Variant #0000929807 (NC_000011.9:g.118895624T>G, NM_001164277.1:c.1287A>C (SLC37A4))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.118895624T>G
DNA change (hg38) -
Published as SLC37A4(NM_001164277.1):c.1286A>C (p.E429A)
ISCN -
DB-ID TRAPPC4_000007
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) 0.00011 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 2023-07-07 10:10:56 +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.1287A>C r.(?) p.?
TRAPPC4 NM_016146.4 ?/. - c.*1515T>G r.(=) p.(=)


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