Variant #0000525934 (NC_000005.9:g.68692391_68692392dup, NC_000005.9(NM_133344.1):c.1572+18_1572+19dup (RAD17))

Chromosome 5
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.68692391_68692392dup
DNA change (hg38) g.69396564_69396565dup
Published as RAD17(NM_002873.1):c.1572+17_1572+18dupAA
ISCN -
DB-ID TAF9_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF9 NM_016283.4 -/. - c.-27060_-27059dup r.(?) p.(=)
RAD17 NM_133344.1 -/. - c.1572+18_1572+19dup r.(=) p.(=)


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