Variant #0000728960 (NC_000023.10:g.48382197C>G, NM_203475.1:c.*3333C>G (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.48382197C>G
DNA change (hg38) -
Published as EBP(NM_006579.2):c.38C>G (p.P13R), EBP(NM_006579.3):c.38C>G (p.P13R)
ISCN -
DB-ID EBP_000054 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) 0.00011 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.38C>G r.(?) p.(Pro13Arg)
PORCN NM_203475.1 ?/. - c.*3333C>G r.(=) p.(=)


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