Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8405 |
| ensemblid | ENSG00000121067.19 |
| hgncid | 11254 |
| symbol | SPOP |
| name | speckle type BTB/POZ protein |
| refseq_nuc | NM_001007228.2 |
| refseq_prot | NP_001007229.1 |
| ensembl_nuc | ENST00000504102.6 |
| ensembl_prot | ENSP00000425905.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 49598884 |
| end | 49678097 |
| strand | - |
| ver | v1.2 |
| region | chr17:49598884-49678097 |
| region5000 | chr17:49593884-49683097 |
| regionname0 | SPOP_chr17_49598884_49678097 |
| regionname5000 | SPOP_chr17_49593884_49683097 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1122 | 388 | 94 | 79 | 162 | 10 | 41 | SPOP_chr17_49593884_49683097 | SPOP | ATGTC others(1117): Show |
chr17 | 49593884 | 49683097 | ||
| a0001c0002 | 0/0 | 1122 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | ATGTC others(1117): Show |
chr17 | 49593884 | 49683097 | ||
| a0001c0003 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | ATGTC others(1117): Show |
chr17 | 49593884 | 49683097 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2850 | 112 | 33 | 23 | 40 | 1 | 14 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2845): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0002 | 0/0 | 2849 | 58 | 9 | 11 | 30 | 2 | 6 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2844): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0003 | 0/0 | 2851 | 44 | 16 | 18 | 3 | 2 | 5 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2846): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0004 | 0/0 | 2852 | 34 | 4 | 1 | 28 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2847): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0005 | 0/0 | 2852 | 34 | 1 | 5 | 25 | 0 | 3 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2847): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0006 | 0/1 | 2849 | 33 | 0 | 7 | 15 | 2 | 8 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2844): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0007 | 0/0 | 2850 | 20 | 0 | 1 | 17 | 0 | 2 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2845): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0008 | 0/0 | 2850 | 11 | 9 | 2 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2845): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0009 | 0/0 | 2849 | 8 | 6 | 1 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2844): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0010 | 0/0 | 2851 | 6 | 4 | 1 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2846): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0011 | 0/0 | 2849 | 6 | 0 | 4 | 0 | 1 | 1 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2844): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0012 | 0/0 | 2852 | 4 | 3 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2847): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0013 | 0/0 | 2851 | 3 | 1 | 0 | 0 | 1 | 1 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2846): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0014 | 0/0 | 2850 | 3 | 3 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2845): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0015 | 0/0 | 2849 | 2 | 1 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2844): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0016 | 0/0 | 2850 | 2 | 2 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2845): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0017 | 0/0 | 2852 | 2 | 0 | 0 | 2 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2847): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0018 | 0/0 | 2851 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2846): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0019 | 0/0 | 2851 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2846): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0020 | 0/0 | 2849 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2844): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0021 | 0/0 | 2851 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2846): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0022 | 0/0 | 2850 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2845): Show |
chr17 | 49593884 | 49683097 |
| a0001c0001t0023 | 0/0 | 2850 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2845): Show |
chr17 | 49593884 | 49683097 |
| a0001c0002t0003 | 0/0 | 2851 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2846): Show |
chr17 | 49593884 | 49683097 |
| a0001c0003t0001 | 0/0 | 2850 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | GACGC others(2845): Show |
chr17 | 49593884 | 49683097 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0183 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0005g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0008g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0009g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0009g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0010g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0010g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0010g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0011g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0011g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0011g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0011g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0012g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0012g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0012g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0013g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0013g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0013g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0014g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0014g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0014g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0015g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0016g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0016g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0017g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0017g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0018g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0019g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0020g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0021g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0022g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0001t0023g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| a0001c0003t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0288 | EUR | GBR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0127 | EUR | GBR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | FIN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0141 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0260 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0369 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0362 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00642 | hp2 | a0001 | c0001 | t0012 | g0287 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | CHS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0285 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0375 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0286 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0061 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0284 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0062 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01081 | hp2 | a0001 | c0001 | t0019 | g0308 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0292 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0339 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0379 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01167 | hp1 | a0001 | c0001 | t0011 | g0119 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0123 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01175 | hp1 | a0001 | c0001 | t0022 | g0022 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0310 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01243 | hp2 | a0001 | c0001 | t0015 | g0012 | AMR | PUR | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01257 | hp1 | a0001 | c0001 | t0023 | g0367 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0220 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01258 | hp1 | a0001 | c0001 | t0010 | g0366 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0300 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0322 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0146 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0102 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0023 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0374 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0376 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0294 | EUR | IBS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0031 | EUR | IBS | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0377 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01934 | hp1 | a0001 | c0001 | t0007 | g0261 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0380 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0137 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0349 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0296 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0373 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0262 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0074 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0363 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02056 | hp2 | a0001 | c0001 | t0009 | g0361 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0266 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0037 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0237 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0172 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0162 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0314 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02148 | hp2 | a0001 | c0001 | t0011 | g0126 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | CDX | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0304 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02273 | hp1 | a0001 | c0001 | t0006 | g0027 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0312 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0378 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0034 | AMR | PEL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0058 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02451 | hp2 | a0001 | c0001 | t0016 | g0327 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0291 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0281 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0365 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0193 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0060 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0344 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0318 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0057 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0068 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0306 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0035 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0368 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02698 | hp2 | a0001 | c0001 | t0013 | g0324 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02717 | hp1 | a0001 | c0001 | t0021 | g0329 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0309 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0313 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0364 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0331 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0056 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02818 | hp2 | a0001 | c0001 | t0014 | g0356 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0319 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0307 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02922 | hp2 | a0001 | c0001 | t0018 | g0326 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0080 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0343 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0067 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0371 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0355 | AFR | ESN | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0311 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0297 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0136 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0372 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0079 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03486 | hp2 | a0001 | c0001 | t0015 | g0011 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0213 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0092 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0353 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0301 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0370 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0051 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0040 | SAS | STU | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | STU | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0382 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0179 | SAS | BEB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | BEB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0043 | SAS | BEB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0053 | SAS | BEB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0206 | SAS | BEB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0042 | SAS | BEB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0024 | SAS | BEB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0381 | SAS | STU | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | STU | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | STU | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0032 | SAS | STU | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0315 | SAS | STU | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | YRI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | YRI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18612 | hp1 | a0001 | c0001 | t0017 | g0250 | EAS | CHB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | CHB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | CHB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | CHB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0328 | AFR | YRI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18941 | hp2 | a0001 | c0001 | t0007 | g0186 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18948 | hp2 | a0001 | c0001 | t0017 | g0152 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0255 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0359 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18980 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | g0265 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19009 | hp1 | a0001 | c0001 | t0007 | g0267 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0268 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | LWK | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0290 | AFR | LWK | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | LWK | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19058 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19066 | hp2 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0269 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19076 | hp1 | a0001 | c0001 | t0005 | g0134 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19076 | hp2 | a0001 | c0001 | t0006 | g0046 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0256 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19082 | hp1 | a0001 | c0001 | t0007 | g0264 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19082 | hp2 | a0001 | c0001 | t0007 | g0071 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19086 | hp2 | a0001 | c0001 | t0007 | g0258 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19087 | hp2 | a0001 | c0001 | t0020 | g0090 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0354 | AFR | YRI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ASW | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0316 | AFR | ASW | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0026 | EUR | TSI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20752 | hp2 | a0001 | c0001 | t0013 | g0325 | EUR | TSI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0293 | EUR | TSI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0360 | EUR | TSI | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | GIH | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0039 | SAS | GIH | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01123 | hp1 | a0001 | c0001 | t0011 | g0128 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0305 | AMR | CLM | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0317 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0109 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0323 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0059 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | MSL | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0302 | AFR | USA | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | USA | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | USA | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | USA | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0334 | AFR | LWK | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0350 | AFR | LWK | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0038 | REF | REF | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0183 | REF | REF | SPOP_chr17_49593884_49683097 | SPOP | chr17 | 49593884 | 49683097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:49601942 | G | A | 1 | a0001c0002 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.903C>T | p.Asn301Asn | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 9/10 | 1134/2850 | 903/1125 | 301/374 | chr17 | 49601942 | |||
| chr17:49611361 | G | A | 1 | a0001c0003 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.577C>T | p.Leu193Leu | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/10 | 808/2850 | 577/1125 | 193/374 | chr17 | 49611361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:49598924 | T | C | 1 | a0001c0001t0008 | 11 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1454A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 1454 | chr17 | 49598924 | ||||||
| chr17:49598933 | G | C | 3 | a0001c0001t0016 a0001c0001t0018 a0001c0001t0021 |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1445C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 1445 | chr17 | 49598933 | ||||||
| chr17:49599083 | G | A | 1 | a0001c0001t0013 | 3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1295C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 1295 | chr17 | 49599083 | ||||||
| chr17:49599506 | G | GT | 5 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0021 others(2): Show |
48 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*871dupA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 871 | chr17 | 49599506 | ||||||
| chr17:49599506 | G | GTT | 2 | a0001c0001t0005 a0001c0001t0012 |
38 | HG00408.hp2 HG00642.hp2 HG00673.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*870_*871dupAA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 871 | chr17 | 49599506 | ||||||
| chr17:49599506 | GT | G | 1 | a0001c0001t0009 | 8 | HG01358.hp2 HG02056.hp2 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*871delA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 871 | chr17 | 49599506 | ||||||
| chr17:49599514 | T | TG | 4 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0019 others(1): Show |
11 | HG01081.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*863_*864insC | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 863 | chr17 | 49599514 | ||||||
| chr17:49599514 | T | TTG | 2 | a0001c0001t0004 a0001c0001t0017 |
36 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*863_*864insCA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 863 | chr17 | 49599514 | ||||||
| chr17:49599516 | T | G | 2 | a0001c0001t0014 a0001c0001t0020 |
4 | HG02818.hp2 HG03195.hp2 NA19087.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*862A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 862 | chr17 | 49599516 | ||||||
| chr17:49599517 | T | G | 1 | a0001c0001t0007 | 20 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*861A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 861 | chr17 | 49599517 | ||||||
| chr17:49599517 | TG | T | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0015 others(1): Show |
67 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*860delC | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 860 | chr17 | 49599517 | ||||||
| chr17:49599518 | G | GT | 1 | a0001c0001t0001 | 7 | HG02723.hp2 HG02886.hp1 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*859dupA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 859 | chr17 | 49599518 | ||||||
| chr17:49599518 | G | T | 7 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(4): Show |
49 | HG00544.hp1 HG01106.hp2 HG01109.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*860C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 860 | chr17 | 49599518 | ||||||
| chr17:49599620 | G | A | 2 | a0001c0001t0005 a0001c0001t0017 |
36 | HG00408.hp2 HG00673.hp2 HG01256.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*758C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 758 | chr17 | 49599620 | ||||||
| chr17:49599829 | T | C | 1 | a0001c0001t0011 | 6 | HG00140.hp2 HG00642.hp1 HG01123.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*549A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 549 | chr17 | 49599829 | ||||||
| chr17:49600005 | CT | C | 3 | a0001c0001t0006 a0001c0001t0022 a0001c0001t0023 |
34 | HG00621.hp2 HG00673.hp1 HG01167.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*372delA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 372 | chr17 | 49600005 | ||||||
| chr17:49600089 | C | T | 1 | a0001c0001t0019 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*289G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 289 | chr17 | 49600089 | ||||||
| chr17:49600174 | A | G | 1 | a0001c0001t0018 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 204 | chr17 | 49600174 | ||||||
| chr17:49600354 | C | T | 1 | a0001c0001t0015 | 2 | HG01243.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*24G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 10/10 | 24 | chr17 | 49600354 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:49600728 | A | G | 1 | a0001c0001t0006g0026 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.981-206T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 9/9 | chr17 | 49600728 | |||||||
| chr17:49600946 | G | A | 1 | a0001c0001t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.981-424C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 9/9 | chr17 | 49600946 | |||||||
| chr17:49601283 | C | T | 2 | a0001c0001t0005g0004 a0001c0001t0005g0146 |
3 | HG01256.hp2 HG01258.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.980+582G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 9/9 | chr17 | 49601283 | |||||||
| chr17:49601339 | C | A | 14 | a0001c0001t0001g0341 a0001c0001t0001g0368 a0001c0001t0001g0369 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.980+526G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 9/9 | chr17 | 49601339 | |||||||
| chr17:49601684 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.980+181A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 9/9 | chr17 | 49601684 | |||||||
| chr17:49601778 | C | T | 1 | a0001c0001t0019g0308 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.980+87G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 9/9 | chr17 | 49601778 | |||||||
| chr17:49601788 | C | T | 1 | a0001c0001t0004g0182 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.980+77G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 9/9 | chr17 | 49601788 | |||||||
| chr17:49602701 | G | A | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.838-694C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49602701 | |||||||
| chr17:49602760 | TTTCAGTT others(7): Show |
T | 1 | a0001c0001t0002g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.838-767_838-754del others(14): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49602760 | |||||||
| chr17:49602844 | T | C | 1 | a0001c0001t0004g0170 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.838-837A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49602844 | |||||||
| chr17:49603141 | G | A | 12 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(9): Show |
12 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.838-1134C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49603141 | |||||||
| chr17:49603168 | C | G | 12 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(9): Show |
12 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.838-1161G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49603168 | |||||||
| chr17:49603548 | A | G | 2 | a0001c0001t0003g0297 a0001c0001t0003g0314 |
2 | HG02148.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.838-1541T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49603548 | |||||||
| chr17:49603580 | T | C | 1 | a0001c0001t0005g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.838-1573A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49603580 | |||||||
| chr17:49603693 | G | A | 1 | a0001c0001t0006g0031 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.838-1686C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49603693 | |||||||
| chr17:49603820 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0274 a0001c0001t0001g0275 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-1813C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49603820 | |||||||
| chr17:49603953 | G | A | 6 | a0001c0001t0004g0163 a0001c0001t0004g0166 a0001c0001t0004g0169 others(3): Show |
6 | HG02165.hp1 NA18977.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-1946C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49603953 | |||||||
| chr17:49604216 | T | G | 10 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(7): Show |
10 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.838-2209A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49604216 | |||||||
| chr17:49604258 | T | C | 67 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0132 others(64): Show |
67 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.838-2251A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49604258 | |||||||
| chr17:49604322 | A | G | 1 | a0001c0001t0004g0363 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.838-2315T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49604322 | |||||||
| chr17:49604694 | G | A | 1 | a0001c0001t0004g0363 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.837+2556C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49604694 | |||||||
| chr17:49604908 | T | C | 1 | a0001c0001t0006g0220 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.837+2342A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49604908 | |||||||
| chr17:49604937 | G | A | 1 | a0001c0001t0004g0140 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.837+2313C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49604937 | |||||||
| chr17:49604967 | T | C | 32 | a0001c0001t0004g0033 a0001c0001t0006g0016 a0001c0001t0006g0017 others(29): Show |
32 | HG00621.hp2 HG00673.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.837+2283A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49604967 | |||||||
| chr17:49605096 | G | A | 3 | a0001c0001t0007g0186 a0001c0001t0007g0258 a0001c0001t0007g0267 |
3 | NA18941.hp2 NA19009.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.837+2154C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605096 | |||||||
| chr17:49605111 | A | G | 1 | a0001c0001t0001g0358 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.837+2139T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605111 | |||||||
| chr17:49605218 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.837+2032A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605218 | |||||||
| chr17:49605289 | C | T | 1 | a0001c0001t0001g0380 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.837+1961G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605289 | |||||||
| chr17:49605433 | T | C | 1 | a0001c0001t0018g0326 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.837+1817A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605433 | |||||||
| chr17:49605544 | G | T | 6 | a0001c0001t0001g0236 a0001c0001t0002g0231 a0001c0001t0002g0232 others(3): Show |
6 | HG02280.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+1706C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605544 | |||||||
| chr17:49605720 | G | A | 1 | a0001c0001t0018g0326 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.837+1530C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605720 | |||||||
| chr17:49605721 | C | T | 30 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(27): Show |
31 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.837+1529G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605721 | |||||||
| chr17:49605860 | C | T | 4 | a0001c0001t0006g0020 a0001c0001t0006g0021 a0001c0001t0006g0023 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+1390G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605860 | |||||||
| chr17:49605989 | C | CA | 19 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(16): Show |
20 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.837+1260dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605989 | |||||||
| chr17:49605989 | C | G | 1 | a0001c0001t0014g0356 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.837+1261G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49605989 | |||||||
| chr17:49606003 | T | A | 8 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+1247A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49606003 | |||||||
| chr17:49606371 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.837+879C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49606371 | |||||||
| chr17:49606382 | C | T | 11 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(8): Show |
11 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+868G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49606382 | |||||||
| chr17:49606484 | G | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0189 a0001c0001t0001g0238 others(9): Show |
13 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.837+766C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49606484 | |||||||
| chr17:49606488 | CTTTTTTC others(1): Show |
C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0189 a0001c0001t0001g0238 others(9): Show |
13 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.837+754_837+761del others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49606488 | |||||||
| chr17:49606495 | CT | C | 322 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(319): Show |
328 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.837+754delA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49606495 | |||||||
| chr17:49606495 | CTT | C | 25 | a0001c0001t0001g0330 a0001c0001t0001g0341 a0001c0001t0001g0346 others(22): Show |
25 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.837+753_837+754del others(2): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49606495 | |||||||
| chr17:49606503 | T | C | 1 | a0001c0001t0006g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.837+747A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49606503 | |||||||
| chr17:49606691 | C | T | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.837+559G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 8/9 | chr17 | 49606691 | |||||||
| chr17:49607450 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.715-78C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 7/9 | chr17 | 49607450 | |||||||
| chr17:49607544 | A | C | 6 | a0001c0001t0001g0185 a0001c0001t0001g0191 a0001c0001t0001g0210 others(3): Show |
6 | NA18946.hp2 NA18961.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-172T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 7/9 | chr17 | 49607544 | |||||||
| chr17:49607570 | C | G | 1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.715-198G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 7/9 | chr17 | 49607570 | |||||||
| chr17:49607648 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0002g0063 |
2 | HG01256.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.714+226T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 7/9 | chr17 | 49607648 | |||||||
| chr17:49607688 | T | G | 83 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(80): Show |
85 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.714+186A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 7/9 | chr17 | 49607688 | |||||||
| chr17:49607838 | C | G | 2 | a0001c0001t0006g0031 a0001c0001t0006g0042 |
2 | HG01516.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.714+36G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 7/9 | chr17 | 49607838 | |||||||
| chr17:49608115 | AATAC | A | 4 | a0001c0001t0003g0025 a0001c0001t0003g0292 a0001c0001t0003g0298 others(1): Show |
4 | HG00733.hp2 HG01099.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.659-190_659-187del others(4): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608115 | |||||||
| chr17:49608302 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.659-373A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608302 | |||||||
| chr17:49608393 | C | T | 1 | a0001c0001t0006g0043 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.659-464G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608393 | |||||||
| chr17:49608409 | G | A | 1 | a0001c0001t0003g0289 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.659-480C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608409 | |||||||
| chr17:49608609 | G | T | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.659-680C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608609 | |||||||
| chr17:49608701 | C | T | 1 | a0001c0001t0005g0237 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.659-772G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608701 | |||||||
| chr17:49608803 | G | T | 1 | a0001c0001t0001g0002 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.659-874C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608803 | |||||||
| chr17:49608827 | A | G | 182 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0050 others(179): Show |
185 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.659-898T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608827 | |||||||
| chr17:49608865 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.659-936A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608865 | |||||||
| chr17:49608953 | G | C | 1 | a0001c0001t0004g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.659-1024C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49608953 | |||||||
| chr17:49609194 | C | A | 2 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.659-1265G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49609194 | |||||||
| chr17:49609286 | G | C | 5 | a0001c0001t0003g0303 a0001c0001t0012g0281 a0001c0001t0012g0287 others(2): Show |
5 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.659-1357C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49609286 | |||||||
| chr17:49609461 | G | A | 1 | a0001c0001t0003g0310 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.659-1532C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49609461 | |||||||
| chr17:49609482 | GGGA | G | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.659-1556_659-1554d others(5): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49609482 | |||||||
| chr17:49609669 | A | G | 1 | a0001c0001t0009g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.658+1611T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49609669 | |||||||
| chr17:49609761 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0154 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.658+1519C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49609761 | |||||||
| chr17:49609816 | A | G | 1 | a0001c0001t0003g0286 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.658+1464T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49609816 | |||||||
| chr17:49609969 | C | T | 1 | a0001c0001t0011g0119 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.658+1311G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49609969 | |||||||
| chr17:49610034 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.658+1246G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610034 | |||||||
| chr17:49610072 | T | C | 1 | a0001c0001t0011g0119 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.658+1208A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610072 | |||||||
| chr17:49610164 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.658+1116C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610164 | |||||||
| chr17:49610222 | G | T | 3 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 |
3 | HG01993.hp2 NA18968.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.658+1058C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610222 | |||||||
| chr17:49610292 | C | T | 1 | a0001c0001t0003g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.658+988G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610292 | |||||||
| chr17:49610366 | A | G | 69 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0175 others(66): Show |
72 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.658+914T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610366 | |||||||
| chr17:49610438 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.658+842G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610438 | |||||||
| chr17:49610807 | G | A | 5 | a0001c0001t0003g0331 a0001c0001t0003g0343 a0001c0001t0003g0344 others(2): Show |
5 | HG02615.hp2 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.658+473C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610807 | |||||||
| chr17:49610899 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.658+381A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610899 | |||||||
| chr17:49610943 | C | T | 1 | a0001c0001t0018g0326 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.658+337G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49610943 | |||||||
| chr17:49611115 | T | G | 1 | a0001c0001t0009g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.658+165A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49611115 | |||||||
| chr17:49611164 | C | T | 31 | a0001c0001t0001g0330 a0001c0001t0001g0341 a0001c0001t0001g0342 others(28): Show |
31 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.658+116G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 6/9 | chr17 | 49611164 | |||||||
| chr17:49611519 | T | TAGAG | 280 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(277): Show |
284 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.481-63_481-62insCT others(2): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49611519 | |||||||
| chr17:49611556 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-99A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49611556 | |||||||
| chr17:49611567 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0002g0063 |
2 | HG01256.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.481-110T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49611567 | |||||||
| chr17:49611669 | A | G | 1 | a0001c0001t0001g0378 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.481-212T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49611669 | |||||||
| chr17:49611886 | C | CT | 333 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(330): Show |
341 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(338): Show |
intron_variant | MODIFIER | c.481-430dupA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49611886 | |||||||
| chr17:49611886 | C | CTT | 7 | a0001c0001t0001g0236 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG02055.hp2 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-431_481-430dup others(2): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49611886 | |||||||
| chr17:49611966 | T | C | 2 | a0001c0001t0002g0203 a0001c0001t0002g0226 |
2 | NA18941.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.481-509A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49611966 | |||||||
| chr17:49612100 | G | A | 1 | a0001c0001t0006g0037 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.481-643C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49612100 | |||||||
| chr17:49612144 | A | G | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.481-687T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49612144 | |||||||
| chr17:49612702 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.481-1245G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49612702 | |||||||
| chr17:49612712 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.481-1255A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49612712 | |||||||
| chr17:49612889 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.481-1432G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49612889 | |||||||
| chr17:49612906 | A | C | 1 | a0001c0001t0007g0266 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.481-1449T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49612906 | |||||||
| chr17:49613274 | T | A | 1 | a0001c0001t0002g0234 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.481-1817A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49613274 | |||||||
| chr17:49613274 | T | TA | 7 | a0001c0001t0001g0211 a0001c0001t0002g0089 a0001c0001t0002g0105 others(4): Show |
7 | HG04115.hp2 NA18612.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1818dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49613274 | |||||||
| chr17:49613274 | TA | T | 32 | a0001c0001t0001g0187 a0001c0001t0001g0191 a0001c0001t0001g0207 others(29): Show |
32 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.481-1818delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49613274 | |||||||
| chr17:49613466 | A | G | 2 | a0001c0001t0001g0364 a0001c0001t0003g0190 |
2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.481-2009T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49613466 | |||||||
| chr17:49613681 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.481-2224A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49613681 | |||||||
| chr17:49613953 | T | C | 2 | a0001c0001t0003g0295 a0001c0001t0003g0302 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.481-2496A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49613953 | |||||||
| chr17:49614150 | A | G | 1 | a0001c0001t0003g0331 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.481-2693T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614150 | |||||||
| chr17:49614450 | T | C | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-2993A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614450 | |||||||
| chr17:49614802 | A | AGT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0073 a0001c0001t0002g0112 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-3347_481-3346d others(4): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | A | AGTGT | 11 | a0001c0001t0001g0189 a0001c0001t0001g0239 a0001c0001t0001g0270 others(8): Show |
11 | HG00642.hp2 HG01106.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.481-3349_481-3346d others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | A | AGTGTGT | 10 | a0001c0001t0001g0050 a0001c0001t0001g0241 a0001c0001t0001g0242 others(7): Show |
10 | HG02145.hp1 HG02717.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-3351_481-3346d others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | A | AGTGTGTG others(1): Show |
21 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0279 others(18): Show |
22 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.481-3353_481-3346d others(10): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | A | AGTGTGTG others(3): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0333 a0001c0001t0003g0289 others(4): Show |
8 | HG02080.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-3355_481-3346d others(12): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.481-3357_481-3346d others(14): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | A | AGTGTGTG others(7): Show |
2 | a0001c0001t0001g0332 a0001c0001t0003g0334 |
2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.481-3359_481-3346d others(16): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | AGT | A | 55 | a0001c0001t0001g0049 a0001c0001t0001g0064 a0001c0001t0001g0101 others(52): Show |
56 | HG00140.hp1 HG00408.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.481-3347_481-3346d others(4): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | AGTGT | A | 127 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0110 others(124): Show |
129 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.481-3349_481-3346d others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | AGTGTGT | A | 44 | a0001c0001t0001g0191 a0001c0001t0001g0210 a0001c0001t0001g0211 others(41): Show |
46 | HG00408.hp2 HG01256.hp2 HG01258.hp2 others(43): Show |
intron_variant | MODIFIER | c.481-3351_481-3346d others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | AGTGTGTG others(1): Show |
A | 15 | a0001c0001t0001g0336 a0001c0001t0001g0380 a0001c0001t0003g0331 others(12): Show |
15 | HG00673.hp2 HG01934.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.481-3353_481-3346d others(10): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | AGTGTGTG others(3): Show |
A | 55 | a0001c0001t0001g0330 a0001c0001t0001g0341 a0001c0001t0001g0342 others(52): Show |
55 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.481-3355_481-3346d others(12): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0001g0370 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.481-3357_481-3346d others(14): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614802 | AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0003g0293 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.481-3361_481-3346d others(18): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614802 | |||||||
| chr17:49614849 | A | G | 1 | a0001c0001t0015g0011 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.481-3392T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614849 | |||||||
| chr17:49614879 | G | T | 2 | a0001c0001t0015g0011 a0001c0001t0015g0012 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.481-3422C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49614879 | |||||||
| chr17:49615109 | T | C | 1 | a0001c0001t0006g0220 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.481-3652A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615109 | |||||||
| chr17:49615117 | C | T | 1 | a0001c0001t0005g0142 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.481-3660G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615117 | |||||||
| chr17:49615346 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.480+3635G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615346 | |||||||
| chr17:49615467 | A | T | 1 | a0001c0001t0001g0333 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.480+3514T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615467 | |||||||
| chr17:49615490 | C | CTATT | 4 | a0001c0001t0008g0061 a0001c0001t0008g0062 a0001c0001t0010g0036 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+3487_480+3490d others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615490 | |||||||
| chr17:49615516 | T | A | 11 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(8): Show |
11 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+3465A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615516 | |||||||
| chr17:49615626 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480+3355C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615626 | |||||||
| chr17:49615706 | A | G | 1 | a0001c0001t0016g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.480+3275T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615706 | |||||||
| chr17:49615729 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.480+3252A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615729 | |||||||
| chr17:49615735 | C | A | 1 | a0001c0001t0003g0198 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.480+3246G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615735 | |||||||
| chr17:49615878 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.480+3103G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615878 | |||||||
| chr17:49615905 | AATGAAGA others(20): Show |
A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0214 a0001c0001t0003g0201 |
3 | HG00323.hp2 HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.480+3049_480+3075d others(29): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49615905 | |||||||
| chr17:49616324 | G | T | 56 | a0001c0001t0001g0138 a0001c0001t0001g0175 a0001c0001t0003g0227 others(53): Show |
59 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.480+2657C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49616324 | |||||||
| chr17:49616341 | A | C | 1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.480+2640T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49616341 | |||||||
| chr17:49616944 | T | C | 1 | a0001c0001t0012g0307 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.480+2037A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49616944 | |||||||
| chr17:49617610 | T | C | 148 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(145): Show |
150 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.480+1371A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49617610 | |||||||
| chr17:49617881 | G | A | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.480+1100C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49617881 | |||||||
| chr17:49617923 | C | CA | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0110 others(19): Show |
23 | HG00642.hp2 HG01167.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.480+1057dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49617923 | |||||||
| chr17:49617923 | CA | C | 14 | a0001c0001t0001g0191 a0001c0001t0001g0196 a0001c0001t0001g0245 others(11): Show |
14 | HG01070.hp2 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.480+1057delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49617923 | |||||||
| chr17:49617949 | A | C | 1 | a0001c0001t0006g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.480+1032T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49617949 | |||||||
| chr17:49618107 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0002g0100 |
2 | NA18973.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.480+874A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618107 | |||||||
| chr17:49618120 | G | C | 5 | a0001c0001t0001g0282 a0001c0001t0002g0083 a0001c0001t0002g0095 others(2): Show |
5 | NA18747.hp2 NA18947.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+861C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618120 | |||||||
| chr17:49618161 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0209 |
2 | HG00438.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.480+820G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618161 | |||||||
| chr17:49618345 | T | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+636A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618345 | |||||||
| chr17:49618350 | G | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+631C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618350 | |||||||
| chr17:49618351 | A | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+630T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618351 | |||||||
| chr17:49618352 | A | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+629T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618352 | |||||||
| chr17:49618354 | T | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+627A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618354 | |||||||
| chr17:49618356 | T | TTAACTGA others(17): Show |
1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+624_480+625ins others(24): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618356 | |||||||
| chr17:49618365 | G | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+616C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618365 | |||||||
| chr17:49618366 | C | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+615G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618366 | |||||||
| chr17:49618371 | C | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+610G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618371 | |||||||
| chr17:49618372 | C | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+609G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618372 | |||||||
| chr17:49618373 | T | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+608A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618373 | |||||||
| chr17:49618374 | G | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+607C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618374 | |||||||
| chr17:49618377 | A | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+604T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618377 | |||||||
| chr17:49618380 | C | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+601G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618380 | |||||||
| chr17:49618382 | G | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+599C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618382 | |||||||
| chr17:49618383 | G | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+598C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618383 | |||||||
| chr17:49618388 | A | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+593T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618388 | |||||||
| chr17:49618389 | G | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+592C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618389 | |||||||
| chr17:49618392 | C | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+589G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618392 | |||||||
| chr17:49618393 | T | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+588A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618393 | |||||||
| chr17:49618394 | T | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+587A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618394 | |||||||
| chr17:49618397 | G | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+584C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618397 | |||||||
| chr17:49618403 | G | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+578C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618403 | |||||||
| chr17:49618416 | T | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+565A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618416 | |||||||
| chr17:49618426 | C | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+555G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618426 | |||||||
| chr17:49618439 | T | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+542A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618439 | |||||||
| chr17:49618444 | G | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+537C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618444 | |||||||
| chr17:49618452 | T | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+529A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618452 | |||||||
| chr17:49618454 | A | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+527T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618454 | |||||||
| chr17:49618455 | G | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+526C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618455 | |||||||
| chr17:49618477 | T | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+504A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618477 | |||||||
| chr17:49618482 | C | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+499G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618482 | |||||||
| chr17:49618486 | A | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+495T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618486 | |||||||
| chr17:49618487 | A | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+494T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618487 | |||||||
| chr17:49618489 | A | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+492T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618489 | |||||||
| chr17:49618490 | A | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+491T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618490 | |||||||
| chr17:49618494 | T | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+487A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618494 | |||||||
| chr17:49618495 | G | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+486C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618495 | |||||||
| chr17:49618496 | G | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+485C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618496 | |||||||
| chr17:49618501 | C | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+480G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618501 | |||||||
| chr17:49618503 | C | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+478G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618503 | |||||||
| chr17:49618505 | T | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+476A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618505 | |||||||
| chr17:49618506 | T | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+475A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618506 | |||||||
| chr17:49618507 | CTTATTTC others(34): Show |
C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+433_480+473del others(41): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618507 | |||||||
| chr17:49618551 | T | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+430A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618551 | |||||||
| chr17:49618560 | G | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+421C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618560 | |||||||
| chr17:49618569 | T | A | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+412A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618569 | |||||||
| chr17:49618570 | C | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+411G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618570 | |||||||
| chr17:49618571 | A | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+410T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618571 | |||||||
| chr17:49618573 | A | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+408T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618573 | |||||||
| chr17:49618574 | G | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+407C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618574 | |||||||
| chr17:49618576 | G | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+405C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618576 | |||||||
| chr17:49618577 | C | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+404G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618577 | |||||||
| chr17:49618578 | A | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+403T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618578 | |||||||
| chr17:49618580 | A | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+401T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618580 | |||||||
| chr17:49618581 | A | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+400T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618581 | |||||||
| chr17:49618583 | A | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+398T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618583 | |||||||
| chr17:49618598 | A | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+383T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618598 | |||||||
| chr17:49618602 | A | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+379T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618602 | |||||||
| chr17:49618604 | A | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+377T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618604 | |||||||
| chr17:49618606 | A | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+375T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618606 | |||||||
| chr17:49618607 | T | C | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+374A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618607 | |||||||
| chr17:49618610 | C | T | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.480+371G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618610 | |||||||
| chr17:49618708 | T | C | 19 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(16): Show |
20 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.480+273A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618708 | |||||||
| chr17:49618844 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.480+137A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 5/9 | chr17 | 49618844 | |||||||
| chr17:49619224 | GA | G | 3 | a0001c0001t0006g0031 a0001c0001t0006g0042 a0001c0001t0010g0036 |
3 | HG01516.hp2 HG02055.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.352+9delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 4/9 | chr17 | 49619224 | |||||||
| chr17:49619458 | G | A | 82 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(79): Show |
84 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.201-73C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49619458 | |||||||
| chr17:49619497 | G | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0204 a0001c0001t0001g0229 |
3 | HG00544.hp2 NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.201-112C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49619497 | |||||||
| chr17:49619504 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0006g0123 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.201-119T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49619504 | |||||||
| chr17:49619523 | T | G | 15 | a0001c0001t0001g0104 a0001c0001t0002g0069 a0001c0001t0002g0070 others(12): Show |
15 | HG00558.hp1 HG00609.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.201-138A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49619523 | |||||||
| chr17:49619571 | C | T | 82 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(79): Show |
84 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.201-186G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49619571 | |||||||
| chr17:49619577 | G | A | 19 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(16): Show |
20 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.201-192C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49619577 | |||||||
| chr17:49619957 | G | A | 1 | a0001c0001t0006g0039 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.201-572C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49619957 | |||||||
| chr17:49620105 | G | C | 1 | a0001c0001t0005g0055 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.201-720C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620105 | |||||||
| chr17:49620184 | A | G | 1 | a0001c0001t0006g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.201-799T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620184 | |||||||
| chr17:49620328 | C | A | 3 | a0001c0001t0011g0126 a0001c0001t0011g0127 a0001c0001t0011g0128 |
3 | HG00140.hp2 HG01123.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.201-943G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620328 | |||||||
| chr17:49620344 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.201-959A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620344 | |||||||
| chr17:49620365 | G | A | 1 | a0001c0001t0003g0296 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.201-980C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620365 | |||||||
| chr17:49620417 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.201-1032C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620417 | |||||||
| chr17:49620447 | G | A | 6 | a0001c0001t0001g0225 a0001c0001t0003g0025 a0001c0001t0003g0292 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.201-1062C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620447 | |||||||
| chr17:49620467 | C | CA | 15 | a0001c0001t0001g0204 a0001c0001t0001g0230 a0001c0001t0001g0333 others(12): Show |
15 | HG00642.hp1 HG01175.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.201-1083dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620467 | |||||||
| chr17:49620467 | CA | C | 9 | a0001c0001t0001g0236 a0001c0001t0002g0096 a0001c0001t0002g0231 others(6): Show |
9 | HG00544.hp1 HG02083.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.201-1083delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620467 | |||||||
| chr17:49620468 | A | C | 1 | a0001c0001t0008g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.201-1083T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620468 | |||||||
| chr17:49620519 | A | C | 2 | a0001c0001t0010g0366 a0001c0001t0023g0367 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.201-1134T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620519 | |||||||
| chr17:49620658 | T | G | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-1273A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620658 | |||||||
| chr17:49620791 | T | C | 12 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(9): Show |
12 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.200+1155A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620791 | |||||||
| chr17:49620797 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0004g0133 |
2 | NA18965.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.200+1149G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49620797 | |||||||
| chr17:49621053 | G | A | 6 | a0001c0001t0001g0236 a0001c0001t0002g0231 a0001c0001t0002g0232 others(3): Show |
6 | HG02280.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.200+893C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49621053 | |||||||
| chr17:49621168 | C | T | 1 | a0001c0001t0003g0343 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.200+778G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49621168 | |||||||
| chr17:49621241 | A | C | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.200+705T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49621241 | |||||||
| chr17:49621659 | G | C | 1 | a0001c0001t0005g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.200+287C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 3/9 | chr17 | 49621659 | |||||||
| chr17:49622949 | T | G | 31 | a0001c0001t0001g0330 a0001c0001t0001g0341 a0001c0001t0001g0342 others(28): Show |
31 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.-66-73A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49622949 | |||||||
| chr17:49622953 | G | A | 82 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(79): Show |
84 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-66-77C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49622953 | |||||||
| chr17:49623077 | G | T | 1 | a0001c0001t0001g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-66-201C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623077 | |||||||
| chr17:49623158 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-66-282G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623158 | |||||||
| chr17:49623225 | C | T | 2 | a0001c0001t0001g0368 a0001c0001t0001g0370 |
2 | HG02698.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-66-349G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623225 | |||||||
| chr17:49623434 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-66-558G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623434 | |||||||
| chr17:49623524 | C | T | 2 | a0001c0001t0003g0297 a0001c0001t0003g0314 |
2 | HG02148.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-66-648G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623524 | |||||||
| chr17:49623529 | G | T | 1 | a0001c0001t0002g0081 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-66-653C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623529 | |||||||
| chr17:49623642 | T | C | 3 | a0001c0001t0008g0316 a0001c0001t0008g0317 a0001c0001t0008g0318 |
3 | HG02109.hp1 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-66-766A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623642 | |||||||
| chr17:49623652 | C | T | 1 | a0001c0001t0003g0345 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-66-776G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623652 | |||||||
| chr17:49623788 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0189 a0001c0001t0001g0238 others(9): Show |
13 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.-66-912A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623788 | |||||||
| chr17:49623827 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-66-951C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623827 | |||||||
| chr17:49623940 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-1064C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49623940 | |||||||
| chr17:49624053 | G | A | 7 | a0001c0001t0002g0360 a0001c0001t0011g0092 a0001c0001t0011g0119 others(4): Show |
7 | HG00140.hp2 HG00642.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-66-1177C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624053 | |||||||
| chr17:49624091 | C | T | 32 | a0001c0001t0004g0033 a0001c0001t0006g0016 a0001c0001t0006g0017 others(29): Show |
32 | HG00621.hp2 HG00673.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.-66-1215G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624091 | |||||||
| chr17:49624234 | ATAC | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0277 a0001c0001t0001g0279 others(1): Show |
5 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-66-1361_-66-1359d others(5): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624234 | |||||||
| chr17:49624305 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0154 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-66-1429C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624305 | |||||||
| chr17:49624319 | A | ACG | 13 | a0001c0001t0001g0008 a0001c0001t0001g0064 a0001c0001t0001g0273 others(10): Show |
14 | HG01243.hp2 HG01255.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.-66-1445_-66-1444d others(4): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624319 | |||||||
| chr17:49624319 | A | G | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-1443T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624319 | |||||||
| chr17:49624321 | G | A | 1 | a0001c0001t0017g0250 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-66-1445C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624321 | |||||||
| chr17:49624327 | G | A | 18 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(15): Show |
19 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.-66-1451C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624327 | |||||||
| chr17:49624331 | G | A | 8 | a0001c0001t0001g0332 a0001c0001t0001g0335 a0001c0001t0001g0336 others(5): Show |
8 | HG01106.hp1 HG01884.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-66-1455C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | G | GCA | 21 | a0001c0001t0001g0154 a0001c0001t0001g0197 a0001c0001t0001g0212 others(18): Show |
21 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-66-1457_-66-1456d others(4): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | G | GCACA | 17 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(14): Show |
17 | HG00733.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-66-1459_-66-1456d others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | G | GCACACA | 12 | a0001c0001t0001g0365 a0001c0001t0002g0082 a0001c0001t0003g0288 others(9): Show |
12 | HG00140.hp1 HG01099.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.-66-1461_-66-1456d others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | G | GCACACAC others(1): Show |
3 | a0001c0001t0003g0322 a0001c0001t0010g0290 a0001c0001t0012g0287 |
3 | HG00642.hp2 HG01346.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-66-1463_-66-1456d others(10): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | G | GCGCACAC others(3): Show |
1 | a0001c0001t0016g0328 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-66-1456_-66-1455i others(12): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | G | GCGCACAC others(9): Show |
1 | a0001c0001t0018g0326 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-66-1456_-66-1455i others(18): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | GCA | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0101 others(118): Show |
123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-66-1457_-66-1456d others(4): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | GCACA | G | 38 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0239 others(35): Show |
39 | HG01109.hp1 HG01167.hp1 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.-66-1459_-66-1456d others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | GCACACA | G | 10 | a0001c0001t0001g0009 a0001c0001t0001g0369 a0001c0001t0001g0375 others(7): Show |
10 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-66-1461_-66-1456d others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | GCACACAC others(1): Show |
G | 5 | a0001c0001t0006g0017 a0001c0001t0006g0023 a0001c0001t0006g0042 others(2): Show |
5 | HG01433.hp1 HG02080.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-66-1463_-66-1456d others(10): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | GCACACAC others(3): Show |
G | 26 | a0001c0001t0004g0033 a0001c0001t0006g0016 a0001c0001t0006g0018 others(23): Show |
26 | HG00621.hp2 HG00673.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.-66-1465_-66-1456d others(12): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | GCACACAC others(5): Show |
G | 2 | a0001c0001t0006g0019 a0001c0001t0006g0039 |
2 | NA19063.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-66-1467_-66-1456d others(14): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624331 | GCACACAC others(9): Show |
G | 1 | a0001c0001t0003g0323 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-66-1471_-66-1456d others(18): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624331 | |||||||
| chr17:49624333 | A | G | 69 | a0001c0001t0001g0008 a0001c0001t0001g0132 a0001c0001t0001g0138 others(66): Show |
74 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.-66-1457T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624333 | |||||||
| chr17:49624335 | A | G | 47 | a0001c0001t0001g0189 a0001c0001t0001g0214 a0001c0001t0001g0244 others(44): Show |
48 | HG00408.hp2 HG00673.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.-66-1459T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624335 | |||||||
| chr17:49624337 | A | G | 16 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(13): Show |
16 | HG01891.hp1 HG02027.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.-66-1461T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624337 | |||||||
| chr17:49624339 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-66-1463T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624339 | |||||||
| chr17:49624341 | A | G | 1 | a0001c0001t0006g0023 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-66-1465T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624341 | |||||||
| chr17:49624343 | A | G | 2 | a0001c0001t0006g0029 a0001c0001t0006g0040 |
2 | HG03688.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-66-1467T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624343 | |||||||
| chr17:49624513 | G | C | 2 | a0001c0001t0002g0124 a0001c0001t0002g0125 |
2 | HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-66-1637C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624513 | |||||||
| chr17:49624775 | C | T | 82 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(79): Show |
84 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-66-1899G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624775 | |||||||
| chr17:49624936 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-66-2060A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49624936 | |||||||
| chr17:49625012 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-66-2136G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49625012 | |||||||
| chr17:49625351 | G | A | 20 | a0001c0001t0001g0138 a0001c0001t0001g0175 a0001c0001t0003g0227 others(17): Show |
21 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.-66-2475C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49625351 | |||||||
| chr17:49625430 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-66-2554C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49625430 | |||||||
| chr17:49625475 | G | A | 1 | a0001c0001t0006g0017 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-66-2599C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49625475 | |||||||
| chr17:49625523 | G | A | 1 | a0001c0001t0004g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-66-2647C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49625523 | |||||||
| chr17:49625672 | T | TA | 8 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-2797dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49625672 | |||||||
| chr17:49625776 | A | G | 1 | a0001c0001t0004g0176 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-66-2900T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49625776 | |||||||
| chr17:49625980 | T | A | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-3104A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49625980 | |||||||
| chr17:49626006 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0189 a0001c0001t0001g0238 others(9): Show |
13 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.-66-3130G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49626006 | |||||||
| chr17:49626043 | C | A | 1 | a0001c0001t0003g0331 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-66-3167G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49626043 | |||||||
| chr17:49626080 | G | C | 82 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(79): Show |
84 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-66-3204C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49626080 | |||||||
| chr17:49626231 | A | G | 1 | a0001c0001t0016g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-66-3355T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49626231 | |||||||
| chr17:49626592 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-66-3716C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49626592 | |||||||
| chr17:49627006 | T | C | 14 | a0001c0001t0001g0341 a0001c0001t0001g0368 a0001c0001t0001g0369 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-66-4130A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627006 | |||||||
| chr17:49627025 | G | A | 366 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(363): Show |
374 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.-66-4149C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627025 | |||||||
| chr17:49627040 | A | G | 1 | a0001c0001t0002g0086 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-66-4164T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627040 | |||||||
| chr17:49627051 | A | G | 1 | a0001c0001t0005g0172 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-66-4175T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627051 | |||||||
| chr17:49627061 | G | A | 1 | a0001c0001t0001g0379 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-66-4185C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627061 | |||||||
| chr17:49627063 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-66-4187T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627063 | |||||||
| chr17:49627084 | C | G | 1 | a0001c0001t0007g0071 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-66-4208G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627084 | |||||||
| chr17:49627133 | G | A | 2 | a0001c0001t0003g0295 a0001c0001t0003g0302 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-66-4257C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627133 | |||||||
| chr17:49627139 | A | G | 2 | a0001c0001t0003g0295 a0001c0001t0003g0302 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-66-4263T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627139 | |||||||
| chr17:49627254 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-66-4378G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627254 | |||||||
| chr17:49627494 | A | G | 19 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(16): Show |
20 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.-66-4618T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627494 | |||||||
| chr17:49627574 | C | G | 2 | a0001c0001t0005g0144 a0001c0001t0005g0237 |
2 | HG02132.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.-66-4698G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627574 | |||||||
| chr17:49627776 | T | G | 16 | a0001c0001t0001g0365 a0001c0001t0003g0025 a0001c0001t0003g0198 others(13): Show |
16 | HG00140.hp1 HG00733.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-66-4900A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627776 | |||||||
| chr17:49627903 | A | C | 68 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0132 others(65): Show |
68 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-66-5027T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49627903 | |||||||
| chr17:49628077 | C | A | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-66-5201G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49628077 | |||||||
| chr17:49628530 | C | CA | 21 | a0001c0001t0001g0270 a0001c0001t0001g0282 a0001c0001t0001g0382 others(18): Show |
22 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.-66-5655dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49628530 | |||||||
| chr17:49628530 | CA | C | 13 | a0001c0001t0001g0332 a0001c0001t0001g0335 a0001c0001t0001g0336 others(10): Show |
13 | HG01106.hp2 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-66-5655delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49628530 | |||||||
| chr17:49628742 | G | A | 1 | a0001c0001t0003g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-66-5866C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49628742 | |||||||
| chr17:49628781 | T | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-5905A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49628781 | |||||||
| chr17:49628812 | T | C | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-66-5936A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49628812 | |||||||
| chr17:49628887 | C | G | 1 | a0001c0001t0001g0191 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-66-6011G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49628887 | |||||||
| chr17:49629099 | G | A | 34 | a0001c0001t0005g0004 a0001c0001t0005g0006 a0001c0001t0005g0051 others(31): Show |
36 | HG00408.hp2 HG00673.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.-66-6223C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49629099 | |||||||
| chr17:49629325 | A | G | 1 | a0001c0001t0010g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-66-6449T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49629325 | |||||||
| chr17:49629863 | C | G | 1 | a0001c0001t0009g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-66-6987G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49629863 | |||||||
| chr17:49630032 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-66-7156A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630032 | |||||||
| chr17:49630092 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-66-7216G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630092 | |||||||
| chr17:49630184 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0257 |
2 | HG00558.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-66-7308A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630184 | |||||||
| chr17:49630261 | C | T | 2 | a0001c0001t0004g0139 a0001c0001t0004g0182 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-66-7385G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630261 | |||||||
| chr17:49630265 | T | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-7389A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630265 | |||||||
| chr17:49630462 | A | C | 1 | a0001c0001t0002g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-66-7586T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630462 | |||||||
| chr17:49630607 | C | CTTTCT | 333 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(330): Show |
341 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(338): Show |
intron_variant | MODIFIER | c.-66-7732_-66-7731i others(7): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630607 | |||||||
| chr17:49630611 | A | T | 1 | a0001c0001t0004g0130 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-66-7735T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630611 | |||||||
| chr17:49630614 | T | A | 1 | a0001c0001t0004g0130 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-66-7738A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630614 | |||||||
| chr17:49630622 | A | T | 20 | a0001c0001t0001g0270 a0001c0001t0003g0334 a0001c0001t0007g0007 others(17): Show |
21 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.-66-7746T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630622 | |||||||
| chr17:49630691 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-7815T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49630691 | |||||||
| chr17:49631187 | G | A | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-66-8311C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49631187 | |||||||
| chr17:49631187 | G | C | 1 | a0001c0001t0017g0152 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-66-8311C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49631187 | |||||||
| chr17:49631843 | T | C | 1 | a0001c0001t0014g0356 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-66-8967A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49631843 | |||||||
| chr17:49632018 | A | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-9142T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49632018 | |||||||
| chr17:49632044 | G | A | 12 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(9): Show |
12 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-66-9168C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49632044 | |||||||
| chr17:49632175 | T | A | 1 | a0001c0001t0004g0147 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-66-9299A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49632175 | |||||||
| chr17:49632326 | C | T | 1 | a0001c0001t0009g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-66-9450G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49632326 | |||||||
| chr17:49632495 | C | CT | 8 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(5): Show |
8 | HG02451.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-9620dupA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49632495 | |||||||
| chr17:49632585 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-9709G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49632585 | |||||||
| chr17:49632586 | G | A | 1 | a0001c0001t0006g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-66-9710C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49632586 | |||||||
| chr17:49632777 | A | G | 1 | a0001c0001t0003g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-66-9901T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49632777 | |||||||
| chr17:49633543 | A | G | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-10667T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49633543 | |||||||
| chr17:49633614 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-66-10738T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49633614 | |||||||
| chr17:49633841 | C | T | 11 | a0001c0001t0001g0332 a0001c0001t0001g0335 a0001c0001t0001g0336 others(8): Show |
11 | HG01106.hp2 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-66-10965G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49633841 | |||||||
| chr17:49633858 | G | C | 1 | a0001c0001t0010g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-66-10982C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49633858 | |||||||
| chr17:49633872 | T | C | 1 | a0001c0001t0007g0264 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-66-10996A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49633872 | |||||||
| chr17:49633897 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-66-11021C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49633897 | |||||||
| chr17:49634016 | T | TA | 20 | a0001c0001t0001g0204 a0001c0001t0001g0217 a0001c0001t0001g0238 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.-66-11141dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49634016 | |||||||
| chr17:49634085 | C | T | 1 | a0001c0001t0003g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-66-11209G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49634085 | |||||||
| chr17:49634106 | T | C | 47 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0116 others(44): Show |
48 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-66-11230A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49634106 | |||||||
| chr17:49634522 | C | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-11646G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49634522 | |||||||
| chr17:49634673 | A | T | 1 | a0001c0001t0002g0076 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-66-11797T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49634673 | |||||||
| chr17:49634766 | C | T | 19 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(16): Show |
20 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.-66-11890G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49634766 | |||||||
| chr17:49634976 | T | C | 277 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(274): Show |
281 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.-66-12100A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49634976 | |||||||
| chr17:49635065 | T | C | 1 | a0001c0001t0012g0281 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-66-12189A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49635065 | |||||||
| chr17:49635632 | C | CT | 84 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(81): Show |
84 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.-66-12757dupA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49635632 | |||||||
| chr17:49635658 | G | A | 2 | a0001c0001t0005g0173 a0001c0001t0017g0152 |
2 | HG02027.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-66-12782C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49635658 | |||||||
| chr17:49635658 | G | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-12782C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49635658 | |||||||
| chr17:49635698 | G | C | 4 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0001g0230 others(1): Show |
4 | HG01261.hp2 HG02155.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-12822C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49635698 | |||||||
| chr17:49635751 | C | T | 6 | a0001c0001t0001g0236 a0001c0001t0002g0231 a0001c0001t0002g0232 others(3): Show |
6 | HG02280.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-66-12875G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49635751 | |||||||
| chr17:49635794 | T | C | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-66-12918A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49635794 | |||||||
| chr17:49635815 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-66-12939C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49635815 | |||||||
| chr17:49635897 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0154 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-66-13021C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49635897 | |||||||
| chr17:49636074 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-13198G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49636074 | |||||||
| chr17:49636207 | A | G | 1 | a0001c0001t0001g0008 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-66-13331T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49636207 | |||||||
| chr17:49636640 | A | G | 1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-66-13764T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49636640 | |||||||
| chr17:49636811 | T | C | 2 | a0001c0001t0004g0065 a0001c0001t0004g0161 |
2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-66-13935A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49636811 | |||||||
| chr17:49636983 | T | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-14107A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49636983 | |||||||
| chr17:49637216 | C | G | 1 | a0001c0001t0001g0002 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-66-14340G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49637216 | |||||||
| chr17:49637508 | G | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-66-14632C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49637508 | |||||||
| chr17:49637588 | T | C | 1 | a0001c0001t0003g0198 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-66-14712A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49637588 | |||||||
| chr17:49637630 | C | T | 5 | a0001c0001t0003g0331 a0001c0001t0003g0343 a0001c0001t0003g0344 others(2): Show |
5 | HG02615.hp2 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-66-14754G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49637630 | |||||||
| chr17:49637724 | AC | A | 4 | a0001c0001t0007g0261 a0001c0001t0007g0262 a0001c0001t0007g0263 others(1): Show |
4 | HG01934.hp1 HG02040.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-14849delG | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49637724 | |||||||
| chr17:49637910 | C | T | 56 | a0001c0001t0001g0138 a0001c0001t0001g0175 a0001c0001t0003g0227 others(53): Show |
59 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-66-15034G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49637910 | |||||||
| chr17:49637971 | G | C | 19 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(16): Show |
20 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.-66-15095C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49637971 | |||||||
| chr17:49638197 | T | A | 3 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 |
3 | HG01993.hp2 NA18968.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-66-15321A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49638197 | |||||||
| chr17:49638458 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-66-15582C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49638458 | |||||||
| chr17:49638495 | A | G | 3 | a0001c0001t0001g0351 a0001c0001t0001g0352 a0001c0001t0001g0353 |
3 | HG01081.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-66-15619T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49638495 | |||||||
| chr17:49638578 | T | C | 345 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(342): Show |
353 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(350): Show |
intron_variant | MODIFIER | c.-66-15702A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49638578 | |||||||
| chr17:49638583 | CA | C | 327 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(324): Show |
335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.-66-15708delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49638583 | |||||||
| chr17:49638817 | G | A | 1 | a0001c0001t0005g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-66-15941C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49638817 | |||||||
| chr17:49638948 | A | G | 276 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(273): Show |
280 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.-66-16072T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49638948 | |||||||
| chr17:49638957 | G | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-16081C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49638957 | |||||||
| chr17:49638983 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-16107G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49638983 | |||||||
| chr17:49639100 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-16224T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49639100 | |||||||
| chr17:49639267 | A | C | 1 | a0001c0001t0002g0086 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-66-16391T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49639267 | |||||||
| chr17:49639471 | ACAAT | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0277 a0001c0001t0001g0279 others(1): Show |
5 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-66-16599_-66-1659 others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49639471 | |||||||
| chr17:49639510 | G | T | 1 | a0001c0001t0001g0270 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-66-16634C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49639510 | |||||||
| chr17:49639547 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-16671T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49639547 | |||||||
| chr17:49639872 | GT | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0225 a0001c0001t0001g0238 others(9): Show |
13 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.-66-16997delA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49639872 | |||||||
| chr17:49639899 | A | G | 1 | a0001c0001t0003g0286 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-66-17023T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49639899 | |||||||
| chr17:49639998 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-66-17122G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49639998 | |||||||
| chr17:49640040 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-66-17164T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49640040 | |||||||
| chr17:49640060 | G | T | 3 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0171 |
3 | NA18977.hp1 NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-66-17184C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49640060 | |||||||
| chr17:49640369 | A | T | 111 | a0001c0001t0001g0009 a0001c0001t0001g0064 a0001c0001t0001g0101 others(108): Show |
113 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-66-17493T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49640369 | |||||||
| chr17:49640429 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-66-17553A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49640429 | |||||||
| chr17:49640723 | A | C | 1 | a0001c0001t0001g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-66-17847T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49640723 | |||||||
| chr17:49640799 | C | T | 1 | a0001c0001t0003g0313 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-66-17923G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49640799 | |||||||
| chr17:49640826 | A | G | 275 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(272): Show |
279 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.-66-17950T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49640826 | |||||||
| chr17:49641108 | C | T | 146 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(143): Show |
148 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.-66-18232G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641108 | |||||||
| chr17:49641149 | G | C | 1 | a0001c0001t0001g0013 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-66-18273C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641149 | |||||||
| chr17:49641263 | C | CA | 31 | a0001c0001t0001g0104 a0001c0001t0001g0116 a0001c0001t0001g0189 others(28): Show |
31 | HG00558.hp1 HG01106.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-66-18388dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641263 | |||||||
| chr17:49641263 | CA | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0050 others(196): Show |
206 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.-66-18388delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641263 | |||||||
| chr17:49641264 | A | C | 3 | a0001c0001t0001g0236 a0001c0001t0002g0234 a0001c0001t0002g0235 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-66-18388T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641264 | |||||||
| chr17:49641482 | C | A | 1 | a0001c0001t0004g0130 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-66-18606G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641482 | |||||||
| chr17:49641532 | G | A | 2 | a0001c0001t0005g0173 a0001c0001t0017g0152 |
2 | HG02027.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-66-18656C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641532 | |||||||
| chr17:49641749 | C | T | 1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-66-18873G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641749 | |||||||
| chr17:49641755 | C | T | 2 | a0001c0001t0015g0011 a0001c0001t0015g0012 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-66-18879G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641755 | |||||||
| chr17:49641880 | G | A | 2 | a0001c0001t0002g0252 a0001c0001t0004g0174 |
2 | NA18952.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-66-19004C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641880 | |||||||
| chr17:49641901 | T | C | 1 | a0001c0001t0009g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-66-19025A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49641901 | |||||||
| chr17:49642021 | G | T | 1 | a0001c0001t0001g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-66-19145C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642021 | |||||||
| chr17:49642074 | G | A | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-66-19198C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642074 | |||||||
| chr17:49642085 | C | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-19209G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642085 | |||||||
| chr17:49642183 | A | G | 1 | a0001c0001t0006g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-66-19307T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642183 | |||||||
| chr17:49642211 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-66-19335T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642211 | |||||||
| chr17:49642252 | A | C | 1 | a0001c0001t0004g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-66-19376T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642252 | |||||||
| chr17:49642335 | G | A | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0180 |
3 | NA18956.hp1 NA18957.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-66-19459C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642335 | |||||||
| chr17:49642422 | G | A | 11 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0141 others(8): Show |
11 | HG00408.hp2 HG00673.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-66-19546C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642422 | |||||||
| chr17:49642593 | T | A | 1 | a0001c0001t0006g0043 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-66-19717A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642593 | |||||||
| chr17:49642623 | C | T | 6 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(3): Show |
6 | HG01358.hp2 HG02109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-66-19747G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642623 | |||||||
| chr17:49642665 | C | T | 2 | a0001c0001t0015g0011 a0001c0001t0015g0012 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-66-19789G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642665 | |||||||
| chr17:49642736 | T | C | 141 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(138): Show |
143 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.-66-19860A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642736 | |||||||
| chr17:49642800 | T | C | 1 | a0001c0001t0001g0378 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-66-19924A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642800 | |||||||
| chr17:49642854 | G | T | 1 | a0001c0001t0011g0119 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-66-19978C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642854 | |||||||
| chr17:49642884 | T | G | 1 | a0001c0001t0004g0140 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-66-20008A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642884 | |||||||
| chr17:49642889 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0221 a0001c0001t0003g0198 |
3 | HG00741.hp1 HG00741.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-66-20013A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642889 | |||||||
| chr17:49642933 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-66-20057C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49642933 | |||||||
| chr17:49643003 | C | T | 2 | a0001c0001t0005g0144 a0001c0001t0005g0237 |
2 | HG02132.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.-66-20127G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643003 | |||||||
| chr17:49643259 | G | T | 3 | a0001c0001t0001g0104 a0001c0001t0002g0085 a0001c0001t0002g0252 |
3 | NA18985.hp2 NA18993.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-66-20383C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643259 | |||||||
| chr17:49643261 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0257 |
2 | HG00558.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-66-20385A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643261 | |||||||
| chr17:49643387 | A | G | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-66-20511T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643387 | |||||||
| chr17:49643457 | C | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-20581G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643457 | |||||||
| chr17:49643577 | TAAG | T | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-66-20704_-66-2070 others(7): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643577 | |||||||
| chr17:49643650 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0245 a0001c0001t0001g0246 others(2): Show |
5 | HG01070.hp2 HG01943.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.-66-20774C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643650 | |||||||
| chr17:49643653 | A | G | 334 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(331): Show |
342 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(339): Show |
intron_variant | MODIFIER | c.-66-20777T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643653 | |||||||
| chr17:49643702 | G | C | 1 | a0001c0001t0007g0255 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-66-20826C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643702 | |||||||
| chr17:49643706 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-20830C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643706 | |||||||
| chr17:49643821 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-66-20945A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643821 | |||||||
| chr17:49643932 | G | GA | 24 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(21): Show |
24 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-66-21057dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643932 | |||||||
| chr17:49643950 | A | T | 1 | a0001c0001t0006g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-66-21074T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49643950 | |||||||
| chr17:49644101 | C | G | 1 | a0001c0001t0006g0039 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-66-21225G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49644101 | |||||||
| chr17:49644264 | C | T | 1 | a0001c0001t0010g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-66-21388G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49644264 | |||||||
| chr17:49644647 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0209 |
2 | HG00438.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-66-21771C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49644647 | |||||||
| chr17:49644782 | G | T | 1 | a0001c0001t0019g0308 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-66-21906C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49644782 | |||||||
| chr17:49644927 | T | C | 3 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 |
3 | HG02647.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-66-22051A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49644927 | |||||||
| chr17:49645031 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-66-22155A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645031 | |||||||
| chr17:49645066 | T | C | 3 | a0001c0001t0006g0017 a0001c0001t0006g0018 a0001c0001t0006g0028 |
3 | HG00621.hp2 HG02080.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-66-22190A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645066 | |||||||
| chr17:49645143 | T | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-22267A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645143 | |||||||
| chr17:49645200 | C | G | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-22324G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645200 | |||||||
| chr17:49645270 | A | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-22394T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645270 | |||||||
| chr17:49645323 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0006g0123 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-66-22447C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645323 | |||||||
| chr17:49645363 | G | A | 1 | a0001c0001t0004g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-66-22487C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645363 | |||||||
| chr17:49645547 | G | A | 1 | a0001c0001t0005g0172 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-66-22671C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645547 | |||||||
| chr17:49645564 | G | A | 1 | a0001c0001t0006g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-66-22688C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645564 | |||||||
| chr17:49645574 | C | A | 1 | a0001c0001t0007g0255 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-66-22698G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645574 | |||||||
| chr17:49645587 | G | A | 12 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(9): Show |
12 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-66-22711C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645587 | |||||||
| chr17:49645642 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-66-22766A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645642 | |||||||
| chr17:49645867 | CTGT | C | 114 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(111): Show |
116 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.-66-22994_-66-2299 others(7): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645867 | |||||||
| chr17:49645948 | A | AT | 5 | a0001c0001t0003g0331 a0001c0001t0003g0343 a0001c0001t0003g0344 others(2): Show |
5 | HG02615.hp2 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-66-23073dupA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49645948 | |||||||
| chr17:49646082 | T | C | 1 | a0001c0001t0005g0137 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-66-23206A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646082 | |||||||
| chr17:49646161 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-66-23285G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646161 | |||||||
| chr17:49646249 | T | G | 2 | a0001c0001t0008g0058 a0001c0001t0008g0059 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-66-23373A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646249 | |||||||
| chr17:49646290 | G | A | 11 | a0001c0001t0001g0116 a0001c0001t0002g0077 a0001c0001t0002g0111 others(8): Show |
11 | HG00639.hp2 HG00738.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-66-23414C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646290 | |||||||
| chr17:49646292 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-23416C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646292 | |||||||
| chr17:49646488 | C | T | 7 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-66-23612G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646488 | |||||||
| chr17:49646519 | C | CA | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(4): Show |
7 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-66-23644dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646519 | |||||||
| chr17:49646519 | CA | C | 10 | a0001c0001t0001g0189 a0001c0001t0001g0195 a0001c0001t0002g0075 others(7): Show |
10 | HG00323.hp2 HG02698.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.-66-23644delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646519 | |||||||
| chr17:49646533 | A | AAG | 14 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(11): Show |
14 | HG01106.hp2 HG01884.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-66-23659_-66-2365 others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646533 | |||||||
| chr17:49646818 | T | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-23942A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646818 | |||||||
| chr17:49646850 | C | T | 34 | a0001c0001t0005g0004 a0001c0001t0005g0006 a0001c0001t0005g0051 others(31): Show |
36 | HG00408.hp2 HG00673.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.-66-23974G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646850 | |||||||
| chr17:49646898 | A | T | 1 | a0001c0001t0005g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-66-24022T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646898 | |||||||
| chr17:49646977 | G | C | 1 | a0001c0001t0008g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-66-24101C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49646977 | |||||||
| chr17:49647115 | C | A | 34 | a0001c0001t0001g0167 a0001c0001t0001g0185 a0001c0001t0001g0187 others(31): Show |
34 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-66-24239G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647115 | |||||||
| chr17:49647195 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-66-24319G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647195 | |||||||
| chr17:49647223 | G | A | 2 | a0001c0001t0003g0301 a0001c0001t0003g0313 |
2 | HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-66-24347C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647223 | |||||||
| chr17:49647259 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-24383C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647259 | |||||||
| chr17:49647267 | G | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-24391C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647267 | |||||||
| chr17:49647297 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-66-24421C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647297 | |||||||
| chr17:49647305 | T | C | 335 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(332): Show |
343 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.-66-24429A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647305 | |||||||
| chr17:49647308 | C | T | 1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-66-24432G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647308 | |||||||
| chr17:49647312 | T | C | 1 | a0001c0001t0001g0377 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-66-24436A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647312 | |||||||
| chr17:49647313 | T | TA | 87 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0154 others(84): Show |
90 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-66-24438dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647313 | |||||||
| chr17:49647313 | T | TAA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0217 a0001c0001t0001g0254 others(16): Show |
20 | HG00673.hp2 HG01358.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.-66-24439_-66-2443 others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647313 | |||||||
| chr17:49647313 | TA | T | 59 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 others(56): Show |
59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-66-24438delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647313 | |||||||
| chr17:49647313 | TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0002g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-66-24451_-66-2443 others(18): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647313 | |||||||
| chr17:49647313 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-24452_-66-2443 others(19): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647313 | |||||||
| chr17:49647447 | C | T | 1 | a0001c0003t0001g0349 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-66-24571G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647447 | |||||||
| chr17:49647476 | A | T | 2 | a0001c0001t0005g0173 a0001c0001t0005g0184 |
2 | HG02027.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.-66-24600T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647476 | |||||||
| chr17:49647549 | C | T | 1 | a0001c0001t0003g0298 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-66-24673G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647549 | |||||||
| chr17:49647735 | C | A | 19 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(16): Show |
20 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.-66-24859G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647735 | |||||||
| chr17:49647819 | C | T | 346 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(343): Show |
354 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(351): Show |
intron_variant | MODIFIER | c.-66-24943G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49647819 | |||||||
| chr17:49648023 | T | A | 1 | a0001c0001t0002g0233 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-66-25147A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49648023 | |||||||
| chr17:49648130 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-66-25254A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49648130 | |||||||
| chr17:49648883 | G | A | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-66-26007C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49648883 | |||||||
| chr17:49648982 | C | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0189 a0001c0001t0001g0225 others(10): Show |
14 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-66-26106G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49648982 | |||||||
| chr17:49649096 | G | A | 4 | a0001c0001t0008g0311 a0001c0001t0008g0316 a0001c0001t0008g0317 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-26220C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649096 | |||||||
| chr17:49649265 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-66-26389G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649265 | |||||||
| chr17:49649331 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-66-26455C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649331 | |||||||
| chr17:49649472 | G | A | 1 | a0001c0001t0020g0090 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-66-26596C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649472 | |||||||
| chr17:49649608 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-26732T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649608 | |||||||
| chr17:49649625 | C | T | 3 | a0001c0001t0001g0351 a0001c0001t0001g0352 a0001c0001t0001g0353 |
3 | HG01081.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-66-26749G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649625 | |||||||
| chr17:49649653 | C | T | 1 | a0001c0001t0003g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-66-26777G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649653 | |||||||
| chr17:49649662 | T | C | 3 | a0001c0001t0002g0070 a0001c0001t0002g0098 a0001c0001t0004g0099 |
3 | NA18945.hp2 NA18950.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.-66-26786A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649662 | |||||||
| chr17:49649793 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0004g0253 |
2 | NA18969.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-66-26917G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649793 | |||||||
| chr17:49649945 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-27069T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649945 | |||||||
| chr17:49649947 | A | G | 2 | a0001c0001t0008g0058 a0001c0001t0008g0059 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-66-27071T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49649947 | |||||||
| chr17:49650027 | G | T | 1 | a0001c0001t0002g0091 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-66-27151C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650027 | |||||||
| chr17:49650028 | A | T | 1 | a0001c0001t0002g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-66-27152T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650028 | |||||||
| chr17:49650110 | T | C | 21 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(18): Show |
21 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.-66-27234A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650110 | |||||||
| chr17:49650235 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-66-27359C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650235 | |||||||
| chr17:49650288 | T | C | 1 | a0001c0001t0002g0089 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-66-27412A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650288 | |||||||
| chr17:49650631 | G | A | 16 | a0001c0001t0007g0007 a0001c0001t0007g0186 a0001c0001t0007g0255 others(13): Show |
17 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.-67+27302C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650631 | |||||||
| chr17:49650682 | A | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+27251T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650682 | |||||||
| chr17:49650737 | T | C | 143 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(140): Show |
145 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.-67+27196A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650737 | |||||||
| chr17:49650774 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-67+27159A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650774 | |||||||
| chr17:49650900 | T | C | 1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-67+27033A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49650900 | |||||||
| chr17:49651197 | A | G | 70 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0132 others(67): Show |
70 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-67+26736T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49651197 | |||||||
| chr17:49651241 | G | C | 70 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0132 others(67): Show |
70 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-67+26692C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49651241 | |||||||
| chr17:49651496 | C | T | 2 | a0001c0001t0003g0301 a0001c0001t0003g0313 |
2 | HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-67+26437G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49651496 | |||||||
| chr17:49651761 | G | A | 3 | a0001c0001t0011g0126 a0001c0001t0011g0127 a0001c0001t0011g0128 |
3 | HG00140.hp2 HG01123.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-67+26172C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49651761 | |||||||
| chr17:49651880 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0277 a0001c0001t0001g0279 others(1): Show |
5 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67+26053C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49651880 | |||||||
| chr17:49651888 | G | A | 2 | a0001c0001t0008g0058 a0001c0001t0008g0059 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-67+26045C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49651888 | |||||||
| chr17:49651974 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0002g0100 |
2 | NA18973.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-67+25959C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49651974 | |||||||
| chr17:49652276 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0002g0252 |
2 | HG02809.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-67+25657A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49652276 | |||||||
| chr17:49652644 | C | A | 18 | a0001c0001t0001g0365 a0001c0001t0003g0025 a0001c0001t0003g0286 others(15): Show |
18 | HG00140.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.-67+25289G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49652644 | |||||||
| chr17:49652866 | A | C | 4 | a0001c0001t0007g0261 a0001c0001t0007g0262 a0001c0001t0007g0263 others(1): Show |
4 | HG01934.hp1 HG02040.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+25067T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49652866 | |||||||
| chr17:49652907 | A | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0122 |
2 | NA18967.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-67+25026T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49652907 | |||||||
| chr17:49652950 | A | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0254 |
2 | HG01099.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-67+24983T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49652950 | |||||||
| chr17:49653027 | C | G | 1 | a0001c0001t0006g0037 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-67+24906G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49653027 | |||||||
| chr17:49653210 | T | A | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-67+24723A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49653210 | |||||||
| chr17:49653347 | G | C | 2 | a0001c0001t0003g0295 a0001c0001t0003g0302 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-67+24586C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49653347 | |||||||
| chr17:49653499 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-67+24434G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49653499 | |||||||
| chr17:49653611 | T | G | 1 | a0001c0001t0003g0286 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-67+24322A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49653611 | |||||||
| chr17:49653820 | A | G | 1 | a0001c0001t0020g0090 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-67+24113T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49653820 | |||||||
| chr17:49653853 | A | G | 2 | a0001c0001t0003g0283 a0001c0001t0003g0284 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-67+24080T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49653853 | |||||||
| chr17:49653969 | A | G | 12 | a0001c0001t0001g0365 a0001c0001t0003g0025 a0001c0001t0003g0292 others(9): Show |
12 | HG00733.hp2 HG01099.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.-67+23964T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49653969 | |||||||
| chr17:49654202 | G | C | 2 | a0001c0001t0001g0101 a0001c0001t0002g0100 |
2 | NA18973.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-67+23731C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49654202 | |||||||
| chr17:49654388 | C | A | 3 | a0001c0001t0005g0162 a0001c0001t0005g0249 a0001c0001t0017g0250 |
3 | HG02135.hp1 NA18612.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-67+23545G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49654388 | |||||||
| chr17:49654600 | C | T | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-67+23333G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49654600 | |||||||
| chr17:49654848 | A | C | 1 | a0001c0001t0006g0040 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-67+23085T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49654848 | |||||||
| chr17:49655079 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+22854T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49655079 | |||||||
| chr17:49655419 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-67+22514C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49655419 | |||||||
| chr17:49655433 | C | T | 12 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(9): Show |
12 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-67+22500G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49655433 | |||||||
| chr17:49655498 | G | A | 1 | a0001c0001t0012g0281 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-67+22435C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49655498 | |||||||
| chr17:49655587 | C | A | 6 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(3): Show |
6 | HG01358.hp2 HG02109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67+22346G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49655587 | |||||||
| chr17:49655818 | A | C | 1 | a0001c0001t0008g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-67+22115T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49655818 | |||||||
| chr17:49655819 | T | A | 3 | a0001c0001t0001g0167 a0001c0001t0005g0153 a0001c0001t0005g0159 |
3 | NA18947.hp2 NA18998.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-67+22114A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49655819 | |||||||
| chr17:49655927 | C | T | 9 | a0001c0001t0001g0167 a0001c0001t0001g0188 a0001c0001t0001g0194 others(6): Show |
9 | HG00408.hp1 HG00438.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-67+22006G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49655927 | |||||||
| chr17:49656031 | C | T | 30 | a0001c0001t0001g0330 a0001c0001t0001g0341 a0001c0001t0001g0342 others(27): Show |
30 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-67+21902G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49656031 | |||||||
| chr17:49656042 | C | T | 2 | a0001c0001t0003g0297 a0001c0001t0003g0314 |
2 | HG02148.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-67+21891G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49656042 | |||||||
| chr17:49656485 | A | C | 5 | a0001c0001t0003g0331 a0001c0001t0003g0343 a0001c0001t0003g0344 others(2): Show |
5 | HG02615.hp2 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67+21448T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49656485 | |||||||
| chr17:49656574 | AC | A | 21 | a0001c0001t0001g0138 a0001c0001t0001g0154 a0001c0001t0001g0175 others(18): Show |
22 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-67+21358delG | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49656574 | |||||||
| chr17:49656696 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-67+21237T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49656696 | |||||||
| chr17:49657057 | C | T | 1 | a0001c0001t0005g0151 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-67+20876G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657057 | |||||||
| chr17:49657058 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-67+20875C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657058 | |||||||
| chr17:49657059 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-67+20874G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657059 | |||||||
| chr17:49657130 | AGCCGAGA others(4): Show |
A | 3 | a0001c0001t0002g0103 a0001c0001t0015g0011 a0001c0001t0015g0012 |
3 | HG01243.hp2 HG03486.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-67+20792_-67+2080 others(15): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657130 | |||||||
| chr17:49657134 | G | C | 1 | a0001c0001t0004g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-67+20799C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657134 | |||||||
| chr17:49657153 | G | A | 2 | a0001c0001t0007g0193 a0001c0001t0007g0206 |
2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-67+20780C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657153 | |||||||
| chr17:49657468 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-67+20465C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657468 | |||||||
| chr17:49657614 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-67+20319C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657614 | |||||||
| chr17:49657643 | C | T | 1 | a0001c0003t0001g0349 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-67+20290G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657643 | |||||||
| chr17:49657686 | C | T | 1 | a0001c0001t0003g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-67+20247G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657686 | |||||||
| chr17:49657696 | C | CT | 79 | a0001c0001t0001g0185 a0001c0001t0001g0204 a0001c0001t0001g0205 others(76): Show |
82 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-67+20236dupA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657696 | |||||||
| chr17:49657696 | CT | C | 30 | a0001c0001t0003g0303 a0001c0001t0003g0331 a0001c0001t0004g0033 others(27): Show |
30 | HG00673.hp1 HG01168.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.-67+20236delA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657696 | |||||||
| chr17:49657696 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0004g0155 a0001c0001t0013g0312 a0001c0001t0013g0324 others(1): Show |
4 | HG02071.hp2 HG02280.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+20226_-67+2023 others(15): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657696 | |||||||
| chr17:49657761 | C | T | 4 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+20172G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657761 | |||||||
| chr17:49657783 | T | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+20150A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657783 | |||||||
| chr17:49657848 | C | T | 1 | a0001c0001t0005g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-67+20085G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657848 | |||||||
| chr17:49657922 | C | A | 1 | a0001c0001t0017g0250 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-67+20011G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657922 | |||||||
| chr17:49657993 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+19940C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49657993 | |||||||
| chr17:49658309 | T | C | 4 | a0001c0001t0002g0105 a0001c0001t0002g0108 a0001c0001t0002g0122 others(1): Show |
4 | NA18612.hp2 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+19624A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658309 | |||||||
| chr17:49658452 | C | G | 1 | a0001c0001t0006g0027 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-67+19481G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658452 | |||||||
| chr17:49658470 | A | C | 1 | a0001c0001t0003g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-67+19463T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658470 | |||||||
| chr17:49658511 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-67+19422T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658511 | |||||||
| chr17:49658646 | G | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+19287C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658646 | |||||||
| chr17:49658654 | G | A | 12 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(9): Show |
12 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-67+19279C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658654 | |||||||
| chr17:49658660 | T | G | 1 | a0001c0001t0003g0201 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-67+19273A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658660 | |||||||
| chr17:49658695 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-67+19238T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658695 | |||||||
| chr17:49658719 | C | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+19214G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658719 | |||||||
| chr17:49658916 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-67+19017G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49658916 | |||||||
| chr17:49659007 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-67+18926T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659007 | |||||||
| chr17:49659163 | A | G | 11 | a0001c0001t0001g0341 a0001c0001t0001g0369 a0001c0001t0001g0373 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67+18770T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659163 | |||||||
| chr17:49659234 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0001c0001t0004g0133 |
3 | HG03098.hp1 NA18965.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-67+18699G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659234 | |||||||
| chr17:49659257 | G | A | 1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-67+18676C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659257 | |||||||
| chr17:49659293 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-67+18640T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659293 | |||||||
| chr17:49659294 | A | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+18639T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659294 | |||||||
| chr17:49659425 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+18508C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659425 | |||||||
| chr17:49659481 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+18452G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659481 | |||||||
| chr17:49659673 | G | A | 4 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0340 others(1): Show |
4 | HG01106.hp2 HG02486.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+18260C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659673 | |||||||
| chr17:49659701 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+18232G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659701 | |||||||
| chr17:49659974 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-67+17959G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49659974 | |||||||
| chr17:49660021 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+17912G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660021 | |||||||
| chr17:49660040 | G | GCAGAGAT others(134): Show |
1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-67+17892_-67+1789 others(145): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660040 | |||||||
| chr17:49660067 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-67+17866C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660067 | |||||||
| chr17:49660294 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+17639A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660294 | |||||||
| chr17:49660367 | T | C | 346 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(343): Show |
354 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(351): Show |
intron_variant | MODIFIER | c.-67+17566A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660367 | |||||||
| chr17:49660443 | C | T | 3 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 |
3 | HG01993.hp2 NA18968.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-67+17490G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660443 | |||||||
| chr17:49660482 | C | T | 1 | a0001c0001t0003g0227 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-67+17451G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660482 | |||||||
| chr17:49660587 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+17346G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660587 | |||||||
| chr17:49660740 | G | A | 108 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(105): Show |
110 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.-67+17193C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660740 | |||||||
| chr17:49660897 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-67+17036G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660897 | |||||||
| chr17:49660952 | C | A | 1 | a0001c0001t0001g0378 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-67+16981G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49660952 | |||||||
| chr17:49661129 | C | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+16804G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49661129 | |||||||
| chr17:49661184 | C | T | 32 | a0001c0001t0004g0033 a0001c0001t0006g0016 a0001c0001t0006g0017 others(29): Show |
32 | HG00621.hp2 HG00673.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.-67+16749G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49661184 | |||||||
| chr17:49661209 | A | C | 1 | a0001c0001t0005g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-67+16724T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49661209 | |||||||
| chr17:49661347 | CTCT | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+16583_-67+1658 others(7): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49661347 | |||||||
| chr17:49661576 | A | G | 1 | a0001c0001t0005g0172 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-67+16357T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49661576 | |||||||
| chr17:49661680 | A | G | 82 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(79): Show |
84 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-67+16253T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49661680 | |||||||
| chr17:49661698 | T | C | 2 | a0001c0001t0015g0011 a0001c0001t0015g0012 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-67+16235A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49661698 | |||||||
| chr17:49661881 | T | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+16052A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49661881 | |||||||
| chr17:49661942 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+15991C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49661942 | |||||||
| chr17:49662013 | CA | C | 94 | a0001c0001t0001g0104 a0001c0001t0001g0132 a0001c0001t0001g0138 others(91): Show |
97 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-67+15919delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662013 | |||||||
| chr17:49662013 | CAA | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(260): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.-67+15918_-67+1591 others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662013 | |||||||
| chr17:49662013 | CAAA | C | 14 | a0001c0001t0001g0187 a0001c0001t0001g0257 a0001c0001t0001g0282 others(11): Show |
14 | HG01169.hp1 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-67+15917_-67+1591 others(7): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662013 | |||||||
| chr17:49662152 | T | G | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+15781A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662152 | |||||||
| chr17:49662162 | C | G | 115 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(112): Show |
117 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.-67+15771G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662162 | |||||||
| chr17:49662398 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+15535G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662398 | |||||||
| chr17:49662498 | A | G | 1 | a0001c0001t0003g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-67+15435T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662498 | |||||||
| chr17:49662591 | G | A | 4 | a0001c0001t0002g0105 a0001c0001t0002g0108 a0001c0001t0002g0122 others(1): Show |
4 | NA18612.hp2 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+15342C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662591 | |||||||
| chr17:49662602 | G | A | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+15331C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662602 | |||||||
| chr17:49662673 | G | C | 13 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(10): Show |
13 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-67+15260C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662673 | |||||||
| chr17:49662846 | A | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+15087T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662846 | |||||||
| chr17:49662903 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+15030T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49662903 | |||||||
| chr17:49663150 | A | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+14783T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49663150 | |||||||
| chr17:49663274 | A | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+14659T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49663274 | |||||||
| chr17:49663401 | G | C | 1 | a0001c0001t0003g0345 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-67+14532C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49663401 | |||||||
| chr17:49663450 | G | A | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-67+14483C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49663450 | |||||||
| chr17:49663614 | A | C | 2 | a0001c0001t0001g0371 a0001c0001t0001g0372 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-67+14319T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49663614 | |||||||
| chr17:49663689 | T | C | 1 | a0001c0001t0003g0198 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-67+14244A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49663689 | |||||||
| chr17:49663795 | T | G | 1 | a0001c0001t0006g0037 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-67+14138A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49663795 | |||||||
| chr17:49664041 | A | G | 1 | a0001c0001t0003g0321 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-67+13892T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664041 | |||||||
| chr17:49664057 | T | C | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+13876A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664057 | |||||||
| chr17:49664337 | T | G | 3 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0021g0329 |
3 | HG02451.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-67+13596A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664337 | |||||||
| chr17:49664490 | A | G | 11 | a0001c0001t0003g0289 a0001c0001t0003g0320 a0001c0001t0003g0321 others(8): Show |
11 | HG01346.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67+13443T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664490 | |||||||
| chr17:49664632 | C | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0189 a0001c0001t0001g0225 others(10): Show |
14 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-67+13301G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664632 | |||||||
| chr17:49664683 | A | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+13250T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664683 | |||||||
| chr17:49664715 | G | A | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+13218C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664715 | |||||||
| chr17:49664730 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-67+13203G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664730 | |||||||
| chr17:49664915 | T | C | 30 | a0001c0001t0001g0330 a0001c0001t0001g0341 a0001c0001t0001g0342 others(27): Show |
30 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-67+13018A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664915 | |||||||
| chr17:49664922 | G | A | 3 | a0001c0001t0005g0149 a0001c0001t0005g0150 a0001c0001t0005g0181 |
3 | HG00673.hp2 HG02071.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-67+13011C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664922 | |||||||
| chr17:49664994 | A | G | 3 | a0001c0001t0014g0354 a0001c0001t0014g0355 a0001c0001t0014g0356 |
3 | HG02818.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-67+12939T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49664994 | |||||||
| chr17:49665136 | T | C | 59 | a0001c0001t0001g0138 a0001c0001t0001g0154 a0001c0001t0001g0175 others(56): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-67+12797A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665136 | |||||||
| chr17:49665277 | T | C | 72 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0132 others(69): Show |
72 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-67+12656A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665277 | |||||||
| chr17:49665338 | G | A | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+12595C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665338 | |||||||
| chr17:49665341 | G | A | 1 | a0001c0001t0005g0173 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-67+12592C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665341 | |||||||
| chr17:49665386 | G | A | 4 | a0001c0001t0004g0182 a0001c0001t0013g0312 a0001c0001t0013g0324 others(1): Show |
4 | HG02280.hp2 HG02698.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+12547C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665386 | |||||||
| chr17:49665431 | A | G | 2 | a0001c0001t0003g0295 a0001c0001t0003g0302 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-67+12502T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665431 | |||||||
| chr17:49665442 | G | A | 1 | a0001c0001t0003g0293 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-67+12491C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665442 | |||||||
| chr17:49665479 | G | T | 58 | a0001c0001t0001g0138 a0001c0001t0001g0154 a0001c0001t0001g0175 others(55): Show |
61 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.-67+12454C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665479 | |||||||
| chr17:49665484 | A | G | 1 | a0001c0001t0010g0291 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-67+12449T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665484 | |||||||
| chr17:49665532 | G | A | 1 | a0001c0001t0010g0291 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-67+12401C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665532 | |||||||
| chr17:49665649 | G | GAC | 56 | a0001c0001t0001g0073 a0001c0001t0001g0138 a0001c0001t0001g0191 others(53): Show |
58 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-67+12282_-67+1228 others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACAC | 27 | a0001c0001t0001g0002 a0001c0001t0001g0175 a0001c0001t0001g0211 others(24): Show |
27 | HG00544.hp1 HG00735.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-67+12280_-67+1228 others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACAC | 25 | a0001c0001t0001g0132 a0001c0001t0001g0154 a0001c0001t0001g0210 others(22): Show |
25 | HG00544.hp2 HG01069.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.-67+12278_-67+1228 others(10): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(1): Show |
27 | a0001c0001t0001g0002 a0001c0001t0001g0187 a0001c0001t0001g0192 others(24): Show |
27 | HG00558.hp2 HG01261.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.-67+12276_-67+1228 others(12): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(3): Show |
22 | a0001c0001t0001g0185 a0001c0001t0001g0194 a0001c0001t0001g0195 others(19): Show |
22 | HG00323.hp2 HG00438.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-67+12274_-67+1228 others(14): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(5): Show |
8 | a0001c0001t0001g0167 a0001c0001t0001g0223 a0001c0001t0003g0198 others(5): Show |
8 | HG00673.hp1 HG00741.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67+12272_-67+1228 others(16): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(7): Show |
13 | a0001c0001t0001g0188 a0001c0001t0001g0207 a0001c0001t0001g0209 others(10): Show |
13 | HG00408.hp1 HG00621.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.-67+12270_-67+1228 others(18): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(9): Show |
5 | a0001c0001t0001g0200 a0001c0001t0001g0246 a0001c0001t0006g0028 others(2): Show |
5 | HG01943.hp1 NA18980.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67+12268_-67+1228 others(20): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(11): Show |
3 | a0001c0001t0006g0030 a0001c0001t0006g0031 a0001c0001t0006g0034 |
3 | HG01516.hp2 HG02027.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-67+12266_-67+1228 others(22): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(13): Show |
6 | a0001c0001t0001g0197 a0001c0001t0001g0221 a0001c0001t0006g0016 others(3): Show |
6 | HG00741.hp2 HG02004.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67+12264_-67+1228 others(24): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(15): Show |
4 | a0001c0001t0001g0202 a0001c0001t0001g0208 a0001c0001t0006g0039 others(1): Show |
4 | HG02280.hp2 NA18971.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+12262_-67+1228 others(26): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(17): Show |
1 | a0001c0001t0006g0037 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-67+12260_-67+1228 others(28): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | G | GACACACA others(19): Show |
2 | a0001c0001t0006g0019 a0001c0001t0006g0024 |
2 | HG03942.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-67+12258_-67+1228 others(30): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | GAC | G | 7 | a0001c0001t0001g0049 a0001c0001t0001g0238 a0001c0001t0001g0243 others(4): Show |
7 | HG01884.hp1 HG02132.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+12282_-67+1228 others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | GACAC | G | 12 | a0001c0001t0001g0189 a0001c0001t0001g0225 a0001c0001t0001g0239 others(9): Show |
12 | HG01069.hp2 HG01071.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.-67+12280_-67+1228 others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | GACACAC | G | 19 | a0001c0001t0001g0008 a0001c0001t0001g0277 a0001c0001t0001g0279 others(16): Show |
20 | HG01106.hp2 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-67+12278_-67+1228 others(10): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | GACACACA others(1): Show |
G | 6 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 others(3): Show |
6 | HG01993.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67+12276_-67+1228 others(12): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | GACACACA others(3): Show |
G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0274 a0001c0001t0001g0275 others(32): Show |
36 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-67+12274_-67+1228 others(14): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | GACACACA others(5): Show |
G | 74 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(71): Show |
75 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-67+12272_-67+1228 others(16): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | GACACACA others(7): Show |
G | 1 | a0001c0001t0001g0368 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-67+12270_-67+1228 others(18): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665649 | GACACACA others(9): Show |
G | 4 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+12268_-67+1228 others(20): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665649 | |||||||
| chr17:49665655 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-67+12278G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665655 | |||||||
| chr17:49665659 | C | G | 1 | a0001c0001t0002g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-67+12274G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665659 | |||||||
| chr17:49665699 | T | A | 32 | a0001c0001t0004g0033 a0001c0001t0006g0016 a0001c0001t0006g0017 others(29): Show |
32 | HG00621.hp2 HG00673.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.-67+12234A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665699 | |||||||
| chr17:49665722 | T | G | 13 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(10): Show |
13 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-67+12211A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665722 | |||||||
| chr17:49665755 | G | A | 1 | a0001c0001t0003g0322 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-67+12178C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665755 | |||||||
| chr17:49665784 | G | C | 1 | a0001c0001t0009g0361 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-67+12149C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665784 | |||||||
| chr17:49665978 | C | CA | 17 | a0001c0001t0001g0110 a0001c0001t0001g0219 a0001c0001t0001g0270 others(14): Show |
17 | HG01109.hp1 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-67+11954dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665978 | |||||||
| chr17:49665996 | T | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0073 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+11937A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49665996 | |||||||
| chr17:49666077 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-67+11856G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666077 | |||||||
| chr17:49666115 | A | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+11818T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666115 | |||||||
| chr17:49666161 | A | G | 17 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(14): Show |
18 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.-67+11772T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666161 | |||||||
| chr17:49666448 | G | GAC | 15 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0001g0215 others(12): Show |
16 | HG01952.hp2 HG02015.hp1 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.-67+11483_-67+1148 others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666448 | |||||||
| chr17:49666448 | G | GACAC | 8 | a0001c0001t0001g0175 a0001c0001t0001g0185 a0001c0001t0001g0218 others(5): Show |
8 | HG01261.hp2 HG01516.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.-67+11481_-67+1148 others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666448 | |||||||
| chr17:49666448 | GAC | G | 70 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0132 others(67): Show |
72 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.-67+11483_-67+1148 others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666448 | |||||||
| chr17:49666448 | GACAC | G | 59 | a0001c0001t0001g0116 a0001c0001t0001g0194 a0001c0001t0001g0195 others(56): Show |
59 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.-67+11481_-67+1148 others(8): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666448 | |||||||
| chr17:49666448 | GACACAC | G | 44 | a0001c0001t0001g0013 a0001c0001t0001g0110 a0001c0001t0001g0138 others(41): Show |
44 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.-67+11479_-67+1148 others(10): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666448 | |||||||
| chr17:49666448 | GACACACA others(1): Show |
G | 105 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(102): Show |
107 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.-67+11477_-67+1148 others(12): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666448 | |||||||
| chr17:49666448 | GACACACA others(3): Show |
G | 9 | a0001c0001t0002g0001 a0001c0001t0002g0063 a0001c0001t0006g0019 others(6): Show |
10 | HG01243.hp2 HG01256.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-67+11475_-67+1148 others(14): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666448 | |||||||
| chr17:49666448 | GACACACA others(5): Show |
G | 2 | a0001c0001t0007g0260 a0001c0001t0009g0079 |
2 | HG00544.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-67+11473_-67+1148 others(16): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666448 | |||||||
| chr17:49666448 | GACACACA others(9): Show |
G | 1 | a0001c0001t0003g0078 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-67+11469_-67+1148 others(20): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666448 | |||||||
| chr17:49666452 | C | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0189 a0001c0001t0001g0277 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67+11481G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666452 | |||||||
| chr17:49666454 | C | G | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+11479G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666454 | |||||||
| chr17:49666456 | C | G | 5 | a0001c0001t0003g0278 a0001c0001t0007g0261 a0001c0001t0007g0262 others(2): Show |
5 | HG01934.hp1 HG02040.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67+11477G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666456 | |||||||
| chr17:49666460 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-67+11473G>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666460 | |||||||
| chr17:49666493 | A | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0212 a0001c0001t0001g0223 others(2): Show |
5 | HG02602.hp2 HG03710.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67+11440T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666493 | |||||||
| chr17:49666503 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+11430C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666503 | |||||||
| chr17:49666521 | G | A | 2 | a0001c0001t0010g0366 a0001c0001t0023g0367 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-67+11412C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666521 | |||||||
| chr17:49666593 | C | T | 1 | a0001c0001t0005g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-67+11340G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666593 | |||||||
| chr17:49666763 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-67+11170C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666763 | |||||||
| chr17:49666783 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+11150C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666783 | |||||||
| chr17:49666977 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-67+10956C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49666977 | |||||||
| chr17:49667115 | T | C | 1 | a0001c0001t0005g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-67+10818A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667115 | |||||||
| chr17:49667149 | G | A | 1 | a0001c0002t0003g0315 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-67+10784C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667149 | |||||||
| chr17:49667178 | T | TA | 109 | a0001c0001t0001g0013 a0001c0001t0001g0132 a0001c0001t0001g0167 others(106): Show |
110 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-67+10754dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667178 | |||||||
| chr17:49667178 | T | TAA | 7 | a0001c0001t0001g0009 a0001c0001t0001g0219 a0001c0001t0001g0364 others(4): Show |
7 | HG02622.hp1 HG02738.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+10753_-67+1075 others(6): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667178 | |||||||
| chr17:49667178 | TA | T | 22 | a0001c0001t0001g0073 a0001c0001t0001g0238 a0001c0001t0001g0341 others(19): Show |
22 | HG01069.hp2 HG01070.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-67+10754delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667178 | |||||||
| chr17:49667243 | A | T | 3 | a0001c0001t0010g0074 a0001c0001t0015g0011 a0001c0001t0015g0012 |
3 | HG01243.hp2 HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-67+10690T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667243 | |||||||
| chr17:49667293 | T | TA | 44 | a0001c0001t0001g0221 a0001c0001t0003g0289 a0001c0001t0003g0320 others(41): Show |
44 | HG00621.hp2 HG00673.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.-67+10639dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667293 | |||||||
| chr17:49667293 | TA | T | 26 | a0001c0001t0001g0270 a0001c0001t0002g0226 a0001c0001t0005g0134 others(23): Show |
27 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.-67+10639delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667293 | |||||||
| chr17:49667417 | T | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+10516A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667417 | |||||||
| chr17:49667450 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+10483C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667450 | |||||||
| chr17:49667476 | C | A | 1 | a0001c0001t0001g0364 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-67+10457G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667476 | |||||||
| chr17:49667513 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-67+10420A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667513 | |||||||
| chr17:49667516 | G | A | 3 | a0001c0001t0013g0312 a0001c0001t0013g0324 a0001c0001t0013g0325 |
3 | HG02280.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-67+10417C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667516 | |||||||
| chr17:49667533 | G | A | 12 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(9): Show |
12 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-67+10400C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667533 | |||||||
| chr17:49667931 | G | A | 81 | a0001c0001t0001g0064 a0001c0001t0001g0101 a0001c0001t0001g0104 others(78): Show |
83 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-67+10002C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667931 | |||||||
| chr17:49667940 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-67+9993A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667940 | |||||||
| chr17:49667947 | A | C | 1 | a0001c0001t0009g0361 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-67+9986T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49667947 | |||||||
| chr17:49668004 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+9929T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668004 | |||||||
| chr17:49668393 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-67+9540G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668393 | |||||||
| chr17:49668431 | A | T | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+9502T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668431 | |||||||
| chr17:49668472 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0004g0133 |
2 | NA18965.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-67+9461T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668472 | |||||||
| chr17:49668595 | A | G | 17 | a0001c0001t0001g0270 a0001c0001t0007g0007 a0001c0001t0007g0186 others(14): Show |
18 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.-67+9338T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668595 | |||||||
| chr17:49668596 | T | G | 1 | a0001c0001t0002g0251 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-67+9337A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668596 | |||||||
| chr17:49668746 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-67+9187C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668746 | |||||||
| chr17:49668759 | T | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+9174A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668759 | |||||||
| chr17:49668771 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0274 a0001c0001t0001g0275 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+9162T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668771 | |||||||
| chr17:49668774 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-67+9159A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668774 | |||||||
| chr17:49668775 | C | CT | 20 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(17): Show |
20 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-67+9157dupA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668775 | |||||||
| chr17:49668775 | CT | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG01243.hp1 HG01257.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67+9157delA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668775 | |||||||
| chr17:49668839 | C | T | 1 | a0001c0001t0003g0288 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-67+9094G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668839 | |||||||
| chr17:49668943 | A | T | 1 | a0001c0001t0002g0251 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-67+8990T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668943 | |||||||
| chr17:49668980 | G | A | 1 | a0001c0001t0005g0173 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-67+8953C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668980 | |||||||
| chr17:49668981 | T | A | 1 | a0001c0001t0004g0174 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-67+8952A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668981 | |||||||
| chr17:49668989 | G | A | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-67+8944C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49668989 | |||||||
| chr17:49669021 | C | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-67+8912G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669021 | |||||||
| chr17:49669062 | C | T | 1 | a0001c0001t0005g0359 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-67+8871G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669062 | |||||||
| chr17:49669067 | C | T | 1 | a0001c0001t0007g0071 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-67+8866G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669067 | |||||||
| chr17:49669075 | CT | C | 335 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(332): Show |
343 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.-67+8857delA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669075 | |||||||
| chr17:49669228 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-67+8705C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669228 | |||||||
| chr17:49669297 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-67+8636G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669297 | |||||||
| chr17:49669429 | TA | T | 89 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0154 others(86): Show |
92 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-67+8503delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669429 | |||||||
| chr17:49669465 | TA | T | 6 | a0001c0001t0001g0245 a0001c0001t0001g0274 a0001c0001t0003g0283 others(3): Show |
6 | HG01069.hp1 HG01070.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67+8467delT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669465 | |||||||
| chr17:49669466 | A | T | 1 | a0001c0001t0003g0289 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-67+8467T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669466 | |||||||
| chr17:49669690 | G | A | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-67+8243C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669690 | |||||||
| chr17:49669701 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-67+8232C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669701 | |||||||
| chr17:49669763 | C | CA | 285 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0049 others(282): Show |
292 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.-67+8169dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669763 | |||||||
| chr17:49669763 | C | CAA | 71 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(68): Show |
71 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-67+8168_-67+8169d others(4): Show |
SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669763 | |||||||
| chr17:49669922 | A | AT | 71 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0154 others(68): Show |
74 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.-67+8010dupA | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49669922 | |||||||
| chr17:49670187 | T | G | 1 | a0001c0001t0012g0281 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-67+7746A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49670187 | |||||||
| chr17:49670286 | C | T | 115 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0101 others(112): Show |
117 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.-67+7647G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49670286 | |||||||
| chr17:49670296 | T | C | 1 | a0001c0001t0006g0048 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-67+7637A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49670296 | |||||||
| chr17:49670593 | T | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+7340A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49670593 | |||||||
| chr17:49670826 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-67+7107T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49670826 | |||||||
| chr17:49670982 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-67+6951G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49670982 | |||||||
| chr17:49671107 | A | C | 1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-67+6826T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671107 | |||||||
| chr17:49671213 | C | T | 1 | a0001c0001t0002g0001 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-67+6720G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671213 | |||||||
| chr17:49671388 | T | C | 6 | a0001c0001t0001g0236 a0001c0001t0002g0231 a0001c0001t0002g0232 others(3): Show |
6 | HG02280.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67+6545A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671388 | |||||||
| chr17:49671530 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-67+6403G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671530 | |||||||
| chr17:49671551 | G | A | 1 | a0001c0001t0005g0237 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-67+6382C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671551 | |||||||
| chr17:49671561 | G | A | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+6372C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671561 | |||||||
| chr17:49671694 | C | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0245 a0001c0001t0001g0246 others(2): Show |
5 | HG01070.hp2 HG01943.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67+6239G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671694 | |||||||
| chr17:49671774 | G | A | 2 | a0001c0001t0005g0249 a0001c0001t0017g0250 |
2 | NA18612.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-67+6159C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671774 | |||||||
| chr17:49671867 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+6066T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671867 | |||||||
| chr17:49671982 | T | C | 1 | a0001c0001t0002g0251 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-67+5951A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49671982 | |||||||
| chr17:49672286 | T | C | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+5647A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49672286 | |||||||
| chr17:49672523 | C | T | 1 | a0001c0001t0009g0361 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-67+5410G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49672523 | |||||||
| chr17:49672613 | G | T | 1 | a0001c0001t0004g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-67+5320C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49672613 | |||||||
| chr17:49672682 | C | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01884.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-67+5251G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49672682 | |||||||
| chr17:49672723 | A | G | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+5210T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49672723 | |||||||
| chr17:49672899 | A | T | 1 | a0001c0001t0006g0017 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-67+5034T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49672899 | |||||||
| chr17:49672947 | G | GA | 20 | a0001c0001t0001g0254 a0001c0001t0001g0257 a0001c0001t0001g0270 others(17): Show |
21 | HG00544.hp1 HG01934.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.-67+4985dupT | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49672947 | |||||||
| chr17:49673199 | T | A | 1 | a0001c0001t0008g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-67+4734A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673199 | |||||||
| chr17:49673215 | T | C | 2 | a0001c0001t0008g0061 a0001c0001t0008g0062 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-67+4718A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673215 | |||||||
| chr17:49673224 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+4709C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673224 | |||||||
| chr17:49673234 | G | A | 3 | a0001c0001t0014g0354 a0001c0001t0014g0355 a0001c0001t0014g0356 |
3 | HG02818.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-67+4699C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673234 | |||||||
| chr17:49673321 | T | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG02015.hp1 HG02083.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-67+4612A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673321 | |||||||
| chr17:49673374 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0002g0063 |
2 | HG01256.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-67+4559G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673374 | |||||||
| chr17:49673438 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0274 a0001c0001t0001g0275 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+4495C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673438 | |||||||
| chr17:49673461 | G | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+4472C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673461 | |||||||
| chr17:49673470 | C | T | 7 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+4463G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673470 | |||||||
| chr17:49673659 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-67+4274T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49673659 | |||||||
| chr17:49674006 | C | T | 1 | a0001c0001t0005g0055 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-67+3927G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49674006 | |||||||
| chr17:49674153 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-67+3780T>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49674153 | |||||||
| chr17:49674157 | T | A | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+3776A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49674157 | |||||||
| chr17:49674538 | T | C | 1 | a0001c0001t0003g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-67+3395A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49674538 | |||||||
| chr17:49674745 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0277 a0001c0001t0001g0279 others(1): Show |
5 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67+3188C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49674745 | |||||||
| chr17:49674789 | G | T | 1 | a0001c0001t0006g0016 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-67+3144C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49674789 | |||||||
| chr17:49675043 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-67+2890G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675043 | |||||||
| chr17:49675117 | T | G | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+2816A>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675117 | |||||||
| chr17:49675170 | A | G | 3 | a0001c0001t0005g0051 a0001c0001t0005g0052 a0001c0001t0005g0053 |
3 | HG01981.hp2 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-67+2763T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675170 | |||||||
| chr17:49675238 | T | C | 1 | a0001c0001t0006g0043 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-67+2695A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675238 | |||||||
| chr17:49675253 | G | T | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+2680C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675253 | |||||||
| chr17:49675307 | T | C | 5 | a0001c0001t0006g0044 a0001c0001t0006g0045 a0001c0001t0006g0046 others(2): Show |
5 | NA18959.hp1 NA18962.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67+2626A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675307 | |||||||
| chr17:49675407 | A | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01884.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-67+2526T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675407 | |||||||
| chr17:49675434 | T | A | 1 | a0001c0001t0004g0280 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-67+2499A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675434 | |||||||
| chr17:49675458 | G | C | 45 | a0001c0001t0001g0365 a0001c0001t0003g0283 a0001c0001t0003g0284 others(42): Show |
45 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-67+2475C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675458 | |||||||
| chr17:49675567 | A | G | 32 | a0001c0001t0003g0025 a0001c0001t0004g0033 a0001c0001t0006g0016 others(29): Show |
32 | HG00621.hp2 HG00673.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.-67+2366T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675567 | |||||||
| chr17:49675575 | A | G | 2 | a0001c0001t0003g0015 a0001c0001t0004g0010 |
2 | NA18948.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-67+2358T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675575 | |||||||
| chr17:49675630 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-67+2303G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675630 | |||||||
| chr17:49675770 | A | G | 1 | a0001c0001t0001g0368 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-67+2163T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49675770 | |||||||
| chr17:49676097 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-67+1836A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49676097 | |||||||
| chr17:49676257 | G | A | 44 | a0001c0001t0001g0365 a0001c0001t0003g0283 a0001c0001t0003g0284 others(41): Show |
44 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.-67+1676C>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49676257 | |||||||
| chr17:49676365 | T | C | 4 | a0001c0001t0003g0320 a0001c0001t0003g0321 a0001c0001t0003g0322 others(1): Show |
4 | HG01346.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+1568A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49676365 | |||||||
| chr17:49676439 | G | T | 1 | a0001c0001t0001g0013 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-67+1494C>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49676439 | |||||||
| chr17:49676551 | T | A | 2 | a0001c0001t0013g0324 a0001c0001t0013g0325 |
2 | HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-67+1382A>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49676551 | |||||||
| chr17:49676562 | G | C | 4 | a0001c0001t0016g0327 a0001c0001t0016g0328 a0001c0001t0018g0326 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+1371C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49676562 | |||||||
| chr17:49676837 | T | C | 42 | a0001c0001t0001g0330 a0001c0001t0001g0332 a0001c0001t0001g0333 others(39): Show |
42 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-67+1096A>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49676837 | |||||||
| chr17:49677146 | A | G | 2 | a0001c0001t0015g0011 a0001c0001t0015g0012 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-67+787T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49677146 | |||||||
| chr17:49677213 | C | A | 1 | a0001c0001t0002g0357 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-67+720G>T | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49677213 | |||||||
| chr17:49677271 | A | G | 1 | a0001c0001t0002g0360 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-67+662T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49677271 | |||||||
| chr17:49677389 | A | G | 1 | a0001c0001t0005g0359 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-67+544T>C | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49677389 | |||||||
| chr17:49677588 | A | C | 1 | a0001c0001t0004g0010 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-67+345T>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49677588 | |||||||
| chr17:49677654 | G | C | 1 | a0001c0001t0001g0382 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-67+279C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49677654 | |||||||
| chr17:49677695 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-67+238G>A | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49677695 | |||||||
| chr17:49677796 | G | C | 1 | a0001c0001t0001g0358 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-67+137C>G | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49677796 | |||||||
| chr17:49677875 | G | GC | 24 | a0001c0001t0001g0364 a0001c0001t0001g0365 a0001c0001t0001g0368 others(21): Show |
24 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.-67+57dupG | SPOP | ENSG00000121067.19 | transcript | ENST00000504102.6 | protein_coding | 1/9 | chr17 | 49677875 |