Variant #0001015408 (NC_000016.9:g.67691645G>T, NC_000016.9(NM_022914.2):c.1547+20C>A (ACD))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67691645G>T
DNA change (hg38) -
Published as ACD(NM_001082486.2):c.1298+20C>A
ISCN -
DB-ID ACD_000073
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) 0.10859 View details
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2024-10-29 21:08:56 +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.*224G>T r.(=) p.(=)
PARD6A NM_016948.2 -/. - c.-3297G>T r.(?) p.(=)
ACD NM_022914.2 -/. - c.1547+20C>A r.(=) p.(=)


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