Variant #0000574969 (NC_000023.10:g.153792168T>C, NM_000402.3:c.-17083A>G (G6PD))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153792168T>C
DNA change (hg38) g.154563953=
Published as IKBKG(NM_001099857.4):c.1056-6T>C, IKBKG(NM_001099857.5):c.1056-6T>C
ISCN -
DB-ID IKBKG_000082 See all 2 reported entries
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) 0.14988 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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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.-17083A>G r.(?) p.(=) - -
G6PD NM_001042351.1 -/. - c.-16494A>G r.(?) p.(=) - -
IKBKG NM_003639.3 -/. - c.1056-6T>C r.(=) p.(=) - -


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