Variant #0000320721 (NC_000001.10:g.32800688T>C, NM_004964.2:c.*2043T>C (HDAC1))

Chromosome 1
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.32800688T>C
DNA change (hg38) g.32335087T>C
Published as MARCKSL1(NM_023009.6):c.98A>G (p.(His33Arg))
ISCN -
DB-ID MARCKSL1_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDAC1 NM_004964.2 ?/. - c.*2043T>C r.(=) p.(=)
MARCKSL1 NM_023009.6 ?/. - c.98A>G r.(?) p.(His33Arg)


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