Variant #0000973896 (NC_000001.10:g.34071065C>T, NM_052896.3:c.6355G>A (CSMD2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34071065C>T
DNA change (hg38) -
Published as CSMD2(NM_001281956.2):c.6349G>A (p.(Glu2117Lys))
ISCN -
DB-ID CSMD2_000013
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) 0.00129 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 2024-04-19 20:20:39 +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.6355G>A r.(?) p.(Glu2119Lys)
HMGB4 NM_145205.4 -?/. - c.-256754C>T r.(?) p.(=)


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