chr5:147828066:A>C Detail (hg38) (SPINK1)

Information

Genome

Assembly Position
hg19 chr5:147,207,629-147,207,629 View the variant detail on this assembly version.
hg38 chr5:147,828,066-147,828,066

HGVS

Type Transcript Protein
RefSeq NM_003122.4:c.150T>G NP_003113.2:p.Asp50Glu
Ensemble ENST00000296695.10:c.150T>G ENST00000296695.10:p.Asp50Glu
ENST00000510027.2:c.150T>G ENST00000510027.2:p.Asp50Glu
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance not provided
Review star
Show details
Links
Type Database ID Link
Gene MIM 167790 OMIM
HGNC 11244 HGNC
Ensembl ENSG00000164266 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
not provided no assertion provided Hereditary pancreatitis germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.245 Hereditary pancreatitis NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_001379610.1(SPINK1):c.150T>G (p.Asp50Glu) AND Hereditary pancreatitis 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
rs515726206 dbSNP
Genome
hg38
Position
chr5:147,828,066-147,828,066
Variant Type
snv
Reference Allele
A
Alternative Allele
C
Genome browser