Variant #0000802325 (NC_000006.11:g.135777066del, NC_000006.11(NM_001134831.1):c.1152-2del (AHI1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.135777066del
DNA change (hg38) -
Published as AHI1(NM_001134831.1):c.1152-2delA (p.?), AHI1(NM_001350503.1):c.1152-2delA
ISCN -
DB-ID AHI1_000193 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHI1 NM_001134831.1 +?/. - c.1152-2del r.spl? p.?
AHI1 NM_017651.4 +?/. - c.1152-2del r.spl? p.?


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