Variant #0000290198 (NC_000010.10:g.70748491_70748493delinsAGT, NM_015634.3:c.-98_-96delinsAGT (KIAA1279))

Chromosome 10
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.70748491_70748493delinsAGT
DNA change (hg38) g.68988735_68988737delinsAGT
Published as KIAA1279(NM_015634.3):c.-98_-96delGCAinsAGT
ISCN -
DB-ID KIAA1279_000024
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX21 NM_004728.3 ?/. - c.*5923_*5925delinsAGT r.(=) p.(=)
KIAA1279 NM_015634.3 ?/. - c.-98_-96delinsAGT r.(?) p.(=)


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