Variant #0000326355 (NC_000019.9:g.19042820C>A, NM_001145721.1:c.655G>T (HOMER3))

Chromosome 19
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.19042820C>A
DNA change (hg38) g.18932011C>A
Published as HOMER3(NM_001145721.1):c.655G>T (p.(Ala219Ser))
ISCN -
DB-ID HOMER3_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     
HOMER3 NM_001145721.1 ?/. - c.655G>T r.(?) p.(Ala219Ser)
DDX49 NM_019070.4 ?/. - c.*3695C>A r.(=) p.(=)


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