Variant #0000891711 (NC_000014.8:g.23882972G>A, NM_000257.2:c.5786C>T (MYH7))

Chromosome 14
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.23882972G>A
DNA change (hg38) -
Published as MYH7(NM_000257.2):c.5786C>T (p.T1929M), MYH7(NM_000257.4):c.5786C>T (p.T1929M)
ISCN -
DB-ID MYH7_000036 See all 6 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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH7 NM_000257.2 ?/. - c.5786C>T r.(?) p.(Thr1929Met)
MYH6 NM_002471.3 ?/. - c.-5557C>T r.(?) p.(=)


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