chrX:153764371:A>G Detail (hg19) (G6PD)

Information

Genome

Assembly Position
hg19 chrX:153,764,371-153,764,371
hg38 chrX:154,536,156-154,536,156 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000402.4:c.143T>C NP_000393.4:p.Ile48Thr
NM_001042351.2:c.143T>C NP_001035810.1:p.Ile48Thr
Ensemble ENST00000369620.6:c.143T>C ENST00000369620.6:p.Ile48Thr
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 Pathogenic Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 305900 OMIM
HGNC 4057 HGNC
Ensembl ENSG00000160211 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
other 2013-04-18 no assertion criteria provided germline Detail
Pathogenic 2023-04-08 criteria provided, multiple submitters, no conflicts not provided germline Detail
Pathogenic Likely pathogenic 2024-03-17 criteria provided, multiple submitters, no conflicts Anemia, nonspherocytic hemolytic, due to G6PD deficiency germline unknown Detail
Pathogenic 2021-06-16 criteria provided, single submitter G6PD deficiency unknown Detail
Likely pathogenic 2022-08-12 criteria provided, single submitter Anemia, nonspherocytic hemolytic, due to G6PD deficiency unknown Detail
Likely pathogenic 2022-08-12 criteria provided, single submitter Anemia, nonspherocytic hemolytic, due to G6PD deficiency unknown Detail
Likely pathogenic 2021-11-11 criteria provided, single submitter Anemia, nonspherocytic hemolytic, due to G6PD deficiency,Malaria, susceptibility to unknown Detail
Likely pathogenic 2021-11-11 criteria provided, single submitter Anemia, nonspherocytic hemolytic, due to G6PD deficiency,Malaria, susceptibility to unknown Detail
Pathogenic 2023-10-26 criteria provided, single submitter Malaria, susceptibility to unknown Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr) AND G6PD AURES ClinVar Detail
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr) AND not provided ClinVar Detail
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr) AND Anemia, nonspherocytic hemolytic, due to G6PD deficiency ClinVar Detail
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr) AND G6PD deficiency ClinVar Detail
NM_001360016.2(G6PD):c.[143T>C;202G>A] AND Anemia, nonspherocytic hemolytic, due to G6PD deficiency ClinVar Detail
NM_001360016.2(G6PD):c.[143T>C;563C>T] AND Anemia, nonspherocytic hemolytic, due to G6PD deficiency ClinVar Detail
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr) AND multiple conditions ClinVar Detail
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr) AND multiple conditions ClinVar Detail
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr) AND Malaria, susceptibility to ClinVar 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
rs76645461 dbSNP
Genome
hg19
Position
chrX:153,764,371-153,764,371
Variant Type
snv
Reference Allele
A
Alternative Allele
G
East Asian Chromosome Counts (ExAC)
6635
East Asian Allele Counts (ExAC)
1
East Asian Heterozygous Counts (ExAC)
1
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
1.5071590052750564E-4
Chromosome Counts in All Race (ExAC)
87386
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)
1.1443480649074222E-5
East Asian Hemizygous Counts (ExAC)
0
Hemizygous Counts in All Race (ExAC)
0
Genome browser