Variant #0000016706 (NC_000014.8:g.23245403C>A, NC_000014.8(NM_001126105.2):c.894+1G>T (SLC7A7))

Chromosome 14
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23245403C>A
DNA change (hg38) g.22776194C>A
Published as IVS6 +1G>T in donor of intron 6: no RNA studies
ISCN -
DB-ID SLC7A7_000029
Variant remarks 1 Japanese LPI family (com-het)
Reference PubMed: Sperandeo et al. 2000
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-12-04 16:25:21 +01:00 (CET)
Date last edited 2020-07-04 15:17:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC7A7 NM_001126105.2 +?/+? i06 c.894+1G>T r.spl? p.?


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