Variant #0001045684 (NC_000001.10:g.43223453C>A, NC_000001.10(NM_022356.3):c.1080+1G>T (P3H1))

Chromosome 1
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.43223453C>A
DNA change (hg38) -
Published as P3H1(NM_022356.3):c.1080+1G>T, P3H1(NM_022356.4):c.1080+1G>T
ISCN -
DB-ID P3H1_000001 See all 41 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) 0.0002 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +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     
P3H1 NM_022356.3 +/. - c.1080+1G>T r.spl? p.?


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