Variant #0000523853 (NC_000005.9:g.112676258A>C, NM_152624.5:c.*327077A>C (DCP2))

Chromosome 5
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.112676258A>C
DNA change (hg38) g.113340561A>C
Published as MCC(NM_001085377.1):c.585T>G (p.I195M)
ISCN -
DB-ID DCP2_000006
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 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCC NM_001085377.1 -?/. - c.585T>G r.(?) p.(Ile195Met)
TSSK1B NM_032028.3 -?/. - c.*93175T>G r.(=) p.(=)
DCP2 NM_152624.5 -?/. - c.*327077A>C r.(=) p.(=)


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