Variant #0000961049 (NC_000001.10:g.43228263C>T, NC_000001.10(NM_022356.3):c.466-117G>A (P3H1))

Chromosome 1
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.43228263C>T
DNA change (hg38) -
Published as P3H1(NM_022356.3):c.466-117G>A
ISCN -
DB-ID P3H1_000132
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +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     
P3H1 NM_022356.3 -?/. - c.466-117G>A r.(=) p.(=)
C1orf50 NM_024097.3 -?/. - c.-4720C>T r.(?) p.(=)


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