Variant #0000517178 (NC_000002.11:g.97426765_97426791del, NM_020184.3:c.29_55del (CNNM4))

Chromosome 2
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.97426765_97426791del
DNA change (hg38) g.96761028_96761054del
Published as CNNM4(NM_020184.3):c.29_55delCGGTCGGCGGACCGGCCCGCGGGCGCC (p.P10_R18del)
ISCN -
DB-ID CNNM4_000017
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_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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNNM4 NM_020184.3 ?/. - c.29_55del r.(?) p.(Pro10_Arg18del)


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