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Variant : CV83820 (NM_001303508.1(ISX):c.72G>A (p.Pro24=)) Homo sapiens

Symbol: CV83820
Name: NM_001303508.1(ISX):c.72G>A (p.Pro24=)
Condition: Malignant melanoma [RCV000063901]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: ISX   ISX-AS1  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NC_000022.11:g.35067159G>A
NC_000022.10:g.35463152G>A
NC_000022.9:g.33793152G>A
NM_001303508.1:c.72G>A
NP_001290437.1:p.Pro24=
Position
Human AssemblyChrPosition (strand)Source
GRCh382235,067,159 - 35,067,159CLINVAR
GRCh372235,463,152 - 35,463,152CLINVAR
Build 362233,793,152 - 33,793,152CLINVAR
Cytogenetic Map2222q12.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8628676
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.