Variant #0000528958 (NC_000006.11:g.44219845G>T, NM_178148.2:c.*2598C>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.44219845G>T
DNA change (hg38) g.44252108G>T
Published as HSP90AB1(NM_001271969.1):c.1572G>T (p.Q524H)
ISCN -
DB-ID SLC35B2_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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSP90AB1 NM_007355.2 -?/. - c.1572G>T r.(?) p.(Gln524His)
SLC35B2 NM_178148.2 -?/. - c.*2598C>A r.(=) p.(=)


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