Variant #0000948658 (NC_000006.11:g.135784291dup, NM_001134831.1:c.910dup (AHI1))

Chromosome 6
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.135784291dup
DNA change (hg38) -
Published as AHI1(NM_017651.4):c.910dupA (p.T304Nfs*6)
ISCN -
DB-ID AHI1_000171 See all 15 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHI1 NM_001134831.1 +/. - c.910dup r.(?) p.(Thr304Asnfs*6)
AHI1 NM_017651.4 +/. - c.910dup r.(?) p.(Thr304Asnfs*6)


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