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Reference SNP (refSNP) Cluster Report: rs371429653                 ** With Uncertain significance allele **
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:138/151
Map to Genome Build:108/Weight 1
Validation Status:byCluster
Citation:PubMedLitVarNEW
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:A/G (FWD)
Allele Origin:A:germline
G:germline
Ancestral Allele:G
Variation Viewer:link to VariationViewer
Clinical Significance:With Uncertain significance allele [ClinVar]
MAF/MinorAlleleCount:A=0.00001/1 (ExAC)
A=0.00008/1 (GO-ESP)
A=0.00002/2 (TOPMED)
HGVS Names
  • CM000678.2:g.88841971G>A
  • NC_000016.10:g.88841971G>A
  • NC_000016.9:g.88908379G>A
  • NG_008667.1:g.19996C>T
  • NM_000512.4:c.245C>T
  • NM_001323543.1:c.-311C>T
  • NM_001323544.1:c.263C>T
  • NP_000503.1:p.Ser82Leu
  • NP_001310473.1:p.Ser88Leu
  • XP_005256358.1:p.Ser82Leu
  • XP_005256359.1:p.Ser88Leu
  • XP_011521284.1:p.Ser88Leu
  • XP_016878600.1:p.Ser88Leu
  • XP_016878601.1:p.Ser88Leu
Links
SNP Details are organized in the following sections:
GeneView Map Submission Fasta Resource Diversity Validation

  Integrated Maps (Hint: click on 'Chr Pos' to see variant in the new NCBI variation viewer) back to top

  GeneView back to top

GeneView via direct blast against RefSeq sequences (used when no gene model is available): N/A


  Submitter records for this RefSNP Cluster back to top
The submission ss713332045 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs371429653 during BLAST analysis for the current build.


NCBI
Assay ID
Handle|Submitter IDValidation
Status
ss to rs
Orientation
/Strand
Alleles5' Near Seq 30 bp3' Near Seq 30 bpEntry
Date
Update
Date
Build
Added
Molecule
Type
Freq
Warning
Ancestral
Allele
Success
Rate
ss713332045NHLBI-ESP|ESP6500SI-chr16-88908379fwd/TA/Gggtagccgtcctgtgagcagtgccgccctcctatgtggaggtgacagaaacagaaactgg02/20/1302/20/13138Genomicunknown
ss947847146EGL|SCV000110902rev/BC/Tccagtttctgtttctgtcacctccacataggagggcggcactgctcacaggacggctacc01/23/1401/23/14138Genomicunknown
ss1692468383EVA_EXAC|EXAC_0.3.16:g88908379g>afwd/A/Gccgtcctgtgagcagtgccgccctcctatgtggaggtgacagaaacagaa03/04/1503/04/15144Genomicunknown
ss1946423674ILLUMINA|HumanCoreExome-12v1-0_C_variant.42816-1_B_R_2113334545fwd/TA/Gccgtcctgtgagcagtgccgccctcctatgtggaggtgacagaaacagaa10/29/1510/29/15147Genomicunknown
ss1959710077ILLUMINA|variant.42816-1_B_R_2113334545fwd/TA/Gccgtcctgtgagcagtgccgccctcctatgtggaggtgacagaaacagaa11/13/1511/13/15147Genomicunknown
ss2379553076TOPMED|16_88908379_G/Afwd/A/Gccgtcctgtgagcagtgccgccctcctatgtggaggtgacagaaacagaa11/19/1611/19/16150Genomicunknown
ss2742241045GNOMAD|exomes_rs371429653fwd/A/Gccgtcctgtgagcagtgccgccctcctatgtggaggtgacagaaacagaa05/17/1705/17/17151Genomicunknown
ss2985079779AFFY|Axiom_PsorMich_Affx-80254952fwd/A/Gccgtcctgtgagcagtgccgccctcctatgtggaggtgacagaaacagaa05/24/1705/24/17151Genomicunknown
ss3021740344ILLUMINA|MEGA_Consortium_v2_15070954_A2_variant.42816-1_B_R_2113334545fwd/A/Gccgtcctgtgagcagtgccgccctcctatgtggaggtgacagaaacagaa06/28/1706/28/17151Genomicunknown
ss3254721479TOPMED|TOPMed_freeze_5?chr16:88,841,971fwd/A/Gccgtcctgtgagcagtgccgccctcctatgtggaggtgacagaaacagaa10/01/1710/01/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs371429653|allelePos=101|totalLen=201|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=151
 GTCCCTGGAG GCGGTGGGCA GCCTACCGTT TCTGGCATGG GCGTTGGTGG TGTAGAAGCC
 ATTGCGGATG GGTAGCCGTC CTGTGAGCAG TGCCGCCCTC
 R
 CTATGTGGAG GTGACAGAAA CAGAAACTGG ATAAGAAGGG TGTGGCTCAG ACCCCGGGCG
 TCAACAAGAG CCCCAACGAG TAGACAGACG CGTGACAGAC

  NCBI Resource Links back to top
Submitter-Referenced
dbSNP Blast Analysis
3D structure mapping
NP_000503  

  Population Diversity (Alleles in RefSNP orientation) back to top

Sample AscertainmentGenotypesAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceHWPA
G
ss1692468383ExAc_Aggregated_Populations120994AF 0.000008260.99999171

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.000+/-0.0030000

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterUNKNOWNUNKNOWNUNKNOWN

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