Variant #0000327170 (NC_000002.11:g.97482487C>T, NM_020184.3:c.*7233C>T (CNNM4))

Chromosome 2
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.97482487C>T
DNA change (hg38) g.96816750C>T
Published as CNNM3(NM_017623.4):c.473C>T (p.(Ala158Val))
ISCN -
DB-ID CNNM3_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNNM3 NM_017623.4 -?/. - c.473C>T r.(?) p.(Ala158Val)
CNNM4 NM_020184.3 -?/. - c.*7233C>T r.(=) p.(=)


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