Variant #0000575423 (NC_000023.10:g.26157782G>C, MAGEB18(NM_173699.3):c.680G>C)

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.26157782G>C
DNA change (hg38) g.26139665G>C
Published as MAGEB18(NM_173699.3):c.680G>C (p.G227A)
ISCN -
DB-ID MAGEB18_000008
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) 3.0E-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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEB18 NM_173699.3 -?/. - c.680G>C r.(?) p.(Gly227Ala)