Variant #0000574998 (NC_000023.10:g.154009534G>A, NM_001363.3:c.*4392G>A (DKC1))

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.154009534G>A
DNA change (hg38) g.154781259G>A
Published as MPP1(NM_001166460.1):c.1153C>T (p.(Pro385Ser))
ISCN -
DB-ID DKC1_000094
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     

P-domain     
DKC1 NM_001363.3 ?/. - c.*4392G>A r.(=) p.(=) -
MPP1 NM_002436.3 ?/. - c.1204C>T r.(?) p.(Pro402Ser) -


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