Variant #0000682632 (NC_000023.10:g.73744491A>T, NM_006517.4:c.873A>T (SLC16A2))

Chromosome X
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.73744491A>T
DNA change (hg38) -
Published as SLC16A2(NM_006517.4):c.873A>T (p.P291=), SLC16A2(NM_006517.5):c.873A>T (p.P291=)
ISCN -
DB-ID SLC16A2_000050 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) 0.0024 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 2020-08-06 14:59:34 +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     
SLC16A2 NM_006517.4 -/. - c.873A>T r.(?) p.(Pro291=)


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