040.3:c.533-1465del	XM_011537040.3:c.533-1465dup	XM_011537040.3:c.533-1466_533-1465dup	XM_011537040.3:c.533-1467_533-1465dup	XM_011537040.3:c.533-1470_533-1465dup	XM_011537040.3:c.533-1465_533-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant X2	XM_017021528.3:c.593-1476=	XM_017021528.3:c.593-1466_593-1465del	XM_017021528.3:c.593-1465del	XM_017021528.3:c.593-1465dup	XM_017021528.3:c.593-1466_593-1465dup	XM_017021528.3:c.593-1467_593-1465dup	XM_017021528.3:c.593-1470_593-1465dup	XM_017021528.3:c.593-1465_593-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant X1	XM_024449672.2:c.611-1476=	XM_024449672.2:c.611-1466_611-1465del	XM_024449672.2:c.611-1465del	XM_024449672.2:c.611-1465dup	XM_024449672.2:c.611-1466_611-1465dup	XM_024449672.2:c.611-1467_611-1465dup	XM_024449672.2:c.611-1470_611-1465dup	XM_024449672.2:c.611-1465_611-1464insTTTTTTTTTTTTTTT
PPP4R4 transcript variant X4	XM_024449673.2:c.533-1476=	XM_024449673.2:c.533-1466_533-1465del	XM_024449673.2:c.533-1465del	XM_024449673.2:c.533-1465dup	XM_024449673.2:c.533-1466_533-1465dup	XM_024449673.2:c.533-1467_533-1465dup	XM_024449673.2:c.533-1470_533-1465dup	XM_024449673.2:c.533-1465_533-1464insTTTTTTTTTTTTTTT

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#.

34 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79904864	Apr 25, 2013 (138)
2	PJP	ss294845195	May 31, 2013 (138)
3	1000GENOMES	ss1374474677	Aug 21, 2014 (142)
4	1000GENOMES	ss1374474679	Aug 21, 2014 (142)
5	EVA_GENOME_DK	ss1574809552	Apr 01, 2015 (144)
6	MCHAISSO	ss3065571246	Nov 08, 2017 (151)
7	BIOINF_KMB_FNS_UNIBA	ss3645364613	Oct 12, 2018 (152)
8	EVA_DECODE	ss3697276565	Jul 13, 2019 (153)
9	EVA_DECODE	ss3697276566	Jul 13, 2019 (153)
10	EVA_DECODE	ss3697276567	Jul 13, 2019 (153)
11	ACPOP	ss3740649343	Jul 13, 2019 (153)
12	ACPOP	ss3740649344	Jul 13, 2019 (153)
13	PACBIO	ss3787751109	Jul 13, 2019 (153)
14	KHV_HUMAN_GENOMES	ss3818021058	Jul 13, 2019 (153)
15	KHV_HUMAN_GENOMES	ss3818021059	Jul 13, 2019 (153)
16	EVA	ss3834075116	Apr 27, 2020 (154)
17	VINODS	ss4031548471	Apr 26, 2021 (155)
18	GNOMAD	ss4283214723	Apr 26, 2021 (155)
19	GNOMAD	ss4283214724	Apr 26, 2021 (155)
20	GNOMAD	ss4283214725	Apr 26, 2021 (155)
21	GNOMAD	ss4283214726	Apr 26, 2021 (155)
22	GNOMAD	ss4283214728	Apr 26, 2021 (155)
23	GNOMAD	ss4283214729	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5214590696	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5214590697	Apr 26, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5297275997	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5297275998	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5297275999	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5491221067	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5491221068	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5491221069	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5767784551	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5767784552	Oct 16, 2022 (156)
34	YY_MCH	ss5815013343	Oct 16, 2022 (156)
35	1000Genomes	NC_000014.8 - 94705534	Oct 12, 2018 (152)
36	The Danish reference pan genome	NC_000014.8 - 94705534	Apr 27, 2020 (154)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 459829934 (NC_000014.9:94239196::T 19190/133618) Row 459829935 (NC_000014.9:94239196::TT 112/133774) Row 459829936 (NC_000014.9:94239196::TTT 15/133774)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 459829934 (NC_000014.9:94239196::T 19190/133618) Row 459829935 (NC_000014.9:94239196::TT 112/133774) Row 459829936 (NC_000014.9:94239196::TTT 15/133774)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 459829934 (NC_000014.9:94239196::T 19190/133618) Row 459829935 (NC_000014.9:94239196::TT 112/133774) Row 459829936 (NC_000014.9:94239196::TTT 15/133774)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 459829934 (NC_000014.9:94239196::T 19190/133618) Row 459829935 (NC_000014.9:94239196::TT 112/133774) Row 459829936 (NC_000014.9:94239196::TTT 15/133774)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 459829934 (NC_000014.9:94239196::T 19190/133618) Row 459829935 (NC_000014.9:94239196::TT 112/133774) Row 459829936 (NC_000014.9:94239196::TTT 15/133774)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 459829934 (NC_000014.9:94239196::T 19190/133618) Row 459829935 (NC_000014.9:94239196::TT 112/133774) Row 459829936 (NC_000014.9:94239196::TTT 15/133774)...	-	Apr 26, 2021 (155)
43	Northern Sweden Submission ignored due to conflicting rows: Row 13934208 (NC_000014.8:94705533:T: 11/600) Row 13934209 (NC_000014.8:94705533::T 21/600)	-	Jul 13, 2019 (153)
44	Northern Sweden Submission ignored due to conflicting rows: Row 13934208 (NC_000014.8:94705533:T: 11/600) Row 13934209 (NC_000014.8:94705533::T 21/600)	-	Jul 13, 2019 (153)
45	8.3KJPN Submission ignored due to conflicting rows: Row 72560003 (NC_000014.8:94705533::T 312/16756) Row 72560004 (NC_000014.8:94705533:T: 40/16756)	-	Apr 26, 2021 (155)
46	8.3KJPN Submission ignored due to conflicting rows: Row 72560003 (NC_000014.8:94705533::T 312/16756) Row 72560004 (NC_000014.8:94705533:T: 40/16756)	-	Apr 26, 2021 (155)
47	14KJPN Submission ignored due to conflicting rows: Row 101621655 (NC_000014.9:94239196::T 456/28022) Row 101621656 (NC_000014.9:94239196:T: 45/28022)	-	Oct 16, 2022 (156)
48	14KJPN Submission ignored due to conflicting rows: Row 101621655 (NC_000014.9:94239196::T 456/28022) Row 101621656 (NC_000014.9:94239196:T: 45/28022)	-	Oct 16, 2022 (156)
49	ALFA	NC_000014.9 - 94239197	Apr 26, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3697276565, ss4283214729	NC_000014.9:94239196:TT:	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTT	(self)
9930998160	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTT	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTT	(self)
65229561, ss1374474677, ss3740649343, ss3787751109, ss3834075116, ss5214590697	NC_000014.8:94705533:T:	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3065571246, ss3645364613, ss3818021058, ss4283214728, ss5297275998, ss5491221067, ss5767784552	NC_000014.9:94239196:T:	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
9930998160	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3697276566	NC_000014.9:94239197:T:	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss294845195	NC_000014.7:93775293::T	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
469899, ss1574809552, ss3740649344, ss5214590696	NC_000014.8:94705533::T	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss1374474679	NC_000014.8:94705534::T	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4283214723, ss5297275997, ss5491221068, ss5767784551, ss5815013343	NC_000014.9:94239196::T	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9930998160	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3818021059	NC_000014.9:94239197::T	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3697276567	NC_000014.9:94239198::T	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss79904864	NT_026437.12:75705545::T	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4031548471	NT_187601.1:1353758::T	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4283214724, ss5297275999, ss5491221069	NC_000014.9:94239196::TT	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9930998160	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4283214725	NC_000014.9:94239196::TTT	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
9930998160	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4283214726	NC_000014.9:94239196::TTTTTT	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9930998160	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:94239196:TTTTTTTTTTTT:… NC_000014.9:94239196:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs370068876

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

rs370068876