Variant #0000551025 (NC_000013.10:g.60385060_60385061insTTAC, NC_000013.10(NM_001042517.1):c.3028-4_3028-3insGTAA (DIAPH3))

Chromosome 13
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.60385060_60385061insTTAC
DNA change (hg38) g.59810926_59810927insTTAC
Published as DIAPH3(NM_001042517.1):c.3028-4_3028-3insGTAA, DIAPH3(NM_001042517.2):c.3028-4_3028-3insGTAA
ISCN -
DB-ID DIAPH3_000017 See all 3 reported entries
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) 0.99035 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +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     
DIAPH3 NM_001042517.1 -?/. - c.3028-4_3028-3insGTAA r.spl? p.?


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