Variant #0000351442 (NC_000014.8:g.93676305T>C, NC_000014.8(NM_175748.3):c.284+2T>C (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.93676305T>C
DNA change (hg38) g.93209959T>C
Published as -
ISCN -
DB-ID UBR7_000003
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-05 16:42:01 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C14orf142 NM_032490.4 ?/. - c.-2923A>G r.(?) p.(=)
UBR7 NM_175748.3 ?/. - c.284+2T>C r.spl? p.?


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