Variant #0000524575 (NC_000005.9:g.140907278_140907289dup, NC_000005.9(NM_005219.4):c.3149-14_3149-3dup (DIAPH1))

Chromosome 5
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.140907278_140907289dup
DNA change (hg38) g.141527711_141527722dup
Published as DIAPH1(NM_001079812.2):c.3122-3_3122-2insTTTTTTTTTTTT (p.?)
ISCN -
DB-ID DIAPH1_000040
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 2020-06-17 18:06:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DIAPH1 NM_005219.4 -?/. - c.3149-14_3149-3dup r.spl? p.?


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