Variant #0000889655 (NC_000011.9:g.118895957C>G, NM_001164277.1:c.1067G>C (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.118895957C>G
DNA change (hg38) -
Published as SLC37A4(NM_001164277.1):c.1067G>C (p.S356T)
ISCN -
DB-ID SLC37A4_000054 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) 0.0011 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 2022-11-01 13:01:21 +01:00 (CET)
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.1067G>C r.(?) p.(Ser356Thr)
TRAPPC4 NM_016146.4 -?/. - c.*1848C>G r.(=) p.(=)


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