Variant #0000984519 (NC_000023.10:g.151900650G>C, NM_001102576.1:c.-2690G>C (CSAG1))

Chromosome X
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.151900650G>C
DNA change (hg38) -
Published as MAGEA12(NM_001166387.4):c.151C>G (p.(Arg51Gly))
ISCN -
DB-ID MAGEA12_000023
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) 0.00255 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSAG1 NM_001102576.1 -?/. - c.-2690G>C r.(?) p.(=)
MAGEA12 NM_005367.5 -?/. - c.151C>G r.(?) p.(Arg51Gly)
CSAG4 NR_073432.1 -?/. - n.33+2454C>G r.(?) -


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