Variant #0000984711 (NC_000023.10:g.48375575T>C, NM_203475.1:c.1178T>C (PORCN))

Chromosome X
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.48375575T>C
DNA change (hg38) -
Published as PORCN(NM_203475.3):c.1178T>C (p.(Leu393Pro))
ISCN -
DB-ID EBP_000061
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) 3.0E-5 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 2024-04-19 20:27:30 +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     
EBP NM_006579.2 ?/. - c.-4794T>C r.(?) p.(=)
PORCN NM_203475.1 ?/. - c.1178T>C r.(?) p.(Leu393Pro)


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