Variant #0000659244 (NC_000023.10:g.21874871A>G, NC_000023.10(NM_015884.3):c.670+3250A>G (MBTPS2))

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.21874871A>G
DNA change (hg38) g.21856753A>G
Published as YY2(NM_206923.3):c.269A>G (p.Y90C)
ISCN -
DB-ID MBTPS2_000071
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) 2.0E-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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBTPS2 NM_015884.3 -?/. - c.670+3250A>G r.(=) p.(=)
YY2 NM_206923.3 -?/. - c.269A>G r.(?) p.(Tyr90Cys)


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