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Gene | RET |
Variant | M918X |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | RET M918X indicates any Ret missense mutation that results in replacement of the methionine (M) at amino acid 918 by a different amino acid. |
Associated Drug Resistance | |
Category Variants Paths |
RET mutant RET M918X |
Transcript | NM_020975.6 |
gDNA | chr10:g.43121967_43121969 |
cDNA | c.2752_2754 |
Protein | p.M918 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_020975.5 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_001406744.1 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_020975.6 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_001406743.1 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_020975 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_020630.5 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_001406759.1 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_020630 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_001406771.1 | chr10:g.43128114_43128116 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_020630.7 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
NM_001406760.1 | chr10:g.43121967_43121969 | c.2752_2754 | p.M918 | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
RET M918X | unknown |