Variant #0000679073 (NC_000011.9:g.118899102A>G, NM_001164277.1:c.183T>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.118899102A>G
DNA change (hg38) -
Published as SLC37A4(NM_001164277.1):c.183T>C (p.(=))
ISCN -
DB-ID SLC37A4_000061
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) 0.01099 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.183T>C r.(?) p.(Ala61=)
TRAPPC4 NM_016146.4 -?/. - c.*4993A>G r.(=) p.(=)


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