Variant #0000993532 (NC_000003.11:g.196434771G>T, NM_032898.3:c.155C>A (CEP19))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.196434771G>T
DNA change (hg38) -
Published as CEP19(NM_032898.3):c.155C>A (p.(Ala52Asp))
ISCN -
DB-ID CEP19_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGX NM_017861.3 ?/. - c.-4633G>T r.(?) p.(=)
CEP19 NM_032898.3 ?/. - c.155C>A r.(?) p.(Ala52Asp)


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