Variant #0000275016 (NC_000005.9:g.140953595_140953597del, NM_005219.4:c.1851_1853del (DIAPH1))

Chromosome 5
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.140953595_140953597del
DNA change (hg38) g.141574028_141574030del
Published as DIAPH1(NM_005219.4):c.1851_1853delTCC (p.P620del), DIAPH1(NM_005219.5):c.1851_1853delTCC (p.P620del)
ISCN -
DB-ID DIAPH1_000014 See all 2 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) 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 2018-01-15 20:58:59 +01:00 (CET)
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     
DIAPH1 NM_005219.4 -/. - c.1851_1853del r.(?) p.(Pro620del)


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