Variant #0000298029 (NC_000002.11:g.167163482T>G, SCN9A(NM_002977.3):c.361A>C)
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.167163482T>G |
DNA change (hg38) |
g.166306972T>G |
Published as |
SCN9A(NM_002977.3):c.361A>C (p.K121Q) |
ISCN |
- |
DB-ID |
SCN9A_000152 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 |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00018 View details |
Owner |
VKGL-NL_Groningen |

Variant on transcripts
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