Variant #0000896264 (NC_000023.10:g.48752372G>A, NM_001032383.1:c.-3023G>A (PQBP1))

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.48752372G>A
DNA change (hg38) -
Published as TIMM17B(NM_001167947.1):c.289C>T (p.(Arg97Trp)), TIMM17B(NM_001167947.2):c.289C>T (p.R97W)
ISCN -
DB-ID TIMM17B_000004 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) 0.0006 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 2022-11-01 13:41:49 +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     
PQBP1 NM_001032383.1 -?/. - c.-3023G>A r.(?) p.(=)
PQBP1 NM_005710.2 -?/. - c.-3421G>A r.(?) p.(=)
TIMM17B NM_005834.3 -?/. - c.139C>T r.(?) p.(Arg47Trp)


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