Variant #0000566700 (NC_000019.9:g.19042805C>A, NM_001145721.1:c.670G>T (HOMER3))

Chromosome 19
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.19042805C>A
DNA change (hg38) g.18931996C>A
Published as HOMER3(NM_001145721.1):c.670G>T (p.(Ala224Ser))
ISCN -
DB-ID DDX49_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) 0.00291 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     
HOMER3 NM_001145721.1 -?/. - c.670G>T r.(?) p.(Ala224Ser)
DDX49 NM_019070.4 -?/. - c.*3680C>A r.(=) p.(=)


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