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Variant : CV90677 (NM_022473.2(ZNF106):c.2276A>T (p.Asn759Ile)) Homo sapiens

Symbol: CV90677
Name: NM_022473.2(ZNF106):c.2276A>T (p.Asn759Ile)
Condition: Malignant melanoma [RCV000070775]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: ZNF106  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000015.8:g.40529417T>A
NC_000015.10:g.42449927T>A
NC_000015.9:g.42742125T>A
NP_071918.1:p.Asn759Ile
NM_022473.2:c.2276A>T
NM_022473.1:c.2276A>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381542,449,927 - 42,449,927CLINVAR
GRCh371542,742,125 - 42,742,125CLINVAR
Build 361540,529,417 - 40,529,417CLINVAR
Cytogenetic Map1515q15.1CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8635456
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.