Variant #0000692617 (NC_000018.9:g.47810410C>T, NM_015846.3:c.-2703G>A (MBD1))

Chromosome 18
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.47810410C>T
DNA change (hg38) -
Published as CXXC1(NM_001101654.1):c.1279G>A (p.E427K)
ISCN -
DB-ID CXXC1_000004
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXXC1 NM_014593.3 ?/. - c.1267G>A r.(?) p.(Glu423Lys)
MBD1 NM_015846.3 ?/. - c.-2703G>A r.(?) p.(=)


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