Variant #0000564762 (NC_000018.9:g.42456670_42456671insTCTT, NC_000018.9(NM_015559.2):c.540+7422_540+7423insTCTT (SETBP1))

Chromosome 18
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.42456670_42456671insTCTT
DNA change (hg38) g.44876705_44876706insTCTT
Published as SETBP1(NM_001130110.2):c.681_682insTCTT (p.T228Sfs*8)
ISCN -
DB-ID SETBP1_000034 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) 0.52088 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SETBP1 NM_015559.2 -/. - c.540+7422_540+7423insTCTT r.(=) p.(=)


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