Variant #0000503516 (NC_000001.10:g.154562881C>T, NM_001111.4:c.2275G>A (ADAR))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.154562881C>T
DNA change (hg38) g.154590405C>T
Published as ADAR(NM_001025107.2):c.1390G>A (p.(Val464Ile)), ADAR(NM_001193495.2):c.1390G>A (p.V464I)
ISCN -
DB-ID ADAR_000022 See all 3 reported entries
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) 0.00013 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAR NM_001111.4 -?/. - c.2275G>A r.(?) p.(Val759Ile)


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