rs_ID |
Location |
Functional Annotation |
rs30634 |
Chr5:14300033(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs42204 |
Chr5:14301803(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs42405 |
Chr5:14312410(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs154154 |
Chr5:14317307(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs42551 |
Chr5:14321785(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs247142 |
Chr5:14325654(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs247143 |
Chr5:14325944(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs154152 |
Chr5:14380324(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs30770 |
Chr5:14378068(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs30769 |
Chr5:14377962(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs409214 |
Chr5:14373284(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1664507 |
Chr5:14371539(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs256417 |
Chr5:14371180(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs30784 |
Chr5:14366840(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs30783 |
Chr5:14366369(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs42407 |
Chr5:14361471(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs154161 |
Chr5:14356028(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs476930 |
Chr5:14352595(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs256423 |
Chr5:14351024(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs247140 |
Chr5:14344689(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs247134 |
Chr5:14337460(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs39857 |
Chr5:14329966(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs247144 |
Chr5:14326476(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs30612 |
Chr5:14420027(Fwd) |
NMD_transcript_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
rs10513177 |
Chr5:14389545(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs39866 |
Chr5:14361009(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs256416 |
Chr5:14370831(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs30792 |
Chr5:14386494(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs154159 |
Chr5:14354827(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |