Variant #0001006781 (NC_000023.10:g.48374469C>T, NM_203475.1:c.1108C>T (PORCN))

Chromosome X
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.48374469C>T
DNA change (hg38) -
Published as PORCN(NM_001282167.1):c.862C>T (p.R288W), PORCN(NM_203475.1):c.1108C>T (p.(Arg370Trp))
ISCN -
DB-ID EBP_000052 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) 1.0E-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 2024-08-28 13:16:32 +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.-5900C>T r.(?) p.(=)
PORCN NM_203475.1 -?/. - c.1108C>T r.(?) p.(Arg370Trp)


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