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

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 164761 OMIM
HGNC 9967 HGNC
Ensembl ENSG00000165731 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM981 COSMIC
MONDO
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

DescrptionSourceLinks
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
Genome browser