Variant #0000991182 (NC_000001.10:g.34166245C>G, NM_052896.3:c.3485G>C (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.34166245C>G
DNA change (hg38) -
Published as CSMD2(NM_001281956.1):c.3605G>C (p.(Arg1202Pro))
ISCN -
DB-ID CSMD2_000016
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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSMD2 NM_052896.3 ?/. - c.3485G>C r.(?) p.(Arg1162Pro)
HMGB4 NM_145205.4 ?/. - c.-161574C>G r.(?) p.(=)


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