Variant #0000333928 (NC_000023.10:g.47485521G>A, NM_002621.2:c.1180C>T (CFP))

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.47485521G>A
DNA change (hg38) g.47626122G>A
Published as CFP(NM_001145252.1):c.1180C>T (p.(Pro394Ser)), CFP(NM_002621.2):c.1180C>T (p.P394S)
ISCN -
DB-ID CFP_000019 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) 6.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFP NM_002621.2 ?/. - c.1180C>T r.(?) p.(Pro394Ser)


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