chrX:154535190:G>C Detail (hg38) (G6PD)
Information
Genome
Assembly | Position |
---|---|
hg19 | chrX:153,763,405-153,763,405 View the variant detail on this assembly version. |
hg38 | chrX:154,535,190-154,535,190 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000402.4:c.463C>G | NP_000393.4:p.His155Asp |
NM_001042351.2:c.463C>G | NP_001035810.1:p.His155Asp | |
Ensemble | ENST00000369620.6:c.463C>G | ENST00000369620.6:p.His155Asp |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2022-08-12 | criteria provided, single submitter | Anemia, nonspherocytic hemolytic, due to G6PD deficiency |
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Detail |
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2023-07-29 | criteria provided, multiple submitters, no conflicts | Anemia, nonspherocytic hemolytic, due to G6PD deficiency |
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Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_001360016.2(G6PD):c.[376A>G;463C>G] AND Anemia, nonspherocytic hemolytic, due to G6PD deficiency | ClinVar | Detail |
NM_001360016.2(G6PD):c.463C>G (p.His155Asp) AND Anemia, nonspherocytic hemolytic, due to G6PD defici... | 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
- rs1050829 dbSNP
- Genome
- hg38
- Position
- chrX:154,535,190-154,535,190
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- C
Genome browser