Variant #0000262109 (NC_000006.11:g.135784390T>G, NM_001134831.1:c.804A>C (AHI1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135784390T>G
DNA change (hg38) g.135463252T>G
Published as AHI1(NM_001134831.1):c.804A>C (p.S268=), AHI1(NM_017651.4):c.804A>C (p.S268=)
ISCN -
DB-ID AHI1_000060 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) 0.00259 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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHI1 NM_001134831.1 -?/. - c.804A>C r.(?) p.(Ser268=)
AHI1 NM_017651.4 -?/. - c.804A>C r.(?) p.(Ser268=)


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