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Variant : CV91560 (NM_006678.4(CD300C):c.196G>A (p.Asp66Asn)) Homo sapiens

Symbol: CV91560
Name: NM_006678.4(CD300C):c.196G>A (p.Asp66Asn)
Condition: Malignant melanoma [RCV000071658]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: CD300C  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NC_000017.9:g.70052547C>T
NC_000017.11:g.74544813C>T
NC_000017.10:g.72540952C>T
NM_006678.4:c.196G>A
NM_006678.3:c.196G>A
NP_006669.1:p.Asp66Asn
Position
Human AssemblyChrPosition (strand)Source
GRCh381774,544,813 - 74,544,813CLINVAR
GRCh371772,540,952 - 72,540,952CLINVAR
Build 361770,052,547 - 70,052,547CLINVAR
Cytogenetic Map1717q25.1CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8636337
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.