Variant #0000864889 (NC_000016.9:g.67693171A>G, NC_000016.9(NM_022914.2):c.708-5T>C (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.67693171A>G
DNA change (hg38) -
Published as ACD(NM_001082486.2):c.459-5T>C
ISCN -
DB-ID ACD_000050
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) 2.0E-5 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 2022-05-09 16:01:56 +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     
RLTPR NM_001013838.1 -?/. - c.*1750A>G r.(=) p.(=)
PARD6A NM_016948.2 -?/. - c.-1771A>G r.(?) p.(=)
ACD NM_022914.2 -?/. - c.708-5T>C r.spl? p.?
ENKD1 NM_032140.1 -?/. - c.*3893T>C r.(=) p.(=)


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