Variant #0000892166 (NC_000015.9:g.57931723G>A, NM_001018090.4:c.1099G>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.57931723G>A
DNA change (hg38) -
Published as MYZAP(NM_001018100.5):c.1099G>A (p.V367I)
ISCN -
DB-ID GCOM1_000033
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) 0.00024 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 2022-11-01 13:41:49 +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.1099G>A r.(?) p.(Val367Ile)
MYZAP NM_001018100.3 ?/. - c.1099G>A r.(?) p.(Val367Ile)
POLR2M NM_001018102.1 ?/. - c.-67318G>A r.(?) p.(=)


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