Variant #0000251852 (NC_000015.9:g.57929927A>G, NM_001018090.4:c.968A>G (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.57929927A>G
DNA change (hg38) g.57637729A>G
Published as MYZAP(NM_001018100.5):c.968A>G (p.H323R)
ISCN -
DB-ID GCOM1_000005
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) 0.00077 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCOM1 NM_001018090.4 -?/. - c.968A>G r.(?) p.(His323Arg)
MYZAP NM_001018100.3 -?/. - c.968A>G r.(?) p.(His323Arg)
POLR2M NM_001018102.1 -?/. - c.-69114A>G r.(?) p.(=)


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