Variant #0000528960 (NC_000006.11:g.44223123C>T, NM_178148.2:c.619G>A (SLC35B2))

Chromosome 6
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.44223123C>T
DNA change (hg38) g.44255386C>T
Published as SLC35B2(NM_178148.2):c.619G>A (p.(Val207Ile))
ISCN -
DB-ID NFKBIE_000002
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) 0.00067 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFKBIE NM_004556.2 -?/. - c.*3833G>A r.(=) p.(=)
HSP90AB1 NM_007355.2 -?/. - c.*1788C>T r.(=) p.(=)
SLC35B2 NM_178148.2 -?/. - c.619G>A r.(?) p.(Val207Ile)


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