Variant #0000322429 (NC_000011.9:g.77921469_77921470del, NM_080491.2:c.*8850_*8851del (GAB2))

Chromosome 11
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.77921469_77921470del
DNA change (hg38) g.78210423_78210424del
Published as USP35(NM_020798.2):c.2568_2569delGT (p.(Ser857fs))
ISCN -
DB-ID USP35_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP35 NM_020798.2 ?/. - c.2568_2569del r.(?) p.(Ser857PhefsTer12)
GAB2 NM_080491.2 ?/. - c.*8850_*8851del r.(=) p.(=)


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