chr10:43609069:T>C Detail (hg19) (RET)

Information

Genome

Assembly Position
hg19 chr10:43,609,069-43,609,069
hg38 chr10:43,113,621-43,113,621 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_020975.4:c.1825T>C NP_066124.1:p.Cys609Arg
NM_020630.4:c.1825T>C NP_065681.1:p.Cys609Arg
Ensemble ENST00000355710.8:c.1825T>C ENST00000355710.8:p.Cys609Arg
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
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
Pathogenic 2000-09-04 no assertion criteria provided familial medullary thyroid carcinoma germline Detail
Pathogenic 2015-06-16 criteria provided, single submitter not provided germline Detail
Likely pathogenic 2013-01-01 no assertion criteria provided Aganglionic megacolon unknown Detail
Pathogenic 2019-07-02 criteria provided, single submitter Hereditary cancer-predisposing syndrome germline Detail
Pathogenic 2023-04-29 criteria provided, single submitter Multiple endocrine neoplasia, type 2 germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.614 multiple endocrine neoplasia type 2A NA CLINVAR Detail
0.522 familial medullary thyroid carcinoma NA CLINVAR Detail
0.320 Medullary carcinoma of thyroid Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with... BeFree 16343103 Detail
0.006 Hyperparathyroidism, Primary In conclusion, at variance from what already known, in this large kindred the Cy... BeFree 19475497 Detail
0.605 pheochromocytoma In conclusion, at variance from what already known, in this large kindred the Cy... BeFree 19475497 Detail
0.320 Medullary carcinoma of thyroid In conclusion, at variance from what already known, in this large kindred the Cy... BeFree 19475497 Detail
0.614 multiple endocrine neoplasia type 2A In this short review article, we comment on our previous report of a large multi... BeFree 22584703 Detail
0.605 pheochromocytoma Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with... BeFree 16343103 Detail
<0.001 Hirschsprung disease 1 Four subjects (aged 31-50 years) with co-occurring RET mutations in exons 10 (C6... BeFree 23744765 Detail
0.006 Hyperparathyroidism, Primary In this short review article, we comment on our previous report of a large multi... BeFree 22584703 Detail
<0.001 Hirschsprung Disease Four subjects (aged 31-50 years) with co-occurring RET mutations in exons 10 (C6... BeFree 23744765 Detail
0.305 multiple endocrine neoplasia Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with... BeFree 16343103 Detail
0.320 Medullary carcinoma of thyroid In this short review article, we comment on our previous report of a large multi... BeFree 22584703 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_020975.6(RET):c.1825T>C (p.Cys609Arg) AND Familial medullary thyroid carcinoma ClinVar Detail
NM_020975.6(RET):c.1825T>C (p.Cys609Arg) AND not provided ClinVar Detail
NM_020975.6(RET):c.1825T>C (p.Cys609Arg) AND Aganglionic megacolon ClinVar Detail
NM_020975.6(RET):c.1825T>C (p.Cys609Arg) AND Hereditary cancer-predisposing syndrome ClinVar Detail
NM_020975.6(RET):c.1825T>C (p.Cys609Arg) AND Multiple endocrine neoplasia, type 2 ClinVar Detail
NA DisGeNET Detail
NA DisGeNET Detail
Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma an... DisGeNET Detail
In conclusion, at variance from what already known, in this large kindred the Cys609Ser RET mutation... DisGeNET Detail
In conclusion, at variance from what already known, in this large kindred the Cys609Ser RET mutation... DisGeNET Detail
In conclusion, at variance from what already known, in this large kindred the Cys609Ser RET mutation... DisGeNET Detail
In this short review article, we comment on our previous report of a large multiple endocrine neopla... DisGeNET Detail
Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma an... DisGeNET Detail
Four subjects (aged 31-50 years) with co-occurring RET mutations in exons 10 (C609R; n=1) and 13 (Y7... DisGeNET Detail
In this short review article, we comment on our previous report of a large multiple endocrine neopla... DisGeNET Detail
Four subjects (aged 31-50 years) with co-occurring RET mutations in exons 10 (C609R; n=1) and 13 (Y7... DisGeNET Detail
Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma an... DisGeNET Detail
In this short review article, we comment on our previous report of a large multiple endocrine neopla... 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
rs77558292 dbSNP
Genome
hg19
Position
chr10:43,609,069-43,609,069
Variant Type
snv
Reference Allele
T
Alternative Allele
C
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