Variant #0000525566 (NC_000005.9:g.36677074T>C, SLC1A3(NM_004172.4):c.648T>C)

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36677074T>C
DNA change (hg38) g.36676972T>C
Published as SLC1A3(NM_004172.4):c.648T>C (p.N216=), SLC1A3(NM_004172.5):c.648T>C (p.N216=)
ISCN -
DB-ID SLC1A3_000004 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) 0.00115 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC1A3 NM_004172.4 -?/. - c.648T>C r.(?) p.(Asn216=)