Variant #0001027047 (NC_000017.10:g.66391276G>A, NM_001267727.1:c.1154G>A (ARSG))

Chromosome 17
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.66391276G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC16A6_000017
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) 0.06646 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 -/. - c.1154G>A r.(?) p.(Arg385His)
SLC16A6 NM_004694.4 -/. - c.-104057C>T r.(?) p.(=)
ARSG NM_014960.4 -/. - c.1154G>A r.(?) p.(Arg385His)
WIPI1 NM_017983.5 -/. - c.*26638C>T r.(=) p.(=)


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