Variant #0001026732 (NC_000016.9:g.67681421C>T, NM_022914.2:c.*10088G>A (ACD))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.67681421C>T
DNA change (hg38) -
Published as CARMIL2(NM_001013838.3):c.787C>T (p.R263*)
ISCN -
DB-ID ACD_000076
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +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.787C>T r.(?) p.(Arg263*)
ACD NM_022914.2 +/. - c.*10088G>A r.(=) p.(=)


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