Variant #0000619140 (NC_000023.10:g.151900113C>T, NM_001102576.1:c.-3227C>T (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.151900113C>T
DNA change (hg38) g.152736847=
Published as MAGEA12(NM_001166386.3):c.688G>A (p.A230T)
ISCN -
DB-ID MAGEA12_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) 6.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSAG1 NM_001102576.1 -?/. - c.-3227C>T r.(?) p.(=)
MAGEA12 NM_005367.5 -?/. - c.688G>A r.(?) p.(Ala230Thr)
CSAG4 NR_073432.1 -?/. - n.34-2835G>A r.(?) -


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