Variant #0001046571 (NC_000016.9:g.66788947G>A, NM_006141.2:c.-3453C>T (DYNC1LI2))

Chromosome 16
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.66788947G>A
DNA change (hg38) -
Published as TERB1(NM_001136505.2):c.2116C>T (p.R706W)
ISCN -
DB-ID CCDC79_000005
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) 0.00132 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC79 NM_001136505.1 ?/. - c.2116C>T r.(?) p.(Arg706Trp)
DYNC1LI2 NM_006141.2 ?/. - c.-3453C>T r.(?) p.(=)


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