Variant #0001033776 (NC_000003.11:g.157146184G>C, NM_024621.2:c.623C>G (VEPH1))

Chromosome 3
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.157146184G>C
DNA change (hg38) -
Published as VEPH1(NM_001167912.2):c.623C>G (p.(Ser208Cys))
ISCN -
DB-ID PTX3_000007
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) 0.00123 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 2025-05-05 21:14:00 +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     
PTX3 NM_002852.3 -?/. - c.-8539G>C r.(?) p.(=)
VEPH1 NM_024621.2 -?/. - c.623C>G r.(?) p.(Ser208Cys)


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