Variant #0000262108 (NC_000006.11:g.135786977G>A, NM_001134831.1:c.724C>T (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.135786977G>A
DNA change (hg38) g.135465839G>A
Published as AHI1(NM_001134831.1):c.724C>T (p.P242S), AHI1(NM_001350503.2):c.724C>T (p.P242S), AHI1(NM_017651.4):c.724C>T (p.P242S)
ISCN -
DB-ID AHI1_000061 See all 3 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) 0.00096 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 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHI1 NM_001134831.1 -/. - c.724C>T r.(?) p.(Pro242Ser)
AHI1 NM_017651.4 -/. - c.724C>T r.(?) p.(Pro242Ser)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.