chr10:43118392:G>A Detail (hg38) (RET)

Information

Genome

Assembly Position
hg19 chr10:43,613,840-43,613,840 View the variant detail on this assembly version.
hg38 chr10:43,118,392-43,118,392

HGVS

Type Transcript Protein
RefSeq NM_020630.4:c.2304G>A NP_065681.1:p.Glu768=
NM_020975.4:c.2304G>A NP_066124.1:p.Glu768=
Ensemble ENST00000340058.6:c.2304G>A ENST00000340058.6:p.Glu768=
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Likely benign
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
Likely benign 2023-02-23 criteria provided, single submitter Hereditary cancer-predisposing syndrome germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.522 familial medullary thyroid carcinoma NA CLINVAR Detail
0.031 Malignant neoplasm of thyroid The RET E768D mutation is associated with MTC with a later age at presentation, ... BeFree 16736292 Detail
0.522 familial medullary thyroid carcinoma RET mutations in exons 13 and 14 of FMTC patients. UNIPROT 7784092 Detail
0.522 familial medullary thyroid carcinoma The RET mutation E768D confers a late-onset familial medullary thyroid carcinoma... BeFree 16736292 Detail
0.320 Medullary carcinoma of thyroid RET mutation analysis confirmed an E768D mutation in exon 13 in 8 family members... BeFree 16736292 Detail
0.109 Thyroid carcinoma The RET E768D mutation is associated with MTC with a later age at presentation, ... BeFree 16736292 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_020975.6(RET):c.2304G>A (p.Glu768=) AND Hereditary cancer-predisposing syndrome ClinVar Detail
NA DisGeNET Detail
The RET E768D mutation is associated with MTC with a later age at presentation, incomplete penetranc... DisGeNET Detail
RET mutations in exons 13 and 14 of FMTC patients. DisGeNET Detail
The RET mutation E768D confers a late-onset familial medullary thyroid carcinoma -- only phenotype w... DisGeNET Detail
RET mutation analysis confirmed an E768D mutation in exon 13 in 8 family members, 3 affected with me... DisGeNET Detail
The RET E768D mutation is associated with MTC with a later age at presentation, incomplete penetranc... 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
-
Genome
hg38
Position
chr10:43,118,392-43,118,392
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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