Variant #0000275357 (NC_000009.11:g.34500821G>A, NM_012144.3:c.1003G>A (DNAI1))

Chromosome 9
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.34500821G>A
DNA change (hg38) g.34500823G>A
Published as DNAI1(NM_012144.3):c.1003G>A (p.V335I), DNAI1(NM_012144.4):c.1003G>A (p.V335I)
ISCN -
DB-ID DNAI1_000006 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) 0.15301 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
DNAI1 NM_012144.3 -/. - c.1003G>A r.(?) p.(Val335Ile)


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