Variant #0000507492 (NC_000001.10:g.43228001G>T, NM_022356.3:c.611C>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.43228001G>T
DNA change (hg38) g.42762330G>T
Published as LEPRE1(NM_001146289.1):c.611C>A (p.(Pro204His)), P3H1(NM_022356.3):c.611C>A (p.P204H)
ISCN -
DB-ID P3H1_000103 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) 0.00175 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-05-16 12:02:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
P3H1 NM_022356.3 -?/. - c.611C>A r.(?) p.(Pro204His)
C1orf50 NM_024097.3 -?/. - c.-4982G>T r.(?) p.(=)


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