Variant #0001040464 (NC_000015.9:g.57953648A>T, NM_001018090.4:c.1120A>T (GCOM1))

Chromosome 15
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.57953648A>T
DNA change (hg38) -
Published as GCOM1(NM_001018090.4):c.1120A>T (p.(Ile374Phe)), MYZAP(NM_001018100.5):c.1120A>T (p.I374F)
ISCN -
DB-ID GCOM1_000007 See all 3 reported entries
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) 0.00028 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 2025-05-05 21:14:00 +02:00 (CEST)
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.1120A>T r.(?) p.(Ile374Phe)
MYZAP NM_001018100.3 -?/. - c.1120A>T r.(?) p.(Ile374Phe)
POLR2M NM_001018102.1 -?/. - c.-45393A>T r.(?) p.(=)


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