Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23012 |
| ensemblid | ENSG00000211455.8 |
| hgncid | 17848 |
| symbol | STK38L |
| name | serine/threonine kinase 38 like |
| refseq_nuc | NM_015000.4 |
| refseq_prot | NP_055815.1 |
| ensembl_nuc | ENST00000389032.8 |
| ensembl_prot | ENSP00000373684.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 27244286 |
| end | 27325959 |
| strand | + |
| ver | v1.2 |
| region | chr12:27244286-27325959 |
| region5000 | chr12:27239286-27330959 |
| regionname0 | STK38L_chr12_27244286_27325959 |
| regionname5000 | STK38L_chr12_27239286_27330959 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1392 | 354 | 73 | 60 | 178 | 8 | 34 | STK38L_chr12_27239286_27330959 | STK38L | ATGGC others(1387): Show |
chr12 | 27239286 | 27330959 | ||
| a0001c0002 | 0/0 | 1392 | 13 | 12 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | ATGGC others(1387): Show |
chr12 | 27239286 | 27330959 | ||
| a0001c0003 | 1/0 | 1392 | 7 | 1 | 3 | 0 | 0 | 2 | STK38L_chr12_27239286_27330959 | STK38L | ATGGC others(1387): Show |
chr12 | 27239286 | 27330959 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4959 | 114 | 21 | 31 | 50 | 3 | 9 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0002 | 0/0 | 4959 | 85 | 14 | 6 | 57 | 1 | 7 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0003 | 0/0 | 4959 | 72 | 2 | 5 | 58 | 0 | 7 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0004 | 0/0 | 4957 | 42 | 6 | 15 | 9 | 4 | 8 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4952): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0005 | 0/0 | 4959 | 6 | 6 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0006 | 0/1 | 4959 | 12 | 6 | 2 | 0 | 0 | 3 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0007 | 0/0 | 4959 | 6 | 6 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0008 | 0/0 | 4959 | 3 | 3 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0009 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0010 | 0/0 | 4957 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4952): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0011 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0012 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0013 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0014 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0015 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0016 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0017 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0001t0018 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0002t0001 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0002t0005 | 0/0 | 4959 | 12 | 11 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0003t0002 | 0/0 | 4959 | 6 | 1 | 3 | 0 | 0 | 2 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4954): Show |
chr12 | 27239286 | 27330959 |
| a0001c0003t0004 | 1/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | GCGGT others(4952): Show |
chr12 | 27239286 | 27330959 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0010g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0010g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0012g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0012g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0013g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0014g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0015g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0016g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0017g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0018g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0004g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0244 | EUR | GBR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0256 | EUR | GBR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0243 | EUR | FIN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | FIN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0249 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0013 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0259 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00741 | hp1 | a0001 | c0002 | t0005 | g0344 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0258 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0334 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0333 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0332 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0240 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01361 | hp1 | a0001 | c0001 | t0017 | g0264 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0111 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0254 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0013 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0248 | EUR | IBS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0279 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0297 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0300 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | CDX | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0343 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0340 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0049 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02451 | hp2 | a0001 | c0002 | t0005 | g0345 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0327 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0316 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0123 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0182 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0325 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0057 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0051 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0339 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0342 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0116 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02976 | hp1 | a0001 | c0002 | t0005 | g0338 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0317 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0224 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0329 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0225 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03209 | hp1 | a0001 | c0001 | t0018 | g0108 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0006 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0337 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0110 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0124 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0319 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0341 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0324 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0281 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0336 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0128 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0252 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0120 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0191 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0330 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0257 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0221 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | CHB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0006 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18946 | hp1 | a0001 | c0001 | t0010 | g0215 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0078 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0289 | AFR | LWK | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0268 | AFR | LWK | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19058 | hp1 | a0001 | c0001 | t0016 | g0056 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19078 | hp1 | a0001 | c0001 | t0010 | g0320 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19240 | hp2 | a0001 | c0002 | t0005 | g0006 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | ASW | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ASW | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | GIH | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | GIH | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0331 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0022 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0335 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | USA | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0326 | AFR | USA | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | USA | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0179 | REF | REF | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0004 | g0241 | REF | REF | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27297738 | G | T | 1 | a0001c0002 | 13 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
synonymous_variant | LOW | c.18G>T | p.Gly6Gly | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/14 | 76/4957 | 18/1395 | 6/464 | chr12 | 27297738 | |||
| chr12:27317933 | G | A | 2 | a0001c0001 a0001c0002 |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
synonymous_variant | LOW | c.993G>A | p.Thr331Thr | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/14 | 1051/4957 | 993/1395 | 331/464 | chr12 | 27317933 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27297714 | C | T | 1 | a0001c0001t0018 | 1 | HG03209.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/14 | chr12 | 27297714 | |||||||
| chr12:27322519 | C | T | 1 | a0001c0001t0007 | 6 | HG01891.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*64C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 64 | chr12 | 27322519 | ||||||
| chr12:27322788 | A | G | 2 | a0001c0001t0006 a0001c0001t0008 |
14 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*333A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 333 | chr12 | 27322788 | ||||||
| chr12:27323025 | T | C | 1 | a0001c0001t0009 | 2 | HG01891.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*570T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 570 | chr12 | 27323025 | ||||||
| chr12:27323201 | T | G | 1 | a0001c0001t0010 | 2 | NA18946.hp1 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*746T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 746 | chr12 | 27323201 | ||||||
| chr12:27323612 | A | G | 5 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0012 others(2): Show |
120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1157A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 1157 | chr12 | 27323612 | ||||||
| chr12:27324166 | A | T | 1 | a0001c0001t0016 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1711A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 1711 | chr12 | 27324166 | ||||||
| chr12:27324174 | C | T | 10 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(7): Show |
131 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1719C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 1719 | chr12 | 27324174 | ||||||
| chr12:27324249 | A | ACT | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(16): Show |
328 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*1795_*1796dupCT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 1797 | INFO_REALIGN_3_PRIME | chr12 | 27324249 | |||||
| chr12:27324564 | G | A | 1 | a0001c0001t0011 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2109G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2109 | chr12 | 27324564 | ||||||
| chr12:27324702 | T | G | 2 | a0001c0001t0005 a0001c0002t0005 |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2247T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2247 | chr12 | 27324702 | ||||||
| chr12:27324814 | G | A | 1 | a0001c0001t0012 | 2 | HG02258.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2359G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2359 | chr12 | 27324814 | ||||||
| chr12:27324866 | A | G | 1 | a0001c0001t0013 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2411A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2411 | chr12 | 27324866 | ||||||
| chr12:27325051 | T | C | 1 | a0001c0001t0014 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2596T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2596 | chr12 | 27325051 | ||||||
| chr12:27325060 | T | C | 1 | a0001c0001t0017 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2605T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2605 | chr12 | 27325060 | ||||||
| chr12:27325928 | G | C | 1 | a0001c0001t0015 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3473G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 3473 | chr12 | 27325928 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27244406 | A | T | 24 | a0001c0001t0001g0328 a0001c0001t0004g0021 a0001c0001t0004g0324 others(21): Show |
27 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-12+74A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244406 | |||||||
| chr12:27244433 | G | A | 1 | a0001c0003t0002g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12+101G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244433 | |||||||
| chr12:27244456 | C | T | 5 | a0001c0001t0003g0020 a0001c0001t0003g0323 a0001c0001t0004g0321 others(2): Show |
6 | HG00609.hp2 NA19007.hp2 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+124C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244456 | |||||||
| chr12:27244540 | A | G | 2 | a0001c0001t0001g0318 a0001c0001t0008g0319 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-12+208A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244540 | |||||||
| chr12:27244589 | C | A | 23 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(20): Show |
23 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+257C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244589 | |||||||
| chr12:27244859 | T | C | 212 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0068 others(209): Show |
234 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.-12+527T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244859 | |||||||
| chr12:27245015 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-12+683G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245015 | |||||||
| chr12:27245196 | G | A | 15 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(12): Show |
15 | HG01069.hp2 HG01071.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+864G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245196 | |||||||
| chr12:27245313 | C | T | 62 | a0001c0001t0001g0214 a0001c0001t0001g0223 a0001c0001t0002g0001 others(59): Show |
75 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-12+981C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245313 | |||||||
| chr12:27245545 | A | C | 238 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0068 others(235): Show |
263 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.-12+1213A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245545 | |||||||
| chr12:27245676 | C | A | 1 | a0001c0001t0006g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-12+1344C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245676 | |||||||
| chr12:27245774 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-12+1442A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245774 | |||||||
| chr12:27246018 | A | G | 23 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(20): Show |
23 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+1686A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246018 | |||||||
| chr12:27246070 | A | G | 314 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(311): Show |
341 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(338): Show |
intron_variant | MODIFIER | c.-12+1738A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246070 | |||||||
| chr12:27246224 | G | A | 1 | a0001c0003t0002g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12+1892G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246224 | |||||||
| chr12:27246311 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-12+1979A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246311 | |||||||
| chr12:27246328 | T | TTG | 314 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(311): Show |
341 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(338): Show |
intron_variant | MODIFIER | c.-12+2007_-12+2008d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27246328 | ||||||
| chr12:27246358 | G | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0265 others(50): Show |
55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+2026G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246358 | |||||||
| chr12:27246440 | A | G | 314 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(311): Show |
341 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(338): Show |
intron_variant | MODIFIER | c.-12+2108A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246440 | |||||||
| chr12:27246548 | T | G | 1 | a0001c0001t0015g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+2216T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246548 | |||||||
| chr12:27246692 | C | A | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+2360C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246692 | |||||||
| chr12:27246750 | G | GCACT | 238 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0068 others(235): Show |
263 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.-12+2419_-12+2422d others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27246750 | ||||||
| chr12:27246848 | A | G | 238 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0068 others(235): Show |
263 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.-12+2516A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246848 | |||||||
| chr12:27246912 | C | T | 2 | a0001c0001t0005g0316 a0001c0001t0005g0317 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+2580C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246912 | |||||||
| chr12:27247167 | C | T | 1 | a0001c0001t0008g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12+2835C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247167 | |||||||
| chr12:27247219 | A | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0265 others(50): Show |
55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+2887A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247219 | |||||||
| chr12:27247313 | G | A | 1 | a0001c0001t0004g0181 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-12+2981G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247313 | |||||||
| chr12:27247531 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+3199G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247531 | |||||||
| chr12:27247656 | C | A | 314 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(311): Show |
341 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(338): Show |
intron_variant | MODIFIER | c.-12+3324C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247656 | |||||||
| chr12:27247814 | A | AT | 68 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(65): Show |
69 | HG00408.hp1 HG00544.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.-12+3502dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27247814 | ||||||
| chr12:27247814 | A | ATTT | 9 | a0001c0001t0012g0340 a0001c0002t0005g0006 a0001c0002t0005g0338 others(6): Show |
11 | HG00741.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+3500_-12+3502d others(5): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27247814 | ||||||
| chr12:27247814 | AT | A | 65 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(62): Show |
68 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.-12+3502delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27247814 | ||||||
| chr12:27247879 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+3547A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247879 | |||||||
| chr12:27247918 | G | A | 1 | a0001c0001t0008g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+3586G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247918 | |||||||
| chr12:27247973 | C | T | 9 | a0001c0001t0001g0223 a0001c0001t0002g0220 a0001c0001t0002g0226 others(6): Show |
10 | HG00639.hp2 HG01192.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+3641C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247973 | |||||||
| chr12:27248039 | T | G | 1 | a0001c0001t0004g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12+3707T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248039 | |||||||
| chr12:27248203 | C | G | 1 | a0001c0001t0001g0318 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-12+3871C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248203 | |||||||
| chr12:27248414 | C | T | 137 | a0001c0001t0001g0109 a0001c0001t0001g0125 a0001c0001t0001g0126 others(134): Show |
152 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-12+4082C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248414 | |||||||
| chr12:27248484 | C | T | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+4152C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248484 | |||||||
| chr12:27248498 | G | A | 1 | a0001c0003t0002g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12+4166G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248498 | |||||||
| chr12:27248534 | C | A | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+4202C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248534 | |||||||
| chr12:27248637 | GT | G | 27 | a0001c0001t0001g0315 a0001c0001t0001g0328 a0001c0001t0004g0021 others(24): Show |
30 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.-12+4308delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27248637 | ||||||
| chr12:27248678 | A | G | 3 | a0001c0001t0005g0327 a0001c0001t0006g0012 a0001c0001t0008g0134 |
4 | HG02257.hp1 HG02717.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+4346A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248678 | |||||||
| chr12:27248767 | G | A | 18 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0136 others(15): Show |
18 | HG00733.hp2 HG00741.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+4435G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248767 | |||||||
| chr12:27248948 | A | C | 1 | a0001c0001t0006g0012 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-12+4616A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248948 | |||||||
| chr12:27249254 | A | G | 2 | a0001c0001t0005g0316 a0001c0001t0005g0317 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+4922A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249254 | |||||||
| chr12:27249330 | TTTTATTT others(1): Show |
T | 3 | a0001c0001t0005g0327 a0001c0001t0006g0012 a0001c0001t0008g0134 |
4 | HG02257.hp1 HG02717.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+5014_-12+5021d others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27249330 | ||||||
| chr12:27249584 | C | T | 22 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0308 others(19): Show |
24 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12+5252C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249584 | |||||||
| chr12:27249716 | T | A | 1 | a0001c0001t0006g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-12+5384T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249716 | |||||||
| chr12:27249776 | G | A | 209 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0068 others(206): Show |
230 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.-12+5444G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249776 | |||||||
| chr12:27249826 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02486.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-12+5494G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249826 | |||||||
| chr12:27249829 | C | T | 2 | a0001c0001t0005g0316 a0001c0001t0005g0317 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+5497C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249829 | |||||||
| chr12:27249898 | C | G | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+5566C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249898 | |||||||
| chr12:27250254 | C | T | 209 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0068 others(206): Show |
230 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.-12+5922C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250254 | |||||||
| chr12:27250281 | C | T | 2 | a0001c0001t0005g0316 a0001c0001t0005g0317 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+5949C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250281 | |||||||
| chr12:27250318 | A | G | 7 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(4): Show |
7 | HG00438.hp1 HG00609.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+5986A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250318 | |||||||
| chr12:27250342 | C | T | 2 | a0001c0001t0001g0301 a0001c0002t0001g0300 |
2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-12+6010C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250342 | |||||||
| chr12:27250529 | T | G | 1 | a0001c0001t0003g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-12+6197T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250529 | |||||||
| chr12:27250631 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-12+6299G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250631 | |||||||
| chr12:27250827 | C | T | 23 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(20): Show |
23 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+6495C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250827 | |||||||
| chr12:27250883 | C | T | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+6551C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250883 | |||||||
| chr12:27250973 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-12+6641T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250973 | |||||||
| chr12:27250991 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-12+6659T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250991 | |||||||
| chr12:27250996 | C | CA | 24 | a0001c0001t0001g0315 a0001c0001t0001g0328 a0001c0001t0004g0021 others(21): Show |
27 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-12+6684dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27250996 | ||||||
| chr12:27250996 | CA | C | 28 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(25): Show |
29 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.-12+6684delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27250996 | ||||||
| chr12:27250996 | CAA | C | 204 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0068 others(201): Show |
225 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.-12+6683_-12+6684d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27250996 | ||||||
| chr12:27251054 | A | G | 27 | a0001c0001t0001g0315 a0001c0001t0001g0328 a0001c0001t0004g0021 others(24): Show |
30 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.-12+6722A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251054 | |||||||
| chr12:27251068 | C | T | 1 | a0001c0001t0005g0327 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+6736C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251068 | |||||||
| chr12:27251114 | T | A | 1 | a0001c0001t0006g0111 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-12+6782T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251114 | |||||||
| chr12:27251241 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-12+6909A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251241 | |||||||
| chr12:27251346 | G | A | 313 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(310): Show |
339 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(336): Show |
intron_variant | MODIFIER | c.-12+7014G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251346 | |||||||
| chr12:27251432 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-12+7100A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251432 | |||||||
| chr12:27251704 | T | C | 1 | a0001c0001t0017g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-12+7372T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251704 | |||||||
| chr12:27251723 | G | A | 15 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(12): Show |
15 | HG01069.hp2 HG01071.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+7391G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251723 | |||||||
| chr12:27251835 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+7503G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251835 | |||||||
| chr12:27251870 | C | T | 23 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(20): Show |
23 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+7538C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251870 | |||||||
| chr12:27251929 | G | A | 25 | a0001c0001t0001g0315 a0001c0001t0001g0328 a0001c0001t0004g0021 others(22): Show |
28 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+7597G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251929 | |||||||
| chr12:27251977 | T | C | 1 | a0001c0001t0006g0110 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-12+7645T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251977 | |||||||
| chr12:27251987 | C | CT | 54 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0265 others(51): Show |
56 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.-12+7665dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27251987 | ||||||
| chr12:27252010 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-12+7678C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252010 | |||||||
| chr12:27252072 | C | T | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+7740C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252072 | |||||||
| chr12:27252201 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-12+7869A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252201 | |||||||
| chr12:27252215 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0265 others(50): Show |
55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+7883G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252215 | |||||||
| chr12:27252274 | C | T | 1 | a0001c0001t0003g0323 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-12+7942C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252274 | |||||||
| chr12:27252420 | A | AC | 140 | a0001c0001t0001g0109 a0001c0001t0001g0125 a0001c0001t0001g0126 others(137): Show |
155 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.-12+8089dupC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27252420 | ||||||
| chr12:27252504 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+8172T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252504 | |||||||
| chr12:27252677 | C | T | 3 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
3 | NA18961.hp2 NA18964.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-12+8345C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252677 | |||||||
| chr12:27252698 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12+8366G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252698 | |||||||
| chr12:27253069 | T | C | 58 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0068 others(55): Show |
62 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.-12+8737T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253069 | |||||||
| chr12:27253076 | T | C | 53 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0265 others(50): Show |
55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+8744T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253076 | |||||||
| chr12:27253129 | G | C | 25 | a0001c0001t0001g0315 a0001c0001t0001g0328 a0001c0001t0004g0021 others(22): Show |
28 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+8797G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253129 | |||||||
| chr12:27253214 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+8882T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253214 | |||||||
| chr12:27253304 | G | A | 5 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(2): Show |
5 | HG02257.hp2 HG02895.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+8972G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253304 | |||||||
| chr12:27253392 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-12+9060G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253392 | |||||||
| chr12:27253444 | C | CTCCTT | 340 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(337): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-12+9114_-12+9115i others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27253444 | ||||||
| chr12:27253733 | T | C | 71 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0068 others(68): Show |
77 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-12+9401T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253733 | |||||||
| chr12:27253785 | A | G | 2 | a0001c0001t0011g0051 a0001c0001t0011g0057 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12+9453A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253785 | |||||||
| chr12:27253786 | C | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0265 others(50): Show |
55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+9454C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253786 | |||||||
| chr12:27253801 | G | T | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+9469G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253801 | |||||||
| chr12:27253814 | G | A | 67 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0175 others(64): Show |
80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-12+9482G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253814 | |||||||
| chr12:27253826 | G | A | 2 | a0001c0001t0001g0262 a0001c0001t0004g0244 |
2 | HG00099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-12+9494G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253826 | |||||||
| chr12:27253834 | G | A | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | NA18971.hp1 NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-12+9502G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253834 | |||||||
| chr12:27253943 | C | T | 1 | a0001c0001t0004g0261 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12+9611C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253943 | |||||||
| chr12:27254022 | T | C | 25 | a0001c0001t0001g0315 a0001c0001t0001g0328 a0001c0001t0004g0021 others(22): Show |
28 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+9690T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254022 | |||||||
| chr12:27254084 | A | G | 2 | a0001c0001t0002g0115 a0001c0001t0014g0116 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-12+9752A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254084 | |||||||
| chr12:27254093 | T | G | 25 | a0001c0001t0001g0315 a0001c0001t0001g0328 a0001c0001t0004g0021 others(22): Show |
28 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+9761T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254093 | |||||||
| chr12:27254330 | A | G | 1 | a0001c0001t0005g0327 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+9998A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254330 | |||||||
| chr12:27254389 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-12+10057A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254389 | |||||||
| chr12:27254401 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+10069G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254401 | |||||||
| chr12:27254435 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-12+10103C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254435 | |||||||
| chr12:27254436 | C | G | 1 | a0001c0001t0002g0114 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-12+10104C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254436 | |||||||
| chr12:27254642 | A | T | 31 | a0001c0001t0001g0132 a0001c0001t0001g0328 a0001c0001t0002g0217 others(28): Show |
34 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12+10310A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254642 | |||||||
| chr12:27254722 | C | T | 183 | a0001c0001t0001g0109 a0001c0001t0001g0125 a0001c0001t0001g0126 others(180): Show |
201 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.-12+10390C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254722 | |||||||
| chr12:27254740 | G | GA | 13 | a0001c0001t0001g0125 a0001c0001t0001g0154 a0001c0001t0001g0155 others(10): Show |
13 | HG02015.hp1 HG02074.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+10411dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27254740 | ||||||
| chr12:27254788 | G | T | 311 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(308): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-12+10456G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254788 | |||||||
| chr12:27254806 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-12+10474G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254806 | |||||||
| chr12:27254924 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-12+10592C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254924 | |||||||
| chr12:27254977 | A | G | 4 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(1): Show |
5 | HG02145.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+10645A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254977 | |||||||
| chr12:27255054 | A | C | 57 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0216 others(54): Show |
61 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-12+10722A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255054 | |||||||
| chr12:27255091 | T | C | 4 | a0001c0001t0001g0318 a0001c0001t0002g0011 a0001c0001t0002g0107 others(1): Show |
5 | HG02717.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+10759T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255091 | |||||||
| chr12:27255228 | G | A | 1 | a0001c0001t0004g0329 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12+10896G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255228 | |||||||
| chr12:27255263 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-12+10931T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255263 | |||||||
| chr12:27255454 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-12+11122A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255454 | |||||||
| chr12:27255823 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-12+11491C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255823 | |||||||
| chr12:27255824 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0006g0222 |
2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12+11492G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255824 | |||||||
| chr12:27255845 | T | C | 167 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(164): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-12+11513T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255845 | |||||||
| chr12:27255978 | G | A | 6 | a0001c0001t0001g0245 a0001c0001t0001g0318 a0001c0001t0006g0048 others(3): Show |
6 | HG02723.hp2 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+11646G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255978 | |||||||
| chr12:27255980 | G | A | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+11648G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255980 | |||||||
| chr12:27256077 | C | G | 1 | a0001c0001t0003g0192 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-12+11745C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256077 | |||||||
| chr12:27256143 | G | A | 251 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(248): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-12+11811G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256143 | |||||||
| chr12:27256153 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-12+11821T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256153 | |||||||
| chr12:27256171 | A | G | 1 | a0001c0001t0004g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-12+11839A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256171 | |||||||
| chr12:27256280 | A | G | 1 | a0001c0001t0005g0327 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+11948A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256280 | |||||||
| chr12:27256367 | C | G | 1 | a0001c0001t0004g0004 | 3 | HG03669.hp1 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+12035C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256367 | |||||||
| chr12:27256569 | G | A | 25 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(22): Show |
28 | HG00741.hp1 HG01123.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+12237G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256569 | |||||||
| chr12:27256951 | G | C | 10 | a0001c0002t0005g0006 a0001c0002t0005g0325 a0001c0002t0005g0326 others(7): Show |
12 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+12619G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256951 | |||||||
| chr12:27257083 | A | G | 2 | a0001c0001t0001g0315 a0001c0001t0012g0340 |
2 | HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-12+12751A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257083 | |||||||
| chr12:27257175 | G | T | 2 | a0001c0001t0002g0115 a0001c0001t0014g0116 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-12+12843G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257175 | |||||||
| chr12:27257231 | G | C | 252 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(249): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-12+12899G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257231 | |||||||
| chr12:27257236 | C | A | 1 | a0001c0001t0004g0330 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-12+12904C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257236 | |||||||
| chr12:27257247 | T | C | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-12+12915T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257247 | |||||||
| chr12:27257286 | G | C | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+12954G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257286 | |||||||
| chr12:27257489 | T | C | 61 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0003g0008 others(58): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+13157T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257489 | |||||||
| chr12:27257540 | C | T | 3 | a0001c0001t0005g0327 a0001c0001t0006g0007 a0001c0001t0006g0012 |
5 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+13208C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257540 | |||||||
| chr12:27257600 | C | G | 70 | a0001c0001t0001g0318 a0001c0001t0002g0063 a0001c0001t0002g0064 others(67): Show |
75 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-12+13268C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257600 | |||||||
| chr12:27257691 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12+13359G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257691 | |||||||
| chr12:27257809 | A | G | 70 | a0001c0001t0001g0318 a0001c0001t0002g0063 a0001c0001t0002g0064 others(67): Show |
75 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-12+13477A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257809 | |||||||
| chr12:27257833 | G | A | 111 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(108): Show |
113 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-12+13501G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257833 | |||||||
| chr12:27257864 | C | CT | 63 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0178 others(60): Show |
67 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+13548dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27257864 | ||||||
| chr12:27257864 | CT | C | 46 | a0001c0001t0001g0314 a0001c0001t0002g0117 a0001c0001t0002g0118 others(43): Show |
51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.-12+13548delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27257864 | ||||||
| chr12:27258113 | TC | T | 3 | a0001c0001t0005g0327 a0001c0001t0006g0007 a0001c0001t0006g0012 |
5 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+13784delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27258113 | ||||||
| chr12:27258135 | G | T | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+13803G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258135 | |||||||
| chr12:27258307 | G | A | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+13975G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258307 | |||||||
| chr12:27258482 | C | A | 1 | a0001c0001t0002g0185 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-12+14150C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258482 | |||||||
| chr12:27258510 | G | A | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+14178G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258510 | |||||||
| chr12:27258609 | G | GT | 9 | a0001c0001t0001g0318 a0001c0001t0005g0014 a0001c0001t0005g0131 others(6): Show |
10 | HG02145.hp2 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+14278dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27258609 | ||||||
| chr12:27258667 | G | A | 11 | a0001c0001t0001g0223 a0001c0001t0002g0047 a0001c0001t0002g0217 others(8): Show |
12 | HG00639.hp2 HG01192.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+14335G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258667 | |||||||
| chr12:27258710 | A | G | 263 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(260): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-12+14378A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258710 | |||||||
| chr12:27258767 | T | A | 60 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+14435T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258767 | |||||||
| chr12:27258804 | G | A | 1 | a0001c0001t0003g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-12+14472G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258804 | |||||||
| chr12:27258960 | C | A | 1 | a0001c0001t0001g0318 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-12+14628C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258960 | |||||||
| chr12:27258969 | C | CTT | 258 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(255): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-12+14638_-12+1463 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27258969 | ||||||
| chr12:27259158 | G | T | 1 | a0001c0001t0005g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-12+14826G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259158 | |||||||
| chr12:27259284 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0269 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-12+14952G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259284 | |||||||
| chr12:27259322 | G | A | 247 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(244): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-12+14990G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259322 | |||||||
| chr12:27259369 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-12+15037C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259369 | |||||||
| chr12:27259401 | T | C | 59 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(56): Show |
63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12+15069T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259401 | |||||||
| chr12:27259436 | C | T | 1 | a0001c0001t0006g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12+15104C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259436 | |||||||
| chr12:27259471 | A | G | 1 | a0001c0001t0015g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+15139A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259471 | |||||||
| chr12:27259531 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-12+15199G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259531 | |||||||
| chr12:27259580 | G | T | 4 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(1): Show |
4 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+15248G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259580 | |||||||
| chr12:27259641 | C | T | 2 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-12+15309C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259641 | |||||||
| chr12:27259693 | G | A | 199 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(196): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-12+15361G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259693 | |||||||
| chr12:27259754 | A | G | 7 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0005g0317 others(4): Show |
7 | HG02809.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+15422A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259754 | |||||||
| chr12:27259959 | T | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(162): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-12+15627T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259959 | |||||||
| chr12:27259966 | T | C | 19 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0026 others(16): Show |
19 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12+15634T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259966 | |||||||
| chr12:27260108 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA18964.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-12+15776A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260108 | |||||||
| chr12:27260190 | A | G | 1 | a0001c0001t0002g0213 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-12+15858A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260190 | |||||||
| chr12:27260293 | A | G | 2 | a0001c0001t0004g0321 a0001c0001t0004g0322 |
2 | NA19062.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-12+15961A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260293 | |||||||
| chr12:27260390 | G | A | 162 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(159): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.-12+16058G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260390 | |||||||
| chr12:27260483 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+16151C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260483 | |||||||
| chr12:27260554 | C | T | 59 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(56): Show |
63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12+16222C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260554 | |||||||
| chr12:27260563 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-12+16231G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260563 | |||||||
| chr12:27260832 | G | A | 2 | a0001c0001t0005g0014 a0001c0001t0005g0131 |
3 | HG02145.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-12+16500G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260832 | |||||||
| chr12:27261117 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
9 | NA18942.hp2 NA18953.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+16785G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261117 | |||||||
| chr12:27261151 | A | G | 14 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(11): Show |
17 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-12+16819A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261151 | |||||||
| chr12:27261166 | T | C | 122 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(119): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-12+16834T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261166 | |||||||
| chr12:27261216 | T | G | 338 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(335): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.-12+16884T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261216 | |||||||
| chr12:27261252 | A | G | 10 | a0001c0001t0001g0223 a0001c0001t0005g0327 a0001c0001t0006g0007 others(7): Show |
12 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12+16920A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261252 | |||||||
| chr12:27261272 | T | C | 122 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(119): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-12+16940T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261272 | |||||||
| chr12:27261612 | G | C | 257 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(254): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-12+17280G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261612 | |||||||
| chr12:27261779 | A | G | 256 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(253): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-12+17447A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261779 | |||||||
| chr12:27261939 | T | A | 10 | a0001c0002t0005g0006 a0001c0002t0005g0325 a0001c0002t0005g0326 others(7): Show |
12 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+17607T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261939 | |||||||
| chr12:27261944 | T | C | 61 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0003g0008 others(58): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+17612T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261944 | |||||||
| chr12:27262172 | A | AAATCTC | 35 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+17842_-12+1784 others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262172 | ||||||
| chr12:27262277 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+17945A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262277 | |||||||
| chr12:27262400 | C | T | 259 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(256): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-12+18068C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262400 | |||||||
| chr12:27262429 | A | G | 167 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(164): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-12+18097A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262429 | |||||||
| chr12:27262470 | A | G | 1 | a0001c0001t0015g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+18138A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262470 | |||||||
| chr12:27262641 | G | C | 5 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(2): Show |
5 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+18309G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262641 | |||||||
| chr12:27262673 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0269 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-12+18341C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262673 | |||||||
| chr12:27262698 | C | CT | 61 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0003g0008 others(58): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+18367dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262698 | ||||||
| chr12:27262704 | C | G | 6 | a0001c0001t0001g0158 a0001c0001t0001g0245 a0001c0001t0002g0112 others(3): Show |
6 | HG02257.hp2 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+18372C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262704 | |||||||
| chr12:27262709 | T | TA | 58 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0003g0008 others(55): Show |
62 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.-12+18393dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262709 | ||||||
| chr12:27262709 | TA | T | 203 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(200): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-12+18393delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262709 | ||||||
| chr12:27262800 | A | AT | 125 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(122): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-12+18484dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262800 | ||||||
| chr12:27262800 | A | ATT | 35 | a0001c0001t0001g0153 a0001c0001t0001g0170 a0001c0001t0001g0262 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+18483_-12+1848 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262800 | ||||||
| chr12:27262800 | AT | A | 60 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0003g0008 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+18484delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262800 | ||||||
| chr12:27262851 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+18519C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262851 | |||||||
| chr12:27262869 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-12+18537G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262869 | |||||||
| chr12:27263022 | C | T | 3 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0219 |
3 | HG00423.hp2 HG02132.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-12+18690C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263022 | |||||||
| chr12:27263168 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-12+18836T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263168 | |||||||
| chr12:27263349 | G | T | 154 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(151): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.-12+19017G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263349 | |||||||
| chr12:27263365 | C | T | 177 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-12+19033C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263365 | |||||||
| chr12:27263404 | C | CATGA | 61 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0003g0008 others(58): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+19073_-12+1907 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27263404 | ||||||
| chr12:27263404 | C | G | 1 | a0001c0001t0001g0242 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-12+19072C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263404 | |||||||
| chr12:27263482 | G | T | 35 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+19150G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263482 | |||||||
| chr12:27263502 | G | A | 6 | a0001c0001t0001g0158 a0001c0001t0001g0245 a0001c0001t0002g0112 others(3): Show |
6 | HG02257.hp2 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+19170G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263502 | |||||||
| chr12:27263560 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-12+19228C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263560 | |||||||
| chr12:27263648 | A | G | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+19316A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263648 | |||||||
| chr12:27263835 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0006g0222 |
2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12+19503C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263835 | |||||||
| chr12:27263899 | T | G | 1 | a0001c0001t0002g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-12+19567T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263899 | |||||||
| chr12:27263948 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+19616C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263948 | |||||||
| chr12:27263977 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-12+19645G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263977 | |||||||
| chr12:27264289 | C | T | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+19957C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264289 | |||||||
| chr12:27264357 | A | G | 62 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0003g0008 others(59): Show |
66 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12+20025A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264357 | |||||||
| chr12:27264442 | C | G | 118 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(115): Show |
120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-12+20110C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264442 | |||||||
| chr12:27264594 | A | G | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+20262A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264594 | |||||||
| chr12:27264765 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+20433G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264765 | |||||||
| chr12:27265178 | T | A | 1 | a0001c0001t0004g0321 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-12+20846T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265178 | |||||||
| chr12:27265266 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-12+20934G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265266 | |||||||
| chr12:27265277 | T | G | 121 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(118): Show |
123 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-12+20945T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265277 | |||||||
| chr12:27265315 | T | G | 2 | a0001c0001t0005g0316 a0001c0001t0005g0317 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+20983T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265315 | |||||||
| chr12:27265323 | C | T | 1 | a0001c0001t0006g0012 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-12+20991C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265323 | |||||||
| chr12:27265434 | T | C | 59 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(56): Show |
63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12+21102T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265434 | |||||||
| chr12:27265579 | T | C | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+21247T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265579 | |||||||
| chr12:27265601 | A | T | 1 | a0001c0001t0002g0212 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-12+21269A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265601 | |||||||
| chr12:27265629 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-12+21297A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265629 | |||||||
| chr12:27265736 | G | A | 1 | a0001c0001t0004g0261 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12+21404G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265736 | |||||||
| chr12:27265800 | T | C | 2 | a0001c0001t0002g0011 a0001c0001t0002g0107 |
3 | HG02717.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-12+21468T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265800 | |||||||
| chr12:27265897 | A | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | NA18947.hp1 NA18964.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-12+21565A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265897 | |||||||
| chr12:27266129 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+21797T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266129 | |||||||
| chr12:27266190 | A | T | 5 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(2): Show |
5 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+21858A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266190 | |||||||
| chr12:27266479 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-12+22147C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266479 | |||||||
| chr12:27266545 | T | G | 1 | a0001c0001t0001g0313 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-12+22213T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266545 | |||||||
| chr12:27266900 | C | G | 5 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(2): Show |
5 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+22568C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266900 | |||||||
| chr12:27267106 | T | A | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG01070.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-12+22774T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267106 | |||||||
| chr12:27267318 | A | G | 9 | a0001c0001t0001g0223 a0001c0001t0006g0007 a0001c0001t0006g0012 others(6): Show |
11 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+22986A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267318 | |||||||
| chr12:27267354 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-12+23022G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267354 | |||||||
| chr12:27267388 | T | A | 1 | a0001c0002t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-12+23056T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267388 | |||||||
| chr12:27267414 | C | T | 1 | a0001c0001t0004g0330 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-12+23082C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267414 | |||||||
| chr12:27267488 | G | C | 262 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(259): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-12+23156G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267488 | |||||||
| chr12:27267577 | T | A | 8 | a0001c0001t0002g0002 a0001c0001t0002g0195 a0001c0001t0002g0196 others(5): Show |
10 | HG00544.hp1 HG02040.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+23245T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267577 | |||||||
| chr12:27267592 | A | G | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-12+23260A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267592 | |||||||
| chr12:27267639 | G | A | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+23307G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267639 | |||||||
| chr12:27267731 | T | C | 1 | a0001c0001t0004g0332 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-12+23399T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267731 | |||||||
| chr12:27267737 | T | G | 263 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(260): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-12+23405T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267737 | |||||||
| chr12:27267738 | TC | T | 263 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(260): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-12+23407delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267738 | |||||||
| chr12:27267773 | T | C | 255 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(252): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-12+23441T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267773 | |||||||
| chr12:27267780 | A | T | 1 | a0001c0001t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-12+23448A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267780 | |||||||
| chr12:27268089 | C | T | 6 | a0001c0001t0001g0158 a0001c0001t0001g0245 a0001c0001t0002g0112 others(3): Show |
6 | HG02257.hp2 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+23757C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268089 | |||||||
| chr12:27268170 | TGTTA | T | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+23843_-12+2384 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27268170 | ||||||
| chr12:27268193 | T | TATACATA others(8): Show |
4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+23861_-12+2386 others(19): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268193 | |||||||
| chr12:27268218 | T | G | 35 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+23886T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268218 | |||||||
| chr12:27268223 | C | T | 20 | a0001c0001t0004g0004 a0001c0001t0004g0235 a0001c0001t0004g0243 others(17): Show |
22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.-12+23891C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268223 | |||||||
| chr12:27268362 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-12+24030T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268362 | |||||||
| chr12:27268487 | A | G | 2 | a0001c0001t0001g0301 a0001c0002t0001g0300 |
2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-12+24155A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268487 | |||||||
| chr12:27268541 | C | G | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+24209C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268541 | |||||||
| chr12:27268566 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-12+24234C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268566 | |||||||
| chr12:27268571 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+24239A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268571 | |||||||
| chr12:27268804 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0006g0007 a0001c0001t0006g0012 others(1): Show |
6 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+24472C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268804 | |||||||
| chr12:27268857 | C | G | 2 | a0001c0001t0001g0223 a0001c0001t0006g0222 |
2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12+24525C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268857 | |||||||
| chr12:27268891 | G | A | 9 | a0001c0001t0001g0223 a0001c0001t0006g0007 a0001c0001t0006g0012 others(6): Show |
11 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+24559G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268891 | |||||||
| chr12:27268904 | T | G | 269 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(266): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-12+24572T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268904 | |||||||
| chr12:27268910 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+24578A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268910 | |||||||
| chr12:27268914 | C | A | 2 | a0001c0001t0006g0007 a0001c0001t0006g0058 |
3 | HG02055.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-12+24582C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268914 | |||||||
| chr12:27268962 | G | T | 2 | a0001c0001t0005g0014 a0001c0001t0005g0131 |
3 | HG02145.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-12+24630G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268962 | |||||||
| chr12:27269180 | A | T | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+24848A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269180 | |||||||
| chr12:27269232 | C | A | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+24900C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269232 | |||||||
| chr12:27269262 | T | G | 231 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(228): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-12+24930T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269262 | |||||||
| chr12:27269314 | G | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.-12+24982G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269314 | |||||||
| chr12:27269334 | T | C | 2 | a0001c0001t0004g0249 a0001c0001t0004g0258 |
2 | HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-12+25002T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269334 | |||||||
| chr12:27269625 | G | A | 5 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(2): Show |
5 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+25293G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269625 | |||||||
| chr12:27269708 | T | A | 61 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0003g0008 others(58): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+25376T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269708 | |||||||
| chr12:27269808 | G | A | 265 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(262): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-12+25476G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269808 | |||||||
| chr12:27269840 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0006g0222 |
2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12+25508G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269840 | |||||||
| chr12:27269844 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-12+25512T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269844 | |||||||
| chr12:27269850 | C | A | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+25518C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269850 | |||||||
| chr12:27269898 | C | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0175 |
3 | NA18960.hp2 NA19010.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.-12+25566C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269898 | |||||||
| chr12:27269912 | A | C | 1 | a0001c0001t0004g0084 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-12+25580A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269912 | |||||||
| chr12:27269925 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-12+25593G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269925 | |||||||
| chr12:27269953 | C | T | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+25621C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269953 | |||||||
| chr12:27270010 | C | A | 115 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(112): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+25678C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270010 | |||||||
| chr12:27270085 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-12+25753C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270085 | |||||||
| chr12:27270268 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12+25936T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270268 | |||||||
| chr12:27270678 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+26346C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270678 | |||||||
| chr12:27270682 | T | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG01243.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-12+26350T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270682 | |||||||
| chr12:27270737 | C | A | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-12+26405C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270737 | |||||||
| chr12:27270786 | T | A | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+26454T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270786 | |||||||
| chr12:27270809 | T | C | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+26477T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270809 | |||||||
| chr12:27271001 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+26669A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271001 | |||||||
| chr12:27271097 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-26613A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271097 | |||||||
| chr12:27271131 | C | T | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-26579C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271131 | |||||||
| chr12:27271338 | C | T | 266 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(263): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-11-26372C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271338 | |||||||
| chr12:27271464 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-11-26246G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271464 | |||||||
| chr12:27271535 | G | C | 8 | a0001c0001t0001g0223 a0001c0001t0006g0007 a0001c0001t0006g0012 others(5): Show |
10 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-26175G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271535 | |||||||
| chr12:27271598 | T | A | 35 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-11-26112T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271598 | |||||||
| chr12:27271645 | A | T | 1 | a0001c0001t0001g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-11-26065A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271645 | |||||||
| chr12:27271658 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-11-26052A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271658 | |||||||
| chr12:27271726 | G | C | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(169): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-11-25984G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271726 | |||||||
| chr12:27271844 | C | T | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-25866C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271844 | |||||||
| chr12:27271854 | C | T | 1 | a0001c0001t0004g0261 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11-25856C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271854 | |||||||
| chr12:27272135 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-11-25575T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272135 | |||||||
| chr12:27272433 | T | C | 157 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(154): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-11-25277T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272433 | |||||||
| chr12:27272457 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-11-25253A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272457 | |||||||
| chr12:27272479 | TC | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0107 |
3 | HG02717.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11-25228delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27272479 | ||||||
| chr12:27272555 | A | G | 4 | a0001c0001t0001g0276 a0001c0001t0003g0035 a0001c0001t0003g0036 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-25155A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272555 | |||||||
| chr12:27272943 | G | A | 1 | a0001c0001t0006g0012 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-11-24767G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272943 | |||||||
| chr12:27272986 | A | C | 60 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-11-24724A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272986 | |||||||
| chr12:27273273 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-11-24437C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273273 | |||||||
| chr12:27273470 | G | C | 5 | a0001c0001t0003g0010 a0001c0001t0003g0052 a0001c0001t0003g0055 others(2): Show |
6 | NA18948.hp1 NA18975.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-24240G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273470 | |||||||
| chr12:27273546 | A | G | 239 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(236): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-11-24164A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273546 | |||||||
| chr12:27273705 | AAATCTGG others(1): Show |
A | 20 | a0001c0001t0001g0262 a0001c0001t0004g0004 a0001c0001t0004g0243 others(17): Show |
22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11-24002_-11-2399 others(12): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27273705 | ||||||
| chr12:27273865 | A | G | 15 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(12): Show |
16 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-23845A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273865 | |||||||
| chr12:27273905 | G | T | 21 | a0001c0001t0001g0262 a0001c0001t0004g0004 a0001c0001t0004g0235 others(18): Show |
23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.-11-23805G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273905 | |||||||
| chr12:27273977 | G | T | 6 | a0001c0001t0006g0058 a0001c0001t0006g0110 a0001c0001t0006g0111 others(3): Show |
6 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-23733G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273977 | |||||||
| chr12:27274129 | G | T | 268 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(265): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-11-23581G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274129 | |||||||
| chr12:27274192 | G | T | 1 | a0001c0001t0002g0174 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-11-23518G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274192 | |||||||
| chr12:27274233 | C | CA | 21 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(18): Show |
24 | HG00741.hp1 HG01361.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11-23462dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27274233 | ||||||
| chr12:27274233 | C | CAA | 147 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.-11-23463_-11-2346 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27274233 | ||||||
| chr12:27274233 | C | CAAA | 90 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(87): Show |
95 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-11-23464_-11-2346 others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27274233 | ||||||
| chr12:27274472 | C | A | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-23238C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274472 | |||||||
| chr12:27274722 | G | A | 15 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(12): Show |
16 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-22988G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274722 | |||||||
| chr12:27274773 | A | G | 1 | a0001c0001t0004g0021 | 2 | HG01358.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-11-22937A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274773 | |||||||
| chr12:27274880 | C | T | 1 | a0001c0001t0003g0102 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-11-22830C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274880 | |||||||
| chr12:27274929 | T | C | 1 | a0001c0001t0004g0061 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-11-22781T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274929 | |||||||
| chr12:27274984 | A | G | 83 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0185 others(80): Show |
87 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-11-22726A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274984 | |||||||
| chr12:27275023 | A | G | 116 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-11-22687A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275023 | |||||||
| chr12:27275037 | A | T | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-22673A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275037 | |||||||
| chr12:27275267 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-11-22443A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275267 | |||||||
| chr12:27275342 | C | CT | 171 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0040 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-11-22350dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27275342 | ||||||
| chr12:27275637 | A | C | 260 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(257): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-11-22073A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275637 | |||||||
| chr12:27275799 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-21911A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275799 | |||||||
| chr12:27275987 | C | T | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-21723C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275987 | |||||||
| chr12:27276021 | T | C | 36 | a0001c0001t0001g0262 a0001c0001t0002g0117 a0001c0001t0002g0118 others(33): Show |
39 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-11-21689T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276021 | |||||||
| chr12:27276034 | A | G | 36 | a0001c0001t0001g0262 a0001c0001t0002g0117 a0001c0001t0002g0118 others(33): Show |
39 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-11-21676A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276034 | |||||||
| chr12:27276112 | T | G | 1 | a0001c0001t0003g0071 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-11-21598T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276112 | |||||||
| chr12:27276318 | T | C | 1 | a0001c0001t0003g0090 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-11-21392T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276318 | |||||||
| chr12:27276597 | G | A | 22 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0003g0023 others(19): Show |
22 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11-21113G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276597 | |||||||
| chr12:27276939 | C | T | 1 | a0001c0001t0004g0255 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-11-20771C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276939 | |||||||
| chr12:27277060 | T | A | 3 | a0001c0001t0008g0134 a0001c0001t0008g0268 a0001c0001t0008g0319 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11-20650T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277060 | |||||||
| chr12:27277233 | ATTAC | A | 24 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0044 others(21): Show |
24 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-20475_-11-2047 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277233 | ||||||
| chr12:27277240 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0269 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11-20470G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277240 | |||||||
| chr12:27277242 | A | G | 57 | a0001c0001t0001g0158 a0001c0001t0001g0245 a0001c0001t0001g0262 others(54): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-11-20468A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277242 | |||||||
| chr12:27277326 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-20384G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277326 | |||||||
| chr12:27277354 | A | AAC | 232 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(229): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.-11-20342_-11-2034 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277354 | ||||||
| chr12:27277392 | C | CCA | 5 | a0001c0001t0005g0316 a0001c0001t0005g0317 a0001c0003t0002g0013 others(2): Show |
6 | HG00735.hp1 HG01433.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-20289_-11-2028 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | ||||||
| chr12:27277392 | CCA | C | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(115): Show |
133 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11-20289_-11-2028 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | ||||||
| chr12:27277392 | CCACA | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0125 others(10): Show |
13 | HG01346.hp2 HG01358.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-20291_-11-2028 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | ||||||
| chr12:27277392 | CCACACA | C | 175 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(172): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-11-20293_-11-2028 others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | ||||||
| chr12:27277392 | CCACACAC others(3): Show |
C | 2 | a0001c0001t0001g0223 a0001c0001t0006g0222 |
2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-11-20297_-11-2028 others(14): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | ||||||
| chr12:27277400 | A | C | 1 | a0001c0001t0004g0257 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-11-20310A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277400 | |||||||
| chr12:27277563 | A | T | 1 | a0001c0001t0015g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11-20147A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277563 | |||||||
| chr12:27277623 | T | A | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-20087T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277623 | |||||||
| chr12:27277791 | T | A | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-19919T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277791 | |||||||
| chr12:27277938 | G | A | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11-19772G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277938 | |||||||
| chr12:27278004 | C | T | 3 | a0001c0001t0001g0223 a0001c0001t0006g0007 a0001c0001t0006g0222 |
4 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-19706C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278004 | |||||||
| chr12:27278413 | A | T | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-11-19297A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278413 | |||||||
| chr12:27278532 | A | G | 26 | a0001c0001t0001g0158 a0001c0001t0001g0245 a0001c0001t0002g0112 others(23): Show |
29 | HG00741.hp1 HG01361.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.-11-19178A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278532 | |||||||
| chr12:27278645 | G | A | 26 | a0001c0001t0001g0158 a0001c0001t0001g0245 a0001c0001t0002g0112 others(23): Show |
29 | HG00741.hp1 HG01361.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.-11-19065G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278645 | |||||||
| chr12:27278929 | A | C | 1 | a0001c0001t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11-18781A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278929 | |||||||
| chr12:27278989 | T | G | 263 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(260): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-11-18721T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278989 | |||||||
| chr12:27279067 | G | T | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-18643G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279067 | |||||||
| chr12:27279104 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-11-18606C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279104 | |||||||
| chr12:27279452 | T | C | 260 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(257): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-11-18258T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279452 | |||||||
| chr12:27279485 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-11-18225G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279485 | |||||||
| chr12:27279506 | C | T | 1 | a0001c0001t0004g0331 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-11-18204C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279506 | |||||||
| chr12:27279688 | A | AT | 174 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(171): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-11-18005dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27279688 | ||||||
| chr12:27279688 | A | ATT | 59 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0267 others(56): Show |
63 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-18006_-11-1800 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27279688 | ||||||
| chr12:27279688 | A | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0328 a0001c0001t0003g0089 others(1): Show |
4 | HG00738.hp1 HG00738.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-18022A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279688 | |||||||
| chr12:27279709 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
8 | NA18942.hp2 NA18953.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-18001A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279709 | |||||||
| chr12:27280098 | G | A | 10 | a0001c0002t0005g0006 a0001c0002t0005g0325 a0001c0002t0005g0326 others(7): Show |
12 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-17612G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280098 | |||||||
| chr12:27280281 | A | G | 8 | a0001c0001t0002g0002 a0001c0001t0002g0195 a0001c0001t0002g0196 others(5): Show |
10 | HG00544.hp1 HG02040.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-17429A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280281 | |||||||
| chr12:27280334 | G | T | 1 | a0001c0001t0004g0181 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-11-17376G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280334 | |||||||
| chr12:27280819 | T | G | 9 | a0001c0001t0001g0223 a0001c0001t0006g0007 a0001c0001t0006g0012 others(6): Show |
11 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-16891T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280819 | |||||||
| chr12:27280955 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-11-16755T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280955 | |||||||
| chr12:27280997 | G | A | 5 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(2): Show |
5 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-16713G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280997 | |||||||
| chr12:27281054 | TGGCTTTA others(324): Show |
T | 266 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(263): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-11-16639_-11-1630 others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281054 | ||||||
| chr12:27281067 | G | GT | 24 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0017 others(21): Show |
25 | HG00544.hp1 HG00735.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-11-16607dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | ||||||
| chr12:27281067 | G | GTT | 19 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0018 others(16): Show |
22 | HG01192.hp1 HG02071.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11-16608_-11-1660 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | ||||||
| chr12:27281067 | G | GTTT | 13 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0129 others(10): Show |
13 | HG00597.hp2 HG02559.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-16609_-11-1660 others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | ||||||
| chr12:27281067 | G | GTTTT | 6 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0180 others(3): Show |
6 | HG02809.hp2 NA18948.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-16610_-11-1660 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | ||||||
| chr12:27281067 | G | GTTTTT | 7 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0150 others(4): Show |
8 | HG00438.hp2 HG01943.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11-16611_-11-1660 others(9): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | ||||||
| chr12:27281067 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0002g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11-16617_-11-1660 others(15): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | ||||||
| chr12:27281074 | T | G | 1 | a0001c0001t0002g0015 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-11-16636T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281074 | |||||||
| chr12:27281155 | G | T | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-16555G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281155 | |||||||
| chr12:27281736 | G | T | 5 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(2): Show |
5 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-15974G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281736 | |||||||
| chr12:27281834 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-11-15876A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281834 | |||||||
| chr12:27281865 | T | A | 121 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(118): Show |
123 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-11-15845T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281865 | |||||||
| chr12:27281905 | G | A | 257 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(254): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-11-15805G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281905 | |||||||
| chr12:27281918 | C | G | 4 | a0001c0001t0006g0048 a0001c0001t0008g0134 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-15792C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281918 | |||||||
| chr12:27281937 | G | C | 2 | a0001c0001t0011g0051 a0001c0001t0011g0057 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-11-15773G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281937 | |||||||
| chr12:27281953 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-11-15757T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281953 | |||||||
| chr12:27282008 | C | A | 1 | a0001c0001t0004g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11-15702C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282008 | |||||||
| chr12:27282065 | A | C | 115 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(112): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-11-15645A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282065 | |||||||
| chr12:27282358 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-11-15352G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282358 | |||||||
| chr12:27282424 | A | G | 266 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(263): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-11-15286A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282424 | |||||||
| chr12:27282459 | A | G | 1 | a0001c0001t0004g0261 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11-15251A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282459 | |||||||
| chr12:27282468 | A | G | 257 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(254): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-11-15242A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282468 | |||||||
| chr12:27282530 | G | GT | 59 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(56): Show |
63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-15170dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27282530 | ||||||
| chr12:27282653 | G | A | 59 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(56): Show |
63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-15057G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282653 | |||||||
| chr12:27282954 | T | C | 266 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(263): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-11-14756T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282954 | |||||||
| chr12:27283112 | A | G | 266 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(263): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-11-14598A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283112 | |||||||
| chr12:27283227 | T | C | 1 | a0001c0001t0004g0251 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-11-14483T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283227 | |||||||
| chr12:27283265 | T | C | 4 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(1): Show |
4 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-14445T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283265 | |||||||
| chr12:27283273 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-11-14437T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283273 | |||||||
| chr12:27283394 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-11-14316T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283394 | |||||||
| chr12:27283422 | A | G | 237 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(234): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-11-14288A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283422 | |||||||
| chr12:27283446 | T | C | 258 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(255): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-11-14264T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283446 | |||||||
| chr12:27283542 | C | A | 1 | a0001c0001t0002g0205 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-11-14168C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283542 | |||||||
| chr12:27283566 | A | T | 1 | a0001c0001t0015g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11-14144A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283566 | |||||||
| chr12:27283811 | T | A | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-13899T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283811 | |||||||
| chr12:27283866 | A | G | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-13844A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283866 | |||||||
| chr12:27284203 | C | T | 1 | a0001c0001t0006g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-11-13507C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27284203 | |||||||
| chr12:27284235 | G | GGGGTA | 4 | a0001c0001t0001g0223 a0001c0001t0006g0007 a0001c0001t0006g0058 others(1): Show |
5 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-13473_-11-1346 others(9): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27284235 | ||||||
| chr12:27284610 | G | A | 1 | a0001c0001t0009g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11-13100G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27284610 | |||||||
| chr12:27284902 | C | T | 3 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0219 |
3 | HG00423.hp2 HG02132.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-11-12808C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27284902 | |||||||
| chr12:27285101 | A | G | 16 | a0001c0001t0001g0295 a0001c0001t0003g0035 a0001c0001t0003g0036 others(13): Show |
16 | HG00642.hp2 HG00673.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-12609A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285101 | |||||||
| chr12:27285125 | A | T | 1 | a0001c0001t0004g0243 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-11-12585A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285125 | |||||||
| chr12:27285159 | T | C | 1 | a0001c0001t0002g0206 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-11-12551T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285159 | |||||||
| chr12:27285387 | A | G | 12 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0048 others(9): Show |
14 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11-12323A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285387 | |||||||
| chr12:27285501 | T | A | 1 | a0001c0002t0005g0326 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-11-12209T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285501 | |||||||
| chr12:27285541 | C | G | 1 | a0001c0001t0003g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-11-12169C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285541 | |||||||
| chr12:27285606 | AG | A | 2 | a0001c0001t0005g0014 a0001c0001t0005g0131 |
3 | HG02145.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-11-12101delG | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27285606 | ||||||
| chr12:27285623 | C | G | 1 | a0001c0001t0002g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-11-12087C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285623 | |||||||
| chr12:27285765 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-11-11945A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285765 | |||||||
| chr12:27285863 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11-11847T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285863 | |||||||
| chr12:27285946 | A | G | 1 | a0001c0001t0004g0261 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11-11764A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285946 | |||||||
| chr12:27286083 | G | T | 117 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(114): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-11627G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286083 | |||||||
| chr12:27286224 | T | C | 5 | a0001c0001t0004g0329 a0001c0001t0004g0333 a0001c0001t0004g0334 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-11486T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286224 | |||||||
| chr12:27286242 | T | C | 1 | a0001c0001t0002g0015 | 2 | NA18954.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-11-11468T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286242 | |||||||
| chr12:27286335 | T | C | 30 | a0001c0001t0004g0004 a0001c0001t0004g0061 a0001c0001t0004g0062 others(27): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.-11-11375T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286335 | |||||||
| chr12:27286398 | CTGTT | C | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11307_-11-1130 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27286398 | ||||||
| chr12:27286408 | A | G | 11 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0048 others(8): Show |
13 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11-11302A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286408 | |||||||
| chr12:27286424 | C | G | 8 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0048 others(5): Show |
10 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-11286C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286424 | |||||||
| chr12:27286723 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-11-10987C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286723 | |||||||
| chr12:27286747 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-11-10963G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286747 | |||||||
| chr12:27286833 | C | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02486.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-11-10877C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286833 | |||||||
| chr12:27286910 | G | A | 8 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0048 others(5): Show |
10 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-10800G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286910 | |||||||
| chr12:27287018 | C | T | 42 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0061 others(39): Show |
45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-10692C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27287018 | |||||||
| chr12:27287101 | C | CT | 28 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(25): Show |
31 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.-11-10593dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27287101 | ||||||
| chr12:27287163 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11-10547G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27287163 | |||||||
| chr12:27287191 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11-10519C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27287191 | |||||||
| chr12:27287251 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11-10459G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27287251 | |||||||
| chr12:27287758 | A | AT | 2 | a0001c0001t0001g0170 a0001c0001t0004g0004 |
4 | HG03669.hp1 HG04204.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-9946dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27287758 | ||||||
| chr12:27288008 | G | A | 21 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(18): Show |
24 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11-9702G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288008 | |||||||
| chr12:27288192 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-11-9518C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288192 | |||||||
| chr12:27288290 | T | A | 1 | a0001c0001t0001g0262 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11-9420T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288290 | |||||||
| chr12:27288500 | A | G | 1 | a0001c0001t0002g0234 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-11-9210A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288500 | |||||||
| chr12:27288578 | C | T | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-9132C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288578 | |||||||
| chr12:27288724 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-8986T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288724 | |||||||
| chr12:27288763 | C | A | 30 | a0001c0001t0004g0004 a0001c0001t0004g0061 a0001c0001t0004g0062 others(27): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.-11-8947C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288763 | |||||||
| chr12:27288825 | C | T | 4 | a0001c0001t0007g0182 a0001c0001t0007g0221 a0001c0001t0007g0224 others(1): Show |
4 | HG02809.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-8885C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288825 | |||||||
| chr12:27288826 | G | A | 1 | a0001c0001t0005g0327 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-11-8884G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288826 | |||||||
| chr12:27288899 | A | G | 262 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(259): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-11-8811A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288899 | |||||||
| chr12:27288968 | C | A | 3 | a0001c0001t0003g0087 a0001c0001t0003g0092 a0001c0001t0003g0093 |
3 | HG00423.hp1 NA18612.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-11-8742C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288968 | |||||||
| chr12:27289139 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0270 a0001c0001t0001g0271 others(8): Show |
13 | NA18942.hp2 NA18951.hp1 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-8571A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27289139 | |||||||
| chr12:27289229 | G | T | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(63): Show |
79 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-11-8481G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27289229 | |||||||
| chr12:27289301 | C | CTCTTAAT others(3): Show |
20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-8407_-11-8398d others(12): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27289301 | ||||||
| chr12:27289356 | T | A | 2 | a0001c0001t0004g0249 a0001c0001t0004g0258 |
2 | HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-11-8354T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27289356 | |||||||
| chr12:27289357 | A | T | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11-8353A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27289357 | |||||||
| chr12:27290025 | G | A | 4 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(1): Show |
4 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-7685G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290025 | |||||||
| chr12:27290136 | G | A | 12 | a0001c0001t0004g0021 a0001c0001t0004g0324 a0001c0001t0004g0329 others(9): Show |
13 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-7574G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290136 | |||||||
| chr12:27290244 | A | G | 1 | a0001c0001t0004g0181 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-11-7466A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290244 | |||||||
| chr12:27290365 | G | A | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-11-7345G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290365 | |||||||
| chr12:27290697 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-11-7013G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290697 | |||||||
| chr12:27290826 | T | G | 1 | a0001c0001t0004g0261 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11-6884T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290826 | |||||||
| chr12:27291017 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-11-6693A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291017 | |||||||
| chr12:27291019 | C | T | 117 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(114): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-6691C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291019 | |||||||
| chr12:27291226 | A | G | 1 | a0001c0001t0004g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-11-6484A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291226 | |||||||
| chr12:27291313 | C | G | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-6397C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291313 | |||||||
| chr12:27291584 | A | G | 1 | a0001c0001t0006g0012 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-11-6126A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291584 | |||||||
| chr12:27291640 | A | C | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-6070A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291640 | |||||||
| chr12:27291641 | G | T | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-6069G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291641 | |||||||
| chr12:27291745 | T | G | 4 | a0001c0001t0002g0016 a0001c0001t0002g0188 a0001c0001t0002g0207 others(1): Show |
5 | NA18975.hp2 NA18981.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-5965T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291745 | |||||||
| chr12:27291876 | C | T | 2 | a0001c0001t0003g0009 a0001c0001t0003g0079 |
3 | NA18943.hp2 NA18988.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-11-5834C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291876 | |||||||
| chr12:27291991 | G | A | 1 | a0001c0001t0004g0321 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-11-5719G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291991 | |||||||
| chr12:27292151 | T | C | 2 | a0001c0001t0005g0316 a0001c0001t0005g0317 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-11-5559T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292151 | |||||||
| chr12:27292338 | TTCTTGTT others(11): Show |
T | 26 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(23): Show |
30 | HG00597.hp1 HG00673.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-11-5331_-11-5314d others(20): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27292338 | ||||||
| chr12:27292404 | A | G | 1 | a0001c0001t0003g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11-5306A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292404 | |||||||
| chr12:27292599 | A | G | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-11-5111A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292599 | |||||||
| chr12:27292605 | T | G | 3 | a0001c0001t0008g0134 a0001c0001t0008g0268 a0001c0001t0008g0319 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11-5105T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292605 | |||||||
| chr12:27292615 | C | CTACT | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-11-5094_-11-5091d others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27292615 | ||||||
| chr12:27292901 | T | C | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-4809T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292901 | |||||||
| chr12:27292954 | T | C | 89 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(86): Show |
106 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.-11-4756T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292954 | |||||||
| chr12:27293262 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-11-4448A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293262 | |||||||
| chr12:27293346 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0014g0116 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-11-4364G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293346 | |||||||
| chr12:27293597 | GGGCCAGA others(23): Show |
G | 117 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(114): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-4112_-11-4083d others(32): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293597 | |||||||
| chr12:27293696 | A | G | 1 | a0001c0001t0004g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-11-4014A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293696 | |||||||
| chr12:27293872 | T | G | 301 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(298): Show |
327 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.-11-3838T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293872 | |||||||
| chr12:27293913 | T | A | 1 | a0001c0001t0004g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-11-3797T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293913 | |||||||
| chr12:27293996 | CAG | C | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-3712_-11-3711d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27293996 | ||||||
| chr12:27294118 | A | G | 2 | a0001c0002t0005g0339 a0001c0002t0005g0345 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-11-3592A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294118 | |||||||
| chr12:27294317 | C | T | 23 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(20): Show |
26 | HG00741.hp1 HG02145.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.-11-3393C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294317 | |||||||
| chr12:27294349 | A | T | 1 | a0001c0001t0002g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11-3361A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294349 | |||||||
| chr12:27294433 | GGAGGTGG others(1160): Show |
G | 1 | a0001c0001t0002g0296 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-11-3275_-11-2109d others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294433 | ||||||
| chr12:27294463 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-11-3247C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294463 | |||||||
| chr12:27294504 | C | CA | 7 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-3188dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294504 | ||||||
| chr12:27294504 | CA | C | 88 | a0001c0001t0001g0159 a0001c0001t0001g0307 a0001c0001t0002g0001 others(85): Show |
103 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.-11-3188delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294504 | ||||||
| chr12:27294504 | CAA | C | 19 | a0001c0001t0002g0001 a0001c0001t0002g0183 a0001c0001t0003g0023 others(16): Show |
19 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.-11-3189_-11-3188d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294504 | ||||||
| chr12:27294526 | G | A | 8 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0058 others(5): Show |
10 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-3184G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294526 | |||||||
| chr12:27294710 | CT | C | 8 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0048 others(5): Show |
10 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-2987delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294710 | ||||||
| chr12:27294879 | T | TA | 34 | a0001c0001t0001g0170 a0001c0001t0001g0315 a0001c0001t0003g0075 others(31): Show |
36 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-11-2815dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294879 | ||||||
| chr12:27294879 | TA | T | 6 | a0001c0001t0001g0312 a0001c0001t0002g0003 a0001c0001t0002g0203 others(3): Show |
7 | HG00438.hp1 HG03209.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-2815delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294879 | ||||||
| chr12:27294897 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11-2813T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294897 | |||||||
| chr12:27294990 | G | C | 1 | a0001c0001t0001g0283 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-11-2720G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294990 | |||||||
| chr12:27295542 | G | A | 1 | a0001c0001t0004g0329 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-11-2168G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295542 | |||||||
| chr12:27295563 | A | G | 117 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(114): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-2147A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295563 | |||||||
| chr12:27295735 | C | T | 1 | a0001c0001t0004g0254 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-11-1975C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295735 | |||||||
| chr12:27295890 | T | G | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-1820T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295890 | |||||||
| chr12:27295959 | T | C | 4 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(1): Show |
4 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-1751T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295959 | |||||||
| chr12:27296276 | A | G | 3 | a0001c0001t0008g0134 a0001c0001t0008g0268 a0001c0001t0008g0319 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11-1434A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296276 | |||||||
| chr12:27296523 | A | G | 1 | a0001c0001t0012g0340 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-11-1187A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296523 | |||||||
| chr12:27296610 | G | A | 1 | a0001c0001t0004g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11-1100G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296610 | |||||||
| chr12:27296643 | G | T | 1 | a0001c0001t0001g0282 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-11-1067G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296643 | |||||||
| chr12:27296881 | G | A | 252 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(249): Show |
274 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.-11-829G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296881 | |||||||
| chr12:27297091 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-11-619T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27297091 | |||||||
| chr12:27297400 | T | G | 1 | a0001c0001t0002g0201 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-11-310T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27297400 | |||||||
| chr12:27297663 | G | C | 11 | a0001c0001t0004g0021 a0001c0001t0004g0329 a0001c0001t0004g0330 others(8): Show |
12 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-47G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27297663 | |||||||
| chr12:27297666 | G | T | 1 | a0001c0001t0003g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-11-44G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27297666 | |||||||
| chr12:27298001 | A | T | 11 | a0001c0002t0001g0300 a0001c0002t0005g0006 a0001c0002t0005g0325 others(8): Show |
13 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.134+147A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298001 | |||||||
| chr12:27298066 | G | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(115): Show |
120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.134+212G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298066 | |||||||
| chr12:27298073 | A | G | 93 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(90): Show |
110 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.134+219A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298073 | |||||||
| chr12:27298252 | A | G | 1 | a0001c0001t0004g0253 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.134+398A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298252 | |||||||
| chr12:27298288 | A | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(111): Show |
134 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.134+434A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298288 | |||||||
| chr12:27298296 | G | A | 1 | a0001c0001t0005g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.134+442G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298296 | |||||||
| chr12:27298358 | GAAGGCAG others(9): Show |
G | 1 | a0001c0001t0001g0305 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.134+510_134+525del others(16): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 27298358 | ||||||
| chr12:27298513 | A | G | 13 | a0001c0001t0004g0004 a0001c0001t0004g0061 a0001c0001t0004g0062 others(10): Show |
15 | HG00642.hp2 HG00673.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.134+659A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298513 | |||||||
| chr12:27298667 | A | T | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.134+813A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298667 | |||||||
| chr12:27298685 | CAG | C | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.134+832_134+833del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298685 | |||||||
| chr12:27298703 | G | T | 8 | a0001c0001t0003g0008 a0001c0001t0003g0053 a0001c0001t0003g0054 others(5): Show |
9 | HG00408.hp2 HG00423.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.134+849G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298703 | |||||||
| chr12:27298769 | G | C | 1 | a0001c0001t0003g0097 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.134+915G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298769 | |||||||
| chr12:27298807 | G | A | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.134+953G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298807 | |||||||
| chr12:27298872 | C | G | 81 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(78): Show |
96 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.134+1018C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298872 | |||||||
| chr12:27299096 | G | T | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.134+1242G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299096 | |||||||
| chr12:27299159 | A | C | 1 | a0001c0001t0002g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.134+1305A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299159 | |||||||
| chr12:27299430 | A | C | 4 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(1): Show |
4 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+1576A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299430 | |||||||
| chr12:27299512 | A | G | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134+1658A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299512 | |||||||
| chr12:27299576 | C | T | 81 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(78): Show |
96 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.134+1722C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299576 | |||||||
| chr12:27299609 | C | T | 2 | a0001c0001t0006g0007 a0001c0001t0006g0222 |
3 | HG00639.hp2 HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.134+1755C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299609 | |||||||
| chr12:27300079 | A | G | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.135-2058A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300079 | |||||||
| chr12:27300318 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.135-1819G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300318 | |||||||
| chr12:27300478 | A | G | 12 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0048 others(9): Show |
14 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.135-1659A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300478 | |||||||
| chr12:27300488 | A | G | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.135-1649A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300488 | |||||||
| chr12:27300720 | G | C | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.135-1417G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300720 | |||||||
| chr12:27300852 | T | A | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135-1285T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300852 | |||||||
| chr12:27301344 | C | T | 1 | a0001c0001t0010g0320 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.135-793C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301344 | |||||||
| chr12:27301345 | G | A | 8 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0058 others(5): Show |
10 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.135-792G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301345 | |||||||
| chr12:27301481 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135-656C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301481 | |||||||
| chr12:27301595 | T | C | 1 | a0001c0001t0003g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.135-542T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301595 | |||||||
| chr12:27301903 | G | A | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.135-234G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301903 | |||||||
| chr12:27301917 | A | T | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.135-220A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301917 | |||||||
| chr12:27302018 | GT | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0330 a0001c0001t0004g0331 others(2): Show |
6 | HG01123.hp1 HG01255.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.135-106delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 27302018 | ||||||
| chr12:27302204 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.186+16A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302204 | |||||||
| chr12:27302234 | C | G | 1 | a0001c0001t0001g0295 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.186+46C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302234 | |||||||
| chr12:27302384 | C | T | 2 | a0001c0001t0005g0014 a0001c0001t0005g0131 |
3 | HG02145.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.186+196C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302384 | |||||||
| chr12:27302509 | A | G | 12 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0048 others(9): Show |
14 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.186+321A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302509 | |||||||
| chr12:27302561 | C | G | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.186+373C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302561 | |||||||
| chr12:27302615 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG00738.hp2 HG01169.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+427G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302615 | |||||||
| chr12:27302742 | C | T | 1 | a0001c0001t0004g0254 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.186+554C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302742 | |||||||
| chr12:27302762 | T | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | NA18747.hp1 NA18939.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.186+574T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302762 | |||||||
| chr12:27302873 | A | G | 113 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(110): Show |
133 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.186+685A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302873 | |||||||
| chr12:27302918 | C | T | 1 | a0001c0001t0003g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.186+730C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302918 | |||||||
| chr12:27302945 | A | G | 118 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(115): Show |
120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.186+757A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302945 | |||||||
| chr12:27303012 | TA | T | 190 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(187): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.186+846delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27303012 | ||||||
| chr12:27303012 | TAA | T | 87 | a0001c0001t0001g0042 a0001c0001t0001g0147 a0001c0001t0001g0170 others(84): Show |
102 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.186+845_186+846del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27303012 | ||||||
| chr12:27303012 | TAAA | T | 21 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(18): Show |
24 | HG00741.hp1 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.186+844_186+846del others(3): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27303012 | ||||||
| chr12:27303101 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.186+913C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303101 | |||||||
| chr12:27303113 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.186+925G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303113 | |||||||
| chr12:27303125 | T | C | 118 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(115): Show |
120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.186+937T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303125 | |||||||
| chr12:27303186 | T | A | 30 | a0001c0001t0004g0004 a0001c0001t0004g0061 a0001c0001t0004g0062 others(27): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.186+998T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303186 | |||||||
| chr12:27303229 | G | C | 2 | a0001c0001t0011g0051 a0001c0001t0011g0057 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.186+1041G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303229 | |||||||
| chr12:27303316 | T | C | 3 | a0001c0001t0008g0134 a0001c0001t0008g0268 a0001c0001t0008g0319 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.186+1128T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303316 | |||||||
| chr12:27303462 | G | A | 8 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0058 others(5): Show |
10 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.186+1274G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303462 | |||||||
| chr12:27303463 | C | G | 4 | a0001c0001t0006g0048 a0001c0001t0008g0134 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+1275C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303463 | |||||||
| chr12:27303590 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.186+1402A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303590 | |||||||
| chr12:27303648 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.186+1460C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303648 | |||||||
| chr12:27303876 | T | C | 1 | a0001c0001t0003g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.186+1688T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303876 | |||||||
| chr12:27304091 | G | C | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.186+1903G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304091 | |||||||
| chr12:27304194 | G | T | 1 | a0001c0001t0002g0201 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.186+2006G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304194 | |||||||
| chr12:27304250 | G | A | 2 | a0001c0001t0006g0058 a0001c0001t0018g0108 |
2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.186+2062G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304250 | |||||||
| chr12:27304258 | C | CA | 30 | a0001c0001t0001g0133 a0001c0001t0001g0152 a0001c0001t0001g0294 others(27): Show |
34 | HG00735.hp1 HG01346.hp1 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.186+2092dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27304258 | ||||||
| chr12:27304258 | C | CAA | 11 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0048 others(8): Show |
13 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.186+2091_186+2092d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27304258 | ||||||
| chr12:27304258 | CA | C | 65 | a0001c0001t0001g0038 a0001c0001t0001g0274 a0001c0001t0003g0008 others(62): Show |
69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.186+2092delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27304258 | ||||||
| chr12:27304289 | A | G | 81 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(78): Show |
96 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.186+2101A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304289 | |||||||
| chr12:27304384 | T | C | 30 | a0001c0001t0004g0004 a0001c0001t0004g0061 a0001c0001t0004g0062 others(27): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.186+2196T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304384 | |||||||
| chr12:27304491 | A | T | 1 | a0001c0001t0001g0262 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.186+2303A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304491 | |||||||
| chr12:27304890 | AT | A | 12 | a0001c0001t0001g0043 a0001c0001t0006g0007 a0001c0001t0006g0012 others(9): Show |
14 | HG00639.hp2 HG00738.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.186+2712delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27304890 | ||||||
| chr12:27304916 | T | C | 20 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(17): Show |
23 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.186+2728T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304916 | |||||||
| chr12:27304982 | T | C | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.186+2794T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304982 | |||||||
| chr12:27305033 | T | C | 251 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(248): Show |
273 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.186+2845T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305033 | |||||||
| chr12:27305342 | T | C | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.187-2997T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305342 | |||||||
| chr12:27305411 | A | T | 1 | a0001c0001t0001g0290 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.187-2928A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305411 | |||||||
| chr12:27305423 | TA | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(111): Show |
134 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.187-2910delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27305423 | ||||||
| chr12:27305450 | CTTA | C | 5 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0027 others(2): Show |
5 | NA18968.hp2 NA18989.hp1 NA19078.hp2 others(2): Show |
intron_variant | MODIFIER | c.187-2882_187-2880d others(5): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27305450 | ||||||
| chr12:27305471 | A | G | 1 | a0001c0001t0004g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.187-2868A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305471 | |||||||
| chr12:27305627 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187-2712C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305627 | |||||||
| chr12:27305666 | C | T | 102 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
120 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.187-2673C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305666 | |||||||
| chr12:27305680 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.187-2659G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305680 | |||||||
| chr12:27305894 | A | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(111): Show |
134 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.187-2445A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305894 | |||||||
| chr12:27306064 | T | A | 3 | a0001c0001t0008g0134 a0001c0001t0008g0268 a0001c0001t0008g0319 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.187-2275T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306064 | |||||||
| chr12:27306272 | A | G | 1 | a0001c0001t0004g0254 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.187-2067A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306272 | |||||||
| chr12:27306353 | T | TA | 65 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0068 others(62): Show |
69 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.187-1977dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306353 | ||||||
| chr12:27306354 | A | T | 1 | a0001c0001t0008g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187-1985A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306354 | |||||||
| chr12:27306427 | A | G | 1 | a0001c0001t0006g0007 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.187-1912A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306427 | |||||||
| chr12:27306589 | T | C | 1 | a0001c0001t0003g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.187-1750T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306589 | |||||||
| chr12:27306614 | T | G | 118 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(115): Show |
120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.187-1725T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306614 | |||||||
| chr12:27306712 | T | TCACACAC others(20): Show |
1 | a0001c0001t0001g0315 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.187-1627_187-1626i others(29): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306712 | |||||||
| chr12:27306714 | A | AAC | 14 | a0001c0001t0001g0158 a0001c0001t0002g0117 a0001c0001t0003g0008 others(11): Show |
15 | HG00408.hp2 HG02132.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.187-1587_187-1586d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACAC | 28 | a0001c0001t0002g0208 a0001c0001t0002g0211 a0001c0001t0003g0009 others(25): Show |
30 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.187-1589_187-1586d others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACAC | 11 | a0001c0001t0001g0169 a0001c0001t0001g0245 a0001c0001t0003g0010 others(8): Show |
12 | HG00673.hp1 HG02602.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.187-1591_187-1586d others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(1): Show |
7 | a0001c0001t0001g0171 a0001c0001t0001g0242 a0001c0001t0001g0273 others(4): Show |
7 | HG00408.hp1 HG01099.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.187-1593_187-1586d others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(3): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0132 a0001c0001t0001g0270 others(5): Show |
10 | HG03669.hp2 NA18942.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-1595_187-1586d others(12): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(5): Show |
8 | a0001c0001t0001g0046 a0001c0001t0001g0236 a0001c0001t0001g0238 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.187-1597_187-1586d others(14): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(7): Show |
14 | a0001c0001t0001g0126 a0001c0001t0001g0146 a0001c0001t0001g0148 others(11): Show |
14 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.187-1599_187-1586d others(16): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(9): Show |
13 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0068 others(10): Show |
13 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.187-1601_187-1586d others(18): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(11): Show |
11 | a0001c0001t0001g0044 a0001c0001t0001g0135 a0001c0001t0001g0157 others(8): Show |
11 | HG01109.hp2 HG01243.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.187-1603_187-1586d others(20): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(13): Show |
13 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0139 others(10): Show |
13 | HG00438.hp1 HG00733.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.187-1605_187-1586d others(22): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(15): Show |
7 | a0001c0001t0001g0038 a0001c0001t0001g0136 a0001c0001t0001g0138 others(4): Show |
7 | HG01928.hp2 HG02486.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.187-1607_187-1586d others(24): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(17): Show |
6 | a0001c0001t0001g0161 a0001c0001t0001g0167 a0001c0001t0001g0175 others(3): Show |
6 | HG01168.hp2 HG02083.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.187-1609_187-1586d others(26): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(19): Show |
6 | a0001c0001t0001g0109 a0001c0001t0001g0125 a0001c0001t0001g0142 others(3): Show |
6 | HG02071.hp1 HG02300.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.187-1611_187-1586d others(28): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(21): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0165 others(2): Show |
5 | HG01069.hp1 HG02148.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.187-1613_187-1586d others(30): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(23): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0001t0001g0283 |
3 | HG01496.hp1 HG02818.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.187-1615_187-1586d others(32): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(25): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0160 |
2 | HG00738.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.187-1617_187-1586d others(34): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(27): Show |
3 | a0001c0001t0001g0159 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG02015.hp1 NA18979.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.187-1619_187-1586d others(36): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | AACACACA others(29): Show |
1 | a0001c0001t0001g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.187-1621_187-1586d others(38): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | A | ACACACAC others(6): Show |
2 | a0001c0001t0001g0155 a0001c0001t0001g0223 |
2 | HG03927.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.187-1625_187-1624i others(15): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | |||||||
| chr12:27306714 | A | ACACACAC others(10): Show |
2 | a0001c0001t0001g0069 a0001c0001t0001g0276 |
2 | HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.187-1625_187-1624i others(19): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | |||||||
| chr12:27306714 | A | ACACACAC others(12): Show |
1 | a0001c0001t0001g0040 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.187-1625_187-1624i others(21): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | |||||||
| chr12:27306714 | A | ACACACAC others(14): Show |
1 | a0001c0001t0001g0154 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.187-1625_187-1624i others(23): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | |||||||
| chr12:27306714 | A | ACACACAC others(18): Show |
1 | a0001c0001t0001g0153 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.187-1625_187-1624i others(27): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | |||||||
| chr12:27306714 | A | ACACACAC others(20): Show |
1 | a0001c0001t0012g0289 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187-1625_187-1624i others(29): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | |||||||
| chr12:27306714 | A | C | 1 | a0001c0001t0001g0315 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.187-1625A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | |||||||
| chr12:27306714 | AAC | A | 80 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0011 others(77): Show |
90 | HG00544.hp1 HG00735.hp1 HG01069.hp2 others(87): Show |
intron_variant | MODIFIER | c.187-1587_187-1586d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | AACAC | A | 37 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0130 others(34): Show |
41 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.187-1589_187-1586d others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | AACACAC | A | 25 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(22): Show |
31 | HG00597.hp2 HG02004.hp2 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.187-1591_187-1586d others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306714 | AACACACA others(1): Show |
A | 7 | a0001c0001t0004g0061 a0001c0001t0004g0062 a0001c0001t0004g0082 others(4): Show |
8 | HG00642.hp2 HG00673.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.187-1593_187-1586d others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | ||||||
| chr12:27306740 | C | T | 2 | a0001c0001t0002g0115 a0001c0001t0014g0116 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.187-1599C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306740 | |||||||
| chr12:27306750 | C | T | 1 | a0001c0001t0004g0251 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.187-1589C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306750 | |||||||
| chr12:27306754 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.187-1585T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306754 | |||||||
| chr12:27306887 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.187-1452C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306887 | |||||||
| chr12:27306922 | G | A | 2 | a0001c0001t0003g0190 a0001c0001t0003g0191 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.187-1417G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306922 | |||||||
| chr12:27307049 | A | G | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.187-1290A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307049 | |||||||
| chr12:27307113 | A | G | 1 | a0001c0001t0003g0100 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187-1226A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307113 | |||||||
| chr12:27307424 | A | G | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.187-915A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307424 | |||||||
| chr12:27307468 | T | G | 301 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(298): Show |
327 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.187-871T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307468 | |||||||
| chr12:27307575 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.187-764A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307575 | |||||||
| chr12:27307676 | C | G | 2 | a0001c0001t0001g0301 a0001c0002t0001g0300 |
2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.187-663C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307676 | |||||||
| chr12:27307899 | A | C | 1 | a0001c0002t0005g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.187-440A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307899 | |||||||
| chr12:27307967 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.187-372A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307967 | |||||||
| chr12:27308077 | A | C | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-262A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27308077 | |||||||
| chr12:27308095 | C | CAT | 161 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(158): Show |
183 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.187-230_187-229dup others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27308095 | ||||||
| chr12:27308095 | C | CATAT | 126 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(123): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.187-232_187-229dup others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27308095 | ||||||
| chr12:27308095 | C | CATATAT | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0175 |
3 | NA18960.hp2 NA19010.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.187-234_187-229dup others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27308095 | ||||||
| chr12:27308857 | A | AT | 9 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0048 others(6): Show |
11 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.310-257_310-256ins others(1): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308857 | |||||||
| chr12:27308857 | AAAATATA others(9): Show |
A | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.310-242_310-227del others(16): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308857 | ||||||
| chr12:27308859 | A | T | 15 | a0001c0001t0001g0265 a0001c0001t0002g0002 a0001c0001t0002g0198 others(12): Show |
18 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.310-255A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308859 | |||||||
| chr12:27308861 | T | A | 1 | a0001c0001t0002g0184 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.310-253T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308861 | |||||||
| chr12:27308875 | AAT | A | 4 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(1): Show |
4 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-231_310-230del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308875 | ||||||
| chr12:27308889 | T | C | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.310-225T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308889 | |||||||
| chr12:27308897 | T | TAAATATA others(24): Show |
1 | a0001c0001t0003g0191 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.310-196_310-166dup others(31): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308897 | ||||||
| chr12:27308921 | T | TATATATA others(25): Show |
1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.310-182_310-151dup others(32): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308921 | ||||||
| chr12:27308926 | A | G | 82 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(79): Show |
97 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.310-188A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308926 | |||||||
| chr12:27308929 | A | T | 3 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0327 |
4 | HG02145.hp2 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-185A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308929 | |||||||
| chr12:27308942 | T | TATATATA others(11): Show |
1 | a0001c0001t0003g0106 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.310-165_310-164ins others(18): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308942 | ||||||
| chr12:27308953 | C | A | 1 | a0001c0001t0003g0106 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.310-161C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308953 | |||||||
| chr12:27308953 | CAT | C | 29 | a0001c0001t0004g0004 a0001c0001t0004g0061 a0001c0001t0004g0062 others(26): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.310-155_310-154del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308953 | ||||||
| chr12:27308969 | T | G | 2 | a0001c0001t0006g0058 a0001c0001t0018g0108 |
2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.310-145T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308969 | |||||||
| chr12:27308989 | T | G | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.310-125T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308989 | |||||||
| chr12:27309051 | T | C | 332 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(329): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.310-63T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27309051 | |||||||
| chr12:27309242 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.393+45C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309242 | |||||||
| chr12:27309677 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.393+480T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309677 | |||||||
| chr12:27309705 | T | C | 116 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(113): Show |
133 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.393+508T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309705 | |||||||
| chr12:27309742 | G | T | 117 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(114): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.393+545G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309742 | |||||||
| chr12:27309814 | A | G | 302 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(299): Show |
328 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.393+617A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309814 | |||||||
| chr12:27310182 | G | C | 2 | a0001c0001t0002g0209 a0001c0001t0002g0218 |
2 | HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.393+985G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310182 | |||||||
| chr12:27310229 | A | G | 3 | a0001c0001t0008g0134 a0001c0001t0008g0268 a0001c0001t0008g0319 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.393+1032A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310229 | |||||||
| chr12:27310341 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.393+1144A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310341 | |||||||
| chr12:27310382 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.393+1185C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310382 | |||||||
| chr12:27310510 | G | A | 4 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(1): Show |
4 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+1313G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310510 | |||||||
| chr12:27310513 | A | G | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.393+1316A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310513 | |||||||
| chr12:27310546 | G | A | 112 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(109): Show |
132 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.393+1349G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310546 | |||||||
| chr12:27310546 | G | T | 2 | a0001c0001t0003g0075 a0001c0001t0003g0076 |
2 | NA19010.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.393+1349G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310546 | |||||||
| chr12:27310568 | TAAATA | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(76): Show |
94 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.393+1374_393+1378d others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27310568 | ||||||
| chr12:27310569 | A | T | 15 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0068 others(12): Show |
15 | HG00099.hp2 HG00140.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+1372A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310569 | |||||||
| chr12:27310683 | G | C | 3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 |
3 | HG02647.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.393+1486G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310683 | |||||||
| chr12:27310763 | G | C | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.393+1566G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310763 | |||||||
| chr12:27311126 | C | A | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.394-1423C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311126 | |||||||
| chr12:27311198 | C | G | 1 | a0001c0001t0003g0045 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.394-1351C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311198 | |||||||
| chr12:27311302 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.394-1247A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311302 | |||||||
| chr12:27311459 | C | T | 2 | a0001c0001t0002g0209 a0001c0001t0002g0218 |
2 | HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.394-1090C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311459 | |||||||
| chr12:27311587 | T | TATAAAAT others(615): Show |
1 | a0001c0001t0017g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.394-775_394-774ins others(622): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27311587 | ||||||
| chr12:27311587 | T | TATAAAAT others(633): Show |
1 | a0001c0001t0001g0280 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.394-775_394-774ins others(640): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27311587 | ||||||
| chr12:27311587 | T | TATAAAAT others(635): Show |
1 | a0001c0001t0001g0314 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.394-775_394-774ins others(642): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27311587 | ||||||
| chr12:27311591 | A | C | 50 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
54 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.394-958A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311591 | |||||||
| chr12:27311597 | T | C | 2 | a0001c0001t0005g0316 a0001c0001t0005g0317 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.394-952T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311597 | |||||||
| chr12:27311710 | T | G | 2 | a0001c0003t0002g0013 a0001c0003t0002g0240 |
3 | HG00735.hp1 HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.394-839T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311710 | |||||||
| chr12:27311745 | TAA | T | 82 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(79): Show |
97 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.394-802_394-801del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27311745 | ||||||
| chr12:27312132 | GC | G | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.394-415delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27312132 | ||||||
| chr12:27312159 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0242 |
2 | HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.394-390G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312159 | |||||||
| chr12:27312167 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.394-382C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312167 | |||||||
| chr12:27312174 | C | T | 2 | a0001c0001t0006g0110 a0001c0001t0006g0111 |
2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.394-375C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312174 | |||||||
| chr12:27312257 | G | T | 15 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(12): Show |
18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.394-292G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312257 | |||||||
| chr12:27312319 | G | A | 21 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0044 others(18): Show |
21 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.394-230G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312319 | |||||||
| chr12:27312777 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.517+105T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27312777 | |||||||
| chr12:27312815 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517+143T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27312815 | |||||||
| chr12:27312949 | C | T | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.517+277C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27312949 | |||||||
| chr12:27312986 | C | T | 1 | a0001c0001t0004g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.517+314C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27312986 | |||||||
| chr12:27313068 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517+396G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313068 | |||||||
| chr12:27313173 | G | A | 2 | a0001c0001t0010g0215 a0001c0001t0010g0320 |
2 | NA18946.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.517+501G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313173 | |||||||
| chr12:27313189 | A | C | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.517+517A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313189 | |||||||
| chr12:27313248 | C | CA | 17 | a0001c0001t0002g0187 a0001c0001t0003g0071 a0001c0001t0003g0094 others(14): Show |
19 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.517+594dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27313248 | ||||||
| chr12:27313248 | CA | C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(137): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.517+594delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27313248 | ||||||
| chr12:27313266 | AT | A | 40 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0061 others(37): Show |
43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.517+595delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313266 | |||||||
| chr12:27313267 | T | A | 1 | a0001c0001t0004g0330 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.517+595T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313267 | |||||||
| chr12:27313365 | GGTTTT | G | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.517+709_517+713del others(5): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27313365 | ||||||
| chr12:27313677 | C | CT | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.518-826dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27313677 | ||||||
| chr12:27313813 | G | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(100): Show |
121 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.518-691G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313813 | |||||||
| chr12:27313826 | T | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(114): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.518-678T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313826 | |||||||
| chr12:27314007 | T | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(112): Show |
135 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.518-497T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27314007 | |||||||
| chr12:27314243 | A | G | 1 | a0001c0003t0002g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.518-261A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27314243 | |||||||
| chr12:27314281 | A | G | 1 | a0001c0001t0008g0268 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.518-223A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27314281 | |||||||
| chr12:27314391 | A | C | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-113A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27314391 | |||||||
| chr12:27314401 | C | CA | 135 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.518-85dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27314401 | ||||||
| chr12:27315377 | T | G | 2 | a0001c0001t0006g0007 a0001c0001t0006g0058 |
3 | HG02055.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.837+27T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315377 | |||||||
| chr12:27315380 | A | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(112): Show |
135 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.837+30A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315380 | |||||||
| chr12:27315573 | A | G | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(64): Show |
80 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.837+223A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315573 | |||||||
| chr12:27315750 | T | C | 15 | a0001c0001t0004g0004 a0001c0001t0004g0061 a0001c0001t0004g0062 others(12): Show |
17 | HG00642.hp2 HG00673.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.837+400T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315750 | |||||||
| chr12:27315939 | T | A | 2 | a0001c0001t0002g0227 a0001c0001t0002g0296 |
2 | NA18963.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.837+589T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315939 | |||||||
| chr12:27316071 | C | T | 1 | a0001c0001t0018g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.837+721C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316071 | |||||||
| chr12:27316340 | C | T | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.837+990C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316340 | |||||||
| chr12:27316353 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.838-983G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316353 | |||||||
| chr12:27316411 | AC | A | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.838-924delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316411 | |||||||
| chr12:27316413 | A | G | 3 | a0001c0001t0003g0045 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.838-923A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316413 | |||||||
| chr12:27316486 | G | A | 1 | a0001c0001t0007g0224 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.838-850G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316486 | |||||||
| chr12:27316595 | A | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(112): Show |
135 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.838-741A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316595 | |||||||
| chr12:27316597 | A | C | 3 | a0001c0001t0008g0134 a0001c0001t0008g0268 a0001c0001t0008g0319 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.838-739A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316597 | |||||||
| chr12:27316607 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.838-729C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316607 | |||||||
| chr12:27316648 | G | C | 82 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(79): Show |
97 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.838-688G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316648 | |||||||
| chr12:27316807 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.838-529C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316807 | |||||||
| chr12:27316858 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.838-478C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316858 | |||||||
| chr12:27317090 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.838-246C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27317090 | |||||||
| chr12:27317272 | C | G | 1 | a0001c0001t0005g0327 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.838-64C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27317272 | |||||||
| chr12:27317556 | T | C | 20 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.955+103T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 10/13 | chr12 | 27317556 | |||||||
| chr12:27317596 | T | C | 30 | a0001c0001t0004g0004 a0001c0001t0004g0061 a0001c0001t0004g0062 others(27): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.955+143T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 10/13 | chr12 | 27317596 | |||||||
| chr12:27317749 | C | T | 260 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(257): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.956-147C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 10/13 | chr12 | 27317749 | |||||||
| chr12:27317855 | C | T | 41 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0061 others(38): Show |
44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.956-41C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 10/13 | chr12 | 27317855 | |||||||
| chr12:27318108 | G | A | 2 | a0001c0001t0003g0075 a0001c0001t0003g0076 |
2 | NA19010.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1079+89G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318108 | |||||||
| chr12:27318284 | G | C | 1 | a0001c0001t0002g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1079+265G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318284 | |||||||
| chr12:27318584 | C | T | 4 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0120 others(1): Show |
4 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079+565C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318584 | |||||||
| chr12:27318729 | T | C | 340 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(337): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1080-599T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318729 | |||||||
| chr12:27318730 | G | A | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1080-598G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318730 | |||||||
| chr12:27318788 | A | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(112): Show |
135 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.1080-540A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318788 | |||||||
| chr12:27318848 | G | A | 49 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1080-480G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318848 | |||||||
| chr12:27318851 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0002g0122 |
2 | HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1080-477C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318851 | |||||||
| chr12:27318920 | G | A | 1 | a0001c0001t0003g0100 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1080-408G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318920 | |||||||
| chr12:27318978 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1080-350G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318978 | |||||||
| chr12:27319022 | A | C | 118 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(115): Show |
120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1080-306A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27319022 | |||||||
| chr12:27319161 | G | A | 16 | a0001c0001t0005g0014 a0001c0001t0005g0131 a0001c0001t0005g0316 others(13): Show |
19 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1080-167G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27319161 | |||||||
| chr12:27319609 | G | C | 9 | a0001c0001t0003g0008 a0001c0001t0003g0053 a0001c0001t0003g0054 others(6): Show |
10 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.1175+186G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27319609 | |||||||
| chr12:27319660 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1175+237T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27319660 | |||||||
| chr12:27319803 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1175+380C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27319803 | |||||||
| chr12:27319986 | T | G | 1 | a0001c0001t0002g0232 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1175+563T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27319986 | |||||||
| chr12:27320018 | T | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(112): Show |
135 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.1175+595T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320018 | |||||||
| chr12:27320178 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1175+755C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320178 | |||||||
| chr12:27320293 | G | T | 17 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1175+870G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320293 | |||||||
| chr12:27320353 | A | C | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175+930A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320353 | |||||||
| chr12:27320384 | A | C | 117 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0039 others(114): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1175+961A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320384 | |||||||
| chr12:27320442 | A | AT | 180 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0040 others(177): Show |
198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1175+1041dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320442 | ||||||
| chr12:27320442 | A | ATT | 64 | a0001c0001t0001g0038 a0001c0001t0001g0132 a0001c0001t0001g0133 others(61): Show |
68 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1175+1040_1175+104 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320442 | ||||||
| chr12:27320442 | A | ATTT | 12 | a0001c0001t0001g0223 a0001c0001t0002g0119 a0001c0001t0003g0066 others(9): Show |
12 | HG00423.hp1 HG02040.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1175+1039_1175+104 others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320442 | ||||||
| chr12:27320442 | AT | A | 31 | a0001c0001t0004g0004 a0001c0001t0004g0061 a0001c0001t0004g0062 others(28): Show |
34 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175+1041delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320442 | ||||||
| chr12:27320445 | T | A | 1 | a0001c0001t0004g0250 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1175+1022T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320445 | |||||||
| chr12:27320561 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1175+1138G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320561 | |||||||
| chr12:27320660 | T | A | 23 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0044 others(20): Show |
23 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1175+1237T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320660 | |||||||
| chr12:27320686 | T | C | 23 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0044 others(20): Show |
23 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1175+1263T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320686 | |||||||
| chr12:27320780 | A | AT | 60 | a0001c0001t0001g0144 a0001c0001t0001g0154 a0001c0001t0001g0165 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1176-1344dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320780 | ||||||
| chr12:27320780 | AT | A | 13 | a0001c0001t0001g0139 a0001c0001t0002g0112 a0001c0001t0002g0113 others(10): Show |
14 | HG01361.hp2 HG02257.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1176-1344delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320780 | ||||||
| chr12:27320816 | C | G | 1 | a0001c0001t0002g0207 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1176-1327C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320816 | |||||||
| chr12:27320939 | C | T | 1 | a0001c0001t0006g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1176-1204C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320939 | |||||||
| chr12:27320957 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1176-1186A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320957 | |||||||
| chr12:27320984 | T | C | 2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | NA18986.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1176-1159T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320984 | |||||||
| chr12:27321359 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1176-784A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27321359 | |||||||
| chr12:27321373 | T | C | 2 | a0001c0001t0003g0099 a0001c0001t0003g0101 |
2 | HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1176-770T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27321373 | |||||||
| chr12:27321758 | T | C | 112 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(109): Show |
132 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1176-385T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27321758 |