Genomic variant #0000016728

Chromosome 14
Allele Parent #1
Affects function (reported) Probably affects function
Affects function (concluded) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.23242890A>G
DNA change (hg38) -
Published as TCA>CCA: S489P
ISCN -
DB-ID SLC7A7_000051
Variant remarks 1 Japanese LPI family (com-het)
Reference PubMed: Shoji et al. 2002
dbSNP ID -
Germline/Somatic/De novo SUMMARY record
Segregation yes
Frequency 0/50 JAP CON
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Anne Polvi




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Class.     

RNA change     

Protein     
SLC7A7 NM_001126105.2 +?/+? 11 c.1465T>C - r.1465u>c p.(Ser489Pro)