Variant #0000711831 (NC_000017.10:g.?, NM_014336.3:c.? (AIPL1))
Chromosome |
17 |
Allele |
Parent #1 |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
DNA change (hg38) |
- |
Published as |
AF148864:287C>T (TGC?TGT) Cys89Cys |
ISCN |
- |
DB-ID |
MYH2_000008 See all 80 reported entries |
Variant remarks |
- |
Reference |
PubMed: Sohocki 2001 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Julia Lopez |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2021-01-14 12:40:33 +01:00 (CET) |
Date last edited |
N/A |
Variant on transcripts
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