Variant #0000551562 (NC_000014.8:g.23243580G>A, NM_001126105.2:c.1228C>T (SLC7A7))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23243580G>A
DNA change (hg38) g.22774371G>A
Published as SLC7A7(NM_001126106.2):c.1228C>T (p.R410*)
ISCN -
DB-ID SLC7A7_000041 See all 2 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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-04 15:16:46 +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 +/. - c.1228C>T r.(?) p.(Arg410Ter)
OXA1L NM_005015.3 +/. - c.*2813G>A r.(=) p.(=)


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