Variant #0000569446 (NC_000020.10:g.33033087_33033089dup, NC_000020.10(NM_001257137.1):c.1089-5_1089-3dup (ITCH))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33033087_33033089dup
DNA change (hg38) g.34445282_34445284dup
Published as ITCH(NM_001257137.1):c.1089-6_1089-5insTTT (p.?)
ISCN -
DB-ID ITCH_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 16:38:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITCH NM_001257137.1 -?/. - c.1089-5_1089-3dup r.spl? p.?


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