RGD:8624775 Rat Genome Database

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Variant: RGD:8624775 -  Homo sapiens

RGD ID: 8624775
ClinVar ID: CV79889
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: APOA2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 161,193,162
GRCh38 1 161,223,372
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001643.1:c.30C>T
NG_012043.1:g.5257C>T
NC_000001.11:g.161223372G>A
NC_000001.10:g.161193162G>A
More...
synonymous variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:APOA2
Accession:NM_001643
Location:EXON
Amino Acid Prediction: L to L (synonymous)
Amino Acid Position: 10
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKLLAATVLLLTICSLEGALVRRQAKEPCVESLVSQYFQTVTDYGKDLMEKVKSPELQAEAKSYFEKSKEQLTPLIKKAG
TELVNFLSYFVELGTQPATQ*

Variant Samples