Variant #0000527280 (NC_000006.11:g.135778690T>G, NM_001134831.1:c.1093A>C (AHI1))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.135778690T>G
DNA change (hg38) g.135457552T>G
Published as AHI1(NM_001350503.2):c.1093A>C (p.M365L)
ISCN -
DB-ID AHI1_000101
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHI1 NM_001134831.1 ?/. - c.1093A>C r.(?) p.(Met365Leu)
AHI1 NM_017651.4 ?/. - c.1093A>C r.(?) p.(Met365Leu)


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