Variant #0000855808 (NC_000020.10:g.33583145G>C, NM_020884.3:c.2833G>C (MYH7B))

Chromosome 20
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.33583145G>C
DNA change (hg38) -
Published as MYH7B(NM_020884.4):c.2833G>C (p.D945H)
ISCN -
DB-ID MYH7B_000099
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPC4AP NM_015638.2 ?/. - c.*7804C>G r.(=) p.(=)
MYH7B NM_020884.3 ?/. - c.2833G>C r.(?) p.(Asp945His)


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