chr2:190428903:T>G Detail (hg19) (SLC40A1)

Information

Genome

Assembly Position
hg19 chr2:190,428,903-190,428,903
hg38 chr2:189,564,177-189,564,177 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_014585.5:c.809A>C NP_055400.1:p.Asp270Ala
Ensemble ENST00000261024.7:c.809A>C ENST00000261024.7:p.Asp270Ala
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 604653 OMIM
HGNC 10909 HGNC
Ensembl ENSG00000138449 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
0.562 HEMOCHROMATOSIS, TYPE 4 NA CLINVAR Detail
0.141 Iron Overload Mild iron overload in an African American man with SLC40A1 D270V. BeFree 22584997 Detail
0.141 Iron Overload We identified a novel D270V mutation in the SLC40A1 gene in a Black South Africa... BeFree 15338274 Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
Mild iron overload in an African American man with SLC40A1 D270V. DisGeNET Detail
We identified a novel D270V mutation in the SLC40A1 gene in a Black South African female with iron o... 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
hg19
Position
chr2:190,428,903-190,428,903
Variant Type
snv
Reference Allele
T
Alternative Allele
G
East Asian Chromosome Counts (ExAC)
8652
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
121216
Allele Counts in All Race (ExAC)
1
Heterozygous Counts in All Race (ExAC)
1
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
8.249736008447729E-6
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