The Variant Effect Prediction table provides variant annotation information, including variant consequences, predicted variant effects and variant allele frequencies. To view live NCBI ALFA allele frequencies for a particular variant, click on the ALFA Frequency link in the table.
Variant Name: NM_001165963:c.4172A>G
Ensembl canonical HGVSC: NM_001353948.2:c.4172A>G
Reference genome: GRCh37
Transcript ID: NM_001165963
Chromosome: 2
Genomic start position: 166859094
Genomic end position: 166859094
Reference allele: T
Alternate allele: C
Disease association with reference allele: False
Variant type: SNV
Gene: SCN1A
| Consequence terms | Polyphen2 hvar score | Polyphen2 hvar prediction | SIFT score | SIFT prediction | SIFT4G score | SIFT4G prediction | FATHMM score | FATHMM prediction | CADD raw | CADD phred | MutationTaster effect prediction | MutationTaster query model | 1000 Genomes global allele frequency | 1000 Genomes allele frequency EUR | 1000 Genomes allele frequency AFR | 1000 Genomes allele frequency AMR | 1000 Genomes allele frequency SAS | 1000 Genomes allele frequency EAS | ExAC global allele frequency | ExAC allele frequency NFE | ExAC allele frequency AFR | ExAC allele frequency AMR | ExAC allele frequency EAS | ExAC allele frequency SAS | gnomAD global allele frequency | gnomAD allele frequency AFR | gnomAD allele frequency EAS | Live ALFA allele frequency |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| missense_variant | 0.079,0.012,0.079,0.012,0.012 | B,B,B,B,B | 0.03 | deleterious | 0.134,0.134,0.123,0.117 | ,T,T,T,T | -3.99,-3.99,-3.94,-3.92 | D,D,D,D | 2.768207 | 24.1 | disease causing | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | No ALFA allele frequency available |