Variant #0000298020 (NC_000002.11:g.167168093C>T, SCN9A(NM_002977.3):c.174G>A)
Chromosome |
2 |
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.167168093C>T |
DNA change (hg38) |
g.166311583C>T |
Published as |
SCN9A(NM_002977.3):c.174G>A (p.Q58=) |
ISCN |
- |
DB-ID |
SCN9A_000008 See all 5 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.57612 View details |
Owner |
VKGL-NL_Groningen |

Variant on transcripts
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