Variant #0000614869 (NC_000014.8:g.23883309C>T, NM_000257.2:c.5562G>A (MYH7))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.23883309C>T
DNA change (hg38) g.23414100C>T
Published as MYH7(NM_000257.2):c.5562G>A (p.T1854=), MYH7(NM_000257.4):c.5562G>A (p.T1854=)
ISCN -
DB-ID MYH6_000535 See all 2 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) 0.00011 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH7 NM_000257.2 -/. - c.5562G>A r.(?) p.(Thr1854=)
MYH6 NM_002471.3 -/. - c.-5894G>A r.(?) p.(=)


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