chr10:43615567:AGC>TTT Detail (hg19) (RET)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr10:43,615,567-43,615,569 |
hg38 | chr10:43,120,119-43,120,121 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_020630.4:c.2646_2648delinsTTT | NP_065681.1:p.Ala883Phe |
NM_020975.4:c.2646_2648delinsTTT | NP_066124.1:p.Ala883Phe | |
Ensemble | ENST00000713926.1:c.2382_2384delinsTTT | ENST00000713926.1:p.Ala795Phe |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.320 | Medullary carcinoma of thyroid | Multiple endocrine neoplasia type 2B with a RET proto-oncogene A883F mutation di... | BeFree | 21186952 | Detail |
0.614 | multiple endocrine neoplasia type 2A | Like RET with the M918T or A883F MEN 2B mutation, the transforming activity of R... | BeFree | 10679286 | Detail |
0.592 | multiple endocrine neoplasia type 2B | Multiple endocrine neoplasia type 2B with a RET proto-oncogene A883F mutation di... | BeFree | 21186952 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Multiple endocrine neoplasia type 2B with a RET proto-oncogene A883F mutation displays a more indole... | DisGeNET | Detail |
Like RET with the M918T or A883F MEN 2B mutation, the transforming activity of RET with the V804M/Y8... | DisGeNET | Detail |
Multiple endocrine neoplasia type 2B with a RET proto-oncogene A883F mutation displays a more indole... | DisGeNET | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs121913306 dbSNP
- Genome
- hg19
- Position
- chr10:43,615,567-43,615,569
- Variant Type
- snv
- Reference Allele
- AGC
- Alternative Allele
- TTT
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