Variant #0000557833 (NC_000016.9:g.30012811C>A, NM_003586.2:c.*4696G>T (DOC2A))

Chromosome 16
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.30012811C>A
DNA change (hg38) g.30001490C>A
Published as INO80E(NM_173618.1):c.473C>A (p.(Pro158His))
ISCN -
DB-ID DOC2A_000004
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) 0.00042 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
DOC2A NM_003586.2 -?/. - c.*4696G>T r.(=) p.(=)
INO80E NM_173618.1 -?/. - c.473C>A r.(?) p.(Pro158His)


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