Variant #0000618070 (NC_000020.10:g.33574702_33574705del, NM_020884.3:c.1044_1047del (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.33574702_33574705del
DNA change (hg38) g.34986899_34986902del
Published as -
ISCN -
DB-ID MYH7B_000046
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-16 16:45:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPC4AP NM_015638.2 ?/. - c.*16247_*16250del r.(=) p.(=)
MYH7B NM_020884.3 ?/. - c.1044_1047del r.(?) p.(Ser349Ter)


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