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Variant : CV91476 (NM_032559.4(KIF2B):c.1861G>A (p.Glu621Lys)) Homo sapiens

Symbol: CV91476
Name: NM_032559.4(KIF2B):c.1861G>A (p.Glu621Lys)
Condition: Malignant melanoma [RCV000071574]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: KIF2B   MIR548AJ2  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NM_032559.4:c.1861G>A
NC_000017.11:g.53824894G>A
NC_000017.10:g.51902255G>A
NR_039674.1:c.57-68870C>T
NP_115948.4:p.Glu621Lys
NC_000017.9:g.49257254G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381753,824,894 - 53,824,894CLINVAR
GRCh371751,902,255 - 51,902,255CLINVAR
Build 361749,257,254 - 49,257,254CLINVAR
Cytogenetic Map1717q22CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8636252
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.