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Variant : CV85460 (NM_017910.3(TRMT61B):c.1348C>T (p.Pro450Ser)) Homo sapiens

Symbol: CV85460
Name: NM_017910.3(TRMT61B):c.1348C>T (p.Pro450Ser)
Condition: Malignant melanoma [RCV000065543]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: SPDYA   TRMT61B  
Variant Type: single nucleotide variant (SO:0001624)
Source: CLINVAR
Molecular Consequence: utr-3|missense variant|3 prime utr variant
Evidence: literature only|not provided
HGVS Name(s): NM_001142634.1:c.*429G>A
NM_182756.3:c.*429G>A
NM_017910.3:c.1348C>T
NC_000002.12:g.28850370G>A
NC_000002.11:g.29073236G>A
NM_182756.2:c.*429G>A
NM_017910.2:c.1348C>T
NP_060380.3:p.Pro450Ser
NC_000002.10:g.28926740G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38228,850,370 - 28,850,370CLINVAR
GRCh37229,073,236 - 29,073,236CLINVAR
Build 36228,926,740 - 28,926,740CLINVAR
Cytogenetic Map22p23.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8630305
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.