Variant #0000288182 (NC_000016.9:g.88923175G>A, NM_000512.4:c.111C>T (GALNS))

Chromosome 16
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.88923175G>A
DNA change (hg38) g.88856767G>A
Published as GALNS(NM_000512.4):c.111C>T (p.L37=)
ISCN -
DB-ID GALNS_000030
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_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 2023-11-27 17:27:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALNS NM_000512.4 -?/. - c.111C>T r.(?) p.(Leu37=)
TRAPPC2L NM_001318525.1 -?/. - c.-384G>A r.(?) p.(=)
TRAPPC2L NM_016209.3 -?/. - c.-384G>A r.(?) p.(=)


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