Variant #0000805718 (NC_000012.11:g.48192428A>G, NM_001098416.2:c.266T>C (HDAC7))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48192428A>G
DNA change (hg38) -
Published as HDAC7(NM_001308090.1):c.215T>C (p.M72T)
ISCN -
DB-ID HDAC7_000005
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) 0.00021 View details
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     
HDAC7 NM_001098416.2 ?/. - c.266T>C r.(?) p.(Met89Thr)
SLC48A1 NM_017842.2 ?/. - c.*18364A>G r.(=) p.(=)


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