Variants | Substitution | Transcript ID | db SNP (b153 v2) | Variation type | 1000 genomes allele frequency | Position |
---|---|---|---|---|---|---|
rs138979590 | G>C G>T | NG_011779.2 | Novel | SNV, intron | not present | chr1:92833927 |
rs558220259 | A>G | NG_011779.2 | Novel | SNV, intron | not present | chr1:92833948 |
rs576892621 | A>G | NG_011779.2 | Novel | SNV, intron | not present | chr1:92833969 |
rs182018447 | G>A | NG_011779.2 | Novel | SNV, intron | not present | chr1:92834024 |
rs559377519 | A>T | NG_011779.2 | Novel | SNV, intron | not present | chr1:92834047 |
Ch1: chromosome 1, SNV: single nucleotide variant, SNP: single nucleotide polymorphism.