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Variant : CV93005 (NM_173078.4(SLITRK4):c.1019C>A (p.Thr340Lys)) Homo sapiens

Symbol: CV93005
Name: NM_173078.4(SLITRK4):c.1019C>A (p.Thr340Lys)
Condition: Malignant melanoma [RCV000073103]
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.1019C>A
NG_021344.2:g.11022C>A
NC_000023.11:g.143630090G>T
NC_000023.10:g.142717906G>T
NM_173078.3:c.1019C>A
NM_173078.2:c.1019C>A
NP_775101.1:p.Thr340Lys
NM_001184750.2:c.1019C>A
NM_001184749.2:c.1019C>A
NM_001184749.1:c.1019C>A
NM_001184750.1:c.1019C>A
NP_001171678.1:p.Thr340Lys
NP_001171679.1:p.Thr340Lys
NC_000023.9:g.142545572G>T
Position
Human AssemblyChrPosition (strand)Source
GRCh38X143,630,090 - 143,630,090CLINVAR
GRCh37X142,717,906 - 142,717,906CLINVAR
Build 36X142,545,572 - 142,545,572CLINVAR
Cytogenetic MapXXq27.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8637779
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.