Variant #0000810716 (NC_000023.10:g.95940165G>T, NM_006729.4:c.108G>T (DIAPH2))

Chromosome X
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.95940165G>T
DNA change (hg38) -
Published as DIAPH2(NM_006729.4):c.108G>T (p.E36D)
ISCN -
DB-ID DIAPH2_000046
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DIAPH2 NM_006729.4 -?/. - c.108G>T r.(?) p.(Glu36Asp)
RPA4 NM_013347.4 -?/. - c.-199145G>T r.(?) p.(=)


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