Variant #0000016681 (NC_000014.8:g.23282502_23282504del, NM_001126105.2:c.106_108del (SLC7A7))

Chromosome 14
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23282502_23282504del
DNA change (hg38) g.22813293_22813295del
Published as deletion of nucleotides 104–106 from the first methionine of the SLC7A7 cDNA: E36del; c.104_106delGGA p.E36del
ISCN -
DB-ID SLC7A7_000004
Variant remarks 1 Greek LPI patient (com-het); Functional studies: mutated protein failed to show transport activity
Reference PubMed: Sperandeo et al. 2005
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 15:17:31 +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 +/+ 03 c.106_108del r.(?) p.(Glu36del)


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