Variant #0001014177 (NC_000006.11:g.135788730T>C, NM_001134831.1:c.178A>G (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.135788730T>C
DNA change (hg38) -
Published as AHI1(NM_001350503.2):c.178A>G (p.T60A), AHI1(NM_017651.4):c.178A>G (p.T60A)
ISCN -
DB-ID AHI1_000243 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) 0.0008 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 21:08:56 +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.178A>G r.(?) p.(Thr60Ala)
AHI1 NM_017651.4 -?/. - c.178A>G r.(?) p.(Thr60Ala)


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