Variant #0000951725 (NC_000023.10:g.153780338C>G, NM_000402.3:c.-5253G>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.153780338C>G
DNA change (hg38) -
Published as IKBKG(NM_001099857.4):c.121C>G (p.L41V)
ISCN -
DB-ID IKBKG_000154
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) 4.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
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.-5253G>C r.(?) p.(=) - -
G6PD NM_001042351.1 -?/. - c.-4664G>C r.(?) p.(=) - -
IKBKG NM_003639.3 -?/. - c.121C>G r.(?) p.(Leu41Val) - -


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