Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 956 |
| ensemblid | ENSG00000168032.10 |
| hgncid | 3365 |
| symbol | ENTPD3 |
| name | ectonucleoside triphosphate diphosphohydrolase 3 |
| refseq_nuc | NM_001248.4 |
| refseq_prot | NP_001239.2 |
| ensembl_nuc | ENST00000301825.8 |
| ensembl_prot | ENSP00000301825.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 40387184 |
| end | 40428744 |
| strand | + |
| ver | v1.2 |
| region | chr3:40387184-40428744 |
| region5000 | chr3:40382184-40433744 |
| regionname0 | ENTPD3_chr3_40387184_40428744 |
| regionname5000 | ENTPD3_chr3_40382184_40433744 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 529 | 242 | 84 | 32 | 90 | 10 | 25 | 72 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0002 | 0/1 | 529 | 112 | 7 | 21 | 62 | 4 | 17 | 48 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0003 | 0/0 | 529 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0004 | 0/0 | 529 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0005 | 0/0 | 529 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0006 | 0/0 | 529 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0007 | 0/0 | 529 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0008 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0009 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0010 | 0/0 | 494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(489): Show |
chr3 | 40382184 | 40433744 |
| a0011 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| a0012 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | MFTVL others(524): Show |
chr3 | 40382184 | 40433744 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1587 | 234 | 78 | 32 | 88 | 10 | 25 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0001c0004 | 0/0 | 1587 | 5 | 5 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0001c0005 | 0/0 | 1587 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0001c0011 | 0/0 | 1696 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1691): Show |
chr3 | 40382184 | 40433744 | ||
| a0002c0002 | 0/1 | 1587 | 112 | 7 | 21 | 62 | 4 | 17 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0003c0003 | 0/0 | 1587 | 8 | 0 | 0 | 8 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0004c0006 | 0/0 | 1587 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0005c0007 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0006c0008 | 0/0 | 1587 | 2 | 0 | 0 | 0 | 0 | 2 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0007c0012 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0008c0014 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0009c0010 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0010c0015 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1477): Show |
chr3 | 40382184 | 40433744 | ||
| a0011c0009 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 | ||
| a0012c0013 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | ATGTT others(1582): Show |
chr3 | 40382184 | 40433744 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2916 | 164 | 31 | 23 | 81 | 8 | 20 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0002 | 0/0 | 2916 | 12 | 9 | 3 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0003 | 0/0 | 2916 | 35 | 19 | 4 | 7 | 1 | 4 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0004 | 0/0 | 2916 | 9 | 9 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0005 | 0/0 | 2916 | 5 | 5 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0006 | 0/0 | 2916 | 3 | 0 | 1 | 0 | 1 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0007 | 0/0 | 2916 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0009 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0010 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0011 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0001t0013 | 0/0 | 2916 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0004t0002 | 0/0 | 2916 | 5 | 5 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0005t0003 | 0/0 | 2916 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0001c0011t0002 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(3020): Show |
chr3 | 40382184 | 40433744 |
| a0002c0002t0002 | 0/1 | 2916 | 109 | 7 | 19 | 62 | 4 | 16 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0002c0002t0008 | 0/0 | 2916 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0002c0002t0012 | 0/0 | 2916 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0003c0003t0001 | 0/0 | 2916 | 8 | 0 | 0 | 8 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0004c0006t0001 | 0/0 | 2916 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0005c0007t0002 | 0/0 | 2916 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0006c0008t0001 | 0/0 | 2916 | 2 | 0 | 0 | 0 | 0 | 2 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0007c0012t0001 | 0/0 | 2916 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0008c0014t0003 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0009c0010t0002 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0010c0015t0001 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2806): Show |
chr3 | 40382184 | 40433744 |
| a0011c0009t0001 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| a0012c0013t0002 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | GCTGA others(2911): Show |
chr3 | 40382184 | 40433744 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 2 | 7 | 11 | 0 | 3 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0003 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0007 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0002g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0001t0013g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0004t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0004t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0004t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0004t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0005t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0005t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0001c0011t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0002 | 0/0 | 18 | 0 | 4 | 10 | 2 | 2 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0006 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0011 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0008g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0002c0002t0012g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0003c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0004c0006t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0004c0006t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0005c0007t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0005c0007t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0006c0008t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0007c0012t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0008c0014t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0009c0010t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0010c0015t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0011c0009t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| a0012c0013t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0152 | EUR | GBR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0011 | EUR | FIN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00558 | hp2 | a0004 | c0006 | t0001 | g0110 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00642 | hp1 | a0001 | c0001 | t0013 | g0095 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00738 | hp1 | a0002 | c0002 | t0008 | g0113 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0150 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0196 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01175 | hp1 | a0002 | c0002 | t0008 | g0107 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01257 | hp1 | a0007 | c0012 | t0001 | g0195 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0124 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0123 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | IBS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0218 | EUR | IBS | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0154 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02027 | hp2 | a0008 | c0014 | t0003 | g0089 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0227 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | KHV | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0137 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02165 | hp1 | a0009 | c0010 | t0002 | g0076 | EAS | CDX | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0121 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0045 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02615 | hp2 | a0005 | c0007 | t0002 | g0040 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0092 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02630 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02683 | hp2 | a0006 | c0008 | t0001 | g0025 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02717 | hp1 | a0005 | c0007 | t0002 | g0009 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02735 | hp2 | a0002 | c0002 | t0012 | g0146 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0078 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02809 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0101 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0103 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0041 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0118 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0097 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0144 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03486 | hp2 | a0001 | c0004 | t0002 | g0046 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0069 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0071 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0047 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03516 | hp2 | a0010 | c0015 | t0001 | g0190 | AFR | ESN | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03579 | hp1 | a0001 | c0011 | t0002 | g0061 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03688 | hp1 | a0006 | c0008 | t0001 | g0025 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0109 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0136 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0080 | SAS | BEB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0016 | SAS | BEB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0068 | SAS | BEB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0105 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | STU | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18956 | hp1 | a0011 | c0009 | t0001 | g0210 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18982 | hp1 | a0003 | c0003 | t0001 | g0207 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18985 | hp1 | a0003 | c0003 | t0001 | g0208 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18985 | hp2 | a0012 | c0013 | t0002 | g0115 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19006 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0220 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | LWK | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | LWK | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0229 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19075 | hp1 | a0001 | c0005 | t0003 | g0093 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19079 | hp2 | a0003 | c0003 | t0001 | g0205 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0209 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19082 | hp2 | a0004 | c0006 | t0001 | g0141 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0060 | AFR | YRI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | ASW | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | TSI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | TSI | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0201 | SAS | GIH | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0016 | SAS | GIH | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | USA | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18955 | hp1 | a0001 | c0005 | t0003 | g0094 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | USA | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0102 | AFR | USA | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0151 | AFR | LWK | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | LWK | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0066 | REF | REF | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0007 | REF | REF | ENTPD3_chr3_40382184_40433744 | ENTPD3 | chr3 | 40382184 | 40433744 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:40388046 | C | G | 1 | a0001 | 1 | HG00642.hp1 | splice_region_variant | LOW | c.-12C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/11 | chr3 | 40388046 | |||||||
| chr3:40388095 | C | A | 2 | a0003 a0011 |
9 | HG02129.hp2 NA18956.hp1 NA18973.hp1 others(6): Show |
missense_variant&splice_region_variant | MODERATE | c.38C>A | p.Ala13Glu | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/11 | 128/2916 | 38/1590 | 13/529 | chr3 | 40388095 | |||
| chr3:40397267 | CTGAACAG others(3724): Show |
C | 1 | a0010 | 1 | HG03516.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.169-3624_275del | p.Tyr57fs | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/11 | 169/1590 | 57/529 | INFO_REALIGN_3_PRIME | chr3 | 40397267 | |||
| chr3:40411951 | G | T | 1 | a0008 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.426G>T | p.Met142Ile | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/11 | 516/2916 | 426/1590 | 142/529 | chr3 | 40411951 | |||
| chr3:40415883 | C | A | 1 | a0008 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.641C>A | p.Thr214Asn | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/11 | 731/2916 | 641/1590 | 214/529 | chr3 | 40415883 | |||
| chr3:40415885 | A | C | 1 | a0011 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.643A>C | p.Thr215Pro | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/11 | 733/2916 | 643/1590 | 215/529 | chr3 | 40415885 | |||
| chr3:40415886 | C | T | 1 | a0006 | 2 | HG02683.hp2 HG03688.hp1 |
missense_variant | MODERATE | c.644C>T | p.Thr215Met | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/11 | 734/2916 | 644/1590 | 215/529 | chr3 | 40415886 | |||
| chr3:40415943 | A | G | 1 | a0012 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.701A>G | p.Lys234Arg | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/11 | 791/2916 | 701/1590 | 234/529 | chr3 | 40415943 | |||
| chr3:40415996 | T | A | 1 | a0004 | 2 | HG00558.hp2 NA19082.hp2 |
missense_variant | MODERATE | c.754T>A | p.Tyr252Asn | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/11 | 844/2916 | 754/1590 | 252/529 | chr3 | 40415996 | |||
| chr3:40422872 | T | C | 1 | a0005 | 2 | HG02615.hp2 HG02717.hp1 |
missense_variant | MODERATE | c.854T>C | p.Leu285Pro | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 8/11 | 944/2916 | 854/1590 | 285/529 | chr3 | 40422872 | |||
| chr3:40422881 | C | T | 1 | a0007 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.863C>T | p.Pro288Leu | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 8/11 | 953/2916 | 863/1590 | 288/529 | chr3 | 40422881 | |||
| chr3:40422972 | C | A | 1 | a0009 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.954C>A | p.Asn318Lys | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 8/11 | 1044/2916 | 954/1590 | 318/529 | chr3 | 40422972 | |||
| chr3:40427405 | C | T | 3 | a0002 a0009 a0012 |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
missense_variant | MODERATE | c.1487C>T | p.Ala496Val | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 1577/2916 | 1487/1590 | 496/529 | chr3 | 40427405 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:40411870 | G | A | 1 | a0001c0005 | 2 | NA18955.hp1 NA19075.hp1 |
synonymous_variant | LOW | c.345G>A | p.Glu115Glu | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/11 | 435/2916 | 345/1590 | 115/529 | chr3 | 40411870 | |||
| chr3:40415884 | C | A | 1 | a0011c0009 | 1 | NA18956.hp1 | synonymous_variant | LOW | c.642C>A | p.Thr214Thr | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/11 | 732/2916 | 642/1590 | 214/529 | chr3 | 40415884 | |||
| chr3:40415944 | G | A | 1 | a0012c0013 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.702G>A | p.Lys234Lys | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/11 | 792/2916 | 702/1590 | 234/529 | chr3 | 40415944 | |||
| chr3:40422978 | T | C | 1 | a0001c0004 | 5 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
synonymous_variant | LOW | c.960T>C | p.Asn320Asn | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 8/11 | 1050/2916 | 960/1590 | 320/529 | chr3 | 40422978 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:40387215 | G | A | 1 | a0001c0001t0006 | 3 | HG01168.hp2 HG01516.hp2 NA20905.hp1 |
5_prime_UTR_variant | MODIFIER | c.-59G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/11 | 843 | chr3 | 40387215 | ||||||
| chr3:40427477 | A | ATGCCTTT others(102): Show |
1 | a0001c0011t0002 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.1566_*84dupTGACCAT others(102): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 85 | INFO_REALIGN_3_PRIME | chr3 | 40427477 | |||||
| chr3:40427560 | G | A | 5 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 others(2): Show |
41 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*52G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 52 | chr3 | 40427560 | ||||||
| chr3:40427578 | T | C | 1 | a0001c0001t0005 | 5 | HG02895.hp1 HG02896.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*70T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 70 | chr3 | 40427578 | ||||||
| chr3:40427744 | C | T | 1 | a0001c0001t0005 | 5 | HG02895.hp1 HG02896.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*236C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 236 | chr3 | 40427744 | ||||||
| chr3:40427763 | G | T | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
188 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*255G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 255 | chr3 | 40427763 | ||||||
| chr3:40427841 | C | G | 1 | a0002c0002t0008 | 2 | HG00738.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*333C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 333 | chr3 | 40427841 | ||||||
| chr3:40427893 | C | G | 1 | a0002c0002t0012 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 385 | chr3 | 40427893 | ||||||
| chr3:40427893 | C | T | 1 | a0001c0001t0009 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 385 | chr3 | 40427893 | ||||||
| chr3:40427946 | C | G | 1 | a0001c0001t0011 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 438 | chr3 | 40427946 | ||||||
| chr3:40428113 | A | G | 2 | a0001c0001t0004 a0001c0001t0005 |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*605A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 605 | chr3 | 40428113 | ||||||
| chr3:40428137 | G | A | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*629G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 11/11 | 629 | chr3 | 40428137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:40387447 | T | G | 138 | a0001c0001t0001g0065 a0001c0001t0001g0138 a0001c0001t0002g0008 others(135): Show |
193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-13+186T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387447 | |||||||
| chr3:40387455 | T | G | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(6): Show |
14 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+194T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387455 | |||||||
| chr3:40387479 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-13+218C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387479 | |||||||
| chr3:40387484 | G | T | 1 | a0001c0001t0004g0156 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-13+223G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387484 | |||||||
| chr3:40387553 | G | T | 1 | a0001c0001t0003g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-13+292G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387553 | |||||||
| chr3:40387554 | T | G | 1 | a0001c0001t0003g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-13+293T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387554 | |||||||
| chr3:40387651 | A | G | 8 | a0001c0001t0001g0037 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
9 | HG00423.hp2 HG02809.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+390A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387651 | |||||||
| chr3:40387692 | A | G | 138 | a0001c0001t0001g0065 a0001c0001t0001g0138 a0001c0001t0002g0008 others(135): Show |
193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-12-354A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387692 | |||||||
| chr3:40387713 | G | C | 1 | a0002c0002t0002g0044 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-12-333G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387713 | |||||||
| chr3:40387847 | T | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(242): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-12-199T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387847 | |||||||
| chr3:40387867 | A | G | 147 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0138 others(144): Show |
203 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.-12-179A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387867 | |||||||
| chr3:40387943 | T | C | 29 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(26): Show |
36 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.-12-103T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387943 | |||||||
| chr3:40387948 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-12-98G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387948 | |||||||
| chr3:40387953 | T | C | 2 | a0002c0002t0002g0062 a0002c0002t0002g0063 |
2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-12-93T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387953 | |||||||
| chr3:40387982 | G | A | 1 | a0002c0002t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-12-64G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 1/10 | chr3 | 40387982 | |||||||
| chr3:40388139 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.40+42T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388139 | |||||||
| chr3:40388247 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.40+150G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388247 | |||||||
| chr3:40388316 | A | G | 1 | a0001c0001t0007g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40+219A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388316 | |||||||
| chr3:40388379 | G | A | 4 | a0001c0004t0002g0021 a0001c0004t0002g0045 a0001c0004t0002g0046 others(1): Show |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+282G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388379 | |||||||
| chr3:40388390 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG00423.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.40+293C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388390 | |||||||
| chr3:40388572 | GCACACAC others(7): Show |
G | 11 | a0002c0002t0002g0014 a0002c0002t0002g0044 a0002c0002t0002g0067 others(8): Show |
13 | HG00438.hp2 HG01256.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.40+488_40+501delGA others(12): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388572 | ||||||
| chr3:40388572 | GCACACAC others(9): Show |
G | 2 | a0002c0002t0002g0077 a0009c0010t0002g0076 |
2 | HG00544.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.40+488_40+503delGA others(14): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388572 | ||||||
| chr3:40388573 | CACACACA others(5): Show |
C | 51 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(48): Show |
73 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.40+488_40+499delGA others(10): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388573 | ||||||
| chr3:40388575 | CACACACA others(3): Show |
C | 12 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(9): Show |
14 | HG00140.hp2 HG00408.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.40+488_40+497delGA others(8): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388575 | ||||||
| chr3:40388577 | CACACACA others(1): Show |
C | 10 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0011 others(7): Show |
11 | HG00323.hp1 HG00642.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.40+488_40+495delGA others(6): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388577 | ||||||
| chr3:40388585 | G | C | 1 | a0002c0002t0002g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.40+488G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388585 | |||||||
| chr3:40388585 | G | GAC | 48 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0019 others(45): Show |
59 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.40+527_40+528dupAC | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | G | GACAC | 23 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0031 others(20): Show |
29 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.40+525_40+528dupAC others(2): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | G | GACACAC | 27 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
49 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.40+523_40+528dupAC others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | G | GACACACA others(1): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0159 others(2): Show |
5 | HG00323.hp2 HG02109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+521_40+528dupAC others(6): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | G | GACACACA others(3): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0214 |
8 | HG00673.hp1 HG01496.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+519_40+528dupAC others(8): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | G | GACACACA others(5): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0226 |
2 | HG00733.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.40+517_40+528dupAC others(10): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | G | GAGAC | 3 | a0001c0001t0001g0157 a0001c0001t0001g0197 a0001c0001t0001g0215 |
3 | NA18951.hp2 NA19010.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.40+489_40+490insGA others(2): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | GAC | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(13): Show |
21 | HG00423.hp1 HG01943.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.40+527_40+528delAC | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | GACAC | G | 22 | a0001c0001t0001g0238 a0001c0001t0002g0008 a0001c0001t0002g0009 others(19): Show |
34 | HG00639.hp1 HG01109.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+525_40+528delAC others(2): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | GACACAC | G | 10 | a0001c0001t0001g0065 a0001c0001t0001g0251 a0001c0001t0002g0038 others(7): Show |
11 | HG00621.hp1 HG00642.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.40+523_40+528delAC others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | GACACACA others(1): Show |
G | 7 | a0001c0001t0003g0099 a0001c0001t0005g0049 a0001c0001t0005g0050 others(4): Show |
7 | HG01192.hp1 HG01934.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+521_40+528delAC others(6): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | GACACACA others(3): Show |
G | 8 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(5): Show |
8 | HG00423.hp2 HG03209.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.40+519_40+528delAC others(8): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | GACACACA others(5): Show |
G | 2 | a0001c0001t0001g0158 a0001c0001t0002g0043 |
2 | HG01255.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.40+517_40+528delAC others(10): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388585 | GACACACA others(7): Show |
G | 4 | a0001c0004t0002g0021 a0001c0004t0002g0045 a0001c0004t0002g0046 others(1): Show |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+515_40+528delAC others(12): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40388585 | ||||||
| chr3:40388601 | C | G | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.40+504C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388601 | |||||||
| chr3:40388610 | ACACACAC others(6): Show |
A | 1 | a0002c0002t0002g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.40+514_40+526delCA others(11): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388610 | |||||||
| chr3:40388638 | C | T | 1 | a0001c0011t0002g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.40+541C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388638 | |||||||
| chr3:40388641 | G | A | 29 | a0001c0001t0001g0065 a0001c0001t0003g0004 a0001c0001t0003g0005 others(26): Show |
40 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.40+544G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388641 | |||||||
| chr3:40388642 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.40+545C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388642 | |||||||
| chr3:40388647 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.40+550C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388647 | |||||||
| chr3:40388919 | T | C | 1 | a0001c0001t0003g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.40+822T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40388919 | |||||||
| chr3:40389155 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.40+1058C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40389155 | |||||||
| chr3:40389338 | TA | T | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(6): Show |
14 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.40+1242delA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40389338 | |||||||
| chr3:40389347 | T | C | 1 | a0001c0001t0004g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.40+1250T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40389347 | |||||||
| chr3:40389480 | G | A | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.40+1383G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40389480 | |||||||
| chr3:40389506 | A | G | 1 | a0002c0002t0002g0153 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.40+1409A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40389506 | |||||||
| chr3:40389612 | T | C | 1 | a0001c0011t0002g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.40+1515T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40389612 | |||||||
| chr3:40389807 | C | T | 4 | a0002c0002t0002g0075 a0002c0002t0002g0150 a0002c0002t0002g0151 others(1): Show |
4 | HG00140.hp2 HG00738.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+1710C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40389807 | |||||||
| chr3:40389913 | G | A | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.40+1816G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40389913 | |||||||
| chr3:40390098 | A | C | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.41-1925A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40390098 | |||||||
| chr3:40390114 | G | A | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-1909G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40390114 | |||||||
| chr3:40390168 | T | C | 3 | a0002c0002t0002g0101 a0002c0002t0002g0102 a0002c0002t0002g0103 |
3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.41-1855T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40390168 | |||||||
| chr3:40390238 | T | C | 2 | a0002c0002t0002g0104 a0002c0002t0002g0153 |
2 | NA19002.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.41-1785T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40390238 | |||||||
| chr3:40390455 | C | T | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-1568C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40390455 | |||||||
| chr3:40390593 | C | T | 146 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0138 others(143): Show |
202 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.41-1430C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40390593 | |||||||
| chr3:40390944 | T | G | 1 | a0001c0001t0003g0080 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.41-1079T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40390944 | |||||||
| chr3:40391087 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0236 |
3 | HG01496.hp2 HG02004.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.41-936C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40391087 | |||||||
| chr3:40391154 | T | G | 107 | a0001c0001t0001g0138 a0001c0001t0002g0008 a0001c0001t0002g0009 others(104): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.41-869T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40391154 | |||||||
| chr3:40391443 | G | A | 5 | a0001c0001t0005g0049 a0001c0001t0005g0050 a0001c0001t0005g0051 others(2): Show |
5 | HG02895.hp1 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-580G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40391443 | |||||||
| chr3:40391446 | A | G | 137 | a0001c0001t0001g0065 a0001c0001t0001g0138 a0001c0001t0002g0008 others(134): Show |
192 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.41-577A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40391446 | |||||||
| chr3:40391452 | A | G | 1 | a0001c0004t0002g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.41-571A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40391452 | |||||||
| chr3:40391503 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.41-520C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40391503 | |||||||
| chr3:40391536 | C | T | 1 | a0001c0001t0003g0100 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.41-487C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40391536 | |||||||
| chr3:40391537 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.41-486G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40391537 | |||||||
| chr3:40391633 | G | A | 9 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(6): Show |
10 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.41-390G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | chr3 | 40391633 | |||||||
| chr3:40391675 | C | CA | 9 | a0001c0001t0001g0238 a0001c0001t0003g0004 a0001c0001t0003g0023 others(6): Show |
15 | HG01884.hp2 HG01891.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.41-333dupA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 40391675 | ||||||
| chr3:40392189 | G | T | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+39G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392189 | |||||||
| chr3:40392286 | T | A | 1 | a0002c0002t0002g0067 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.168+136T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392286 | |||||||
| chr3:40392292 | G | A | 15 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(12): Show |
21 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.168+142G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392292 | |||||||
| chr3:40392343 | T | C | 15 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(12): Show |
21 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.168+193T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392343 | |||||||
| chr3:40392464 | A | C | 14 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(11): Show |
15 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+314A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392464 | |||||||
| chr3:40392498 | G | A | 1 | a0001c0001t0003g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.168+348G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392498 | |||||||
| chr3:40392499 | A | G | 1 | a0001c0001t0003g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.168+349A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392499 | |||||||
| chr3:40392553 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.168+403C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392553 | |||||||
| chr3:40392574 | C | CA | 10 | a0001c0001t0001g0160 a0001c0001t0002g0059 a0001c0001t0004g0022 others(7): Show |
11 | HG00438.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+442dupA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40392574 | ||||||
| chr3:40392574 | CA | C | 12 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(9): Show |
13 | HG01496.hp2 HG02683.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+442delA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40392574 | ||||||
| chr3:40392574 | CAAAAAAA | C | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(6): Show |
14 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+436_168+442del others(7): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40392574 | ||||||
| chr3:40392581 | A | G | 6 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG00423.hp2 NA18941.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+431A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392581 | |||||||
| chr3:40392591 | A | T | 1 | a0001c0001t0001g0037 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.168+441A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392591 | |||||||
| chr3:40392592 | AT | A | 3 | a0001c0001t0003g0081 a0001c0001t0003g0086 a0001c0001t0003g0087 |
3 | HG02486.hp2 HG02897.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.168+445delT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40392592 | ||||||
| chr3:40392593 | T | A | 26 | a0001c0001t0001g0065 a0001c0001t0003g0004 a0001c0001t0003g0005 others(23): Show |
37 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.168+443T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392593 | |||||||
| chr3:40392599 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+449G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392599 | |||||||
| chr3:40392605 | T | C | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+455T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392605 | |||||||
| chr3:40392671 | C | T | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.168+521C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392671 | |||||||
| chr3:40392722 | G | A | 1 | a0001c0001t0003g0088 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.168+572G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392722 | |||||||
| chr3:40392730 | A | T | 1 | a0001c0001t0001g0235 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.168+580A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392730 | |||||||
| chr3:40392742 | G | C | 1 | a0002c0002t0002g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.168+592G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392742 | |||||||
| chr3:40392819 | A | T | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.168+669A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392819 | |||||||
| chr3:40392969 | C | T | 8 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(5): Show |
9 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+819C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40392969 | |||||||
| chr3:40392989 | CA | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0230 a0001c0001t0001g0231 others(3): Show |
8 | HG01167.hp2 HG01169.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+855delA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40392989 | ||||||
| chr3:40393040 | C | T | 1 | a0003c0003t0001g0229 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.168+890C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40393040 | |||||||
| chr3:40393163 | G | A | 1 | a0002c0002t0002g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.168+1013G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40393163 | |||||||
| chr3:40393200 | T | G | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.168+1050T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40393200 | |||||||
| chr3:40393484 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.168+1334G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40393484 | |||||||
| chr3:40393603 | G | A | 2 | a0002c0002t0002g0105 a0002c0002t0002g0106 |
2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.168+1453G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40393603 | |||||||
| chr3:40393654 | TA | T | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.168+1513delA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40393654 | ||||||
| chr3:40393680 | A | C | 1 | a0003c0003t0001g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.168+1530A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40393680 | |||||||
| chr3:40393790 | A | G | 1 | a0002c0002t0002g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.168+1640A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40393790 | |||||||
| chr3:40393816 | G | A | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.168+1666G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40393816 | |||||||
| chr3:40393905 | G | T | 107 | a0001c0001t0001g0138 a0001c0001t0002g0008 a0001c0001t0002g0009 others(104): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.168+1755G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40393905 | |||||||
| chr3:40394048 | C | CA | 24 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(21): Show |
31 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.168+1924dupA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40394048 | ||||||
| chr3:40394048 | C | CAA | 7 | a0001c0001t0002g0039 a0001c0001t0004g0057 a0001c0001t0005g0049 others(4): Show |
7 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+1923_168+1924d others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40394048 | ||||||
| chr3:40394048 | CA | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(125): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.168+1924delA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40394048 | ||||||
| chr3:40394048 | CAA | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0235 a0001c0001t0001g0237 others(4): Show |
8 | HG02683.hp2 HG02698.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+1923_168+1924d others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40394048 | ||||||
| chr3:40394048 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.168+1915_168+1924d others(12): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40394048 | ||||||
| chr3:40394166 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(243): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.168+2016A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40394166 | |||||||
| chr3:40394399 | A | G | 108 | a0001c0001t0001g0138 a0001c0001t0002g0008 a0001c0001t0002g0009 others(105): Show |
151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.168+2249A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40394399 | |||||||
| chr3:40394409 | A | G | 29 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(26): Show |
36 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.168+2259A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40394409 | |||||||
| chr3:40394613 | T | A | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.168+2463T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40394613 | |||||||
| chr3:40394808 | T | C | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0191 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+2658T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40394808 | |||||||
| chr3:40394955 | C | G | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.168+2805C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40394955 | |||||||
| chr3:40395028 | A | G | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.168+2878A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40395028 | |||||||
| chr3:40395439 | G | A | 14 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(11): Show |
15 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+3289G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40395439 | |||||||
| chr3:40395506 | C | G | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+3356C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40395506 | |||||||
| chr3:40395508 | G | A | 30 | a0001c0001t0001g0065 a0001c0001t0003g0004 a0001c0001t0003g0005 others(27): Show |
42 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.168+3358G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40395508 | |||||||
| chr3:40395560 | G | T | 1 | a0002c0002t0002g0149 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.168+3410G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40395560 | |||||||
| chr3:40395764 | G | A | 14 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(11): Show |
15 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+3614G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40395764 | |||||||
| chr3:40395803 | A | G | 147 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0138 others(144): Show |
203 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.168+3653A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40395803 | |||||||
| chr3:40396048 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.168+3898A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40396048 | |||||||
| chr3:40396049 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.168+3899A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40396049 | |||||||
| chr3:40396050 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.168+3900T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40396050 | |||||||
| chr3:40396147 | G | A | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.168+3997G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40396147 | |||||||
| chr3:40396235 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0167 |
5 | HG02080.hp1 NA18950.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+4085G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40396235 | |||||||
| chr3:40396385 | AC | A | 4 | a0002c0002t0002g0026 a0002c0002t0002g0114 a0002c0002t0008g0107 others(1): Show |
5 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+4237delC | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40396385 | ||||||
| chr3:40396629 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0224 |
4 | HG01256.hp1 HG01346.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-4265C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40396629 | |||||||
| chr3:40396854 | A | G | 1 | a0004c0006t0001g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.169-4040A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40396854 | |||||||
| chr3:40397060 | G | C | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.169-3834G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40397060 | |||||||
| chr3:40397119 | C | CTT | 26 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0031 others(23): Show |
32 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.169-3756_169-3755d others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | C | CTTT | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(64): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.169-3757_169-3755d others(5): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | C | CTTTT | 5 | a0001c0001t0001g0035 a0001c0001t0001g0164 a0001c0001t0001g0189 others(2): Show |
6 | HG04199.hp1 NA18947.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-3758_169-3755d others(6): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | C | CTTTTTTT | 8 | a0001c0001t0005g0049 a0002c0002t0002g0011 a0002c0002t0002g0069 others(5): Show |
11 | HG00323.hp1 HG00408.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-3761_169-3755d others(9): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | C | CTTTTTTT others(1): Show |
67 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(64): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.169-3762_169-3755d others(10): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | C | CTTTTTTT others(2): Show |
23 | a0001c0001t0001g0138 a0001c0001t0002g0008 a0001c0001t0002g0038 others(20): Show |
28 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.169-3763_169-3755d others(11): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0009 a0002c0002t0002g0102 a0005c0007t0002g0009 others(1): Show |
6 | HG00639.hp1 HG01109.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-3764_169-3755d others(12): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | C | CTTTTTTT others(6): Show |
3 | a0001c0004t0002g0021 a0001c0004t0002g0045 a0001c0004t0002g0046 |
4 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-3767_169-3755d others(15): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | C | CTTTTTTT others(7): Show |
1 | a0001c0004t0002g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.169-3768_169-3755d others(16): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | CT | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0003g0080 others(4): Show |
8 | HG00621.hp1 HG00642.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-3755delT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397119 | CTT | C | 22 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0023 others(19): Show |
34 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.169-3756_169-3755d others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397119 | ||||||
| chr3:40397151 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-3743G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40397151 | |||||||
| chr3:40397495 | G | GTATGA | 14 | a0001c0001t0001g0034 a0001c0001t0001g0216 a0001c0001t0001g0217 others(11): Show |
15 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.169-3376_169-3372d others(7): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40397495 | ||||||
| chr3:40397615 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.169-3279C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40397615 | |||||||
| chr3:40397701 | C | A | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.169-3193C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40397701 | |||||||
| chr3:40397826 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.169-3068C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40397826 | |||||||
| chr3:40397900 | G | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0224 |
2 | HG01346.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.169-2994G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40397900 | |||||||
| chr3:40397935 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.169-2959C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40397935 | |||||||
| chr3:40398074 | G | T | 2 | a0002c0002t0002g0002 a0002c0002t0002g0128 |
2 | NA18961.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.169-2820G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398074 | |||||||
| chr3:40398082 | C | T | 2 | a0002c0002t0002g0117 a0002c0002t0002g0129 |
2 | NA18964.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.169-2812C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398082 | |||||||
| chr3:40398096 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169-2798G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398096 | |||||||
| chr3:40398123 | G | A | 80 | a0001c0001t0001g0138 a0001c0001t0001g0183 a0002c0002t0002g0002 others(77): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.169-2771G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398123 | |||||||
| chr3:40398345 | C | T | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.169-2549C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398345 | |||||||
| chr3:40398378 | C | A | 1 | a0001c0011t0002g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.169-2516C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398378 | |||||||
| chr3:40398379 | G | A | 6 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG00423.hp2 NA18941.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-2515G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398379 | |||||||
| chr3:40398390 | G | C | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.169-2504G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398390 | |||||||
| chr3:40398625 | G | A | 42 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(39): Show |
59 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.169-2269G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398625 | |||||||
| chr3:40398859 | T | C | 2 | a0001c0001t0001g0245 a0002c0002t0002g0154 |
2 | HG01934.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.169-2035T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398859 | |||||||
| chr3:40398876 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169-2018A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398876 | |||||||
| chr3:40398961 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169-1933G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398961 | |||||||
| chr3:40398971 | C | A | 2 | a0001c0001t0001g0180 a0007c0012t0001g0195 |
2 | HG01257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.169-1923C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40398971 | |||||||
| chr3:40399023 | A | T | 1 | a0001c0001t0001g0037 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169-1871A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399023 | |||||||
| chr3:40399255 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.169-1639G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399255 | |||||||
| chr3:40399262 | C | T | 1 | a0001c0011t0002g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.169-1632C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399262 | |||||||
| chr3:40399263 | G | A | 1 | a0002c0002t0002g0016 | 2 | HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.169-1631G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399263 | |||||||
| chr3:40399290 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169-1604G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399290 | |||||||
| chr3:40399378 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(94): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169-1516T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399378 | |||||||
| chr3:40399540 | C | A | 1 | a0003c0003t0001g0207 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.169-1354C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399540 | |||||||
| chr3:40399559 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.169-1335G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399559 | |||||||
| chr3:40399578 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169-1316G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399578 | |||||||
| chr3:40399646 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.169-1248C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399646 | |||||||
| chr3:40399789 | T | G | 42 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(39): Show |
59 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.169-1105T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399789 | |||||||
| chr3:40399854 | G | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(95): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.169-1040G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399854 | |||||||
| chr3:40399987 | G | A | 7 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00423.hp2 HG03471.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-907G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399987 | |||||||
| chr3:40399993 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.169-901G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40399993 | |||||||
| chr3:40400002 | C | T | 1 | a0002c0002t0002g0002 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.169-892C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400002 | |||||||
| chr3:40400023 | G | C | 1 | a0004c0006t0001g0110 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.169-871G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400023 | |||||||
| chr3:40400035 | C | A | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-859C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400035 | |||||||
| chr3:40400251 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169-643G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400251 | |||||||
| chr3:40400264 | C | CA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0189 a0001c0001t0001g0192 others(10): Show |
14 | HG00544.hp2 HG00741.hp2 HG03579.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-613dupA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40400264 | ||||||
| chr3:40400264 | CA | C | 41 | a0001c0001t0001g0233 a0001c0001t0003g0004 a0001c0001t0003g0005 others(38): Show |
53 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.169-613delA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 40400264 | ||||||
| chr3:40400370 | G | C | 4 | a0001c0004t0002g0021 a0001c0004t0002g0045 a0001c0004t0002g0046 others(1): Show |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-524G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400370 | |||||||
| chr3:40400417 | C | T | 106 | a0001c0001t0001g0138 a0001c0001t0003g0004 a0001c0001t0003g0005 others(103): Show |
153 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.169-477C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400417 | |||||||
| chr3:40400789 | G | A | 1 | a0003c0003t0001g0199 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.169-105G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400789 | |||||||
| chr3:40400789 | G | T | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.169-105G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400789 | |||||||
| chr3:40400799 | G | A | 1 | a0002c0002t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.169-95G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400799 | |||||||
| chr3:40400874 | C | G | 27 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0023 others(24): Show |
38 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.169-20C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 3/10 | chr3 | 40400874 | |||||||
| chr3:40401083 | AGAGGTCC | A | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.286+73_286+79delGA others(5): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40401083 | |||||||
| chr3:40401288 | T | G | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+277T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40401288 | |||||||
| chr3:40401343 | T | C | 5 | a0001c0001t0005g0049 a0001c0001t0005g0050 a0001c0001t0005g0051 others(2): Show |
5 | HG02895.hp1 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+332T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40401343 | |||||||
| chr3:40401344 | T | G | 1 | a0001c0001t0006g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.286+333T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40401344 | |||||||
| chr3:40401684 | A | C | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.286+673A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40401684 | |||||||
| chr3:40401946 | TG | T | 7 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00423.hp2 HG03471.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+936delG | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40401946 | |||||||
| chr3:40401965 | TTC | T | 8 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(5): Show |
9 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.286+956_286+957del others(2): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40401965 | ||||||
| chr3:40402101 | A | C | 1 | a0002c0002t0002g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.286+1090A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40402101 | |||||||
| chr3:40402114 | T | TTTTTTTT others(4): Show |
8 | a0002c0002t0002g0072 a0002c0002t0002g0112 a0002c0002t0002g0131 others(5): Show |
8 | HG00438.hp2 HG02071.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+1111_286+1112i others(13): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40402114 | ||||||
| chr3:40402115 | T | TTTTTTTT others(3): Show |
68 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(65): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.286+1111_286+1112i others(12): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40402115 | ||||||
| chr3:40402115 | T | TTTTTTTT others(4): Show |
1 | a0002c0002t0002g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.286+1111_286+1112i others(13): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40402115 | ||||||
| chr3:40402117 | T | TTTTTTTC | 53 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(50): Show |
71 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.286+1111_286+1112i others(9): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40402117 | ||||||
| chr3:40402123 | C | CTTTTTTT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(89): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.286+1119_286+1125d others(9): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40402123 | ||||||
| chr3:40402123 | C | CTTTTTTT others(1): Show |
11 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0185 others(8): Show |
11 | HG01934.hp1 HG03516.hp2 HG04199.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+1118_286+1125d others(10): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40402123 | ||||||
| chr3:40402123 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.286+1116_286+1125d others(12): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40402123 | ||||||
| chr3:40402123 | C | T | 139 | a0001c0001t0001g0065 a0001c0001t0001g0138 a0001c0001t0001g0200 others(136): Show |
194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.286+1112C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40402123 | |||||||
| chr3:40402137 | G | T | 1 | a0001c0001t0003g0099 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.286+1126G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40402137 | |||||||
| chr3:40402139 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.286+1128G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40402139 | |||||||
| chr3:40402197 | C | T | 1 | a0001c0001t0006g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.286+1186C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40402197 | |||||||
| chr3:40402252 | G | A | 1 | a0002c0002t0002g0119 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.286+1241G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40402252 | |||||||
| chr3:40402339 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.286+1328G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40402339 | |||||||
| chr3:40402436 | T | C | 134 | a0001c0001t0001g0138 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
188 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.286+1425T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40402436 | |||||||
| chr3:40402613 | T | C | 9 | a0001c0001t0001g0158 a0001c0001t0004g0022 a0001c0001t0004g0048 others(6): Show |
10 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+1602T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40402613 | |||||||
| chr3:40403054 | C | T | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.286+2043C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40403054 | |||||||
| chr3:40403212 | C | T | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.286+2201C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40403212 | |||||||
| chr3:40403485 | T | G | 44 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0031 others(41): Show |
63 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.286+2474T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40403485 | |||||||
| chr3:40403610 | G | A | 2 | a0002c0002t0002g0101 a0002c0002t0002g0103 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.286+2599G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40403610 | |||||||
| chr3:40403627 | A | G | 27 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0023 others(24): Show |
38 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.286+2616A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40403627 | |||||||
| chr3:40403653 | A | AT | 120 | a0001c0001t0001g0034 a0001c0001t0001g0138 a0001c0001t0001g0162 others(117): Show |
171 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.286+2659dupT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40403653 | ||||||
| chr3:40403653 | A | ATT | 7 | a0001c0001t0002g0008 a0001c0001t0002g0039 a0002c0002t0002g0069 others(4): Show |
10 | HG02135.hp2 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.286+2658_286+2659d others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40403653 | ||||||
| chr3:40403653 | AT | A | 6 | a0001c0001t0001g0168 a0001c0001t0001g0211 a0001c0001t0001g0245 others(3): Show |
6 | HG01516.hp2 HG01943.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.286+2659delT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40403653 | ||||||
| chr3:40403865 | T | C | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.286+2854T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40403865 | |||||||
| chr3:40403895 | T | C | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.286+2884T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40403895 | |||||||
| chr3:40403947 | C | T | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.286+2936C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40403947 | |||||||
| chr3:40404062 | TCA | T | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.286+3053_286+3054d others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40404062 | ||||||
| chr3:40404593 | GAGGCCA | G | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.286+3583_286+3588d others(8): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40404593 | |||||||
| chr3:40404670 | G | T | 7 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0039 others(4): Show |
12 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.286+3659G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40404670 | |||||||
| chr3:40404880 | A | G | 2 | a0003c0003t0001g0209 a0011c0009t0001g0210 |
2 | NA18956.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.286+3869A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40404880 | |||||||
| chr3:40404912 | G | T | 4 | a0001c0004t0002g0021 a0001c0004t0002g0045 a0001c0004t0002g0046 others(1): Show |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+3901G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40404912 | |||||||
| chr3:40404937 | C | A | 7 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00423.hp2 HG03471.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+3926C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40404937 | |||||||
| chr3:40404948 | G | A | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+3937G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40404948 | |||||||
| chr3:40404967 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.286+3956G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40404967 | |||||||
| chr3:40405275 | C | T | 1 | a0001c0001t0003g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.286+4264C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40405275 | |||||||
| chr3:40405295 | A | G | 2 | a0002c0002t0002g0117 a0002c0002t0002g0129 |
2 | NA18964.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.286+4284A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40405295 | |||||||
| chr3:40405504 | C | CA | 120 | a0001c0001t0001g0138 a0001c0001t0002g0008 a0001c0001t0002g0009 others(117): Show |
173 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.286+4505dupA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40405504 | ||||||
| chr3:40405604 | T | C | 1 | a0007c0012t0001g0195 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.286+4593T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40405604 | |||||||
| chr3:40405689 | G | A | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.286+4678G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40405689 | |||||||
| chr3:40405798 | C | T | 2 | a0002c0002t0002g0062 a0002c0002t0002g0063 |
2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.286+4787C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40405798 | |||||||
| chr3:40405871 | C | T | 145 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0138 others(142): Show |
201 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.286+4860C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40405871 | |||||||
| chr3:40405945 | ATACGAAC others(6): Show |
A | 1 | a0002c0002t0002g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.286+4936_286+4948d others(15): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40405945 | ||||||
| chr3:40406034 | G | A | 1 | a0002c0002t0002g0120 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.286+5023G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406034 | |||||||
| chr3:40406057 | G | A | 55 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(52): Show |
73 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.286+5046G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406057 | |||||||
| chr3:40406129 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0236 |
3 | HG01496.hp2 HG02004.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.286+5118T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406129 | |||||||
| chr3:40406141 | C | T | 8 | a0001c0001t0001g0037 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
9 | HG00423.hp2 HG02809.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.286+5130C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406141 | |||||||
| chr3:40406186 | C | T | 1 | a0002c0002t0002g0128 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.286+5175C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406186 | |||||||
| chr3:40406233 | C | T | 78 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(75): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.286+5222C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406233 | |||||||
| chr3:40406263 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.286+5252G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406263 | |||||||
| chr3:40406441 | C | T | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(6): Show |
14 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-5371C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406441 | |||||||
| chr3:40406477 | T | C | 42 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(39): Show |
59 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.287-5335T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406477 | |||||||
| chr3:40406576 | C | T | 3 | a0001c0001t0003g0086 a0001c0001t0003g0087 a0002c0002t0002g0154 |
3 | HG01934.hp2 HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.287-5236C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406576 | |||||||
| chr3:40406579 | G | C | 1 | a0001c0001t0001g0219 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.287-5233G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406579 | |||||||
| chr3:40406645 | C | A | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-5167C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406645 | |||||||
| chr3:40406689 | T | C | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.287-5123T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406689 | |||||||
| chr3:40406906 | G | A | 79 | a0001c0001t0001g0138 a0002c0002t0002g0002 a0002c0002t0002g0006 others(76): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.287-4906G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406906 | |||||||
| chr3:40406990 | A | G | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.287-4822A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40406990 | |||||||
| chr3:40407043 | C | G | 4 | a0001c0004t0002g0021 a0001c0004t0002g0045 a0001c0004t0002g0046 others(1): Show |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-4769C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407043 | |||||||
| chr3:40407120 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.287-4692T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407120 | |||||||
| chr3:40407156 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0011g0060 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.287-4656G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407156 | |||||||
| chr3:40407331 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.287-4481C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407331 | |||||||
| chr3:40407332 | A | G | 1 | a0001c0011t0002g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.287-4480A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407332 | |||||||
| chr3:40407359 | T | G | 1 | a0002c0002t0002g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.287-4453T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407359 | |||||||
| chr3:40407373 | T | A | 1 | a0009c0010t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.287-4439T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407373 | |||||||
| chr3:40407552 | G | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0079 |
3 | HG01891.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.287-4260G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407552 | |||||||
| chr3:40407603 | C | T | 2 | a0001c0001t0003g0081 a0001c0001t0003g0082 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.287-4209C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407603 | |||||||
| chr3:40407820 | A | G | 1 | a0002c0002t0002g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.287-3992A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407820 | |||||||
| chr3:40407860 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(199): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.287-3952C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407860 | |||||||
| chr3:40407886 | C | T | 1 | a0002c0002t0002g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.287-3926C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40407886 | |||||||
| chr3:40408045 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.287-3767G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40408045 | |||||||
| chr3:40408407 | A | C | 1 | a0001c0001t0002g0043 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.287-3405A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40408407 | |||||||
| chr3:40408603 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.287-3209A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40408603 | |||||||
| chr3:40408927 | TTTC | T | 39 | a0001c0001t0002g0038 a0001c0001t0003g0004 a0001c0001t0003g0005 others(36): Show |
51 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.287-2882_287-2880d others(5): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40408927 | ||||||
| chr3:40408928 | TTC | T | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0039 others(16): Show |
25 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-2882_287-2881d others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40408928 | ||||||
| chr3:40408946 | T | C | 4 | a0002c0002t0002g0062 a0002c0002t0002g0063 a0002c0002t0002g0121 others(1): Show |
4 | HG00735.hp2 HG01175.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-2866T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40408946 | |||||||
| chr3:40409064 | C | A | 1 | a0002c0002t0002g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.287-2748C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409064 | |||||||
| chr3:40409113 | C | A | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.287-2699C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409113 | |||||||
| chr3:40409129 | G | A | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.287-2683G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409129 | |||||||
| chr3:40409184 | G | A | 12 | a0001c0001t0001g0138 a0001c0001t0001g0241 a0001c0001t0001g0243 others(9): Show |
12 | HG00423.hp2 HG01074.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.287-2628G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409184 | |||||||
| chr3:40409374 | C | A | 1 | a0001c0001t0001g0202 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.287-2438C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409374 | |||||||
| chr3:40409397 | C | T | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.287-2415C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409397 | |||||||
| chr3:40409496 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.287-2316C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409496 | |||||||
| chr3:40409542 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.287-2270T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409542 | |||||||
| chr3:40409650 | T | C | 2 | a0004c0006t0001g0110 a0004c0006t0001g0141 |
2 | HG00558.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.287-2162T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409650 | |||||||
| chr3:40409659 | C | T | 1 | a0001c0001t0005g0052 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.287-2153C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409659 | |||||||
| chr3:40409715 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.287-2097T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409715 | |||||||
| chr3:40409862 | G | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0159 a0001c0001t0001g0221 |
4 | HG00280.hp2 HG03942.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-1950G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409862 | |||||||
| chr3:40409863 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.287-1949T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40409863 | |||||||
| chr3:40410052 | C | T | 76 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(73): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.287-1760C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40410052 | |||||||
| chr3:40410114 | G | A | 8 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(5): Show |
9 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-1698G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40410114 | |||||||
| chr3:40410211 | C | T | 4 | a0003c0003t0001g0207 a0003c0003t0001g0208 a0003c0003t0001g0220 others(1): Show |
4 | NA18982.hp1 NA18985.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-1601C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40410211 | |||||||
| chr3:40410275 | T | C | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.287-1537T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40410275 | |||||||
| chr3:40410348 | C | A | 1 | a0002c0002t0002g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.287-1464C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40410348 | |||||||
| chr3:40410443 | G | GA | 95 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0138 others(92): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.287-1354dupA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40410443 | ||||||
| chr3:40410443 | GA | G | 34 | a0001c0001t0001g0157 a0001c0001t0001g0179 a0001c0001t0001g0184 others(31): Show |
45 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.287-1354delA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40410443 | ||||||
| chr3:40410524 | A | G | 1 | a0002c0002t0002g0140 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.287-1288A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40410524 | |||||||
| chr3:40410783 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287-1029G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40410783 | |||||||
| chr3:40410799 | TAGAC | T | 59 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(56): Show |
77 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.287-1009_287-1006d others(6): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40410799 | ||||||
| chr3:40410897 | T | C | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.287-915T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40410897 | |||||||
| chr3:40411117 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.287-695C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411117 | |||||||
| chr3:40411135 | C | A | 1 | a0001c0001t0006g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.287-677C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411135 | |||||||
| chr3:40411151 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.287-661C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411151 | |||||||
| chr3:40411199 | G | A | 2 | a0002c0002t0002g0069 a0002c0002t0002g0071 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.287-613G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411199 | |||||||
| chr3:40411308 | A | AAAAAAAG | 135 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(132): Show |
189 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.287-499_287-498ins others(7): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40411308 | ||||||
| chr3:40411310 | A | AAAAGAAA others(3): Show |
1 | a0002c0002t0002g0127 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.287-494_287-493ins others(10): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 40411310 | ||||||
| chr3:40411350 | A | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0031 others(38): Show |
60 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.287-462A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411350 | |||||||
| chr3:40411469 | T | C | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.287-343T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411469 | |||||||
| chr3:40411533 | T | C | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.287-279T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411533 | |||||||
| chr3:40411581 | C | T | 1 | a0001c0001t0004g0022 | 2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.287-231C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411581 | |||||||
| chr3:40411680 | C | A | 1 | a0004c0006t0001g0110 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.287-132C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411680 | |||||||
| chr3:40411697 | C | T | 1 | a0001c0001t0003g0100 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.287-115C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411697 | |||||||
| chr3:40411764 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.287-48C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 4/10 | chr3 | 40411764 | |||||||
| chr3:40412031 | G | A | 1 | a0002c0002t0002g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.437+69G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412031 | |||||||
| chr3:40412110 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0011g0060 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.437+148G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412110 | |||||||
| chr3:40412118 | A | G | 1 | a0001c0001t0001g0013 | 4 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.437+156A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412118 | |||||||
| chr3:40412160 | A | G | 4 | a0002c0002t0002g0062 a0002c0002t0002g0063 a0002c0002t0002g0121 others(1): Show |
4 | HG00735.hp2 HG01175.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+198A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412160 | |||||||
| chr3:40412170 | C | A | 45 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(42): Show |
62 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.437+208C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412170 | |||||||
| chr3:40412604 | T | A | 2 | a0001c0001t0001g0065 a0006c0008t0001g0025 |
3 | HG02683.hp2 HG03098.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.437+642T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412604 | |||||||
| chr3:40412645 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.437+683G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412645 | |||||||
| chr3:40412650 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0213 |
2 | NA18966.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.437+688T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412650 | |||||||
| chr3:40412802 | T | C | 1 | a0001c0001t0013g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.437+840T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412802 | |||||||
| chr3:40412947 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
6 | HG01167.hp2 HG01169.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.437+985A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412947 | |||||||
| chr3:40412992 | A | T | 1 | a0011c0009t0001g0210 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.437+1030A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412992 | |||||||
| chr3:40412993 | T | A | 1 | a0011c0009t0001g0210 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.437+1031T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412993 | |||||||
| chr3:40412994 | A | T | 1 | a0011c0009t0001g0210 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.437+1032A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40412994 | |||||||
| chr3:40413048 | C | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0164 |
2 | NA19000.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.437+1086C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40413048 | |||||||
| chr3:40413128 | G | A | 1 | a0001c0001t0003g0100 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.437+1166G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40413128 | |||||||
| chr3:40413280 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.437+1318A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40413280 | |||||||
| chr3:40413738 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.438-943C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40413738 | |||||||
| chr3:40413864 | G | A | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.438-817G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40413864 | |||||||
| chr3:40413899 | A | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(247): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.438-782A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40413899 | |||||||
| chr3:40414325 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.438-356A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40414325 | |||||||
| chr3:40414437 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0186 |
4 | HG03490.hp1 HG03492.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-244C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40414437 | |||||||
| chr3:40414489 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.438-192T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40414489 | |||||||
| chr3:40414535 | T | C | 45 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(42): Show |
62 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.438-146T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40414535 | |||||||
| chr3:40414538 | T | G | 1 | a0002c0002t0002g0127 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.438-143T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40414538 | |||||||
| chr3:40414539 | G | T | 1 | a0002c0002t0002g0127 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.438-142G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40414539 | |||||||
| chr3:40414622 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.438-59T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40414622 | |||||||
| chr3:40414629 | T | A | 1 | a0001c0001t0001g0245 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.438-52T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 5/10 | chr3 | 40414629 | |||||||
| chr3:40414904 | C | T | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.597+64C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 6/10 | chr3 | 40414904 | |||||||
| chr3:40414930 | G | C | 3 | a0002c0002t0002g0104 a0002c0002t0002g0122 a0002c0002t0002g0153 |
3 | NA18998.hp1 NA19002.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.597+90G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 6/10 | chr3 | 40414930 | |||||||
| chr3:40415142 | G | T | 7 | a0001c0001t0003g0005 a0001c0001t0003g0088 a0001c0001t0003g0097 others(4): Show |
11 | HG01168.hp1 HG01169.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+302G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 6/10 | chr3 | 40415142 | |||||||
| chr3:40415248 | C | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA18950.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.597+408C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 6/10 | chr3 | 40415248 | |||||||
| chr3:40415547 | T | C | 138 | a0001c0001t0001g0065 a0001c0001t0002g0008 a0001c0001t0002g0009 others(135): Show |
193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.598-293T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 6/10 | chr3 | 40415547 | |||||||
| chr3:40415568 | T | C | 12 | a0001c0001t0001g0138 a0001c0001t0001g0241 a0001c0001t0001g0243 others(9): Show |
12 | HG00423.hp2 HG01074.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-272T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 6/10 | chr3 | 40415568 | |||||||
| chr3:40415593 | C | A | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.598-247C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 6/10 | chr3 | 40415593 | |||||||
| chr3:40415789 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.598-51C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 6/10 | chr3 | 40415789 | |||||||
| chr3:40416164 | C | T | 1 | a0009c0010t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.831+91C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416164 | |||||||
| chr3:40416218 | G | A | 2 | a0001c0001t0003g0023 a0001c0001t0003g0079 |
3 | HG01891.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.831+145G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416218 | |||||||
| chr3:40416225 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.831+152G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416225 | |||||||
| chr3:40416304 | C | T | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.831+231C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416304 | |||||||
| chr3:40416500 | T | C | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+427T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416500 | |||||||
| chr3:40416550 | T | C | 136 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(133): Show |
190 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.831+477T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416550 | |||||||
| chr3:40416572 | C | T | 6 | a0001c0001t0002g0059 a0001c0001t0011g0060 a0001c0004t0002g0021 others(3): Show |
7 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+499C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416572 | |||||||
| chr3:40416630 | A | C | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+557A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416630 | |||||||
| chr3:40416889 | A | T | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+816A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416889 | |||||||
| chr3:40416956 | C | T | 1 | a0002c0002t0002g0116 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.831+883C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40416956 | |||||||
| chr3:40416967 | GT | G | 14 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(11): Show |
15 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.831+896delT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40416967 | ||||||
| chr3:40417031 | A | G | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+958A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417031 | |||||||
| chr3:40417032 | G | A | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+959G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417032 | |||||||
| chr3:40417144 | A | T | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+1071A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417144 | |||||||
| chr3:40417189 | T | C | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.831+1116T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417189 | |||||||
| chr3:40417319 | G | C | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+1246G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417319 | |||||||
| chr3:40417320 | C | G | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+1247C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417320 | |||||||
| chr3:40417392 | C | T | 1 | a0001c0001t0006g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.831+1319C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417392 | |||||||
| chr3:40417448 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0011g0060 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+1375C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417448 | |||||||
| chr3:40417472 | G | A | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.831+1399G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417472 | |||||||
| chr3:40417546 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.831+1473C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417546 | |||||||
| chr3:40417552 | C | T | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.831+1479C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417552 | |||||||
| chr3:40417560 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0011g0060 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+1487G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417560 | |||||||
| chr3:40417765 | G | A | 1 | a0002c0002t0002g0128 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.831+1692G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417765 | |||||||
| chr3:40417778 | A | G | 1 | a0002c0002t0002g0128 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.831+1705A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417778 | |||||||
| chr3:40417791 | T | A | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.831+1718T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417791 | |||||||
| chr3:40417797 | T | C | 2 | a0001c0001t0005g0052 a0001c0001t0005g0053 |
2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.831+1724T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417797 | |||||||
| chr3:40417847 | A | G | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+1774A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417847 | |||||||
| chr3:40417848 | G | A | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+1775G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417848 | |||||||
| chr3:40417897 | G | T | 2 | a0001c0001t0003g0024 a0001c0001t0003g0098 |
3 | HG02559.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.831+1824G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417897 | |||||||
| chr3:40417914 | G | C | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+1841G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417914 | |||||||
| chr3:40417915 | C | G | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+1842C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417915 | |||||||
| chr3:40417921 | T | C | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.831+1848T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417921 | |||||||
| chr3:40417946 | A | T | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+1873A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417946 | |||||||
| chr3:40417992 | T | G | 2 | a0001c0005t0003g0093 a0001c0005t0003g0094 |
2 | NA18955.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.831+1919T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40417992 | |||||||
| chr3:40418041 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(94): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.831+1968A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418041 | |||||||
| chr3:40418141 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.831+2068C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418141 | |||||||
| chr3:40418224 | T | C | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+2151T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418224 | |||||||
| chr3:40418233 | A | G | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.831+2160A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418233 | |||||||
| chr3:40418348 | C | A | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+2275C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418348 | |||||||
| chr3:40418365 | A | C | 1 | a0002c0002t0002g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.831+2292A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418365 | |||||||
| chr3:40418394 | T | C | 1 | a0003c0003t0001g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.831+2321T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418394 | |||||||
| chr3:40418588 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.831+2515C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418588 | |||||||
| chr3:40418654 | G | A | 135 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(132): Show |
189 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.831+2581G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418654 | |||||||
| chr3:40418714 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0160 others(74): Show |
112 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.831+2641T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418714 | |||||||
| chr3:40418778 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.831+2705T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418778 | |||||||
| chr3:40418861 | C | T | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.831+2788C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418861 | |||||||
| chr3:40418892 | G | A | 152 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0138 others(149): Show |
208 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.831+2819G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418892 | |||||||
| chr3:40418963 | A | T | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+2890A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40418963 | |||||||
| chr3:40419276 | T | C | 136 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(133): Show |
190 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.831+3203T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40419276 | |||||||
| chr3:40419299 | G | C | 2 | a0001c0001t0002g0059 a0001c0001t0011g0060 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+3226G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40419299 | |||||||
| chr3:40419320 | A | T | 1 | a0012c0013t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.831+3247A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40419320 | |||||||
| chr3:40419367 | CTAA | C | 76 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(73): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.831+3301_831+3303d others(5): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40419367 | ||||||
| chr3:40419540 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA18950.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.832-3310G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40419540 | |||||||
| chr3:40419577 | C | T | 2 | a0002c0002t0002g0150 a0002c0002t0002g0152 |
2 | HG00140.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.832-3273C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40419577 | |||||||
| chr3:40419763 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.832-3087A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40419763 | |||||||
| chr3:40419825 | T | A | 1 | a0001c0001t0001g0037 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.832-3025T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40419825 | |||||||
| chr3:40419865 | G | A | 1 | a0007c0012t0001g0195 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.832-2985G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40419865 | |||||||
| chr3:40420122 | A | G | 12 | a0001c0001t0001g0138 a0001c0001t0001g0241 a0001c0001t0001g0243 others(9): Show |
12 | HG00423.hp2 HG01074.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-2728A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420122 | |||||||
| chr3:40420152 | A | G | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(6): Show |
14 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.832-2698A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420152 | |||||||
| chr3:40420241 | C | CT | 14 | a0001c0001t0002g0042 a0001c0001t0004g0022 a0001c0001t0004g0048 others(11): Show |
15 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.832-2598dupT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40420241 | ||||||
| chr3:40420281 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.832-2569G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420281 | |||||||
| chr3:40420284 | G | GGA | 43 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(40): Show |
80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.832-2564_832-2563d others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40420284 | ||||||
| chr3:40420431 | G | A | 2 | a0002c0002t0002g0015 a0002c0002t0002g0142 |
4 | NA19009.hp2 NA19011.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-2419G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420431 | |||||||
| chr3:40420461 | G | A | 1 | a0001c0001t0002g0008 | 4 | HG02559.hp2 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-2389G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420461 | |||||||
| chr3:40420481 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(94): Show |
147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.832-2369C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420481 | |||||||
| chr3:40420516 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0231 a0001c0001t0001g0232 |
5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-2334C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420516 | |||||||
| chr3:40420520 | T | G | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.832-2330T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420520 | |||||||
| chr3:40420535 | C | G | 137 | a0001c0001t0001g0138 a0001c0001t0001g0206 a0001c0001t0002g0008 others(134): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.832-2315C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420535 | |||||||
| chr3:40420643 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.832-2207T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420643 | |||||||
| chr3:40420671 | C | T | 151 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0138 others(148): Show |
207 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.832-2179C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420671 | |||||||
| chr3:40420742 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.832-2108T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420742 | |||||||
| chr3:40420867 | T | C | 5 | a0002c0002t0002g0028 a0002c0002t0002g0070 a0002c0002t0002g0077 others(2): Show |
6 | HG00544.hp2 NA18951.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-1983T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420867 | |||||||
| chr3:40420978 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.832-1872G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40420978 | |||||||
| chr3:40421019 | A | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(94): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.832-1831A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421019 | |||||||
| chr3:40421025 | A | AT | 34 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0182 others(31): Show |
45 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.832-1809dupT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40421025 | ||||||
| chr3:40421025 | A | ATT | 16 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(13): Show |
22 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.832-1810_832-1809d others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40421025 | ||||||
| chr3:40421025 | AT | A | 9 | a0001c0001t0001g0065 a0001c0001t0001g0165 a0001c0001t0001g0243 others(6): Show |
10 | HG01346.hp2 HG01934.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.832-1809delT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40421025 | ||||||
| chr3:40421026 | T | A | 10 | a0002c0002t0002g0006 a0002c0002t0002g0015 a0002c0002t0002g0068 others(7): Show |
16 | HG01255.hp2 HG01928.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.832-1824T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421026 | |||||||
| chr3:40421092 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.832-1758C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421092 | |||||||
| chr3:40421390 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0206 |
2 | HG00140.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.832-1460T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421390 | |||||||
| chr3:40421494 | T | C | 8 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(5): Show |
9 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.832-1356T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421494 | |||||||
| chr3:40421499 | A | G | 1 | a0001c0001t0005g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.832-1351A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421499 | |||||||
| chr3:40421572 | G | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(53): Show |
96 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.832-1278G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421572 | |||||||
| chr3:40421631 | T | C | 45 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(42): Show |
62 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.832-1219T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421631 | |||||||
| chr3:40421791 | T | G | 11 | a0001c0001t0001g0138 a0001c0001t0001g0241 a0001c0001t0001g0243 others(8): Show |
11 | HG00423.hp2 HG01074.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-1059T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421791 | |||||||
| chr3:40421836 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.832-1014G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421836 | |||||||
| chr3:40421912 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.832-938C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421912 | |||||||
| chr3:40421939 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.832-911C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421939 | |||||||
| chr3:40421980 | A | G | 138 | a0001c0001t0001g0065 a0001c0001t0002g0008 a0001c0001t0002g0009 others(135): Show |
193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.832-870A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40421980 | |||||||
| chr3:40422092 | T | C | 11 | a0001c0001t0001g0138 a0001c0001t0001g0241 a0001c0001t0001g0243 others(8): Show |
11 | HG00423.hp2 HG01074.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-758T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422092 | |||||||
| chr3:40422110 | G | A | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.832-740G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422110 | |||||||
| chr3:40422134 | T | TCA | 39 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0039 others(36): Show |
55 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.832-692_832-691dup others(2): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40422134 | ||||||
| chr3:40422134 | TCA | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(115): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.832-692_832-691del others(2): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40422134 | ||||||
| chr3:40422139 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.832-711C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422139 | |||||||
| chr3:40422168 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0042 a0001c0001t0010g0041 others(2): Show |
7 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-682C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422168 | |||||||
| chr3:40422201 | T | A | 7 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0039 others(4): Show |
12 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.832-649T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422201 | |||||||
| chr3:40422249 | T | C | 2 | a0001c0005t0003g0093 a0001c0005t0003g0094 |
2 | NA18955.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.832-601T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422249 | |||||||
| chr3:40422263 | T | TAGAG | 59 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(56): Show |
77 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.832-584_832-583ins others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40422263 | ||||||
| chr3:40422263 | T | TGGAG | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.832-587_832-586ins others(4): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422263 | |||||||
| chr3:40422286 | T | G | 16 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0023 others(13): Show |
26 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.832-564T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422286 | |||||||
| chr3:40422325 | CT | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(214): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.832-509delT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 40422325 | ||||||
| chr3:40422444 | T | C | 1 | a0002c0002t0002g0124 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.832-406T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422444 | |||||||
| chr3:40422464 | G | A | 1 | a0002c0002t0002g0073 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.832-386G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422464 | |||||||
| chr3:40422494 | C | T | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.832-356C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422494 | |||||||
| chr3:40422514 | C | A | 30 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0023 others(27): Show |
41 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.832-336C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422514 | |||||||
| chr3:40422514 | C | T | 4 | a0001c0001t0005g0049 a0001c0001t0005g0050 a0001c0001t0005g0052 others(1): Show |
4 | HG02895.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-336C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422514 | |||||||
| chr3:40422525 | A | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0042 a0001c0001t0010g0041 others(2): Show |
7 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-325A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 7/10 | chr3 | 40422525 | |||||||
| chr3:40423141 | G | C | 1 | a0002c0002t0002g0140 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1104+19G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 8/10 | chr3 | 40423141 | |||||||
| chr3:40423159 | T | C | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1104+37T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 8/10 | chr3 | 40423159 | |||||||
| chr3:40423206 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1104+84A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 8/10 | chr3 | 40423206 | |||||||
| chr3:40423230 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1105-61T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 8/10 | chr3 | 40423230 | |||||||
| chr3:40423421 | G | C | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(6): Show |
14 | HG00639.hp1 HG01109.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1215+20G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 9/10 | chr3 | 40423421 | |||||||
| chr3:40423468 | G | A | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1215+67G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 9/10 | chr3 | 40423468 | |||||||
| chr3:40423558 | G | A | 1 | a0002c0002t0002g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1215+157G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 9/10 | chr3 | 40423558 | |||||||
| chr3:40424198 | C | T | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1353+235C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40424198 | |||||||
| chr3:40424343 | A | C | 1 | a0001c0001t0001g0250 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1353+380A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40424343 | |||||||
| chr3:40424393 | C | T | 7 | a0001c0001t0003g0024 a0001c0001t0003g0086 a0001c0001t0003g0087 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1353+430C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40424393 | |||||||
| chr3:40424458 | A | G | 2 | a0001c0001t0004g0022 a0001c0001t0004g0055 |
3 | HG02622.hp1 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1353+495A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40424458 | |||||||
| chr3:40424602 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1353+639T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40424602 | |||||||
| chr3:40424794 | G | A | 1 | a0002c0002t0002g0125 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1353+831G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40424794 | |||||||
| chr3:40424817 | C | T | 12 | a0001c0001t0001g0138 a0001c0001t0001g0241 a0001c0001t0001g0243 others(9): Show |
12 | HG00423.hp2 HG01074.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1353+854C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40424817 | |||||||
| chr3:40425183 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1353+1220C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425183 | |||||||
| chr3:40425204 | G | A | 1 | a0001c0011t0002g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1353+1241G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425204 | |||||||
| chr3:40425336 | C | A | 1 | a0002c0002t0002g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1353+1373C>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425336 | |||||||
| chr3:40425358 | G | A | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1353+1395G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425358 | |||||||
| chr3:40425488 | G | A | 151 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0138 others(148): Show |
207 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1353+1525G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425488 | |||||||
| chr3:40425619 | G | A | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0010 others(74): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1354-1653G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425619 | |||||||
| chr3:40425729 | T | C | 1 | a0001c0011t0002g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1354-1543T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425729 | |||||||
| chr3:40425892 | T | C | 136 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(133): Show |
190 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1354-1380T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425892 | |||||||
| chr3:40425897 | C | CA | 9 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0173 others(6): Show |
9 | HG01934.hp2 HG02040.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1354-1359dupA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 40425897 | ||||||
| chr3:40425897 | CA | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(109): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1354-1359delA | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 40425897 | ||||||
| chr3:40425916 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1354-1356A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425916 | |||||||
| chr3:40425937 | G | A | 1 | a0002c0002t0002g0145 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1354-1335G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40425937 | |||||||
| chr3:40426026 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1354-1246A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426026 | |||||||
| chr3:40426069 | T | A | 45 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(42): Show |
62 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.1354-1203T>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426069 | |||||||
| chr3:40426107 | C | CT | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(97): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1354-1146dupT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 40426107 | ||||||
| chr3:40426107 | C | CTT | 6 | a0001c0001t0001g0065 a0001c0001t0001g0173 a0001c0001t0001g0214 others(3): Show |
6 | HG03098.hp2 HG03579.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-1147_1354-114 others(6): Show |
ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 40426107 | ||||||
| chr3:40426107 | CT | C | 14 | a0001c0001t0001g0242 a0001c0001t0004g0022 a0001c0001t0004g0048 others(11): Show |
15 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1354-1146delT | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 40426107 | ||||||
| chr3:40426108 | T | C | 1 | a0002c0002t0002g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1354-1164T>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426108 | |||||||
| chr3:40426240 | C | G | 2 | a0001c0001t0001g0065 a0006c0008t0001g0025 |
3 | HG02683.hp2 HG03098.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1354-1032C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426240 | |||||||
| chr3:40426270 | G | C | 59 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(56): Show |
77 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1354-1002G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426270 | |||||||
| chr3:40426387 | G | A | 2 | a0001c0001t0006g0196 a0001c0001t0006g0218 |
2 | HG01168.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1354-885G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426387 | |||||||
| chr3:40426409 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1354-863A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426409 | |||||||
| chr3:40426457 | G | C | 2 | a0001c0001t0002g0059 a0001c0001t0011g0060 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1354-815G>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426457 | |||||||
| chr3:40426469 | A | C | 1 | a0001c0011t0002g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1354-803A>C | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426469 | |||||||
| chr3:40426715 | T | G | 59 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0038 others(56): Show |
77 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1354-557T>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426715 | |||||||
| chr3:40426751 | G | T | 5 | a0001c0001t0005g0049 a0001c0001t0005g0050 a0001c0001t0005g0051 others(2): Show |
5 | HG02895.hp1 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1354-521G>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426751 | |||||||
| chr3:40426813 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1354-459C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426813 | |||||||
| chr3:40426822 | A | G | 1 | a0006c0008t0001g0025 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1354-450A>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426822 | |||||||
| chr3:40426915 | G | A | 138 | a0001c0001t0001g0065 a0001c0001t0002g0008 a0001c0001t0002g0009 others(135): Show |
193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1354-357G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426915 | |||||||
| chr3:40426918 | C | G | 13 | a0001c0001t0004g0022 a0001c0001t0004g0048 a0001c0001t0004g0054 others(10): Show |
14 | HG01891.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-354C>G | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426918 | |||||||
| chr3:40426986 | A | T | 1 | a0001c0001t0005g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1354-286A>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40426986 | |||||||
| chr3:40427128 | G | A | 5 | a0001c0001t0005g0049 a0001c0001t0005g0050 a0001c0001t0005g0051 others(2): Show |
5 | HG02895.hp1 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1354-144G>A | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40427128 | |||||||
| chr3:40427135 | C | T | 3 | a0001c0001t0004g0022 a0001c0001t0004g0054 a0001c0001t0004g0055 |
4 | HG02622.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-137C>T | ENTPD3 | ENSG00000168032.10 | transcript | ENST00000301825.8 | protein_coding | 10/10 | chr3 | 40427135 |