Variant #0000967189 (NC_000013.10:g.30829772_30829776dup, NC_000013.10(NM_032116.4):c.324-10_324-6dup (KATNAL1))

Chromosome 13
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.30829772_30829776dup
DNA change (hg38) -
Published as KATNAL1(NM_032116.5):c.324-10_324-6dupTTTTT
ISCN -
DB-ID KATNAL1_000006
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KATNAL1 NM_032116.4 -/. - c.324-10_324-6dup r.(=) p.(=)


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