SNP | Position (GRCh38.p12) | Consequence | GenomAD reported MAF | Context sequence |
---|---|---|---|---|
rs5128 (C3238G) | chr11:116832924 g.8017G > C | 3’UTR Variant | G = 0.16051 (39,468/245886) | AAGTCCACCTGCCTATCCATCCTGC [C/G]AGCTCCTTGGGTCCTGCAATCTCCA |
rs2854117 (C-482 T) | chr11:116829426 g.4519 T > C | 5’UTR Transcript Variant | C = 0 0.4163 (12,835/30834) | AGGCCTTGCCGGAGCCACTGATGCC [T/C]GGTCTTCTGTGCCTTTACTCCAAAC |
rs2070668 (T528G) | chr11:11683043 g.5530 T > G | Intron (1) Variant | G = 0.4314 (13,268/30758) | [T/G]AGCAGGGAGCCGGCCCCTACTCCTT |
KUAPOC3N2 | chr11:116700819 g.5196 A > G | Intron (1) Variant | N/A | Custom Designed NovelSNP2: Forward: GGTCCTCAGTGCCTGCTG Reverse:TCTAGGGATGAACTGAGCAGACA |
KUAPOC3N3 | chr11:116701159 g. 5536G > A | Intron (1) Variant | N/A | Custom Designed NovelSNP3: Forward: CCCCCACCCCTCATCATAAC Reverse: CTATGTAGCTTTGGGCAAGTGA |