Variant #0000862331 (NC_000011.9:g.118895635G>A, NM_001164277.1:c.1275C>T (SLC37A4))

Chromosome 11
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.118895635G>A
DNA change (hg38) -
Published as SLC37A4(NM_001164277.1):c.1275C>T (p.S425=)
ISCN -
DB-ID SLC37A4_000059 See all 3 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) 0.0057 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC37A4 NM_001164277.1 -/. - c.1275C>T r.(?) p.(Ser425=)
TRAPPC4 NM_016146.4 -/. - c.*1526G>A r.(=) p.(=)


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