Variant #0001054947 (NC_000014.8:g.93686751A>G, NM_175748.3:c.1117A>G (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.93686751A>G
DNA change (hg38) -
Published as UBR7(NM_175748.4):c.1117A>G (p.(Ile373Val))
ISCN -
DB-ID C14orf142_000006
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 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C14orf142 NM_032490.4 ?/. - c.-13369T>C r.(?) p.(=)
UBR7 NM_175748.3 ?/. - c.1117A>G r.(?) p.(Ile373Val)


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