Variant #0000553427 (NC_000014.8:g.93673776C>A, NM_175748.3:c.140C>A (UBR7))

Chromosome 14
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.93673776C>A
DNA change (hg38) g.93207431C>A
Published as UBR7(NM_175748.3):c.140C>A (p.S47Y)
ISCN -
DB-ID C14orf142_000001
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) Retrieve
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     
C14orf142 NM_032490.4 ?/. - c.-394G>T r.(?) p.(=)
UBR7 NM_175748.3 ?/. - c.140C>A r.(?) p.(Ser47Tyr)


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