chr9:136149722:G>A Detail (hg19) (ABO)

Information

Genome

Assembly Position
hg19 chr9:136,149,722-136,149,722
hg38 chr9:133,274,306-133,274,306 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_020469.2:c.28+856C>T
Ensemble ENST00000538324.2:c.28+856C>T
ENST00000611156.4:c.28+856C>T
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 110300 OMIM
HGNC 79 HGNC
Ensembl ENSG00000175164 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
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.129 Pancreatic Neoplasm NA GAD Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs630014 dbSNP
Genome
hg19
Position
chr9:136,149,722-136,149,722
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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