Variant #0001026814 (NC_000017.10:g.10432638_10432639del, NC_000017.10(NM_017534.5):c.3263+14_3263+15del (MYH2))

Chromosome 17
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.10432638_10432639del
DNA change (hg38) -
Published as MYH2(NM_001100112.1):c.3263+14_3263+15del (p.(=))
ISCN -
DB-ID MYH2_000092
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) 0.00032 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-02-07 18:57:27 +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     
MYH2 NM_017534.5 -?/. - c.3263+14_3263+15del r.(=) p.(=)


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