Variant #0000312936 (NC_000014.8:g.93686585_93686586del, NC_000014.8(NM_175748.3):c.961-10_961-9del (UBR7))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.93686585_93686586del
DNA change (hg38) g.93220239_93220240del
Published as UBR7(NM_175748.4):c.961-10_961-9delTT
ISCN -
DB-ID UBR7_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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-13188_-13187del r.(?) p.(=)
UBR7 NM_175748.3 -/. - c.961-10_961-9del r.(=) p.(=)


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