Variant #0000558749 (NC_000016.9:g.67692863T>C, NM_022914.2:c.862A>G (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.67692863T>C
DNA change (hg38) g.67658960T>C
Published as ACD(NM_001082486.2):c.613A>G (p.T205A)
ISCN -
DB-ID ACD_000016 See all 3 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) 0.00139 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RLTPR NM_001013838.1 ?/. - c.*1442T>C r.(=) p.(=)
PARD6A NM_016948.2 ?/. - c.-2079T>C r.(?) p.(=)
ACD NM_022914.2 ?/. - c.862A>G r.(?) p.(Thr288Ala)
ENKD1 NM_032140.1 ?/. - c.*4201A>G r.(=) p.(=)


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