Variant #0000802616 (NC_000006.11:g.44222986C>T, NM_178148.2:c.756G>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.44222986C>T
DNA change (hg38) -
Published as SLC35B2(NM_001286520.1):c.357G>A (p.M119I)
ISCN -
DB-ID HSP90AB1_000001
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
NFKBIE NM_004556.2 -?/. - c.*3970G>A r.(=) p.(=)
HSP90AB1 NM_007355.2 -?/. - c.*1651C>T r.(=) p.(=)
SLC35B2 NM_178148.2 -?/. - c.756G>A r.(?) p.(Met252Ile)


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