Variant #0000332097 (NC_000008.10:g.38091918G>A, NM_015214.2:c.227G>A (DDHD2))

Chromosome 8
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.38091918G>A
DNA change (hg38) g.38234400G>A
Published as DDHD2(NM_001164232.1):c.227G>A (p.(Gly76Asp)), DDHD2(NM_001362912.1):c.227G>A (p.G76D)
ISCN -
DB-ID DDHD2_000006 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) 0.00118 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDHD2 NM_015214.2 ?/. - c.227G>A r.(?) p.(Gly76Asp)


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