Variant #0000967864 (NC_000015.9:g.57925929G>A, NM_001018090.4:c.923G>A (GCOM1))

Chromosome 15
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.57925929G>A
DNA change (hg38) -
Published as MYZAP(NM_001018100.5):c.923G>A (p.R308H)
ISCN -
DB-ID GCOM1_000041
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) 5.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCOM1 NM_001018090.4 ?/. - c.923G>A r.(?) p.(Arg308His)
MYZAP NM_001018100.3 ?/. - c.923G>A r.(?) p.(Arg308His)
POLR2M NM_001018102.1 ?/. - c.-73112G>A r.(?) p.(=)


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