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Variant : CV87769 (NM_001077653.2(TBX20):c.250C>T (p.Pro84Ser)) Homo sapiens

Symbol: CV87769
Name: NM_001077653.2(TBX20):c.250C>T (p.Pro84Ser)
Condition: Malignant melanoma [RCV000067861]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: TBX20  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NP_001159692.1:p.Pro84Ser
NM_001166220.1:c.250C>T
NM_001077653.2:c.250C>T
NG_015805.1:g.9019C>T
NC_000007.14:g.35250081G>A
NC_000007.13:g.35289693G>A
NM_001077653.1:c.250C>T
NP_001071121.1:p.Pro84Ser
NC_000007.12:g.35256218G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38735,250,081 - 35,250,081CLINVAR
GRCh37735,289,693 - 35,289,693CLINVAR
Build 36735,256,218 - 35,256,218CLINVAR
Cytogenetic Map77p14.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8632561
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.