Variant #0001041261 (NC_000016.9:g.67693911G>A, NM_022914.2:c.386C>T (ACD))

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.67693911G>A
DNA change (hg38) -
Published as ACD(NM_001082486.1):c.395C>T (p.(Ser132Phe))
ISCN -
DB-ID ACD_000081
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) 1.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RLTPR NM_001013838.1 ?/. - c.*2490G>A r.(=) p.(=)
PARD6A NM_016948.2 ?/. - c.-1031G>A r.(?) p.(=)
ACD NM_022914.2 ?/. - c.386C>T r.(?) p.(Ser129Phe)
ENKD1 NM_032140.1 ?/. - c.*3153C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.