Variant #0000726635 (NC_000017.10:g.66391335G>A, NC_000017.10(NM_001267727.1):c.1212+1G>A (ARSG))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66391335G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC16A6_000008 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 +?/. - c.1212+1G>A r.spl? p.?
SLC16A6 NM_004694.4 +?/. - c.-104116C>T r.(?) p.(=)
ARSG NM_014960.3 +?/. - c.1212+1G>A r.spl? p.?
ARSG NM_014960.4 +?/. - c.1212+1G>A r.spl? p.?
WIPI1 NM_017983.5 +?/. - c.*26579C>T r.(=) p.(=)


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