Variant #0000253819 (NC_000007.13:g.65426068del, NC_000007.13(NM_000181.3):c.1790-5del (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.65426068del
DNA change (hg38) g.65961081del
Published as GUSB(NM_000181.3):c.1790-5del (p.?), GUSB(NM_000181.3):c.1790-5delT
ISCN -
DB-ID GUSB_000005 See all 2 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-22 17:34:37 +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.1790-5del r.spl? p.?
VKORC1L1 NM_173517.3 -/. - c.*6781del r.(?) p.(=)


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