Variant #0000688147 (NC_000001.10:g.34092131C>T, NM_052896.3:c.5131G>A (CSMD2))

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.34092131C>T
DNA change (hg38) -
Published as CSMD2(NM_001281956.1):c.5251G>A (p.A1751T)
ISCN -
DB-ID CSMD2_000008
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) 0.00015 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSMD2 NM_052896.3 ?/. - c.5131G>A r.(?) p.(Ala1711Thr)
HMGB4 NM_145205.4 ?/. - c.-235688C>T r.(?) p.(=)


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