Variant #0000542626 (NC_000011.9:g.118898370T>A, NM_001164277.1:c.593A>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.118898370T>A
DNA change (hg38) g.119027660T>A
Published as SLC37A4(NM_001164277.1):c.593A>T (p.N198I, p.(Asn198Ile))
ISCN -
DB-ID SLC37A4_000052 See all 5 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) 0.00362 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC37A4 NM_001164277.1 -?/. - c.593A>T r.(?) p.(Asn198Ile)
TRAPPC4 NM_016146.4 -?/. - c.*4261T>A r.(=) p.(=)


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