Variant #0000690958 (NC_000011.9:g.118895632C>T, NM_001164277.1:c.1278G>A (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.118895632C>T
DNA change (hg38) -
Published as SLC37A4(NM_001164277.1):c.1278G>A (p.(Lys426=))
ISCN -
DB-ID SLC37A4_000058 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) 0.00398 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-09-15 15:50:26 +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.1278G>A r.(?) p.(Lys426=)
TRAPPC4 NM_016146.4 -/. - c.*1523C>T r.(=) p.(=)


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