Variant #0001055624 (NC_000016.9:g.67693916G>A, NM_022914.2:c.381C>T (ACD))

Chromosome 16
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.67693916G>A
DNA change (hg38) -
Published as ACD(NM_001082486.1):c.390C>T (p.(Gly130=)), ACD(NM_001082486.2):c.132C>T (p.G44=)
ISCN -
DB-ID ACD_000035 See all 2 reported entries
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) 0.00254 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RLTPR NM_001013838.1 -?/. - c.*2495G>A r.(=) p.(=)
PARD6A NM_016948.2 -?/. - c.-1026G>A r.(?) p.(=)
ACD NM_022914.2 -?/. - c.381C>T r.(?) p.(Gly127=)
ENKD1 NM_032140.1 -?/. - c.*3148C>T r.(=) p.(=)


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