Variant #0000510049 (NC_000002.11:g.167145106C>A, SCN9A(NM_002977.3):c.1155G>T)
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.167145106C>A |
DNA change (hg38) |
g.166288596C>A |
Published as |
SCN9A(NM_002977.3):c.1155G>T (p.V385=) |
ISCN |
- |
DB-ID |
SCN9A_000147 See all 3 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) |
0.01494 View details |
Owner |
VKGL-NL_Nijmegen |

Variant on transcripts
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