View all transcript variants in gene RET

Information The variants shown are described using the NM_020975.4 transcript reference sequence.

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Effect     

AscendingDNA change (cDNA)     

Protein     

GVS function     

Position     

Exon     

PolyPhen     

RNA change     

SIFT     

Chr     

Allele     

Type     

DNA change (genomic) (hg19)     

Published as     

GERP     

Segregation     

DB-ID     

MSCV     

dbSNP ID     

Frequency     

Sources     

Reference     

Variant remarks     

Genetic origin     

Owner     
+/+ c.2753T>C p.(Met918Thr) missense_variant - 16/19 probably_damaging(1) r.(?) deleterious(0) 10 Unknown subst g.43617416T>C - 5.430 - RET_000007 MSCV_0000200 rs74799832 - ; clinvar; 15531714;18252215;7824936;9620546;23757202;7977365;2660074;3078962;7536460;7911697;{PMID:7906417:79064 - - -
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