Variant #0000557794 (NC_000016.9:g.28997868T>C, NM_001014987.1:c.318T>C (LAT))

Chromosome 16
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.28997868T>C
DNA change (hg38) g.28986547T>C
Published as LAT(NM_014387.3):c.318T>C (p.S106=), LAT(NM_014387.4):c.318T>C (p.S106=)
ISCN -
DB-ID LAT_000001 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) 0.00275 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAT NM_001014987.1 -?/. - c.318T>C r.(?) p.(Ser106=)
SPNS1 NM_032038.2 -?/. - c.*2248T>C r.(=) p.(=)


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