Genomic variant #0000016699

Chromosome 14
Allele Paternal (confirmed)
Affects function (reported) Probably affects function
Affects function (concluded) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.23249134C>G
DNA change (hg38) -
Published as c.625+1G>C: p.C167_G209delinsX
ISCN -
DB-ID SLC7A7_000022
Variant remarks 1 English/Argentinean LPI family (com-het)
Reference PubMed: Font-Llitjos et al. 2009
dbSNP ID -
Germline/Somatic/De novo SUMMARY record
Segregation yes
Frequency 0/50 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 +?/+? i04 c.625+1G>C - r.spl? p.?