Variant #0000621078 (NC_000002.11:g.44586754G>A, NM_000341.3:c.*38976G>A (SLC3A1))

Chromosome 2
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.44586754G>A
DNA change (hg38) g.44359615G>A
Published as PREPL(NM_006036.4):c.101C>T (p.A34V)
ISCN -
DB-ID SLC3A1_000045
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) 3.0E-5 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC3A1 NM_000341.3 -?/. - c.*38976G>A r.(=) p.(=)
PREPL NM_006036.4 -?/. - c.101C>T r.(?) p.(Ala34Val)
CAMKMT NM_024766.4 -?/. - c.-2393G>A r.(?) p.(=)


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