Variant #0000996157 (NC_000007.13:g.122114500A>C, NM_017954.10:c.1933T>G (CADPS2))

Chromosome 7
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.122114500A>C
DNA change (hg38) -
Published as CADPS2(NM_017954.10):c.1933T>G (p.(Phe645Val))
ISCN -
DB-ID CADPS2_000009
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) 0.0005 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 2024-08-28 13:16:32 +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     
CADPS2 NM_017954.10 -?/. - c.1933T>G r.(?) p.(Phe645Val)
RNF133 NM_139175.1 -?/. - c.*223342T>G r.(=) p.(=)
RNF148 NM_198085.1 -?/. - c.*227387T>G r.(=) p.(=)


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