Variant #0000893119 (NC_000016.9:g.67692863T>C, NM_022914.2:c.862A>G (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.67692863T>C
DNA change (hg38) -
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.*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.