Variant #0000576271 (NC_000023.10:g.48688123A>G, HDAC6(NM_006044.2):c.*5101A>G)

Chromosome X
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.48688123A>G
DNA change (hg38) g.48829713A>G
Published as ERAS(NM_181532.3):c.590A>G (p.H197R)
ISCN -
DB-ID HDAC6_000044
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 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDAC6 NM_006044.2 -?/. - c.*5101A>G r.(=) p.(=)
PCSK1N NM_013271.2 -?/. - c.*1547T>C r.(=) p.(=)
ERAS NM_181532.2 -?/. - c.590A>G r.(?) p.(His197Arg)