Variant #0000260687 (NC_000006.11:g.135784293G>T, NM_001134831.1:c.901C>A (AHI1))

Chromosome 6
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.135784293G>T
DNA change (hg38) g.135463155G>T
Published as AHI1(NM_017651.4):c.901C>A (p.P301T)
ISCN -
DB-ID AHI1_000059
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.901C>A r.(?) p.(Pro301Thr)
AHI1 NM_017651.4 -/. - c.901C>A r.(?) p.(Pro301Thr)


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