Variant #0000302525 (NC_000022.10:g.36745275G>C, NM_002473.4:c.7C>G (MYH9))

Chromosome 22
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.36745275G>C
DNA change (hg38) g.36349230G>C
Published as MYH9(NM_002473.4):c.7C>G (p.(Gln3Glu)), MYH9(NM_002473.5):c.7C>G (p.Q3E)
ISCN -
DB-ID MYH9_000080 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) 0.00156 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH9 NM_002473.4 -?/. - c.7C>G r.(?) p.(Gln3Glu)


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