Variant #0000810168 (NC_000023.10:g.153775047T>G, NM_000402.3:c.39A>C (G6PD))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153775047T>G
DNA change (hg38) -
Published as G6PD(NM_000402.4):c.39A>C (p.T13=)
ISCN -
DB-ID IKBKG_000145
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     

Protein level     
G6PD NM_000402.3 -?/. - c.39A>C r.(?) p.(Thr13=) - -
G6PD NM_001042351.1 -?/. - c.-9+636A>C r.(=) p.(=) - -
IKBKG NM_003639.3 -?/. - c.-1273T>G r.(?) p.(=) - -


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