View genomic variant #0000000841

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.157435621T>C
Published as -
GERP 5.890
Segregation -
DB-ID GPD2_000001 See all 2 reported entries
MSCV MSCV_0000841
dbSNP ID rs121918407
Frequency -
Sources ; clinVar; Ensembl;
Reference 9070847
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
GPD2 00000781 NM_000408.4 0000000841 +/+ - 15/17 c.1904T>C p.(Phe635Ser) benign(0.368) missense_variant - deleterious(0.01)
GPD2 00000780 NM_001083112.2 0000000841 +/+ - 15/17 c.1904T>C p.(Phe635Ser) benign(0.368) missense_variant - deleterious(0.01)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000017461;
Chromosome 2:157435621..157435621
ClinVar Allele ID 31120
Disease database name and identifier Human Phenotype Ontology:HP:0005965, Human Phenotype Ontology:HP:0005978, Human Phenotype Ontology:HP:0100652, MONDO:MONDO:0005148, MeSH:D003924, MedGen:C0011860, OMIM:125853
ClinVar preferred disease name Type II diabetes mellitus
HGVS variant names NC 000002.11:g.157435621T>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA126187|OMIM:138430.0001
Gene symbol:Gene id. GPD2:2820
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121918407
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None