Variant #0000892909 (NC_000016.9:g.28997041C>T, NM_001014987.1:c.108C>T (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.28997041C>T
DNA change (hg38) -
Published as LAT(NM_001014987.2):c.108C>T (p.Y36=), LAT(NM_014387.3):c.108C>T (p.Y36=)
ISCN -
DB-ID LAT_000012 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) 0.00039 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAT NM_001014987.1 -?/. - c.108C>T r.(?) p.(Tyr36=)
SPNS1 NM_032038.2 -?/. - c.*1421C>T r.(=) p.(=)


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