Variant #0000518475 (NC_000003.11:g.170198959G>C, NC_000003.11(NM_020949.2):c.1116-4C>G (SLC7A14))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.170198959G>C
DNA change (hg38) g.170481170G>C
Published as SLC7A14(NM_020949.2):c.1116-4C>G, SLC7A14(NM_020949.3):c.1116-4C>G
ISCN -
DB-ID SLC7A14_000006 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) 0.00038 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC7A14 NM_020949.2 -/. - c.1116-4C>G r.spl? p.?


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