Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5746 |
| ensemblid | ENSG00000144407.10 |
| hgncid | 9609 |
| symbol | PTH2R |
| name | parathyroid hormone 2 receptor |
| refseq_nuc | NM_005048.4 |
| refseq_prot | NP_005039.1 |
| ensembl_nuc | ENST00000272847.7 |
| ensembl_prot | ENSP00000272847.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 208406792 |
| end | 208494506 |
| strand | + |
| ver | v1.2 |
| region | chr2:208406792-208494506 |
| region5000 | chr2:208401792-208499506 |
| regionname0 | PTH2R_chr2_208406792_208494506 |
| regionname5000 | PTH2R_chr2_208401792_208499506 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 550 | 281 | 79 | 30 | 126 | 11 | 33 | 92 | PTH2R_chr2_208401792_208499506 | PTH2R | MAGLG others(545): Show |
chr2 | 208401792 | 208499506 |
| a0002 | 0/0 | 550 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | MAGLG others(545): Show |
chr2 | 208401792 | 208499506 |
| a0003 | 0/0 | 550 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | MAGLG others(545): Show |
chr2 | 208401792 | 208499506 |
| a0004 | 0/0 | 550 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PTH2R_chr2_208401792_208499506 | PTH2R | MAGLG others(545): Show |
chr2 | 208401792 | 208499506 |
| a0005 | 0/0 | 81 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | MAGLG others(76): Show |
chr2 | 208401792 | 208499506 |
| a0006 | 0/0 | 550 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | MAGLG others(545): Show |
chr2 | 208401792 | 208499506 |
| a0007 | 0/0 | 550 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | MAGLG others(545): Show |
chr2 | 208401792 | 208499506 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1650 | 149 | 29 | 17 | 76 | 7 | 19 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0001c0002 | 1/0 | 1650 | 84 | 15 | 6 | 47 | 2 | 13 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0001c0003 | 0/0 | 1650 | 42 | 30 | 7 | 2 | 2 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0001c0006 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0001c0008 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0001c0010 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0001c0011 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0002c0004 | 0/0 | 1650 | 5 | 5 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0003c0005 | 0/0 | 1650 | 3 | 0 | 2 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0004c0007 | 0/0 | 1650 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0005c0009 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0006c0012 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 | ||
| a0007c0013 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | ATGGC others(1645): Show |
chr2 | 208401792 | 208499506 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2753 | 121 | 18 | 15 | 67 | 6 | 14 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2748): Show |
chr2 | 208401792 | 208499506 |
| a0001c0001t0003 | 0/0 | 2752 | 23 | 8 | 2 | 8 | 1 | 4 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0001t0005 | 0/0 | 2752 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0001t0006 | 0/0 | 2752 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0001t0007 | 0/0 | 2753 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2748): Show |
chr2 | 208401792 | 208499506 |
| a0001c0001t0010 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2748): Show |
chr2 | 208401792 | 208499506 |
| a0001c0002t0002 | 1/0 | 2752 | 83 | 14 | 6 | 47 | 2 | 13 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0002t0008 | 0/0 | 2752 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0003t0003 | 0/0 | 2752 | 41 | 29 | 7 | 2 | 2 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0003t0009 | 0/0 | 2752 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0006t0001 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2748): Show |
chr2 | 208401792 | 208499506 |
| a0001c0006t0005 | 0/0 | 2752 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0008t0003 | 0/0 | 2752 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0010t0002 | 0/0 | 2752 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0001c0011t0004 | 0/0 | 2752 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0002c0004t0004 | 0/0 | 2752 | 5 | 5 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0003c0005t0002 | 0/0 | 2752 | 3 | 0 | 2 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0004c0007t0001 | 0/0 | 2753 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2748): Show |
chr2 | 208401792 | 208499506 |
| a0005c0009t0001 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2748): Show |
chr2 | 208401792 | 208499506 |
| a0006c0012t0003 | 0/0 | 2752 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2747): Show |
chr2 | 208401792 | 208499506 |
| a0007c0013t0001 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | AGGAC others(2748): Show |
chr2 | 208401792 | 208499506 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0001t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0002t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0003t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0006t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0006t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0008t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0008t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0010t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0001c0011t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0002c0004t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0002c0004t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0002c0004t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0002c0004t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0002c0004t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0003c0005t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0003c0005t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0003c0005t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0004c0007t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0005c0009t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0006c0012t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| a0007c0013t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | GBR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0051 | EUR | GBR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0041 | EUR | GBR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00280 | hp1 | a0001 | c0003 | t0003 | g0264 | EUR | FIN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00735 | hp1 | a0001 | c0003 | t0003 | g0015 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01069 | hp2 | a0001 | c0003 | t0003 | g0012 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0076 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0015 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0267 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0269 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0094 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01255 | hp1 | a0003 | c0005 | t0002 | g0050 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01261 | hp1 | a0001 | c0003 | t0003 | g0270 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01261 | hp2 | a0003 | c0005 | t0002 | g0049 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01433 | hp2 | a0001 | c0003 | t0003 | g0034 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0266 | EUR | IBS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02132 | hp1 | a0001 | c0003 | t0003 | g0263 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02145 | hp2 | a0001 | c0003 | t0003 | g0191 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | CDX | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | CDX | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02165 | hp2 | a0001 | c0003 | t0003 | g0259 | EAS | CDX | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0209 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02258 | hp1 | a0001 | c0006 | t0005 | g0199 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0198 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0207 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02451 | hp1 | a0001 | c0008 | t0003 | g0202 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0138 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0027 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02622 | hp2 | a0001 | c0003 | t0003 | g0031 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02630 | hp2 | a0001 | c0003 | t0003 | g0205 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02647 | hp1 | a0001 | c0003 | t0003 | g0223 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02647 | hp2 | a0001 | c0003 | t0003 | g0195 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02717 | hp1 | a0001 | c0006 | t0001 | g0186 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0155 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0093 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0105 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02809 | hp1 | a0002 | c0004 | t0004 | g0272 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0024 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02886 | hp2 | a0001 | c0003 | t0003 | g0224 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02895 | hp2 | a0001 | c0003 | t0003 | g0023 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02896 | hp2 | a0002 | c0004 | t0004 | g0273 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02922 | hp1 | a0001 | c0003 | t0003 | g0022 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02922 | hp2 | a0001 | c0003 | t0003 | g0203 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0029 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02976 | hp1 | a0001 | c0011 | t0004 | g0193 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03041 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03098 | hp1 | a0002 | c0004 | t0004 | g0274 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0254 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03139 | hp1 | a0001 | c0003 | t0009 | g0206 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0200 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0194 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0012 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03239 | hp1 | a0005 | c0009 | t0001 | g0157 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0108 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03516 | hp2 | a0001 | c0003 | t0003 | g0210 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0180 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0082 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0081 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0092 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0090 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03834 | hp2 | a0006 | c0012 | t0003 | g0217 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03927 | hp1 | a0007 | c0013 | t0001 | g0183 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0100 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0054 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04115 | hp2 | a0001 | c0003 | t0003 | g0204 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0087 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0061 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0107 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0208 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | CHB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18952 | hp2 | a0004 | c0007 | t0001 | g0013 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18995 | hp1 | a0001 | c0010 | t0002 | g0187 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19001 | hp1 | a0004 | c0007 | t0001 | g0013 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19030 | hp1 | a0001 | c0003 | t0003 | g0032 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0120 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19240 | hp1 | a0002 | c0004 | t0004 | g0268 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA19240 | hp2 | a0001 | c0002 | t0008 | g0039 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA20752 | hp1 | a0003 | c0005 | t0002 | g0230 | EUR | TSI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0212 | EUR | TSI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | GIH | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0033 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02486 | hp1 | a0001 | c0003 | t0003 | g0025 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03471 | hp1 | a0002 | c0004 | t0004 | g0271 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| HG03471 | hp2 | a0001 | c0003 | t0003 | g0028 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | USA | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| NA21309 | hp2 | a0001 | c0008 | t0003 | g0201 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0222 | REF | REF | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0192 | REF | REF | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:208407092 | G | T | 1 | a0007 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.49G>T | p.Gly17Cys | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/13 | 301/2752 | 49/1653 | 17/550 | chr2 | 208407092 | |||
| chr2:208437603 | C | A | 1 | a0005 | 1 | HG03239.hp1 | stop_gained | HIGH | c.245C>A | p.Ser82* | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 3/13 | 497/2752 | 245/1653 | 82/550 | chr2 | 208437603 | |||
| chr2:208442379 | C | T | 1 | a0003 | 3 | HG01255.hp1 HG01261.hp2 NA20752.hp1 |
missense_variant | MODERATE | c.427C>T | p.Arg143Cys | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/13 | 679/2752 | 427/1653 | 143/550 | chr2 | 208442379 | |||
| chr2:208443511 | G | T | 1 | a0006 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.673G>T | p.Ala225Ser | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/13 | 925/2752 | 673/1653 | 225/550 | chr2 | 208443511 | |||
| chr2:208481137 | T | C | 1 | a0004 | 2 | NA18952.hp2 NA19001.hp1 |
missense_variant | MODERATE | c.1049T>C | p.Val350Ala | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/13 | 1301/2752 | 1049/1653 | 350/550 | chr2 | 208481137 | |||
| chr2:208493309 | G | A | 1 | a0002 | 5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.1303G>A | p.Val435Met | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 1555/2752 | 1303/1653 | 435/550 | chr2 | 208493309 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:208442396 | T | C | 1 | a0001c0010 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.444T>C | p.Tyr148Tyr | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/13 | 696/2752 | 444/1653 | 148/550 | chr2 | 208442396 | |||
| chr2:208444736 | C | T | 1 | a0001c0008 | 2 | HG02451.hp1 NA21309.hp2 |
splice_region_variant&synonymous_variant | LOW | c.702C>T | p.Ile234Ile | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/13 | 954/2752 | 702/1653 | 234/550 | chr2 | 208444736 | |||
| chr2:208459943 | G | A | 1 | a0001c0006 | 2 | HG02258.hp1 HG02717.hp1 |
synonymous_variant | LOW | c.963G>A | p.Pro321Pro | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/13 | 1215/2752 | 963/1653 | 321/550 | chr2 | 208459943 | |||
| chr2:208489072 | C | T | 1 | a0001c0011 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1137C>T | p.Phe379Phe | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/13 | 1389/2752 | 1137/1653 | 379/550 | chr2 | 208489072 | |||
| chr2:208489075 | A | G | 2 | a0001c0003 a0001c0008 |
44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
synonymous_variant | LOW | c.1140A>G | p.Val380Val | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/13 | 1392/2752 | 1140/1653 | 380/550 | chr2 | 208489075 | |||
| chr2:208493302 | C | T | 10 | a0001c0001 a0001c0003 a0001c0006 others(7): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
synonymous_variant | LOW | c.1296C>T | p.Asn432Asn | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 1548/2752 | 1296/1653 | 432/550 | chr2 | 208493302 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:208406841 | C | T | 1 | a0001c0001t0010 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-203C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/13 | 203 | chr2 | 208406841 | ||||||
| chr2:208406995 | C | T | 1 | a0001c0003t0009 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-49C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/13 | 49 | chr2 | 208406995 | ||||||
| chr2:208493690 | G | C | 2 | a0001c0011t0004 a0002c0004t0004 |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*31G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 31 | chr2 | 208493690 | ||||||
| chr2:208493691 | G | T | 2 | a0001c0011t0004 a0002c0004t0004 |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*32G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 32 | chr2 | 208493691 | ||||||
| chr2:208493884 | C | G | 1 | a0001c0002t0008 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 225 | chr2 | 208493884 | ||||||
| chr2:208493920 | A | AT | 7 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(4): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*268dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 269 | INFO_REALIGN_3_PRIME | chr2 | 208493920 | |||||
| chr2:208494011 | T | A | 2 | a0001c0001t0005 a0001c0006t0005 |
3 | HG02258.hp1 HG02630.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*352T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 352 | chr2 | 208494011 | ||||||
| chr2:208494226 | C | T | 7 | a0001c0001t0003 a0001c0003t0003 a0001c0003t0009 others(4): Show |
74 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*567C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 567 | chr2 | 208494226 | ||||||
| chr2:208494337 | T | C | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(14): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*678T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 678 | chr2 | 208494337 | ||||||
| chr2:208494437 | T | G | 1 | a0001c0001t0007 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 778 | chr2 | 208494437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:208407566 | G | T | 1 | a0001c0001t0003g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75+448G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208407566 | |||||||
| chr2:208407814 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(3): Show |
8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+696T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208407814 | |||||||
| chr2:208407835 | T | C | 1 | a0001c0003t0003g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+717T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208407835 | |||||||
| chr2:208407870 | A | G | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+752A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208407870 | |||||||
| chr2:208408196 | G | A | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+1078G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408196 | |||||||
| chr2:208408534 | GA | G | 17 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(14): Show |
18 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+1426delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408534 | ||||||
| chr2:208408603 | T | C | 1 | a0001c0003t0003g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+1485T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408603 | |||||||
| chr2:208408719 | G | GGAAAGAG others(15): Show |
6 | a0001c0001t0001g0265 a0001c0003t0003g0015 a0001c0003t0003g0205 others(3): Show |
7 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(22): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408719 | ||||||
| chr2:208408719 | G | GGAAAGAG others(17): Show |
1 | a0001c0001t0003g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(24): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408719 | ||||||
| chr2:208408721 | A | AAAGAGAG others(14): Show |
1 | a0001c0003t0003g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(21): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408721 | ||||||
| chr2:208408722 | A | AAGAG | 25 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0229 others(22): Show |
29 | HG00597.hp1 HG02148.hp2 HG02630.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+1618_75+1621dup others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408722 | A | AAGAGAGA others(17): Show |
5 | a0001c0003t0003g0012 a0001c0003t0003g0207 a0001c0003t0003g0208 others(2): Show |
6 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(24): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408722 | A | AAGAGAGA others(19): Show |
10 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(7): Show |
10 | HG01175.hp1 HG01261.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(26): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408722 | A | AAGAGAGA others(21): Show |
5 | a0001c0001t0003g0218 a0001c0001t0003g0219 a0001c0001t0003g0220 others(2): Show |
5 | HG02615.hp1 HG03017.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(28): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408722 | A | AAGAGAGA others(23): Show |
7 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(4): Show |
7 | HG01496.hp2 HG01884.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(30): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408722 | A | AAGAGAGA others(25): Show |
4 | a0001c0001t0001g0250 a0001c0001t0003g0251 a0002c0004t0004g0272 others(1): Show |
4 | HG02809.hp1 HG02896.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(32): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408722 | A | AAGAGAGA others(27): Show |
1 | a0001c0001t0003g0252 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(34): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408722 | A | AAGAGAGA others(29): Show |
2 | a0001c0001t0003g0253 a0002c0004t0004g0274 |
2 | HG02080.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(36): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408722 | A | AAGAGAGA others(20): Show |
1 | a0001c0001t0003g0255 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(27): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408722 | A | AAGAGAGA others(22): Show |
1 | a0001c0001t0003g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | ||||||
| chr2:208408724 | G | GAGAGAGA others(13): Show |
14 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(11): Show |
14 | HG00280.hp1 HG01433.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408724 | ||||||
| chr2:208408724 | G | GAGAGAGA others(15): Show |
1 | a0001c0001t0003g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(22): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408724 | ||||||
| chr2:208408726 | G | GAGAGAGA others(11): Show |
7 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(4): Show |
7 | HG02486.hp1 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(18): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408726 | ||||||
| chr2:208408726 | G | GAGAGAGA others(13): Show |
1 | a0001c0003t0003g0033 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408726 | ||||||
| chr2:208408728 | G | GAGAGAGA others(9): Show |
3 | a0001c0003t0003g0198 a0001c0003t0003g0200 a0001c0006t0005g0199 |
3 | HG02258.hp1 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(16): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408728 | ||||||
| chr2:208408732 | G | GAGAGAGA others(5): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
6 | HG02257.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(12): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408732 | ||||||
| chr2:208408736 | G | GAGAGAGA others(1): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 |
4 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(8): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408736 | ||||||
| chr2:208408740 | A | AAGAGAGA others(11): Show |
1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+1630_75+1647dup others(18): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408740 | ||||||
| chr2:208408740 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.75+1622A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408740 | |||||||
| chr2:208408742 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.75+1624G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408742 | |||||||
| chr2:208408742 | G | GAA | 80 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0067 others(77): Show |
85 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.75+1625_75+1626ins others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408742 | ||||||
| chr2:208408742 | G | GAGAA | 78 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0113 others(75): Show |
84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.75+1627_75+1628ins others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408742 | ||||||
| chr2:208408744 | G | A | 1 | a0001c0002t0002g0036 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.75+1626G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408744 | |||||||
| chr2:208408746 | G | A | 1 | a0001c0003t0003g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+1628G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408746 | |||||||
| chr2:208408765 | A | AGAGAGAG others(10): Show |
1 | a0001c0003t0003g0254 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+1647_75+1648ins others(17): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408765 | |||||||
| chr2:208408766 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(5): Show |
10 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+1648A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408766 | |||||||
| chr2:208408768 | T | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(5): Show |
10 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+1650T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408768 | |||||||
| chr2:208408788 | A | G | 6 | a0001c0003t0003g0015 a0001c0003t0003g0264 a0001c0003t0003g0266 others(3): Show |
7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1670A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408788 | |||||||
| chr2:208408907 | T | C | 33 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(30): Show |
34 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.75+1789T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408907 | |||||||
| chr2:208408969 | C | T | 3 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 |
3 | HG01433.hp2 HG02258.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.75+1851C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408969 | |||||||
| chr2:208409048 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.75+1930G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409048 | |||||||
| chr2:208409058 | A | G | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.75+1940A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409058 | |||||||
| chr2:208409094 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.75+1976C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409094 | |||||||
| chr2:208409104 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.75+1986C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409104 | |||||||
| chr2:208409126 | T | C | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+2008T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409126 | |||||||
| chr2:208409264 | A | G | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.75+2146A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409264 | |||||||
| chr2:208409306 | A | G | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+2188A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409306 | |||||||
| chr2:208409314 | T | C | 2 | a0001c0001t0001g0196 a0001c0001t0005g0197 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.75+2196T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409314 | |||||||
| chr2:208409500 | G | A | 1 | a0001c0003t0003g0259 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.75+2382G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409500 | |||||||
| chr2:208409542 | T | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(185): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.75+2424T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409542 | |||||||
| chr2:208409550 | A | G | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+2432A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409550 | |||||||
| chr2:208409786 | A | C | 1 | a0001c0003t0003g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.75+2668A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409786 | |||||||
| chr2:208409834 | A | G | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.75+2716A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409834 | |||||||
| chr2:208409975 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.75+2857C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409975 | |||||||
| chr2:208410074 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(184): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.75+2956C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410074 | |||||||
| chr2:208410149 | G | A | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+3031G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410149 | |||||||
| chr2:208410245 | C | T | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.75+3127C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410245 | |||||||
| chr2:208410314 | A | G | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+3196A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410314 | |||||||
| chr2:208410451 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(3): Show |
8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+3333T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410451 | |||||||
| chr2:208410684 | A | T | 1 | a0001c0001t0003g0216 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.75+3566A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410684 | |||||||
| chr2:208410746 | A | T | 1 | a0001c0001t0003g0216 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.75+3628A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410746 | |||||||
| chr2:208410762 | T | TTG | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(22): Show |
28 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.75+3662_75+3663dup others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208410762 | ||||||
| chr2:208411067 | G | A | 1 | a0001c0002t0002g0038 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.75+3949G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411067 | |||||||
| chr2:208411323 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.75+4205T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411323 | |||||||
| chr2:208411334 | GA | G | 10 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0215 others(7): Show |
10 | HG02080.hp2 HG02523.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+4217delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411334 | |||||||
| chr2:208411428 | G | A | 1 | a0001c0003t0003g0012 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.75+4310G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411428 | |||||||
| chr2:208411579 | G | A | 32 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(29): Show |
33 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.75+4461G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411579 | |||||||
| chr2:208411752 | T | C | 15 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0203 others(12): Show |
15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+4634T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411752 | |||||||
| chr2:208411898 | G | T | 2 | a0001c0003t0003g0012 a0001c0006t0001g0186 |
3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.75+4780G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411898 | |||||||
| chr2:208412116 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.75+4998T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412116 | |||||||
| chr2:208412390 | A | C | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+5272A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412390 | |||||||
| chr2:208412713 | T | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(3): Show |
8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+5595T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412713 | |||||||
| chr2:208412743 | A | T | 1 | a0001c0002t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+5625A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412743 | |||||||
| chr2:208412754 | A | G | 1 | a0001c0001t0003g0228 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.75+5636A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412754 | |||||||
| chr2:208412867 | G | A | 2 | a0001c0003t0003g0034 a0001c0003t0003g0204 |
2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.75+5749G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412867 | |||||||
| chr2:208413014 | T | C | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+5896T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413014 | |||||||
| chr2:208413141 | C | CCA | 12 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(9): Show |
12 | HG01099.hp1 HG01943.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+6052_75+6053dup others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | ||||||
| chr2:208413141 | C | CCACA | 29 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0215 others(26): Show |
29 | HG01433.hp2 HG01884.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.75+6050_75+6053dup others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | ||||||
| chr2:208413141 | C | CCACACA | 7 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(4): Show |
7 | HG02572.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+6048_75+6053dup others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | ||||||
| chr2:208413141 | C | CCACACAC others(3): Show |
1 | a0001c0003t0003g0198 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+6044_75+6053dup others(10): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | ||||||
| chr2:208413141 | C | CCACACAC others(5): Show |
1 | a0001c0001t0001g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.75+6042_75+6053dup others(12): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | ||||||
| chr2:208413141 | CCA | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(9): Show |
13 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.75+6052_75+6053del others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | ||||||
| chr2:208413141 | CCACA | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(173): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.75+6050_75+6053del others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | ||||||
| chr2:208413172 | G | C | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.75+6054G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413172 | |||||||
| chr2:208413200 | G | A | 1 | a0001c0002t0002g0043 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.75+6082G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413200 | |||||||
| chr2:208413320 | C | A | 4 | a0001c0003t0003g0205 a0001c0003t0003g0207 a0001c0008t0003g0201 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+6202C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413320 | |||||||
| chr2:208413331 | A | G | 23 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.75+6213A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413331 | |||||||
| chr2:208413998 | C | T | 2 | a0001c0003t0003g0200 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.75+6880C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413998 | |||||||
| chr2:208414288 | A | G | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.75+7170A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208414288 | |||||||
| chr2:208414545 | T | C | 5 | a0002c0004t0004g0268 a0002c0004t0004g0271 a0002c0004t0004g0272 others(2): Show |
5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+7427T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208414545 | |||||||
| chr2:208414547 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(3): Show |
8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+7429G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208414547 | |||||||
| chr2:208414862 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.75+7744C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208414862 | |||||||
| chr2:208415072 | G | A | 1 | a0001c0003t0003g0012 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.75+7954G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415072 | |||||||
| chr2:208415076 | G | A | 1 | a0001c0002t0002g0044 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.75+7958G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415076 | |||||||
| chr2:208415104 | A | C | 2 | a0001c0001t0003g0221 a0001c0001t0003g0228 |
2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.75+7986A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415104 | |||||||
| chr2:208415148 | T | C | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.75+8030T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415148 | |||||||
| chr2:208415204 | T | C | 8 | a0001c0003t0003g0203 a0001c0003t0003g0208 a0001c0003t0003g0209 others(5): Show |
8 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+8086T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415204 | |||||||
| chr2:208415374 | T | A | 2 | a0001c0001t0001g0196 a0001c0001t0005g0197 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.75+8256T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415374 | |||||||
| chr2:208415428 | G | A | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+8310G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415428 | |||||||
| chr2:208415655 | C | A | 1 | a0001c0003t0003g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.75+8537C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415655 | |||||||
| chr2:208415831 | C | G | 15 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+8713C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415831 | |||||||
| chr2:208415836 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.75+8718G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415836 | |||||||
| chr2:208415978 | A | T | 1 | a0007c0013t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.75+8860A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415978 | |||||||
| chr2:208416066 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.75+8948C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416066 | |||||||
| chr2:208416091 | G | C | 7 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(4): Show |
7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+8973G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416091 | |||||||
| chr2:208416132 | G | A | 1 | a0001c0002t0002g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.75+9014G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416132 | |||||||
| chr2:208416155 | G | T | 26 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(23): Show |
26 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.75+9037G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416155 | |||||||
| chr2:208416206 | T | C | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+9088T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416206 | |||||||
| chr2:208416343 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(3): Show |
8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+9225T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416343 | |||||||
| chr2:208416363 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.75+9245C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416363 | |||||||
| chr2:208416460 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.75+9342C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416460 | |||||||
| chr2:208416703 | G | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(38): Show |
48 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.75+9585G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416703 | |||||||
| chr2:208416790 | T | C | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+9672T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416790 | |||||||
| chr2:208416962 | C | T | 12 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+9844C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416962 | |||||||
| chr2:208416981 | C | T | 6 | a0001c0003t0003g0015 a0001c0003t0003g0264 a0001c0003t0003g0266 others(3): Show |
7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+9863C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416981 | |||||||
| chr2:208417075 | T | C | 1 | a0001c0002t0002g0046 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.75+9957T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417075 | |||||||
| chr2:208417233 | C | T | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.75+10115C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417233 | |||||||
| chr2:208417234 | G | A | 3 | a0001c0003t0003g0203 a0001c0003t0003g0254 a0001c0011t0004g0193 |
3 | HG02922.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.75+10116G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417234 | |||||||
| chr2:208417541 | C | CT | 9 | a0001c0001t0001g0106 a0001c0001t0001g0247 a0001c0002t0002g0093 others(6): Show |
9 | HG00597.hp1 HG01175.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+10452dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | ||||||
| chr2:208417541 | CT | C | 127 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(124): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.75+10452delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | ||||||
| chr2:208417541 | CTT | C | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG01255.hp2 HG01993.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+10451_75+10452d others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | ||||||
| chr2:208417541 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0235 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.75+10442_75+10452d others(13): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | ||||||
| chr2:208417541 | CTTTTTTT others(8): Show |
C | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+10438_75+10452d others(17): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | ||||||
| chr2:208417541 | CTTTTTTT others(9): Show |
C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(44): Show |
49 | HG01433.hp2 HG01496.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.75+10437_75+10452d others(18): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | ||||||
| chr2:208417572 | T | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.75+10454T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417572 | |||||||
| chr2:208417651 | G | A | 1 | a0001c0001t0003g0253 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.75+10533G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417651 | |||||||
| chr2:208417731 | A | G | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.76-10470A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417731 | |||||||
| chr2:208417963 | C | A | 7 | a0001c0003t0003g0203 a0001c0003t0003g0208 a0001c0003t0003g0209 others(4): Show |
7 | HG02257.hp1 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-10238C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417963 | |||||||
| chr2:208418282 | C | T | 1 | a0001c0002t0002g0122 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.76-9919C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418282 | |||||||
| chr2:208418363 | A | AT | 17 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(14): Show |
18 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-9827dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208418363 | ||||||
| chr2:208418363 | AT | A | 41 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(38): Show |
41 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(38): Show |
intron_variant | MODIFIER | c.76-9827delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208418363 | ||||||
| chr2:208418377 | G | A | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.76-9824G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418377 | |||||||
| chr2:208418529 | C | T | 3 | a0001c0001t0003g0212 a0001c0001t0003g0218 a0006c0012t0003g0217 |
3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.76-9672C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418529 | |||||||
| chr2:208418576 | T | C | 1 | a0001c0003t0003g0012 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.76-9625T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418576 | |||||||
| chr2:208418623 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.76-9578C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418623 | |||||||
| chr2:208418667 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.76-9534G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418667 | |||||||
| chr2:208418868 | C | T | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.76-9333C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418868 | |||||||
| chr2:208418884 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(185): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.76-9317A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418884 | |||||||
| chr2:208419391 | T | G | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-8810T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208419391 | |||||||
| chr2:208419457 | C | T | 5 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(2): Show |
5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-8744C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208419457 | |||||||
| chr2:208419792 | T | C | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-8409T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208419792 | |||||||
| chr2:208420210 | C | T | 1 | a0001c0002t0002g0044 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.76-7991C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420210 | |||||||
| chr2:208420441 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.76-7760G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420441 | |||||||
| chr2:208420534 | ATTAAC | A | 12 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(9): Show |
13 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-7662_76-7658del others(5): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208420534 | ||||||
| chr2:208420655 | G | A | 5 | a0001c0001t0003g0211 a0001c0001t0003g0225 a0001c0001t0003g0226 others(2): Show |
5 | HG01496.hp2 HG01884.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-7546G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420655 | |||||||
| chr2:208420707 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.76-7494A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420707 | |||||||
| chr2:208420744 | A | G | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-7457A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420744 | |||||||
| chr2:208420781 | T | G | 23 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-7420T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420781 | |||||||
| chr2:208420807 | C | T | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-7394C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420807 | |||||||
| chr2:208420983 | C | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(38): Show |
48 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.76-7218C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420983 | |||||||
| chr2:208421016 | C | T | 4 | a0001c0003t0003g0028 a0001c0003t0003g0029 a0001c0003t0003g0031 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-7185C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421016 | |||||||
| chr2:208421049 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.76-7152T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421049 | |||||||
| chr2:208421094 | G | C | 69 | a0001c0001t0001g0067 a0001c0001t0003g0089 a0001c0002t0002g0006 others(66): Show |
72 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.76-7107G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421094 | |||||||
| chr2:208421240 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0005g0197 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.76-6961C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421240 | |||||||
| chr2:208421365 | G | GGT | 23 | a0001c0001t0001g0171 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-6815_76-6814dup others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208421365 | ||||||
| chr2:208421365 | G | T | 2 | a0001c0003t0003g0012 a0001c0006t0001g0186 |
3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.76-6836G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421365 | |||||||
| chr2:208421417 | G | T | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.76-6784G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421417 | |||||||
| chr2:208421508 | A | G | 61 | a0001c0001t0001g0067 a0001c0001t0003g0089 a0001c0002t0002g0006 others(58): Show |
64 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.76-6693A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421508 | |||||||
| chr2:208421601 | A | G | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6600A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421601 | |||||||
| chr2:208421895 | C | T | 5 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(2): Show |
5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-6306C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421895 | |||||||
| chr2:208422082 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(183): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.76-6119C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422082 | |||||||
| chr2:208422122 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.76-6079G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422122 | |||||||
| chr2:208422202 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.76-5999A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422202 | |||||||
| chr2:208422271 | A | G | 4 | a0001c0003t0003g0205 a0001c0003t0003g0207 a0001c0008t0003g0201 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-5930A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422271 | |||||||
| chr2:208422495 | C | T | 8 | a0001c0003t0003g0203 a0001c0003t0003g0208 a0001c0003t0003g0209 others(5): Show |
8 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-5706C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422495 | |||||||
| chr2:208422516 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.76-5685G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422516 | |||||||
| chr2:208422525 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.76-5676T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422525 | |||||||
| chr2:208422601 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-5600C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422601 | |||||||
| chr2:208422739 | A | G | 1 | a0001c0002t0002g0129 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.76-5462A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422739 | |||||||
| chr2:208422883 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(268): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.76-5318G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422883 | |||||||
| chr2:208422934 | A | G | 1 | a0001c0003t0003g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.76-5267A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422934 | |||||||
| chr2:208423157 | G | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.76-5044G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423157 | |||||||
| chr2:208423167 | G | A | 1 | a0001c0003t0003g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.76-5034G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423167 | |||||||
| chr2:208423346 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(183): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.76-4855T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423346 | |||||||
| chr2:208423348 | G | A | 1 | a0001c0002t0002g0055 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.76-4853G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423348 | |||||||
| chr2:208423477 | C | G | 69 | a0001c0001t0001g0067 a0001c0001t0003g0089 a0001c0002t0002g0006 others(66): Show |
72 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.76-4724C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423477 | |||||||
| chr2:208423738 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-4463A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423738 | |||||||
| chr2:208423765 | GCT | G | 15 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0203 others(12): Show |
15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.76-4433_76-4432del others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208423765 | ||||||
| chr2:208423808 | T | C | 2 | a0001c0001t0001g0196 a0001c0001t0005g0197 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.76-4393T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423808 | |||||||
| chr2:208423960 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(183): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.76-4241G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423960 | |||||||
| chr2:208424058 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(38): Show |
48 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.76-4143G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424058 | |||||||
| chr2:208424080 | G | A | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.76-4121G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424080 | |||||||
| chr2:208424081 | C | T | 1 | a0001c0002t0002g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.76-4120C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424081 | |||||||
| chr2:208424090 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.76-4111C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424090 | |||||||
| chr2:208424470 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.76-3731C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424470 | |||||||
| chr2:208424877 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(2): Show |
7 | HG02257.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-3324G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424877 | |||||||
| chr2:208425025 | T | G | 2 | a0001c0003t0003g0200 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.76-3176T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208425025 | |||||||
| chr2:208425521 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.76-2680A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208425521 | |||||||
| chr2:208426130 | A | G | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.76-2071A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426130 | |||||||
| chr2:208426210 | C | T | 2 | a0001c0001t0003g0212 a0001c0001t0003g0218 |
2 | HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.76-1991C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426210 | |||||||
| chr2:208426403 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.76-1798T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426403 | |||||||
| chr2:208426420 | T | C | 4 | a0001c0002t0002g0056 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1781T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426420 | |||||||
| chr2:208426591 | A | G | 1 | a0002c0004t0004g0274 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-1610A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426591 | |||||||
| chr2:208426614 | T | C | 1 | a0001c0003t0003g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.76-1587T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426614 | |||||||
| chr2:208426639 | A | G | 23 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-1562A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426639 | |||||||
| chr2:208426674 | T | G | 1 | a0001c0003t0003g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.76-1527T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426674 | |||||||
| chr2:208426703 | C | T | 15 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-1498C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426703 | |||||||
| chr2:208426719 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(185): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.76-1482G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426719 | |||||||
| chr2:208426785 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(2): Show |
7 | HG02257.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-1416A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426785 | |||||||
| chr2:208426909 | T | C | 6 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(3): Show |
6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-1292T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426909 | |||||||
| chr2:208427210 | G | GA | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(2): Show |
7 | HG02257.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-984dupA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208427210 | ||||||
| chr2:208427230 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.76-971A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427230 | |||||||
| chr2:208427233 | C | T | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-968C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427233 | |||||||
| chr2:208427318 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.76-883C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427318 | |||||||
| chr2:208427468 | A | G | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.76-733A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427468 | |||||||
| chr2:208427542 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.76-659T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427542 | |||||||
| chr2:208427599 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18940.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.76-602A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427599 | |||||||
| chr2:208427628 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.76-573G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427628 | |||||||
| chr2:208427649 | A | G | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-552A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427649 | |||||||
| chr2:208427723 | A | C | 13 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(10): Show |
13 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.76-478A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427723 | |||||||
| chr2:208428443 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.178+140C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428443 | |||||||
| chr2:208428468 | C | G | 6 | a0001c0001t0003g0211 a0001c0001t0003g0219 a0001c0001t0003g0225 others(3): Show |
6 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+165C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428468 | |||||||
| chr2:208428556 | C | G | 5 | a0002c0004t0004g0268 a0002c0004t0004g0271 a0002c0004t0004g0272 others(2): Show |
5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+253C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428556 | |||||||
| chr2:208428574 | G | T | 2 | a0001c0001t0001g0196 a0001c0001t0005g0197 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+271G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428574 | |||||||
| chr2:208428612 | C | T | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.178+309C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428612 | |||||||
| chr2:208428639 | G | A | 2 | a0001c0003t0003g0012 a0001c0006t0001g0186 |
3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.178+336G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428639 | |||||||
| chr2:208428772 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.178+469A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428772 | |||||||
| chr2:208428813 | G | A | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+510G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428813 | |||||||
| chr2:208428862 | A | G | 2 | a0001c0002t0002g0081 a0001c0002t0002g0082 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.178+559A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428862 | |||||||
| chr2:208428951 | G | A | 2 | a0001c0003t0003g0200 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.178+648G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428951 | |||||||
| chr2:208429011 | G | C | 4 | a0001c0003t0003g0194 a0001c0003t0003g0195 a0001c0003t0003g0203 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+708G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429011 | |||||||
| chr2:208429025 | C | T | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+722C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429025 | |||||||
| chr2:208429026 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.178+723G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429026 | |||||||
| chr2:208429039 | C | T | 145 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(142): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.178+736C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429039 | |||||||
| chr2:208429084 | CA | C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(160): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.178+799delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208429084 | ||||||
| chr2:208429084 | CAA | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
106 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.178+798_178+799del others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208429084 | ||||||
| chr2:208429229 | G | C | 4 | a0001c0003t0003g0205 a0001c0003t0003g0207 a0001c0008t0003g0201 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+926G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429229 | |||||||
| chr2:208429252 | A | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(45): Show |
57 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.178+949A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429252 | |||||||
| chr2:208429307 | C | T | 1 | a0001c0002t0002g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.178+1004C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429307 | |||||||
| chr2:208429362 | T | G | 1 | a0001c0001t0003g0213 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.178+1059T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429362 | |||||||
| chr2:208429440 | T | C | 23 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.178+1137T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429440 | |||||||
| chr2:208429486 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.178+1183C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429486 | |||||||
| chr2:208429572 | T | C | 1 | a0001c0003t0003g0012 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.178+1269T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429572 | |||||||
| chr2:208429652 | A | T | 1 | a0001c0002t0002g0080 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.178+1349A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429652 | |||||||
| chr2:208429694 | A | T | 15 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.178+1391A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429694 | |||||||
| chr2:208430093 | T | A | 31 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(28): Show |
32 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.178+1790T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430093 | |||||||
| chr2:208430291 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.178+1988A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430291 | |||||||
| chr2:208430460 | C | A | 1 | a0001c0002t0002g0059 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.178+2157C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430460 | |||||||
| chr2:208430546 | C | CT | 42 | a0001c0001t0001g0166 a0001c0001t0001g0260 a0001c0001t0001g0261 others(39): Show |
43 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.178+2261dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208430546 | ||||||
| chr2:208430555 | T | TC | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(43): Show |
55 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.178+2252_178+2253i others(3): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430555 | |||||||
| chr2:208430893 | A | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0229 a0001c0001t0001g0243 others(1): Show |
5 | NA18942.hp1 NA18950.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+2590A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430893 | |||||||
| chr2:208430911 | T | C | 145 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(142): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.178+2608T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430911 | |||||||
| chr2:208430981 | T | C | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+2678T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430981 | |||||||
| chr2:208431004 | C | T | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.178+2701C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431004 | |||||||
| chr2:208431102 | T | C | 1 | a0001c0003t0003g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178+2799T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431102 | |||||||
| chr2:208431290 | A | G | 1 | a0001c0003t0003g0012 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.178+2987A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431290 | |||||||
| chr2:208431345 | A | G | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.178+3042A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431345 | |||||||
| chr2:208431411 | G | A | 7 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(4): Show |
7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+3108G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431411 | |||||||
| chr2:208431702 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.178+3399A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431702 | |||||||
| chr2:208431780 | T | C | 2 | a0001c0003t0003g0200 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.178+3477T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431780 | |||||||
| chr2:208432218 | G | T | 67 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(64): Show |
69 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.178+3915G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432218 | |||||||
| chr2:208432301 | G | A | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+3998G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432301 | |||||||
| chr2:208432532 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.178+4229T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432532 | |||||||
| chr2:208432594 | T | C | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+4291T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432594 | |||||||
| chr2:208432615 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(39): Show |
50 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.178+4312C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432615 | |||||||
| chr2:208432679 | G | A | 2 | a0001c0002t0002g0081 a0001c0002t0002g0082 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.178+4376G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432679 | |||||||
| chr2:208432941 | G | A | 1 | a0001c0002t0002g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.179-4596G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432941 | |||||||
| chr2:208432985 | G | A | 23 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.179-4552G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432985 | |||||||
| chr2:208432992 | G | A | 7 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(4): Show |
7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-4545G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432992 | |||||||
| chr2:208433078 | G | C | 13 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(10): Show |
13 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-4459G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433078 | |||||||
| chr2:208433079 | G | A | 5 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(2): Show |
5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-4458G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433079 | |||||||
| chr2:208433106 | A | T | 8 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(5): Show |
8 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-4431A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433106 | |||||||
| chr2:208433305 | T | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(39): Show |
49 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.179-4232T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433305 | |||||||
| chr2:208433411 | A | G | 7 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(4): Show |
7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-4126A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433411 | |||||||
| chr2:208433688 | C | T | 2 | a0001c0003t0003g0012 a0001c0006t0001g0186 |
3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.179-3849C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433688 | |||||||
| chr2:208433908 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(45): Show |
57 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.179-3629T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433908 | |||||||
| chr2:208434040 | G | A | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.179-3497G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434040 | |||||||
| chr2:208434095 | C | T | 1 | a0001c0003t0003g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-3442C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434095 | |||||||
| chr2:208434130 | A | G | 2 | a0001c0003t0003g0200 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.179-3407A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434130 | |||||||
| chr2:208434214 | T | C | 1 | a0001c0003t0003g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.179-3323T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434214 | |||||||
| chr2:208434299 | C | CA | 8 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0170 others(5): Show |
8 | HG01884.hp2 HG02071.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-3225dupA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208434299 | ||||||
| chr2:208434390 | A | G | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-3147A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434390 | |||||||
| chr2:208434641 | C | T | 4 | a0001c0003t0003g0028 a0001c0003t0003g0029 a0001c0003t0003g0031 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2896C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434641 | |||||||
| chr2:208434706 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0178 |
2 | NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.179-2831C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434706 | |||||||
| chr2:208434744 | T | G | 1 | a0001c0003t0003g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.179-2793T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434744 | |||||||
| chr2:208434805 | A | T | 1 | a0001c0002t0002g0078 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.179-2732A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434805 | |||||||
| chr2:208435005 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0265 |
3 | HG01099.hp1 HG02015.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.179-2532G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435005 | |||||||
| chr2:208435183 | A | G | 1 | a0001c0003t0003g0254 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.179-2354A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435183 | |||||||
| chr2:208435206 | G | A | 1 | a0001c0002t0002g0088 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.179-2331G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435206 | |||||||
| chr2:208435353 | G | A | 2 | a0001c0003t0003g0012 a0001c0006t0001g0186 |
3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.179-2184G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435353 | |||||||
| chr2:208435410 | G | A | 23 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.179-2127G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435410 | |||||||
| chr2:208435437 | G | A | 2 | a0001c0003t0003g0012 a0001c0006t0001g0186 |
3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.179-2100G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435437 | |||||||
| chr2:208435546 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.179-1991A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435546 | |||||||
| chr2:208435563 | C | T | 3 | a0001c0001t0003g0212 a0001c0001t0003g0218 a0006c0012t0003g0217 |
3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.179-1974C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435563 | |||||||
| chr2:208435721 | C | A | 1 | a0001c0001t0001g0245 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.179-1816C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435721 | |||||||
| chr2:208435833 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.179-1704C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435833 | |||||||
| chr2:208435893 | A | C | 1 | a0001c0001t0003g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.179-1644A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435893 | |||||||
| chr2:208436052 | G | A | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0123 |
3 | HG00423.hp2 HG00621.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.179-1485G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436052 | |||||||
| chr2:208436066 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.179-1471C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436066 | |||||||
| chr2:208436242 | G | A | 2 | a0001c0003t0003g0012 a0001c0006t0001g0186 |
3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.179-1295G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436242 | |||||||
| chr2:208436288 | AG | A | 147 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(144): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.179-1246delG | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208436288 | ||||||
| chr2:208436480 | A | G | 23 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.179-1057A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436480 | |||||||
| chr2:208436506 | C | T | 3 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 |
3 | HG01433.hp2 HG02258.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.179-1031C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436506 | |||||||
| chr2:208436541 | A | T | 1 | a0001c0001t0003g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.179-996A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436541 | |||||||
| chr2:208436698 | G | A | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.179-839G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436698 | |||||||
| chr2:208436726 | G | C | 15 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.179-811G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436726 | |||||||
| chr2:208436918 | G | A | 1 | a0001c0001t0007g0120 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.179-619G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436918 | |||||||
| chr2:208436920 | C | T | 1 | a0002c0004t0004g0268 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.179-617C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436920 | |||||||
| chr2:208436959 | G | A | 13 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(10): Show |
13 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-578G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436959 | |||||||
| chr2:208437057 | A | G | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
4 | HG01099.hp1 HG01943.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-480A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437057 | |||||||
| chr2:208437062 | T | C | 2 | a0001c0003t0003g0203 a0001c0003t0003g0254 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.179-475T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437062 | |||||||
| chr2:208437194 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0164 |
2 | NA19010.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.179-343A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437194 | |||||||
| chr2:208437381 | T | A | 4 | a0001c0003t0003g0194 a0001c0003t0003g0195 a0001c0003t0003g0203 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-156T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437381 | |||||||
| chr2:208437438 | C | T | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.179-99C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437438 | |||||||
| chr2:208437748 | A | G | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.290-12A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 3/12 | chr2 | 208437748 | |||||||
| chr2:208438148 | C | CA | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.411+267_411+268ins others(1): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438148 | |||||||
| chr2:208438161 | A | T | 1 | a0001c0002t0002g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.411+280A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438161 | |||||||
| chr2:208438265 | G | A | 1 | a0001c0003t0003g0198 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.411+384G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438265 | |||||||
| chr2:208438646 | A | G | 15 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0203 others(12): Show |
15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.411+765A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438646 | |||||||
| chr2:208438657 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.411+776A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438657 | |||||||
| chr2:208439025 | A | G | 4 | a0001c0001t0001g0126 a0001c0001t0001g0140 a0001c0001t0001g0163 others(1): Show |
4 | HG02027.hp1 HG02071.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1144A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439025 | |||||||
| chr2:208439183 | A | G | 17 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(14): Show |
18 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.411+1302A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439183 | |||||||
| chr2:208439511 | A | G | 1 | a0001c0003t0003g0023 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.411+1630A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439511 | |||||||
| chr2:208439533 | A | G | 1 | a0001c0002t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411+1652A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439533 | |||||||
| chr2:208439619 | C | G | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.411+1738C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439619 | |||||||
| chr2:208439722 | G | T | 2 | a0001c0003t0003g0200 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.411+1841G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439722 | |||||||
| chr2:208439771 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.411+1890T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439771 | |||||||
| chr2:208439941 | A | G | 2 | a0001c0002t0002g0077 a0001c0002t0002g0083 |
2 | NA18955.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.411+2060A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439941 | |||||||
| chr2:208439992 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.411+2111C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439992 | |||||||
| chr2:208440165 | C | T | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412-2199C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440165 | |||||||
| chr2:208440378 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 |
4 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-1986T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440378 | |||||||
| chr2:208440529 | A | G | 1 | a0001c0001t0003g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412-1835A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440529 | |||||||
| chr2:208440557 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0190 |
2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.412-1807A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440557 | |||||||
| chr2:208440689 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.412-1675A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440689 | |||||||
| chr2:208440804 | G | T | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412-1560G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440804 | |||||||
| chr2:208440960 | C | G | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.412-1404C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440960 | |||||||
| chr2:208441082 | AGCCAATT others(10): Show |
A | 1 | a0001c0002t0002g0060 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.412-1278_412-1262d others(19): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 208441082 | ||||||
| chr2:208441206 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.412-1158G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441206 | |||||||
| chr2:208441230 | A | G | 1 | a0001c0003t0003g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.412-1134A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441230 | |||||||
| chr2:208441253 | C | T | 1 | a0001c0001t0003g0213 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.412-1111C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441253 | |||||||
| chr2:208441254 | A | G | 17 | a0001c0001t0003g0211 a0001c0001t0003g0213 a0001c0001t0003g0214 others(14): Show |
17 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.412-1110A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441254 | |||||||
| chr2:208441350 | A | G | 2 | a0001c0003t0003g0203 a0001c0003t0003g0254 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.412-1014A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441350 | |||||||
| chr2:208441479 | G | A | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.412-885G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441479 | |||||||
| chr2:208441603 | T | C | 1 | a0002c0004t0004g0273 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.412-761T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441603 | |||||||
| chr2:208441671 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG00140.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.412-693G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441671 | |||||||
| chr2:208441768 | T | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0178 |
2 | NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.412-596T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441768 | |||||||
| chr2:208441854 | G | A | 15 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.412-510G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441854 | |||||||
| chr2:208441981 | C | T | 1 | a0007c0013t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.412-383C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441981 | |||||||
| chr2:208442068 | G | C | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.412-296G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442068 | |||||||
| chr2:208442096 | C | T | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412-268C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442096 | |||||||
| chr2:208442201 | T | C | 4 | a0001c0003t0003g0205 a0001c0003t0003g0207 a0001c0008t0003g0201 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-163T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442201 | |||||||
| chr2:208442204 | A | G | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412-160A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442204 | |||||||
| chr2:208442216 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.412-148C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442216 | |||||||
| chr2:208442729 | G | A | 2 | a0001c0003t0003g0034 a0001c0003t0003g0204 |
2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.509+268G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208442729 | |||||||
| chr2:208442814 | A | G | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+353A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208442814 | |||||||
| chr2:208442988 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.510-360A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208442988 | |||||||
| chr2:208443143 | A | G | 23 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.510-205A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208443143 | |||||||
| chr2:208443155 | T | C | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510-193T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208443155 | |||||||
| chr2:208443160 | T | A | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510-188T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208443160 | |||||||
| chr2:208443762 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.699+225G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208443762 | |||||||
| chr2:208443837 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 |
4 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+300C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208443837 | |||||||
| chr2:208444056 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.699+519G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208444056 | |||||||
| chr2:208444405 | C | T | 1 | a0001c0002t0002g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.700-329C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208444405 | |||||||
| chr2:208444672 | A | C | 1 | a0001c0003t0003g0012 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.700-62A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208444672 | |||||||
| chr2:208444721 | T | G | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.700-13T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208444721 | |||||||
| chr2:208444995 | C | G | 2 | a0001c0003t0003g0200 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.853+108C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208444995 | |||||||
| chr2:208445070 | C | T | 17 | a0001c0001t0003g0211 a0001c0001t0003g0213 a0001c0001t0003g0214 others(14): Show |
17 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.853+183C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445070 | |||||||
| chr2:208445076 | G | C | 1 | a0001c0002t0002g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.853+189G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445076 | |||||||
| chr2:208445108 | T | A | 17 | a0001c0003t0003g0012 a0001c0003t0003g0021 a0001c0003t0003g0022 others(14): Show |
18 | HG01069.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.853+221T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445108 | |||||||
| chr2:208445462 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
54 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.853+575C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445462 | |||||||
| chr2:208445639 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.853+752C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445639 | |||||||
| chr2:208445699 | C | G | 1 | a0001c0001t0005g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.853+812C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445699 | |||||||
| chr2:208445939 | A | G | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853+1052A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445939 | |||||||
| chr2:208446154 | A | G | 1 | a0001c0003t0003g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.853+1267A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446154 | |||||||
| chr2:208446284 | C | T | 13 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.853+1397C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446284 | |||||||
| chr2:208446327 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.853+1440G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446327 | |||||||
| chr2:208446455 | G | A | 2 | a0001c0003t0003g0012 a0001c0006t0001g0186 |
3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.853+1568G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446455 | |||||||
| chr2:208446499 | T | C | 7 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(4): Show |
7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+1612T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446499 | |||||||
| chr2:208446661 | T | C | 7 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(4): Show |
7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+1774T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446661 | |||||||
| chr2:208446867 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.853+1980A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446867 | |||||||
| chr2:208446916 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.853+2029C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446916 | |||||||
| chr2:208447257 | C | T | 1 | a0001c0002t0002g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853+2370C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447257 | |||||||
| chr2:208447433 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.853+2546A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447433 | |||||||
| chr2:208447449 | G | A | 12 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+2562G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447449 | |||||||
| chr2:208447491 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.853+2604A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447491 | |||||||
| chr2:208447587 | C | CA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
77 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.853+2710dupA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447587 | ||||||
| chr2:208447587 | CA | C | 15 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0200 others(12): Show |
15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.853+2710delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447587 | ||||||
| chr2:208447606 | A | AAAAT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(63): Show |
74 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.853+2754_853+2757d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447606 | ||||||
| chr2:208447606 | AAAAT | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(161): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.853+2754_853+2757d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447606 | ||||||
| chr2:208447606 | AAAATAAA others(5): Show |
A | 4 | a0001c0003t0003g0194 a0001c0003t0003g0195 a0001c0003t0003g0203 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+2746_853+2757d others(14): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447606 | ||||||
| chr2:208447791 | T | C | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.853+2904T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447791 | |||||||
| chr2:208447913 | T | C | 72 | a0001c0001t0001g0067 a0001c0001t0001g0124 a0001c0001t0001g0143 others(69): Show |
75 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.854-2836T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447913 | |||||||
| chr2:208448046 | C | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(268): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.854-2703C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448046 | |||||||
| chr2:208448162 | C | T | 17 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(14): Show |
18 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.854-2587C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448162 | |||||||
| chr2:208448284 | T | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.854-2465T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448284 | |||||||
| chr2:208448315 | T | A | 1 | a0001c0003t0003g0012 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.854-2434T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448315 | |||||||
| chr2:208448377 | A | G | 1 | a0001c0001t0003g0252 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.854-2372A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448377 | |||||||
| chr2:208448566 | G | A | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.854-2183G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448566 | |||||||
| chr2:208448582 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.854-2167C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448582 | |||||||
| chr2:208449132 | A | G | 1 | a0001c0003t0003g0012 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.854-1617A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449132 | |||||||
| chr2:208449244 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.854-1505T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449244 | |||||||
| chr2:208449300 | G | A | 6 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(3): Show |
6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-1449G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449300 | |||||||
| chr2:208449437 | T | TGATA | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.854-1299_854-1296d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449437 | ||||||
| chr2:208449437 | T | TGATAGAT others(1): Show |
113 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(110): Show |
124 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.854-1303_854-1296d others(10): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449437 | ||||||
| chr2:208449437 | T | TGATAGAT others(5): Show |
51 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0101 others(48): Show |
53 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.854-1307_854-1296d others(14): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449437 | ||||||
| chr2:208449437 | T | TGATAGAT others(9): Show |
5 | a0001c0001t0001g0159 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG00597.hp2 HG02027.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.854-1311_854-1296d others(18): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449437 | ||||||
| chr2:208449446 | GATAGATA others(1): Show |
G | 3 | a0001c0001t0001g0196 a0001c0001t0005g0197 a0001c0001t0005g0249 |
3 | HG02486.hp2 HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.854-1295_854-1288d others(10): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449446 | ||||||
| chr2:208449450 | GATAA | G | 3 | a0001c0001t0003g0212 a0001c0001t0003g0221 a0001c0003t0003g0224 |
3 | HG02886.hp2 HG03017.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.854-1295_854-1292d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449450 | ||||||
| chr2:208449454 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.854-1295A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449454 | |||||||
| chr2:208449480 | A | T | 1 | a0001c0003t0003g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.854-1269A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449480 | |||||||
| chr2:208449800 | A | C | 1 | a0001c0002t0002g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.854-949A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449800 | |||||||
| chr2:208449822 | A | G | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.854-927A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449822 | |||||||
| chr2:208450132 | T | C | 3 | a0001c0002t0002g0105 a0001c0002t0002g0107 a0001c0002t0002g0108 |
3 | HG02738.hp2 HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.854-617T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450132 | |||||||
| chr2:208450185 | T | C | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.854-564T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450185 | |||||||
| chr2:208450211 | A | C | 2 | a0001c0003t0003g0203 a0001c0003t0003g0254 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.854-538A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450211 | |||||||
| chr2:208450296 | A | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
52 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.854-453A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450296 | |||||||
| chr2:208450370 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.854-379C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450370 | |||||||
| chr2:208450397 | A | C | 4 | a0001c0003t0003g0194 a0001c0003t0003g0195 a0001c0003t0003g0203 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.854-352A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450397 | |||||||
| chr2:208450473 | T | C | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.854-276T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450473 | |||||||
| chr2:208450720 | C | T | 1 | a0001c0002t0008g0039 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.854-29C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450720 | |||||||
| chr2:208450721 | T | C | 15 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0203 others(12): Show |
15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.854-28T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450721 | |||||||
| chr2:208450722 | A | T | 15 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0203 others(12): Show |
15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.854-27A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450722 | |||||||
| chr2:208450723 | G | T | 15 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0203 others(12): Show |
15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.854-26G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450723 | |||||||
| chr2:208450848 | G | A | 146 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(143): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.914+39G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208450848 | |||||||
| chr2:208451249 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
52 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.914+440C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451249 | |||||||
| chr2:208451373 | G | T | 4 | a0001c0003t0003g0194 a0001c0003t0003g0195 a0001c0003t0003g0203 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+564G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451373 | |||||||
| chr2:208451571 | T | C | 5 | a0001c0002t0002g0064 a0001c0002t0002g0072 a0001c0002t0002g0078 others(2): Show |
5 | HG02083.hp1 NA18940.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.914+762T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451571 | |||||||
| chr2:208451680 | A | G | 1 | a0001c0003t0003g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.914+871A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451680 | |||||||
| chr2:208451857 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 |
4 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+1048T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451857 | |||||||
| chr2:208451995 | C | T | 1 | a0001c0002t0002g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.914+1186C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451995 | |||||||
| chr2:208452035 | A | G | 216 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(213): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.914+1226A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452035 | |||||||
| chr2:208452468 | C | T | 1 | a0001c0002t0002g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.914+1659C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452468 | |||||||
| chr2:208452627 | G | A | 1 | a0001c0003t0003g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.914+1818G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452627 | |||||||
| chr2:208452694 | G | T | 1 | a0001c0002t0002g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.914+1885G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452694 | |||||||
| chr2:208452762 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.914+1953A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452762 | |||||||
| chr2:208452847 | G | C | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.914+2038G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452847 | |||||||
| chr2:208452857 | G | A | 23 | a0001c0001t0001g0250 a0001c0001t0003g0211 a0001c0001t0003g0212 others(20): Show |
23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.914+2048G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452857 | |||||||
| chr2:208452925 | G | A | 1 | a0001c0003t0003g0263 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.914+2116G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452925 | |||||||
| chr2:208453068 | G | A | 148 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(145): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.914+2259G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453068 | |||||||
| chr2:208453112 | C | T | 4 | a0001c0003t0003g0205 a0001c0003t0003g0207 a0001c0008t0003g0201 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+2303C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453112 | |||||||
| chr2:208453153 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.914+2344C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453153 | |||||||
| chr2:208453475 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.914+2666A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453475 | |||||||
| chr2:208453609 | G | T | 27 | a0001c0001t0001g0196 a0001c0001t0001g0250 a0001c0001t0003g0211 others(24): Show |
27 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.914+2800G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453609 | |||||||
| chr2:208453661 | A | G | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.914+2852A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453661 | |||||||
| chr2:208453676 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.914+2867G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453676 | |||||||
| chr2:208453718 | A | G | 2 | a0001c0002t0002g0081 a0001c0002t0002g0082 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.914+2909A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453718 | |||||||
| chr2:208453733 | C | T | 46 | a0001c0001t0001g0196 a0001c0001t0001g0250 a0001c0001t0003g0211 others(43): Show |
46 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(43): Show |
intron_variant | MODIFIER | c.914+2924C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453733 | |||||||
| chr2:208453769 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.914+2960A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453769 | |||||||
| chr2:208453927 | C | T | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.914+3118C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453927 | |||||||
| chr2:208453934 | T | A | 5 | a0002c0004t0004g0268 a0002c0004t0004g0271 a0002c0004t0004g0272 others(2): Show |
5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.914+3125T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453934 | |||||||
| chr2:208454165 | CT | C | 6 | a0001c0003t0003g0195 a0001c0003t0003g0224 a0001c0006t0001g0186 others(3): Show |
6 | HG01255.hp1 HG01261.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.914+3366delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 208454165 | ||||||
| chr2:208454204 | G | C | 7 | a0001c0001t0001g0084 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG00609.hp1 NA18939.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.914+3395G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454204 | |||||||
| chr2:208454324 | A | G | 8 | a0001c0002t0002g0002 a0001c0002t0002g0135 a0001c0002t0002g0136 others(5): Show |
10 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.914+3515A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454324 | |||||||
| chr2:208454461 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.914+3652G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454461 | |||||||
| chr2:208454541 | C | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.914+3732C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454541 | |||||||
| chr2:208454708 | T | C | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.914+3899T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454708 | |||||||
| chr2:208454967 | A | G | 4 | a0001c0003t0003g0205 a0001c0003t0003g0207 a0001c0008t0003g0201 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+4158A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454967 | |||||||
| chr2:208455268 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.914+4459G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455268 | |||||||
| chr2:208455455 | T | G | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.915-4440T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455455 | |||||||
| chr2:208455475 | C | T | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(221): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.915-4420C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455475 | |||||||
| chr2:208455551 | C | G | 1 | a0005c0009t0001g0157 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.915-4344C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455551 | |||||||
| chr2:208455573 | G | T | 6 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(3): Show |
6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.915-4322G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455573 | |||||||
| chr2:208455575 | A | T | 6 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(3): Show |
6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.915-4320A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455575 | |||||||
| chr2:208455783 | ATTT | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 |
4 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.915-4111_915-4109d others(5): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455783 | |||||||
| chr2:208455883 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.915-4012A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455883 | |||||||
| chr2:208455904 | T | G | 1 | a0001c0001t0001g0035 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.915-3991T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455904 | |||||||
| chr2:208455931 | T | C | 8 | a0001c0002t0002g0065 a0001c0002t0002g0066 a0001c0002t0002g0073 others(5): Show |
8 | HG00438.hp1 HG00621.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.915-3964T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455931 | |||||||
| chr2:208456103 | G | A | 2 | a0001c0002t0002g0078 a0001c0003t0003g0030 |
2 | HG02145.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.915-3792G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456103 | |||||||
| chr2:208456107 | T | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0260 a0001c0001t0001g0261 others(14): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.915-3788T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456107 | |||||||
| chr2:208456113 | G | A | 1 | a0001c0002t0002g0074 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.915-3782G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456113 | |||||||
| chr2:208456167 | G | C | 3 | a0001c0001t0001g0196 a0001c0001t0005g0197 a0001c0001t0005g0249 |
3 | HG02486.hp2 HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.915-3728G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456167 | |||||||
| chr2:208456231 | G | A | 28 | a0001c0001t0001g0196 a0001c0001t0001g0250 a0001c0001t0003g0089 others(25): Show |
28 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.915-3664G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456231 | |||||||
| chr2:208456253 | G | A | 28 | a0001c0001t0001g0196 a0001c0001t0001g0250 a0001c0001t0003g0089 others(25): Show |
28 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.915-3642G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456253 | |||||||
| chr2:208456369 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.915-3526G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456369 | |||||||
| chr2:208456421 | A | G | 1 | a0001c0001t0001g0004 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.915-3474A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456421 | |||||||
| chr2:208456876 | T | A | 1 | a0001c0001t0001g0239 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.915-3019T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456876 | |||||||
| chr2:208457196 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.915-2699C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457196 | |||||||
| chr2:208457271 | G | T | 1 | a0001c0002t0002g0048 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.915-2624G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457271 | |||||||
| chr2:208457387 | A | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.915-2508A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457387 | |||||||
| chr2:208457461 | G | T | 1 | a0001c0002t0002g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.915-2434G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457461 | |||||||
| chr2:208457482 | T | C | 42 | a0001c0001t0001g0250 a0001c0001t0001g0260 a0001c0001t0001g0261 others(39): Show |
43 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.915-2413T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457482 | |||||||
| chr2:208457530 | A | G | 7 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(4): Show |
7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.915-2365A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457530 | |||||||
| chr2:208457587 | G | A | 3 | a0001c0001t0003g0212 a0001c0001t0003g0218 a0006c0012t0003g0217 |
3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.915-2308G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457587 | |||||||
| chr2:208457825 | G | A | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.915-2070G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457825 | |||||||
| chr2:208457991 | T | A | 1 | a0001c0002t0002g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.915-1904T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457991 | |||||||
| chr2:208458119 | G | A | 1 | a0001c0002t0002g0078 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.915-1776G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458119 | |||||||
| chr2:208458257 | C | CA | 24 | a0001c0001t0001g0250 a0001c0001t0003g0089 a0001c0001t0003g0211 others(21): Show |
24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.915-1633dupA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 208458257 | ||||||
| chr2:208458320 | C | T | 3 | a0001c0001t0003g0212 a0001c0001t0003g0218 a0006c0012t0003g0217 |
3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.915-1575C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458320 | |||||||
| chr2:208458326 | A | G | 2 | a0001c0006t0001g0186 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.915-1569A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458326 | |||||||
| chr2:208458338 | C | T | 1 | a0001c0002t0002g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.915-1557C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458338 | |||||||
| chr2:208458478 | A | C | 4 | a0001c0002t0002g0009 a0001c0002t0002g0062 a0001c0002t0002g0063 others(1): Show |
5 | NA18945.hp2 NA18971.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.915-1417A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458478 | |||||||
| chr2:208458495 | G | A | 4 | a0001c0001t0001g0196 a0001c0001t0005g0197 a0001c0001t0005g0249 others(1): Show |
4 | HG02486.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.915-1400G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458495 | |||||||
| chr2:208458599 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.915-1296T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458599 | |||||||
| chr2:208458610 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.915-1285C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458610 | |||||||
| chr2:208458693 | C | T | 151 | a0001c0001t0001g0250 a0001c0001t0001g0260 a0001c0001t0001g0261 others(148): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.915-1202C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458693 | |||||||
| chr2:208458828 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.915-1067G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458828 | |||||||
| chr2:208458848 | C | T | 2 | a0001c0006t0001g0186 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.915-1047C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458848 | |||||||
| chr2:208458889 | A | G | 2 | a0001c0003t0003g0012 a0001c0003t0003g0200 |
3 | HG01069.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.915-1006A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458889 | |||||||
| chr2:208458974 | A | G | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.915-921A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458974 | |||||||
| chr2:208458998 | GTTC | G | 77 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(74): Show |
83 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.915-891_915-889del others(3): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 208458998 | ||||||
| chr2:208459074 | G | A | 5 | a0002c0004t0004g0268 a0002c0004t0004g0271 a0002c0004t0004g0272 others(2): Show |
5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.915-821G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459074 | |||||||
| chr2:208459078 | A | G | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.915-817A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459078 | |||||||
| chr2:208459175 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.915-720T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459175 | |||||||
| chr2:208459216 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.915-679G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459216 | |||||||
| chr2:208459530 | G | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.915-365G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459530 | |||||||
| chr2:208459685 | T | A | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.915-210T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459685 | |||||||
| chr2:208459964 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | splice_region_variant&intron_variant | LOW | c.981+3A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208459964 | |||||||
| chr2:208460036 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.981+75C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208460036 | |||||||
| chr2:208460140 | A | G | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+179A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208460140 | |||||||
| chr2:208460905 | G | C | 1 | a0001c0001t0003g0213 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.981+944G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208460905 | |||||||
| chr2:208461479 | T | C | 1 | a0001c0002t0002g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.981+1518T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461479 | |||||||
| chr2:208461561 | G | A | 24 | a0001c0001t0001g0250 a0001c0001t0003g0089 a0001c0001t0003g0211 others(21): Show |
24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.981+1600G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461561 | |||||||
| chr2:208461627 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.981+1666T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461627 | |||||||
| chr2:208461659 | T | C | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.981+1698T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461659 | |||||||
| chr2:208461738 | G | A | 1 | a0001c0003t0003g0264 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.981+1777G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461738 | |||||||
| chr2:208461792 | C | T | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+1831C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461792 | |||||||
| chr2:208461830 | T | G | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.981+1869T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461830 | |||||||
| chr2:208462116 | G | A | 2 | a0001c0003t0003g0203 a0001c0003t0003g0254 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.981+2155G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462116 | |||||||
| chr2:208462125 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.981+2164A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462125 | |||||||
| chr2:208462634 | C | T | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.981+2673C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462634 | |||||||
| chr2:208462880 | G | A | 12 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(9): Show |
13 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+2919G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462880 | |||||||
| chr2:208462979 | G | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.981+3018G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462979 | |||||||
| chr2:208462997 | G | A | 5 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(2): Show |
5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+3036G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462997 | |||||||
| chr2:208463126 | A | G | 1 | a0001c0001t0010g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.981+3165A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463126 | |||||||
| chr2:208463353 | C | T | 1 | a0005c0009t0001g0157 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.981+3392C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463353 | |||||||
| chr2:208463470 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0123 |
2 | HG00423.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.981+3509G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463470 | |||||||
| chr2:208463768 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+3807T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463768 | |||||||
| chr2:208463817 | T | A | 1 | a0007c0013t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.981+3856T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463817 | |||||||
| chr2:208463817 | T | C | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+3856T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463817 | |||||||
| chr2:208463858 | G | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.981+3897G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463858 | |||||||
| chr2:208463903 | G | A | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+3942G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463903 | |||||||
| chr2:208463968 | A | T | 33 | a0001c0003t0003g0012 a0001c0003t0003g0021 a0001c0003t0003g0022 others(30): Show |
34 | HG01069.hp2 HG01433.hp2 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.981+4007A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463968 | |||||||
| chr2:208463988 | A | T | 66 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(63): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.981+4027A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463988 | |||||||
| chr2:208463989 | A | G | 1 | a0001c0003t0003g0263 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.981+4028A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463989 | |||||||
| chr2:208464036 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.981+4075G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464036 | |||||||
| chr2:208464231 | A | G | 2 | a0001c0001t0005g0197 a0001c0001t0005g0249 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.981+4270A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464231 | |||||||
| chr2:208464238 | A | G | 18 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+4277A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464238 | |||||||
| chr2:208464275 | G | A | 1 | a0001c0003t0003g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.981+4314G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464275 | |||||||
| chr2:208464329 | A | G | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.981+4368A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464329 | |||||||
| chr2:208464408 | C | T | 2 | a0001c0003t0003g0034 a0001c0003t0003g0204 |
2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.981+4447C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464408 | |||||||
| chr2:208464453 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.981+4492A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464453 | |||||||
| chr2:208464527 | G | A | 4 | a0001c0002t0002g0127 a0001c0002t0002g0231 a0001c0002t0002g0232 others(1): Show |
4 | NA18960.hp1 NA18990.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+4566G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464527 | |||||||
| chr2:208464568 | G | A | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.981+4607G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464568 | |||||||
| chr2:208464599 | C | T | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.981+4638C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464599 | |||||||
| chr2:208464614 | T | C | 6 | a0001c0003t0003g0015 a0001c0003t0003g0264 a0001c0003t0003g0266 others(3): Show |
7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.981+4653T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464614 | |||||||
| chr2:208464718 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.981+4757A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464718 | |||||||
| chr2:208464736 | G | A | 1 | a0001c0003t0003g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.981+4775G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464736 | |||||||
| chr2:208464794 | G | A | 1 | a0001c0002t0002g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.981+4833G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464794 | |||||||
| chr2:208464882 | A | T | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+4921A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464882 | |||||||
| chr2:208464938 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.981+4977T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464938 | |||||||
| chr2:208464958 | C | T | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.981+4997C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464958 | |||||||
| chr2:208465119 | G | A | 1 | a0001c0002t0002g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.981+5158G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465119 | |||||||
| chr2:208465272 | A | G | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.981+5311A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465272 | |||||||
| chr2:208465306 | T | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.981+5345T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465306 | |||||||
| chr2:208465332 | C | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.981+5371C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465332 | |||||||
| chr2:208465388 | C | CT | 12 | a0001c0002t0002g0052 a0001c0002t0002g0054 a0001c0002t0002g0057 others(9): Show |
12 | HG00423.hp1 HG00438.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.981+5459dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | ||||||
| chr2:208465388 | C | CTT | 9 | a0001c0002t0002g0063 a0001c0002t0002g0066 a0001c0002t0002g0072 others(6): Show |
9 | HG02027.hp2 HG02083.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+5458_981+5459d others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | ||||||
| chr2:208465388 | CT | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
61 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.981+5459delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | ||||||
| chr2:208465388 | CTT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.981+5458_981+5459d others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | ||||||
| chr2:208465388 | CTTT | C | 18 | a0001c0001t0001g0085 a0001c0003t0003g0020 a0001c0003t0003g0023 others(15): Show |
18 | HG01433.hp2 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.981+5457_981+5459d others(5): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | ||||||
| chr2:208465388 | CTTTT | C | 10 | a0001c0001t0005g0249 a0001c0003t0003g0021 a0001c0003t0003g0022 others(7): Show |
10 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.981+5456_981+5459d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | ||||||
| chr2:208465663 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.981+5702A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465663 | |||||||
| chr2:208465715 | T | A | 9 | a0001c0001t0005g0197 a0001c0002t0002g0062 a0001c0002t0002g0063 others(6): Show |
9 | HG02486.hp1 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+5754T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465715 | |||||||
| chr2:208465893 | TA | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0246 |
3 | HG01516.hp1 HG02895.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.981+5937delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465893 | ||||||
| chr2:208465894 | A | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.981+5933A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465894 | |||||||
| chr2:208465895 | A | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.981+5934A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465895 | |||||||
| chr2:208466090 | T | G | 2 | a0001c0006t0001g0186 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.981+6129T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466090 | |||||||
| chr2:208466385 | T | C | 1 | a0001c0001t0003g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.981+6424T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466385 | |||||||
| chr2:208466391 | T | C | 1 | a0001c0002t0002g0086 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.981+6430T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466391 | |||||||
| chr2:208466548 | G | A | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+6587G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466548 | |||||||
| chr2:208466763 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.981+6802C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466763 | |||||||
| chr2:208466776 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.981+6815A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466776 | |||||||
| chr2:208466862 | T | C | 1 | a0001c0003t0003g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.981+6901T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466862 | |||||||
| chr2:208466918 | G | A | 3 | a0001c0001t0003g0212 a0001c0001t0003g0218 a0006c0012t0003g0217 |
3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.981+6957G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466918 | |||||||
| chr2:208467202 | T | A | 2 | a0001c0003t0003g0012 a0001c0003t0003g0200 |
3 | HG01069.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.981+7241T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467202 | |||||||
| chr2:208467408 | A | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG02257.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+7447A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467408 | |||||||
| chr2:208467473 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0229 others(15): Show |
22 | HG00597.hp1 HG02148.hp2 NA18940.hp2 others(19): Show |
intron_variant | MODIFIER | c.981+7512A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467473 | |||||||
| chr2:208467706 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.981+7745G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467706 | |||||||
| chr2:208467730 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.981+7769T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467730 | |||||||
| chr2:208467737 | CA | C | 24 | a0001c0001t0001g0250 a0001c0001t0003g0089 a0001c0001t0003g0211 others(21): Show |
24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.981+7777delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467737 | |||||||
| chr2:208467796 | AAAG | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0162 |
3 | HG02083.hp2 NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.981+7837_981+7839d others(5): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208467796 | ||||||
| chr2:208467801 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0162 |
3 | HG02083.hp2 NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.981+7840C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467801 | |||||||
| chr2:208467854 | A | G | 1 | a0007c0013t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.981+7893A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467854 | |||||||
| chr2:208468373 | A | T | 2 | a0001c0006t0001g0186 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.981+8412A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468373 | |||||||
| chr2:208468454 | G | A | 24 | a0001c0001t0001g0250 a0001c0001t0003g0089 a0001c0001t0003g0211 others(21): Show |
24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.981+8493G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468454 | |||||||
| chr2:208468533 | C | T | 2 | a0001c0002t0002g0007 a0001c0002t0002g0112 |
3 | HG02109.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.981+8572C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468533 | |||||||
| chr2:208468689 | C | T | 25 | a0001c0001t0001g0139 a0001c0001t0001g0250 a0001c0001t0003g0089 others(22): Show |
25 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.981+8728C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468689 | |||||||
| chr2:208468770 | T | C | 2 | a0001c0002t0002g0081 a0001c0002t0002g0082 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.981+8809T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468770 | |||||||
| chr2:208468937 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.981+8976T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468937 | |||||||
| chr2:208469407 | T | A | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.981+9446T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208469407 | |||||||
| chr2:208469704 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG02257.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+9743A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208469704 | |||||||
| chr2:208469903 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.981+9942G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208469903 | |||||||
| chr2:208469943 | A | G | 2 | a0001c0006t0001g0186 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.981+9982A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208469943 | |||||||
| chr2:208470046 | T | C | 2 | a0001c0006t0001g0186 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.981+10085T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470046 | |||||||
| chr2:208470135 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.981+10174C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470135 | |||||||
| chr2:208470205 | C | T | 1 | a0001c0001t0001g0014 | 2 | NA18942.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.981+10244C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470205 | |||||||
| chr2:208470206 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0189 |
2 | NA18970.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.981+10245G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470206 | |||||||
| chr2:208470253 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.981+10292A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470253 | |||||||
| chr2:208470361 | A | G | 1 | a0001c0002t0002g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.981+10400A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470361 | |||||||
| chr2:208470402 | ATCTCATC others(255): Show |
A | 1 | a0001c0003t0003g0198 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.981+10444_982-1040 others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208470402 | ||||||
| chr2:208470487 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.981+10526C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470487 | |||||||
| chr2:208470565 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.982-10505C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470565 | |||||||
| chr2:208470621 | G | T | 2 | a0001c0006t0001g0186 a0001c0006t0005g0199 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.982-10449G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470621 | |||||||
| chr2:208470699 | C | G | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982-10371C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470699 | |||||||
| chr2:208470771 | G | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0249 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-10299G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470771 | |||||||
| chr2:208470964 | G | A | 1 | a0001c0001t0003g0214 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.982-10106G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470964 | |||||||
| chr2:208471044 | A | C | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982-10026A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208471044 | |||||||
| chr2:208471458 | T | A | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.982-9612T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208471458 | |||||||
| chr2:208472036 | A | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.982-9034A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208472036 | |||||||
| chr2:208472247 | G | A | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982-8823G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208472247 | |||||||
| chr2:208472688 | T | A | 37 | a0001c0003t0003g0015 a0001c0003t0003g0020 a0001c0003t0003g0021 others(34): Show |
38 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.982-8382T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208472688 | |||||||
| chr2:208472744 | A | G | 1 | a0001c0001t0005g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.982-8326A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208472744 | |||||||
| chr2:208472895 | TA | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.982-8173delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208472895 | ||||||
| chr2:208473012 | T | G | 2 | a0001c0003t0003g0203 a0001c0003t0003g0254 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.982-8058T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208473012 | |||||||
| chr2:208473674 | C | T | 2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.982-7396C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208473674 | |||||||
| chr2:208473888 | G | A | 6 | a0001c0011t0004g0193 a0002c0004t0004g0268 a0002c0004t0004g0271 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.982-7182G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208473888 | |||||||
| chr2:208474010 | C | G | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.982-7060C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474010 | |||||||
| chr2:208474033 | A | G | 42 | a0001c0003t0003g0012 a0001c0003t0003g0015 a0001c0003t0003g0020 others(39): Show |
44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.982-7037A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474033 | |||||||
| chr2:208474166 | T | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0249 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-6904T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474166 | |||||||
| chr2:208474258 | A | G | 12 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.982-6812A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474258 | |||||||
| chr2:208474274 | C | CA | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.982-6796_982-6795i others(3): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474274 | |||||||
| chr2:208474477 | A | T | 1 | a0001c0003t0003g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.982-6593A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474477 | |||||||
| chr2:208474488 | C | G | 45 | a0001c0001t0005g0197 a0001c0001t0005g0249 a0001c0003t0003g0012 others(42): Show |
47 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.982-6582C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474488 | |||||||
| chr2:208474526 | G | A | 8 | a0001c0001t0001g0124 a0001c0001t0001g0141 a0001c0001t0001g0143 others(5): Show |
8 | HG01943.hp1 HG01993.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-6544G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474526 | |||||||
| chr2:208474792 | G | T | 3 | a0001c0001t0005g0197 a0001c0001t0005g0249 a0001c0006t0005g0199 |
3 | HG02258.hp1 HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-6278G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474792 | |||||||
| chr2:208474919 | A | T | 1 | a0001c0001t0010g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.982-6151A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474919 | |||||||
| chr2:208474978 | C | T | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982-6092C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474978 | |||||||
| chr2:208475092 | A | G | 2 | a0001c0003t0003g0034 a0001c0003t0003g0204 |
2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.982-5978A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208475092 | |||||||
| chr2:208475187 | A | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.982-5883A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208475187 | |||||||
| chr2:208475188 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.982-5882A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208475188 | |||||||
| chr2:208475732 | T | C | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982-5338T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208475732 | |||||||
| chr2:208476057 | G | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0249 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-5013G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476057 | |||||||
| chr2:208476130 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.982-4940A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476130 | |||||||
| chr2:208476162 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.982-4908A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476162 | |||||||
| chr2:208476199 | G | C | 5 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(2): Show |
5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.982-4871G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476199 | |||||||
| chr2:208476280 | T | C | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.982-4790T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476280 | |||||||
| chr2:208476423 | A | G | 2 | a0001c0003t0003g0029 a0001c0003t0003g0031 |
2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.982-4647A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476423 | |||||||
| chr2:208476501 | G | T | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.982-4569G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476501 | |||||||
| chr2:208476790 | G | A | 24 | a0001c0001t0001g0250 a0001c0001t0003g0089 a0001c0001t0003g0211 others(21): Show |
24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.982-4280G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476790 | |||||||
| chr2:208477369 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.982-3701A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477369 | |||||||
| chr2:208477392 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.982-3678C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477392 | |||||||
| chr2:208477458 | T | G | 1 | a0005c0009t0001g0157 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.982-3612T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477458 | |||||||
| chr2:208477581 | C | A | 15 | a0001c0003t0003g0021 a0001c0003t0003g0022 a0001c0003t0003g0023 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.982-3489C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477581 | |||||||
| chr2:208477690 | T | C | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.982-3380T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477690 | |||||||
| chr2:208477764 | CTTTGT | C | 8 | a0001c0003t0003g0015 a0001c0003t0003g0259 a0001c0003t0003g0263 others(5): Show |
9 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.982-3300_982-3296d others(7): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477764 | ||||||
| chr2:208477880 | T | TTACTACT others(11): Show |
10 | a0001c0002t0002g0002 a0001c0002t0002g0135 a0001c0002t0002g0136 others(7): Show |
12 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-3142_982-3125d others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477880 | ||||||
| chr2:208477880 | TTACTACT others(11): Show |
T | 2 | a0001c0001t0005g0197 a0001c0002t0002g0088 |
2 | NA18950.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-3142_982-3125d others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477880 | ||||||
| chr2:208477882 | A | G | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.982-3188A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477882 | |||||||
| chr2:208477896 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.982-3174C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477896 | |||||||
| chr2:208477916 | C | CTACTACT others(20): Show |
1 | a0001c0003t0003g0223 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.982-3151_982-3125d others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477916 | ||||||
| chr2:208477937 | CTACTAGT others(20): Show |
C | 2 | a0001c0003t0003g0203 a0001c0003t0003g0254 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.982-3124_982-3098d others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477937 | ||||||
| chr2:208477946 | G | C | 6 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(3): Show |
6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.982-3124G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477946 | |||||||
| chr2:208477946 | G | GTACTAGC others(20): Show |
8 | a0001c0002t0002g0065 a0001c0002t0002g0066 a0001c0002t0002g0073 others(5): Show |
8 | HG00438.hp1 HG00621.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-3091_982-3065d others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477946 | ||||||
| chr2:208477946 | GTACTAGC others(20): Show |
G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.982-3091_982-3065d others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477946 | ||||||
| chr2:208477953 | C | T | 6 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(3): Show |
6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.982-3117C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477953 | |||||||
| chr2:208477964 | G | GTACTAGC others(5): Show |
1 | a0001c0001t0001g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.982-3100_982-3099i others(14): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477964 | ||||||
| chr2:208477970 | GTACTACT others(8): Show |
G | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982-3094_982-3080d others(17): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477970 | ||||||
| chr2:208477973 | C | CTACTAGT others(11): Show |
2 | a0001c0003t0003g0194 a0001c0003t0003g0195 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.982-3091_982-3090i others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477973 | ||||||
| chr2:208477973 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.982-3097C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477973 | |||||||
| chr2:208477973 | CTACTAGC others(11): Show |
C | 1 | a0001c0003t0003g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.982-3090_982-3073d others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477973 | ||||||
| chr2:208477980 | C | T | 67 | a0001c0001t0001g0250 a0001c0001t0003g0089 a0001c0001t0003g0211 others(64): Show |
69 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.982-3090C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477980 | |||||||
| chr2:208478284 | C | T | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982-2786C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478284 | |||||||
| chr2:208478493 | G | A | 6 | a0001c0011t0004g0193 a0002c0004t0004g0268 a0002c0004t0004g0271 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.982-2577G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478493 | |||||||
| chr2:208478534 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0190 |
2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.982-2536C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478534 | |||||||
| chr2:208478739 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.982-2331C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478739 | |||||||
| chr2:208478804 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.982-2266C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478804 | |||||||
| chr2:208479141 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.982-1929G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479141 | |||||||
| chr2:208479184 | G | T | 6 | a0001c0001t0003g0211 a0001c0001t0003g0219 a0001c0001t0003g0225 others(3): Show |
6 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.982-1886G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479184 | |||||||
| chr2:208479196 | C | T | 1 | a0001c0002t0002g0046 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.982-1874C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479196 | |||||||
| chr2:208479242 | G | T | 2 | a0001c0002t0002g0046 a0001c0002t0002g0074 |
2 | NA18952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.982-1828G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479242 | |||||||
| chr2:208479288 | G | A | 6 | a0001c0003t0003g0015 a0001c0003t0003g0264 a0001c0003t0003g0266 others(3): Show |
7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.982-1782G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479288 | |||||||
| chr2:208479490 | C | T | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982-1580C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479490 | |||||||
| chr2:208479645 | C | T | 1 | a0001c0002t0002g0076 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.982-1425C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479645 | |||||||
| chr2:208480069 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.982-1001C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480069 | |||||||
| chr2:208480259 | G | A | 7 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 others(4): Show |
7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.982-811G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480259 | |||||||
| chr2:208480271 | A | G | 8 | a0001c0002t0002g0002 a0001c0002t0002g0135 a0001c0002t0002g0136 others(5): Show |
10 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.982-799A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480271 | |||||||
| chr2:208480583 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.982-487G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480583 | |||||||
| chr2:208480632 | C | T | 1 | a0001c0001t0010g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.982-438C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480632 | |||||||
| chr2:208480789 | A | G | 1 | a0001c0003t0003g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.982-281A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480789 | |||||||
| chr2:208480941 | T | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.982-129T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480941 | |||||||
| chr2:208481219 | CT | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1076+72delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 208481219 | ||||||
| chr2:208481219 | CTT | C | 27 | a0001c0001t0001g0126 a0001c0001t0001g0162 a0001c0001t0001g0229 others(24): Show |
27 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.1076+71_1076+72del others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 208481219 | ||||||
| chr2:208481295 | T | TGCAACCT others(1): Show |
191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1076+131_1076+132i others(10): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481295 | |||||||
| chr2:208481304 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG00323.hp1 HG01106.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1076+140G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481304 | |||||||
| chr2:208481360 | G | A | 1 | a0001c0003t0003g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1076+196G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481360 | |||||||
| chr2:208481622 | A | G | 42 | a0001c0003t0003g0012 a0001c0003t0003g0015 a0001c0003t0003g0020 others(39): Show |
44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1076+458A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481622 | |||||||
| chr2:208481864 | G | C | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1076+700G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481864 | |||||||
| chr2:208481939 | T | C | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1076+775T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481939 | |||||||
| chr2:208482083 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1076+919T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482083 | |||||||
| chr2:208482267 | T | C | 1 | a0001c0003t0003g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+1103T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482267 | |||||||
| chr2:208482282 | C | T | 5 | a0002c0004t0004g0268 a0002c0004t0004g0271 a0002c0004t0004g0272 others(2): Show |
5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076+1118C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482282 | |||||||
| chr2:208482379 | A | G | 4 | a0001c0002t0002g0036 a0001c0002t0002g0038 a0001c0002t0002g0060 others(1): Show |
4 | HG00609.hp2 NA18983.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+1215A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482379 | |||||||
| chr2:208482522 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1076+1358A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482522 | |||||||
| chr2:208482745 | T | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1076+1581T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482745 | |||||||
| chr2:208482918 | C | T | 1 | a0001c0002t0002g0122 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1076+1754C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482918 | |||||||
| chr2:208483079 | G | T | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1076+1915G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483079 | |||||||
| chr2:208483081 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1076+1917G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483081 | |||||||
| chr2:208483380 | G | T | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1076+2216G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483380 | |||||||
| chr2:208483417 | T | A | 33 | a0001c0003t0003g0012 a0001c0003t0003g0021 a0001c0003t0003g0022 others(30): Show |
34 | HG01069.hp2 HG01433.hp2 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1076+2253T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483417 | |||||||
| chr2:208483456 | G | A | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1076+2292G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483456 | |||||||
| chr2:208483575 | G | A | 24 | a0001c0001t0001g0250 a0001c0001t0003g0089 a0001c0001t0003g0211 others(21): Show |
24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.1076+2411G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483575 | |||||||
| chr2:208483586 | A | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1076+2422A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483586 | |||||||
| chr2:208483672 | C | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1076+2508C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483672 | |||||||
| chr2:208483673 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1076+2509A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483673 | |||||||
| chr2:208483687 | T | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1076+2523T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483687 | |||||||
| chr2:208483899 | G | A | 1 | a0001c0003t0003g0254 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1076+2735G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483899 | |||||||
| chr2:208484170 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1076+3006T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484170 | |||||||
| chr2:208484178 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1076+3014A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484178 | |||||||
| chr2:208484203 | C | T | 1 | a0001c0002t0002g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1076+3039C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484203 | |||||||
| chr2:208484314 | G | A | 1 | a0001c0006t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1076+3150G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484314 | |||||||
| chr2:208484498 | T | C | 14 | a0001c0003t0003g0015 a0001c0003t0003g0020 a0001c0003t0003g0259 others(11): Show |
15 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1076+3334T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484498 | |||||||
| chr2:208485252 | G | C | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1077-3760G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485252 | |||||||
| chr2:208485339 | C | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1077-3673C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485339 | |||||||
| chr2:208485403 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1077-3609G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485403 | |||||||
| chr2:208485575 | G | T | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1077-3437G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485575 | |||||||
| chr2:208485582 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0149 others(15): Show |
22 | HG00597.hp1 HG02148.hp2 NA18940.hp2 others(19): Show |
intron_variant | MODIFIER | c.1077-3430C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485582 | |||||||
| chr2:208485583 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1077-3429A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485583 | |||||||
| chr2:208485658 | G | T | 5 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(2): Show |
5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077-3354G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485658 | |||||||
| chr2:208485707 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1077-3305C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485707 | |||||||
| chr2:208485901 | C | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1077-3111C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485901 | |||||||
| chr2:208486021 | G | A | 1 | a0001c0011t0004g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1077-2991G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208486021 | |||||||
| chr2:208486600 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1077-2412A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208486600 | |||||||
| chr2:208486611 | A | T | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1077-2401A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208486611 | |||||||
| chr2:208486732 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1077-2280A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208486732 | |||||||
| chr2:208487211 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1077-1801A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487211 | |||||||
| chr2:208487433 | C | T | 1 | a0001c0003t0003g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1077-1579C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487433 | |||||||
| chr2:208487600 | C | T | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-1412C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487600 | |||||||
| chr2:208487687 | G | C | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-1325G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487687 | |||||||
| chr2:208487725 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1077-1287C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487725 | |||||||
| chr2:208487776 | A | G | 25 | a0001c0001t0001g0250 a0001c0001t0003g0089 a0001c0001t0003g0211 others(22): Show |
25 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1077-1236A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487776 | |||||||
| chr2:208487813 | C | T | 25 | a0001c0001t0001g0250 a0001c0001t0003g0089 a0001c0001t0003g0211 others(22): Show |
25 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1077-1199C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487813 | |||||||
| chr2:208487874 | G | A | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-1138G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487874 | |||||||
| chr2:208488141 | G | A | 1 | a0001c0003t0003g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1077-871G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488141 | |||||||
| chr2:208488210 | C | T | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-802C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488210 | |||||||
| chr2:208488447 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1077-565A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488447 | |||||||
| chr2:208488487 | A | AT | 2 | a0001c0001t0001g0005 a0001c0001t0001g0019 |
3 | HG02257.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1077-521dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 208488487 | ||||||
| chr2:208488526 | G | A | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-486G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488526 | |||||||
| chr2:208488702 | C | T | 3 | a0001c0003t0003g0034 a0001c0003t0003g0198 a0001c0003t0003g0204 |
3 | HG01433.hp2 HG02258.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1077-310C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488702 | |||||||
| chr2:208488826 | G | C | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-186G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488826 | |||||||
| chr2:208488833 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1077-179C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488833 | |||||||
| chr2:208488882 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1077-130A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488882 | |||||||
| chr2:208488931 | GT | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1077-71delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 208488931 | ||||||
| chr2:208488951 | C | A | 6 | a0001c0002t0002g0002 a0001c0002t0002g0136 a0001c0002t0002g0137 others(3): Show |
8 | HG02055.hp1 HG02451.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077-61C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488951 | |||||||
| chr2:208488969 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1077-43G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488969 | |||||||
| chr2:208489719 | T | G | 1 | a0001c0001t0006g0100 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1215+569T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/12 | chr2 | 208489719 | |||||||
| chr2:208490132 | C | T | 1 | a0001c0003t0003g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1216-507C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/12 | chr2 | 208490132 | |||||||
| chr2:208490580 | T | C | 4 | a0001c0003t0003g0205 a0001c0003t0003g0207 a0001c0008t0003g0201 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-59T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/12 | chr2 | 208490580 | |||||||
| chr2:208490853 | A | G | 8 | a0001c0002t0002g0002 a0001c0002t0002g0135 a0001c0002t0002g0136 others(5): Show |
10 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257+173A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208490853 | |||||||
| chr2:208490939 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1257+259A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208490939 | |||||||
| chr2:208491203 | A | G | 1 | a0001c0002t0002g0138 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1257+523A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491203 | |||||||
| chr2:208491215 | G | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0249 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1257+535G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491215 | |||||||
| chr2:208491222 | G | A | 9 | a0001c0003t0003g0015 a0001c0003t0003g0020 a0001c0003t0003g0259 others(6): Show |
10 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257+542G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491222 | |||||||
| chr2:208491252 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1257+572G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491252 | |||||||
| chr2:208491529 | A | G | 2 | a0001c0002t0002g0061 a0001c0002t0002g0092 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1257+849A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491529 | |||||||
| chr2:208491675 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1257+995C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491675 | |||||||
| chr2:208491676 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1257+996C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491676 | |||||||
| chr2:208491683 | C | G | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1257+1003C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491683 | |||||||
| chr2:208491691 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1257+1011C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491691 | |||||||
| chr2:208491847 | A | C | 2 | a0001c0003t0003g0015 a0001c0003t0003g0267 |
3 | HG00735.hp1 HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1257+1167A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491847 | |||||||
| chr2:208492195 | C | T | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1258-1069C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492195 | |||||||
| chr2:208492198 | G | A | 1 | a0001c0006t0005g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1258-1066G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492198 | |||||||
| chr2:208492268 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0007g0120 |
2 | NA18978.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1258-996T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492268 | |||||||
| chr2:208492554 | C | T | 1 | a0001c0001t0005g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1258-710C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492554 | |||||||
| chr2:208492729 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1258-535T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492729 | |||||||
| chr2:208492746 | A | G | 5 | a0002c0004t0004g0268 a0002c0004t0004g0271 a0002c0004t0004g0272 others(2): Show |
5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-518A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492746 | |||||||
| chr2:208492898 | G | A | 1 | a0004c0007t0001g0013 | 2 | NA18952.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1258-366G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492898 | |||||||
| chr2:208492918 | A | G | 1 | a0001c0003t0003g0259 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1258-346A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492918 | |||||||
| chr2:208492947 | C | G | 42 | a0001c0003t0003g0012 a0001c0003t0003g0015 a0001c0003t0003g0020 others(39): Show |
44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1258-317C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492947 | |||||||
| chr2:208493145 | G | A | 42 | a0001c0003t0003g0012 a0001c0003t0003g0015 a0001c0003t0003g0020 others(39): Show |
44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1258-119G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208493145 |