Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3781 |
| ensemblid | ENSG00000080709.17 |
| hgncid | 6291 |
| symbol | KCNN2 |
| name | potassium calcium-activated channel subfamily N member 2 |
| refseq_nuc | NM_021614.4 |
| refseq_prot | NP_067627.3 |
| ensembl_nuc | ENST00000673685.1 |
| ensembl_prot | ENSP00000501239.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 114362070 |
| end | 114496496 |
| strand | + |
| ver | v1.2 |
| region | chr5:114362070-114496496 |
| region5000 | chr5:114357070-114501496 |
| regionname0 | KCNN2_chr5_114362070_114496496 |
| regionname5000 | KCNN2_chr5_114357070_114501496 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 791 | 114 | 43 | 29 | 15 | 11 | 15 | 13 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(786): Show |
chr5 | 114357070 | 114501496 |
| a0002 | 0/1 | 792 | 109 | 21 | 25 | 43 | 3 | 16 | 33 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(787): Show |
chr5 | 114357070 | 114501496 |
| a0003 | 0/0 | 791 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(786): Show |
chr5 | 114357070 | 114501496 |
| a0004 | 0/0 | 793 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(788): Show |
chr5 | 114357070 | 114501496 |
| a0005 | 0/0 | 792 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(787): Show |
chr5 | 114357070 | 114501496 |
| a0006 | 0/0 | 792 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(787): Show |
chr5 | 114357070 | 114501496 |
| a0007 | 0/0 | 791 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(786): Show |
chr5 | 114357070 | 114501496 |
| a0008 | 0/0 | 792 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(787): Show |
chr5 | 114357070 | 114501496 |
| a0009 | 0/0 | 791 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(786): Show |
chr5 | 114357070 | 114501496 |
| a0010 | 0/0 | 792 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | METPL others(787): Show |
chr5 | 114357070 | 114501496 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2373 | 105 | 37 | 28 | 14 | 10 | 15 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0001c0006 | 0/0 | 2373 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0001c0015 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0001c0018 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0001c0019 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0001c0020 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0001c0021 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0002c0002 | 0/1 | 2376 | 100 | 16 | 23 | 41 | 3 | 16 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 | ||
| a0002c0005 | 0/0 | 2376 | 4 | 3 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 | ||
| a0002c0011 | 0/0 | 2376 | 2 | 1 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 | ||
| a0002c0014 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 | ||
| a0002c0016 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 | ||
| a0002c0017 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 | ||
| a0003c0003 | 0/0 | 2373 | 6 | 6 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0003c0009 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0004c0008 | 0/0 | 2379 | 3 | 3 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2374): Show |
chr5 | 114357070 | 114501496 | ||
| a0004c0012 | 0/0 | 2379 | 2 | 0 | 2 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2374): Show |
chr5 | 114357070 | 114501496 | ||
| a0005c0004 | 0/0 | 2376 | 5 | 5 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 | ||
| a0006c0007 | 0/0 | 2376 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 | ||
| a0007c0010 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0008c0013 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 | ||
| a0009c0022 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2368): Show |
chr5 | 114357070 | 114501496 | ||
| a0010c0023 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | ATGGA others(2371): Show |
chr5 | 114357070 | 114501496 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2760 | 104 | 37 | 28 | 14 | 10 | 14 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0001c0001t0002 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0001c0006t0001 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0001c0015t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0001c0018t0001 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0001c0019t0001 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0001c0020t0001 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0001c0021t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0002c0002t0001 | 0/1 | 2763 | 100 | 16 | 23 | 41 | 3 | 16 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| a0002c0005t0001 | 0/0 | 2763 | 4 | 3 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| a0002c0011t0001 | 0/0 | 2763 | 2 | 1 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| a0002c0014t0001 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| a0002c0016t0003 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| a0002c0017t0001 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| a0003c0003t0001 | 0/0 | 2760 | 6 | 6 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0003c0009t0001 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0004c0008t0001 | 0/0 | 2766 | 3 | 3 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2761): Show |
chr5 | 114357070 | 114501496 |
| a0004c0012t0001 | 0/0 | 2766 | 2 | 0 | 2 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2761): Show |
chr5 | 114357070 | 114501496 |
| a0005c0004t0001 | 0/0 | 2763 | 5 | 5 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| a0006c0007t0001 | 0/0 | 2763 | 4 | 4 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| a0007c0010t0001 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0008c0013t0001 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| a0009c0022t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2755): Show |
chr5 | 114357070 | 114501496 |
| a0010c0023t0001 | 0/0 | 2763 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | GCTCC others(2758): Show |
chr5 | 114357070 | 114501496 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0006t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0015t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0018t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0019t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0020t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0001c0021t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0005t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0005t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0011t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0011t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0014t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0016t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0002c0017t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0009t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0003c0009t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0008t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0008t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0012t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0004c0012t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0005c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0006c0007t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0006c0007t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0006c0007t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0006c0007t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0007c0010t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0007c0010t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0008c0013t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0009c0022t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| a0010c0023t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0208 | EUR | GBR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0141 | EUR | GBR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | FIN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0206 | EUR | FIN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | CHS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | CHS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01070 | hp1 | a0004 | c0012 | t0001 | g0143 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01243 | hp1 | a0002 | c0011 | t0001 | g0241 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01243 | hp2 | a0002 | c0005 | t0001 | g0013 | AMR | PUR | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01256 | hp2 | a0004 | c0012 | t0001 | g0142 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01261 | hp1 | a0001 | c0019 | t0001 | g0234 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01516 | hp2 | a0001 | c0020 | t0001 | g0232 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0225 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02040 | hp1 | a0001 | c0018 | t0001 | g0029 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02055 | hp1 | a0001 | c0006 | t0001 | g0095 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0098 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0159 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | PEL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02451 | hp1 | a0002 | c0011 | t0001 | g0239 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02451 | hp2 | a0002 | c0005 | t0001 | g0015 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | KHV | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02572 | hp1 | a0002 | c0014 | t0001 | g0017 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02622 | hp1 | a0006 | c0007 | t0001 | g0104 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02630 | hp1 | a0001 | c0021 | t0001 | g0220 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02809 | hp1 | a0003 | c0009 | t0001 | g0194 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02818 | hp1 | a0005 | c0004 | t0001 | g0149 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02886 | hp2 | a0008 | c0013 | t0001 | g0237 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02895 | hp1 | a0007 | c0010 | t0001 | g0191 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02895 | hp2 | a0001 | c0006 | t0001 | g0097 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02896 | hp1 | a0004 | c0008 | t0001 | g0012 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02897 | hp1 | a0007 | c0010 | t0001 | g0192 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02897 | hp2 | a0004 | c0008 | t0001 | g0011 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0200 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02965 | hp2 | a0001 | c0015 | t0001 | g0219 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02976 | hp2 | a0002 | c0005 | t0001 | g0016 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03098 | hp1 | a0002 | c0005 | t0001 | g0014 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03098 | hp2 | a0006 | c0007 | t0001 | g0221 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0197 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03139 | hp1 | a0009 | c0022 | t0001 | g0071 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0198 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03225 | hp2 | a0005 | c0004 | t0001 | g0148 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0199 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0204 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03704 | hp2 | a0010 | c0023 | t0001 | g0160 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0180 | SAS | BEB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | BEB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0128 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18522 | hp1 | a0006 | c0007 | t0001 | g0223 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18522 | hp2 | a0003 | c0009 | t0001 | g0195 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0093 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18999 | hp1 | a0002 | c0017 | t0001 | g0178 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | LWK | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0196 | AFR | LWK | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19077 | hp2 | a0002 | c0016 | t0003 | g0177 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA19240 | hp2 | a0005 | c0004 | t0001 | g0176 | AFR | YRI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20129 | hp1 | a0004 | c0008 | t0001 | g0010 | AFR | ASW | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0193 | AFR | ASW | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02486 | hp2 | a0005 | c0004 | t0001 | g0147 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG02559 | hp2 | a0005 | c0004 | t0001 | g0146 | AFR | ACB | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG06807 | hp1 | a0006 | c0007 | t0001 | g0222 | AFR | USA | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | USA | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0116 | AFR | USA | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0113 | REF | REF | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0077 | REF | REF | KCNN2_chr5_114357070_114501496 | KCNN2 | chr5 | 114357070 | 114501496 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:114362339 | T | A | 1 | a0008 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.200T>A | p.Leu67His | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 270/2760 | 200/2376 | 67/791 | chr5 | 114362339 | |||
| chr5:114362471 | C | CCTG | 1 | a0004 | 5 | HG01070.hp1 HG01256.hp2 HG02896.hp1 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.350_352dupGCT | p.Cys117dup | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 423/2760 | 353/2376 | 118/791 | INFO_REALIGN_3_PRIME | chr5 | 114362471 | ||
| chr5:114362474 | G | C | 1 | a0005 | 5 | HG02486.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
missense_variant | MODERATE | c.335G>C | p.Cys112Ser | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 405/2760 | 335/2376 | 112/791 | chr5 | 114362474 | |||
| chr5:114362567 | A | C | 1 | a0010 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.428A>C | p.Tyr143Ser | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 498/2760 | 428/2376 | 143/791 | chr5 | 114362567 | |||
| chr5:114362625 | C | G | 1 | a0009 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.486C>G | p.Ser162Arg | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 556/2760 | 486/2376 | 162/791 | chr5 | 114362625 | |||
| chr5:114362675 | G | C | 2 | a0003 a0007 |
10 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
missense_variant | MODERATE | c.536G>C | p.Gly179Ala | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 606/2760 | 536/2376 | 179/791 | chr5 | 114362675 | |||
| chr5:114362677 | C | G | 1 | a0006 | 4 | HG02622.hp1 HG03098.hp2 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.538C>G | p.Pro180Ala | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 608/2760 | 538/2376 | 180/791 | chr5 | 114362677 | |||
| chr5:114362704 | C | T | 1 | a0007 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.565C>T | p.Pro189Ser | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 635/2760 | 565/2376 | 189/791 | chr5 | 114362704 | |||
| chr5:114362934 | T | TGCC | 6 | a0002 a0004 a0005 others(3): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
disruptive_inframe_insertion | MODERATE | c.807_809dupCGC | p.Ala270dup | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 880/2760 | 810/2376 | 270/791 | INFO_REALIGN_3_PRIME | chr5 | 114362934 | ||
| chr5:114495971 | T | A | 1 | a0002 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.2165T>A | p.Leu722Gln | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 2235/2760 | 2165/2376 | 722/791 | chr5 | 114495971 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:114362439 | G | A | 4 | a0001c0015 a0002c0005 a0002c0014 others(1): Show |
9 | HG01243.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.300G>A | p.Arg100Arg | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 370/2760 | 300/2376 | 100/791 | chr5 | 114362439 | |||
| chr5:114362847 | G | C | 12 | a0002c0002 a0002c0005 a0002c0011 others(9): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
synonymous_variant | LOW | c.708G>C | p.Leu236Leu | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 778/2760 | 708/2376 | 236/791 | chr5 | 114362847 | |||
| chr5:114362964 | C | G | 1 | a0001c0021 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.825C>G | p.Ala275Ala | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/8 | 895/2760 | 825/2376 | 275/791 | chr5 | 114362964 | |||
| chr5:114473092 | A | G | 1 | a0008c0013 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1818A>G | p.Ala606Ala | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/8 | 1888/2760 | 1818/2376 | 606/791 | chr5 | 114473092 | |||
| chr5:114473125 | C | T | 1 | a0001c0020 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.1851C>T | p.His617His | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/8 | 1921/2760 | 1851/2376 | 617/791 | chr5 | 114473125 | |||
| chr5:114493424 | G | A | 5 | a0001c0006 a0001c0015 a0002c0011 others(2): Show |
10 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
synonymous_variant | LOW | c.2040G>A | p.Glu680Glu | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/8 | 2110/2760 | 2040/2376 | 680/791 | chr5 | 114493424 | |||
| chr5:114495999 | T | C | 1 | a0002c0017 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.2193T>C | p.Gly731Gly | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 2263/2760 | 2193/2376 | 731/791 | chr5 | 114495999 | |||
| chr5:114496059 | C | T | 1 | a0001c0019 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.2253C>T | p.Phe751Phe | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 2323/2760 | 2253/2376 | 751/791 | chr5 | 114496059 | |||
| chr5:114496092 | C | T | 1 | a0001c0018 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.2286C>T | p.His762His | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 2356/2760 | 2286/2376 | 762/791 | chr5 | 114496092 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:114496223 | A | T | 1 | a0002c0016t0003 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 41 | chr5 | 114496223 | ||||||
| chr5:114496407 | C | T | 1 | a0001c0001t0002 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 8/8 | 225 | chr5 | 114496407 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:114363418 | G | C | 1 | a0002c0002t0001g0002 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1122+157G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363418 | |||||||
| chr5:114363435 | G | T | 1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1122+174G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363435 | |||||||
| chr5:114363503 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1122+242C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363503 | |||||||
| chr5:114363586 | A | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | NA18964.hp2 NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1123-320A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363586 | |||||||
| chr5:114363642 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1123-264C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363642 | |||||||
| chr5:114363675 | C | T | 1 | a0002c0002t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1123-231C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363675 | |||||||
| chr5:114363846 | C | A | 1 | a0002c0002t0001g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1123-60C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 1/7 | chr5 | 114363846 | |||||||
| chr5:114364088 | C | G | 6 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218+87C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364088 | |||||||
| chr5:114364249 | C | A | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+248C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364249 | |||||||
| chr5:114364507 | C | T | 9 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(6): Show |
9 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+506C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364507 | |||||||
| chr5:114364616 | C | CT | 26 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+629dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114364616 | ||||||
| chr5:114364616 | CT | C | 5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0002c0002t0001g0005 others(2): Show |
5 | HG02922.hp1 HG03491.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+629delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114364616 | ||||||
| chr5:114364685 | A | G | 100 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(97): Show |
100 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1218+684A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364685 | |||||||
| chr5:114364863 | G | C | 9 | a0002c0002t0001g0110 a0002c0002t0001g0111 a0002c0002t0001g0112 others(6): Show |
9 | HG00738.hp2 HG01192.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218+862G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364863 | |||||||
| chr5:114364882 | T | A | 1 | a0002c0002t0001g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1218+881T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114364882 | |||||||
| chr5:114364896 | GT | G | 11 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0118 others(8): Show |
11 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+906delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114364896 | ||||||
| chr5:114365101 | G | A | 29 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 others(26): Show |
29 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1218+1100G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365101 | |||||||
| chr5:114365257 | G | C | 1 | a0002c0002t0001g0145 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1218+1256G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365257 | |||||||
| chr5:114365335 | C | A | 4 | a0005c0004t0001g0146 a0005c0004t0001g0147 a0005c0004t0001g0148 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+1334C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365335 | |||||||
| chr5:114365559 | G | A | 9 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(6): Show |
9 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+1558G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365559 | |||||||
| chr5:114365934 | A | G | 6 | a0002c0002t0001g0139 a0002c0002t0001g0140 a0002c0002t0001g0141 others(3): Show |
6 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+1933A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114365934 | |||||||
| chr5:114366014 | A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2013A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366014 | |||||||
| chr5:114366172 | A | G | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+2171A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366172 | |||||||
| chr5:114366201 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1218+2200G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366201 | |||||||
| chr5:114366205 | A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2204A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366205 | |||||||
| chr5:114366309 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1218+2308A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366309 | |||||||
| chr5:114366322 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+2321C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366322 | |||||||
| chr5:114366351 | G | C | 1 | a0002c0002t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1218+2350G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366351 | |||||||
| chr5:114366361 | C | A | 85 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(82): Show |
85 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1218+2360C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366361 | |||||||
| chr5:114366366 | C | G | 5 | a0001c0021t0001g0220 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+2365C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366366 | |||||||
| chr5:114366435 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(65): Show |
69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1218+2434G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366435 | |||||||
| chr5:114366537 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(190): Show |
194 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.1218+2536C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366537 | |||||||
| chr5:114366603 | G | A | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2602G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366603 | |||||||
| chr5:114366649 | A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2648A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366649 | |||||||
| chr5:114366767 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+2766T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366767 | |||||||
| chr5:114366795 | G | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1218+2794G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366795 | |||||||
| chr5:114366917 | T | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+2916T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114366917 | |||||||
| chr5:114367111 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+3110C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367111 | |||||||
| chr5:114367184 | T | A | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1218+3183T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367184 | |||||||
| chr5:114367357 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1218+3356C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367357 | |||||||
| chr5:114367376 | C | G | 1 | a0001c0015t0001g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1218+3375C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367376 | |||||||
| chr5:114367576 | T | C | 132 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1218+3575T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367576 | |||||||
| chr5:114367650 | A | AT | 13 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(10): Show |
13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1218+3663dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114367650 | ||||||
| chr5:114367650 | A | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+3649A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367650 | |||||||
| chr5:114367931 | C | G | 34 | a0001c0021t0001g0220 a0002c0002t0001g0004 a0002c0002t0001g0008 others(31): Show |
34 | HG00099.hp1 HG00280.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1218+3930C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114367931 | |||||||
| chr5:114367968 | AAC | A | 5 | a0002c0002t0001g0238 a0002c0002t0001g0240 a0002c0011t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218+3969_1218+397 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114367968 | ||||||
| chr5:114368094 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1218+4093G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368094 | |||||||
| chr5:114368270 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1218+4269A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368270 | |||||||
| chr5:114368308 | G | C | 12 | a0002c0002t0001g0110 a0002c0002t0001g0111 a0002c0002t0001g0112 others(9): Show |
12 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1218+4307G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368308 | |||||||
| chr5:114368449 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1218+4448G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368449 | |||||||
| chr5:114368494 | G | T | 8 | a0002c0002t0001g0004 a0002c0002t0001g0236 a0002c0002t0001g0238 others(5): Show |
8 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1218+4493G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368494 | |||||||
| chr5:114368657 | C | T | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+4656C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368657 | |||||||
| chr5:114368815 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1218+4814A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114368815 | |||||||
| chr5:114368870 | A | AT | 206 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1218+4878dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114368870 | ||||||
| chr5:114369034 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(65): Show |
69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1218+5033G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369034 | |||||||
| chr5:114369071 | G | A | 1 | a0002c0002t0001g0002 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1218+5070G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369071 | |||||||
| chr5:114369136 | G | T | 2 | a0003c0003t0001g0196 a0003c0009t0001g0195 |
2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1218+5135G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369136 | |||||||
| chr5:114369347 | C | A | 1 | a0002c0002t0001g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1218+5346C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369347 | |||||||
| chr5:114369444 | A | G | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+5443A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369444 | |||||||
| chr5:114369448 | G | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+5447G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369448 | |||||||
| chr5:114369498 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1218+5497C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369498 | |||||||
| chr5:114369772 | T | G | 140 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1218+5771T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369772 | |||||||
| chr5:114369820 | A | G | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+5819A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369820 | |||||||
| chr5:114369894 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1218+5893A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369894 | |||||||
| chr5:114369986 | G | A | 10 | a0003c0003t0001g0193 a0003c0003t0001g0196 a0003c0003t0001g0197 others(7): Show |
10 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+5985G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114369986 | |||||||
| chr5:114370147 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1218+6146T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114370147 | |||||||
| chr5:114370237 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1218+6236C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114370237 | |||||||
| chr5:114370576 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1218+6575C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114370576 | |||||||
| chr5:114370642 | A | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1218+6641A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114370642 | |||||||
| chr5:114370970 | T | TAGAG | 140 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1218+6971_1218+697 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114370970 | ||||||
| chr5:114371481 | G | A | 10 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+7480G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371481 | |||||||
| chr5:114371602 | T | A | 130 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(127): Show |
130 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1218+7601T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371602 | |||||||
| chr5:114371724 | A | T | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1218+7723A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371724 | |||||||
| chr5:114371752 | T | C | 1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1218+7751T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371752 | |||||||
| chr5:114371846 | A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1218+7845A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114371846 | |||||||
| chr5:114372144 | A | G | 119 | a0001c0021t0001g0220 a0002c0002t0001g0002 a0002c0002t0001g0003 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1218+8143A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372144 | |||||||
| chr5:114372146 | C | T | 6 | a0002c0002t0001g0238 a0002c0002t0001g0240 a0002c0011t0001g0239 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+8145C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372146 | |||||||
| chr5:114372180 | G | A | 2 | a0002c0002t0001g0008 a0002c0002t0001g0009 |
2 | HG02523.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1218+8179G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372180 | |||||||
| chr5:114372203 | C | A | 3 | a0004c0008t0001g0010 a0004c0008t0001g0011 a0004c0008t0001g0012 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1218+8202C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372203 | |||||||
| chr5:114372206 | G | T | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+8205G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372206 | |||||||
| chr5:114372419 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1218+8418G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372419 | |||||||
| chr5:114372561 | A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+8560A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372561 | |||||||
| chr5:114372614 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1218+8613A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372614 | |||||||
| chr5:114372752 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(190): Show |
194 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.1218+8751C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372752 | |||||||
| chr5:114372957 | A | T | 6 | a0002c0002t0001g0238 a0002c0002t0001g0240 a0002c0011t0001g0239 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+8956A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114372957 | |||||||
| chr5:114373078 | T | C | 1 | a0002c0002t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1218+9077T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373078 | |||||||
| chr5:114373421 | A | G | 7 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(4): Show |
7 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+9420A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373421 | |||||||
| chr5:114373450 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1218+9449G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373450 | |||||||
| chr5:114373640 | T | A | 1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1218+9639T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373640 | |||||||
| chr5:114373640 | T | TATATATA others(38): Show |
1 | a0002c0002t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1218+9639_1218+964 others(49): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373640 | |||||||
| chr5:114373640 | T | TTA | 7 | a0001c0001t0001g0109 a0002c0002t0001g0120 a0002c0002t0001g0157 others(4): Show |
7 | HG00099.hp1 HG01169.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218+9656_1218+965 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATA | 5 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0004c0008t0001g0010 others(2): Show |
5 | HG01358.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+9654_1218+965 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATA | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0002c0002t0001g0121 |
3 | NA19009.hp2 NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1218+9652_1218+965 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(3): Show |
1 | a0002c0002t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1218+9648_1218+965 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(7): Show |
1 | a0002c0002t0001g0110 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1218+9644_1218+965 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(9): Show |
1 | a0002c0002t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1218+9642_1218+965 others(20): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(11): Show |
8 | a0002c0002t0001g0004 a0002c0002t0001g0122 a0002c0002t0001g0236 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1218+9640_1218+965 others(22): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(13): Show |
2 | a0002c0002t0001g0117 a0008c0013t0001g0237 |
2 | HG01261.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(15): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0247 a0002c0002t0001g0123 others(2): Show |
5 | HG01070.hp2 HG02559.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(17): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0248 a0002c0002t0001g0118 others(3): Show |
6 | HG01192.hp1 HG01943.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(28): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(19): Show |
2 | a0002c0002t0001g0125 a0002c0002t0001g0158 |
2 | NA18959.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(21): Show |
2 | a0002c0002t0001g0111 a0002c0002t0001g0159 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(32): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(34): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(25): Show |
7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG01099.hp1 HG01978.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(36): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(27): Show |
2 | a0002c0002t0001g0161 a0010c0023t0001g0160 |
2 | HG03704.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(38): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(29): Show |
2 | a0001c0001t0001g0055 a0002c0002t0001g0145 |
2 | HG02109.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(40): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(31): Show |
2 | a0001c0001t0001g0001 a0005c0004t0001g0147 |
3 | HG02486.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(42): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(33): Show |
6 | a0001c0001t0001g0031 a0001c0001t0001g0244 a0002c0002t0001g0152 others(3): Show |
6 | HG01361.hp2 HG02300.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(44): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(35): Show |
9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01081.hp2 HG01257.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(46): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(37): Show |
19 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0053 others(16): Show |
19 | HG00558.hp2 HG00741.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(48): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(39): Show |
13 | a0001c0001t0001g0037 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
13 | HG00642.hp2 HG00738.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(41): Show |
20 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(17): Show |
20 | HG01074.hp2 HG01169.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(52): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(43): Show |
16 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(13): Show |
16 | HG00438.hp2 HG01192.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(54): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(45): Show |
8 | a0001c0001t0001g0050 a0002c0002t0001g0116 a0002c0002t0001g0136 others(5): Show |
8 | HG01070.hp1 HG01433.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(56): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(47): Show |
6 | a0001c0019t0001g0234 a0002c0002t0001g0141 a0002c0002t0001g0144 others(3): Show |
6 | HG00099.hp2 HG01261.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(58): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(49): Show |
3 | a0001c0001t0001g0051 a0002c0002t0001g0002 a0002c0002t0001g0185 |
3 | HG02080.hp1 NA18942.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(60): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(51): Show |
2 | a0001c0001t0001g0235 a0002c0002t0001g0186 |
2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(62): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(39): Show |
1 | a0001c0001t0001g0063 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1218+9650_1218+965 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTATATAT others(43): Show |
1 | a0001c0001t0001g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1218+9650_1218+965 others(54): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTTATATA others(24): Show |
1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(35): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTTTATAT others(3): Show |
1 | a0003c0009t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTTTATAT others(19): Show |
1 | a0003c0003t0001g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTTTATAT others(35): Show |
1 | a0003c0003t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(46): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTTTATAT others(37): Show |
1 | a0003c0003t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(48): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTTTATAT others(39): Show |
1 | a0003c0003t0001g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTTTATAT others(43): Show |
1 | a0003c0009t0001g0195 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(54): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373640 | T | TTTTATAT others(45): Show |
1 | a0003c0003t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1218+9640_1218+964 others(56): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373640 | ||||||
| chr5:114373645 | T | TATATATA others(33): Show |
1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(44): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373645 | ||||||
| chr5:114373645 | T | TATATATA others(39): Show |
1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373645 | ||||||
| chr5:114373657 | T | TATATATA others(3): Show |
10 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0096 others(7): Show |
10 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | ||||||
| chr5:114373657 | T | TATATATA others(29): Show |
1 | a0001c0018t0001g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(40): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | ||||||
| chr5:114373657 | T | TATATATA others(35): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0227 |
2 | HG01346.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(46): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | ||||||
| chr5:114373657 | T | TATATATA others(39): Show |
1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(50): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | ||||||
| chr5:114373657 | T | TATATATA others(43): Show |
1 | a0001c0001t0001g0039 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(54): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373657 | ||||||
| chr5:114373658 | A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(47): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373658 | |||||||
| chr5:114373658 | A | ATATATAT others(42): Show |
2 | a0002c0002t0001g0179 a0002c0017t0001g0178 |
2 | NA18999.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1218+9657_1218+965 others(53): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373658 | |||||||
| chr5:114373658 | A | ATATATAT others(48): Show |
1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1218+9657_1218+965 others(59): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114373658 | |||||||
| chr5:114373798 | AT | A | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(10): Show |
13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1218+9808delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114373798 | ||||||
| chr5:114374010 | A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+10009A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374010 | |||||||
| chr5:114374128 | A | C | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1218+10127A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374128 | |||||||
| chr5:114374144 | A | T | 3 | a0004c0008t0001g0010 a0004c0008t0001g0011 a0004c0008t0001g0012 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1218+10143A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374144 | |||||||
| chr5:114374547 | G | A | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+10546G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374547 | |||||||
| chr5:114374569 | C | T | 11 | a0002c0002t0001g0004 a0003c0003t0001g0193 a0003c0003t0001g0196 others(8): Show |
11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+10568C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374569 | |||||||
| chr5:114374661 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(87): Show |
91 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(88): Show |
intron_variant | MODIFIER | c.1218+10660C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374661 | |||||||
| chr5:114374741 | A | G | 2 | a0002c0002t0001g0139 a0002c0002t0001g0140 |
2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1218+10740A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374741 | |||||||
| chr5:114374787 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1218+10786C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374787 | |||||||
| chr5:114374805 | C | T | 1 | a0002c0002t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1218+10804C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374805 | |||||||
| chr5:114374912 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(190): Show |
194 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.1218+10911G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374912 | |||||||
| chr5:114374954 | G | A | 11 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+10953G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114374954 | |||||||
| chr5:114375064 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1218+11063T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114375064 | |||||||
| chr5:114375485 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1218+11484A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114375485 | |||||||
| chr5:114375692 | G | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(104): Show |
108 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1218+11691G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114375692 | |||||||
| chr5:114375694 | T | A | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+11693T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114375694 | |||||||
| chr5:114375952 | G | GTA | 7 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
7 | HG01109.hp1 HG01358.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218+11975_1218+11 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATA | 6 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0003c0003t0001g0197 others(3): Show |
6 | HG01516.hp1 HG01517.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218+11973_1218+11 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(3): Show |
1 | a0002c0002t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1218+11967_1218+11 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(5): Show |
2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1218+11965_1218+11 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(7): Show |
1 | a0002c0011t0001g0241 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1218+11963_1218+11 others(20): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(9): Show |
11 | a0001c0001t0001g0092 a0002c0002t0001g0004 a0002c0002t0001g0005 others(8): Show |
11 | HG01070.hp1 HG01361.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+11961_1218+11 others(22): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(11): Show |
26 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0002c0002t0001g0119 others(23): Show |
26 | HG00741.hp1 HG01175.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+11959_1218+11 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(13): Show |
26 | a0001c0006t0001g0097 a0001c0006t0001g0098 a0002c0002t0001g0110 others(23): Show |
26 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1218+11957_1218+11 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(15): Show |
18 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0111 others(15): Show |
18 | HG00099.hp1 HG00642.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1218+11955_1218+11 others(28): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(17): Show |
16 | a0001c0001t0001g0096 a0002c0002t0001g0117 a0002c0002t0001g0120 others(13): Show |
16 | HG00741.hp2 HG01070.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+11953_1218+11 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(19): Show |
7 | a0001c0006t0001g0095 a0002c0002t0001g0006 a0002c0002t0001g0127 others(4): Show |
7 | HG02055.hp1 HG02523.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218+11976_1218+11 others(32): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(21): Show |
3 | a0001c0001t0001g0094 a0002c0002t0001g0151 a0002c0002t0001g0166 |
3 | HG02040.hp2 HG02559.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1218+11976_1218+11 others(34): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTATATAT others(23): Show |
2 | a0001c0006t0001g0093 a0002c0002t0001g0165 |
2 | HG02080.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1218+11976_1218+11 others(36): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | G | GTGTATAT others(11): Show |
1 | a0002c0002t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1218+11952_1218+11 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | GTA | G | 27 | a0001c0001t0001g0034 a0001c0001t0001g0054 a0001c0001t0001g0055 others(24): Show |
27 | HG01081.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1218+11975_1218+11 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375952 | GTATA | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(60): Show |
64 | HG00280.hp1 HG01081.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.1218+11973_1218+11 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375952 | ||||||
| chr5:114375974 | A | ATATATAT others(15): Show |
1 | a0005c0004t0001g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1218+11976_1218+11 others(28): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375974 | ||||||
| chr5:114375974 | A | ATATATAT others(11): Show |
1 | a0002c0002t0001g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1218+11976_1218+11 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114375974 | ||||||
| chr5:114376006 | C | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1218+12005C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376006 | |||||||
| chr5:114376090 | A | G | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+12089A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376090 | |||||||
| chr5:114376111 | T | TAC | 18 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0008 others(15): Show |
18 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.1218+12113_1218+12 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114376111 | ||||||
| chr5:114376115 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1218+12114C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376115 | |||||||
| chr5:114376188 | T | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(40): Show |
44 | HG01081.hp2 HG01099.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.1218+12187T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376188 | |||||||
| chr5:114376194 | G | A | 10 | a0003c0003t0001g0193 a0003c0003t0001g0196 a0003c0003t0001g0197 others(7): Show |
10 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+12193G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376194 | |||||||
| chr5:114376258 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(63): Show |
67 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.1218+12257G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376258 | |||||||
| chr5:114376267 | T | C | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+12266T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376267 | |||||||
| chr5:114376315 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(103): Show |
107 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1218+12314G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376315 | |||||||
| chr5:114376326 | G | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(65): Show |
69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1218+12325G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376326 | |||||||
| chr5:114376454 | C | A | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1218+12453C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376454 | |||||||
| chr5:114376470 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(144): Show |
148 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1218+12469T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376470 | |||||||
| chr5:114376475 | A | G | 1 | a0002c0002t0001g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1218+12474A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376475 | |||||||
| chr5:114376662 | G | C | 56 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1218+12661G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376662 | |||||||
| chr5:114376778 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1218+12777A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376778 | |||||||
| chr5:114376877 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(104): Show |
108 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1218+12876G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114376877 | |||||||
| chr5:114377057 | G | T | 23 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0083 others(20): Show |
23 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1218+13056G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377057 | |||||||
| chr5:114377067 | G | A | 5 | a0001c0021t0001g0220 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+13066G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377067 | |||||||
| chr5:114377085 | A | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(87): Show |
91 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(88): Show |
intron_variant | MODIFIER | c.1218+13084A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377085 | |||||||
| chr5:114377157 | C | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1218+13156C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377157 | |||||||
| chr5:114377434 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(40): Show |
44 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.1218+13433C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377434 | |||||||
| chr5:114377584 | G | A | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+13583G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377584 | |||||||
| chr5:114377666 | T | C | 3 | a0004c0008t0001g0010 a0004c0008t0001g0011 a0004c0008t0001g0012 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1218+13665T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377666 | |||||||
| chr5:114377680 | T | C | 46 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0083 others(43): Show |
46 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1218+13679T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377680 | |||||||
| chr5:114377730 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1218+13729G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377730 | |||||||
| chr5:114377730 | G | C | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1218+13729G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377730 | |||||||
| chr5:114377747 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1218+13746C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377747 | |||||||
| chr5:114377918 | G | A | 1 | a0002c0002t0001g0166 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1218+13917G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114377918 | |||||||
| chr5:114378171 | A | G | 18 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(15): Show |
18 | HG01243.hp1 HG01243.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1218+14170A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378171 | |||||||
| chr5:114378176 | TA | T | 18 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(15): Show |
18 | HG01243.hp1 HG01243.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1218+14183delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114378176 | ||||||
| chr5:114378209 | C | T | 28 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0083 others(25): Show |
28 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1218+14208C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378209 | |||||||
| chr5:114378280 | A | G | 7 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(4): Show |
7 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+14279A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378280 | |||||||
| chr5:114378372 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
80 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.1218+14371G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378372 | |||||||
| chr5:114378406 | A | G | 1 | a0002c0002t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+14405A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378406 | |||||||
| chr5:114378489 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1218+14488T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378489 | |||||||
| chr5:114378542 | C | T | 9 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0005t0001g0013 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+14541C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378542 | |||||||
| chr5:114378544 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.1218+14543G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378544 | |||||||
| chr5:114378551 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1218+14550G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378551 | |||||||
| chr5:114378558 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1218+14557A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378558 | |||||||
| chr5:114378723 | TAGTGTCA others(11): Show |
T | 6 | a0002c0002t0001g0238 a0002c0002t0001g0240 a0002c0011t0001g0239 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+14725_1218+14 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114378723 | ||||||
| chr5:114378756 | T | C | 17 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(14): Show |
17 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1218+14755T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378756 | |||||||
| chr5:114378902 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1218+14901G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114378902 | |||||||
| chr5:114379052 | A | G | 10 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+15051A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379052 | |||||||
| chr5:114379066 | C | A | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1218+15065C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379066 | |||||||
| chr5:114379078 | G | T | 29 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(26): Show |
29 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1218+15077G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379078 | |||||||
| chr5:114379095 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1218+15094A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379095 | |||||||
| chr5:114379140 | T | C | 1 | a0002c0002t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1218+15139T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379140 | |||||||
| chr5:114379296 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1218+15295T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379296 | |||||||
| chr5:114379299 | C | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0061 |
2 | HG01099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1218+15298C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379299 | |||||||
| chr5:114379361 | T | C | 1 | a0002c0002t0001g0173 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1218+15360T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379361 | |||||||
| chr5:114379422 | A | AATATTAT others(25): Show |
2 | a0002c0002t0001g0115 a0002c0002t0001g0150 |
2 | HG02132.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1218+15510_1218+15 others(38): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379422 | ||||||
| chr5:114379422 | AATATTAT others(25): Show |
A | 6 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0006t0001g0093 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218+15510_1218+15 others(38): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379422 | ||||||
| chr5:114379422 | AATATTAT others(57): Show |
A | 16 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(13): Show |
16 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+15478_1218+15 others(70): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379422 | ||||||
| chr5:114379451 | G | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(36): Show |
40 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.1218+15450G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379451 | |||||||
| chr5:114379477 | TTTATAGA others(56): Show |
T | 10 | a0001c0001t0001g0069 a0001c0001t0001g0229 a0001c0001t0001g0231 others(7): Show |
10 | HG00099.hp1 HG00280.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+15510_1218+15 others(69): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379477 | ||||||
| chr5:114379477 | TTTATAGA others(87): Show |
T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0090 others(4): Show |
7 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+15511_1218+15 others(100): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379477 | ||||||
| chr5:114379496 | A | G | 11 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+15495A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379496 | |||||||
| chr5:114379507 | TATTTATA others(88): Show |
T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0018t0001g0029 |
3 | HG02040.hp1 NA19060.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1218+15507_1218+15 others(101): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379507 | |||||||
| chr5:114379508 | AT | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(85): Show |
89 | HG00280.hp2 HG01074.hp1 HG01081.hp2 others(86): Show |
intron_variant | MODIFIER | c.1218+15510delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379508 | ||||||
| chr5:114379534 | TTATATAT others(115): Show |
T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG01978.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218+15542_1218+15 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379534 | ||||||
| chr5:114379540 | A | AT | 81 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(78): Show |
82 | HG00280.hp2 HG01074.hp1 HG01081.hp2 others(79): Show |
intron_variant | MODIFIER | c.1218+15541dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379540 | ||||||
| chr5:114379541 | TTATAGAA others(23): Show |
T | 2 | a0001c0001t0001g0230 a0001c0019t0001g0234 |
2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1218+15542_1218+15 others(36): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379541 | ||||||
| chr5:114379543 | A | ATATAACA others(13): Show |
4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+15544_1218+15 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379543 | ||||||
| chr5:114379543 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(76): Show |
80 | HG00280.hp2 HG01074.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.1218+15542A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379543 | |||||||
| chr5:114379565 | TTATATAT others(84): Show |
T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(80): Show |
84 | HG00280.hp2 HG01074.hp1 HG01081.hp2 others(81): Show |
intron_variant | MODIFIER | c.1218+15573_1218+15 others(97): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379565 | ||||||
| chr5:114379571 | A | AT | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(17): Show |
20 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1218+15572dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379571 | ||||||
| chr5:114379574 | A | G | 22 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(19): Show |
22 | HG01081.hp1 HG01099.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1218+15573A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379574 | |||||||
| chr5:114379593 | ATAT | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG01433.hp2 HG01993.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+15596_1218+15 others(9): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379593 | ||||||
| chr5:114379596 | TTATATAT others(53): Show |
T | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1218+15605_1218+15 others(66): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379596 | ||||||
| chr5:114379601 | TA | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG01433.hp2 HG01993.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+15601delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379601 | |||||||
| chr5:114379605 | T | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0045 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+15604T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379605 | |||||||
| chr5:114379605 | T | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG01433.hp2 HG01993.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+15604T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379605 | |||||||
| chr5:114379605 | T | TG | 39 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0057 others(36): Show |
39 | HG00280.hp1 HG01081.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1218+15604_1218+15 others(7): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379605 | |||||||
| chr5:114379605 | T | TGTAGAAT others(23): Show |
1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1218+15604_1218+15 others(36): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379605 | |||||||
| chr5:114379610 | A | T | 1 | a0002c0002t0001g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1218+15609A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379610 | |||||||
| chr5:114379624 | ATAT | A | 9 | a0002c0002t0001g0102 a0002c0002t0001g0103 a0002c0005t0001g0013 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+15627_1218+15 others(9): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379624 | ||||||
| chr5:114379625 | TATTATAT others(24): Show |
T | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1218+15625_1218+15 others(37): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379625 | |||||||
| chr5:114379637 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1218+15636G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379637 | |||||||
| chr5:114379637 | GTAGAATA others(22): Show |
G | 4 | a0002c0014t0001g0017 a0007c0010t0001g0191 a0007c0010t0001g0192 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+15659_1218+15 others(35): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379637 | ||||||
| chr5:114379656 | A | ATAT | 45 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(42): Show |
45 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1218+15656_1218+15 others(9): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379656 | ||||||
| chr5:114379656 | A | ATATATAT others(89): Show |
1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1218+15664_1218+15 others(102): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379656 | ||||||
| chr5:114379656 | A | ATATTATA others(28): Show |
3 | a0003c0003t0001g0193 a0003c0003t0001g0196 a0003c0009t0001g0195 |
3 | NA18522.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1218+15658_1218+15 others(41): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379656 | ||||||
| chr5:114379666 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(124): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1218+15665A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379666 | |||||||
| chr5:114379698 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(124): Show |
128 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(125): Show |
intron_variant | MODIFIER | c.1218+15697A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379698 | |||||||
| chr5:114379730 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(112): Show |
116 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(113): Show |
intron_variant | MODIFIER | c.1218+15729A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379730 | |||||||
| chr5:114379748 | CATATTAT others(27): Show |
C | 9 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(6): Show |
9 | HG00280.hp2 HG01256.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218+15752_1218+15 others(40): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379748 | ||||||
| chr5:114379762 | A | G | 14 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0091 others(11): Show |
14 | HG02055.hp1 HG02145.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1218+15761A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379762 | |||||||
| chr5:114379780 | CAT | C | 48 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(45): Show |
48 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1218+15786_1218+15 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114379780 | ||||||
| chr5:114379781 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1218+15780A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379781 | |||||||
| chr5:114379882 | G | A | 27 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1218+15881G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379882 | |||||||
| chr5:114379897 | G | T | 1 | a0002c0002t0001g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1218+15896G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379897 | |||||||
| chr5:114379947 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1218+15946G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379947 | |||||||
| chr5:114379964 | T | C | 3 | a0002c0002t0001g0144 a0004c0012t0001g0142 a0004c0012t0001g0143 |
3 | HG01070.hp1 HG01256.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1218+15963T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114379964 | |||||||
| chr5:114380017 | A | G | 10 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+16016A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380017 | |||||||
| chr5:114380248 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1218+16247G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380248 | |||||||
| chr5:114380373 | T | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(40): Show |
44 | HG01081.hp2 HG01099.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.1218+16372T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380373 | |||||||
| chr5:114380378 | C | G | 26 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0066 others(23): Show |
26 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+16377C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380378 | |||||||
| chr5:114380461 | G | C | 1 | a0002c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1218+16460G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380461 | |||||||
| chr5:114380785 | G | T | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+16784G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380785 | |||||||
| chr5:114380807 | T | C | 1 | a0002c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1218+16806T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380807 | |||||||
| chr5:114380835 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(143): Show |
147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1218+16834G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380835 | |||||||
| chr5:114380991 | G | A | 4 | a0002c0002t0001g0122 a0002c0002t0001g0130 a0002c0002t0001g0133 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+16990G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114380991 | |||||||
| chr5:114381030 | G | T | 1 | a0001c0001t0001g0028 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1218+17029G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381030 | |||||||
| chr5:114381044 | C | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+17043C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381044 | |||||||
| chr5:114381238 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1218+17237C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381238 | |||||||
| chr5:114381340 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1218+17339A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381340 | |||||||
| chr5:114381560 | C | A | 1 | a0002c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1218+17559C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381560 | |||||||
| chr5:114381564 | T | C | 1 | a0002c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1218+17563T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381564 | |||||||
| chr5:114381591 | G | T | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1218+17590G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381591 | |||||||
| chr5:114381700 | C | T | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1218+17699C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381700 | |||||||
| chr5:114381735 | G | A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218+17734G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381735 | |||||||
| chr5:114381774 | G | A | 9 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0009 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+17773G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114381774 | |||||||
| chr5:114382020 | G | A | 20 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(17): Show |
20 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.1218+18019G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382020 | |||||||
| chr5:114382078 | G | A | 1 | a0002c0002t0001g0157 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1218+18077G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382078 | |||||||
| chr5:114382194 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1218+18193C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382194 | |||||||
| chr5:114382445 | G | C | 1 | a0002c0002t0001g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1218+18444G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382445 | |||||||
| chr5:114382631 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1218+18630C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382631 | |||||||
| chr5:114382632 | C | A | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1218+18631C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382632 | |||||||
| chr5:114382737 | C | G | 5 | a0001c0021t0001g0220 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+18736C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382737 | |||||||
| chr5:114382760 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(41): Show |
45 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.1218+18759G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382760 | |||||||
| chr5:114382921 | T | C | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+18920T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114382921 | |||||||
| chr5:114383139 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1218+19138A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383139 | |||||||
| chr5:114383235 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19234A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383235 | |||||||
| chr5:114383250 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19249G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383250 | |||||||
| chr5:114383290 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19289G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383290 | |||||||
| chr5:114383302 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1218+19301G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383302 | |||||||
| chr5:114383431 | G | C | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1218+19430G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383431 | |||||||
| chr5:114383434 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19433G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383434 | |||||||
| chr5:114383448 | T | G | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0003c0009t0001g0194 |
3 | HG02809.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+19447T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383448 | |||||||
| chr5:114383464 | C | CT | 20 | a0001c0001t0001g0070 a0001c0001t0001g0079 a0001c0001t0001g0080 others(17): Show |
20 | HG00438.hp1 HG01109.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1218+19487dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114383464 | ||||||
| chr5:114383464 | CT | C | 70 | a0001c0001t0001g0066 a0001c0001t0001g0083 a0001c0001t0001g0084 others(67): Show |
70 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1218+19487delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114383464 | ||||||
| chr5:114383464 | CTT | C | 12 | a0001c0001t0001g0087 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.1218+19486_1218+19 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114383464 | ||||||
| chr5:114383464 | CTTTTTTT others(5): Show |
C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(65): Show |
69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1218+19476_1218+19 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114383464 | ||||||
| chr5:114383594 | A | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1218+19593A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383594 | |||||||
| chr5:114383615 | G | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1218+19614G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383615 | |||||||
| chr5:114383641 | T | G | 11 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218+19640T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383641 | |||||||
| chr5:114383654 | G | A | 6 | a0001c0001t0001g0090 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
6 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+19653G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383654 | |||||||
| chr5:114383940 | T | C | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1218+19939T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383940 | |||||||
| chr5:114383955 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02280.hp1 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1218+19954C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114383955 | |||||||
| chr5:114384045 | A | G | 2 | a0002c0002t0001g0130 a0002c0002t0001g0137 |
2 | HG02109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1218+20044A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384045 | |||||||
| chr5:114384255 | C | T | 1 | a0002c0002t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1219-20183C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384255 | |||||||
| chr5:114384504 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(127): Show |
131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1219-19934G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384504 | |||||||
| chr5:114384517 | A | C | 1 | a0002c0002t0001g0072 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1219-19921A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384517 | |||||||
| chr5:114384667 | A | G | 1 | a0003c0003t0001g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1219-19771A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114384667 | |||||||
| chr5:114384961 | CTTAA | C | 9 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(6): Show |
9 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-19473_1219-19 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114384961 | ||||||
| chr5:114385234 | C | T | 15 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0004 others(12): Show |
15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-19204C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385234 | |||||||
| chr5:114385244 | T | C | 11 | a0001c0001t0001g0248 a0003c0003t0001g0193 a0003c0003t0001g0196 others(8): Show |
11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-19194T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385244 | |||||||
| chr5:114385310 | T | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG02886.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1219-19128T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385310 | |||||||
| chr5:114385501 | C | T | 15 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0004 others(12): Show |
15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18937C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385501 | |||||||
| chr5:114385514 | T | TGC | 9 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0230 others(6): Show |
9 | HG01109.hp1 HG01192.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1219-18919_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385514 | ||||||
| chr5:114385514 | T | TGCGC | 3 | a0001c0001t0001g0028 a0001c0001t0001g0050 a0001c0015t0001g0219 |
3 | HG02965.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1219-18921_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385514 | ||||||
| chr5:114385514 | TGC | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0002c0005t0001g0013 others(1): Show |
4 | HG01099.hp2 HG01243.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-18919_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385514 | ||||||
| chr5:114385514 | TGCGC | T | 9 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0008 others(6): Show |
9 | HG02523.hp1 HG02630.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-18921_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385514 | ||||||
| chr5:114385515 | GCGCGCAC others(7): Show |
G | 1 | a0006c0007t0001g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1219-18921_1219-18 others(20): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385515 | ||||||
| chr5:114385517 | G | A | 2 | a0002c0002t0001g0004 a0002c0005t0001g0015 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1219-18921G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385517 | |||||||
| chr5:114385517 | G | GCA | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(6): Show |
9 | HG01433.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-18920_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385517 | ||||||
| chr5:114385519 | G | A | 16 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(13): Show |
16 | HG01081.hp1 HG01243.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-18919G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385519 | |||||||
| chr5:114385519 | G | GCA | 10 | a0001c0001t0001g0066 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
10 | HG00642.hp1 HG00738.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1219-18882_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385519 | G | GCACA | 9 | a0001c0001t0001g0076 a0002c0002t0001g0201 a0002c0002t0001g0202 others(6): Show |
9 | HG00099.hp1 HG00280.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-18884_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385519 | G | GCACACA | 4 | a0001c0001t0001g0083 a0002c0002t0001g0205 a0002c0002t0001g0236 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-18886_1219-18 others(12): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385519 | G | GCACACAC others(3): Show |
1 | a0002c0002t0001g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1219-18890_1219-18 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385519 | G | GCGCA | 39 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(36): Show |
39 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1219-18918_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385519 | G | GCGCACA | 4 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0215 others(1): Show |
5 | HG02273.hp2 HG02886.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-18918_1219-18 others(12): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385519 | G | GCGCACAC others(1): Show |
3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0218 |
3 | HG01074.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1219-18918_1219-18 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385519 | G | GCGCACAC others(3): Show |
4 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0216 others(1): Show |
4 | HG02486.hp1 HG02615.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-18918_1219-18 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385519 | GCA | G | 81 | a0001c0001t0001g0034 a0001c0001t0001g0086 a0001c0001t0001g0100 others(78): Show |
81 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1219-18882_1219-18 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385519 | GCACA | G | 4 | a0001c0001t0001g0247 a0002c0002t0001g0002 a0002c0002t0001g0167 others(1): Show |
4 | HG01167.hp1 NA18906.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-18884_1219-18 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385519 | ||||||
| chr5:114385521 | A | G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0099 others(5): Show |
8 | HG00280.hp1 HG00738.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-18917A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385521 | |||||||
| chr5:114385523 | A | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0227 a0001c0001t0001g0228 others(7): Show |
10 | HG01081.hp2 HG03139.hp1 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.1219-18915A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385523 | |||||||
| chr5:114385620 | T | C | 1 | a0002c0002t0001g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1219-18818T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385620 | |||||||
| chr5:114385654 | C | G | 11 | a0001c0001t0001g0248 a0003c0003t0001g0193 a0003c0003t0001g0196 others(8): Show |
11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-18784C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385654 | |||||||
| chr5:114385691 | C | G | 15 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0004 others(12): Show |
15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18747C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385691 | |||||||
| chr5:114385734 | T | C | 15 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0004 others(12): Show |
15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18704T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385734 | |||||||
| chr5:114385741 | T | C | 15 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0004 others(12): Show |
15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18697T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385741 | |||||||
| chr5:114385752 | C | T | 33 | a0001c0001t0001g0066 a0001c0001t0001g0083 a0001c0001t0001g0084 others(30): Show |
33 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1219-18686C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385752 | |||||||
| chr5:114385825 | G | GT | 10 | a0002c0002t0001g0123 a0002c0002t0001g0127 a0002c0002t0001g0131 others(7): Show |
10 | HG00741.hp1 HG01070.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1219-18603dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114385825 | ||||||
| chr5:114385929 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1219-18509A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114385929 | |||||||
| chr5:114386014 | T | TA | 15 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0004 others(12): Show |
15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18415dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114386014 | ||||||
| chr5:114386015 | A | G | 22 | a0001c0001t0001g0066 a0001c0001t0001g0083 a0001c0001t0001g0084 others(19): Show |
22 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1219-18423A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386015 | |||||||
| chr5:114386098 | C | T | 1 | a0002c0002t0001g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1219-18340C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386098 | |||||||
| chr5:114386181 | T | TA | 19 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0082 others(16): Show |
19 | HG01243.hp2 HG01981.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1219-18236dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114386181 | ||||||
| chr5:114386181 | TA | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(64): Show |
68 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1219-18236delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114386181 | ||||||
| chr5:114386195 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG01978.hp2 HG01981.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-18243A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386195 | |||||||
| chr5:114386392 | G | GA | 15 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0004 others(12): Show |
15 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1219-18040dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114386392 | ||||||
| chr5:114386401 | A | G | 2 | a0007c0010t0001g0191 a0007c0010t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1219-18037A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386401 | |||||||
| chr5:114386402 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1219-18036T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386402 | |||||||
| chr5:114386660 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-17778G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386660 | |||||||
| chr5:114386938 | A | G | 4 | a0002c0002t0001g0122 a0002c0002t0001g0130 a0002c0002t0001g0133 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-17500A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114386938 | |||||||
| chr5:114387159 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1219-17279A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387159 | |||||||
| chr5:114387238 | A | T | 11 | a0001c0001t0001g0248 a0003c0003t0001g0193 a0003c0003t0001g0196 others(8): Show |
11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-17200A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387238 | |||||||
| chr5:114387282 | G | T | 9 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0009 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-17156G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387282 | |||||||
| chr5:114387294 | C | T | 27 | a0001c0001t0001g0066 a0001c0001t0001g0083 a0001c0001t0001g0084 others(24): Show |
27 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1219-17144C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387294 | |||||||
| chr5:114387302 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-17136T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387302 | |||||||
| chr5:114387509 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1219-16929G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387509 | |||||||
| chr5:114387533 | TA | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1219-16896delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114387533 | ||||||
| chr5:114387743 | C | G | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1219-16695C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387743 | |||||||
| chr5:114387922 | G | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(141): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1219-16516G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114387922 | |||||||
| chr5:114388008 | A | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-16430A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388008 | |||||||
| chr5:114388036 | C | T | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-16402C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388036 | |||||||
| chr5:114388043 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1219-16395C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388043 | |||||||
| chr5:114388127 | A | G | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1219-16311A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388127 | |||||||
| chr5:114388134 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(77): Show |
81 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.1219-16304G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388134 | |||||||
| chr5:114388187 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1219-16251G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388187 | |||||||
| chr5:114388249 | C | T | 2 | a0001c0001t0001g0248 a0003c0009t0001g0194 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1219-16189C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388249 | |||||||
| chr5:114388474 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-15964A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388474 | |||||||
| chr5:114388632 | G | A | 9 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0009 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-15806G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388632 | |||||||
| chr5:114388700 | A | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0061 |
2 | HG01099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1219-15738A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388700 | |||||||
| chr5:114388725 | A | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0062 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1219-15713A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388725 | |||||||
| chr5:114388745 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1219-15693A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388745 | |||||||
| chr5:114388805 | A | T | 4 | a0002c0005t0001g0013 a0002c0005t0001g0014 a0002c0005t0001g0015 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-15633A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114388805 | |||||||
| chr5:114388811 | GT | G | 7 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0009 others(4): Show |
7 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-15619delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114388811 | ||||||
| chr5:114389140 | A | G | 9 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0009 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-15298A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389140 | |||||||
| chr5:114389217 | G | T | 11 | a0001c0001t0001g0248 a0003c0003t0001g0193 a0003c0003t0001g0196 others(8): Show |
11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-15221G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389217 | |||||||
| chr5:114389240 | C | G | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1219-15198C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389240 | |||||||
| chr5:114389492 | G | A | 9 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0009 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-14946G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389492 | |||||||
| chr5:114389649 | A | T | 11 | a0001c0001t0001g0248 a0003c0003t0001g0193 a0003c0003t0001g0196 others(8): Show |
11 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-14789A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389649 | |||||||
| chr5:114389692 | A | G | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1219-14746A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389692 | |||||||
| chr5:114389797 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(134): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1219-14641G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389797 | |||||||
| chr5:114389974 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(77): Show |
81 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.1219-14464A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114389974 | |||||||
| chr5:114390013 | C | G | 29 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(26): Show |
29 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1219-14425C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390013 | |||||||
| chr5:114390177 | A | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0182 |
2 | HG02132.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1219-14261A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390177 | |||||||
| chr5:114390213 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
80 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.1219-14225G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390213 | |||||||
| chr5:114390280 | A | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-14158A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390280 | |||||||
| chr5:114390603 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1219-13835A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390603 | |||||||
| chr5:114390705 | A | C | 50 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(47): Show |
50 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.1219-13733A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390705 | |||||||
| chr5:114390842 | G | A | 18 | a0001c0001t0001g0248 a0002c0002t0001g0201 a0002c0002t0001g0202 others(15): Show |
18 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1219-13596G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390842 | |||||||
| chr5:114390907 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1219-13531G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114390907 | |||||||
| chr5:114391241 | C | A | 14 | a0001c0021t0001g0220 a0002c0002t0001g0004 a0002c0002t0001g0008 others(11): Show |
14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1219-13197C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391241 | |||||||
| chr5:114391292 | A | T | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-13146A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391292 | |||||||
| chr5:114391352 | T | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(54): Show |
58 | HG01081.hp2 HG01099.hp1 HG01175.hp2 others(55): Show |
intron_variant | MODIFIER | c.1219-13086T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391352 | |||||||
| chr5:114391415 | C | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(128): Show |
132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1219-13023C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391415 | |||||||
| chr5:114391457 | G | A | 5 | a0001c0021t0001g0220 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-12981G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391457 | |||||||
| chr5:114391488 | C | G | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1219-12950C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391488 | |||||||
| chr5:114391509 | G | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02280.hp1 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1219-12929G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391509 | |||||||
| chr5:114391662 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1219-12776T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391662 | |||||||
| chr5:114391801 | A | C | 8 | a0002c0002t0001g0129 a0002c0002t0001g0157 a0002c0002t0001g0158 others(5): Show |
8 | HG02132.hp1 NA18959.hp1 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.1219-12637A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391801 | |||||||
| chr5:114391937 | T | C | 9 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
9 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-12501T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114391937 | |||||||
| chr5:114391985 | C | CT | 10 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(7): Show |
10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-12446dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114391985 | ||||||
| chr5:114392442 | C | G | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-11996C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392442 | |||||||
| chr5:114392503 | G | A | 1 | a0004c0012t0001g0143 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1219-11935G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392503 | |||||||
| chr5:114392548 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1219-11890G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392548 | |||||||
| chr5:114392669 | C | T | 1 | a0002c0002t0001g0184 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1219-11769C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392669 | |||||||
| chr5:114392706 | T | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1219-11732T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114392706 | |||||||
| chr5:114392806 | GT | G | 27 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0030 others(24): Show |
27 | HG01081.hp1 HG01099.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.1219-11619delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114392806 | ||||||
| chr5:114392806 | GTT | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(47): Show |
51 | HG00280.hp1 HG01081.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.1219-11620_1219-11 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114392806 | ||||||
| chr5:114393010 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1219-11428C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393010 | |||||||
| chr5:114393340 | T | A | 2 | a0007c0010t0001g0191 a0007c0010t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1219-11098T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393340 | |||||||
| chr5:114393410 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1219-11028G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393410 | |||||||
| chr5:114393778 | CT | C | 3 | a0004c0008t0001g0010 a0004c0008t0001g0011 a0004c0008t0001g0012 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1219-10656delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114393778 | ||||||
| chr5:114393782 | T | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(124): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1219-10656T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393782 | |||||||
| chr5:114393783 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1219-10655A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393783 | |||||||
| chr5:114393860 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1219-10578G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393860 | |||||||
| chr5:114393901 | C | T | 10 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(7): Show |
10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-10537C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393901 | |||||||
| chr5:114393927 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1219-10511A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393927 | |||||||
| chr5:114393970 | A | G | 14 | a0001c0021t0001g0220 a0002c0002t0001g0004 a0002c0002t0001g0008 others(11): Show |
14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1219-10468A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393970 | |||||||
| chr5:114393973 | CAT | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1219-10464_1219-10 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114393973 | |||||||
| chr5:114394005 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(75): Show |
79 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-10433T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394005 | |||||||
| chr5:114394195 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1219-10243A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394195 | |||||||
| chr5:114394202 | A | G | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-10236A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394202 | |||||||
| chr5:114394404 | T | G | 1 | a0002c0002t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1219-10034T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394404 | |||||||
| chr5:114394576 | C | T | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1219-9862C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394576 | |||||||
| chr5:114394710 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(64): Show |
68 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1219-9728G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114394710 | |||||||
| chr5:114395074 | T | C | 2 | a0002c0002t0001g0126 a0002c0002t0001g0158 |
2 | NA18959.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1219-9364T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395074 | |||||||
| chr5:114395272 | C | T | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1219-9166C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395272 | |||||||
| chr5:114395311 | A | G | 2 | a0002c0002t0001g0128 a0002c0002t0001g0132 |
2 | HG01169.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1219-9127A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395311 | |||||||
| chr5:114395315 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1219-9123G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395315 | |||||||
| chr5:114395318 | G | A | 1 | a0002c0002t0001g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1219-9120G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395318 | |||||||
| chr5:114395322 | T | C | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1219-9116T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395322 | |||||||
| chr5:114395381 | A | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(65): Show |
69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1219-9057A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395381 | |||||||
| chr5:114395430 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1219-9008A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395430 | |||||||
| chr5:114395462 | T | C | 5 | a0001c0001t0001g0090 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-8976T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395462 | |||||||
| chr5:114395708 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-8730A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395708 | |||||||
| chr5:114395726 | A | G | 42 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(39): Show |
42 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1219-8712A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395726 | |||||||
| chr5:114395822 | C | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1219-8616C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395822 | |||||||
| chr5:114395826 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(65): Show |
69 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1219-8612C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395826 | |||||||
| chr5:114395877 | C | T | 7 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0009 others(4): Show |
7 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-8561C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395877 | |||||||
| chr5:114395959 | T | C | 3 | a0002c0005t0001g0013 a0002c0005t0001g0014 a0002c0005t0001g0015 |
3 | HG01243.hp2 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1219-8479T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114395959 | |||||||
| chr5:114396054 | A | G | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-8384A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396054 | |||||||
| chr5:114396096 | A | C | 1 | a0002c0002t0001g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1219-8342A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396096 | |||||||
| chr5:114396124 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(63): Show |
67 | HG00280.hp1 HG01081.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.1219-8314A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396124 | |||||||
| chr5:114396141 | G | T | 1 | a0002c0002t0001g0132 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1219-8297G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396141 | |||||||
| chr5:114396142 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1219-8296C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396142 | |||||||
| chr5:114396157 | CTCTT | C | 86 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0003 others(83): Show |
86 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1219-8275_1219-827 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114396157 | ||||||
| chr5:114396204 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1219-8234A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396204 | |||||||
| chr5:114396313 | C | G | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1219-8125C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396313 | |||||||
| chr5:114396313 | CTAAT | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(64): Show |
68 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1219-8121_1219-811 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114396313 | ||||||
| chr5:114396490 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-7948G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396490 | |||||||
| chr5:114396530 | G | A | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1219-7908G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396530 | |||||||
| chr5:114396551 | CT | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(140): Show |
144 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.1219-7872delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114396551 | ||||||
| chr5:114396688 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(42): Show |
46 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(43): Show |
intron_variant | MODIFIER | c.1219-7750A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396688 | |||||||
| chr5:114396717 | T | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-7721T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396717 | |||||||
| chr5:114396830 | C | T | 12 | a0001c0001t0001g0248 a0002c0002t0001g0004 a0003c0003t0001g0193 others(9): Show |
12 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.1219-7608C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396830 | |||||||
| chr5:114396862 | T | A | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1219-7576T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114396862 | |||||||
| chr5:114397033 | C | T | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1219-7405C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397033 | |||||||
| chr5:114397034 | G | A | 10 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(7): Show |
10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-7404G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397034 | |||||||
| chr5:114397084 | A | G | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1219-7354A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397084 | |||||||
| chr5:114397114 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1219-7324C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397114 | |||||||
| chr5:114397167 | A | G | 10 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(7): Show |
10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-7271A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397167 | |||||||
| chr5:114397412 | G | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(59): Show |
63 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.1219-7026G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397412 | |||||||
| chr5:114397542 | A | G | 1 | a0001c0018t0001g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1219-6896A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397542 | |||||||
| chr5:114397548 | G | A | 2 | a0001c0001t0001g0247 a0002c0002t0001g0119 |
2 | HG04115.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1219-6890G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397548 | |||||||
| chr5:114397634 | C | T | 1 | a0002c0002t0001g0152 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1219-6804C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114397634 | |||||||
| chr5:114398039 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1219-6399C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398039 | |||||||
| chr5:114398254 | C | T | 1 | a0002c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1219-6184C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398254 | |||||||
| chr5:114398313 | A | T | 1 | a0010c0023t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1219-6125A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398313 | |||||||
| chr5:114398484 | G | GT | 35 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0083 others(32): Show |
35 | HG00738.hp1 HG01074.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1219-5941dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114398484 | ||||||
| chr5:114398484 | G | GTT | 8 | a0001c0001t0001g0082 a0001c0001t0001g0106 a0001c0006t0001g0098 others(5): Show |
8 | HG00642.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-5942_1219-594 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114398484 | ||||||
| chr5:114398676 | G | A | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1219-5762G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398676 | |||||||
| chr5:114398721 | G | T | 58 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(55): Show |
58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1219-5717G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398721 | |||||||
| chr5:114398780 | A | G | 58 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(55): Show |
58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1219-5658A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398780 | |||||||
| chr5:114398958 | T | G | 1 | a0002c0002t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1219-5480T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398958 | |||||||
| chr5:114398999 | T | A | 1 | a0002c0002t0001g0134 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1219-5439T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114398999 | |||||||
| chr5:114399116 | G | C | 1 | a0002c0002t0001g0141 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1219-5322G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399116 | |||||||
| chr5:114399367 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1219-5071T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399367 | |||||||
| chr5:114399394 | T | G | 13 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(10): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1219-5044T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399394 | |||||||
| chr5:114399431 | C | T | 1 | a0002c0002t0001g0072 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1219-5007C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399431 | |||||||
| chr5:114399530 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1219-4908G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399530 | |||||||
| chr5:114399591 | A | G | 4 | a0002c0002t0001g0236 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-4847A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399591 | |||||||
| chr5:114399616 | A | G | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-4822A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399616 | |||||||
| chr5:114399723 | T | A | 47 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(44): Show |
47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1219-4715T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399723 | |||||||
| chr5:114399773 | C | A | 1 | a0002c0002t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1219-4665C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399773 | |||||||
| chr5:114399833 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0037 |
2 | HG03195.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1219-4605G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399833 | |||||||
| chr5:114399847 | C | T | 1 | a0002c0002t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1219-4591C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399847 | |||||||
| chr5:114399861 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1219-4577A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399861 | |||||||
| chr5:114399929 | T | G | 2 | a0001c0001t0001g0086 a0001c0021t0001g0220 |
2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1219-4509T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399929 | |||||||
| chr5:114399929 | T | TTG | 7 | a0002c0002t0001g0004 a0003c0003t0001g0193 a0003c0003t0001g0196 others(4): Show |
7 | HG02922.hp2 HG03209.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-4509_1219-450 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399929 | |||||||
| chr5:114399930 | G | GT | 51 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0035 others(48): Show |
51 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1219-4496dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114399930 | ||||||
| chr5:114399930 | G | T | 13 | a0001c0001t0001g0086 a0001c0001t0001g0248 a0001c0021t0001g0220 others(10): Show |
13 | HG01884.hp1 HG02630.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1219-4508G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114399930 | |||||||
| chr5:114400081 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1219-4357T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400081 | |||||||
| chr5:114400181 | C | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1219-4257C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400181 | |||||||
| chr5:114400193 | T | C | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1219-4245T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400193 | |||||||
| chr5:114400310 | A | G | 1 | a0002c0002t0001g0152 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1219-4128A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400310 | |||||||
| chr5:114400350 | C | T | 10 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(7): Show |
10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-4088C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400350 | |||||||
| chr5:114400400 | A | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(56): Show |
60 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.1219-4038A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400400 | |||||||
| chr5:114400442 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1219-3996C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400442 | |||||||
| chr5:114400550 | G | C | 8 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-3888G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400550 | |||||||
| chr5:114400571 | C | T | 1 | a0004c0012t0001g0142 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1219-3867C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400571 | |||||||
| chr5:114400719 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(58): Show |
62 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.1219-3719G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400719 | |||||||
| chr5:114400768 | C | A | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1219-3670C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400768 | |||||||
| chr5:114400899 | T | C | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1219-3539T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400899 | |||||||
| chr5:114400969 | CTA | C | 3 | a0001c0001t0001g0080 a0002c0002t0001g0008 a0002c0002t0001g0009 |
3 | HG02523.hp1 HG04204.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1219-3467_1219-346 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114400969 | ||||||
| chr5:114400981 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(134): Show |
138 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.1219-3457T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114400981 | |||||||
| chr5:114401043 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1219-3395C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401043 | |||||||
| chr5:114401053 | G | T | 3 | a0002c0005t0001g0013 a0002c0005t0001g0014 a0002c0005t0001g0015 |
3 | HG01243.hp2 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1219-3385G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401053 | |||||||
| chr5:114401302 | C | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1219-3136C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401302 | |||||||
| chr5:114401365 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(135): Show |
139 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.1219-3073T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401365 | |||||||
| chr5:114401453 | C | G | 1 | a0001c0001t0001g0246 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1219-2985C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401453 | |||||||
| chr5:114401464 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(58): Show |
62 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.1219-2974G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401464 | |||||||
| chr5:114401686 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1219-2752G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114401686 | |||||||
| chr5:114402302 | G | T | 2 | a0001c0006t0001g0093 a0001c0006t0001g0095 |
2 | HG02055.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1219-2136G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402302 | |||||||
| chr5:114402335 | G | T | 1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1219-2103G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402335 | |||||||
| chr5:114402402 | G | C | 1 | a0002c0002t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1219-2036G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402402 | |||||||
| chr5:114402403 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1219-2035G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402403 | |||||||
| chr5:114402502 | A | G | 1 | a0002c0002t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1219-1936A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402502 | |||||||
| chr5:114402570 | TAAGG | T | 5 | a0001c0001t0001g0090 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-1866_1219-186 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 114402570 | ||||||
| chr5:114402615 | T | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1219-1823T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402615 | |||||||
| chr5:114402764 | G | C | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1219-1674G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402764 | |||||||
| chr5:114402829 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1219-1609T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402829 | |||||||
| chr5:114402977 | A | T | 1 | a0001c0001t0001g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1219-1461A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114402977 | |||||||
| chr5:114403017 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(67): Show |
71 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1219-1421G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403017 | |||||||
| chr5:114403213 | A | T | 4 | a0002c0005t0001g0013 a0002c0005t0001g0014 a0002c0005t0001g0015 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-1225A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403213 | |||||||
| chr5:114403266 | C | T | 2 | a0007c0010t0001g0191 a0007c0010t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1219-1172C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403266 | |||||||
| chr5:114403299 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1219-1139T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403299 | |||||||
| chr5:114403580 | C | G | 6 | a0002c0002t0001g0238 a0002c0002t0001g0240 a0002c0011t0001g0239 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1219-858C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403580 | |||||||
| chr5:114403776 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1219-662C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114403776 | |||||||
| chr5:114404333 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1219-105G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 2/7 | chr5 | 114404333 | |||||||
| chr5:114404940 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1637+84G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114404940 | |||||||
| chr5:114405269 | G | A | 6 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0006c0007t0001g0104 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+413G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405269 | |||||||
| chr5:114405314 | T | C | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(10): Show |
13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1637+458T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405314 | |||||||
| chr5:114405356 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1637+500G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405356 | |||||||
| chr5:114405532 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+676T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405532 | |||||||
| chr5:114405584 | C | A | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+728C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405584 | |||||||
| chr5:114405632 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1637+776G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405632 | |||||||
| chr5:114405716 | GT | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(142): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1637+872delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114405716 | ||||||
| chr5:114405773 | C | T | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+917C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405773 | |||||||
| chr5:114405990 | G | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0227 a0001c0001t0001g0229 others(5): Show |
8 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1637+1134G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405990 | |||||||
| chr5:114405996 | C | A | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+1140C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114405996 | |||||||
| chr5:114406000 | G | A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0227 a0001c0001t0001g0229 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1637+1144G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406000 | |||||||
| chr5:114406002 | A | C | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1637+1146A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406002 | |||||||
| chr5:114406016 | T | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+1160T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406016 | |||||||
| chr5:114406208 | T | C | 14 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0008 others(11): Show |
14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1637+1352T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406208 | |||||||
| chr5:114406302 | GCTAT | G | 14 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0008 others(11): Show |
14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1637+1451_1637+145 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114406302 | ||||||
| chr5:114406345 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0046 |
3 | HG01358.hp2 HG03654.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1637+1489T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406345 | |||||||
| chr5:114406390 | A | G | 10 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(7): Show |
10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1637+1534A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406390 | |||||||
| chr5:114406742 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1637+1886T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406742 | |||||||
| chr5:114406860 | AAG | A | 6 | a0002c0002t0001g0238 a0002c0002t0001g0240 a0002c0011t0001g0239 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+2010_1637+201 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114406860 | ||||||
| chr5:114406868 | T | G | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+2012T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406868 | |||||||
| chr5:114406888 | T | A | 12 | a0001c0001t0001g0248 a0002c0002t0001g0004 a0003c0003t0001g0193 others(9): Show |
12 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.1637+2032T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114406888 | |||||||
| chr5:114407056 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+2200G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407056 | |||||||
| chr5:114407075 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+2219T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407075 | |||||||
| chr5:114407083 | C | CACAAGGA others(26): Show |
1 | a0002c0002t0001g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1637+2239_1637+227 others(37): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114407083 | ||||||
| chr5:114407127 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1637+2271A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407127 | |||||||
| chr5:114407172 | G | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(57): Show |
61 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1637+2316G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407172 | |||||||
| chr5:114407434 | T | A | 1 | a0002c0002t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1637+2578T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407434 | |||||||
| chr5:114407757 | A | G | 14 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0002c0002t0001g0008 others(11): Show |
14 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1637+2901A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407757 | |||||||
| chr5:114407766 | C | G | 1 | a0003c0003t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1637+2910C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407766 | |||||||
| chr5:114407787 | A | G | 3 | a0002c0002t0001g0163 a0002c0002t0001g0175 a0002c0017t0001g0178 |
3 | HG00438.hp2 NA18999.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1637+2931A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407787 | |||||||
| chr5:114407931 | C | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(68): Show |
72 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.1637+3075C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407931 | |||||||
| chr5:114407932 | G | A | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+3076G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407932 | |||||||
| chr5:114407956 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(55): Show |
59 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.1637+3100A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114407956 | |||||||
| chr5:114408016 | C | G | 1 | a0006c0007t0001g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1637+3160C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408016 | |||||||
| chr5:114408180 | A | C | 6 | a0002c0002t0001g0238 a0002c0002t0001g0240 a0002c0011t0001g0239 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+3324A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408180 | |||||||
| chr5:114408201 | C | CT | 29 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(26): Show |
29 | HG00099.hp1 HG00280.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1637+3360dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114408201 | ||||||
| chr5:114408311 | G | T | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+3455G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408311 | |||||||
| chr5:114408410 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1637+3554G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408410 | |||||||
| chr5:114408639 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+3783A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408639 | |||||||
| chr5:114408758 | A | C | 39 | a0001c0001t0001g0066 a0001c0001t0001g0083 a0001c0001t0001g0084 others(36): Show |
39 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1637+3902A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408758 | |||||||
| chr5:114408762 | C | T | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+3906C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408762 | |||||||
| chr5:114408851 | C | T | 3 | a0002c0002t0001g0240 a0002c0011t0001g0239 a0002c0011t0001g0241 |
3 | HG01243.hp1 HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1637+3995C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408851 | |||||||
| chr5:114408899 | A | G | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+4043A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114408899 | |||||||
| chr5:114409009 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(45): Show |
49 | HG00741.hp1 HG01070.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.1637+4153C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409009 | |||||||
| chr5:114409084 | A | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0031 |
2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1637+4228A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409084 | |||||||
| chr5:114409174 | C | T | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+4318C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409174 | |||||||
| chr5:114409178 | C | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+4322C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409178 | |||||||
| chr5:114409332 | T | TA | 72 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(69): Show |
73 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1637+4485dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114409332 | ||||||
| chr5:114409715 | T | TAGGAGCA others(3): Show |
2 | a0001c0006t0001g0093 a0001c0006t0001g0095 |
2 | HG02055.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1637+4868_1637+486 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114409715 | ||||||
| chr5:114409771 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1637+4915G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409771 | |||||||
| chr5:114409832 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(71): Show |
75 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.1637+4976T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409832 | |||||||
| chr5:114409867 | T | TTCTC | 2 | a0007c0010t0001g0191 a0007c0010t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1637+5029_1637+503 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114409867 | ||||||
| chr5:114409995 | T | C | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1637+5139T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114409995 | |||||||
| chr5:114410041 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(122): Show |
126 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.1637+5185T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410041 | |||||||
| chr5:114410052 | C | G | 1 | a0009c0022t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1637+5196C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410052 | |||||||
| chr5:114410115 | G | C | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+5259G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410115 | |||||||
| chr5:114410140 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(143): Show |
147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1637+5284C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410140 | |||||||
| chr5:114410219 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1637+5363G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410219 | |||||||
| chr5:114410281 | G | A | 1 | a0005c0004t0001g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1637+5425G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410281 | |||||||
| chr5:114410287 | A | G | 3 | a0002c0002t0001g0153 a0002c0002t0001g0161 a0002c0002t0001g0183 |
3 | NA19001.hp1 NA19001.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1637+5431A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410287 | |||||||
| chr5:114410429 | G | A | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+5573G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410429 | |||||||
| chr5:114410483 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(135): Show |
139 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.1637+5627A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410483 | |||||||
| chr5:114410632 | T | A | 10 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0040 others(7): Show |
10 | HG01978.hp2 HG02080.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.1637+5776T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410632 | |||||||
| chr5:114410894 | A | G | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+6038A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410894 | |||||||
| chr5:114410944 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1637+6088C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114410944 | |||||||
| chr5:114411011 | G | A | 5 | a0001c0021t0001g0220 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+6155G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411011 | |||||||
| chr5:114411251 | T | G | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(10): Show |
13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1637+6395T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411251 | |||||||
| chr5:114411449 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(145): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+6593T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411449 | |||||||
| chr5:114411544 | C | T | 5 | a0001c0021t0001g0220 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+6688C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411544 | |||||||
| chr5:114411545 | C | A | 5 | a0001c0021t0001g0220 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+6689C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411545 | |||||||
| chr5:114411572 | G | C | 13 | a0001c0021t0001g0220 a0002c0002t0001g0008 a0002c0002t0001g0009 others(10): Show |
13 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1637+6716G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411572 | |||||||
| chr5:114411576 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1637+6720A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411576 | |||||||
| chr5:114411671 | A | AG | 8 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0001g0064 others(5): Show |
8 | HG01081.hp1 HG01081.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1637+6820dupG | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114411671 | ||||||
| chr5:114411954 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(145): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+7098T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114411954 | |||||||
| chr5:114412391 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1637+7535A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412391 | |||||||
| chr5:114412438 | A | ATAGAGT | 148 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(145): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+7583_1637+758 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114412438 | ||||||
| chr5:114412523 | A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+7667A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412523 | |||||||
| chr5:114412685 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1637+7829G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412685 | |||||||
| chr5:114412817 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0045 |
2 | HG01943.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1637+7961A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412817 | |||||||
| chr5:114412874 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(129): Show |
133 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1637+8018C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412874 | |||||||
| chr5:114412918 | A | G | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1637+8062A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114412918 | |||||||
| chr5:114413262 | C | CTTGTTTT others(3): Show |
1 | a0002c0002t0001g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1637+8419_1637+842 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114413262 | ||||||
| chr5:114413311 | T | A | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1637+8455T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413311 | |||||||
| chr5:114413346 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(145): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+8490A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413346 | |||||||
| chr5:114413348 | AAT | A | 8 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+8493_1637+849 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413348 | |||||||
| chr5:114413505 | C | G | 6 | a0002c0002t0001g0117 a0002c0002t0001g0152 a0002c0002t0001g0159 others(3): Show |
6 | HG00741.hp2 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+8649C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413505 | |||||||
| chr5:114413641 | T | A | 1 | a0001c0001t0001g0032 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1637+8785T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413641 | |||||||
| chr5:114413733 | A | C | 1 | a0002c0002t0001g0129 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1637+8877A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413733 | |||||||
| chr5:114413763 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(68): Show |
72 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.1637+8907A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413763 | |||||||
| chr5:114413842 | C | A | 1 | a0001c0001t0001g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1637+8986C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413842 | |||||||
| chr5:114413891 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(145): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+9035C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114413891 | |||||||
| chr5:114414042 | T | C | 58 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(55): Show |
58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1637+9186T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414042 | |||||||
| chr5:114414249 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(136): Show |
140 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.1637+9393T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414249 | |||||||
| chr5:114414367 | G | C | 2 | a0002c0002t0001g0155 a0002c0002t0001g0164 |
2 | HG00558.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1637+9511G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414367 | |||||||
| chr5:114414469 | T | C | 2 | a0007c0010t0001g0191 a0007c0010t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1637+9613T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414469 | |||||||
| chr5:114414512 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1637+9656C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414512 | |||||||
| chr5:114414513 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1637+9657G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414513 | |||||||
| chr5:114414748 | T | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(69): Show |
73 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1637+9892T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114414748 | |||||||
| chr5:114415128 | A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+10272A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415128 | |||||||
| chr5:114415328 | C | G | 1 | a0002c0002t0001g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1637+10472C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415328 | |||||||
| chr5:114415424 | C | CGT | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG02886.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1637+10579_1637+10 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114415424 | ||||||
| chr5:114415710 | A | C | 17 | a0001c0001t0001g0082 a0001c0001t0001g0212 a0001c0021t0001g0220 others(14): Show |
17 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1637+10854A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415710 | |||||||
| chr5:114415719 | T | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | NA19088.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1637+10863T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415719 | |||||||
| chr5:114415895 | T | C | 2 | a0007c0010t0001g0191 a0007c0010t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1637+11039T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114415895 | |||||||
| chr5:114416190 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1637+11334A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416190 | |||||||
| chr5:114416395 | C | T | 1 | a0002c0002t0001g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1637+11539C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416395 | |||||||
| chr5:114416420 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(145): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1637+11564T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416420 | |||||||
| chr5:114416663 | G | A | 1 | a0003c0003t0001g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1637+11807G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416663 | |||||||
| chr5:114416827 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1637+11971A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114416827 | |||||||
| chr5:114417226 | C | T | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+12370C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417226 | |||||||
| chr5:114417303 | T | G | 7 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(4): Show |
7 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+12447T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417303 | |||||||
| chr5:114417357 | G | A | 1 | a0006c0007t0001g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1637+12501G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417357 | |||||||
| chr5:114417397 | A | G | 1 | a0001c0015t0001g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1637+12541A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417397 | |||||||
| chr5:114417424 | G | C | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+12568G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417424 | |||||||
| chr5:114417674 | A | T | 15 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(12): Show |
15 | HG00099.hp1 HG00280.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1637+12818A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417674 | |||||||
| chr5:114417740 | T | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+12884T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114417740 | |||||||
| chr5:114418027 | A | G | 3 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0088 |
3 | HG01346.hp2 HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1637+13171A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418027 | |||||||
| chr5:114418107 | G | A | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+13251G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418107 | |||||||
| chr5:114418260 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1637+13404T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418260 | |||||||
| chr5:114418557 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1637+13701T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418557 | |||||||
| chr5:114418749 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1637+13893G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418749 | |||||||
| chr5:114418772 | A | G | 1 | a0002c0002t0001g0175 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1637+13916A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418772 | |||||||
| chr5:114418775 | T | G | 11 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(8): Show |
11 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1637+13919T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114418775 | |||||||
| chr5:114419007 | C | T | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+14151C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114419007 | |||||||
| chr5:114419044 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(58): Show |
62 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.1637+14188G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114419044 | |||||||
| chr5:114419934 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1637+15078G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114419934 | |||||||
| chr5:114419940 | A | G | 1 | a0002c0002t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1637+15084A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114419940 | |||||||
| chr5:114420100 | T | C | 60 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0083 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1637+15244T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420100 | |||||||
| chr5:114420167 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1637+15311C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420167 | |||||||
| chr5:114420236 | C | T | 6 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0006c0007t0001g0104 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+15380C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420236 | |||||||
| chr5:114420262 | T | C | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1637+15406T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420262 | |||||||
| chr5:114420270 | C | G | 4 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0014t0001g0017 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+15414C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420270 | |||||||
| chr5:114420585 | G | A | 9 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1637+15729G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420585 | |||||||
| chr5:114420611 | G | C | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1637+15755G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420611 | |||||||
| chr5:114420740 | T | C | 1 | a0002c0002t0001g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1637+15884T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420740 | |||||||
| chr5:114420824 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1637+15968A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420824 | |||||||
| chr5:114420919 | T | TAAAAATA others(315): Show |
1 | a0002c0002t0001g0123 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1637+16079_1637+16 others(328): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114420919 | ||||||
| chr5:114420927 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1637+16071A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420927 | |||||||
| chr5:114420977 | C | T | 8 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+16121C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114420977 | |||||||
| chr5:114421101 | A | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+16245A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421101 | |||||||
| chr5:114421108 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(69): Show |
73 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1637+16252G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421108 | |||||||
| chr5:114421119 | G | T | 35 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0083 others(32): Show |
35 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1637+16263G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421119 | |||||||
| chr5:114421165 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1637+16309T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421165 | |||||||
| chr5:114421169 | A | G | 4 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0014t0001g0017 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+16313A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421169 | |||||||
| chr5:114421226 | C | CA | 111 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(108): Show |
112 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.1637+16380dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114421226 | ||||||
| chr5:114421226 | C | CAA | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+16379_1637+16 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114421226 | ||||||
| chr5:114421254 | G | T | 3 | a0002c0002t0001g0165 a0002c0002t0001g0166 a0002c0002t0001g0167 |
3 | HG01167.hp1 HG02040.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1637+16398G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421254 | |||||||
| chr5:114421287 | A | T | 44 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(41): Show |
44 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1637+16431A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421287 | |||||||
| chr5:114421342 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(88): Show |
92 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.1637+16486G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421342 | |||||||
| chr5:114421426 | G | A | 4 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0014t0001g0017 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+16570G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421426 | |||||||
| chr5:114421666 | A | G | 27 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(24): Show |
27 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1637+16810A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421666 | |||||||
| chr5:114421750 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01081.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1637+16894C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421750 | |||||||
| chr5:114421784 | A | G | 6 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0006c0007t0001g0104 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+16928A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114421784 | |||||||
| chr5:114422258 | G | A | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1637+17402G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422258 | |||||||
| chr5:114422268 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(137): Show |
141 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(138): Show |
intron_variant | MODIFIER | c.1637+17412A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422268 | |||||||
| chr5:114422298 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1637+17442C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422298 | |||||||
| chr5:114422366 | C | A | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1637+17510C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422366 | |||||||
| chr5:114422410 | A | G | 12 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(9): Show |
12 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1637+17554A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422410 | |||||||
| chr5:114422476 | G | A | 3 | a0002c0002t0001g0238 a0002c0014t0001g0017 a0008c0013t0001g0237 |
3 | HG02572.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1637+17620G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422476 | |||||||
| chr5:114422476 | G | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(141): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1637+17620G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422476 | |||||||
| chr5:114422623 | G | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+17767G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422623 | |||||||
| chr5:114422701 | C | A | 8 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
8 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+17845C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422701 | |||||||
| chr5:114422793 | A | C | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+17937A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422793 | |||||||
| chr5:114422915 | G | A | 4 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0014t0001g0017 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+18059G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114422915 | |||||||
| chr5:114423009 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1637+18153C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423009 | |||||||
| chr5:114423018 | A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+18162A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423018 | |||||||
| chr5:114423028 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(55): Show |
59 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.1637+18172A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423028 | |||||||
| chr5:114423100 | T | C | 3 | a0002c0002t0001g0165 a0002c0002t0001g0166 a0002c0002t0001g0167 |
3 | HG01167.hp1 HG02040.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1637+18244T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423100 | |||||||
| chr5:114423205 | A | T | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+18349A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423205 | |||||||
| chr5:114423275 | G | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(68): Show |
72 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.1637+18419G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423275 | |||||||
| chr5:114423288 | G | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(135): Show |
139 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.1637+18432G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423288 | |||||||
| chr5:114423317 | A | G | 12 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(9): Show |
12 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1637+18461A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423317 | |||||||
| chr5:114423333 | C | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01981.hp1 HG02148.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+18477C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423333 | |||||||
| chr5:114423343 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1637+18487C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423343 | |||||||
| chr5:114423380 | A | G | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+18524A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423380 | |||||||
| chr5:114423400 | G | A | 4 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0014t0001g0017 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+18544G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423400 | |||||||
| chr5:114423618 | G | A | 11 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(8): Show |
11 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1637+18762G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423618 | |||||||
| chr5:114423619 | C | T | 11 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(8): Show |
11 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1637+18763C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423619 | |||||||
| chr5:114423738 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(135): Show |
139 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.1637+18882G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423738 | |||||||
| chr5:114423932 | C | A | 1 | a0002c0002t0001g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1637+19076C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423932 | |||||||
| chr5:114423978 | T | C | 9 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0004c0008t0001g0010 others(6): Show |
9 | HG02622.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1637+19122T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114423978 | |||||||
| chr5:114424003 | A | C | 1 | a0002c0002t0001g0171 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1637+19147A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114424003 | |||||||
| chr5:114424006 | C | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(79): Show |
83 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(80): Show |
intron_variant | MODIFIER | c.1637+19150C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114424006 | |||||||
| chr5:114424223 | T | A | 6 | a0001c0001t0001g0082 a0001c0021t0001g0220 a0006c0007t0001g0104 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+19367T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114424223 | |||||||
| chr5:114425005 | G | A | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+20149G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425005 | |||||||
| chr5:114425200 | T | G | 20 | a0001c0021t0001g0220 a0002c0002t0001g0008 a0002c0002t0001g0009 others(17): Show |
20 | HG00099.hp1 HG00280.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1637+20344T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425200 | |||||||
| chr5:114425303 | T | C | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+20447T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425303 | |||||||
| chr5:114425310 | C | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+20454C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425310 | |||||||
| chr5:114425337 | T | C | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637+20481T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425337 | |||||||
| chr5:114425581 | C | T | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+20725C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425581 | |||||||
| chr5:114425674 | T | C | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+20818T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425674 | |||||||
| chr5:114425974 | G | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+21118G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114425974 | |||||||
| chr5:114426011 | C | T | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+21155C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426011 | |||||||
| chr5:114426017 | C | CA | 13 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1637+21176dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114426017 | ||||||
| chr5:114426017 | CA | C | 18 | a0001c0001t0001g0068 a0001c0001t0001g0090 a0001c0001t0001g0230 others(15): Show |
18 | HG00738.hp2 HG01109.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.1637+21176delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114426017 | ||||||
| chr5:114426160 | C | CA | 12 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(9): Show |
12 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1637+21314dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114426160 | ||||||
| chr5:114426171 | T | A | 5 | a0001c0021t0001g0220 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+21315T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426171 | |||||||
| chr5:114426223 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1637+21367A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426223 | |||||||
| chr5:114426372 | C | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0227 a0001c0001t0001g0229 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1637+21516C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426372 | |||||||
| chr5:114426426 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1637+21570C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426426 | |||||||
| chr5:114426943 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1637+22087C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114426943 | |||||||
| chr5:114427113 | A | G | 101 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(98): Show |
101 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1637+22257A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427113 | |||||||
| chr5:114427159 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1637+22303T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427159 | |||||||
| chr5:114427381 | G | A | 1 | a0002c0002t0001g0124 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1637+22525G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427381 | |||||||
| chr5:114427481 | C | T | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1637+22625C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427481 | |||||||
| chr5:114427541 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0031 |
2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1637+22685G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114427541 | |||||||
| chr5:114428077 | AT | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG01074.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1637+23224delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114428077 | ||||||
| chr5:114428087 | A | T | 1 | a0001c0001t0001g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1637+23231A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428087 | |||||||
| chr5:114428091 | C | T | 8 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
8 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+23235C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428091 | |||||||
| chr5:114428167 | C | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1637+23311C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428167 | |||||||
| chr5:114428208 | A | G | 5 | a0001c0021t0001g0220 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+23352A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428208 | |||||||
| chr5:114428411 | C | T | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+23555C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428411 | |||||||
| chr5:114428445 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+23589T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428445 | |||||||
| chr5:114428749 | C | T | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+23893C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428749 | |||||||
| chr5:114428958 | C | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1637+24102C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114428958 | |||||||
| chr5:114429263 | C | A | 2 | a0005c0004t0001g0147 a0005c0004t0001g0149 |
2 | HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1637+24407C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429263 | |||||||
| chr5:114429285 | A | G | 110 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0001g0067 others(107): Show |
110 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1637+24429A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429285 | |||||||
| chr5:114429354 | T | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(30): Show |
34 | HG01099.hp1 HG01175.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.1637+24498T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429354 | |||||||
| chr5:114429634 | G | A | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(10): Show |
13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1637+24778G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429634 | |||||||
| chr5:114429818 | C | CT | 80 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(77): Show |
80 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1637+24985dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114429818 | ||||||
| chr5:114429818 | C | CTT | 16 | a0001c0001t0001g0065 a0001c0001t0001g0070 a0001c0001t0001g0089 others(13): Show |
16 | HG00099.hp2 HG00642.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1637+24984_1637+24 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114429818 | ||||||
| chr5:114429818 | CT | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(75): Show |
79 | HG00741.hp1 HG01070.hp2 HG01074.hp1 others(76): Show |
intron_variant | MODIFIER | c.1637+24985delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114429818 | ||||||
| chr5:114429818 | CTT | C | 14 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0055 others(11): Show |
14 | HG01433.hp2 HG01993.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1637+24984_1637+24 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114429818 | ||||||
| chr5:114429990 | TA | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0227 a0001c0001t0001g0229 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1637+25135delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114429990 | |||||||
| chr5:114430067 | C | G | 1 | a0010c0023t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1637+25211C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114430067 | |||||||
| chr5:114430849 | T | A | 101 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(98): Show |
101 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1637+25993T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114430849 | |||||||
| chr5:114431129 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1637+26273C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431129 | |||||||
| chr5:114431130 | G | A | 8 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0102 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+26274G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431130 | |||||||
| chr5:114431162 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1637+26306T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431162 | |||||||
| chr5:114431293 | T | A | 3 | a0004c0008t0001g0010 a0004c0008t0001g0011 a0004c0008t0001g0012 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1637+26437T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431293 | |||||||
| chr5:114431383 | T | A | 1 | a0002c0002t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1637+26527T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431383 | |||||||
| chr5:114431402 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1637+26546A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431402 | |||||||
| chr5:114431638 | CT | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(57): Show |
61 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1637+26783delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431638 | |||||||
| chr5:114431886 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+27030T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114431886 | |||||||
| chr5:114432152 | T | C | 2 | a0005c0004t0001g0147 a0005c0004t0001g0149 |
2 | HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1637+27296T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432152 | |||||||
| chr5:114432295 | A | G | 6 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0005t0001g0013 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+27439A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432295 | |||||||
| chr5:114432391 | C | T | 3 | a0002c0002t0001g0145 a0002c0002t0001g0155 a0002c0002t0001g0164 |
3 | HG00558.hp1 HG02523.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1637+27535C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432391 | |||||||
| chr5:114432395 | T | C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | NA18964.hp2 NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1637+27539T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432395 | |||||||
| chr5:114432429 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1637+27573C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432429 | |||||||
| chr5:114432433 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1637+27577G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432433 | |||||||
| chr5:114432469 | T | TA | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+27616dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114432469 | ||||||
| chr5:114432514 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1637+27658G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432514 | |||||||
| chr5:114432550 | C | T | 100 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(97): Show |
100 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1637+27694C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432550 | |||||||
| chr5:114432678 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(202): Show |
206 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.1637+27822A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432678 | |||||||
| chr5:114432714 | C | T | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+27858C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432714 | |||||||
| chr5:114432741 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+27885G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432741 | |||||||
| chr5:114432765 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+27909G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432765 | |||||||
| chr5:114432767 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1637+27911G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432767 | |||||||
| chr5:114432849 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1637+27993G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432849 | |||||||
| chr5:114432916 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1637+28060C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432916 | |||||||
| chr5:114432922 | G | A | 7 | a0002c0002t0001g0236 a0002c0002t0001g0238 a0002c0002t0001g0240 others(4): Show |
7 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+28066G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432922 | |||||||
| chr5:114432963 | A | T | 101 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(98): Show |
101 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1637+28107A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114432963 | |||||||
| chr5:114433353 | C | G | 1 | a0002c0002t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1637+28497C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433353 | |||||||
| chr5:114433559 | G | T | 1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1637+28703G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433559 | |||||||
| chr5:114433714 | T | C | 1 | a0002c0002t0001g0072 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1637+28858T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433714 | |||||||
| chr5:114433728 | A | G | 13 | a0001c0021t0001g0220 a0002c0002t0001g0008 a0002c0002t0001g0009 others(10): Show |
13 | HG01243.hp2 HG02451.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1637+28872A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433728 | |||||||
| chr5:114433780 | C | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1637+28924C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433780 | |||||||
| chr5:114433796 | C | T | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+28940C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433796 | |||||||
| chr5:114433809 | C | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1637+28953C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433809 | |||||||
| chr5:114433877 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(43): Show |
47 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.1637+29021G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433877 | |||||||
| chr5:114433884 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1637+29028C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433884 | |||||||
| chr5:114433997 | A | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1638-29052A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114433997 | |||||||
| chr5:114434119 | T | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(44): Show |
48 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.1638-28930T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434119 | |||||||
| chr5:114434138 | G | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(57): Show |
61 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1638-28911G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434138 | |||||||
| chr5:114434180 | A | AT | 117 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0001g0067 others(114): Show |
117 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1638-28861dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114434180 | ||||||
| chr5:114434230 | A | AT | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0054 others(10): Show |
13 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1638-28810dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114434230 | ||||||
| chr5:114434255 | G | C | 101 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(98): Show |
101 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1638-28794G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434255 | |||||||
| chr5:114434346 | A | G | 9 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1638-28703A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434346 | |||||||
| chr5:114434367 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1638-28682A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434367 | |||||||
| chr5:114434453 | A | G | 8 | a0001c0021t0001g0220 a0004c0008t0001g0010 a0004c0008t0001g0011 others(5): Show |
8 | HG02622.hp1 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-28596A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434453 | |||||||
| chr5:114434575 | A | G | 2 | a0001c0001t0001g0247 a0002c0002t0001g0236 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1638-28474A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434575 | |||||||
| chr5:114434585 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1638-28464G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434585 | |||||||
| chr5:114434877 | A | T | 2 | a0002c0002t0001g0119 a0002c0002t0001g0132 |
2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-28172A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434877 | |||||||
| chr5:114434965 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0031 |
2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1638-28084G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114434965 | |||||||
| chr5:114435177 | C | G | 5 | a0002c0002t0001g0007 a0002c0002t0001g0187 a0002c0002t0001g0188 others(2): Show |
5 | NA18946.hp2 NA18962.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-27872C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435177 | |||||||
| chr5:114435431 | G | A | 5 | a0002c0002t0001g0007 a0002c0002t0001g0187 a0002c0002t0001g0188 others(2): Show |
5 | NA18946.hp2 NA18962.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-27618G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435431 | |||||||
| chr5:114435510 | G | T | 1 | a0005c0004t0001g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1638-27539G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435510 | |||||||
| chr5:114435562 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1638-27487C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435562 | |||||||
| chr5:114435641 | A | G | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0066 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1638-27408A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435641 | |||||||
| chr5:114435726 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1638-27323A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435726 | |||||||
| chr5:114435780 | G | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1638-27269G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435780 | |||||||
| chr5:114435837 | A | G | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1638-27212A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114435837 | |||||||
| chr5:114436081 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1638-26968T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436081 | |||||||
| chr5:114436114 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(205): Show |
209 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1638-26935A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436114 | |||||||
| chr5:114436147 | A | G | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-26902A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436147 | |||||||
| chr5:114436342 | G | T | 3 | a0002c0002t0001g0240 a0002c0011t0001g0239 a0002c0011t0001g0241 |
3 | HG01243.hp1 HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1638-26707G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436342 | |||||||
| chr5:114436413 | C | T | 2 | a0002c0002t0001g0119 a0002c0002t0001g0132 |
2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-26636C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436413 | |||||||
| chr5:114436584 | C | T | 1 | a0002c0002t0001g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1638-26465C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436584 | |||||||
| chr5:114436606 | C | T | 2 | a0002c0002t0001g0119 a0002c0002t0001g0132 |
2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-26443C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436606 | |||||||
| chr5:114436635 | A | G | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1638-26414A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436635 | |||||||
| chr5:114436774 | A | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-26275A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436774 | |||||||
| chr5:114436799 | A | G | 2 | a0002c0002t0001g0119 a0002c0002t0001g0132 |
2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-26250A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114436799 | |||||||
| chr5:114437005 | G | T | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1638-26044G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437005 | |||||||
| chr5:114437076 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1638-25973T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437076 | |||||||
| chr5:114437440 | A | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-25609A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437440 | |||||||
| chr5:114437769 | A | G | 1 | a0002c0002t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1638-25280A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437769 | |||||||
| chr5:114437931 | G | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(9): Show |
12 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-25118G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114437931 | |||||||
| chr5:114438096 | C | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(9): Show |
12 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-24953C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438096 | |||||||
| chr5:114438216 | G | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(9): Show |
12 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-24833G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438216 | |||||||
| chr5:114438435 | AAT | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02280.hp1 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1638-24609_1638-24 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114438435 | ||||||
| chr5:114438480 | A | C | 12 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(9): Show |
12 | HG01081.hp1 HG01099.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-24569A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438480 | |||||||
| chr5:114438819 | C | T | 15 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(12): Show |
15 | HG01081.hp1 HG01099.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1638-24230C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438819 | |||||||
| chr5:114438823 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0096 |
2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1638-24226C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438823 | |||||||
| chr5:114438936 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1638-24113G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114438936 | |||||||
| chr5:114439043 | T | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1638-24006T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439043 | |||||||
| chr5:114439075 | A | T | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0066 others(10): Show |
13 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1638-23974A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439075 | |||||||
| chr5:114439109 | C | T | 10 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0230 others(7): Show |
10 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1638-23940C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439109 | |||||||
| chr5:114439117 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1638-23932G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439117 | |||||||
| chr5:114439220 | A | C | 1 | a0002c0002t0001g0173 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1638-23829A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439220 | |||||||
| chr5:114439372 | C | CA | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0066 others(10): Show |
13 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1638-23676dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114439372 | ||||||
| chr5:114439455 | T | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-23594T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439455 | |||||||
| chr5:114439516 | A | T | 1 | a0002c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1638-23533A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439516 | |||||||
| chr5:114439633 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1638-23416G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439633 | |||||||
| chr5:114439762 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1638-23287A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439762 | |||||||
| chr5:114439812 | G | C | 2 | a0002c0002t0001g0119 a0002c0002t0001g0132 |
2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-23237G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439812 | |||||||
| chr5:114439918 | A | G | 2 | a0003c0003t0001g0196 a0003c0009t0001g0195 |
2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1638-23131A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114439918 | |||||||
| chr5:114440113 | G | C | 2 | a0002c0002t0001g0119 a0002c0002t0001g0132 |
2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-22936G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440113 | |||||||
| chr5:114440173 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(50): Show |
54 | HG00438.hp2 HG00558.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1638-22876C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440173 | |||||||
| chr5:114440304 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG01257.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1638-22745A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440304 | |||||||
| chr5:114440316 | A | G | 11 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0230 others(8): Show |
11 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1638-22733A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440316 | |||||||
| chr5:114440612 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1638-22437T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440612 | |||||||
| chr5:114440617 | CAGGTGTG others(11): Show |
C | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1638-22429_1638-22 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114440617 | ||||||
| chr5:114440834 | CAG | C | 119 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0033 others(116): Show |
119 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1638-22214_1638-22 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440834 | |||||||
| chr5:114440862 | C | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1638-22187C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440862 | |||||||
| chr5:114440871 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1638-22178A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440871 | |||||||
| chr5:114440895 | A | C | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-22154A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440895 | |||||||
| chr5:114440913 | CT | C | 128 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(125): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1638-22128delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114440913 | ||||||
| chr5:114440972 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1638-22077G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114440972 | |||||||
| chr5:114441405 | A | G | 1 | a0002c0002t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1638-21644A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114441405 | |||||||
| chr5:114441893 | G | T | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-21156G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114441893 | |||||||
| chr5:114442186 | C | T | 107 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0033 others(104): Show |
107 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1638-20863C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442186 | |||||||
| chr5:114442247 | C | CATAT | 10 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(7): Show |
10 | HG01169.hp1 HG02523.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1638-20792_1638-20 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114442247 | ||||||
| chr5:114442252 | A | G | 1 | a0002c0002t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1638-20797A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442252 | |||||||
| chr5:114442278 | G | GTA | 16 | a0001c0001t0001g0039 a0001c0001t0001g0108 a0001c0001t0001g0211 others(13): Show |
16 | HG00738.hp1 HG00738.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1638-20764_1638-20 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114442278 | ||||||
| chr5:114442287 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1638-20762G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442287 | |||||||
| chr5:114442289 | G | T | 20 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(17): Show |
20 | HG01169.hp1 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1638-20760G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442289 | |||||||
| chr5:114442366 | GTAGTGAT others(3): Show |
G | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-20682_1638-20 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442366 | |||||||
| chr5:114442378 | A | C | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-20671A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114442378 | |||||||
| chr5:114442974 | G | GT | 110 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(107): Show |
110 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.1638-20068dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114442974 | ||||||
| chr5:114443161 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0002g0038 a0002c0002t0001g0123 others(1): Show |
4 | HG00741.hp1 HG01070.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-19888C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443161 | |||||||
| chr5:114443162 | G | A | 1 | a0009c0022t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1638-19887G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443162 | |||||||
| chr5:114443461 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1638-19588T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443461 | |||||||
| chr5:114443504 | T | C | 5 | a0002c0002t0001g0117 a0002c0002t0001g0152 a0002c0002t0001g0159 others(2): Show |
5 | HG01261.hp2 HG01433.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-19545T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443504 | |||||||
| chr5:114443504 | TGCCTTGC others(24): Show |
T | 1 | a0004c0008t0001g0011 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1638-19543_1638-19 others(37): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114443504 | ||||||
| chr5:114443615 | T | C | 17 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(14): Show |
17 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1638-19434T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443615 | |||||||
| chr5:114443724 | G | A | 98 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0027 others(95): Show |
98 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1638-19325G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443724 | |||||||
| chr5:114443829 | G | T | 1 | a0002c0002t0001g0111 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1638-19220G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443829 | |||||||
| chr5:114443856 | C | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1638-19193C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443856 | |||||||
| chr5:114443919 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1638-19130T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114443919 | |||||||
| chr5:114444083 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1638-18966G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444083 | |||||||
| chr5:114444348 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1638-18701G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444348 | |||||||
| chr5:114444392 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0089 |
2 | HG01099.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1638-18657A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444392 | |||||||
| chr5:114444396 | G | GA | 33 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0057 others(30): Show |
33 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1638-18645dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114444396 | ||||||
| chr5:114444490 | T | G | 99 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(96): Show |
99 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.1638-18559T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444490 | |||||||
| chr5:114444781 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0109 |
3 | HG00642.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1638-18268A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444781 | |||||||
| chr5:114444820 | T | C | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-18229T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114444820 | |||||||
| chr5:114445037 | G | T | 1 | a0006c0007t0001g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1638-18012G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445037 | |||||||
| chr5:114445189 | T | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | HG00280.hp2 HG01358.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-17860T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445189 | |||||||
| chr5:114445190 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | HG00280.hp2 HG01358.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-17859T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445190 | |||||||
| chr5:114445298 | C | T | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-17751C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445298 | |||||||
| chr5:114445312 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1638-17737G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114445312 | |||||||
| chr5:114445423 | T | TA | 6 | a0001c0001t0001g0042 a0002c0002t0001g0007 a0002c0002t0001g0187 others(3): Show |
6 | NA18942.hp2 NA18946.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-17625dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114445423 | ||||||
| chr5:114446124 | C | G | 11 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(8): Show |
11 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1638-16925C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446124 | |||||||
| chr5:114446406 | C | G | 1 | a0003c0003t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1638-16643C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446406 | |||||||
| chr5:114446700 | A | T | 12 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0087 others(9): Show |
12 | HG01169.hp1 HG01175.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1638-16349A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446700 | |||||||
| chr5:114446835 | G | A | 8 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(5): Show |
8 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-16214G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446835 | |||||||
| chr5:114446976 | A | T | 1 | a0003c0003t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1638-16073A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114446976 | |||||||
| chr5:114447076 | G | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.1638-15973G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114447076 | |||||||
| chr5:114447182 | T | C | 1 | a0002c0002t0001g0072 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1638-15867T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114447182 | |||||||
| chr5:114447229 | T | C | 5 | a0002c0005t0001g0013 a0002c0005t0001g0014 a0002c0005t0001g0015 others(2): Show |
5 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-15820T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114447229 | |||||||
| chr5:114448271 | A | G | 1 | a0002c0002t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1638-14778A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448271 | |||||||
| chr5:114448292 | T | C | 32 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0057 others(29): Show |
32 | HG00280.hp1 HG01081.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1638-14757T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448292 | |||||||
| chr5:114448399 | C | A | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-14650C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448399 | |||||||
| chr5:114448400 | A | G | 1 | a0002c0002t0001g0175 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1638-14649A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448400 | |||||||
| chr5:114448412 | CTG | C | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-14633_1638-14 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114448412 | ||||||
| chr5:114448525 | G | A | 5 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0227 others(2): Show |
5 | HG00280.hp2 HG02572.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-14524G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448525 | |||||||
| chr5:114448551 | C | G | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-14498C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114448551 | |||||||
| chr5:114449061 | A | C | 1 | a0002c0002t0001g0009 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1638-13988A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449061 | |||||||
| chr5:114449180 | T | C | 24 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0074 others(21): Show |
24 | HG01081.hp1 HG02055.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1638-13869T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449180 | |||||||
| chr5:114449279 | C | T | 8 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(5): Show |
8 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-13770C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449279 | |||||||
| chr5:114449422 | A | T | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-13627A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449422 | |||||||
| chr5:114449568 | C | T | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1638-13481C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449568 | |||||||
| chr5:114449825 | C | T | 1 | a0002c0002t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1638-13224C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449825 | |||||||
| chr5:114449869 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1638-13180C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449869 | |||||||
| chr5:114449879 | T | TAC | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0235 |
3 | HG00280.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1638-13141_1638-13 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | ||||||
| chr5:114449879 | T | TACAC | 9 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0227 others(6): Show |
9 | HG00280.hp2 HG01081.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1638-13143_1638-13 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | ||||||
| chr5:114449879 | T | TACACAC | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0230 others(1): Show |
4 | HG01081.hp1 HG01515.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-13145_1638-13 others(12): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | ||||||
| chr5:114449879 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0094 others(1): Show |
4 | HG02559.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-13147_1638-13 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | ||||||
| chr5:114449879 | T | TACACACA others(3): Show |
7 | a0001c0001t0001g0092 a0001c0001t0001g0100 a0001c0006t0001g0093 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1638-13149_1638-13 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | ||||||
| chr5:114449879 | T | TACACACA others(5): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0002c0002t0001g0205 others(1): Show |
4 | HG02615.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-13151_1638-13 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | ||||||
| chr5:114449879 | TACAC | T | 18 | a0001c0001t0001g0057 a0001c0001t0001g0065 a0001c0001t0001g0067 others(15): Show |
18 | HG01099.hp2 HG01256.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1638-13143_1638-13 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449879 | ||||||
| chr5:114449898 | ACACACAC others(5): Show |
A | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1638-13149_1638-13 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449898 | ||||||
| chr5:114449900 | ACACACAC others(3): Show |
A | 99 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0027 others(96): Show |
99 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.1638-13147_1638-13 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449900 | ||||||
| chr5:114449902 | ACACACAC others(1): Show |
A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(42): Show |
46 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1638-13145_1638-13 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449902 | ||||||
| chr5:114449904 | A | G | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-13145A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449904 | |||||||
| chr5:114449904 | ACACACG | A | 3 | a0002c0002t0001g0145 a0002c0002t0001g0155 a0002c0002t0001g0164 |
3 | HG00558.hp1 HG02523.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1638-13143_1638-13 others(12): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449904 | ||||||
| chr5:114449906 | A | G | 5 | a0001c0021t0001g0220 a0002c0002t0001g0004 a0004c0008t0001g0010 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-13143A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449906 | |||||||
| chr5:114449908 | A | ACACACAC others(19): Show |
5 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0216 others(2): Show |
5 | HG01074.hp1 HG03225.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(32): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(21): Show |
2 | a0002c0011t0001g0239 a0002c0011t0001g0241 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(34): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(17): Show |
1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(19): Show |
1 | a0001c0001t0001g0215 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(32): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(13): Show |
1 | a0009c0022t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(15): Show |
1 | a0001c0001t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(28): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(17): Show |
3 | a0001c0001t0001g0211 a0002c0002t0001g0119 a0002c0002t0001g0132 |
3 | HG01169.hp1 HG02615.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(30): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(11): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 |
3 | HG03139.hp2 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(13): Show |
1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(26): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(11): Show |
1 | a0002c0002t0001g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(18): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(9): Show |
1 | a0002c0002t0001g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(22): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(3): Show |
3 | a0001c0001t0001g0248 a0007c0010t0001g0191 a0007c0010t0001g0192 |
3 | HG02895.hp1 HG02897.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(9): Show |
1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(22): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(11): Show |
1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1638-13140_1638-13 others(24): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | ACACACAC others(1): Show |
5 | a0003c0003t0001g0193 a0003c0003t0001g0197 a0003c0003t0001g0198 others(2): Show |
5 | HG02809.hp1 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-13140_1638-13 others(14): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114449908 | ||||||
| chr5:114449908 | A | G | 23 | a0001c0001t0001g0057 a0001c0001t0001g0065 a0001c0001t0001g0067 others(20): Show |
23 | HG01099.hp2 HG01256.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1638-13141A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449908 | |||||||
| chr5:114449910 | G | A | 5 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0227 others(2): Show |
5 | HG00280.hp2 HG02572.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-13139G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449910 | |||||||
| chr5:114449912 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0173 |
2 | HG01175.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1638-13137G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449912 | |||||||
| chr5:114449914 | G | A | 3 | a0001c0001t0001g0217 a0002c0002t0001g0005 a0002c0002t0001g0173 |
3 | HG01175.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1638-13135G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449914 | |||||||
| chr5:114449916 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0173 |
2 | HG01175.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1638-13133G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449916 | |||||||
| chr5:114449918 | T | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0173 |
2 | HG01175.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1638-13131T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449918 | |||||||
| chr5:114449920 | G | A | 3 | a0001c0001t0001g0227 a0002c0002t0001g0201 a0002c0002t0001g0206 |
3 | HG00280.hp2 HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1638-13129G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449920 | |||||||
| chr5:114449923 | T | C | 13 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 others(10): Show |
13 | HG01169.hp1 HG01175.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1638-13126T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449923 | |||||||
| chr5:114449925 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1638-13124C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449925 | |||||||
| chr5:114449927 | C | T | 1 | a0002c0002t0001g0181 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1638-13122C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449927 | |||||||
| chr5:114449976 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(45): Show |
49 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1638-13073G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449976 | |||||||
| chr5:114449989 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1638-13060A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449989 | |||||||
| chr5:114449996 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1638-13053C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114449996 | |||||||
| chr5:114450323 | T | G | 3 | a0004c0008t0001g0010 a0006c0007t0001g0222 a0006c0007t0001g0223 |
3 | HG06807.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1638-12726T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450323 | |||||||
| chr5:114450385 | G | A | 1 | a0002c0002t0001g0072 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1638-12664G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450385 | |||||||
| chr5:114450421 | T | A | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-12628T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450421 | |||||||
| chr5:114450572 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1638-12477T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450572 | |||||||
| chr5:114450714 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1638-12335G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450714 | |||||||
| chr5:114450718 | A | G | 17 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(14): Show |
17 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1638-12331A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450718 | |||||||
| chr5:114450791 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(45): Show |
49 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1638-12258C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450791 | |||||||
| chr5:114450806 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0010c0023t0001g0160 |
3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1638-12243G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450806 | |||||||
| chr5:114450819 | C | G | 1 | a0003c0003t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1638-12230C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114450819 | |||||||
| chr5:114451023 | C | T | 1 | a0002c0002t0001g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1638-12026C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451023 | |||||||
| chr5:114451040 | G | A | 11 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(8): Show |
11 | HG01074.hp1 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1638-12009G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451040 | |||||||
| chr5:114451049 | A | G | 1 | a0003c0003t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1638-12000A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451049 | |||||||
| chr5:114451315 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1638-11734T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451315 | |||||||
| chr5:114451358 | G | A | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-11691G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451358 | |||||||
| chr5:114451568 | T | C | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-11481T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451568 | |||||||
| chr5:114451598 | A | G | 2 | a0002c0002t0001g0238 a0002c0014t0001g0017 |
2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1638-11451A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451598 | |||||||
| chr5:114451624 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1638-11425C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451624 | |||||||
| chr5:114451634 | A | C | 21 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(18): Show |
21 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1638-11415A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451634 | |||||||
| chr5:114451635 | G | A | 1 | a0002c0002t0001g0007 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1638-11414G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451635 | |||||||
| chr5:114451663 | A | G | 26 | a0001c0001t0001g0035 a0001c0001t0001g0066 a0001c0001t0001g0069 others(23): Show |
26 | HG01169.hp1 HG02486.hp2 HG02723.hp1 others(23): Show |
intron_variant | MODIFIER | c.1638-11386A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451663 | |||||||
| chr5:114451671 | C | T | 1 | a0003c0009t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1638-11378C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451671 | |||||||
| chr5:114451692 | C | G | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1638-11357C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451692 | |||||||
| chr5:114451693 | A | G | 1 | a0002c0002t0001g0174 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1638-11356A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451693 | |||||||
| chr5:114451766 | G | A | 7 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG01074.hp1 HG02615.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1638-11283G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451766 | |||||||
| chr5:114451820 | C | A | 1 | a0002c0002t0001g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1638-11229C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451820 | |||||||
| chr5:114451854 | G | A | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1638-11195G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451854 | |||||||
| chr5:114451912 | A | G | 31 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0042 others(28): Show |
31 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1638-11137A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451912 | |||||||
| chr5:114451915 | A | G | 4 | a0006c0007t0001g0104 a0006c0007t0001g0221 a0006c0007t0001g0222 others(1): Show |
4 | HG02622.hp1 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-11134A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451915 | |||||||
| chr5:114451942 | G | T | 81 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(78): Show |
81 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1638-11107G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451942 | |||||||
| chr5:114451984 | T | C | 14 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(11): Show |
14 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1638-11065T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114451984 | |||||||
| chr5:114451994 | C | CT | 18 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(15): Show |
18 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1638-11052dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114451994 | ||||||
| chr5:114452104 | A | G | 4 | a0001c0001t0001g0231 a0002c0002t0001g0134 a0002c0002t0001g0173 others(1): Show |
4 | HG01175.hp1 HG01192.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-10945A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452104 | |||||||
| chr5:114452218 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1638-10831G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452218 | |||||||
| chr5:114452233 | G | A | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-10816G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452233 | |||||||
| chr5:114452405 | C | T | 1 | a0002c0002t0001g0006 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1638-10644C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452405 | |||||||
| chr5:114452454 | A | G | 3 | a0002c0002t0001g0114 a0002c0002t0001g0156 a0004c0012t0001g0142 |
3 | HG00738.hp2 HG01256.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1638-10595A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452454 | |||||||
| chr5:114452626 | T | G | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-10423T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452626 | |||||||
| chr5:114452689 | G | A | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1638-10360G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452689 | |||||||
| chr5:114452896 | G | A | 73 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(70): Show |
73 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1638-10153G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114452896 | |||||||
| chr5:114453034 | A | C | 1 | a0001c0001t0001g0031 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1638-10015A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453034 | |||||||
| chr5:114453047 | C | A | 2 | a0001c0001t0001g0108 a0002c0002t0001g0204 |
2 | HG00738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1638-10002C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453047 | |||||||
| chr5:114453058 | C | T | 54 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0033 others(51): Show |
54 | HG00099.hp2 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1638-9991C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453058 | |||||||
| chr5:114453252 | C | A | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1638-9797C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453252 | |||||||
| chr5:114453283 | T | G | 1 | a0002c0002t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1638-9766T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453283 | |||||||
| chr5:114453531 | T | A | 1 | a0002c0005t0001g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1638-9518T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453531 | |||||||
| chr5:114453916 | A | G | 1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1638-9133A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453916 | |||||||
| chr5:114453973 | G | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1638-9076G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114453973 | |||||||
| chr5:114454152 | C | G | 1 | a0001c0001t0001g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1638-8897C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114454152 | |||||||
| chr5:114454380 | A | G | 3 | a0002c0002t0001g0240 a0002c0011t0001g0239 a0002c0011t0001g0241 |
3 | HG01243.hp1 HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1638-8669A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114454380 | |||||||
| chr5:114454693 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1638-8356G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114454693 | |||||||
| chr5:114454699 | C | G | 1 | a0002c0002t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1638-8350C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114454699 | |||||||
| chr5:114455065 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1638-7984C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455065 | |||||||
| chr5:114455098 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1638-7951C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455098 | |||||||
| chr5:114455120 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1638-7929G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455120 | |||||||
| chr5:114455239 | G | A | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1638-7810G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455239 | |||||||
| chr5:114455348 | A | G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0057 others(14): Show |
17 | HG01099.hp2 HG01192.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1638-7701A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455348 | |||||||
| chr5:114455359 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1638-7690A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455359 | |||||||
| chr5:114455365 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1638-7684C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455365 | |||||||
| chr5:114455497 | C | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0002c0002t0001g0008 others(4): Show |
7 | HG00438.hp1 NA18986.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.1638-7552C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455497 | |||||||
| chr5:114455498 | G | A | 1 | a0002c0002t0001g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1638-7551G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455498 | |||||||
| chr5:114455594 | A | G | 197 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(194): Show |
197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1638-7455A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455594 | |||||||
| chr5:114455933 | G | A | 12 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0039 others(9): Show |
12 | HG00099.hp2 HG00738.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-7116G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114455933 | |||||||
| chr5:114456098 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1638-6951A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456098 | |||||||
| chr5:114456213 | C | G | 9 | a0001c0001t0001g0099 a0003c0003t0001g0193 a0003c0003t0001g0197 others(6): Show |
9 | HG02622.hp2 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1638-6836C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456213 | |||||||
| chr5:114456510 | A | C | 38 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0057 others(35): Show |
38 | HG01099.hp2 HG01192.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.1638-6539A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456510 | |||||||
| chr5:114456679 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1638-6370C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456679 | |||||||
| chr5:114456757 | G | C | 2 | a0002c0002t0001g0238 a0002c0014t0001g0017 |
2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1638-6292G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456757 | |||||||
| chr5:114456820 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0002c0002t0001g0008 others(3): Show |
6 | NA18986.hp1 NA19000.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-6229A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456820 | |||||||
| chr5:114456891 | C | A | 195 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(192): Show |
195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1638-6158C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456891 | |||||||
| chr5:114456927 | G | C | 83 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(80): Show |
83 | HG00280.hp1 HG00558.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.1638-6122G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456927 | |||||||
| chr5:114456988 | A | G | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(12): Show |
15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-6061A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114456988 | |||||||
| chr5:114457249 | C | G | 5 | a0001c0001t0001g0099 a0003c0003t0001g0197 a0003c0003t0001g0198 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-5800C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457249 | |||||||
| chr5:114457375 | C | G | 1 | a0001c0015t0001g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1638-5674C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457375 | |||||||
| chr5:114457589 | A | G | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(12): Show |
15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-5460A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457589 | |||||||
| chr5:114457635 | T | G | 197 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(194): Show |
197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1638-5414T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457635 | |||||||
| chr5:114457675 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1638-5374C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457675 | |||||||
| chr5:114457915 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1638-5134G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114457915 | |||||||
| chr5:114458226 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1638-4823C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458226 | |||||||
| chr5:114458390 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1638-4659A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458390 | |||||||
| chr5:114458396 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1638-4653C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458396 | |||||||
| chr5:114458567 | T | C | 4 | a0002c0002t0001g0103 a0002c0005t0001g0016 a0005c0004t0001g0147 others(1): Show |
4 | HG02486.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-4482T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458567 | |||||||
| chr5:114458697 | G | A | 196 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(193): Show |
196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1638-4352G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458697 | |||||||
| chr5:114458941 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1638-4108G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458941 | |||||||
| chr5:114458962 | C | G | 45 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(42): Show |
45 | HG00558.hp1 HG00741.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.1638-4087C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114458962 | |||||||
| chr5:114459248 | T | G | 8 | a0001c0001t0001g0099 a0003c0003t0001g0197 a0003c0003t0001g0198 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-3801T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459248 | |||||||
| chr5:114459250 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0045 |
2 | HG01943.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1638-3799T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459250 | |||||||
| chr5:114459595 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1638-3454T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459595 | |||||||
| chr5:114459734 | T | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0058 others(3): Show |
6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-3315T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459734 | |||||||
| chr5:114459861 | T | C | 63 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1638-3188T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114459861 | |||||||
| chr5:114460169 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1638-2880A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460169 | |||||||
| chr5:114460232 | T | TTTTG | 3 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01358.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1638-2802_1638-279 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114460232 | ||||||
| chr5:114460435 | G | C | 2 | a0001c0001t0001g0019 a0002c0002t0001g0182 |
2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1638-2614G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460435 | |||||||
| chr5:114460555 | T | A | 191 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(188): Show |
191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1638-2494T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460555 | |||||||
| chr5:114460567 | G | A | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1638-2482G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460567 | |||||||
| chr5:114460584 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1638-2465T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460584 | |||||||
| chr5:114460665 | A | T | 112 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(109): Show |
112 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1638-2384A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460665 | |||||||
| chr5:114460763 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1638-2286T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460763 | |||||||
| chr5:114460776 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1638-2273T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460776 | |||||||
| chr5:114460806 | A | G | 6 | a0001c0001t0001g0042 a0002c0002t0001g0007 a0002c0002t0001g0187 others(3): Show |
6 | NA18942.hp2 NA18946.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-2243A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460806 | |||||||
| chr5:114460895 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1638-2154A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114460895 | |||||||
| chr5:114461218 | A | G | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | NA18964.hp2 NA19009.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-1831A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461218 | |||||||
| chr5:114461266 | A | G | 1 | a0002c0002t0001g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1638-1783A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461266 | |||||||
| chr5:114461304 | A | G | 1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1638-1745A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461304 | |||||||
| chr5:114461568 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1638-1481T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461568 | |||||||
| chr5:114461630 | G | A | 1 | a0002c0002t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1638-1419G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461630 | |||||||
| chr5:114461639 | G | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1638-1410G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461639 | |||||||
| chr5:114461730 | G | GA | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(12): Show |
15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1638-1306dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 114461730 | ||||||
| chr5:114461747 | T | C | 68 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(65): Show |
68 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1638-1302T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461747 | |||||||
| chr5:114461847 | C | G | 89 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(86): Show |
89 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1638-1202C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461847 | |||||||
| chr5:114461907 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1638-1142C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461907 | |||||||
| chr5:114461908 | G | A | 90 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(87): Show |
90 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.1638-1141G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114461908 | |||||||
| chr5:114462217 | G | A | 43 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(40): Show |
43 | HG00558.hp1 HG00741.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1638-832G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462217 | |||||||
| chr5:114462319 | G | T | 176 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(173): Show |
176 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1638-730G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462319 | |||||||
| chr5:114462424 | A | C | 2 | a0001c0001t0001g0100 a0005c0004t0001g0146 |
2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1638-625A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462424 | |||||||
| chr5:114462878 | G | A | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1638-171G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462878 | |||||||
| chr5:114462945 | A | G | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1638-104A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 3/7 | chr5 | 114462945 | |||||||
| chr5:114463226 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1779+36C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463226 | |||||||
| chr5:114463244 | A | G | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(12): Show |
15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1779+54A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463244 | |||||||
| chr5:114463289 | C | T | 24 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
24 | HG01169.hp1 HG01358.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1779+99C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463289 | |||||||
| chr5:114463353 | C | T | 24 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
24 | HG01169.hp1 HG01358.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1779+163C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463353 | |||||||
| chr5:114463706 | G | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(88): Show |
91 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.1779+516G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463706 | |||||||
| chr5:114463720 | A | T | 10 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(7): Show |
10 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1779+530A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463720 | |||||||
| chr5:114463851 | C | T | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1779+661C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463851 | |||||||
| chr5:114463881 | A | C | 62 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(59): Show |
62 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1779+691A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114463881 | |||||||
| chr5:114464047 | G | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(88): Show |
91 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.1779+857G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464047 | |||||||
| chr5:114464367 | A | G | 2 | a0002c0002t0001g0139 a0002c0002t0001g0140 |
2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1779+1177A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464367 | |||||||
| chr5:114464467 | G | A | 1 | a0005c0004t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1779+1277G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464467 | |||||||
| chr5:114464627 | G | A | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1779+1437G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464627 | |||||||
| chr5:114464713 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1779+1523A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464713 | |||||||
| chr5:114464803 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1779+1613G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464803 | |||||||
| chr5:114464809 | T | TA | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0089 others(3): Show |
6 | HG02145.hp1 HG02293.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1779+1630dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114464809 | ||||||
| chr5:114464809 | TA | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
31 | HG00099.hp1 HG00558.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1779+1630delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114464809 | ||||||
| chr5:114464822 | G | A | 97 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(94): Show |
97 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.1779+1632G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464822 | |||||||
| chr5:114464837 | CTGTT | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1779+1653_1779+165 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114464837 | ||||||
| chr5:114464858 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1779+1668A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114464858 | |||||||
| chr5:114465004 | G | A | 1 | a0002c0005t0001g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1779+1814G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465004 | |||||||
| chr5:114465141 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1779+1951A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465141 | |||||||
| chr5:114465162 | G | A | 7 | a0001c0001t0001g0099 a0003c0003t0001g0193 a0003c0003t0001g0197 others(4): Show |
7 | HG02622.hp2 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1779+1972G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465162 | |||||||
| chr5:114465253 | T | G | 1 | a0001c0018t0001g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1779+2063T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465253 | |||||||
| chr5:114465333 | C | G | 1 | a0009c0022t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1779+2143C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465333 | |||||||
| chr5:114465350 | C | T | 1 | a0006c0007t0001g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1779+2160C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465350 | |||||||
| chr5:114465381 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1779+2191G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465381 | |||||||
| chr5:114465424 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1779+2234C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465424 | |||||||
| chr5:114465519 | G | A | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1779+2329G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465519 | |||||||
| chr5:114465544 | G | A | 1 | a0002c0002t0001g0203 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1779+2354G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465544 | |||||||
| chr5:114465547 | G | T | 107 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(104): Show |
107 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.1779+2357G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465547 | |||||||
| chr5:114465615 | C | CA | 33 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0073 others(30): Show |
33 | HG01099.hp2 HG01192.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1779+2438dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114465615 | ||||||
| chr5:114465635 | G | A | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0091 others(12): Show |
15 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1779+2445G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465635 | |||||||
| chr5:114465726 | A | G | 100 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(97): Show |
100 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1779+2536A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465726 | |||||||
| chr5:114465934 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1779+2744G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465934 | |||||||
| chr5:114465973 | C | T | 2 | a0007c0010t0001g0191 a0007c0010t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1779+2783C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114465973 | |||||||
| chr5:114466058 | TTACCAAG others(5): Show |
T | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1779+2871_1779+288 others(16): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114466058 | ||||||
| chr5:114466115 | T | G | 1 | a0002c0002t0001g0183 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1779+2925T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466115 | |||||||
| chr5:114466165 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0078 a0002c0002t0001g0208 |
3 | HG00099.hp1 HG01346.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1779+2975A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466165 | |||||||
| chr5:114466175 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1779+2985C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466175 | |||||||
| chr5:114466282 | A | G | 18 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(15): Show |
18 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1779+3092A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466282 | |||||||
| chr5:114466329 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1779+3139G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466329 | |||||||
| chr5:114466444 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1779+3254G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466444 | |||||||
| chr5:114466474 | A | AAT | 4 | a0001c0001t0001g0211 a0002c0005t0001g0013 a0002c0005t0001g0015 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1779+3302_1779+330 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114466474 | ||||||
| chr5:114466474 | AAT | A | 178 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(175): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1779+3302_1779+330 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114466474 | ||||||
| chr5:114466945 | A | G | 181 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(178): Show |
181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1779+3755A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114466945 | |||||||
| chr5:114467013 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1779+3823G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467013 | |||||||
| chr5:114467231 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1779+4041A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467231 | |||||||
| chr5:114467443 | T | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0058 others(3): Show |
6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1779+4253T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467443 | |||||||
| chr5:114467506 | C | T | 180 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(177): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1779+4316C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467506 | |||||||
| chr5:114467563 | T | C | 5 | a0001c0001t0001g0082 a0006c0007t0001g0104 a0006c0007t0001g0221 others(2): Show |
5 | HG02622.hp1 HG03098.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1779+4373T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467563 | |||||||
| chr5:114467747 | A | G | 17 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
17 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1779+4557A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467747 | |||||||
| chr5:114467882 | C | A | 2 | a0002c0002t0001g0103 a0002c0005t0001g0016 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1779+4692C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467882 | |||||||
| chr5:114467974 | A | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0089 a0001c0001t0001g0228 |
3 | HG01099.hp2 HG02145.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1779+4784A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467974 | |||||||
| chr5:114467984 | C | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1779+4794C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114467984 | |||||||
| chr5:114468092 | T | G | 1 | a0002c0002t0001g0153 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1779+4902T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468092 | |||||||
| chr5:114468124 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01081.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1780-4930T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468124 | |||||||
| chr5:114468152 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1780-4902G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468152 | |||||||
| chr5:114468377 | C | G | 18 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(15): Show |
18 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1780-4677C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468377 | |||||||
| chr5:114468443 | A | T | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1780-4611A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468443 | |||||||
| chr5:114468482 | C | T | 1 | a0002c0002t0001g0203 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1780-4572C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468482 | |||||||
| chr5:114468789 | G | A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0073 others(12): Show |
15 | HG01099.hp2 HG01192.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1780-4265G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468789 | |||||||
| chr5:114468797 | T | C | 4 | a0002c0002t0001g0103 a0002c0005t0001g0016 a0005c0004t0001g0147 others(1): Show |
4 | HG02486.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-4257T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468797 | |||||||
| chr5:114468940 | T | C | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1780-4114T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114468940 | |||||||
| chr5:114469133 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1780-3921C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469133 | |||||||
| chr5:114469138 | G | A | 1 | a0002c0002t0001g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1780-3916G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469138 | |||||||
| chr5:114469656 | T | C | 1 | a0002c0005t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1780-3398T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469656 | |||||||
| chr5:114469665 | T | C | 64 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1780-3389T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469665 | |||||||
| chr5:114469814 | A | G | 16 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(13): Show |
16 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1780-3240A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469814 | |||||||
| chr5:114469855 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1780-3199C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469855 | |||||||
| chr5:114469977 | T | A | 199 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(196): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1780-3077T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114469977 | |||||||
| chr5:114470299 | G | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
9 | HG01169.hp1 HG01358.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1780-2755G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114470299 | |||||||
| chr5:114470487 | TG | T | 4 | a0001c0001t0001g0243 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02922.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-2565delG | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114470487 | ||||||
| chr5:114470590 | C | T | 20 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(17): Show |
20 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1780-2464C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114470590 | |||||||
| chr5:114470705 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1780-2349C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114470705 | |||||||
| chr5:114470894 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0109 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1780-2160T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114470894 | |||||||
| chr5:114471109 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1780-1945T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471109 | |||||||
| chr5:114471131 | C | T | 1 | a0001c0019t0001g0234 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1780-1923C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471131 | |||||||
| chr5:114471256 | T | C | 17 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
17 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1780-1798T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471256 | |||||||
| chr5:114471330 | CTT | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1780-1721_1780-172 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114471330 | ||||||
| chr5:114471531 | A | G | 66 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(63): Show |
66 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1780-1523A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471531 | |||||||
| chr5:114471655 | C | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0002c0002t0001g0008 others(4): Show |
7 | HG00438.hp1 NA18986.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.1780-1399C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471655 | |||||||
| chr5:114471904 | T | C | 2 | a0002c0011t0001g0239 a0002c0011t0001g0241 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1780-1150T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471904 | |||||||
| chr5:114471928 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1780-1126T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114471928 | |||||||
| chr5:114472047 | A | G | 63 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1780-1007A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472047 | |||||||
| chr5:114472214 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0046 a0001c0001t0001g0078 others(1): Show |
4 | HG00099.hp1 HG01346.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1780-840C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472214 | |||||||
| chr5:114472239 | TCTTTC | T | 63 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1780-814_1780-810d others(7): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472239 | |||||||
| chr5:114472275 | G | A | 5 | a0002c0002t0001g0103 a0002c0002t0001g0238 a0002c0005t0001g0016 others(2): Show |
5 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1780-779G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472275 | |||||||
| chr5:114472332 | C | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0010c0023t0001g0160 |
3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1780-722C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472332 | |||||||
| chr5:114472334 | T | C | 176 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(173): Show |
176 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1780-720T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472334 | |||||||
| chr5:114472353 | A | G | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1780-701A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472353 | |||||||
| chr5:114472389 | T | C | 1 | a0003c0003t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1780-665T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472389 | |||||||
| chr5:114472395 | A | ATGAAGAT others(26): Show |
1 | a0001c0001t0001g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1780-657_1780-625d others(35): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114472395 | ||||||
| chr5:114472436 | C | T | 202 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(199): Show |
202 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1780-618C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472436 | |||||||
| chr5:114472549 | A | C | 202 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(199): Show |
202 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1780-505A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472549 | |||||||
| chr5:114472550 | C | CTGA | 202 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(199): Show |
202 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1780-503_1780-501d others(5): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 114472550 | ||||||
| chr5:114472558 | G | C | 1 | a0002c0002t0001g0183 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1780-496G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472558 | |||||||
| chr5:114472667 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(16): Show |
20 | HG00099.hp1 HG01099.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1780-387A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472667 | |||||||
| chr5:114472739 | G | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(15): Show |
19 | HG00099.hp1 HG01099.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1780-315G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 4/7 | chr5 | 114472739 | |||||||
| chr5:114473678 | G | T | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1890+514G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114473678 | |||||||
| chr5:114473697 | A | G | 1 | a0002c0002t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1890+533A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114473697 | |||||||
| chr5:114474108 | A | C | 5 | a0001c0001t0001g0243 a0003c0003t0001g0197 a0003c0003t0001g0198 others(2): Show |
5 | HG02922.hp2 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1890+944A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474108 | |||||||
| chr5:114474173 | A | G | 2 | a0002c0002t0001g0003 a0002c0002t0001g0203 |
2 | HG01257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1890+1009A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474173 | |||||||
| chr5:114474265 | G | A | 13 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(10): Show |
13 | HG01081.hp1 HG02622.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1890+1101G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474265 | |||||||
| chr5:114474361 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(41): Show |
45 | HG00099.hp1 HG00558.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.1890+1197T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474361 | |||||||
| chr5:114474629 | A | T | 1 | a0002c0002t0001g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1890+1465A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474629 | |||||||
| chr5:114474828 | A | C | 1 | a0002c0002t0001g0153 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1890+1664A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474828 | |||||||
| chr5:114474933 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1890+1769T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474933 | |||||||
| chr5:114474937 | C | T | 114 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(111): Show |
114 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.1890+1773C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114474937 | |||||||
| chr5:114475172 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1890+2008C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114475172 | |||||||
| chr5:114475347 | C | G | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1890+2183C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114475347 | |||||||
| chr5:114475616 | C | T | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890+2452C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114475616 | |||||||
| chr5:114475748 | G | A | 1 | a0002c0002t0001g0111 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1890+2584G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114475748 | |||||||
| chr5:114476250 | A | G | 63 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1890+3086A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476250 | |||||||
| chr5:114476365 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1890+3201T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476365 | |||||||
| chr5:114476442 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1890+3278T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476442 | |||||||
| chr5:114476490 | A | G | 1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1890+3326A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476490 | |||||||
| chr5:114476496 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0069 |
2 | HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1890+3332G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476496 | |||||||
| chr5:114476695 | A | C | 2 | a0002c0002t0001g0124 a0002c0002t0001g0164 |
2 | NA19065.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1890+3531A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476695 | |||||||
| chr5:114476753 | C | G | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1890+3589C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114476753 | |||||||
| chr5:114477002 | T | TAATTCTA others(35): Show |
61 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(58): Show |
61 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1890+3839_1890+388 others(46): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114477002 | ||||||
| chr5:114477152 | A | AT | 97 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(94): Show |
97 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1890+3994dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114477152 | ||||||
| chr5:114477250 | G | A | 114 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(111): Show |
114 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.1890+4086G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477250 | |||||||
| chr5:114477451 | T | C | 178 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(175): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1890+4287T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477451 | |||||||
| chr5:114477524 | G | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1890+4360G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477524 | |||||||
| chr5:114477534 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1890+4370C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477534 | |||||||
| chr5:114477636 | A | G | 80 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(77): Show |
80 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1890+4472A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477636 | |||||||
| chr5:114477821 | A | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0229 a0002c0002t0001g0122 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1890+4657A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477821 | |||||||
| chr5:114477898 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1890+4734C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114477898 | |||||||
| chr5:114478030 | A | G | 34 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0057 others(31): Show |
34 | HG01099.hp2 HG01169.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.1890+4866A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478030 | |||||||
| chr5:114478162 | C | G | 2 | a0002c0002t0001g0124 a0002c0002t0001g0164 |
2 | NA19065.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1890+4998C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478162 | |||||||
| chr5:114478296 | A | G | 1 | a0002c0002t0001g0072 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1890+5132A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478296 | |||||||
| chr5:114478381 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1890+5217C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478381 | |||||||
| chr5:114478459 | A | C | 1 | a0002c0002t0001g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1890+5295A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478459 | |||||||
| chr5:114478567 | C | G | 11 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(8): Show |
11 | HG01081.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1890+5403C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478567 | |||||||
| chr5:114478657 | C | T | 11 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(8): Show |
11 | HG01081.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1890+5493C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478657 | |||||||
| chr5:114478747 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1890+5583C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478747 | |||||||
| chr5:114478757 | A | G | 64 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1890+5593A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478757 | |||||||
| chr5:114478899 | C | T | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1890+5735C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478899 | |||||||
| chr5:114478992 | A | C | 1 | a0002c0002t0001g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1890+5828A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114478992 | |||||||
| chr5:114479015 | A | G | 11 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0230 others(8): Show |
11 | HG00280.hp1 HG01081.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1890+5851A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479015 | |||||||
| chr5:114479046 | CAATAGT | C | 6 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(3): Show |
6 | HG01074.hp1 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1890+5885_1890+589 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114479046 | ||||||
| chr5:114479084 | A | ATTAAAAG others(68): Show |
7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0002c0002t0001g0008 others(4): Show |
7 | HG00438.hp1 NA18986.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.1890+5921_1890+599 others(79): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114479084 | ||||||
| chr5:114479226 | T | TA | 189 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(186): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1890+6075dupA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114479226 | ||||||
| chr5:114479226 | T | TAA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0058 others(3): Show |
6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1890+6074_1890+607 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114479226 | ||||||
| chr5:114479380 | C | T | 177 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(174): Show |
177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1890+6216C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479380 | |||||||
| chr5:114479388 | A | G | 1 | a0002c0002t0001g0123 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1890+6224A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479388 | |||||||
| chr5:114479833 | T | G | 64 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1890+6669T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479833 | |||||||
| chr5:114479859 | A | G | 1 | a0001c0021t0001g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1890+6695A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479859 | |||||||
| chr5:114479926 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1890+6762C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479926 | |||||||
| chr5:114479976 | A | C | 65 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(62): Show |
65 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1890+6812A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114479976 | |||||||
| chr5:114480454 | A | G | 64 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1891-6596A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480454 | |||||||
| chr5:114480513 | C | G | 9 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
9 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1891-6537C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480513 | |||||||
| chr5:114480588 | C | T | 1 | a0002c0002t0001g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1891-6462C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480588 | |||||||
| chr5:114480759 | C | G | 7 | a0001c0001t0001g0099 a0001c0001t0001g0243 a0002c0002t0001g0240 others(4): Show |
7 | HG02622.hp2 HG02922.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1891-6291C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480759 | |||||||
| chr5:114480784 | G | A | 2 | a0002c0002t0001g0134 a0002c0002t0001g0224 |
2 | HG01192.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1891-6266G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480784 | |||||||
| chr5:114480823 | A | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0044 |
2 | HG01358.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1891-6227A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480823 | |||||||
| chr5:114480829 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1891-6221A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480829 | |||||||
| chr5:114480864 | C | A | 63 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1891-6186C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480864 | |||||||
| chr5:114480867 | C | T | 63 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1891-6183C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480867 | |||||||
| chr5:114480885 | C | G | 1 | a0003c0009t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1891-6165C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480885 | |||||||
| chr5:114480930 | G | A | 49 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(46): Show |
49 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.1891-6120G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114480930 | |||||||
| chr5:114481189 | T | A | 1 | a0003c0003t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1891-5861T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481189 | |||||||
| chr5:114481213 | G | A | 17 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(14): Show |
17 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1891-5837G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481213 | |||||||
| chr5:114481353 | A | G | 22 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0083 others(19): Show |
22 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1891-5697A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481353 | |||||||
| chr5:114481358 | C | G | 13 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(10): Show |
13 | HG01081.hp1 HG02622.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1891-5692C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481358 | |||||||
| chr5:114481673 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0010c0023t0001g0160 |
3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1891-5377C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481673 | |||||||
| chr5:114481746 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1891-5304A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481746 | |||||||
| chr5:114481883 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1891-5167C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481883 | |||||||
| chr5:114481971 | G | A | 1 | a0002c0002t0001g0172 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1891-5079G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481971 | |||||||
| chr5:114481988 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1891-5062C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481988 | |||||||
| chr5:114481994 | T | C | 1 | a0005c0004t0001g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1891-5056T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114481994 | |||||||
| chr5:114482006 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1891-5044T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482006 | |||||||
| chr5:114482028 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1891-5022A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482028 | |||||||
| chr5:114482568 | T | C | 1 | a0009c0022t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1891-4482T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482568 | |||||||
| chr5:114482726 | G | T | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1891-4324G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482726 | |||||||
| chr5:114482823 | T | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0082 |
3 | HG03139.hp2 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1891-4227T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482823 | |||||||
| chr5:114482885 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1891-4165G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482885 | |||||||
| chr5:114482888 | G | C | 63 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1891-4162G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482888 | |||||||
| chr5:114482916 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1891-4134T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482916 | |||||||
| chr5:114482946 | G | C | 64 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1891-4104G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114482946 | |||||||
| chr5:114483072 | C | T | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1891-3978C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483072 | |||||||
| chr5:114483124 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1891-3926T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483124 | |||||||
| chr5:114483231 | T | G | 1 | a0005c0004t0001g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1891-3819T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483231 | |||||||
| chr5:114483273 | CT | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(34): Show |
38 | HG00099.hp1 HG00558.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1891-3758delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483273 | ||||||
| chr5:114483273 | CTT | C | 193 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1891-3759_1891-375 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483273 | ||||||
| chr5:114483273 | CTTT | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0105 a0001c0001t0001g0246 others(3): Show |
6 | HG01517.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1891-3760_1891-375 others(7): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483273 | ||||||
| chr5:114483335 | C | T | 61 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(58): Show |
61 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1891-3715C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483335 | |||||||
| chr5:114483373 | C | G | 16 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(13): Show |
16 | HG01169.hp1 HG01358.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.1891-3677C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483373 | |||||||
| chr5:114483427 | A | G | 4 | a0001c0001t0001g0085 a0002c0005t0001g0013 a0002c0005t0001g0015 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891-3623A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483427 | |||||||
| chr5:114483712 | ACT | A | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1891-3337_1891-333 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483712 | |||||||
| chr5:114483713 | C | CTG | 71 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(68): Show |
71 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1891-3307_1891-330 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | ||||||
| chr5:114483713 | C | CTGTG | 63 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0024 others(60): Show |
64 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1891-3309_1891-330 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | ||||||
| chr5:114483713 | C | CTGTGTG | 8 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0052 others(5): Show |
8 | HG02523.hp1 HG02735.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.1891-3311_1891-330 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | ||||||
| chr5:114483713 | CTG | C | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(15): Show |
18 | HG01081.hp1 HG01169.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1891-3307_1891-330 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | ||||||
| chr5:114483713 | CTGTG | C | 9 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0096 others(6): Show |
9 | HG02280.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1891-3309_1891-330 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | ||||||
| chr5:114483713 | CTGTGTG | C | 9 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(6): Show |
9 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1891-3311_1891-330 others(10): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 114483713 | ||||||
| chr5:114483926 | T | C | 1 | a0002c0002t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1891-3124T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483926 | |||||||
| chr5:114483971 | T | C | 1 | a0002c0002t0001g0184 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1891-3079T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114483971 | |||||||
| chr5:114484145 | A | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(42): Show |
46 | HG00099.hp1 HG00558.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1891-2905A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484145 | |||||||
| chr5:114484283 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1891-2767G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484283 | |||||||
| chr5:114484372 | T | C | 1 | a0002c0002t0001g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1891-2678T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484372 | |||||||
| chr5:114484401 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0058 others(3): Show |
6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1891-2649C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484401 | |||||||
| chr5:114484633 | G | A | 1 | a0002c0002t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1891-2417G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484633 | |||||||
| chr5:114484755 | G | T | 33 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0042 others(30): Show |
33 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1891-2295G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484755 | |||||||
| chr5:114484775 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1891-2275A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484775 | |||||||
| chr5:114484808 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1891-2242T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114484808 | |||||||
| chr5:114485133 | G | A | 3 | a0001c0001t0001g0247 a0002c0002t0001g0236 a0008c0013t0001g0237 |
3 | HG02886.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1891-1917G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485133 | |||||||
| chr5:114485146 | T | C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | NA18964.hp2 NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1891-1904T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485146 | |||||||
| chr5:114485148 | G | A | 1 | a0002c0002t0001g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1891-1902G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485148 | |||||||
| chr5:114485264 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1891-1786G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485264 | |||||||
| chr5:114485298 | G | A | 21 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(18): Show |
21 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1891-1752G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485298 | |||||||
| chr5:114485429 | A | G | 1 | a0002c0002t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1891-1621A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485429 | |||||||
| chr5:114485534 | C | G | 4 | a0001c0001t0001g0085 a0002c0005t0001g0013 a0002c0005t0001g0015 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891-1516C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485534 | |||||||
| chr5:114485899 | G | T | 2 | a0002c0002t0001g0002 a0002c0002t0001g0185 |
2 | NA18942.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1891-1151G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485899 | |||||||
| chr5:114485920 | C | T | 2 | a0002c0002t0001g0119 a0002c0002t0001g0132 |
2 | HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1891-1130C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114485920 | |||||||
| chr5:114486213 | G | A | 21 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(18): Show |
21 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1891-837G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486213 | |||||||
| chr5:114486500 | G | A | 61 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0032 others(58): Show |
61 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1891-550G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486500 | |||||||
| chr5:114486508 | C | T | 176 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(173): Show |
176 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1891-542C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486508 | |||||||
| chr5:114486590 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1891-460A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486590 | |||||||
| chr5:114486880 | C | A | 9 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
9 | HG01074.hp1 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1891-170C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114486880 | |||||||
| chr5:114487009 | G | T | 1 | a0001c0001t0001g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1891-41G>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114487009 | |||||||
| chr5:114487038 | T | C | 1 | a0002c0002t0001g0129 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1891-12T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 5/7 | chr5 | 114487038 | |||||||
| chr5:114487304 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018+127A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114487304 | |||||||
| chr5:114487436 | T | C | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0109 others(1): Show |
4 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018+259T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114487436 | |||||||
| chr5:114488045 | A | G | 2 | a0001c0001t0001g0075 a0005c0004t0001g0176 |
2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2018+868A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488045 | |||||||
| chr5:114488219 | T | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(178): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2018+1042T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488219 | |||||||
| chr5:114488271 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2018+1094C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488271 | |||||||
| chr5:114488279 | G | A | 21 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(18): Show |
21 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.2018+1102G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488279 | |||||||
| chr5:114488391 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(202): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2018+1214T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488391 | |||||||
| chr5:114488432 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(42): Show |
46 | HG00099.hp1 HG00558.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.2018+1255A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488432 | |||||||
| chr5:114488457 | A | C | 1 | a0002c0002t0001g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2018+1280A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488457 | |||||||
| chr5:114488476 | G | C | 1 | a0002c0002t0001g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2018+1299G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488476 | |||||||
| chr5:114488737 | G | C | 2 | a0001c0001t0001g0108 a0002c0002t0001g0204 |
2 | HG00738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2018+1560G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488737 | |||||||
| chr5:114488816 | C | T | 2 | a0002c0002t0001g0136 a0002c0002t0001g0249 |
2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2018+1639C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488816 | |||||||
| chr5:114488823 | A | G | 1 | a0002c0002t0001g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2018+1646A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488823 | |||||||
| chr5:114488910 | A | G | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2018+1733A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488910 | |||||||
| chr5:114488940 | C | T | 1 | a0002c0002t0001g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2018+1763C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114488940 | |||||||
| chr5:114489052 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018+1875T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489052 | |||||||
| chr5:114489159 | A | G | 23 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0083 others(20): Show |
23 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2018+1982A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489159 | |||||||
| chr5:114489189 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2018+2012T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489189 | |||||||
| chr5:114489267 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2018+2090C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489267 | |||||||
| chr5:114489298 | T | G | 17 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
17 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2018+2121T>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489298 | |||||||
| chr5:114489319 | A | G | 23 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0083 others(20): Show |
23 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2018+2142A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489319 | |||||||
| chr5:114489331 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2018+2154T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489331 | |||||||
| chr5:114489360 | A | G | 1 | a0002c0002t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2018+2183A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489360 | |||||||
| chr5:114489485 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.2018+2308T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489485 | |||||||
| chr5:114489554 | A | G | 2 | a0001c0001t0001g0084 a0002c0002t0001g0173 |
2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2018+2377A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489554 | |||||||
| chr5:114489657 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2018+2480C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489657 | |||||||
| chr5:114489789 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018+2612C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489789 | |||||||
| chr5:114489972 | A | C | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2018+2795A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114489972 | |||||||
| chr5:114490014 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2018+2837T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114490014 | |||||||
| chr5:114490114 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2018+2937G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114490114 | |||||||
| chr5:114490935 | T | C | 1 | a0002c0002t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2019-2468T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114490935 | |||||||
| chr5:114491042 | A | G | 65 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(62): Show |
65 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2019-2361A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491042 | |||||||
| chr5:114491423 | C | G | 1 | a0002c0002t0001g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2019-1980C>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491423 | |||||||
| chr5:114491509 | CT | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.2019-1878delT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114491509 | ||||||
| chr5:114491509 | CTT | C | 18 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0076 others(15): Show |
18 | HG00280.hp1 HG01109.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.2019-1879_2019-187 others(6): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114491509 | ||||||
| chr5:114491525 | T | A | 6 | a0001c0001t0001g0069 a0001c0021t0001g0220 a0002c0002t0001g0004 others(3): Show |
6 | HG01361.hp1 HG02630.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2019-1878T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491525 | |||||||
| chr5:114491532 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2019-1871A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491532 | |||||||
| chr5:114491533 | G | A | 2 | a0001c0001t0001g0069 a0004c0008t0001g0012 |
2 | HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2019-1870G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491533 | |||||||
| chr5:114491533 | GA | G | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0067 others(4): Show |
7 | HG01081.hp1 HG01517.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2019-1855delA | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114491533 | ||||||
| chr5:114491534 | A | G | 2 | a0002c0002t0001g0072 a0004c0008t0001g0012 |
2 | HG02896.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2019-1869A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491534 | |||||||
| chr5:114491564 | TAAAG | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0010c0023t0001g0160 |
3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2019-1837_2019-183 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114491564 | ||||||
| chr5:114491590 | A | G | 22 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0083 others(19): Show |
22 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.2019-1813A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491590 | |||||||
| chr5:114491680 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2019-1723C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114491680 | |||||||
| chr5:114492167 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2019-1236T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114492167 | |||||||
| chr5:114492525 | T | TAA | 6 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(3): Show |
6 | HG01074.hp1 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019-876_2019-875d others(4): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114492525 | ||||||
| chr5:114492769 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2019-634A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114492769 | |||||||
| chr5:114492802 | T | C | 10 | a0001c0001t0001g0099 a0001c0001t0001g0243 a0002c0002t0001g0240 others(7): Show |
10 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.2019-601T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114492802 | |||||||
| chr5:114492886 | G | GT | 47 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(44): Show |
48 | HG00099.hp1 HG00558.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.2019-506dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 114492886 | ||||||
| chr5:114492992 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2019-411A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114492992 | |||||||
| chr5:114493224 | T | C | 1 | a0002c0002t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2019-179T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 6/7 | chr5 | 114493224 | |||||||
| chr5:114493510 | T | C | 1 | a0002c0002t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2088+38T>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493510 | |||||||
| chr5:114493551 | A | C | 23 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0083 others(20): Show |
23 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2088+79A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493551 | |||||||
| chr5:114493615 | C | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0229 a0002c0002t0001g0122 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.2088+143C>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493615 | |||||||
| chr5:114493692 | C | T | 1 | a0002c0002t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2088+220C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493692 | |||||||
| chr5:114493705 | A | C | 24 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0083 others(21): Show |
24 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2088+233A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493705 | |||||||
| chr5:114493754 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2088+282A>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493754 | |||||||
| chr5:114493783 | C | T | 1 | a0002c0002t0001g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2088+311C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114493783 | |||||||
| chr5:114494067 | T | A | 1 | a0002c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2088+595T>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494067 | |||||||
| chr5:114494172 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2088+700G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494172 | |||||||
| chr5:114494196 | A | G | 1 | a0002c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2088+724A>G | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494196 | |||||||
| chr5:114494259 | G | GT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.2088+796dupT | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 114494259 | ||||||
| chr5:114494259 | G | GTT | 10 | a0001c0001t0001g0099 a0001c0001t0001g0243 a0002c0002t0001g0153 others(7): Show |
10 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.2088+795_2088+796d others(4): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 114494259 | ||||||
| chr5:114494418 | G | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0058 others(3): Show |
6 | HG01346.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.2088+946G>C | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494418 | |||||||
| chr5:114494508 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
23 | HG00099.hp1 HG00558.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.2088+1036G>A | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494508 | |||||||
| chr5:114494702 | A | T | 2 | a0001c0001t0001g0083 a0002c0002t0001g0209 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2089-1193A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494702 | |||||||
| chr5:114494714 | G | GGACT | 4 | a0002c0002t0001g0004 a0004c0008t0001g0010 a0004c0008t0001g0011 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-1179_2089-117 others(8): Show |
KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 114494714 | ||||||
| chr5:114494879 | A | T | 1 | a0002c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2089-1016A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114494879 | |||||||
| chr5:114495105 | A | T | 62 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(59): Show |
62 | HG00280.hp1 HG00558.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2089-790A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114495105 | |||||||
| chr5:114495454 | A | T | 1 | a0009c0022t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2089-441A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114495454 | |||||||
| chr5:114495466 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0010c0023t0001g0160 |
3 | HG01081.hp1 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2089-429C>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114495466 | |||||||
| chr5:114495707 | A | T | 1 | a0002c0016t0003g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2089-188A>T | KCNN2 | ENSG00000080709.17 | transcript | ENST00000673685.1 | protein_coding | 7/7 | chr5 | 114495707 |