Variant #0000546087 (NC_000011.9:g.93460786_93460789dup, NM_033395.1:c.7144_7147dup (KIAA1731))

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.93460786_93460789dup
DNA change (hg38) g.93727620_93727623dup
Published as CEP295(NM_033395.2):c.7144_7147dupAGCT (p.S2383*)
ISCN -
DB-ID KIAA1731_000005
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 2020-07-01 11:11:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF1D NM_024116.3 ?/. - c.*8538_*8541dup r.(=) p.(=)
KIAA1731 NM_033395.1 ?/. - c.7144_7147dup r.(?) p.(Ser2383Ter)


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