Variant #0000724680 (NC_000014.8:g.23243154G>A, NM_001126105.2:c.1417C>T (SLC7A7))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23243154G>A
DNA change (hg38) -
Published as SLC7A7(NM_001126106.2):c.1417C>T (p.R473*)
ISCN -
DB-ID SLC7A7_000049 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC7A7 NM_001126105.2 +?/. - c.1417C>T r.(?) p.(Arg473Ter)
OXA1L NM_005015.3 +?/. - c.*2387G>A r.(=) p.(=)


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