Variant #0001000871 (NC_000014.8:g.23549549G>C, NM_014977.3:c.1169C>G (ACIN1))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.23549549G>C
DNA change (hg38) -
Published as ACIN1(NM_001164814.1):c.1169C>G (p.(Pro390Arg))
ISCN -
DB-ID ACIN1_000014
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACIN1 NM_014977.3 ?/. - c.1169C>G r.(?) p.(Pro390Arg)
C14orf119 NM_017924.3 ?/. - c.-15281G>C r.(?) p.(=)


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