chr10:43114493:CGA> Detail (hg38) (RET)

Information

Genome

Assembly Position
hg19 chr10:43,609,941-43,609,943 
hg38 chr10:43,114,493-43,114,495

HGVS

Type Transcript Protein
RefSeq NM_020630.4:c.1893_1895delCGA NP_065681.1:p.Asp631del
NM_020975.4:c.1893_1895delCGA NP_066124.1:p.Asp631del
Ensemble ENST00000340058.6:c.1893_1895delCGA ENST00000340058.6:p.Asp631del
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
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.614 multiple endocrine neoplasia type 2A NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NA 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
rs377767435 dbSNP
Genome
hg38
Position
chr10:43,114,493-43,114,495
Variant Type
snv
Reference Allele
CGA
Alternative Allele
-
Genome browser