Variant #0000984578 (NC_000023.10:g.153791864C>T, NM_000402.3:c.-16779G>A (G6PD))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.153791864C>T
DNA change (hg38) -
Published as IKBKG(NM_001099857.5):c.1003C>T (p.Q335*)
ISCN -
DB-ID IKBKG_000157
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +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.-16779G>A r.(?) p.(=) - -
G6PD NM_001042351.1 +/. - c.-16190G>A r.(?) p.(=) - -
IKBKG NM_003639.3 +/. - c.1003C>T r.(?) p.(Gln335*) - -


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