Variant #0001015409 (NC_000016.9:g.67691668A>G, NM_022914.2:c.1544T>C (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.67691668A>G
DNA change (hg38) -
Published as ACD(NM_001082486.2):c.1295T>C (p.V432A)
ISCN -
DB-ID ACD_000074
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) 0.50177 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.*247A>G r.(=) p.(=)
PARD6A NM_016948.2 -/. - c.-3274A>G r.(?) p.(=)
ACD NM_022914.2 -/. - c.1544T>C r.(?) p.(Val515Ala)


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