Variant #0000546929 (NC_000012.11:g.123741445A>G, NM_152269.4:c.368A>G (C12orf65))

Chromosome 12
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.123741445A>G
DNA change (hg38) g.123256898A>G
Published as C12orf65(NM_001143905.2):c.368A>G (p.(Glu123Gly))
ISCN -
DB-ID C12orf65_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
CDK2AP1 NM_004642.3 ?/. - c.*4838T>C r.(=) p.(=)
C12orf65 NM_152269.4 ?/. - c.368A>G r.(?) p.(Glu123Gly)


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