chr19:1221977:G>T Detail (hg38) (STK11)

Information

Genome

Assembly Position
hg19 chr19:1,221,976-1,221,976 View the variant detail on this assembly version.
hg38 chr19:1,221,977-1,221,977

HGVS

Type Transcript Protein
RefSeq NM_000455.4:c.891G>T NP_000446.1:p.Arg297Ser
Ensemble ENST00000326873.12:c.891G>T ENST00000326873.12:p.Arg297Ser
ENST00000585465.3:c.891G>T ENST00000585465.3:p.Arg297Ser
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 602216 OMIM
HGNC 11389 HGNC
Ensembl ENSG00000118046 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM6557208 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2023-06-22 criteria provided, single submitter Peutz-Jeghers syndrome germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.120 Neoplastic Syndromes, Hereditary NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000455.5(STK11):c.891G>T (p.Arg297Ser) AND Peutz-Jeghers syndrome 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
rs730881984 dbSNP
Genome
hg38
Position
chr19:1,221,977-1,221,977
Variant Type
snv
Reference Allele
G
Alternative Allele
T
Genome browser