Variant #0000267472 (NC_000017.10:g.72308319G>A, NM_023036.4:c.1672G>A (DNAI2))

Chromosome 17
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.72308319G>A
DNA change (hg38) g.74312180G>A
Published as DNAI2(NM_023036.5):c.1672G>A (p.A558T), DNAI2(NM_023036.6):c.1672G>A (p.A558T)
ISCN -
DB-ID DNAI2_000009 See all 2 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) 0.86441 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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     
DNAI2 NM_023036.4 -/. - c.1672G>A r.(?) p.(Ala558Thr)


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