Variant #0000728691 (NC_000023.10:g.153774997C>G, NC_000023.10(NM_000402.3):c.82+7G>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.153774997C>G
DNA change (hg38) -
Published as G6PD(NM_000402.4):c.82+7G>C (p.(=))
ISCN -
DB-ID IKBKG_000073 See all 3 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) 0.0007 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +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.82+7G>C r.(=) p.(=) - -
G6PD NM_001042351.1 -?/. - c.-8-619G>C r.(=) p.(=) - -
IKBKG NM_003639.3 -?/. - c.-1323C>G r.(?) p.(=) - -


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