Variant #0000853680 (NC_000013.10:g.44462892G>T, NM_144974.3:c.-9325C>A (CCDC122))

Chromosome 13
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.44462892G>T
DNA change (hg38) -
Published as LACC1(NM_001350641.1):c.908-1G>T
ISCN -
DB-ID CCDC122_000007
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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC122 NM_144974.3 ?/. - c.-9325C>A r.(?) p.(=)
LACC1 NM_153218.2 ?/. - c.908-1G>T r.spl? p.?


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