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 International |
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) |

Variant on transcripts
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