Variant #0000998807 (NC_000011.9:g.118895981_118895982del, NM_001164277.1:c.1043_1044del (SLC37A4))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.118895981_118895982del
DNA change (hg38) -
Published as SLC37A4(NM_001164277.1):c.1042_1043delCT (p.(Leu348fs)), SLC37A4(NM_001164277.1):c.1042_1043delCT (p.L348Vfs*53)
ISCN -
DB-ID SLC37A4_000065 See all 4 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) 0.00018 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +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.1043_1044del r.? p.?
TRAPPC4 NM_016146.4 +?/. - c.*1872_*1873del r.(=) p.(=)


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