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Variant : CV93006 (NM_173078.4(SLITRK4):c.149G>A (p.Arg50Lys)) Homo sapiens

Symbol: CV93006
Name: NM_173078.4(SLITRK4):c.149G>A (p.Arg50Lys)
Condition: Malignant melanoma [RCV000073104]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: SLITRK4  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NM_173078.4:c.149G>A
NG_021344.2:g.10152G>A
NC_000023.11:g.143630960C>T
NC_000023.10:g.142718776C>T
NM_173078.3:c.149G>A
NM_173078.2:c.149G>A
NP_775101.1:p.Arg50Lys
NM_001184749.2:c.149G>A
NM_001184750.2:c.149G>A
NM_001184749.1:c.149G>A
NM_001184750.1:c.149G>A
NP_001171679.1:p.Arg50Lys
NP_001171678.1:p.Arg50Lys
NC_000023.9:g.142546442C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh38X143,630,960 - 143,630,960CLINVAR
GRCh37X142,718,776 - 142,718,776CLINVAR
Build 36X142,546,442 - 142,546,442CLINVAR
Cytogenetic MapXXq27.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8637780
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.