Variant #0000576217 (NC_000023.10:g.48375668C>A, NM_203475.1:c.1271C>A (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.48375668C>A
DNA change (hg38) g.48517280C>A
Published as PORCN(NM_001282167.1):c.1025C>A (p.T342N)
ISCN -
DB-ID EBP_000040
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EBP NM_006579.2 ?/. - c.-4701C>A r.(?) p.(=)
PORCN NM_203475.1 ?/. - c.1271C>A r.(?) p.(Thr424Asn)


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