Variant #0000287507 (NC_000023.10:g.135288752C>T, FHL1(NM_001159702.2):c.156+5C>T)
Chromosome |
X |
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.135288752C>T |
DNA change (hg38) |
g.136206593C>T |
Published as |
FHL1(NM_001159699.1):c.204+5C>T (p.?), FHL1(NM_001159704.1):c.156+5C>T |
ISCN |
- |
DB-ID |
FHL1_000037 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) |
0.00144 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
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