Variant #0000542628 (NC_000011.9:g.118898407G>A, NM_001164277.1:c.556C>T (SLC37A4))

Chromosome 11
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.118898407G>A
DNA change (hg38) g.119027697G>A
Published as SLC37A4(NM_001164277.1):c.556C>T (p.L186F), SLC37A4(NM_001164277.2):c.556C>T (p.(Leu186Phe))
ISCN -
DB-ID SLC37A4_000053 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) 0.00015 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC37A4 NM_001164277.1 -?/. - c.556C>T r.(?) p.(Leu186Phe)
TRAPPC4 NM_016146.4 -?/. - c.*4298G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.