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Variant : CV82980 (NM_152459.4(C16orf89):c.513G>A (p.Thr171=)) Homo sapiens

Symbol: CV82980
Name: NM_152459.4(C16orf89):c.513G>A (p.Thr171=)
Condition: Malignant melanoma [RCV000063060]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: C16orf89  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NC_000016.8:g.5048609C>T
NM_152459.4:c.513G>A
NG_030316.1:g.12539G>A
NC_000016.10:g.5058607C>T
NC_000016.9:g.5108608C>T
NM_152459.3:c.513G>A
NP_689672.4:p.Thr171=
NM_001098514.2:c.513G>A
NM_001098514.1:c.513G>A
NP_001091984.2:p.Thr171=
Position
Human AssemblyChrPosition (strand)Source
GRCh38165,058,607 - 5,058,607CLINVAR
GRCh37165,108,608 - 5,108,608CLINVAR
Build 36165,048,609 - 5,048,609CLINVAR
Cytogenetic Map1616p13.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8627836
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.