Variant #0000690051 (NC_000007.13:g.65426068dup, NC_000007.13(NM_000181.3):c.1790-5dup (GUSB))

Chromosome 7
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.65426068dup
DNA change (hg38) -
Published as GUSB(NM_000181.3):c.1790-5dupT, GUSB(NM_000181.3):c.1790-5dupT (p.?), GUSB(NM_000181.4):c.1790-5dupT
ISCN -
DB-ID GUSB_000006 See all 3 reported entries
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GUSB NM_000181.3 -/. - c.1790-5dup r.spl? p.?
VKORC1L1 NM_173517.3 -/. - c.*6781dup r.(?) p.(=)


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