Variant #0000538015 (NC_000009.11:g.34459053dup, NC_000009.11(NM_012144.3):c.48+2dup (DNAI1))

Chromosome 9
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.34459053dup
DNA change (hg38) g.34459055dup
Published as DNAI1(NM_001281428.1):c.48+2dup (p.?), DNAI1(NM_001281428.1):c.48+2dupT, DNAI1(NM_001281428.2):c.48+2dupT
ISCN -
DB-ID FAM219A_000001 See all 7 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM219A NM_001184940.1 +/. - c.-792dup r.(?) p.(=)
DNAI1 NM_012144.3 +/. - c.48+2dup r.spl? p.?


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