chr10:43597858:G>T Detail (hg19) (RET)

Information

Genome

Assembly Position
hg19 chr10:43,597,858-43,597,858
hg38 chr10:43,102,410-43,102,410 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_020975.4:c.406G>T NP_066124.1:p.Glu136Ter
NM_020630.4:c.406G>T NP_065681.1:p.Glu136Ter
Ensemble ENST00000355710.8:c.406G>T ENST00000355710.8:p.Glu136Ter
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance risk factor
Review star
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
Clinical significance Last evaluated Review status Condition Origin Links
risk factor 1994-01-27 no assertion criteria provided Hirschsprung disease, susceptibility to, 1 germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.156 Hirschsprung disease 1 NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_020975.6(RET):c.406G>T (p.Glu136Ter) AND Hirschsprung disease, susceptibility to, 1 ClinVar Detail
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
rs79014735 dbSNP
Genome
hg19
Position
chr10:43,597,858-43,597,858
Variant Type
snv
Reference Allele
G
Alternative Allele
T
Genome browser