Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV84430 (NM_172362.2(KCNH1):c.2925G>A (p.Arg975=)) Homo sapiens

Symbol: CV84430
Name: NM_172362.2(KCNH1):c.2925G>A (p.Arg975=)
Condition: Malignant melanoma [RCV000064512]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: KCNH1  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_002238.3:c.2844G>A
NM_172362.2:c.2925G>A
NG_029777.1:g.455790G>A
NC_000001.11:g.210683326C>T
NC_000001.10:g.210856668C>T
NM_002238.2:c.2844G>A
NM_172362.1:c.2925G>A
NP_758872.1:p.Arg975=
NP_002229.1:p.Arg948=
NC_000001.9:g.208923291C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381210,683,326 - 210,683,326CLINVAR
GRCh371210,856,668 - 210,856,668CLINVAR
Build 361208,923,291 - 208,923,291CLINVAR
Cytogenetic Map11q32.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8629285
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
Status: ACTIVE



NHLBI Logo

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