Variant #0000692039 (NC_000016.9:g.29816481dup, NM_002383.2:c.-1542dup (MAZ))

Chromosome 16
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.29816481dup
DNA change (hg38) -
Published as KIF22(NM_001256270.1):c.1732dupG (p.E578Gfs*?)
ISCN -
DB-ID KIF22_000016
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 2020-09-15 15:50:26 +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     
MAZ NM_002383.2 ?/. - c.-1542dup r.(?) p.(=)
KIF22 NM_007317.2 ?/. - c.1936dup r.(?) p.(Glu646GlyfsTer?)


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