chr1:206770368:G>A Detail (hg38) (IL10)

Information

Genome

Assembly Position
hg19 chr1:206,943,713-206,943,713 View the variant detail on this assembly version.
hg38 chr1:206,770,368-206,770,368

HGVS

Type Transcript Protein
RefSeq NM_000572.2:c.379-474C>T
Ensemble ENST00000423557.1:c.379-474C>T
ENST00000471071.2:c.124-474C>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 124092 OMIM
HGNC 5962 HGNC
Ensembl ENSG00000136634 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
0.004 Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site Eight single nucleotide polymorphisms were associated with spontaneous productio... BeFree 24628819 Detail
Annotation

Annotations

DescrptionSourceLinks
Eight single nucleotide polymorphisms were associated with spontaneous production of IL-10 in cultur... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs1878672 dbSNP
Genome
hg38
Position
chr1:206,770,368-206,770,368
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser