Variant #0000524594 (NC_000005.9:g.140953592_140953597dup, NM_005219.4:c.1848_1853dup (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.140953592_140953597dup
DNA change (hg38) g.141574025_141574030dup
Published as DIAPH1(NM_005219.4):c.1848_1853dupTCCTCC (p.P619_P620dup), DIAPH1(NM_005219.5):c.1842_1847dupTCCTCC (p.P619_P620dup), DIAPH1(NM_005219.5):c.1848_18...
ISCN -
DB-ID DIAPH1_000057 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +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.1848_1853dup r.(?) p.(Pro619_Pro620dup)


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