Genomic variant #0000000091

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.42329648_42329649delGA
ExAC MAF -
gnomAD MAF -
dbSNP ID -
Segregation -
# Affected Unrelated 1
Zygosity -
ACMG class Pathogenic
Other Classification Authors: pathogenic
Reference [Yamada, 2014]
DB-ID SLC20A2_000041
Average frequency (large NGS studies) Variant not found in online data sets
Owner Coppola Lab UCLA (EMR)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

Exon     

Protein     
SLC20A2 NM_006749.4 +?/. c.260_261delTC 2 p.(Leu87Hisfs*6)