Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9325 |
| ensemblid | ENSG00000103671.10 |
| hgncid | 12310 |
| symbol | TRIP4 |
| name | thyroid hormone receptor interactor 4 |
| refseq_nuc | NM_016213.5 |
| refseq_prot | NP_057297.2 |
| ensembl_nuc | ENST00000261884.8 |
| ensembl_prot | ENSP00000261884.3 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 64387836 |
| end | 64455303 |
| strand | + |
| ver | v1.2 |
| region | chr15:64387836-64455303 |
| region5000 | chr15:64382836-64460303 |
| regionname0 | TRIP4_chr15_64387836_64455303 |
| regionname5000 | TRIP4_chr15_64382836_64460303 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 581 | 217 | 94 | 32 | 39 | 14 | 36 | 25 | TRIP4_chr15_64382836_64460303 | TRIP4 | MAVAG others(576): Show |
chr15 | 64382836 | 64460303 |
| a0002 | 0/0 | 581 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | MAVAG others(576): Show |
chr15 | 64382836 | 64460303 |
| a0003 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | MAVAG others(576): Show |
chr15 | 64382836 | 64460303 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1743 | 123 | 46 | 20 | 27 | 9 | 20 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0001c0002 | 1/0 | 1743 | 53 | 30 | 0 | 11 | 1 | 10 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0001c0003 | 0/0 | 1743 | 16 | 3 | 7 | 1 | 3 | 2 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0001c0004 | 0/0 | 1743 | 9 | 0 | 4 | 0 | 1 | 4 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0001c0005 | 0/0 | 1743 | 6 | 5 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0001c0006 | 0/0 | 1743 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0001c0007 | 0/0 | 1743 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0001c0008 | 0/0 | 1743 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0001c0010 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0002c0009 | 0/0 | 1743 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 | ||
| a0003c0011 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | ATGGC others(1738): Show |
chr15 | 64382836 | 64460303 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2013 | 118 | 41 | 20 | 27 | 9 | 20 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0001c0001t0002 | 0/0 | 2013 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0001c0002t0001 | 1/0 | 2013 | 53 | 30 | 0 | 11 | 1 | 10 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0001c0003t0001 | 0/0 | 2013 | 16 | 3 | 7 | 1 | 3 | 2 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0001c0004t0001 | 0/0 | 2013 | 9 | 0 | 4 | 0 | 1 | 4 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0001c0005t0001 | 0/0 | 2013 | 6 | 5 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0001c0006t0001 | 0/0 | 2013 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0001c0007t0001 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0001c0008t0001 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0001c0010t0001 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0002c0009t0001 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| a0003c0011t0001 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | GCAGC others(2008): Show |
chr15 | 64382836 | 64460303 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0007t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0007t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0008t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0008t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0010t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0002c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0002c0009t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0003c0011t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0153 | EUR | GBR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00323 | hp1 | a0001 | c0004 | t0001 | g0034 | EUR | FIN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0183 | EUR | FIN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0151 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0052 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0146 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01109 | hp2 | a0001 | c0005 | t0001 | g0048 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0218 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0219 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0147 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0032 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0148 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0152 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0035 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0108 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0197 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0081 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0045 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02451 | hp1 | a0001 | c0008 | t0001 | g0046 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0050 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0076 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0031 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0206 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02735 | hp1 | a0001 | c0004 | t0001 | g0036 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02818 | hp2 | a0002 | c0009 | t0001 | g0027 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02886 | hp2 | a0001 | c0007 | t0001 | g0030 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02922 | hp2 | a0001 | c0006 | t0001 | g0075 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03041 | hp1 | a0001 | c0010 | t0001 | g0167 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03130 | hp2 | a0001 | c0008 | t0001 | g0047 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0029 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03453 | hp2 | a0001 | c0005 | t0001 | g0049 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0196 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0111 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0033 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0037 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0107 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18993 | hp2 | a0003 | c0011 | t0001 | g0114 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0051 | AFR | LWK | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | ASW | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0193 | EUR | TSI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0156 | EUR | TSI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | GIH | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0205 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03471 | hp2 | a0002 | c0009 | t0001 | g0026 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | USA | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | USA | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | USA | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | USA | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0149 | AFR | LWK | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0154 | REF | REF | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0082 | REF | REF | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:64397652 | A | G | 1 | a0002 | 2 | HG02818.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.452A>G | p.Asn151Ser | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/13 | 480/2013 | 452/1746 | 151/581 | chr15 | 64397652 | |||
| chr15:64406413 | A | G | 1 | a0003 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.781A>G | p.Lys261Glu | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/13 | 809/2013 | 781/1746 | 261/581 | chr15 | 64406413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:64387884 | G | C | 1 | a0001c0006 | 5 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
synonymous_variant | LOW | c.21G>C | p.Val7Val | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/13 | 49/2013 | 21/1746 | 7/581 | chr15 | 64387884 | |||
| chr15:64394099 | G | A | 1 | a0001c0007 | 2 | HG02886.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.255G>A | p.Gln85Gln | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/13 | 283/2013 | 255/1746 | 85/581 | chr15 | 64394099 | |||
| chr15:64397782 | A | G | 1 | a0001c0008 | 2 | HG02451.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.582A>G | p.Gln194Gln | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/13 | 610/2013 | 582/1746 | 194/581 | chr15 | 64397782 | |||
| chr15:64409766 | C | T | 2 | a0001c0005 a0001c0008 |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
synonymous_variant | LOW | c.981C>T | p.Thr327Thr | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/13 | 1009/2013 | 981/1746 | 327/581 | chr15 | 64409766 | |||
| chr15:64414133 | A | G | 1 | a0001c0004 | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
synonymous_variant | LOW | c.1092A>G | p.Pro364Pro | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/13 | 1120/2013 | 1092/1746 | 364/581 | chr15 | 64414133 | |||
| chr15:64418564 | C | T | 1 | a0001c0010 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.1194C>T | p.Ala398Ala | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/13 | 1222/2013 | 1194/1746 | 398/581 | chr15 | 64418564 | |||
| chr15:64418628 | T | C | 1 | a0001c0003 | 16 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(13): Show |
synonymous_variant | LOW | c.1258T>C | p.Leu420Leu | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/13 | 1286/2013 | 1258/1746 | 420/581 | chr15 | 64418628 | |||
| chr15:64445026 | G | A | 9 | a0001c0001 a0001c0003 a0001c0004 others(6): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
synonymous_variant | LOW | c.1596G>A | p.Glu532Glu | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/13 | 1624/2013 | 1596/1746 | 532/581 | chr15 | 64445026 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:64455254 | G | C | 1 | a0001c0001t0002 | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*190G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 13/13 | 190 | chr15 | 64455254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:64388027 | G | A | 1 | a0001c0003t0001g0002 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.101+63G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388027 | |||||||
| chr15:64388070 | A | T | 2 | a0001c0004t0001g0218 a0001c0004t0001g0219 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.101+106A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388070 | |||||||
| chr15:64388084 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.101+120G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388084 | |||||||
| chr15:64388143 | T | C | 2 | a0001c0004t0001g0218 a0001c0004t0001g0219 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.101+179T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388143 | |||||||
| chr15:64388192 | C | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(23): Show |
27 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.101+228C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388192 | |||||||
| chr15:64388193 | A | G | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+229A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388193 | |||||||
| chr15:64388210 | A | G | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+246A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388210 | |||||||
| chr15:64388353 | C | A | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+389C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388353 | |||||||
| chr15:64388904 | A | G | 3 | a0001c0001t0001g0028 a0002c0009t0001g0026 a0002c0009t0001g0027 |
3 | HG02818.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.101+940A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388904 | |||||||
| chr15:64388969 | A | G | 2 | a0001c0006t0001g0205 a0001c0006t0001g0206 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.101+1005A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388969 | |||||||
| chr15:64389007 | GGTTGGGG others(14): Show |
G | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+1049_101+1069d others(23): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64389007 | ||||||
| chr15:64389031 | T | G | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1067T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389031 | |||||||
| chr15:64389109 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101+1145A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389109 | |||||||
| chr15:64389226 | T | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1262T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389226 | |||||||
| chr15:64389420 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.101+1456C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389420 | |||||||
| chr15:64389578 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.101+1614A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389578 | |||||||
| chr15:64389708 | C | CT | 10 | a0001c0001t0001g0199 a0001c0002t0001g0198 a0001c0002t0001g0200 others(7): Show |
10 | HG00621.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.101+1764dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64389708 | ||||||
| chr15:64389708 | CT | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0001g0041 others(12): Show |
15 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.101+1764delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64389708 | ||||||
| chr15:64389754 | G | A | 1 | a0001c0002t0001g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.101+1790G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389754 | |||||||
| chr15:64389799 | C | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1835C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389799 | |||||||
| chr15:64389848 | C | T | 1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.101+1884C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389848 | |||||||
| chr15:64389993 | C | T | 1 | a0001c0006t0001g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101+2029C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389993 | |||||||
| chr15:64390047 | CAAATATA others(30): Show |
C | 2 | a0001c0002t0001g0044 a0001c0004t0001g0031 |
2 | HG02698.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.101+2136_101+2172d others(39): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64390047 | ||||||
| chr15:64390154 | C | A | 14 | a0001c0001t0001g0204 a0001c0001t0002g0213 a0001c0001t0002g0214 others(11): Show |
14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.101+2190C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390154 | |||||||
| chr15:64390160 | TA | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0213 others(4): Show |
7 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+2206delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64390160 | ||||||
| chr15:64390193 | G | A | 1 | a0001c0003t0001g0052 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.101+2229G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390193 | |||||||
| chr15:64390203 | T | C | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+2239T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390203 | |||||||
| chr15:64390242 | A | G | 12 | a0001c0001t0001g0186 a0001c0002t0001g0044 a0001c0002t0001g0187 others(9): Show |
12 | HG00621.hp1 HG02071.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+2278A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390242 | |||||||
| chr15:64390318 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101+2354C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390318 | |||||||
| chr15:64390442 | C | G | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+2478C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390442 | |||||||
| chr15:64390460 | C | CA | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+2507dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64390460 | ||||||
| chr15:64390505 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0185 |
2 | HG02080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.101+2541A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390505 | |||||||
| chr15:64390537 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.101+2573A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390537 | |||||||
| chr15:64390628 | C | T | 1 | a0001c0002t0001g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.101+2664C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390628 | |||||||
| chr15:64390664 | G | T | 12 | a0001c0001t0001g0186 a0001c0002t0001g0044 a0001c0002t0001g0187 others(9): Show |
12 | HG00621.hp1 HG02071.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+2700G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390664 | |||||||
| chr15:64390720 | G | A | 1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.101+2756G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390720 | |||||||
| chr15:64390861 | C | T | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+2897C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390861 | |||||||
| chr15:64391097 | T | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0086 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.102-2849T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391097 | |||||||
| chr15:64391179 | C | T | 1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.102-2767C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391179 | |||||||
| chr15:64391302 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102-2644G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391302 | |||||||
| chr15:64391359 | G | C | 14 | a0001c0001t0001g0204 a0001c0001t0002g0213 a0001c0001t0002g0214 others(11): Show |
14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.102-2587G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391359 | |||||||
| chr15:64391447 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102-2499A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391447 | |||||||
| chr15:64391450 | C | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.102-2496C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391450 | |||||||
| chr15:64391498 | A | G | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-2448A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391498 | |||||||
| chr15:64391682 | C | A | 12 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0086 others(9): Show |
12 | HG00099.hp2 HG02080.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.102-2264C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391682 | |||||||
| chr15:64391844 | G | A | 1 | a0001c0008t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.102-2102G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391844 | |||||||
| chr15:64391883 | A | G | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-2063A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391883 | |||||||
| chr15:64391889 | T | C | 8 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0055 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-2057T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391889 | |||||||
| chr15:64391911 | C | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-2035C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391911 | |||||||
| chr15:64391970 | C | CA | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0041 others(49): Show |
52 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.102-1952dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64391970 | ||||||
| chr15:64391970 | C | CAA | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG01109.hp1 HG01261.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-1953_102-1952d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64391970 | ||||||
| chr15:64391970 | CA | C | 27 | a0001c0001t0001g0023 a0001c0001t0002g0215 a0001c0001t0002g0216 others(24): Show |
27 | HG00323.hp1 HG00323.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.102-1952delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64391970 | ||||||
| chr15:64391970 | CAA | C | 7 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-1953_102-1952d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64391970 | ||||||
| chr15:64392006 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0097 a0001c0001t0001g0120 others(5): Show |
8 | HG00140.hp2 HG01109.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-1940C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392006 | |||||||
| chr15:64392046 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.102-1900G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392046 | |||||||
| chr15:64392073 | G | C | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.102-1873G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392073 | |||||||
| chr15:64392112 | T | C | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.102-1834T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392112 | |||||||
| chr15:64392306 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102-1640A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392306 | |||||||
| chr15:64392599 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102-1347C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392599 | |||||||
| chr15:64392832 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102-1114C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392832 | |||||||
| chr15:64393005 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.102-941G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393005 | |||||||
| chr15:64393008 | G | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.102-938G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393008 | |||||||
| chr15:64393151 | A | AT | 13 | a0001c0001t0001g0071 a0001c0001t0001g0119 a0001c0001t0001g0181 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.102-775dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64393151 | ||||||
| chr15:64393151 | AT | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(13): Show |
16 | HG00323.hp1 HG00642.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-775delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64393151 | ||||||
| chr15:64393338 | T | TA | 39 | a0001c0001t0001g0041 a0001c0001t0001g0095 a0001c0001t0001g0097 others(36): Show |
39 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-607dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64393338 | ||||||
| chr15:64393446 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0086 a0001c0001t0001g0094 |
3 | HG03491.hp1 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.102-500C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393446 | |||||||
| chr15:64393597 | C | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-349C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393597 | |||||||
| chr15:64393734 | C | T | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-212C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393734 | |||||||
| chr15:64393891 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.102-55T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393891 | |||||||
| chr15:64393908 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.102-38T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393908 | |||||||
| chr15:64394188 | T | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.271+73T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394188 | |||||||
| chr15:64394211 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01071.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.271+96C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394211 | |||||||
| chr15:64394233 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.271+118G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394233 | |||||||
| chr15:64394429 | C | A | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.271+314C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394429 | |||||||
| chr15:64394504 | C | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.271+389C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394504 | |||||||
| chr15:64394567 | T | A | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.271+452T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394567 | |||||||
| chr15:64394591 | C | T | 14 | a0001c0001t0001g0204 a0001c0001t0002g0213 a0001c0001t0002g0214 others(11): Show |
14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.271+476C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394591 | |||||||
| chr15:64394604 | C | CA | 19 | a0001c0001t0001g0071 a0001c0001t0001g0118 a0001c0001t0001g0119 others(16): Show |
19 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.271+507dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 64394604 | ||||||
| chr15:64394724 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.271+609T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394724 | |||||||
| chr15:64395105 | C | CA | 33 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0086 others(30): Show |
33 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(30): Show |
intron_variant | MODIFIER | c.272-290dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 64395105 | ||||||
| chr15:64395360 | CTGTG | C | 2 | a0001c0002t0001g0072 a0001c0002t0001g0073 |
2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.272-28_272-25delGT others(2): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 64395360 | ||||||
| chr15:64395582 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0086 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.405+51G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395582 | |||||||
| chr15:64395585 | T | A | 2 | a0001c0001t0001g0186 a0001c0002t0001g0200 |
2 | HG00621.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.405+54T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395585 | |||||||
| chr15:64395739 | CT | C | 18 | a0001c0002t0001g0074 a0001c0002t0001g0207 a0001c0002t0001g0208 others(15): Show |
18 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.405+224delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64395739 | ||||||
| chr15:64395755 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.405+224T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395755 | |||||||
| chr15:64395804 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.405+273G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395804 | |||||||
| chr15:64395865 | C | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.405+334C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395865 | |||||||
| chr15:64395890 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0185 |
2 | HG02080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.405+359G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395890 | |||||||
| chr15:64395912 | CTT | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.405+394_405+395del others(2): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64395912 | ||||||
| chr15:64395940 | G | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.405+409G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395940 | |||||||
| chr15:64396082 | G | A | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+551G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396082 | |||||||
| chr15:64396124 | G | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+593G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396124 | |||||||
| chr15:64396131 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.405+600G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396131 | |||||||
| chr15:64396201 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.405+670G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396201 | |||||||
| chr15:64396266 | C | CT | 12 | a0001c0001t0001g0014 a0001c0001t0001g0071 a0001c0001t0002g0215 others(9): Show |
12 | HG02055.hp2 HG02071.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.405+763dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | ||||||
| chr15:64396266 | CT | C | 34 | a0001c0001t0001g0007 a0001c0002t0001g0038 a0001c0002t0001g0039 others(31): Show |
34 | HG00323.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.405+763delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | ||||||
| chr15:64396266 | CTTTTTTT | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0145 others(2): Show |
5 | HG02071.hp1 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+757_405+763del others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | ||||||
| chr15:64396266 | CTTTTTTT others(1): Show |
C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.405+756_405+763del others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | ||||||
| chr15:64396266 | CTTTTTTT others(5): Show |
C | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.405+752_405+763del others(12): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | ||||||
| chr15:64396337 | C | T | 7 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.405+806C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396337 | |||||||
| chr15:64396560 | T | A | 21 | a0001c0001t0001g0186 a0001c0002t0001g0044 a0001c0002t0001g0053 others(18): Show |
21 | HG00621.hp1 HG01884.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.405+1029T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396560 | |||||||
| chr15:64396707 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.406-899G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396707 | |||||||
| chr15:64396753 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.406-853G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396753 | |||||||
| chr15:64396842 | A | G | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.406-764A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396842 | |||||||
| chr15:64396923 | C | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.406-683C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396923 | |||||||
| chr15:64396935 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.406-671T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396935 | |||||||
| chr15:64397043 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.406-563T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64397043 | |||||||
| chr15:64397220 | C | T | 22 | a0001c0001t0001g0204 a0001c0001t0002g0213 a0001c0001t0002g0214 others(19): Show |
22 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.406-386C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64397220 | |||||||
| chr15:64397241 | T | C | 2 | a0001c0004t0001g0036 a0001c0004t0001g0037 |
2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.406-365T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64397241 | |||||||
| chr15:64397458 | C | G | 1 | a0001c0003t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.406-148C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64397458 | |||||||
| chr15:64397939 | C | T | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.618+121C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64397939 | |||||||
| chr15:64397975 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.618+157G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64397975 | |||||||
| chr15:64397993 | C | T | 1 | a0001c0008t0001g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.618+175C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64397993 | |||||||
| chr15:64398190 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.618+372C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398190 | |||||||
| chr15:64398322 | C | G | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+504C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398322 | |||||||
| chr15:64398424 | C | CA | 52 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0096 others(49): Show |
52 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.618+632dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398424 | ||||||
| chr15:64398424 | CA | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(13): Show |
17 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.618+632delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398424 | ||||||
| chr15:64398527 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+709C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398527 | |||||||
| chr15:64398555 | G | T | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.618+737G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398555 | |||||||
| chr15:64398561 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.618+743C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398561 | |||||||
| chr15:64398573 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.618+755A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398573 | |||||||
| chr15:64398624 | A | G | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+806A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398624 | |||||||
| chr15:64398667 | G | A | 5 | a0001c0006t0001g0075 a0001c0006t0001g0076 a0001c0006t0001g0196 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+849G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398667 | |||||||
| chr15:64398682 | G | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.618+864G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398682 | |||||||
| chr15:64398939 | C | CT | 6 | a0001c0002t0001g0039 a0001c0002t0001g0068 a0001c0002t0001g0209 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+1149dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | ||||||
| chr15:64398939 | CT | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
53 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.618+1149delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | ||||||
| chr15:64398939 | CTT | C | 19 | a0001c0001t0001g0186 a0001c0001t0002g0213 a0001c0001t0002g0214 others(16): Show |
19 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.618+1148_618+1149d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | ||||||
| chr15:64398939 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0140 |
2 | HG01192.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.618+1139_618+1149d others(13): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | ||||||
| chr15:64398939 | CTTTTTTT others(5): Show |
C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.618+1138_618+1149d others(14): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | ||||||
| chr15:64398972 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0125 others(2): Show |
5 | HG02055.hp1 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+1154C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398972 | |||||||
| chr15:64398982 | C | G | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.618+1164C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398982 | |||||||
| chr15:64398988 | C | T | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.618+1170C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398988 | |||||||
| chr15:64399018 | C | T | 1 | a0001c0003t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.618+1200C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399018 | |||||||
| chr15:64399199 | A | G | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+1381A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399199 | |||||||
| chr15:64399542 | T | G | 1 | a0001c0002t0001g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.619-1201T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399542 | |||||||
| chr15:64399674 | G | T | 1 | a0001c0001t0001g0004 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.619-1069G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399674 | |||||||
| chr15:64399938 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.619-805G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399938 | |||||||
| chr15:64399953 | T | C | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-790T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399953 | |||||||
| chr15:64399995 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.619-748A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399995 | |||||||
| chr15:64400219 | G | T | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-524G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64400219 | |||||||
| chr15:64400408 | A | G | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-335A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64400408 | |||||||
| chr15:64400456 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.619-287A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64400456 | |||||||
| chr15:64400473 | CT | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.619-254delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64400473 | ||||||
| chr15:64400732 | C | G | 3 | a0001c0001t0001g0028 a0002c0009t0001g0026 a0002c0009t0001g0027 |
3 | HG02818.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.619-11C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64400732 | |||||||
| chr15:64400851 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.697+30G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64400851 | |||||||
| chr15:64400884 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.697+63T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64400884 | |||||||
| chr15:64400950 | G | GT | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.697+137dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 64400950 | ||||||
| chr15:64401130 | A | G | 1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.697+309A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401130 | |||||||
| chr15:64401237 | C | A | 1 | a0001c0003t0001g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.697+416C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401237 | |||||||
| chr15:64401426 | C | A | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.697+605C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401426 | |||||||
| chr15:64401427 | G | A | 1 | a0001c0004t0001g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.697+606G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401427 | |||||||
| chr15:64401594 | C | G | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+773C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401594 | |||||||
| chr15:64401925 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.697+1104G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401925 | |||||||
| chr15:64401935 | A | G | 6 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.697+1114A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401935 | |||||||
| chr15:64402026 | T | A | 13 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.697+1205T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402026 | |||||||
| chr15:64402198 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.697+1377A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402198 | |||||||
| chr15:64402305 | C | G | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+1484C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402305 | |||||||
| chr15:64402448 | C | T | 2 | a0001c0004t0001g0218 a0001c0004t0001g0219 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.697+1627C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402448 | |||||||
| chr15:64402524 | T | A | 3 | a0001c0005t0001g0045 a0001c0008t0001g0046 a0001c0008t0001g0047 |
3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.697+1703T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402524 | |||||||
| chr15:64402591 | T | C | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+1770T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402591 | |||||||
| chr15:64402747 | A | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(24): Show |
28 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.697+1926A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402747 | |||||||
| chr15:64402748 | A | ACTC | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.697+1930_697+1932d others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 64402748 | ||||||
| chr15:64402865 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.697+2044G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402865 | |||||||
| chr15:64403180 | G | A | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.697+2359G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403180 | |||||||
| chr15:64403313 | T | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.697+2492T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403313 | |||||||
| chr15:64403405 | C | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.697+2584C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403405 | |||||||
| chr15:64403450 | C | T | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.697+2629C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403450 | |||||||
| chr15:64403511 | G | A | 3 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.697+2690G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403511 | |||||||
| chr15:64403848 | A | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.698-2482A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403848 | |||||||
| chr15:64403914 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG03041.hp2 HG04228.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-2416G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403914 | |||||||
| chr15:64403984 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.698-2346G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403984 | |||||||
| chr15:64404182 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.698-2148C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404182 | |||||||
| chr15:64404207 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.698-2123A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404207 | |||||||
| chr15:64404574 | A | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18962.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.698-1756A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404574 | |||||||
| chr15:64404603 | G | A | 3 | a0001c0002t0001g0078 a0001c0002t0001g0079 a0001c0002t0001g0081 |
3 | HG02258.hp2 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.698-1727G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404603 | |||||||
| chr15:64404712 | G | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.698-1618G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404712 | |||||||
| chr15:64404739 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.698-1591C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404739 | |||||||
| chr15:64404782 | C | G | 4 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0059 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1548C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404782 | |||||||
| chr15:64404863 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.698-1467G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404863 | |||||||
| chr15:64404952 | C | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.698-1378C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404952 | |||||||
| chr15:64404981 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.698-1349C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404981 | |||||||
| chr15:64405223 | C | T | 1 | a0001c0005t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.698-1107C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405223 | |||||||
| chr15:64405242 | C | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.698-1088C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405242 | |||||||
| chr15:64405255 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.698-1075T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405255 | |||||||
| chr15:64405415 | A | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.698-915A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405415 | |||||||
| chr15:64405907 | G | A | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-423G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405907 | |||||||
| chr15:64405915 | C | T | 1 | a0001c0001t0001g0003 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.698-415C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405915 | |||||||
| chr15:64406086 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.698-244G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64406086 | |||||||
| chr15:64406292 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.698-38A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64406292 | |||||||
| chr15:64406637 | A | G | 2 | a0001c0002t0001g0039 a0001c0002t0001g0068 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.827+178A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64406637 | |||||||
| chr15:64406692 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.827+233G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64406692 | |||||||
| chr15:64406736 | C | T | 7 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.827+277C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64406736 | |||||||
| chr15:64406978 | G | C | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.827+519G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64406978 | |||||||
| chr15:64407003 | GA | G | 33 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0086 others(30): Show |
33 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(30): Show |
intron_variant | MODIFIER | c.827+545delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407003 | |||||||
| chr15:64407074 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.827+615C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407074 | |||||||
| chr15:64407166 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18942.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.827+707A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407166 | |||||||
| chr15:64407199 | G | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.827+740G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407199 | |||||||
| chr15:64407355 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.827+896A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407355 | |||||||
| chr15:64407389 | C | T | 2 | a0001c0001t0001g0105 a0001c0002t0001g0099 |
2 | HG00438.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.827+930C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407389 | |||||||
| chr15:64407395 | C | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.827+936C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407395 | |||||||
| chr15:64407398 | T | G | 2 | a0001c0008t0001g0046 a0001c0008t0001g0047 |
2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.827+939T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407398 | |||||||
| chr15:64407559 | C | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.827+1100C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407559 | |||||||
| chr15:64407666 | C | CA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): Show |
49 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.827+1217dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64407666 | ||||||
| chr15:64407814 | C | A | 12 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0125 others(9): Show |
12 | HG01071.hp2 HG02055.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.827+1355C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407814 | |||||||
| chr15:64408024 | G | A | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.827+1565G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408024 | |||||||
| chr15:64408044 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0090 |
2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.828-1569G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408044 | |||||||
| chr15:64408094 | C | CA | 21 | a0001c0001t0001g0159 a0001c0001t0002g0213 a0001c0001t0002g0214 others(18): Show |
21 | HG02055.hp2 HG02083.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.828-1503dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408094 | ||||||
| chr15:64408139 | C | G | 12 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0125 others(9): Show |
12 | HG01071.hp2 HG02055.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.828-1474C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408139 | |||||||
| chr15:64408157 | A | ATT | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.828-1452_828-1451d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408157 | ||||||
| chr15:64408163 | G | GT | 28 | a0001c0001t0001g0204 a0001c0002t0001g0060 a0001c0002t0001g0099 others(25): Show |
28 | HG00323.hp1 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.828-1438dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408163 | ||||||
| chr15:64408163 | G | GTT | 103 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.828-1439_828-1438d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408163 | ||||||
| chr15:64408163 | G | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.828-1450G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408163 | |||||||
| chr15:64408190 | G | A | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.828-1423G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408190 | |||||||
| chr15:64408249 | A | AT | 26 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(23): Show |
26 | HG00621.hp1 HG01192.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.828-1337dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | ||||||
| chr15:64408249 | AT | A | 10 | a0001c0001t0001g0204 a0001c0001t0002g0213 a0001c0001t0002g0215 others(7): Show |
10 | HG02559.hp2 HG02886.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.828-1337delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | ||||||
| chr15:64408249 | ATT | A | 23 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0103 others(20): Show |
23 | HG01071.hp2 HG01169.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.828-1338_828-1337d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | ||||||
| chr15:64408249 | ATTT | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.828-1339_828-1337d others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | ||||||
| chr15:64408249 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.828-1346_828-1337d others(12): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | ||||||
| chr15:64408340 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.828-1273G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408340 | |||||||
| chr15:64408359 | C | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.828-1254C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408359 | |||||||
| chr15:64408539 | GT | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.828-1072delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408539 | ||||||
| chr15:64408547 | A | G | 1 | a0001c0002t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.828-1066A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408547 | |||||||
| chr15:64408695 | G | A | 8 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0055 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.828-918G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408695 | |||||||
| chr15:64408843 | G | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.828-770G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408843 | |||||||
| chr15:64408996 | C | T | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.828-617C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408996 | |||||||
| chr15:64409083 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.828-530C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409083 | |||||||
| chr15:64409170 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.828-443G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409170 | |||||||
| chr15:64409190 | CA | C | 9 | a0001c0002t0001g0099 a0001c0005t0001g0045 a0001c0005t0001g0048 others(6): Show |
9 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.828-409delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64409190 | ||||||
| chr15:64409278 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.828-335G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409278 | |||||||
| chr15:64409528 | T | C | 1 | a0001c0004t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.828-85T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409528 | |||||||
| chr15:64409597 | G | C | 3 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.828-16G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409597 | |||||||
| chr15:64409969 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1043+141G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64409969 | |||||||
| chr15:64410024 | G | GT | 13 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0001g0199 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1043+215dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 64410024 | ||||||
| chr15:64410171 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1043+343G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64410171 | |||||||
| chr15:64410334 | T | A | 1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1043+506T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64410334 | |||||||
| chr15:64410709 | T | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0160 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1043+881T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64410709 | |||||||
| chr15:64411025 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.1043+1197G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411025 | |||||||
| chr15:64411110 | T | A | 14 | a0001c0001t0001g0204 a0001c0001t0002g0213 a0001c0001t0002g0214 others(11): Show |
14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1043+1282T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411110 | |||||||
| chr15:64411492 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1043+1664C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411492 | |||||||
| chr15:64411611 | A | G | 4 | a0001c0002t0001g0209 a0001c0002t0001g0210 a0001c0002t0001g0211 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+1783A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411611 | |||||||
| chr15:64411616 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0128 |
2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1043+1788C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411616 | |||||||
| chr15:64411685 | G | GT | 132 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1043+1869dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 64411685 | ||||||
| chr15:64411741 | G | A | 1 | a0001c0002t0001g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1043+1913G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411741 | |||||||
| chr15:64412063 | A | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1044-2022A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412063 | |||||||
| chr15:64412069 | A | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.1044-2016A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412069 | |||||||
| chr15:64412079 | T | G | 6 | a0001c0002t0001g0044 a0001c0002t0001g0188 a0001c0002t0001g0191 others(3): Show |
6 | NA18962.hp1 NA18972.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044-2006T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412079 | |||||||
| chr15:64412284 | T | G | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1044-1801T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412284 | |||||||
| chr15:64412305 | C | G | 1 | a0001c0004t0001g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1044-1780C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412305 | |||||||
| chr15:64412557 | TA | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1044-1513delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 64412557 | ||||||
| chr15:64412562 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1044-1523A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412562 | |||||||
| chr15:64412645 | A | ATATAT | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1044-1438_1044-143 others(9): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 64412645 | ||||||
| chr15:64412682 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1044-1403C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412682 | |||||||
| chr15:64412742 | G | A | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1044-1343G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412742 | |||||||
| chr15:64413132 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1044-953A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413132 | |||||||
| chr15:64413347 | A | G | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1044-738A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413347 | |||||||
| chr15:64413511 | G | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): Show |
49 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1044-574G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413511 | |||||||
| chr15:64413541 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1044-544G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413541 | |||||||
| chr15:64413596 | T | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1044-489T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413596 | |||||||
| chr15:64413603 | T | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1044-482T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413603 | |||||||
| chr15:64414039 | C | T | 1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1044-46C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64414039 | |||||||
| chr15:64414060 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1044-25G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64414060 | |||||||
| chr15:64414064 | C | T | 2 | a0001c0002t0001g0064 a0001c0002t0001g0067 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1044-21C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64414064 | |||||||
| chr15:64414229 | C | G | 12 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0086 others(9): Show |
12 | HG00099.hp2 HG02080.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.1170+18C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414229 | |||||||
| chr15:64414298 | ATACCAAT others(20): Show |
A | 1 | a0001c0002t0001g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1170+107_1170+133d others(29): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64414298 | ||||||
| chr15:64414403 | T | C | 14 | a0001c0001t0001g0204 a0001c0001t0002g0213 a0001c0001t0002g0214 others(11): Show |
14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1170+192T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414403 | |||||||
| chr15:64414486 | A | G | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+275A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414486 | |||||||
| chr15:64414512 | C | CT | 14 | a0001c0002t0001g0209 a0001c0002t0001g0210 a0001c0002t0001g0211 others(11): Show |
14 | HG00323.hp1 HG00323.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1170+323dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64414512 | ||||||
| chr15:64414512 | C | CTT | 100 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1170+322_1170+323d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64414512 | ||||||
| chr15:64414512 | C | CTTT | 16 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1170+321_1170+323d others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64414512 | ||||||
| chr15:64414512 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0092 |
2 | NA18998.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1170+301C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414512 | |||||||
| chr15:64414578 | A | G | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+367A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414578 | |||||||
| chr15:64414603 | G | A | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1170+392G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414603 | |||||||
| chr15:64414621 | A | G | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+410A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414621 | |||||||
| chr15:64414641 | T | C | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+430T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414641 | |||||||
| chr15:64414718 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): Show |
49 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1170+507C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414718 | |||||||
| chr15:64414744 | C | T | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1170+533C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414744 | |||||||
| chr15:64414760 | A | G | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+549A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414760 | |||||||
| chr15:64414863 | G | A | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1170+652G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414863 | |||||||
| chr15:64414923 | G | A | 1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1170+712G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414923 | |||||||
| chr15:64415001 | G | A | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+790G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415001 | |||||||
| chr15:64415005 | G | A | 2 | a0001c0003t0001g0149 a0001c0003t0001g0150 |
2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1170+794G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415005 | |||||||
| chr15:64415085 | A | G | 6 | a0001c0002t0001g0184 a0001c0006t0001g0075 a0001c0006t0001g0076 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+874A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415085 | |||||||
| chr15:64415093 | T | A | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+882T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415093 | |||||||
| chr15:64415176 | G | A | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+965G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415176 | |||||||
| chr15:64415335 | T | C | 3 | a0001c0005t0001g0045 a0001c0008t0001g0046 a0001c0008t0001g0047 |
3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1170+1124T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415335 | |||||||
| chr15:64415817 | A | C | 3 | a0001c0005t0001g0045 a0001c0008t0001g0046 a0001c0008t0001g0047 |
3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1170+1606A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415817 | |||||||
| chr15:64415828 | C | T | 1 | a0002c0009t0001g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1170+1617C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415828 | |||||||
| chr15:64416123 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1170+1912T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64416123 | |||||||
| chr15:64416226 | A | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(24): Show |
28 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1170+2015A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64416226 | |||||||
| chr15:64416605 | A | C | 1 | a0001c0002t0001g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1171-1936A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64416605 | |||||||
| chr15:64416827 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1171-1714G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64416827 | |||||||
| chr15:64417107 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1171-1434G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64417107 | |||||||
| chr15:64417467 | T | A | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1171-1074T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64417467 | |||||||
| chr15:64417467 | T | TA | 110 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.1171-1068dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64417467 | ||||||
| chr15:64417621 | T | G | 7 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-920T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64417621 | |||||||
| chr15:64417676 | C | G | 1 | a0001c0002t0001g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1171-865C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64417676 | |||||||
| chr15:64418068 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1171-473C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64418068 | |||||||
| chr15:64418379 | T | C | 2 | a0001c0004t0001g0033 a0001c0004t0001g0035 |
2 | HG01934.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1171-162T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64418379 | |||||||
| chr15:64418392 | G | A | 1 | a0001c0002t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1171-149G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64418392 | |||||||
| chr15:64418494 | G | A | 1 | a0001c0002t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1171-47G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64418494 | |||||||
| chr15:64418838 | C | A | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+110C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64418838 | |||||||
| chr15:64418975 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
58 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1358+247C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64418975 | |||||||
| chr15:64419383 | C | T | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1358+655C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419383 | |||||||
| chr15:64419390 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.1358+662T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419390 | |||||||
| chr15:64419391 | G | C | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+663G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419391 | |||||||
| chr15:64419430 | C | G | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358+702C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419430 | |||||||
| chr15:64419787 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1358+1059A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419787 | |||||||
| chr15:64419827 | T | G | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1358+1099T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419827 | |||||||
| chr15:64419857 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
58 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1358+1129C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419857 | |||||||
| chr15:64419960 | C | T | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1358+1232C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419960 | |||||||
| chr15:64419965 | G | A | 3 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1358+1237G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419965 | |||||||
| chr15:64420143 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1358+1415C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420143 | |||||||
| chr15:64420209 | C | T | 2 | a0001c0004t0001g0218 a0001c0004t0001g0219 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1358+1481C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420209 | |||||||
| chr15:64420303 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1358+1575T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420303 | |||||||
| chr15:64420341 | A | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+1613A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420341 | |||||||
| chr15:64420356 | G | A | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358+1628G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420356 | |||||||
| chr15:64420409 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1358+1681A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420409 | |||||||
| chr15:64420433 | C | G | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1358+1705C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420433 | |||||||
| chr15:64420507 | A | G | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1358+1779A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420507 | |||||||
| chr15:64420529 | C | CT | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1358+1813dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64420529 | ||||||
| chr15:64420609 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1358+1881C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420609 | |||||||
| chr15:64420688 | T | C | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+1960T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420688 | |||||||
| chr15:64420754 | G | A | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+2026G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420754 | |||||||
| chr15:64420783 | C | A | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1358+2055C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420783 | |||||||
| chr15:64420812 | G | C | 3 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1358+2084G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420812 | |||||||
| chr15:64420900 | C | G | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1358+2172C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420900 | |||||||
| chr15:64421070 | G | T | 1 | a0001c0008t0001g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1358+2342G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421070 | |||||||
| chr15:64421285 | A | C | 1 | a0001c0002t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1358+2557A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421285 | |||||||
| chr15:64421295 | TATA | T | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+2571_1358+257 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64421295 | ||||||
| chr15:64421326 | T | C | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1358+2598T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421326 | |||||||
| chr15:64421334 | T | A | 1 | a0001c0002t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1358+2606T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421334 | |||||||
| chr15:64421351 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1358+2623T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421351 | |||||||
| chr15:64421405 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1359-2626C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421405 | |||||||
| chr15:64421441 | T | C | 1 | a0001c0002t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1359-2590T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421441 | |||||||
| chr15:64421567 | C | G | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1359-2464C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421567 | |||||||
| chr15:64421883 | A | C | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1359-2148A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421883 | |||||||
| chr15:64421999 | T | C | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1359-2032T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421999 | |||||||
| chr15:64422028 | C | CA | 38 | a0001c0001t0001g0136 a0001c0001t0001g0186 a0001c0002t0001g0039 others(35): Show |
38 | HG00621.hp1 HG01884.hp2 HG02071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1359-1989dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64422028 | ||||||
| chr15:64422265 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG04228.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1359-1766G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422265 | |||||||
| chr15:64422309 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1359-1722T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422309 | |||||||
| chr15:64422573 | A | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1359-1458A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422573 | |||||||
| chr15:64422704 | T | G | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1359-1327T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422704 | |||||||
| chr15:64422807 | T | C | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1359-1224T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422807 | |||||||
| chr15:64423049 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1359-982T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423049 | |||||||
| chr15:64423108 | G | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1359-923G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423108 | |||||||
| chr15:64423428 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1359-603T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423428 | |||||||
| chr15:64423461 | C | CA | 13 | a0001c0002t0001g0062 a0001c0002t0001g0065 a0001c0002t0001g0069 others(10): Show |
13 | HG00323.hp1 HG01169.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1359-544dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64423461 | ||||||
| chr15:64423461 | CA | C | 54 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0086 others(51): Show |
54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.1359-544delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64423461 | ||||||
| chr15:64423461 | CAA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
106 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.1359-545_1359-544d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64423461 | ||||||
| chr15:64423461 | CAAA | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359-546_1359-544d others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64423461 | ||||||
| chr15:64423527 | G | A | 1 | a0001c0003t0001g0111 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1359-504G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423527 | |||||||
| chr15:64423813 | A | C | 4 | a0001c0005t0001g0048 a0001c0005t0001g0049 a0001c0005t0001g0050 others(1): Show |
4 | HG01109.hp2 HG02572.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1359-218A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423813 | |||||||
| chr15:64423865 | T | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359-166T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423865 | |||||||
| chr15:64424312 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1483+157C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64424312 | |||||||
| chr15:64424382 | T | C | 1 | a0001c0003t0001g0183 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1483+227T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64424382 | |||||||
| chr15:64424778 | C | G | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1483+623C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64424778 | |||||||
| chr15:64424900 | C | T | 1 | a0001c0003t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1484-640C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64424900 | |||||||
| chr15:64425241 | G | A | 1 | a0001c0003t0001g0002 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1484-299G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64425241 | |||||||
| chr15:64425273 | T | A | 3 | a0001c0005t0001g0045 a0001c0008t0001g0046 a0001c0008t0001g0047 |
3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1484-267T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64425273 | |||||||
| chr15:64425295 | T | C | 1 | a0001c0003t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1484-245T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64425295 | |||||||
| chr15:64425646 | C | CT | 5 | a0001c0002t0001g0184 a0001c0006t0001g0075 a0001c0006t0001g0076 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+26dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64425646 | ||||||
| chr15:64425666 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0174 a0001c0001t0001g0176 others(4): Show |
7 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+35G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64425666 | |||||||
| chr15:64425792 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1575+161C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64425792 | |||||||
| chr15:64425934 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1575+303T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64425934 | |||||||
| chr15:64426133 | C | T | 1 | a0001c0002t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1575+502C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426133 | |||||||
| chr15:64426140 | C | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0163 |
2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1575+509C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426140 | |||||||
| chr15:64426294 | TTGCCAGG others(4): Show |
T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+669_1575+679d others(13): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64426294 | ||||||
| chr15:64426320 | G | C | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1575+689G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426320 | |||||||
| chr15:64426362 | G | A | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1575+731G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426362 | |||||||
| chr15:64426538 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1575+907A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426538 | |||||||
| chr15:64426563 | G | A | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1575+932G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426563 | |||||||
| chr15:64426573 | G | A | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+942G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426573 | |||||||
| chr15:64426699 | C | CA | 5 | a0001c0001t0001g0023 a0001c0001t0001g0071 a0001c0001t0002g0213 others(2): Show |
5 | HG02129.hp1 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1575+1088dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64426699 | ||||||
| chr15:64426699 | CA | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.1575+1088delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64426699 | ||||||
| chr15:64426893 | G | A | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1575+1262G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426893 | |||||||
| chr15:64426939 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(25): Show |
29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1575+1308G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426939 | |||||||
| chr15:64426948 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1575+1317C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426948 | |||||||
| chr15:64426965 | G | A | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+1334G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426965 | |||||||
| chr15:64426993 | C | T | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1575+1362C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426993 | |||||||
| chr15:64427044 | A | G | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1575+1413A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427044 | |||||||
| chr15:64427105 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1575+1474A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427105 | |||||||
| chr15:64427191 | A | G | 3 | a0001c0006t0001g0076 a0001c0006t0001g0205 a0001c0006t0001g0206 |
3 | HG02486.hp2 HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1575+1560A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427191 | |||||||
| chr15:64427566 | A | G | 1 | a0001c0005t0001g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1575+1935A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427566 | |||||||
| chr15:64427665 | T | C | 24 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0001t0001g0103 others(21): Show |
24 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1575+2034T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427665 | |||||||
| chr15:64427954 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1575+2323C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427954 | |||||||
| chr15:64427954 | C | T | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+2323C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427954 | |||||||
| chr15:64428047 | G | C | 1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1575+2416G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64428047 | |||||||
| chr15:64428234 | C | A | 1 | a0001c0003t0001g0052 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1575+2603C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64428234 | |||||||
| chr15:64428381 | TCTC | T | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1575+2753_1575+275 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64428381 | ||||||
| chr15:64428554 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG04228.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1575+2923G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64428554 | |||||||
| chr15:64428740 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1575+3109C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64428740 | |||||||
| chr15:64429045 | T | C | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1575+3414T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429045 | |||||||
| chr15:64429081 | G | A | 1 | a0001c0002t0001g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1575+3450G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429081 | |||||||
| chr15:64429178 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1575+3547G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429178 | |||||||
| chr15:64429317 | C | CA | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+3694dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64429317 | ||||||
| chr15:64429396 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1575+3765G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429396 | |||||||
| chr15:64429519 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1575+3888G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429519 | |||||||
| chr15:64429546 | C | A | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1575+3915C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429546 | |||||||
| chr15:64429629 | A | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1575+3998A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429629 | |||||||
| chr15:64429684 | A | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18942.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1575+4053A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429684 | |||||||
| chr15:64429728 | G | T | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1575+4097G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429728 | |||||||
| chr15:64430177 | C | T | 1 | a0001c0002t0001g0085 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1575+4546C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430177 | |||||||
| chr15:64430237 | A | G | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+4606A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430237 | |||||||
| chr15:64430242 | C | T | 2 | a0001c0004t0001g0218 a0001c0004t0001g0219 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1575+4611C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430242 | |||||||
| chr15:64430498 | A | T | 2 | a0001c0004t0001g0036 a0001c0004t0001g0037 |
2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1575+4867A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430498 | |||||||
| chr15:64430502 | C | CT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1575+4882dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64430502 | ||||||
| chr15:64430643 | T | C | 1 | a0001c0003t0001g0002 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1575+5012T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430643 | |||||||
| chr15:64430755 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0090 |
2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1575+5124A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430755 | |||||||
| chr15:64430856 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0090 |
2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1575+5225C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430856 | |||||||
| chr15:64431268 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0128 |
3 | HG00140.hp1 HG01515.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1575+5637G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431268 | |||||||
| chr15:64431378 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1575+5747G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431378 | |||||||
| chr15:64431431 | C | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+5800C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431431 | |||||||
| chr15:64431469 | G | A | 3 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1575+5838G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431469 | |||||||
| chr15:64431677 | G | T | 1 | a0001c0003t0001g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1575+6046G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431677 | |||||||
| chr15:64431831 | T | TTA | 3 | a0001c0002t0001g0039 a0001c0002t0001g0056 a0001c0002t0001g0068 |
3 | HG01884.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1575+6216_1575+621 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | ||||||
| chr15:64431831 | T | TTATATAT others(3): Show |
1 | a0001c0001t0002g0214 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1575+6208_1575+621 others(14): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | ||||||
| chr15:64431831 | T | TTATATAT others(19): Show |
1 | a0001c0001t0002g0217 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(30): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | ||||||
| chr15:64431831 | T | TTATATAT others(21): Show |
1 | a0001c0001t0002g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(32): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | ||||||
| chr15:64431831 | T | TTATATAT others(25): Show |
2 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(36): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | ||||||
| chr15:64431833 | A | T | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+6202A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431833 | |||||||
| chr15:64431847 | A | AT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(25): Show |
29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1575+6224dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(37): Show |
1 | a0001c0005t0001g0049 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(48): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(32): Show |
1 | a0001c0005t0001g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(43): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(26): Show |
1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(37): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(30): Show |
1 | a0001c0005t0001g0048 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(41): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(31): Show |
1 | a0001c0005t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(42): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(33): Show |
1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(44): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(22): Show |
1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(33): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(23): Show |
1 | a0001c0008t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(34): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(25): Show |
1 | a0001c0008t0001g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(36): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(16): Show |
1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(27): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(5): Show |
3 | a0001c0004t0001g0033 a0001c0004t0001g0034 a0001c0004t0001g0035 |
3 | HG00323.hp1 HG01934.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(6): Show |
1 | a0001c0004t0001g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(17): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(4): Show |
2 | a0001c0004t0001g0036 a0001c0004t0001g0037 |
2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(15): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(5): Show |
1 | a0001c0004t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATAT others(6): Show |
2 | a0001c0004t0001g0218 a0001c0004t0001g0219 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(17): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATT | 34 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0092 others(31): Show |
34 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(10): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATTT | 6 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG02004.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(11): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATTT others(14): Show |
2 | a0001c0002t0001g0208 a0001c0002t0001g0209 |
2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(25): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATATTT others(15): Show |
2 | a0001c0002t0001g0207 a0001c0002t0001g0210 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(26): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATTTT | 40 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0086 others(37): Show |
40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(10): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATATTTTT others(14): Show |
2 | a0001c0002t0001g0211 a0001c0002t0001g0212 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(25): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | ATTTTTT | 20 | a0001c0001t0001g0093 a0001c0001t0001g0101 a0001c0001t0001g0104 others(17): Show |
20 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1575+6219_1575+622 others(10): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | ||||||
| chr15:64431847 | A | T | 2 | a0001c0002t0001g0066 a0001c0002t0001g0077 |
2 | HG02083.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1575+6216A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431847 | |||||||
| chr15:64431849 | T | A | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+6218T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431849 | |||||||
| chr15:64431851 | T | A | 1 | a0001c0001t0002g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1575+6220T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431851 | |||||||
| chr15:64431877 | C | CT | 10 | a0001c0001t0002g0214 a0001c0002t0001g0057 a0001c0002t0001g0059 others(7): Show |
10 | HG02071.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1575+6270dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | ||||||
| chr15:64431877 | C | CTT | 5 | a0001c0002t0001g0211 a0001c0002t0001g0212 a0001c0005t0001g0048 others(2): Show |
5 | HG01109.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1575+6269_1575+627 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | ||||||
| chr15:64431877 | CT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.1575+6270delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | ||||||
| chr15:64431877 | CTTTTTTT others(2): Show |
C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(24): Show |
28 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1575+6262_1575+627 others(13): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | ||||||
| chr15:64431877 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1575+6261_1575+627 others(14): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | ||||||
| chr15:64431882 | T | TC | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1575+6251_1575+625 others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431882 | |||||||
| chr15:64431884 | T | C | 1 | a0001c0002t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1575+6253T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431884 | |||||||
| chr15:64431885 | T | C | 2 | a0001c0008t0001g0046 a0001c0008t0001g0047 |
2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1575+6254T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431885 | |||||||
| chr15:64431912 | C | T | 2 | a0001c0002t0001g0211 a0001c0002t0001g0212 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1575+6281C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431912 | |||||||
| chr15:64431925 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1575+6294C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431925 | |||||||
| chr15:64431964 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1575+6333G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431964 | |||||||
| chr15:64432047 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0159 a0001c0001t0001g0162 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+6416C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432047 | |||||||
| chr15:64432352 | G | A | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+6721G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432352 | |||||||
| chr15:64432380 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1575+6749G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432380 | |||||||
| chr15:64432436 | A | AAACC | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1575+6805_1575+680 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432436 | |||||||
| chr15:64432497 | C | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1575+6866C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432497 | |||||||
| chr15:64432652 | C | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01071.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1575+7021C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432652 | |||||||
| chr15:64432762 | T | G | 1 | a0001c0002t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1575+7131T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432762 | |||||||
| chr15:64432804 | G | A | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1575+7173G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432804 | |||||||
| chr15:64432825 | C | A | 1 | a0001c0002t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1575+7194C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432825 | |||||||
| chr15:64432868 | G | A | 7 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+7237G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432868 | |||||||
| chr15:64432869 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1575+7238C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432869 | |||||||
| chr15:64432922 | A | AAAATAAA others(1): Show |
5 | a0001c0001t0001g0106 a0001c0001t0001g0140 a0001c0002t0001g0064 others(2): Show |
5 | HG01192.hp2 HG01978.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1575+7311_1575+731 others(12): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64432922 | ||||||
| chr15:64432922 | A | AAAATAAA others(5): Show |
4 | a0001c0005t0001g0048 a0001c0005t0001g0050 a0001c0008t0001g0046 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+7307_1575+731 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64432922 | ||||||
| chr15:64432922 | AAAAT | A | 22 | a0001c0001t0001g0101 a0001c0001t0001g0186 a0001c0002t0001g0044 others(19): Show |
22 | HG00621.hp1 HG01884.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1575+7315_1575+731 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64432922 | ||||||
| chr15:64432946 | T | TAAATAAA others(5): Show |
2 | a0001c0005t0001g0049 a0001c0005t0001g0051 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1575+7318_1575+731 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64432946 | ||||||
| chr15:64433167 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1575+7536A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433167 | |||||||
| chr15:64433416 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1575+7785C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433416 | |||||||
| chr15:64433622 | A | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+7991A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433622 | |||||||
| chr15:64433748 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1575+8117C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433748 | |||||||
| chr15:64433917 | AT | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1575+8297delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64433917 | ||||||
| chr15:64433945 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1575+8314C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433945 | |||||||
| chr15:64434065 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1575+8434T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434065 | |||||||
| chr15:64434392 | T | C | 2 | a0001c0008t0001g0046 a0001c0008t0001g0047 |
2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1575+8761T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434392 | |||||||
| chr15:64434402 | G | GA | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1575+8787dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64434402 | ||||||
| chr15:64434838 | G | A | 3 | a0001c0001t0001g0186 a0001c0002t0001g0099 a0001c0002t0001g0200 |
3 | HG00621.hp1 NA18987.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1575+9207G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434838 | |||||||
| chr15:64434841 | A | G | 3 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1575+9210A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434841 | |||||||
| chr15:64434926 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1575+9295A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434926 | |||||||
| chr15:64435004 | C | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.1575+9373C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435004 | |||||||
| chr15:64435213 | C | CA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1575+9606dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435213 | ||||||
| chr15:64435213 | C | CAA | 17 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0113 others(14): Show |
17 | HG00621.hp2 HG00642.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1575+9605_1575+960 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435213 | ||||||
| chr15:64435213 | CA | C | 6 | a0001c0002t0001g0184 a0001c0006t0001g0075 a0001c0006t0001g0076 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+9606delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435213 | ||||||
| chr15:64435259 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1575+9628C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435259 | |||||||
| chr15:64435260 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1575+9629G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435260 | |||||||
| chr15:64435418 | C | T | 7 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-9588C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435418 | |||||||
| chr15:64435439 | T | A | 1 | a0001c0002t0001g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1576-9567T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435439 | |||||||
| chr15:64435504 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1576-9502C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435504 | |||||||
| chr15:64435525 | C | CAAA | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-9466_1576-946 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435525 | ||||||
| chr15:64435525 | CA | C | 126 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.1576-9464delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435525 | ||||||
| chr15:64435525 | CAA | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0088 a0001c0001t0001g0091 others(2): Show |
5 | HG02109.hp2 HG03471.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-9465_1576-946 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435525 | ||||||
| chr15:64435541 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0109 |
2 | HG02683.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1576-9465A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435541 | |||||||
| chr15:64435541 | AAT | A | 10 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
10 | HG01071.hp2 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1576-9462_1576-946 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435541 | ||||||
| chr15:64435543 | T | A | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-9463T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435543 | |||||||
| chr15:64435656 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1576-9350T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435656 | |||||||
| chr15:64435752 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0128 |
2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1576-9254G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435752 | |||||||
| chr15:64435822 | T | TA | 104 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(101): Show |
104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.1576-9163dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435822 | ||||||
| chr15:64435822 | T | TAA | 23 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(20): Show |
24 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1576-9164_1576-916 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435822 | ||||||
| chr15:64435822 | TA | T | 8 | a0001c0002t0001g0077 a0001c0002t0001g0192 a0001c0002t0001g0211 others(5): Show |
8 | HG00323.hp1 HG02698.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-9163delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435822 | ||||||
| chr15:64435848 | A | G | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1576-9158A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435848 | |||||||
| chr15:64435893 | G | GA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1576-9099dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435893 | ||||||
| chr15:64436364 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1576-8642C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436364 | |||||||
| chr15:64436375 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1576-8631C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436375 | |||||||
| chr15:64436387 | T | C | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1576-8619T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436387 | |||||||
| chr15:64436548 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1576-8458G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436548 | |||||||
| chr15:64436708 | CT | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0040 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1576-8281delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436708 | ||||||
| chr15:64436708 | CTT | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0001t0001g0170 others(7): Show |
10 | HG01074.hp1 HG01074.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1576-8282_1576-828 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436708 | ||||||
| chr15:64436725 | T | A | 3 | a0001c0005t0001g0045 a0001c0008t0001g0046 a0001c0008t0001g0047 |
3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1576-8281T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436725 | |||||||
| chr15:64436760 | T | G | 1 | a0001c0002t0001g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1576-8246T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436760 | |||||||
| chr15:64436763 | C | CT | 17 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 others(14): Show |
17 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1576-8214dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | ||||||
| chr15:64436763 | C | CTT | 6 | a0001c0001t0002g0213 a0001c0001t0002g0217 a0001c0002t0001g0074 others(3): Show |
6 | HG02055.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1576-8215_1576-821 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | ||||||
| chr15:64436763 | C | CTTT | 87 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0042 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.1576-8216_1576-821 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | ||||||
| chr15:64436763 | C | CTTTT | 38 | a0001c0001t0001g0087 a0001c0001t0001g0095 a0001c0001t0001g0097 others(35): Show |
38 | HG00438.hp1 HG00438.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1576-8217_1576-821 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | ||||||
| chr15:64436763 | C | CTTTTTTT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG00733.hp1 HG01069.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1576-8220_1576-821 others(11): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | ||||||
| chr15:64436763 | C | CTTTTTTT others(1): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(9): Show |
13 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1576-8221_1576-821 others(12): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | ||||||
| chr15:64436763 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0086 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1576-8223_1576-821 others(14): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | ||||||
| chr15:64437015 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1576-7991C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437015 | |||||||
| chr15:64437263 | T | TA | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1576-7733dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64437263 | ||||||
| chr15:64437490 | G | A | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-7516G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437490 | |||||||
| chr15:64437498 | G | GT | 29 | a0001c0001t0001g0137 a0001c0001t0001g0186 a0001c0001t0002g0213 others(26): Show |
29 | HG00621.hp1 HG02055.hp2 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1576-7496dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64437498 | ||||||
| chr15:64437602 | C | T | 2 | a0002c0009t0001g0026 a0002c0009t0001g0027 |
2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1576-7404C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437602 | |||||||
| chr15:64437808 | C | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1576-7198C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437808 | |||||||
| chr15:64437821 | A | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(25): Show |
29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1576-7185A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437821 | |||||||
| chr15:64438040 | G | T | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-6966G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438040 | |||||||
| chr15:64438185 | T | C | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-6821T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438185 | |||||||
| chr15:64438381 | A | G | 2 | a0001c0004t0001g0218 a0001c0004t0001g0219 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1576-6625A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438381 | |||||||
| chr15:64438397 | G | T | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-6609G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438397 | |||||||
| chr15:64438571 | G | A | 1 | a0001c0002t0001g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1576-6435G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438571 | |||||||
| chr15:64438623 | G | C | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-6383G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438623 | |||||||
| chr15:64438788 | T | C | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1576-6218T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438788 | |||||||
| chr15:64438834 | G | A | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1576-6172G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438834 | |||||||
| chr15:64438965 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1576-6041A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438965 | |||||||
| chr15:64439326 | A | G | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1576-5680A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64439326 | |||||||
| chr15:64439367 | C | T | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-5639C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64439367 | |||||||
| chr15:64439480 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.1576-5526G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64439480 | |||||||
| chr15:64439496 | A | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1576-5510A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64439496 | |||||||
| chr15:64439512 | C | CTTTT | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1576-5469_1576-546 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64439512 | ||||||
| chr15:64439512 | CT | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0090 others(57): Show |
60 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1576-5466delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64439512 | ||||||
| chr15:64439512 | CTT | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1576-5467_1576-546 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64439512 | ||||||
| chr15:64439512 | CTTT | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0174 others(4): Show |
7 | HG02004.hp1 HG02897.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-5468_1576-546 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64439512 | ||||||
| chr15:64440053 | T | TTA | 33 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(30): Show |
34 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1576-4942_1576-494 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440053 | ||||||
| chr15:64440234 | ATAAT | A | 2 | a0001c0002t0001g0060 a0001c0002t0001g0065 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1576-4763_1576-476 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440234 | ||||||
| chr15:64440459 | C | CT | 168 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1576-4534dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440459 | ||||||
| chr15:64440459 | C | CTT | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(40): Show |
44 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1576-4535_1576-453 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440459 | ||||||
| chr15:64440640 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1576-4366G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64440640 | |||||||
| chr15:64440990 | AT | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(26): Show |
30 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1576-4002delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440990 | ||||||
| chr15:64441005 | A | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0090 |
2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1576-4001A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441005 | |||||||
| chr15:64441024 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0174 a0001c0001t0001g0176 others(4): Show |
7 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-3982G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441024 | |||||||
| chr15:64441089 | C | T | 2 | a0002c0009t0001g0026 a0002c0009t0001g0027 |
2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1576-3917C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441089 | |||||||
| chr15:64441146 | G | A | 1 | a0001c0002t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1576-3860G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441146 | |||||||
| chr15:64441221 | C | G | 1 | a0001c0002t0001g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1576-3785C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441221 | |||||||
| chr15:64441305 | C | T | 2 | a0001c0008t0001g0046 a0001c0008t0001g0047 |
2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1576-3701C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441305 | |||||||
| chr15:64441430 | A | C | 1 | a0001c0005t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1576-3576A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441430 | |||||||
| chr15:64441698 | G | A | 4 | a0001c0005t0001g0048 a0001c0005t0001g0049 a0001c0005t0001g0050 others(1): Show |
4 | HG01109.hp2 HG02572.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576-3308G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441698 | |||||||
| chr15:64442140 | C | T | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-2866C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442140 | |||||||
| chr15:64442198 | CA | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(102): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.1576-2794delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64442198 | ||||||
| chr15:64442263 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01071.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1576-2743G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442263 | |||||||
| chr15:64442514 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1576-2492G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442514 | |||||||
| chr15:64442524 | A | G | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-2482A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442524 | |||||||
| chr15:64442597 | T | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-2409T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442597 | |||||||
| chr15:64442624 | T | TA | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1576-2370dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64442624 | ||||||
| chr15:64443018 | C | T | 2 | a0001c0002t0001g0099 a0001c0002t0001g0200 |
2 | HG00621.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1576-1988C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443018 | |||||||
| chr15:64443081 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1576-1925T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443081 | |||||||
| chr15:64443257 | G | A | 8 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-1749G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443257 | |||||||
| chr15:64443328 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1576-1678G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443328 | |||||||
| chr15:64443892 | A | G | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-1114A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443892 | |||||||
| chr15:64444007 | G | GTT | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1576-997_1576-996d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64444007 | ||||||
| chr15:64444088 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1576-918T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444088 | |||||||
| chr15:64444175 | C | G | 8 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0125 others(5): Show |
8 | HG01071.hp2 HG02055.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-831C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444175 | |||||||
| chr15:64444466 | G | A | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1576-540G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444466 | |||||||
| chr15:64444506 | T | C | 9 | a0001c0002t0001g0039 a0001c0002t0001g0068 a0001c0002t0001g0069 others(6): Show |
9 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1576-500T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444506 | |||||||
| chr15:64444674 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1576-332A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444674 | |||||||
| chr15:64444746 | C | CT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
49 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1576-240dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64444746 | ||||||
| chr15:64444746 | C | CTT | 146 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0086 others(143): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1576-241_1576-240d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64444746 | ||||||
| chr15:64444826 | G | C | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-180G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444826 | |||||||
| chr15:64444904 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1576-102G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444904 | |||||||
| chr15:64445134 | G | A | 8 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0055 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+26G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445134 | |||||||
| chr15:64445173 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1678+65A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445173 | |||||||
| chr15:64445412 | G | A | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+304G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445412 | |||||||
| chr15:64445433 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1678+325C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445433 | |||||||
| chr15:64445474 | CA | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1678+384delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445474 | ||||||
| chr15:64445488 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+380A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445488 | |||||||
| chr15:64445539 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+431A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445539 | |||||||
| chr15:64445584 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1678+476G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445584 | |||||||
| chr15:64445608 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+500A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445608 | |||||||
| chr15:64445638 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01071.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1678+530C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445638 | |||||||
| chr15:64445659 | C | T | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678+551C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445659 | |||||||
| chr15:64445666 | T | TCAAA | 2 | a0001c0001t0001g0004 a0001c0001t0001g0009 |
2 | HG01069.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1678+559_1678+562d others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445666 | ||||||
| chr15:64445667 | C | CA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0042 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.1678+583dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445667 | ||||||
| chr15:64445667 | C | CAA | 10 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0145 others(7): Show |
10 | HG00733.hp2 HG01978.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.1678+582_1678+583d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445667 | ||||||
| chr15:64445667 | C | CAAACA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
25 | HG00642.hp1 HG00733.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1678+562_1678+563i others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445667 | ||||||
| chr15:64445667 | CA | C | 12 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(9): Show |
12 | HG01169.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1678+583delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445667 | ||||||
| chr15:64446002 | G | A | 1 | a0001c0002t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1678+894G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446002 | |||||||
| chr15:64446062 | C | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+954C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446062 | |||||||
| chr15:64446198 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+1090C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446198 | |||||||
| chr15:64446230 | C | A | 3 | a0001c0002t0001g0054 a0001c0002t0001g0057 a0001c0002t0001g0058 |
3 | HG02145.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1678+1122C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446230 | |||||||
| chr15:64446283 | G | A | 1 | a0002c0009t0001g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1678+1175G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446283 | |||||||
| chr15:64446363 | C | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(25): Show |
29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1678+1255C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446363 | |||||||
| chr15:64446381 | C | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(33): Show |
37 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1678+1273C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446381 | |||||||
| chr15:64446406 | A | AT | 9 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0104 others(6): Show |
9 | HG00642.hp2 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+1314dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64446406 | ||||||
| chr15:64446427 | CAG | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+1322_1678+132 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64446427 | ||||||
| chr15:64446523 | C | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1678+1415C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446523 | |||||||
| chr15:64446565 | T | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+1457T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446565 | |||||||
| chr15:64446651 | C | G | 9 | a0001c0002t0001g0039 a0001c0002t0001g0068 a0001c0002t0001g0069 others(6): Show |
9 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1678+1543C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446651 | |||||||
| chr15:64446838 | C | T | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1678+1730C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446838 | |||||||
| chr15:64447134 | CA | C | 21 | a0001c0002t0001g0044 a0001c0002t0001g0053 a0001c0002t0001g0054 others(18): Show |
21 | HG00621.hp1 HG01884.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1678+2034delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64447134 | ||||||
| chr15:64447142 | A | AC | 7 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+2035dupC | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64447142 | ||||||
| chr15:64447204 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(24): Show |
28 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1678+2096C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447204 | |||||||
| chr15:64447397 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+2289A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447397 | |||||||
| chr15:64447431 | C | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.1678+2323C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447431 | |||||||
| chr15:64447526 | A | G | 3 | a0001c0001t0001g0028 a0002c0009t0001g0026 a0002c0009t0001g0027 |
3 | HG02818.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1678+2418A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447526 | |||||||
| chr15:64447991 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1678+2883A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447991 | |||||||
| chr15:64448288 | A | T | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+3180A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448288 | |||||||
| chr15:64448305 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1678+3197A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448305 | |||||||
| chr15:64448367 | T | G | 1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1678+3259T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448367 | |||||||
| chr15:64448559 | G | A | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678+3451G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448559 | |||||||
| chr15:64448611 | G | A | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+3503G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448611 | |||||||
| chr15:64448690 | C | T | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1678+3582C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448690 | |||||||
| chr15:64448771 | G | T | 4 | a0001c0002t0001g0209 a0001c0002t0001g0210 a0001c0002t0001g0211 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+3663G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448771 | |||||||
| chr15:64448893 | A | G | 1 | a0001c0002t0001g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1678+3785A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448893 | |||||||
| chr15:64449054 | T | G | 1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1678+3946T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449054 | |||||||
| chr15:64449212 | TA | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0096 others(21): Show |
24 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1678+4116delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449212 | ||||||
| chr15:64449271 | G | GT | 7 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+4171dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449271 | ||||||
| chr15:64449289 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1678+4181T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449289 | |||||||
| chr15:64449289 | TG | T | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1678+4182delG | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449289 | |||||||
| chr15:64449290 | G | GT | 8 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0092 others(5): Show |
8 | HG00438.hp1 HG00438.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+4194dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449290 | ||||||
| chr15:64449291 | T | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0162 a0001c0001t0001g0172 |
3 | HG01167.hp2 HG01169.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1678+4183T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449291 | |||||||
| chr15:64449296 | T | G | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+4188T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449296 | |||||||
| chr15:64449343 | T | C | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1678+4235T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449343 | |||||||
| chr15:64449444 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0095 others(71): Show |
74 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1678+4336C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449444 | |||||||
| chr15:64449562 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(25): Show |
29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1678+4454G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449562 | |||||||
| chr15:64449571 | C | CAT | 25 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0096 others(22): Show |
25 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1678+4477_1678+447 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449571 | ||||||
| chr15:64449587 | A | T | 2 | a0001c0001t0001g0012 a0001c0005t0001g0048 |
2 | HG01109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1678+4479A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449587 | |||||||
| chr15:64449611 | CTTAAA | C | 4 | a0001c0004t0001g0031 a0001c0004t0001g0033 a0001c0004t0001g0034 others(1): Show |
4 | HG00323.hp1 HG01934.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1678+4509_1678+451 others(9): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449611 | ||||||
| chr15:64449622 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1678+4514G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449622 | |||||||
| chr15:64449866 | A | G | 8 | a0001c0005t0001g0045 a0001c0005t0001g0048 a0001c0005t0001g0049 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+4758A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449866 | |||||||
| chr15:64450068 | A | T | 8 | a0001c0001t0001g0097 a0001c0001t0001g0120 a0001c0001t0001g0121 others(5): Show |
8 | HG00140.hp2 HG01109.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1679-4929A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450068 | |||||||
| chr15:64450151 | T | C | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1679-4846T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450151 | |||||||
| chr15:64450384 | G | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0090 |
2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1679-4613G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450384 | |||||||
| chr15:64450393 | G | GA | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(37): Show |
41 | HG00642.hp1 HG01069.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1679-4583dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64450393 | ||||||
| chr15:64450409 | A | G | 3 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1679-4588A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450409 | |||||||
| chr15:64450411 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1679-4586A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450411 | |||||||
| chr15:64450471 | T | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1679-4526T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450471 | |||||||
| chr15:64450563 | A | T | 1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1679-4434A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450563 | |||||||
| chr15:64451278 | A | G | 1 | a0001c0002t0001g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1679-3719A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451278 | |||||||
| chr15:64451369 | TC | T | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679-3626delC | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451369 | ||||||
| chr15:64451465 | CT | C | 81 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0086 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.1679-3509delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451465 | ||||||
| chr15:64451465 | CTT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(46): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.1679-3510_1679-350 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451465 | ||||||
| chr15:64451465 | CTTT | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0095 others(74): Show |
77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1679-3511_1679-350 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451465 | ||||||
| chr15:64451546 | A | G | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1679-3451A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451546 | |||||||
| chr15:64451584 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1679-3413A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451584 | |||||||
| chr15:64451637 | A | G | 1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1679-3360A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451637 | |||||||
| chr15:64451684 | A | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-3313A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451684 | |||||||
| chr15:64451953 | CA | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1679-3029delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451953 | ||||||
| chr15:64451968 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1679-3029A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451968 | |||||||
| chr15:64452085 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1679-2912T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64452085 | |||||||
| chr15:64452591 | T | C | 9 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0033 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679-2406T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64452591 | |||||||
| chr15:64452680 | G | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0165 a0001c0001t0001g0203 |
3 | NA18972.hp1 NA19084.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1679-2317G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64452680 | |||||||
| chr15:64452889 | T | C | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1679-2108T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64452889 | |||||||
| chr15:64453000 | C | T | 1 | a0001c0002t0001g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1679-1997C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453000 | |||||||
| chr15:64453060 | C | G | 9 | a0001c0001t0001g0118 a0001c0001t0001g0158 a0001c0001t0001g0174 others(6): Show |
9 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679-1937C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453060 | |||||||
| chr15:64453071 | A | AGCTACAG others(5): Show |
1 | a0001c0002t0001g0195 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1679-1921_1679-191 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64453071 | ||||||
| chr15:64453080 | G | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0163 |
2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1679-1917G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453080 | |||||||
| chr15:64453335 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1679-1662A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453335 | |||||||
| chr15:64453424 | G | A | 1 | a0001c0004t0001g0033 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1679-1573G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453424 | |||||||
| chr15:64454217 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1679-780T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454217 | |||||||
| chr15:64454249 | C | G | 2 | a0001c0007t0001g0029 a0001c0007t0001g0030 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1679-748C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454249 | |||||||
| chr15:64454394 | C | G | 1 | a0001c0002t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1679-603C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454394 | |||||||
| chr15:64454598 | CA | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-398delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454598 | |||||||
| chr15:64454600 | T | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-397T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454600 | |||||||
| chr15:64454627 | C | T | 5 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-370C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454627 |