Variant #0000320557 (NC_000001.10:g.15957003T>C, NM_032341.4:c.452T>C (DDI2))

Chromosome 1
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.15957003T>C
DNA change (hg38) g.15630508T>C
Published as DDI2(NM_032341.4):c.452T>C (p.(Leu151Ser))
ISCN -
DB-ID DDI2_000001
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 2018-01-15 20:58:59 +01:00 (CET)
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     
RSC1A1 NM_006511.1 ?/. - c.-29361T>C r.(?) p.(=)
DDI2 NM_032341.4 ?/. - c.452T>C r.(?) p.(Leu151Ser)


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