Variant #0000725898 (NC_000016.9:g.67683941C>A, NM_022914.2:c.*7568G>T (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.67683941C>A
DNA change (hg38) -
Published as CARMIL2(NM_001013838.3):c.2083-11C>A
ISCN -
DB-ID ACD_000032
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) 0.00078 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RLTPR NM_001013838.1 -/. - c.2083-11C>A r.(=) p.(=)
ACD NM_022914.2 -/. - c.*7568G>T r.(=) p.(=)


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