Variant #0000577798 (NC_000023.10:g.96171440_96171442del, NM_006729.4:c.736_738del (DIAPH2))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.96171440_96171442del
DNA change (hg38) g.96916441_96916443del
Published as DIAPH2(NM_006729.4):c.736_738del (p.(Gly246del))
ISCN -
DB-ID DIAPH2_000035
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DIAPH2 NM_006729.4 ?/. - c.736_738del r.(?) p.(Gly246del)
RPA4 NM_013347.4 ?/. - c.*31345_*31347del r.(=) p.(=)


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