Variant #0000719309 (NC_000003.11:g.191107320C>T, NM_178335.2:c.1358C>T (CCDC50))

Chromosome 3
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.191107320C>T
DNA change (hg38) -
Published as CCDC50(NM_178335.2):c.1358C>T (p.A453V)
ISCN -
DB-ID UTS2D_000009
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_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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC50 NM_178335.2 ?/. - c.1358C>T r.(?) p.(Ala453Val)
UTS2D NM_198152.3 ?/. - c.-59782G>A r.(?) p.(=)


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