Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 400451 |
| ensemblid | ENSG00000185442.13 |
| hgncid | 34339 |
| symbol | FAM174B |
| name | family with sequence similarity 174 member B |
| refseq_nuc | NM_207446.3 |
| refseq_prot | NP_997329.2 |
| ensembl_nuc | ENST00000327355.6 |
| ensembl_prot | ENSP00000329040.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 92617448 |
| end | 92655775 |
| strand | - |
| ver | v1.2 |
| region | chr15:92617448-92655775 |
| region5000 | chr15:92612448-92660775 |
| regionname0 | FAM174B_chr15_92617448_92655775 |
| regionname5000 | FAM174B_chr15_92612448_92660775 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 156 | 373 | 78 | 70 | 171 | 11 | 42 | 133 | FAM174B_chr15_92612448_92660775 | FAM174B | MRAVP others(151): Show |
chr15 | 92612448 | 92660775 |
| a0002 | 1/0 | 158 | 13 | 11 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | MRAVP others(153): Show |
chr15 | 92612448 | 92660775 |
| a0003 | 0/0 | 156 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | MRAVP others(151): Show |
chr15 | 92612448 | 92660775 |
| a0004 | 0/0 | 156 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM174B_chr15_92612448_92660775 | FAM174B | MRAVP others(151): Show |
chr15 | 92612448 | 92660775 |
| a0005 | 0/0 | 156 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | MRAVP others(151): Show |
chr15 | 92612448 | 92660775 |
| a0006 | 0/0 | 156 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | MRAVP others(151): Show |
chr15 | 92612448 | 92660775 |
| a0007 | 0/0 | 156 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | MRAVP others(151): Show |
chr15 | 92612448 | 92660775 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 470 | 363 | 71 | 70 | 169 | 11 | 41 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0001c0003 | 0/0 | 470 | 5 | 5 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0001c0006 | 0/0 | 470 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0001c0008 | 0/0 | 470 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0001c0009 | 0/0 | 470 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0001c0010 | 0/0 | 470 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0002c0002 | 1/0 | 476 | 13 | 11 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(471): Show |
chr15 | 92612448 | 92660775 | ||
| a0003c0004 | 0/0 | 470 | 3 | 2 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0004c0005 | 0/0 | 470 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0005c0012 | 0/0 | 470 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0006c0007 | 0/0 | 470 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 | ||
| a0007c0011 | 0/0 | 470 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | ATGCG others(465): Show |
chr15 | 92612448 | 92660775 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2597 | 58 | 5 | 12 | 37 | 0 | 4 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0002 | 0/0 | 2598 | 43 | 4 | 4 | 34 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0003 | 0/1 | 2596 | 33 | 4 | 10 | 9 | 4 | 5 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0004 | 0/0 | 2597 | 22 | 3 | 6 | 4 | 3 | 6 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0005 | 0/0 | 2596 | 27 | 0 | 4 | 18 | 1 | 4 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0006 | 0/0 | 2596 | 23 | 0 | 8 | 14 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0007 | 0/0 | 2596 | 19 | 2 | 5 | 7 | 0 | 5 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0008 | 0/0 | 2597 | 11 | 4 | 0 | 7 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0009 | 0/0 | 2597 | 9 | 8 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0010 | 0/0 | 2582 | 8 | 5 | 2 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2577): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0011 | 0/0 | 2598 | 8 | 7 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0012 | 0/0 | 2596 | 6 | 1 | 2 | 2 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0013 | 0/0 | 2595 | 7 | 0 | 0 | 6 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2590): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0014 | 0/0 | 2595 | 6 | 0 | 5 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2590): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0015 | 0/0 | 2597 | 4 | 4 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0016 | 0/0 | 2598 | 4 | 1 | 0 | 0 | 1 | 2 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0017 | 0/0 | 2597 | 5 | 0 | 0 | 5 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0018 | 0/0 | 2597 | 4 | 0 | 3 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0019 | 0/0 | 2596 | 3 | 0 | 0 | 2 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0020 | 0/0 | 2595 | 3 | 1 | 1 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2590): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0021 | 0/0 | 2598 | 3 | 0 | 0 | 1 | 0 | 2 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0022 | 0/0 | 2595 | 3 | 0 | 2 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2590): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0023 | 0/0 | 2595 | 3 | 0 | 0 | 3 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2590): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0024 | 0/0 | 2596 | 2 | 1 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0025 | 0/0 | 2597 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0026 | 0/0 | 2597 | 2 | 0 | 0 | 0 | 1 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0027 | 0/0 | 2596 | 2 | 1 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0028 | 0/0 | 2595 | 2 | 1 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2590): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0029 | 0/0 | 2597 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0030 | 0/0 | 2597 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0031 | 0/0 | 2599 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2594): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0032 | 0/0 | 2596 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0033 | 0/0 | 2581 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2576): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0034 | 0/0 | 2599 | 2 | 1 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2594): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0035 | 0/0 | 2596 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0036 | 0/0 | 2598 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0037 | 0/0 | 2582 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2577): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0039 | 0/0 | 2597 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0040 | 0/0 | 2596 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0042 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0043 | 0/0 | 2594 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2589): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0044 | 0/0 | 2596 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0045 | 0/0 | 2596 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0046 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0047 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0048 | 0/0 | 2596 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0049 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0050 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0051 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0052 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0053 | 0/0 | 2596 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0054 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2590): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0055 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0056 | 0/0 | 2599 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2594): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0057 | 0/0 | 2598 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0058 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0059 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0060 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0061 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0062 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0063 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0001t0064 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0003t0002 | 0/0 | 2598 | 5 | 5 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0006t0002 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0001c0006t0024 | 0/0 | 2596 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0008t0001 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0001c0009t0005 | 0/0 | 2596 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0001c0010t0012 | 0/0 | 2596 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0002c0002t0004 | 1/0 | 2603 | 6 | 5 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2598): Show |
chr15 | 92612448 | 92660775 |
| a0002c0002t0009 | 0/0 | 2603 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2598): Show |
chr15 | 92612448 | 92660775 |
| a0002c0002t0010 | 0/0 | 2588 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2583): Show |
chr15 | 92612448 | 92660775 |
| a0002c0002t0015 | 0/0 | 2603 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2598): Show |
chr15 | 92612448 | 92660775 |
| a0002c0002t0031 | 0/0 | 2605 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2600): Show |
chr15 | 92612448 | 92660775 |
| a0002c0002t0032 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2597): Show |
chr15 | 92612448 | 92660775 |
| a0003c0004t0004 | 0/0 | 2597 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0003c0004t0016 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2593): Show |
chr15 | 92612448 | 92660775 |
| a0003c0004t0038 | 0/0 | 2596 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0004c0005t0001 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0004c0005t0041 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0005c0012t0003 | 0/0 | 2596 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2591): Show |
chr15 | 92612448 | 92660775 |
| a0006c0007t0001 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| a0007c0011t0025 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | AAGCA others(2592): Show |
chr15 | 92612448 | 92660775 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0015g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0015g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0015g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0015g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0016g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0016g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0016g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0016g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0017g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0017g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0017g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0017g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0018g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0018g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0018g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0018g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0019g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0019g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0019g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0020g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0020g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0020g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0021g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0021g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0021g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0022g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0022g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0022g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0023g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0023g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0023g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0024g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0024g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0025g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0025g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0026g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0026g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0027g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0027g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0028g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0028g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0029g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0029g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0030g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0030g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0031g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0032g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0033g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0033g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0034g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0034g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0035g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0035g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0036g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0036g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0037g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0037g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0039g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0040g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0042g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0043g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0044g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0045g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0046g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0047g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0048g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0049g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0050g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0051g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0052g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0053g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0054g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0055g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0056g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0057g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0058g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0059g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0060g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0061g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0062g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0063g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0064g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0003t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0003t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0003t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0006t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0006t0024g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0008t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0009t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0010t0012g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0006 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0009g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0009g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0010g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0015g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0015g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0031g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0032g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0003c0004t0004g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0003c0004t0016g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0003c0004t0038g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0004c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0004c0005t0041g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0005c0012t0003g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0006c0007t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0007c0011t0025g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0016 | g0341 | EUR | GBR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0201 | EUR | GBR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00140 | hp1 | a0001 | c0001 | t0026 | g0118 | EUR | GBR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00140 | hp2 | a0001 | c0001 | t0010 | g0339 | EUR | GBR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0170 | EUR | FIN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0255 | EUR | FIN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0218 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00438 | hp1 | a0001 | c0001 | t0042 | g0191 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00544 | hp2 | a0001 | c0001 | t0020 | g0345 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00558 | hp1 | a0001 | c0010 | t0012 | g0082 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00597 | hp1 | a0001 | c0001 | t0029 | g0227 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00597 | hp2 | a0001 | c0001 | t0024 | g0209 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0145 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0325 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00642 | hp1 | a0003 | c0004 | t0004 | g0368 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0323 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0215 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00733 | hp1 | a0001 | c0001 | t0010 | g0349 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0103 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0091 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00741 | hp1 | a0001 | c0001 | t0018 | g0262 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0142 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0348 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01074 | hp1 | a0001 | c0001 | t0018 | g0066 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01099 | hp1 | a0001 | c0001 | t0014 | g0241 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0029 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0112 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01167 | hp1 | a0001 | c0001 | t0054 | g0169 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01167 | hp2 | a0001 | c0001 | t0033 | g0336 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01168 | hp1 | a0001 | c0001 | t0022 | g0267 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01168 | hp2 | a0001 | c0001 | t0022 | g0322 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01192 | hp1 | a0001 | c0001 | t0039 | g0281 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0347 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01243 | hp1 | a0001 | c0001 | t0020 | g0110 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01243 | hp2 | a0002 | c0002 | t0010 | g0378 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0256 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01255 | hp2 | a0001 | c0001 | t0014 | g0240 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0265 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0213 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01358 | hp2 | a0001 | c0001 | t0018 | g0154 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0081 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0250 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0334 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0251 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01496 | hp1 | a0001 | c0001 | t0012 | g0085 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0254 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01515 | hp1 | a0005 | c0012 | t0003 | g0380 | EUR | IBS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0274 | EUR | IBS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0069 | EUR | IBS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0276 | EUR | IBS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0128 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0198 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01891 | hp2 | a0001 | c0006 | t0024 | g0102 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01928 | hp2 | a0001 | c0001 | t0014 | g0163 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0305 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01943 | hp1 | a0001 | c0001 | t0014 | g0243 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01943 | hp2 | a0001 | c0001 | t0014 | g0092 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0245 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0242 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0246 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01975 | hp2 | a0001 | c0001 | t0012 | g0350 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0273 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0249 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01993 | hp2 | a0001 | c0001 | t0057 | g0261 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02027 | hp1 | a0001 | c0001 | t0013 | g0149 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0238 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0333 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0360 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02080 | hp2 | a0001 | c0001 | t0013 | g0297 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0159 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02155 | hp1 | a0001 | c0001 | t0007 | g0259 | EAS | CDX | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | CDX | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CDX | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02257 | hp2 | a0001 | c0006 | t0002 | g0013 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02258 | hp1 | a0002 | c0002 | t0031 | g0373 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02258 | hp2 | a0001 | c0001 | t0050 | g0026 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02280 | hp1 | a0001 | c0001 | t0027 | g0335 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0038 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0260 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02451 | hp1 | a0002 | c0002 | t0032 | g0370 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02451 | hp2 | a0001 | c0001 | t0034 | g0342 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02523 | hp1 | a0001 | c0001 | t0025 | g0296 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02523 | hp2 | a0001 | c0001 | t0025 | g0234 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0375 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02602 | hp1 | a0001 | c0001 | t0013 | g0220 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0275 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02615 | hp1 | a0001 | c0001 | t0024 | g0037 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02622 | hp1 | a0001 | c0001 | t0046 | g0364 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02622 | hp2 | a0001 | c0001 | t0047 | g0111 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0123 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0196 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02683 | hp2 | a0001 | c0001 | t0016 | g0352 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02698 | hp1 | a0001 | c0001 | t0019 | g0041 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02698 | hp2 | a0001 | c0001 | t0018 | g0054 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02717 | hp1 | a0002 | c0002 | t0009 | g0371 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0101 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02723 | hp2 | a0003 | c0004 | t0016 | g0366 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0192 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02735 | hp2 | a0001 | c0008 | t0001 | g0011 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02809 | hp1 | a0002 | c0002 | t0004 | g0376 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0343 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0374 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0045 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02896 | hp1 | a0001 | c0001 | t0037 | g0382 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0137 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02897 | hp1 | a0001 | c0001 | t0032 | g0033 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02897 | hp2 | a0001 | c0001 | t0037 | g0381 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02965 | hp1 | a0001 | c0003 | t0002 | g0001 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02965 | hp2 | a0001 | c0001 | t0061 | g0136 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0197 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02976 | hp1 | a0001 | c0001 | t0049 | g0363 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02976 | hp2 | a0001 | c0001 | t0043 | g0108 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0100 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0362 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03041 | hp2 | a0001 | c0001 | t0060 | g0132 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0135 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03098 | hp2 | a0001 | c0001 | t0062 | g0035 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0106 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03130 | hp2 | a0003 | c0004 | t0038 | g0367 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03209 | hp1 | a0002 | c0002 | t0015 | g0379 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03209 | hp2 | a0001 | c0001 | t0035 | g0027 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03225 | hp2 | a0002 | c0002 | t0009 | g0369 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0024 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0107 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03491 | hp1 | a0001 | c0001 | t0012 | g0168 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03491 | hp2 | a0001 | c0001 | t0031 | g0130 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0200 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03492 | hp2 | a0001 | c0001 | t0021 | g0127 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03516 | hp2 | a0001 | c0001 | t0035 | g0030 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03540 | hp1 | a0001 | c0001 | t0015 | g0109 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0046 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03579 | hp1 | a0002 | c0002 | t0015 | g0377 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0044 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03654 | hp1 | a0001 | c0001 | t0044 | g0302 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0252 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0353 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03688 | hp2 | a0001 | c0001 | t0007 | g0179 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0073 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03704 | hp2 | a0001 | c0001 | t0027 | g0328 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0340 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0129 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0190 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03834 | hp1 | a0001 | c0001 | t0034 | g0090 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0131 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03927 | hp1 | a0001 | c0001 | t0064 | g0387 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03927 | hp2 | a0001 | c0001 | t0026 | g0225 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03942 | hp1 | a0001 | c0001 | t0016 | g0351 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0047 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0133 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0068 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0232 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | YRI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18522 | hp2 | a0001 | c0001 | t0045 | g0126 | AFR | YRI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | CHB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0237 | EAS | CHB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18747 | hp2 | a0001 | c0009 | t0005 | g0358 | EAS | CHB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0356 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0272 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18943 | hp2 | a0001 | c0001 | t0007 | g0065 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0331 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0357 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0287 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0311 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0203 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18948 | hp2 | a0001 | c0001 | t0036 | g0293 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18950 | hp1 | a0001 | c0001 | t0023 | g0244 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18953 | hp1 | a0001 | c0001 | t0017 | g0384 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0277 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18954 | hp1 | a0001 | c0001 | t0021 | g0361 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18956 | hp2 | a0001 | c0001 | t0048 | g0043 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18957 | hp2 | a0001 | c0001 | t0028 | g0359 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18961 | hp1 | a0001 | c0001 | t0063 | g0385 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18961 | hp2 | a0001 | c0001 | t0017 | g0007 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18962 | hp1 | a0001 | c0001 | t0008 | g0235 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18968 | hp1 | a0001 | c0001 | t0040 | g0178 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18970 | hp2 | a0001 | c0001 | t0007 | g0117 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0314 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18980 | hp2 | a0001 | c0001 | t0030 | g0165 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18982 | hp2 | a0001 | c0001 | t0030 | g0173 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0078 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18983 | hp2 | a0001 | c0001 | t0013 | g0099 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0050 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18990 | hp1 | a0001 | c0001 | t0013 | g0055 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18990 | hp2 | a0001 | c0001 | t0029 | g0222 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18992 | hp1 | a0001 | c0001 | t0017 | g0007 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18994 | hp2 | a0004 | c0005 | t0001 | g0010 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18997 | hp2 | a0001 | c0001 | t0006 | g0247 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19001 | hp2 | a0001 | c0001 | t0022 | g0061 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0269 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0186 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19003 | hp2 | a0001 | c0001 | t0059 | g0141 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19006 | hp2 | a0001 | c0001 | t0056 | g0207 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0152 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19009 | hp2 | a0001 | c0001 | t0017 | g0386 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19030 | hp1 | a0002 | c0002 | t0004 | g0006 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19043 | hp2 | a0001 | c0001 | t0028 | g0337 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19054 | hp1 | a0001 | c0001 | t0013 | g0264 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19054 | hp2 | a0001 | c0001 | t0012 | g0289 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19055 | hp1 | a0007 | c0011 | t0025 | g0365 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19056 | hp2 | a0001 | c0001 | t0006 | g0332 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19058 | hp1 | a0001 | c0001 | t0019 | g0228 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19060 | hp1 | a0001 | c0001 | t0013 | g0266 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19065 | hp1 | a0001 | c0001 | t0052 | g0057 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19065 | hp2 | a0001 | c0001 | t0012 | g0104 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0062 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19068 | hp2 | a0001 | c0001 | t0014 | g0070 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19083 | hp1 | a0001 | c0001 | t0008 | g0184 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19083 | hp2 | a0004 | c0005 | t0041 | g0009 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19084 | hp2 | a0001 | c0001 | t0023 | g0151 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19090 | hp1 | a0001 | c0001 | t0023 | g0202 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19090 | hp2 | a0001 | c0001 | t0017 | g0383 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19091 | hp1 | a0001 | c0001 | t0036 | g0292 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19091 | hp2 | a0001 | c0001 | t0019 | g0307 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0193 | AFR | YRI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20129 | hp1 | a0001 | c0001 | t0033 | g0028 | AFR | ASW | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0139 | AFR | ASW | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0122 | EUR | TSI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0257 | EUR | TSI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20905 | hp1 | a0001 | c0001 | t0058 | g0329 | SAS | GIH | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0205 | SAS | GIH | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02109 | hp1 | a0002 | c0002 | t0004 | g0372 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02486 | hp2 | a0001 | c0001 | t0051 | g0324 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02559 | hp2 | a0006 | c0007 | t0001 | g0008 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03471 | hp2 | a0001 | c0001 | t0053 | g0138 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG06807 | hp1 | a0001 | c0001 | t0020 | g0143 | AFR | USA | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0338 | AFR | USA | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | USA | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0001 | AFR | USA | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA21309 | hp1 | a0001 | c0001 | t0055 | g0125 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0194 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0172 | REF | REF | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0004 | g0006 | REF | REF | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92630254 | C | A | 1 | a0001 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.436G>T | p.Asp146Tyr | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/3 | 552/2604 | 436/480 | 146/159 | chr15 | 92630254 | |||
| chr15:92630320 | G | A | 1 | a0001 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.370C>T | p.Arg124Cys | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/3 | 486/2604 | 370/480 | 124/159 | chr15 | 92630320 | |||
| chr15:92655448 | TTGGAGC | T | 6 | a0001 a0003 a0004 others(3): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
disruptive_inframe_deletion | MODERATE | c.206_211delGCTCCA | p.Ser69_Ser70del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 327/2604 | 206/480 | 69/159 | chr15 | 92655448 | |||
| chr15:92655521 | G | A | 1 | a0007 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.139C>T | p.Pro47Ser | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 255/2604 | 139/480 | 47/159 | chr15 | 92655521 | |||
| chr15:92655554 | A | G | 5 | a0001 a0004 a0005 others(2): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
missense_variant | MODERATE | c.106T>C | p.Trp36Arg | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 222/2604 | 106/480 | 36/159 | chr15 | 92655554 | |||
| chr15:92655559 | G | T | 1 | a0004 | 2 | NA18994.hp2 NA19083.hp2 |
missense_variant | MODERATE | c.101C>A | p.Ala34Glu | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 217/2604 | 101/480 | 34/159 | chr15 | 92655559 | |||
| chr15:92655620 | G | T | 1 | a0006 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.40C>A | p.Leu14Met | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 156/2604 | 40/480 | 14/159 | chr15 | 92655620 | |||
| chr15:92655635 | G | C | 1 | a0005 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.25C>G | p.Pro9Ala | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 141/2604 | 25/480 | 9/159 | chr15 | 92655635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92630237 | G | C | 1 | a0001c0006 | 2 | HG01891.hp2 HG02257.hp2 |
synonymous_variant | LOW | c.453C>G | p.Ser151Ser | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/3 | 569/2604 | 453/480 | 151/159 | chr15 | 92630237 | |||
| chr15:92630273 | C | T | 1 | a0001c0003 | 5 | HG02630.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.417G>A | p.Ala139Ala | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/3 | 533/2604 | 417/480 | 139/159 | chr15 | 92630273 | |||
| chr15:92655441 | A | G | 10 | a0001c0001 a0001c0003 a0001c0006 others(7): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
synonymous_variant | LOW | c.219T>C | p.Ser73Ser | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 335/2604 | 219/480 | 73/159 | chr15 | 92655441 | |||
| chr15:92655492 | C | T | 1 | a0001c0008 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.168G>A | p.Arg56Arg | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 284/2604 | 168/480 | 56/159 | chr15 | 92655492 | |||
| chr15:92655540 | C | T | 1 | a0001c0008 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.120G>A | p.Glu40Glu | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 236/2604 | 120/480 | 40/159 | chr15 | 92655540 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92617590 | G | A | 3 | a0001c0001t0046 a0001c0001t0047 a0001c0001t0049 |
3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1866C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1866 | chr15 | 92617590 | ||||||
| chr15:92617707 | C | T | 3 | a0001c0001t0058 a0001c0001t0059 a0004c0005t0041 |
3 | NA19003.hp2 NA19083.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1749 | chr15 | 92617707 | ||||||
| chr15:92617719 | C | G | 3 | a0001c0001t0058 a0001c0001t0059 a0004c0005t0041 |
3 | NA19003.hp2 NA19083.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1737G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1737 | chr15 | 92617719 | ||||||
| chr15:92617868 | GC | G | 3 | a0001c0001t0013 a0001c0001t0023 a0001c0001t0052 |
11 | HG02027.hp1 HG02080.hp2 HG02602.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1587delG | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1587 | chr15 | 92617868 | ||||||
| chr15:92617904 | G | A | 2 | a0001c0001t0029 a0001c0001t0040 |
3 | HG00597.hp1 NA18968.hp1 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1552C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1552 | chr15 | 92617904 | ||||||
| chr15:92617966 | G | A | 1 | a0001c0001t0023 | 3 | NA18950.hp1 NA19084.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1490C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1490 | chr15 | 92617966 | ||||||
| chr15:92617990 | C | T | 1 | a0001c0001t0055 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1466G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1466 | chr15 | 92617990 | ||||||
| chr15:92618105 | C | A | 1 | a0001c0001t0042 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1351G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1351 | chr15 | 92618105 | ||||||
| chr15:92618150 | A | G | 3 | a0001c0001t0058 a0001c0001t0059 a0004c0005t0041 |
3 | NA19003.hp2 NA19083.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1306T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1306 | chr15 | 92618150 | ||||||
| chr15:92618160 | T | C | 1 | a0001c0001t0030 | 2 | NA18980.hp2 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1296A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1296 | chr15 | 92618160 | ||||||
| chr15:92618216 | G | A | 1 | a0001c0001t0047 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1240C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1240 | chr15 | 92618216 | ||||||
| chr15:92618261 | A | G | 2 | a0001c0001t0006 a0001c0001t0014 |
29 | HG01099.hp1 HG01255.hp2 HG01346.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1195T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1195 | chr15 | 92618261 | ||||||
| chr15:92618271 | G | T | 9 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0024 others(6): Show |
43 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1185C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1185 | chr15 | 92618271 | ||||||
| chr15:92618414 | C | T | 1 | a0001c0001t0050 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1042G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1042 | chr15 | 92618414 | ||||||
| chr15:92618487 | A | G | 3 | a0001c0001t0046 a0001c0001t0047 a0001c0001t0049 |
3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*969T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 969 | chr15 | 92618487 | ||||||
| chr15:92618493 | G | A | 3 | a0001c0001t0020 a0001c0001t0043 a0001c0001t0045 |
5 | HG00544.hp2 HG01243.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*963C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 963 | chr15 | 92618493 | ||||||
| chr15:92618531 | A | AT | 17 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0017 others(14): Show |
88 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*924dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 924 | chr15 | 92618531 | ||||||
| chr15:92618608 | G | C | 18 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(15): Show |
90 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*848C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 848 | chr15 | 92618608 | ||||||
| chr15:92618695 | A | G | 5 | a0001c0001t0009 a0001c0001t0032 a0001c0001t0055 others(2): Show |
14 | HG01109.hp2 HG02055.hp2 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*761T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 761 | chr15 | 92618695 | ||||||
| chr15:92618718 | TCACACAC others(9): Show |
T | 4 | a0001c0001t0010 a0001c0001t0033 a0001c0001t0037 others(1): Show |
13 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*737delCGTGTG others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 722 | chr15 | 92618718 | ||||||
| chr15:92618728 | GCACACGC others(11): Show |
G | 1 | a0001c0001t0051 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*710_*727delTGCACG others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 710 | chr15 | 92618728 | ||||||
| chr15:92618733 | CGCACACA others(3): Show |
C | 1 | a0001c0001t0027 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*713_*722delACGTGT others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 713 | chr15 | 92618733 | ||||||
| chr15:92618744 | G | GCA | 3 | a0001c0001t0021 a0001c0001t0031 a0002c0002t0031 |
5 | HG02258.hp1 HG02735.hp1 HG03491.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*710_*711dupTG | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 711 | chr15 | 92618744 | ||||||
| chr15:92618744 | GCA | G | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(37): Show |
190 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*710_*711delTG | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 710 | chr15 | 92618744 | ||||||
| chr15:92618746 | A | G | 17 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(14): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*710T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 710 | chr15 | 92618746 | ||||||
| chr15:92618748 | A | G | 1 | a0001c0001t0035 | 2 | HG03209.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*708T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 708 | chr15 | 92618748 | ||||||
| chr15:92618782 | A | C | 1 | a0001c0001t0057 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*674T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 674 | chr15 | 92618782 | ||||||
| chr15:92618786 | T | A | 1 | a0001c0001t0053 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 670 | chr15 | 92618786 | ||||||
| chr15:92618828 | C | CT | 17 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0026 others(14): Show |
81 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*627dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 627 | chr15 | 92618828 | ||||||
| chr15:92618839 | T | A | 2 | a0001c0001t0025 a0007c0011t0025 |
3 | HG02523.hp1 HG02523.hp2 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*617A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 617 | chr15 | 92618839 | ||||||
| chr15:92618839 | T | TA | 13 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0024 others(10): Show |
70 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*616_*617insT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 616 | chr15 | 92618839 | ||||||
| chr15:92618840 | T | A | 21 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(18): Show |
93 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*616A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 616 | chr15 | 92618840 | ||||||
| chr15:92618840 | T | TA | 14 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 others(11): Show |
74 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*615dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 615 | chr15 | 92618840 | ||||||
| chr15:92618840 | T | TAA | 6 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0034 others(3): Show |
23 | HG01109.hp1 HG01109.hp2 HG02055.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*614_*615dupTT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 615 | chr15 | 92618840 | ||||||
| chr15:92618840 | TA | T | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0021 others(3): Show |
57 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*615delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 615 | chr15 | 92618840 | ||||||
| chr15:92618840 | TAA | T | 2 | a0001c0001t0014 a0001c0001t0028 |
8 | HG01099.hp1 HG01255.hp2 HG01928.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*614_*615delTT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 614 | chr15 | 92618840 | ||||||
| chr15:92618841 | A | T | 19 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(16): Show |
96 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*615T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 615 | chr15 | 92618841 | ||||||
| chr15:92618842 | A | T | 5 | a0001c0001t0012 a0001c0001t0026 a0001c0001t0027 others(2): Show |
12 | HG00140.hp1 HG00558.hp1 HG01496.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*614T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 614 | chr15 | 92618842 | ||||||
| chr15:92618844 | A | G | 1 | a0001c0001t0039 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 612 | chr15 | 92618844 | ||||||
| chr15:92618881 | G | A | 2 | a0001c0001t0058 a0001c0001t0059 |
2 | NA19003.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*575C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 575 | chr15 | 92618881 | ||||||
| chr15:92618976 | C | CA | 2 | a0001c0001t0011 a0001c0001t0060 |
9 | HG01109.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*479dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 479 | chr15 | 92618976 | ||||||
| chr15:92619155 | T | A | 1 | a0001c0001t0036 | 2 | NA18948.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*301A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 301 | chr15 | 92619155 | ||||||
| chr15:92619301 | T | C | 1 | a0001c0001t0061 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*155A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 155 | chr15 | 92619301 | ||||||
| chr15:92619310 | C | A | 1 | a0001c0001t0062 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 146 | chr15 | 92619310 | ||||||
| chr15:92619419 | A | G | 1 | a0003c0004t0038 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*37T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 37 | chr15 | 92619419 | ||||||
| chr15:92655666 | G | A | 1 | a0001c0001t0037 | 2 | HG02896.hp1 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-7C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 7 | chr15 | 92655666 | ||||||
| chr15:92655705 | G | C | 2 | a0001c0001t0017 a0001c0001t0063 |
6 | NA18953.hp1 NA18961.hp1 NA18961.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-46C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 46 | chr15 | 92655705 | ||||||
| chr15:92655717 | G | A | 1 | a0001c0001t0064 | 1 | HG03927.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 58 | chr15 | 92655717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92619476 | G | T | 8 | a0001c0001t0011g0024 a0001c0001t0011g0029 a0001c0001t0011g0031 others(5): Show |
8 | HG01109.hp1 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.477-17C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92619476 | |||||||
| chr15:92619672 | C | T | 79 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(76): Show |
80 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.477-213G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92619672 | |||||||
| chr15:92619795 | G | A | 63 | a0001c0001t0001g0309 a0001c0001t0004g0048 a0001c0001t0004g0239 others(60): Show |
65 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.477-336C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92619795 | |||||||
| chr15:92619833 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.477-374C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92619833 | |||||||
| chr15:92620269 | C | T | 13 | a0001c0001t0009g0019 a0001c0001t0009g0021 a0001c0001t0009g0034 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.477-810G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620269 | |||||||
| chr15:92620291 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.477-832C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620291 | |||||||
| chr15:92620477 | A | AAG | 12 | a0001c0001t0005g0238 a0001c0001t0013g0055 a0001c0001t0013g0099 others(9): Show |
12 | HG02027.hp1 HG02027.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.477-1019_477-1018i others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620477 | |||||||
| chr15:92620492 | C | T | 11 | a0001c0001t0013g0055 a0001c0001t0013g0099 a0001c0001t0013g0149 others(8): Show |
11 | HG02027.hp1 HG02080.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.477-1033G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620492 | |||||||
| chr15:92620613 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.477-1154C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620613 | |||||||
| chr15:92620771 | C | T | 11 | a0001c0001t0013g0055 a0001c0001t0013g0099 a0001c0001t0013g0149 others(8): Show |
11 | HG02027.hp1 HG02080.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.477-1312G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620771 | |||||||
| chr15:92620814 | C | CA | 101 | a0001c0001t0001g0124 a0001c0001t0001g0309 a0001c0001t0002g0005 others(98): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.477-1356dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620814 | |||||||
| chr15:92620814 | C | CAA | 84 | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0001g0072 others(81): Show |
85 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.477-1357_477-1356d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620814 | |||||||
| chr15:92620814 | C | CAAA | 32 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0083 others(29): Show |
32 | HG01074.hp2 HG01106.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.477-1358_477-1356d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620814 | |||||||
| chr15:92620814 | CA | C | 58 | a0001c0001t0004g0069 a0001c0001t0004g0081 a0001c0001t0004g0103 others(55): Show |
58 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.477-1356delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620814 | |||||||
| chr15:92620854 | A | C | 1 | a0001c0001t0061g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.477-1395T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620854 | |||||||
| chr15:92620857 | T | C | 2 | a0001c0001t0036g0292 a0001c0001t0036g0293 |
2 | NA18948.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.477-1398A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620857 | |||||||
| chr15:92620883 | G | T | 1 | a0001c0001t0008g0287 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.477-1424C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620883 | |||||||
| chr15:92620984 | T | G | 88 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(85): Show |
89 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.477-1525A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620984 | |||||||
| chr15:92620986 | C | T | 58 | a0001c0001t0003g0042 a0001c0001t0003g0051 a0001c0001t0003g0064 others(55): Show |
58 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.477-1527G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620986 | |||||||
| chr15:92621169 | C | T | 1 | a0001c0001t0026g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.477-1710G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621169 | |||||||
| chr15:92621257 | C | T | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.477-1798G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621257 | |||||||
| chr15:92621261 | C | T | 1 | a0001c0001t0022g0322 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.477-1802G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621261 | |||||||
| chr15:92621347 | C | T | 4 | a0001c0001t0020g0110 a0001c0001t0020g0143 a0001c0001t0020g0345 others(1): Show |
4 | HG00544.hp2 HG01243.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-1888G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621347 | |||||||
| chr15:92621393 | C | T | 1 | a0001c0001t0021g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.477-1934G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621393 | |||||||
| chr15:92621553 | T | C | 2 | a0001c0001t0003g0258 a0001c0001t0007g0275 |
2 | HG02004.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.477-2094A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621553 | |||||||
| chr15:92621594 | G | C | 19 | a0001c0001t0011g0024 a0001c0001t0011g0029 a0001c0001t0011g0031 others(16): Show |
19 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.477-2135C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621594 | |||||||
| chr15:92621608 | C | CA | 82 | a0001c0001t0001g0039 a0001c0001t0001g0158 a0001c0001t0001g0216 others(79): Show |
84 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.477-2150dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621608 | |||||||
| chr15:92621608 | CA | C | 94 | a0001c0001t0001g0088 a0001c0001t0002g0140 a0001c0001t0002g0166 others(91): Show |
94 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.477-2150delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621608 | |||||||
| chr15:92621735 | C | A | 288 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.477-2276G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621735 | |||||||
| chr15:92621736 | A | C | 288 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.477-2277T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621736 | |||||||
| chr15:92621763 | T | C | 87 | a0001c0001t0001g0164 a0001c0001t0004g0048 a0001c0001t0004g0239 others(84): Show |
89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.477-2304A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621763 | |||||||
| chr15:92621928 | C | T | 1 | a0001c0001t0028g0337 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.477-2469G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621928 | |||||||
| chr15:92622114 | G | A | 1 | a0001c0001t0051g0324 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.477-2655C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622114 | |||||||
| chr15:92622269 | G | A | 7 | a0001c0001t0011g0024 a0001c0001t0011g0029 a0001c0001t0011g0031 others(4): Show |
7 | HG01109.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.477-2810C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622269 | |||||||
| chr15:92622304 | G | A | 1 | a0001c0001t0015g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.477-2845C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622304 | |||||||
| chr15:92622366 | A | G | 192 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(189): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.477-2907T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622366 | |||||||
| chr15:92622389 | G | A | 1 | a0001c0001t0053g0138 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.477-2930C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622389 | |||||||
| chr15:92622418 | A | G | 176 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(173): Show |
180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.477-2959T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622418 | |||||||
| chr15:92622526 | T | C | 1 | a0001c0001t0059g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.477-3067A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622526 | |||||||
| chr15:92622556 | TC | T | 41 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(38): Show |
42 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.477-3098delG | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622556 | |||||||
| chr15:92622572 | T | C | 1 | a0001c0001t0059g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.477-3113A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622572 | |||||||
| chr15:92622683 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.477-3224C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622683 | |||||||
| chr15:92622733 | C | T | 160 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.477-3274G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622733 | |||||||
| chr15:92622766 | T | C | 2 | a0001c0001t0001g0093 a0006c0007t0001g0008 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.477-3307A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622766 | |||||||
| chr15:92622808 | G | A | 7 | a0001c0001t0011g0024 a0001c0001t0011g0029 a0001c0001t0011g0031 others(4): Show |
7 | HG01109.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.477-3349C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622808 | |||||||
| chr15:92622867 | T | G | 1 | a0001c0001t0050g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.477-3408A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622867 | |||||||
| chr15:92623223 | G | A | 69 | a0001c0001t0003g0075 a0001c0001t0004g0048 a0001c0001t0004g0239 others(66): Show |
71 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.477-3764C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623223 | |||||||
| chr15:92623471 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.477-4012G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623471 | |||||||
| chr15:92623547 | T | A | 2 | a0001c0001t0020g0110 a0001c0001t0043g0108 |
2 | HG01243.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.477-4088A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623547 | |||||||
| chr15:92623560 | T | G | 186 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(183): Show |
190 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.477-4101A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623560 | |||||||
| chr15:92623644 | G | C | 4 | a0002c0002t0004g0372 a0002c0002t0004g0375 a0002c0002t0004g0376 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.477-4185C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623644 | |||||||
| chr15:92623668 | G | A | 3 | a0001c0001t0005g0068 a0001c0001t0005g0073 a0001c0001t0010g0091 |
3 | HG00735.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.477-4209C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623668 | |||||||
| chr15:92623670 | C | T | 41 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(38): Show |
42 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.477-4211G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623670 | |||||||
| chr15:92623682 | G | A | 3 | a0001c0001t0046g0364 a0001c0001t0047g0111 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.477-4223C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623682 | |||||||
| chr15:92623688 | G | C | 1 | a0001c0001t0002g0195 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.477-4229C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623688 | |||||||
| chr15:92623788 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.477-4329G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623788 | |||||||
| chr15:92623792 | T | G | 182 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(179): Show |
186 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.477-4333A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623792 | |||||||
| chr15:92623804 | C | G | 1 | a0001c0001t0002g0270 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.477-4345G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623804 | |||||||
| chr15:92623820 | C | A | 40 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(37): Show |
41 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.477-4361G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623820 | |||||||
| chr15:92623829 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.477-4370C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623829 | |||||||
| chr15:92623968 | T | C | 2 | a0001c0001t0001g0093 a0006c0007t0001g0008 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.477-4509A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623968 | |||||||
| chr15:92624004 | T | C | 1 | a0001c0001t0003g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.477-4545A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624004 | |||||||
| chr15:92624107 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | NA18963.hp1 NA18968.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.477-4648A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624107 | |||||||
| chr15:92624261 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0093 a0001c0001t0062g0035 others(1): Show |
4 | HG02109.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-4802G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624261 | |||||||
| chr15:92624299 | T | C | 2 | a0001c0001t0020g0143 a0001c0001t0020g0345 |
2 | HG00544.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.477-4840A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624299 | |||||||
| chr15:92624324 | C | T | 11 | a0001c0001t0006g0268 a0001c0001t0006g0269 a0001c0001t0006g0272 others(8): Show |
11 | HG02027.hp1 HG02602.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.477-4865G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624324 | |||||||
| chr15:92624402 | CCATT | C | 64 | a0001c0001t0003g0075 a0001c0001t0004g0048 a0001c0001t0004g0239 others(61): Show |
66 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.477-4947_477-4944d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624402 | |||||||
| chr15:92624570 | T | G | 32 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0204 others(29): Show |
32 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.477-5111A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624570 | |||||||
| chr15:92624627 | C | T | 72 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.477-5168G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624627 | |||||||
| chr15:92624739 | C | T | 198 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(195): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.477-5280G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624739 | |||||||
| chr15:92624758 | C | G | 186 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(183): Show |
190 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.477-5299G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624758 | |||||||
| chr15:92624822 | G | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.477-5363C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624822 | |||||||
| chr15:92624847 | C | T | 1 | a0007c0011t0025g0365 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.476+5367G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624847 | |||||||
| chr15:92624859 | C | T | 148 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(145): Show |
149 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.476+5355G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624859 | |||||||
| chr15:92624897 | C | G | 1 | a0001c0001t0002g0116 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.476+5317G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624897 | |||||||
| chr15:92624899 | C | T | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.476+5315G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624899 | |||||||
| chr15:92624920 | G | A | 21 | a0001c0001t0004g0069 a0001c0001t0004g0081 a0001c0001t0004g0103 others(18): Show |
21 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.476+5294C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624920 | |||||||
| chr15:92624954 | G | A | 70 | a0001c0001t0001g0309 a0001c0001t0003g0075 a0001c0001t0004g0048 others(67): Show |
72 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.476+5260C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624954 | |||||||
| chr15:92624965 | C | G | 2 | a0002c0002t0004g0372 a0002c0002t0031g0373 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.476+5249G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624965 | |||||||
| chr15:92625061 | G | C | 1 | a0001c0001t0048g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.476+5153C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625061 | |||||||
| chr15:92625663 | T | C | 1 | a0001c0001t0053g0138 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.476+4551A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625663 | |||||||
| chr15:92625692 | A | G | 197 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(194): Show |
202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.476+4522T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625692 | |||||||
| chr15:92625710 | G | A | 1 | a0001c0001t0059g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.476+4504C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625710 | |||||||
| chr15:92625717 | G | A | 13 | a0001c0001t0002g0022 a0001c0001t0008g0012 a0001c0001t0008g0014 others(10): Show |
14 | HG00099.hp1 HG02257.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.476+4497C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625717 | |||||||
| chr15:92625751 | C | T | 1 | a0001c0001t0017g0386 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.476+4463G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625751 | |||||||
| chr15:92625786 | T | C | 2 | a0001c0001t0010g0015 a0001c0001t0010g0038 |
2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.476+4428A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625786 | |||||||
| chr15:92625857 | T | A | 1 | a0001c0001t0005g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.476+4357A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625857 | |||||||
| chr15:92625978 | GA | G | 41 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0295 others(38): Show |
41 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.476+4235delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625978 | |||||||
| chr15:92626028 | A | G | 1 | a0001c0001t0059g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.476+4186T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626028 | |||||||
| chr15:92626114 | A | AT | 53 | a0001c0001t0001g0309 a0001c0001t0002g0005 a0001c0001t0002g0053 others(50): Show |
54 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.476+4099dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626114 | |||||||
| chr15:92626114 | A | ATT | 6 | a0001c0001t0006g0272 a0001c0001t0007g0159 a0001c0001t0007g0263 others(3): Show |
6 | HG01071.hp2 HG02027.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.476+4098_476+4099d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626114 | |||||||
| chr15:92626114 | AT | A | 167 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0052 others(164): Show |
170 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.476+4099delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626114 | |||||||
| chr15:92626134 | T | G | 2 | a0001c0001t0003g0150 a0001c0001t0040g0178 |
2 | HG02080.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.476+4080A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626134 | |||||||
| chr15:92626135 | T | A | 2 | a0001c0001t0003g0150 a0001c0001t0040g0178 |
2 | HG02080.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.476+4079A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626135 | |||||||
| chr15:92626139 | A | ACGGAGTC others(12): Show |
351 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(348): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.476+4074_476+4075i others(21): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626139 | |||||||
| chr15:92626139 | A | AGTCTCGC others(8): Show |
2 | a0001c0001t0003g0150 a0001c0001t0040g0178 |
2 | HG02080.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.476+4074_476+4075i others(17): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626139 | |||||||
| chr15:92626159 | C | A | 3 | a0001c0001t0006g0078 a0001c0001t0006g0249 a0001c0001t0014g0243 |
3 | HG01943.hp1 HG01981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.476+4055G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626159 | |||||||
| chr15:92626167 | T | C | 2 | a0001c0001t0003g0002 a0001c0001t0003g0020 |
3 | HG01891.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.476+4047A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626167 | |||||||
| chr15:92626199 | C | T | 71 | a0001c0001t0003g0075 a0001c0001t0004g0048 a0001c0001t0004g0239 others(68): Show |
73 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.476+4015G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626199 | |||||||
| chr15:92626212 | C | T | 5 | a0001c0001t0020g0110 a0001c0001t0043g0108 a0001c0001t0046g0364 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.476+4002G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626212 | |||||||
| chr15:92626230 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.476+3984G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626230 | |||||||
| chr15:92626369 | T | A | 68 | a0001c0001t0003g0075 a0001c0001t0004g0048 a0001c0001t0004g0239 others(65): Show |
70 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.476+3845A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626369 | |||||||
| chr15:92626379 | G | A | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.476+3835C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626379 | |||||||
| chr15:92626414 | T | A | 69 | a0001c0001t0003g0075 a0001c0001t0004g0048 a0001c0001t0004g0133 others(66): Show |
71 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.476+3800A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626414 | |||||||
| chr15:92626415 | A | T | 42 | a0001c0001t0001g0309 a0001c0001t0002g0005 a0001c0001t0002g0053 others(39): Show |
43 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.476+3799T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626415 | |||||||
| chr15:92626462 | A | T | 3 | a0001c0001t0046g0364 a0001c0001t0047g0111 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.476+3752T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626462 | |||||||
| chr15:92626548 | A | C | 69 | a0001c0001t0003g0075 a0001c0001t0004g0048 a0001c0001t0004g0239 others(66): Show |
71 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.476+3666T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626548 | |||||||
| chr15:92626635 | G | A | 4 | a0001c0001t0003g0278 a0001c0001t0046g0364 a0001c0001t0047g0111 others(1): Show |
4 | HG01175.hp1 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+3579C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626635 | |||||||
| chr15:92626827 | T | G | 7 | a0001c0001t0015g0107 a0001c0001t0015g0109 a0001c0001t0015g0197 others(4): Show |
7 | HG02280.hp1 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.476+3387A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626827 | |||||||
| chr15:92626870 | G | A | 2 | a0001c0001t0003g0002 a0001c0001t0003g0020 |
3 | HG01891.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.476+3344C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626870 | |||||||
| chr15:92626929 | G | A | 1 | a0001c0001t0059g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.476+3285C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626929 | |||||||
| chr15:92627027 | G | A | 1 | a0001c0001t0015g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.476+3187C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627027 | |||||||
| chr15:92627068 | C | A | 1 | a0001c0001t0048g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.476+3146G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627068 | |||||||
| chr15:92627082 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.476+3132G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627082 | |||||||
| chr15:92627101 | G | A | 41 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(38): Show |
42 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.476+3113C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627101 | |||||||
| chr15:92627113 | T | C | 1 | a0001c0001t0014g0163 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.476+3101A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627113 | |||||||
| chr15:92627176 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0093 a0001c0001t0062g0035 others(1): Show |
4 | HG02109.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+3038C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627176 | |||||||
| chr15:92627179 | G | A | 8 | a0001c0001t0001g0098 a0001c0001t0001g0161 a0001c0001t0001g0164 others(5): Show |
8 | HG00140.hp1 HG01175.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.476+3035C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627179 | |||||||
| chr15:92627232 | C | G | 43 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(40): Show |
44 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.476+2982G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627232 | |||||||
| chr15:92627306 | T | C | 1 | a0001c0006t0024g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.476+2908A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627306 | |||||||
| chr15:92627355 | C | T | 1 | a0001c0001t0059g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.476+2859G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627355 | |||||||
| chr15:92627389 | C | G | 3 | a0001c0001t0004g0340 a0001c0001t0004g0347 a0001c0001t0050g0026 |
3 | HG01192.hp2 HG02258.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.476+2825G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627389 | |||||||
| chr15:92627426 | G | A | 2 | a0001c0001t0023g0151 a0001c0001t0023g0244 |
2 | NA18950.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.476+2788C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627426 | |||||||
| chr15:92627574 | T | C | 68 | a0001c0001t0002g0005 a0001c0001t0002g0022 a0001c0001t0002g0053 others(65): Show |
70 | HG00099.hp1 HG00639.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.476+2640A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627574 | |||||||
| chr15:92627630 | C | G | 4 | a0001c0001t0010g0333 a0001c0001t0010g0362 a0001c0001t0033g0028 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.476+2584G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627630 | |||||||
| chr15:92627697 | G | A | 1 | a0001c0001t0053g0138 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.476+2517C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627697 | |||||||
| chr15:92627713 | G | C | 1 | a0001c0001t0013g0149 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.476+2501C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627713 | |||||||
| chr15:92627792 | C | T | 2 | a0001c0001t0011g0135 a0001c0001t0061g0136 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.476+2422G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627792 | |||||||
| chr15:92627793 | G | A | 3 | a0002c0002t0009g0369 a0002c0002t0009g0371 a0002c0002t0032g0370 |
3 | HG02451.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.476+2421C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627793 | |||||||
| chr15:92627800 | T | C | 1 | a0003c0004t0038g0367 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.476+2414A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627800 | |||||||
| chr15:92627809 | G | C | 44 | a0001c0001t0001g0309 a0001c0001t0002g0005 a0001c0001t0002g0053 others(41): Show |
45 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.476+2405C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627809 | |||||||
| chr15:92627864 | A | T | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2350T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627864 | |||||||
| chr15:92627866 | G | C | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2348C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627866 | |||||||
| chr15:92627868 | G | A | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2346C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627868 | |||||||
| chr15:92627871 | A | C | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2343T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627871 | |||||||
| chr15:92627874 | G | T | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2340C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627874 | |||||||
| chr15:92627875 | A | T | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2339T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627875 | |||||||
| chr15:92627877 | A | T | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2337T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627877 | |||||||
| chr15:92627879 | A | T | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2335T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627879 | |||||||
| chr15:92627880 | A | C | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2334T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627880 | |||||||
| chr15:92627883 | G | T | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2331C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627883 | |||||||
| chr15:92627892 | T | C | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2322A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627892 | |||||||
| chr15:92627894 | A | C | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2320T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627894 | |||||||
| chr15:92627896 | A | T | 1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2318T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627896 | |||||||
| chr15:92627914 | T | G | 44 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(41): Show |
45 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.476+2300A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627914 | |||||||
| chr15:92627928 | G | A | 2 | a0001c0001t0005g0176 a0001c0001t0005g0183 |
2 | NA18979.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.476+2286C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627928 | |||||||
| chr15:92627930 | A | T | 188 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(185): Show |
192 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.476+2284T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627930 | |||||||
| chr15:92628052 | A | C | 4 | a0001c0001t0016g0351 a0001c0001t0016g0352 a0001c0001t0034g0090 others(1): Show |
4 | HG02451.hp2 HG02683.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.476+2162T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628052 | |||||||
| chr15:92628171 | AT | A | 71 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(68): Show |
72 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.476+2042delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628171 | |||||||
| chr15:92628338 | CT | C | 179 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(176): Show |
181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.476+1875delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628338 | |||||||
| chr15:92628338 | CTT | C | 112 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(109): Show |
114 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.476+1874_476+1875d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628338 | |||||||
| chr15:92628338 | CTTT | C | 38 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(35): Show |
39 | HG00639.hp1 HG01071.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.476+1873_476+1875d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628338 | |||||||
| chr15:92628338 | CTTTTTTT others(5): Show |
C | 1 | a0003c0004t0038g0367 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.476+1864_476+1875d others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628338 | |||||||
| chr15:92628443 | A | G | 43 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(40): Show |
44 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.476+1771T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628443 | |||||||
| chr15:92628537 | G | T | 4 | a0001c0001t0017g0007 a0001c0001t0017g0383 a0001c0001t0017g0384 others(1): Show |
5 | NA18953.hp1 NA18961.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.476+1677C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628537 | |||||||
| chr15:92628538 | A | C | 3 | a0001c0001t0046g0364 a0001c0001t0047g0111 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.476+1676T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628538 | |||||||
| chr15:92628745 | C | T | 2 | a0001c0001t0004g0188 a0001c0001t0004g0208 |
2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.476+1469G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628745 | |||||||
| chr15:92628800 | T | A | 1 | a0001c0001t0003g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.476+1414A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628800 | |||||||
| chr15:92628964 | C | G | 43 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(40): Show |
44 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.476+1250G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628964 | |||||||
| chr15:92629084 | ACCG | A | 8 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0008g0198 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.476+1127_476+1129d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629084 | |||||||
| chr15:92629250 | A | G | 44 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0212 others(41): Show |
45 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.476+964T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629250 | |||||||
| chr15:92629340 | C | T | 4 | a0001c0001t0004g0114 a0001c0001t0046g0364 a0001c0001t0047g0111 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+874G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629340 | |||||||
| chr15:92629346 | A | G | 3 | a0001c0001t0009g0019 a0001c0001t0015g0128 a0003c0004t0038g0367 |
3 | HG01884.hp1 HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.476+868T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629346 | |||||||
| chr15:92629361 | A | G | 2 | a0001c0001t0016g0341 a0001c0001t0020g0345 |
2 | HG00099.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.476+853T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629361 | |||||||
| chr15:92629375 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.476+839A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629375 | |||||||
| chr15:92629445 | C | A | 1 | a0001c0001t0005g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.476+769G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629445 | |||||||
| chr15:92629445 | CGCCACCC others(5): Show |
C | 1 | a0001c0001t0005g0200 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.476+757_476+768del others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629445 | |||||||
| chr15:92629446 | G | A | 10 | a0001c0001t0001g0290 a0001c0001t0002g0053 a0001c0001t0002g0212 others(7): Show |
10 | HG02165.hp1 NA18946.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.476+768C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629446 | |||||||
| chr15:92629537 | C | T | 1 | a0001c0001t0022g0267 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.476+677G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629537 | |||||||
| chr15:92629652 | A | G | 2 | a0001c0001t0023g0151 a0001c0001t0023g0244 |
2 | NA18950.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.476+562T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629652 | |||||||
| chr15:92629783 | C | T | 1 | a0001c0001t0015g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.476+431G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629783 | |||||||
| chr15:92629806 | C | A | 1 | a0001c0001t0011g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.476+408G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629806 | |||||||
| chr15:92629842 | A | G | 270 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(267): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.476+372T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629842 | |||||||
| chr15:92629906 | C | T | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.476+308G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629906 | |||||||
| chr15:92630155 | G | A | 1 | a0001c0001t0022g0322 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.476+59C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92630155 | |||||||
| chr15:92630357 | G | A | 1 | a0001c0001t0004g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.345-12C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630357 | |||||||
| chr15:92630423 | G | A | 49 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(46): Show |
50 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.345-78C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630423 | |||||||
| chr15:92630539 | C | T | 2 | a0001c0001t0037g0381 a0001c0001t0037g0382 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-194G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630539 | |||||||
| chr15:92630601 | G | A | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-256C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630601 | |||||||
| chr15:92630667 | TAATACAC others(1): Show |
T | 8 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-330_345-323del others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630667 | |||||||
| chr15:92630678 | T | C | 8 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-333A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630678 | |||||||
| chr15:92630716 | AT | A | 16 | a0001c0001t0002g0153 a0001c0001t0003g0002 a0001c0001t0003g0020 others(13): Show |
18 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-372delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630716 | |||||||
| chr15:92630717 | T | TA | 80 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(77): Show |
82 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.345-373_345-372ins others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630717 | |||||||
| chr15:92630729 | T | C | 4 | a0001c0001t0003g0334 a0001c0001t0010g0339 a0001c0001t0028g0337 others(1): Show |
4 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-384A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630729 | |||||||
| chr15:92630731 | T | C | 1 | a0001c0001t0006g0062 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.345-386A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630731 | |||||||
| chr15:92630740 | AT | A | 9 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0009g0112 others(6): Show |
9 | HG01109.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-396delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630740 | |||||||
| chr15:92630753 | TATA | T | 6 | a0001c0001t0002g0005 a0001c0001t0003g0334 a0001c0001t0009g0338 others(3): Show |
7 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-411_345-409del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630753 | |||||||
| chr15:92630759 | A | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0087 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.345-414T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630759 | |||||||
| chr15:92630763 | TATA | T | 83 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(80): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.345-421_345-419del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630763 | |||||||
| chr15:92630765 | T | TTTTTTAT others(16): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0087 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.345-421_345-420ins others(23): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630765 | |||||||
| chr15:92630765 | TA | T | 286 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(283): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.345-421delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630765 | |||||||
| chr15:92630766 | A | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0087 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.345-421T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630766 | |||||||
| chr15:92630786 | ATTACATA others(62): Show |
A | 3 | a0001c0001t0007g0129 a0001c0001t0021g0127 a0001c0001t0031g0130 |
3 | HG03491.hp2 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.345-510_345-442del others(69): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630786 | |||||||
| chr15:92630797 | C | T | 1 | a0001c0001t0005g0073 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.345-452G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630797 | |||||||
| chr15:92630801 | TTATATAT others(27): Show |
T | 29 | a0001c0001t0001g0161 a0001c0001t0001g0204 a0001c0001t0001g0216 others(26): Show |
29 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.345-490_345-457del others(34): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630801 | |||||||
| chr15:92630804 | T | C | 3 | a0001c0001t0007g0254 a0001c0001t0007g0260 a0001c0001t0057g0261 |
3 | HG01496.hp2 HG01993.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.345-459A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630804 | |||||||
| chr15:92630805 | A | ATAT | 89 | a0001c0001t0001g0039 a0001c0001t0001g0134 a0001c0001t0001g0164 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.345-463_345-461dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630805 | |||||||
| chr15:92630809 | A | T | 4 | a0001c0001t0002g0153 a0001c0001t0003g0051 a0001c0001t0003g0146 others(1): Show |
4 | HG01258.hp1 NA18973.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-464T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630809 | |||||||
| chr15:92630809 | ATT | A | 5 | a0001c0001t0001g0124 a0001c0001t0008g0012 a0001c0001t0011g0031 others(2): Show |
5 | HG02970.hp2 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-466_345-465del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630809 | |||||||
| chr15:92630811 | T | A | 89 | a0001c0001t0001g0039 a0001c0001t0001g0134 a0001c0001t0001g0164 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.345-466A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630811 | |||||||
| chr15:92630811 | T | TACGTATT others(5): Show |
7 | a0001c0001t0002g0022 a0001c0001t0008g0014 a0001c0001t0008g0137 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-467_345-466ins others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630811 | |||||||
| chr15:92630811 | TTTATATA others(58): Show |
T | 1 | a0001c0001t0016g0352 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.345-531_345-467del others(65): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630811 | |||||||
| chr15:92630811 | TTTATATA others(93): Show |
T | 1 | a0001c0001t0016g0351 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345-566_345-467del others(100): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630811 | |||||||
| chr15:92630813 | T | C | 3 | a0001c0001t0010g0362 a0001c0001t0046g0364 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.345-468A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630813 | |||||||
| chr15:92630815 | T | C | 103 | a0001c0001t0001g0039 a0001c0001t0001g0124 a0001c0001t0001g0134 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.345-470A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630815 | |||||||
| chr15:92630815 | TATATTAC others(23): Show |
T | 4 | a0001c0001t0004g0347 a0001c0001t0012g0350 a0001c0001t0020g0345 others(1): Show |
4 | HG00544.hp2 HG01192.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-500_345-471del others(30): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630815 | |||||||
| chr15:92630816 | A | G | 94 | a0001c0001t0001g0039 a0001c0001t0001g0124 a0001c0001t0001g0134 others(91): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.345-471T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630816 | |||||||
| chr15:92630816 | ATATTACA others(170): Show |
A | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-648_345-472del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630816 | |||||||
| chr15:92630818 | A | G | 89 | a0001c0001t0001g0039 a0001c0001t0001g0134 a0001c0001t0001g0164 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.345-473T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630818 | |||||||
| chr15:92630818 | ATTACATA others(30): Show |
A | 1 | a0001c0001t0010g0349 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.345-510_345-474del others(37): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630818 | |||||||
| chr15:92630822 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-477G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630822 | |||||||
| chr15:92630822 | CATATTAT others(121): Show |
C | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.345-605_345-478del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630822 | |||||||
| chr15:92630823 | A | G | 5 | a0001c0001t0001g0124 a0001c0001t0008g0012 a0001c0001t0011g0031 others(2): Show |
5 | HG02970.hp2 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-478T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630823 | |||||||
| chr15:92630825 | A | G | 14 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0002g0005 others(11): Show |
15 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.345-480T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630825 | |||||||
| chr15:92630829 | T | C | 107 | a0001c0001t0001g0039 a0001c0001t0001g0124 a0001c0001t0001g0134 others(104): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.345-484A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630829 | |||||||
| chr15:92630830 | A | G | 1 | a0001c0001t0001g0346 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.345-485T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630830 | |||||||
| chr15:92630832 | A | T | 1 | a0001c0001t0004g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.345-487T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630832 | |||||||
| chr15:92630833 | T | A | 1 | a0001c0001t0004g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.345-488A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630833 | |||||||
| chr15:92630833 | T | TTA | 91 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(88): Show |
95 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.345-490_345-489dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630833 | |||||||
| chr15:92630833 | TTA | T | 94 | a0001c0001t0001g0039 a0001c0001t0001g0124 a0001c0001t0001g0134 others(91): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.345-490_345-489del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630833 | |||||||
| chr15:92630835 | A | ACATATTA others(271): Show |
1 | a0001c0001t0002g0005 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.345-491_345-490ins others(278): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | |||||||
| chr15:92630835 | A | ACATATTA others(341): Show |
1 | a0001c0001t0001g0344 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.345-491_345-490ins others(348): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | |||||||
| chr15:92630835 | A | ACATATTA others(341): Show |
1 | a0001c0001t0003g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.345-491_345-490ins others(348): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | |||||||
| chr15:92630835 | A | ACATATTA others(306): Show |
2 | a0001c0001t0009g0338 a0001c0001t0010g0339 |
2 | HG00140.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.345-491_345-490ins others(313): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | |||||||
| chr15:92630835 | A | ACATATTA others(271): Show |
1 | a0001c0001t0028g0337 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.345-491_345-490ins others(278): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | |||||||
| chr15:92630835 | A | ACGTATTA others(12): Show |
7 | a0001c0001t0002g0022 a0001c0001t0008g0014 a0001c0001t0008g0137 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-491_345-490ins others(19): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | |||||||
| chr15:92630835 | A | ATATATTA others(19): Show |
1 | a0001c0001t0018g0262 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345-491_345-490ins others(26): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | |||||||
| chr15:92630835 | ATATATAT others(35): Show |
A | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-532_345-491del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | |||||||
| chr15:92630836 | T | TATATATT others(16): Show |
1 | a0001c0001t0008g0311 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.345-514_345-492dup others(23): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630836 | |||||||
| chr15:92630838 | T | C | 17 | a0001c0001t0001g0124 a0001c0001t0001g0161 a0001c0001t0001g0346 others(14): Show |
17 | HG01109.hp1 HG01175.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-493A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630838 | |||||||
| chr15:92630839 | A | G | 1 | a0001c0001t0001g0346 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.345-494T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630839 | |||||||
| chr15:92630845 | C | T | 139 | a0001c0001t0001g0039 a0001c0001t0001g0124 a0001c0001t0001g0134 others(136): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.345-500G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630845 | |||||||
| chr15:92630846 | A | G | 2 | a0001c0001t0001g0346 a0001c0001t0016g0341 |
2 | HG00099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.345-501T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630846 | |||||||
| chr15:92630853 | A | ATGTTACA others(28): Show |
1 | a0001c0001t0009g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.345-543_345-509dup others(35): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630853 | |||||||
| chr15:92630853 | A | G | 145 | a0001c0001t0001g0039 a0001c0001t0001g0124 a0001c0001t0001g0134 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.345-508T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630853 | |||||||
| chr15:92630855 | G | A | 23 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(20): Show |
24 | HG00099.hp1 HG00140.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.345-510C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | G | GTTACATA others(100): Show |
2 | a0001c0001t0005g0073 a0001c0001t0010g0091 |
2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.345-511_345-510ins others(107): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | G | GTTACATA others(135): Show |
3 | a0001c0001t0003g0067 a0001c0001t0005g0068 a0001c0001t0034g0090 |
3 | HG02683.hp1 HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.345-511_345-510ins others(142): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | G | GTTACATA others(135): Show |
1 | a0001c0001t0003g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.345-511_345-510ins others(142): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | G | GTTACATA others(98): Show |
4 | a0001c0001t0004g0069 a0001c0001t0004g0103 a0001c0001t0018g0054 others(1): Show |
4 | HG00735.hp1 HG01074.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-511_345-510ins others(105): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | G | GTTACATA others(21): Show |
3 | a0001c0001t0002g0153 a0001c0001t0003g0146 a0001c0001t0007g0152 |
3 | NA18973.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.345-511_345-510ins others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | G | GTTACATA others(98): Show |
1 | a0001c0001t0013g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.345-511_345-510ins others(105): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | G | GTTACATA others(28): Show |
2 | a0001c0001t0006g0305 a0001c0001t0007g0100 |
2 | HG01934.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.345-545_345-511dup others(35): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | G | GTTACATA others(63): Show |
1 | a0001c0001t0052g0057 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.345-511_345-510ins others(70): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | GTTACATA others(28): Show |
G | 95 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(92): Show |
99 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.345-545_345-511del others(35): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630855 | GTTACATA others(63): Show |
G | 4 | a0001c0001t0004g0347 a0001c0001t0010g0362 a0001c0001t0046g0364 others(1): Show |
4 | HG01192.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-580_345-511del others(70): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | |||||||
| chr15:92630860 | A | G | 20 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(17): Show |
21 | HG00099.hp1 HG00140.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.345-515T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630860 | |||||||
| chr15:92630862 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0010g0349 a0001c0001t0011g0031 |
3 | HG00733.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.345-517T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630862 | |||||||
| chr15:92630866 | CATATTAT others(35): Show |
C | 1 | a0001c0001t0003g0051 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.345-563_345-522del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630866 | |||||||
| chr15:92630867 | A | G | 3 | a0001c0001t0001g0346 a0001c0001t0004g0340 a0001c0001t0016g0341 |
3 | HG00099.hp1 HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.345-522T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630867 | |||||||
| chr15:92630873 | T | C | 9 | a0001c0001t0001g0124 a0001c0001t0001g0346 a0001c0001t0004g0340 others(6): Show |
9 | HG00099.hp1 HG00733.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-528A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630873 | |||||||
| chr15:92630873 | T | TATATTAC others(266): Show |
1 | a0001c0001t0033g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.345-529_345-528ins others(273): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630873 | |||||||
| chr15:92630874 | A | G | 2 | a0001c0001t0001g0346 a0001c0001t0016g0341 |
2 | HG00099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.345-529T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630874 | |||||||
| chr15:92630880 | T | C | 10 | a0001c0001t0001g0346 a0001c0001t0004g0081 a0001c0001t0004g0340 others(7): Show |
10 | HG00099.hp1 HG00544.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-535A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630880 | |||||||
| chr15:92630881 | A | G | 4 | a0001c0001t0001g0346 a0001c0001t0012g0343 a0001c0001t0012g0350 others(1): Show |
4 | HG00099.hp1 HG01175.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-536T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630881 | |||||||
| chr15:92630888 | G | A | 2 | a0001c0001t0004g0081 a0005c0012t0003g0380 |
2 | HG01361.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.345-543C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630888 | |||||||
| chr15:92630890 | A | G | 91 | a0001c0001t0001g0039 a0001c0001t0001g0161 a0001c0001t0001g0164 others(88): Show |
91 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.345-545T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630890 | |||||||
| chr15:92630891 | T | C | 1 | a0001c0001t0005g0073 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.345-546A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630891 | |||||||
| chr15:92630895 | A | G | 25 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.345-550T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630895 | |||||||
| chr15:92630897 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-552T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630897 | |||||||
| chr15:92630901 | CATATTAT others(7): Show |
C | 2 | a0001c0001t0012g0350 a0001c0001t0034g0342 |
2 | HG01975.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.345-570_345-557del others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630901 | |||||||
| chr15:92630902 | A | G | 3 | a0001c0001t0001g0346 a0001c0001t0010g0349 a0001c0001t0016g0341 |
3 | HG00099.hp1 HG00733.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.345-557T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630902 | |||||||
| chr15:92630908 | T | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0346 a0001c0001t0010g0349 others(1): Show |
4 | HG00099.hp1 HG00733.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-563A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630908 | |||||||
| chr15:92630908 | T | TATATTAC others(329): Show |
1 | a0001c0001t0012g0343 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.345-564_345-563ins others(336): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630908 | |||||||
| chr15:92630909 | A | G | 5 | a0001c0001t0001g0346 a0001c0001t0004g0340 a0001c0001t0010g0349 others(2): Show |
5 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-564T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630909 | |||||||
| chr15:92630915 | T | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0004g0081 others(9): Show |
12 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-570A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630915 | |||||||
| chr15:92630916 | A | G | 6 | a0001c0001t0004g0340 a0001c0001t0010g0349 a0001c0001t0012g0350 others(3): Show |
6 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-571T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630916 | |||||||
| chr15:92630922 | C | T | 1 | a0001c0001t0018g0262 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345-577G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630922 | |||||||
| chr15:92630923 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.345-578C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630923 | |||||||
| chr15:92630925 | A | G | 38 | a0001c0001t0001g0211 a0001c0001t0001g0216 a0001c0001t0002g0049 others(35): Show |
38 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.345-580T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630925 | |||||||
| chr15:92630927 | T | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-582A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630927 | |||||||
| chr15:92630929 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-584G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630929 | |||||||
| chr15:92630930 | A | G | 29 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.345-585T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630930 | |||||||
| chr15:92630931 | T | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-586A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630931 | |||||||
| chr15:92630932 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-587T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630932 | |||||||
| chr15:92630932 | A | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-587T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630932 | |||||||
| chr15:92630936 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-591G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630936 | |||||||
| chr15:92630936 | CATATTAT others(7): Show |
C | 1 | a0001c0001t0016g0352 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.345-605_345-592del others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630936 | |||||||
| chr15:92630937 | A | G | 8 | a0001c0001t0001g0346 a0001c0001t0004g0340 a0001c0001t0010g0349 others(5): Show |
8 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-592T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630937 | |||||||
| chr15:92630943 | T | C | 8 | a0001c0001t0001g0124 a0001c0001t0001g0346 a0001c0001t0004g0340 others(5): Show |
8 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-598A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630943 | |||||||
| chr15:92630944 | A | G | 7 | a0001c0001t0001g0346 a0001c0001t0004g0340 a0001c0001t0010g0349 others(4): Show |
7 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-599T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630944 | |||||||
| chr15:92630950 | T | C | 18 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 others(15): Show |
18 | HG00544.hp2 HG00558.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.345-605A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630950 | |||||||
| chr15:92630951 | A | G | 8 | a0001c0001t0001g0083 a0001c0001t0004g0340 a0001c0001t0010g0349 others(5): Show |
8 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-606T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630951 | |||||||
| chr15:92630953 | A | G | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.345-608T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630953 | |||||||
| chr15:92630958 | G | A | 4 | a0001c0001t0007g0348 a0001c0001t0010g0362 a0001c0001t0046g0364 others(1): Show |
4 | HG01071.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-613C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630958 | |||||||
| chr15:92630960 | A | G | 18 | a0001c0001t0002g0224 a0001c0001t0002g0321 a0001c0001t0003g0189 others(15): Show |
18 | HG00733.hp2 HG00741.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-615T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630960 | |||||||
| chr15:92630964 | C | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0315 |
2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-619G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630964 | |||||||
| chr15:92630965 | A | ATATTACA others(56): Show |
1 | a0001c0001t0003g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.345-621_345-620ins others(63): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630965 | |||||||
| chr15:92630965 | A | G | 29 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.345-620T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630965 | |||||||
| chr15:92630967 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0007g0348 |
2 | HG01071.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.345-622T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630967 | |||||||
| chr15:92630971 | CATATTAT others(7): Show |
C | 1 | a0001c0001t0016g0351 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345-640_345-627del others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630971 | |||||||
| chr15:92630971 | CATATTAT others(35): Show |
C | 1 | a0001c0001t0005g0232 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.345-668_345-627del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630971 | |||||||
| chr15:92630972 | A | G | 11 | a0001c0001t0001g0346 a0001c0001t0004g0340 a0001c0001t0004g0347 others(8): Show |
11 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-627T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630972 | |||||||
| chr15:92630977 | ATAT | A | 3 | a0001c0001t0001g0231 a0001c0001t0002g0166 a0001c0001t0024g0209 |
3 | HG00597.hp2 HG01934.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.345-635_345-633del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630977 | |||||||
| chr15:92630978 | T | C | 9 | a0001c0001t0001g0346 a0001c0001t0004g0347 a0001c0001t0007g0348 others(6): Show |
9 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-633A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630978 | |||||||
| chr15:92630978 | T | TATATTAC others(21): Show |
1 | a0001c0001t0012g0085 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.345-634_345-633ins others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630978 | |||||||
| chr15:92630979 | A | G | 8 | a0001c0001t0001g0346 a0001c0001t0004g0347 a0001c0001t0007g0348 others(5): Show |
8 | HG00099.hp1 HG00733.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-634T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630979 | |||||||
| chr15:92630983 | TATATATT others(44): Show |
T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-689_345-639del others(51): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630983 | |||||||
| chr15:92630985 | T | C | 13 | a0001c0001t0001g0040 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG00558.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.345-640A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630985 | |||||||
| chr15:92630986 | A | G | 6 | a0001c0001t0001g0083 a0001c0001t0004g0347 a0001c0001t0007g0348 others(3): Show |
6 | HG01071.hp2 HG01192.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-641T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630986 | |||||||
| chr15:92630993 | GTATTACA others(35): Show |
G | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-690_345-649del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630993 | |||||||
| chr15:92630995 | A | G | 7 | a0001c0001t0002g0180 a0001c0001t0002g0212 a0001c0001t0003g0121 others(4): Show |
7 | HG00733.hp2 HG01099.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-650T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630995 | |||||||
| chr15:92630999 | C | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0315 |
2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-654G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630999 | |||||||
| chr15:92631000 | A | G | 34 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(31): Show |
35 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.345-655T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631000 | |||||||
| chr15:92631002 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-657T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631002 | |||||||
| chr15:92631004 | T | A | 2 | a0001c0001t0001g0308 a0001c0001t0001g0315 |
2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-659A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631004 | |||||||
| chr15:92631006 | C | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0315 |
2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-661G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631006 | |||||||
| chr15:92631007 | A | G | 11 | a0001c0001t0001g0346 a0001c0001t0004g0347 a0001c0001t0007g0348 others(8): Show |
11 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-662T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631007 | |||||||
| chr15:92631012 | A | ATATATTA others(464): Show |
1 | a0001c0001t0001g0087 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.345-668_345-667ins others(471): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631012 | |||||||
| chr15:92631013 | T | C | 15 | a0001c0001t0004g0122 a0001c0001t0004g0347 a0001c0001t0007g0348 others(12): Show |
15 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.345-668A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631013 | |||||||
| chr15:92631013 | T | TATATTAC others(126): Show |
1 | a0001c0001t0001g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.345-669_345-668ins others(133): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631013 | |||||||
| chr15:92631014 | A | G | 5 | a0001c0001t0001g0346 a0001c0001t0004g0347 a0001c0001t0007g0348 others(2): Show |
5 | HG01071.hp2 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-669T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631014 | |||||||
| chr15:92631019 | ATATATTA others(146): Show |
A | 2 | a0001c0001t0001g0308 a0001c0001t0001g0315 |
2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-827_345-675del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631019 | |||||||
| chr15:92631020 | T | C | 13 | a0001c0001t0001g0040 a0001c0001t0001g0083 a0001c0001t0001g0086 others(10): Show |
13 | HG00558.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.345-675A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631020 | |||||||
| chr15:92631021 | A | G | 5 | a0001c0001t0001g0083 a0001c0001t0004g0347 a0001c0001t0007g0348 others(2): Show |
5 | HG01071.hp2 HG01192.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-676T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631021 | |||||||
| chr15:92631030 | A | G | 4 | a0001c0001t0002g0212 a0001c0001t0003g0189 a0001c0001t0007g0254 others(1): Show |
4 | HG00733.hp2 HG01496.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-685T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631030 | |||||||
| chr15:92631035 | A | G | 36 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0124 others(33): Show |
37 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.345-690T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631035 | |||||||
| chr15:92631037 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-692T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631037 | |||||||
| chr15:92631041 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-696G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631041 | |||||||
| chr15:92631042 | A | G | 11 | a0001c0001t0001g0346 a0001c0001t0004g0347 a0001c0001t0007g0348 others(8): Show |
11 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-697T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631042 | |||||||
| chr15:92631045 | TTA | T | 8 | a0001c0001t0001g0216 a0001c0001t0001g0306 a0001c0001t0004g0131 others(5): Show |
8 | HG03710.hp1 HG03834.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-702_345-701del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631045 | |||||||
| chr15:92631046 | T | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-701A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631046 | |||||||
| chr15:92631047 | A | ATATATTA others(289): Show |
1 | a0001c0001t0001g0086 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.345-703_345-702ins others(296): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631047 | |||||||
| chr15:92631047 | A | ATATATTA others(157): Show |
1 | a0001c0010t0012g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.345-703_345-702ins others(164): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631047 | |||||||
| chr15:92631047 | A | ATGTATTA others(328): Show |
1 | a0001c0001t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.345-703_345-702ins others(335): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631047 | |||||||
| chr15:92631047 | ATATATTA others(61): Show |
A | 6 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0009g0112 others(3): Show |
6 | HG01109.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-770_345-703del others(68): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631047 | |||||||
| chr15:92631048 | T | C | 5 | a0001c0001t0001g0084 a0001c0001t0004g0069 a0001c0001t0004g0103 others(2): Show |
5 | HG00735.hp1 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-703A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631048 | |||||||
| chr15:92631049 | A | G | 2 | a0001c0001t0001g0346 a0001c0001t0007g0348 |
2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.345-704T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631049 | |||||||
| chr15:92631055 | T | C | 13 | a0001c0001t0001g0040 a0001c0001t0001g0144 a0001c0001t0001g0226 others(10): Show |
13 | HG01106.hp1 HG01943.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.345-710A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631055 | |||||||
| chr15:92631056 | A | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0226 a0001c0001t0007g0348 others(2): Show |
5 | HG01071.hp2 HG01106.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-711T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631056 | |||||||
| chr15:92631061 | ACG | A | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0340 |
3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-718_345-717del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631061 | |||||||
| chr15:92631063 | G | A | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-718C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631063 | |||||||
| chr15:92631065 | A | G | 1 | a0001c0001t0007g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.345-720T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631065 | |||||||
| chr15:92631067 | T | A | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-722A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631067 | |||||||
| chr15:92631069 | C | T | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0340 |
3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-724G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631069 | |||||||
| chr15:92631070 | A | G | 37 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0086 others(34): Show |
38 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.345-725T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631070 | |||||||
| chr15:92631071 | T | A | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-726A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631071 | |||||||
| chr15:92631072 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-727T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631072 | |||||||
| chr15:92631072 | A | T | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-727T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631072 | |||||||
| chr15:92631076 | C | T | 2 | a0001c0001t0004g0340 a0001c0001t0022g0061 |
2 | HG03710.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.345-731G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631076 | |||||||
| chr15:92631077 | A | G | 10 | a0001c0001t0001g0346 a0001c0001t0004g0347 a0001c0001t0007g0348 others(7): Show |
10 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-732T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631077 | |||||||
| chr15:92631080 | TTA | T | 90 | a0001c0001t0001g0039 a0001c0001t0001g0088 a0001c0001t0001g0134 others(87): Show |
91 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.345-737_345-736del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631080 | |||||||
| chr15:92631082 | A | ACATATTA others(129): Show |
1 | a0001c0001t0004g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.345-738_345-737ins others(136): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | |||||||
| chr15:92631082 | A | ATATATTA others(124): Show |
1 | a0001c0001t0002g0060 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.345-738_345-737ins others(131): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | |||||||
| chr15:92631082 | A | ATATATTA others(89): Show |
1 | a0001c0001t0001g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.345-738_345-737ins others(96): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | |||||||
| chr15:92631082 | A | ATATATTA others(54): Show |
1 | a0001c0001t0022g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.345-738_345-737ins others(61): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | |||||||
| chr15:92631082 | A | ATATATTA others(89): Show |
7 | a0001c0001t0001g0144 a0001c0001t0002g0063 a0001c0001t0002g0077 others(4): Show |
7 | NA18948.hp1 NA18966.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-738_345-737ins others(96): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | |||||||
| chr15:92631082 | A | ATATATTA others(68): Show |
1 | a0001c0001t0001g0303 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345-738_345-737ins others(75): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | |||||||
| chr15:92631082 | A | ATATATTA others(95): Show |
1 | a0001c0001t0002g0320 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.345-738_345-737ins others(102): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | |||||||
| chr15:92631082 | ATATATTA others(26): Show |
A | 2 | a0001c0001t0010g0349 a0001c0001t0012g0350 |
2 | HG00733.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.345-770_345-738del others(33): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | |||||||
| chr15:92631083 | T | C | 2 | a0001c0001t0012g0085 a0005c0012t0003g0380 |
2 | HG01496.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.345-738A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631083 | |||||||
| chr15:92631084 | A | G | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.345-739T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631084 | |||||||
| chr15:92631088 | T | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-743A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631088 | |||||||
| chr15:92631090 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0014g0092 |
2 | HG01106.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.345-745A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631090 | |||||||
| chr15:92631091 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0014g0092 |
2 | HG01106.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.345-746T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631091 | |||||||
| chr15:92631097 | C | T | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0340 |
3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-752G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631097 | |||||||
| chr15:92631098 | G | A | 5 | a0001c0001t0001g0248 a0001c0001t0004g0113 a0001c0001t0004g0114 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-753C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631098 | |||||||
| chr15:92631100 | A | T | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-755T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631100 | |||||||
| chr15:92631101 | T | A | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-756A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631101 | |||||||
| chr15:92631104 | C | T | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-759G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631104 | |||||||
| chr15:92631105 | A | G | 34 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 others(31): Show |
35 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.345-760T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631105 | |||||||
| chr15:92631107 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-762T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631107 | |||||||
| chr15:92631111 | C | T | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0340 |
3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-766G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631111 | |||||||
| chr15:92631111 | CATATTAT others(57): Show |
C | 3 | a0001c0001t0001g0216 a0001c0001t0007g0047 a0001c0001t0036g0292 |
3 | HG04184.hp1 NA19087.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.345-830_345-767del others(64): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631111 | |||||||
| chr15:92631112 | A | G | 2 | a0001c0001t0007g0348 a0001c0001t0016g0341 |
2 | HG00099.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.345-767T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631112 | |||||||
| chr15:92631115 | T | TTA | 165 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0071 others(162): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.345-772_345-771dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631115 | |||||||
| chr15:92631115 | T | TTATATAT others(258): Show |
1 | a0001c0001t0001g0040 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.345-771_345-770ins others(265): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631115 | |||||||
| chr15:92631123 | T | C | 1 | a0001c0001t0014g0092 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.345-778A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631123 | |||||||
| chr15:92631124 | A | G | 1 | a0001c0001t0014g0092 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.345-779T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631124 | |||||||
| chr15:92631128 | T | A | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0340 |
3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-783A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631128 | |||||||
| chr15:92631130 | C | T | 5 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0340 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-785G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631130 | |||||||
| chr15:92631131 | G | A | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0340 |
3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-786C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631131 | |||||||
| chr15:92631137 | C | T | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0340 |
3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-792G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631137 | |||||||
| chr15:92631138 | A | G | 36 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 others(33): Show |
37 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.345-793T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631138 | |||||||
| chr15:92631140 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-795T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631140 | |||||||
| chr15:92631144 | C | T | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0340 |
3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-799G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631144 | |||||||
| chr15:92631144 | CATATTAT others(24): Show |
C | 82 | a0001c0001t0001g0039 a0001c0001t0001g0134 a0001c0001t0001g0161 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.345-830_345-800del others(31): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631144 | |||||||
| chr15:92631145 | A | G | 1 | a0001c0001t0016g0341 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.345-800T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631145 | |||||||
| chr15:92631145 | ATATTATA others(27): Show |
A | 1 | a0001c0001t0024g0209 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.345-834_345-801del others(34): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631145 | |||||||
| chr15:92631147 | A | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-802T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631147 | |||||||
| chr15:92631148 | T | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-803A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | |||||||
| chr15:92631148 | T | TTA | 67 | a0001c0001t0001g0040 a0001c0001t0001g0124 a0001c0001t0001g0144 others(64): Show |
68 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.345-805_345-804dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | |||||||
| chr15:92631148 | T | TTACATAT others(316): Show |
1 | a0001c0001t0012g0085 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.345-804_345-803ins others(323): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | |||||||
| chr15:92631148 | T | TTATATAT others(274): Show |
1 | a0001c0001t0014g0092 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.345-804_345-803ins others(281): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | |||||||
| chr15:92631148 | T | TTATATAT others(215): Show |
1 | a0001c0001t0001g0072 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.345-804_345-803ins others(222): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | |||||||
| chr15:92631148 | T | TTATATAT others(180): Show |
1 | a0001c0001t0002g0089 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.345-804_345-803ins others(187): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | |||||||
| chr15:92631149 | T | TATATATT others(16): Show |
1 | a0001c0001t0001g0288 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.345-805_345-804ins others(23): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | |||||||
| chr15:92631149 | T | TATATATT others(23): Show |
2 | a0001c0001t0015g0107 a0001c0001t0015g0109 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.345-805_345-804ins others(30): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | |||||||
| chr15:92631149 | T | TATATATT others(227): Show |
2 | a0001c0001t0001g0093 a0006c0007t0001g0008 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.345-805_345-804ins others(234): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | |||||||
| chr15:92631149 | T | TATATATT others(91): Show |
1 | a0001c0001t0019g0041 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.345-805_345-804ins others(98): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | |||||||
| chr15:92631149 | T | TATATATT others(157): Show |
1 | a0001c0001t0007g0065 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.345-805_345-804ins others(164): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | |||||||
| chr15:92631149 | T | TATATATT others(56): Show |
1 | a0001c0001t0003g0042 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.345-805_345-804ins others(63): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | |||||||
| chr15:92631149 | T | TATATATT others(84): Show |
1 | a0001c0001t0001g0286 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.345-805_345-804ins others(91): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | |||||||
| chr15:92631149 | T | TATATATT others(89): Show |
8 | a0001c0001t0001g0309 a0001c0001t0002g0053 a0001c0001t0002g0058 others(5): Show |
8 | HG00423.hp1 HG02071.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-805_345-804ins others(96): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | |||||||
| chr15:92631149 | T | TATATATT others(122): Show |
1 | a0001c0001t0005g0314 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.345-805_345-804ins others(129): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | |||||||
| chr15:92631159 | A | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-814T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631159 | |||||||
| chr15:92631160 | T | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-815A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | |||||||
| chr15:92631160 | T | TTA | 4 | a0001c0001t0001g0072 a0001c0001t0002g0089 a0001c0001t0012g0085 others(1): Show |
4 | HG01496.hp1 HG01943.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-817_345-816dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | |||||||
| chr15:92631160 | T | TTACGTAT others(114): Show |
2 | a0001c0001t0007g0100 a0001c0001t0013g0099 |
2 | HG03017.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.345-816_345-815ins others(121): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | |||||||
| chr15:92631160 | T | TTACGTAT others(163): Show |
1 | a0001c0001t0013g0149 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.345-816_345-815ins others(170): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | |||||||
| chr15:92631160 | T | TTACGTAT others(147): Show |
1 | a0001c0001t0002g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.345-816_345-815ins others(154): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | |||||||
| chr15:92631160 | T | TTACGTAT others(182): Show |
1 | a0001c0001t0001g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.345-816_345-815ins others(189): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | |||||||
| chr15:92631160 | T | TTACGTAT others(250): Show |
1 | a0001c0001t0001g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.345-816_345-815ins others(257): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | |||||||
| chr15:92631160 | TTATATAA others(26): Show |
T | 2 | a0001c0001t0001g0326 a0001c0001t0002g0291 |
2 | HG02056.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.345-848_345-816del others(33): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | |||||||
| chr15:92631161 | T | TACGTATT others(9): Show |
1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-817_345-816ins others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631161 | |||||||
| chr15:92631162 | A | ACG | 63 | a0001c0001t0001g0040 a0001c0001t0001g0144 a0001c0001t0001g0177 others(60): Show |
64 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.345-818_345-817ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | |||||||
| chr15:92631162 | A | ACGTATTA others(58): Show |
3 | a0001c0001t0001g0290 a0001c0001t0001g0294 a0001c0001t0012g0289 |
3 | NA18952.hp2 NA18970.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.345-818_345-817ins others(65): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | |||||||
| chr15:92631162 | A | ACGTATTA others(30): Show |
11 | a0001c0001t0001g0317 a0001c0001t0002g0094 a0001c0001t0004g0069 others(8): Show |
11 | HG00735.hp1 HG00735.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-818_345-817ins others(37): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | |||||||
| chr15:92631162 | A | ACGTATTA others(63): Show |
21 | a0001c0001t0001g0071 a0001c0001t0001g0095 a0001c0001t0001g0097 others(18): Show |
21 | HG00558.hp2 HG02683.hp1 HG03669.hp2 others(18): Show |
intron_variant | MODIFIER | c.345-818_345-817ins others(70): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | |||||||
| chr15:92631162 | A | ACGTATTA others(98): Show |
1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-818_345-817ins others(105): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | |||||||
| chr15:92631162 | A | ACGTATTA others(96): Show |
6 | a0001c0001t0001g0052 a0001c0001t0001g0096 a0001c0001t0001g0098 others(3): Show |
6 | HG00408.hp1 HG01515.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-818_345-817ins others(103): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | |||||||
| chr15:92631162 | ATATAATA others(22): Show |
A | 1 | a0001c0001t0009g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.345-846_345-818del others(29): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | |||||||
| chr15:92631162 | ATATAATA others(92): Show |
A | 1 | a0001c0001t0021g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.345-916_345-818del others(99): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | |||||||
| chr15:92631163 | T | C | 10 | a0001c0001t0002g0022 a0001c0001t0002g0116 a0001c0001t0006g0272 others(7): Show |
10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-818A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631163 | |||||||
| chr15:92631163 | TATAATAA others(59): Show |
T | 2 | a0001c0001t0037g0381 a0001c0001t0037g0382 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-884_345-819del others(66): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631163 | |||||||
| chr15:92631163 | TATAATAA others(85): Show |
T | 3 | a0001c0001t0002g0155 a0001c0001t0056g0207 a0007c0011t0025g0365 |
3 | NA18947.hp1 NA19006.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.345-910_345-819del others(92): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631163 | |||||||
| chr15:92631164 | A | G | 10 | a0001c0001t0002g0022 a0001c0001t0002g0116 a0001c0001t0006g0272 others(7): Show |
10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-819T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631164 | |||||||
| chr15:92631164 | ATAATAAT others(50): Show |
A | 1 | a0001c0001t0020g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.345-876_345-820del others(57): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631164 | |||||||
| chr15:92631166 | A | ATATTAC | 4 | a0001c0001t0001g0088 a0001c0001t0001g0306 a0001c0001t0002g0036 others(1): Show |
4 | HG02280.hp2 NA19055.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-822_345-821ins others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | |||||||
| chr15:92631166 | A | ATATTACA others(43): Show |
2 | a0001c0001t0001g0086 a0001c0010t0012g0082 |
2 | HG00558.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.345-822_345-821ins others(50): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | |||||||
| chr15:92631166 | A | ATATTACA others(81): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0087 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.345-822_345-821ins others(88): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | |||||||
| chr15:92631166 | A | T | 106 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(103): Show |
107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.345-821T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | |||||||
| chr15:92631166 | AATAAT | A | 12 | a0001c0001t0002g0022 a0001c0001t0002g0116 a0001c0001t0006g0268 others(9): Show |
12 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-826_345-822del others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | |||||||
| chr15:92631167 | A | ACG | 3 | a0001c0001t0008g0012 a0001c0001t0008g0014 a0001c0001t0033g0028 |
3 | HG02895.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-823_345-822ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631167 | |||||||
| chr15:92631167 | A | T | 18 | a0001c0001t0001g0093 a0001c0001t0001g0286 a0001c0001t0001g0288 others(15): Show |
18 | HG00423.hp1 HG00741.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.345-822T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631167 | |||||||
| chr15:92631168 | T | C | 101 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(98): Show |
102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.345-823A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631168 | |||||||
| chr15:92631169 | A | ACGTATTA others(1): Show |
18 | a0001c0001t0001g0093 a0001c0001t0001g0286 a0001c0001t0001g0288 others(15): Show |
18 | HG00423.hp1 HG00741.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.345-825_345-824ins others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631169 | |||||||
| chr15:92631169 | A | G | 8 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0003g0334 others(5): Show |
9 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-824T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631169 | |||||||
| chr15:92631170 | A | T | 124 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(121): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.345-825T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631170 | |||||||
| chr15:92631171 | T | A | 119 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(116): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.345-826A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631171 | |||||||
| chr15:92631171 | T | TA | 18 | a0001c0001t0001g0093 a0001c0001t0001g0286 a0001c0001t0001g0288 others(15): Show |
18 | HG00423.hp1 HG00741.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.345-827_345-826ins others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631171 | |||||||
| chr15:92631172 | T | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0004g0340 others(4): Show |
7 | HG01928.hp1 HG01978.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-827A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631172 | |||||||
| chr15:92631173 | T | C | 3 | a0001c0001t0008g0012 a0001c0001t0008g0014 a0001c0001t0033g0028 |
3 | HG02895.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-828A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631173 | |||||||
| chr15:92631175 | T | C | 131 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(128): Show |
132 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.345-830A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631175 | |||||||
| chr15:92631176 | A | G | 10 | a0001c0001t0002g0022 a0001c0001t0006g0268 a0001c0001t0006g0269 others(7): Show |
10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-831T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631176 | |||||||
| chr15:92631178 | A | T | 3 | a0001c0001t0008g0012 a0001c0001t0008g0014 a0001c0001t0033g0028 |
3 | HG02895.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-833T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631178 | |||||||
| chr15:92631179 | T | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0308 others(6): Show |
9 | HG00673.hp2 HG01928.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-834A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631179 | |||||||
| chr15:92631179 | T | TTA | 3 | a0001c0001t0004g0131 a0001c0001t0004g0133 a0001c0001t0018g0262 |
3 | HG00741.hp1 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.345-836_345-835dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631179 | |||||||
| chr15:92631179 | TTATATTA | T | 4 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0001c0001t0047g0111 others(1): Show |
4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-841_345-835del others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631179 | |||||||
| chr15:92631179 | TTATATTA others(70): Show |
T | 1 | a0001c0001t0009g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.345-911_345-835del others(77): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631179 | |||||||
| chr15:92631180 | T | TAC | 12 | a0001c0001t0002g0022 a0001c0001t0002g0116 a0001c0001t0006g0268 others(9): Show |
12 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-836_345-835ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631180 | |||||||
| chr15:92631180 | T | TACGTATT others(9): Show |
1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-836_345-835ins others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631180 | |||||||
| chr15:92631187 | T | C | 2 | a0001c0001t0006g0268 a0001c0001t0006g0269 |
2 | NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-842A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631187 | |||||||
| chr15:92631191 | TTATA | T | 7 | a0001c0001t0001g0308 a0001c0001t0001g0315 a0001c0001t0001g0346 others(4): Show |
7 | HG00673.hp2 HG00733.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-850_345-847del others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631191 | |||||||
| chr15:92631191 | TTATATAT others(91): Show |
T | 1 | a0001c0001t0024g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.345-944_345-847del others(98): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631191 | |||||||
| chr15:92631192 | T | A | 16 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0086 others(13): Show |
16 | HG00544.hp1 HG00558.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-847A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631192 | |||||||
| chr15:92631193 | A | ACGTAT | 14 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0003g0334 others(11): Show |
15 | HG00140.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-849_345-848ins others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631193 | |||||||
| chr15:92631193 | A | ATATAT | 5 | a0001c0001t0001g0088 a0001c0001t0001g0306 a0001c0001t0002g0036 others(2): Show |
5 | HG02280.hp2 NA19003.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-853_345-849dup others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631193 | |||||||
| chr15:92631194 | T | TATATA | 10 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0086 others(7): Show |
10 | HG00544.hp1 HG00558.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-854_345-850dup others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631194 | |||||||
| chr15:92631195 | A | AT | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0013g0149 |
3 | HG02027.hp1 HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-851dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631195 | |||||||
| chr15:92631196 | T | C | 16 | a0001c0001t0001g0326 a0001c0001t0001g0344 a0001c0001t0002g0005 others(13): Show |
17 | HG00140.hp2 HG00741.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-851A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631196 | |||||||
| chr15:92631196 | TATATTAC others(48): Show |
T | 5 | a0001c0001t0007g0348 a0001c0001t0016g0341 a0001c0001t0016g0351 others(2): Show |
5 | HG00099.hp1 HG00544.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-906_345-852del others(55): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631196 | |||||||
| chr15:92631197 | A | ATTACG | 10 | a0001c0001t0001g0124 a0001c0001t0002g0022 a0001c0001t0006g0272 others(7): Show |
10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-853_345-852ins others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631197 | |||||||
| chr15:92631197 | A | G | 13 | a0001c0001t0001g0326 a0001c0001t0001g0344 a0001c0001t0002g0005 others(10): Show |
14 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.345-852T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631197 | |||||||
| chr15:92631197 | ATATTACA others(65): Show |
A | 1 | a0001c0001t0006g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-924_345-853del others(72): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631197 | |||||||
| chr15:92631199 | ATTAC | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0004g0340 |
3 | HG01928.hp1 HG01978.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-858_345-855del others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631199 | |||||||
| chr15:92631200 | T | A | 1 | a0001c0001t0014g0070 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.345-855A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631200 | |||||||
| chr15:92631201 | T | A | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0013g0149 |
3 | HG02027.hp1 HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-856A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631201 | |||||||
| chr15:92631201 | TAC | T | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-858_345-857del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631201 | |||||||
| chr15:92631202 | A | ATATAT | 4 | a0001c0001t0001g0088 a0001c0001t0002g0036 a0001c0001t0010g0038 others(1): Show |
4 | HG02280.hp2 NA19003.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-858_345-857ins others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631202 | |||||||
| chr15:92631202 | A | T | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0013g0149 |
3 | HG02027.hp1 HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-857T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631202 | |||||||
| chr15:92631203 | C | A | 7 | a0001c0001t0001g0088 a0001c0001t0002g0036 a0001c0001t0004g0113 others(4): Show |
7 | HG02027.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-858G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | |||||||
| chr15:92631203 | C | CATATATT others(19): Show |
1 | a0002c0002t0004g0374 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.345-884_345-859dup others(26): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | |||||||
| chr15:92631203 | C | CGTGTTAC others(5): Show |
1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-859_345-858ins others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | |||||||
| chr15:92631203 | C | T | 23 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0086 others(20): Show |
23 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.345-858G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | |||||||
| chr15:92631203 | CAT | C | 12 | a0001c0001t0001g0326 a0001c0001t0002g0022 a0001c0001t0002g0116 others(9): Show |
12 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-860_345-859del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | |||||||
| chr15:92631203 | CATATATT others(19): Show |
C | 8 | a0001c0001t0045g0126 a0001c0001t0055g0125 a0002c0002t0004g0372 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-884_345-859del others(26): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | |||||||
| chr15:92631204 | A | ATAT | 12 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0003g0334 others(9): Show |
13 | HG00140.hp2 HG00741.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-862_345-860dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631204 | |||||||
| chr15:92631206 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0002g0116 a0001c0001t0008g0137 others(6): Show |
9 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-861T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631206 | |||||||
| chr15:92631206 | A | T | 92 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(89): Show |
96 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.345-861T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631206 | |||||||
| chr15:92631208 | A | T | 2 | a0001c0001t0008g0012 a0001c0001t0033g0028 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-863T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631208 | |||||||
| chr15:92631209 | T | A | 16 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0086 others(13): Show |
16 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-864A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631209 | |||||||
| chr15:92631212 | T | C | 14 | a0001c0001t0001g0326 a0001c0001t0002g0022 a0001c0001t0002g0116 others(11): Show |
14 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-867A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631212 | |||||||
| chr15:92631213 | A | G | 2 | a0001c0001t0006g0268 a0001c0001t0006g0269 |
2 | NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-868T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631213 | |||||||
| chr15:92631215 | A | T | 15 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0086 others(12): Show |
15 | HG00544.hp1 HG00558.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-870T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631215 | |||||||
| chr15:92631216 | T | A | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0086 others(14): Show |
17 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-871A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | |||||||
| chr15:92631216 | T | TTATATTA others(82): Show |
1 | a0001c0001t0002g0304 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.345-872_345-871ins others(89): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | |||||||
| chr15:92631216 | T | TTATATTA others(129): Show |
1 | a0001c0001t0006g0078 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.345-872_345-871ins others(136): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | |||||||
| chr15:92631216 | TTATATTA others(66): Show |
T | 2 | a0001c0001t0002g0175 a0001c0001t0005g0217 |
2 | NA19001.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.345-944_345-872del others(73): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | |||||||
| chr15:92631216 | TTATATTA others(113): Show |
T | 1 | a0001c0001t0003g0051 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.345-991_345-872del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | |||||||
| chr15:92631217 | T | TACGTATT others(2): Show |
3 | a0001c0001t0004g0131 a0001c0001t0004g0133 a0001c0001t0018g0262 |
3 | HG00741.hp1 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.345-873_345-872ins others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631217 | |||||||
| chr15:92631217 | TATATTAT others(92): Show |
T | 1 | a0001c0001t0062g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.345-971_345-873del others(99): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631217 | |||||||
| chr15:92631219 | T | C | 2 | a0001c0001t0006g0268 a0001c0001t0006g0269 |
2 | NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-874A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631219 | |||||||
| chr15:92631221 | TTATATAT others(181): Show |
T | 1 | a0001c0001t0009g0019 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.345-1064_345-877de others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631221 | |||||||
| chr15:92631222 | T | A | 11 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0003g0334 others(8): Show |
12 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-877A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631222 | |||||||
| chr15:92631223 | A | T | 2 | a0001c0001t0006g0268 a0001c0001t0006g0269 |
2 | NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-878T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631223 | |||||||
| chr15:92631223 | ATATATAA others(104): Show |
A | 69 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(66): Show |
70 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.345-989_345-879del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631223 | |||||||
| chr15:92631224 | T | C | 5 | a0001c0001t0004g0131 a0001c0001t0004g0133 a0001c0001t0008g0012 others(2): Show |
5 | HG00741.hp1 HG03225.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-879A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631224 | |||||||
| chr15:92631224 | TATATAAT others(97): Show |
T | 8 | a0001c0001t0002g0355 a0001c0001t0009g0194 a0001c0001t0015g0197 others(5): Show |
9 | HG02970.hp1 NA18953.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-983_345-880del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631224 | |||||||
| chr15:92631225 | A | G | 2 | a0001c0001t0008g0012 a0001c0001t0033g0028 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-880T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631225 | |||||||
| chr15:92631225 | ATATAATA others(174): Show |
A | 7 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0021 others(4): Show |
9 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-1061_345-881de others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631225 | |||||||
| chr15:92631226 | T | A | 8 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0003g0334 others(5): Show |
9 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-881A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631226 | |||||||
| chr15:92631226 | T | C | 5 | a0001c0001t0001g0124 a0001c0001t0002g0116 a0001c0001t0006g0268 others(2): Show |
5 | HG02895.hp2 NA19002.hp1 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-881A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631226 | |||||||
| chr15:92631226 | TATAATAT others(83): Show |
T | 1 | a0001c0001t0007g0263 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.345-971_345-882del others(90): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631226 | |||||||
| chr15:92631227 | A | T | 10 | a0001c0001t0001g0306 a0001c0001t0001g0344 a0001c0001t0002g0005 others(7): Show |
11 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-882T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631227 | |||||||
| chr15:92631228 | T | A | 2 | a0001c0001t0001g0306 a0001c0001t0020g0143 |
2 | HG06807.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.345-883A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631228 | |||||||
| chr15:92631229 | A | ATT | 3 | a0001c0001t0003g0167 a0001c0001t0003g0274 a0001c0001t0021g0361 |
3 | HG01346.hp1 HG01515.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.345-885_345-884ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631229 | |||||||
| chr15:92631229 | A | C | 1 | a0001c0001t0020g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.345-884T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631229 | |||||||
| chr15:92631229 | A | T | 25 | a0001c0001t0001g0306 a0001c0001t0001g0326 a0001c0001t0001g0344 others(22): Show |
26 | HG00140.hp2 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.345-884T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631229 | |||||||
| chr15:92631230 | A | T | 6 | a0001c0001t0001g0124 a0001c0001t0002g0116 a0001c0001t0006g0268 others(3): Show |
6 | HG00673.hp1 HG02895.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-885T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631230 | |||||||
| chr15:92631231 | T | C | 12 | a0001c0001t0001g0326 a0001c0001t0002g0022 a0001c0001t0002g0291 others(9): Show |
12 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-886A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631231 | |||||||
| chr15:92631232 | A | G | 12 | a0001c0001t0001g0326 a0001c0001t0002g0022 a0001c0001t0002g0291 others(9): Show |
12 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-887T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631232 | |||||||
| chr15:92631232 | ATATTATA others(3): Show |
A | 1 | a0001c0001t0007g0215 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.345-897_345-888del others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631232 | |||||||
| chr15:92631235 | T | A | 1 | a0001c0001t0001g0306 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.345-890A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631235 | |||||||
| chr15:92631236 | T | A | 4 | a0001c0001t0001g0088 a0001c0001t0002g0036 a0001c0001t0006g0272 others(1): Show |
4 | NA18940.hp2 NA19003.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-891A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631236 | |||||||
| chr15:92631236 | T | TATATATT others(54): Show |
1 | a0001c0001t0008g0287 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.345-892_345-891ins others(61): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631236 | |||||||
| chr15:92631236 | TATATATT others(12): Show |
T | 1 | a0001c0001t0001g0211 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.345-910_345-892del others(19): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631236 | |||||||
| chr15:92631237 | A | T | 1 | a0001c0001t0006g0272 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.345-892T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631237 | |||||||
| chr15:92631237 | ATATAT | A | 27 | a0001c0001t0001g0032 a0001c0001t0001g0098 a0001c0001t0001g0134 others(24): Show |
27 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.345-897_345-893del others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631237 | |||||||
| chr15:92631238 | T | C | 14 | a0001c0001t0001g0326 a0001c0001t0002g0022 a0001c0001t0002g0291 others(11): Show |
14 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-893A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631238 | |||||||
| chr15:92631238 | TATATTAT others(71): Show |
T | 5 | a0001c0001t0002g0212 a0001c0001t0002g0321 a0001c0001t0015g0128 others(2): Show |
5 | HG00140.hp1 HG01884.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-971_345-894del others(78): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631238 | |||||||
| chr15:92631239 | A | G | 8 | a0001c0001t0002g0022 a0001c0001t0008g0137 a0001c0001t0010g0015 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-894T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631239 | |||||||
| chr15:92631240 | T | C | 1 | a0001c0001t0006g0272 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.345-895A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631240 | |||||||
| chr15:92631241 | A | T | 8 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0003g0334 others(5): Show |
9 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-896T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631241 | |||||||
| chr15:92631242 | T | A | 10 | a0001c0001t0001g0204 a0001c0001t0001g0306 a0001c0001t0001g0344 others(7): Show |
11 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-897A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631242 | T | TTA | 7 | a0001c0001t0001g0330 a0001c0001t0003g0105 a0001c0001t0006g0247 others(4): Show |
7 | HG02055.hp1 HG04184.hp1 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-899_345-898dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631242 | T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0088 a0001c0001t0002g0036 |
2 | NA19056.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.345-898_345-897ins others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631242 | T | TTATATAT others(21): Show |
3 | a0001c0001t0003g0042 a0001c0001t0019g0041 a0001c0008t0001g0011 |
3 | HG00741.hp2 HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.345-898_345-897ins others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631242 | T | TTATATAT others(53): Show |
1 | a0001c0001t0002g0320 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.345-898_345-897ins others(60): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631242 | T | TTATATAT others(56): Show |
19 | a0001c0001t0001g0071 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
19 | HG00423.hp1 HG01934.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.345-898_345-897ins others(63): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631242 | T | TTATATAT others(77): Show |
2 | a0001c0001t0001g0040 a0001c0001t0006g0062 |
2 | HG01106.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.345-898_345-897ins others(84): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631242 | T | TTATATAT others(54): Show |
1 | a0001c0001t0001g0295 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.345-898_345-897ins others(61): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631242 | T | TTATATAT others(56): Show |
1 | a0001c0001t0001g0303 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345-898_345-897ins others(63): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631242 | T | TTATATAT others(4): Show |
1 | a0001c0001t0059g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.345-898_345-897ins others(11): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | |||||||
| chr15:92631243 | TATATTAT others(5): Show |
T | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-910_345-899del others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631243 | |||||||
| chr15:92631243 | TATATTAT others(31): Show |
T | 3 | a0001c0001t0007g0129 a0001c0001t0021g0127 a0001c0001t0031g0130 |
3 | HG03491.hp2 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.345-936_345-899del others(38): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631243 | |||||||
| chr15:92631244 | A | ACG | 4 | a0001c0001t0001g0124 a0001c0001t0004g0131 a0001c0001t0004g0133 others(1): Show |
4 | HG00741.hp1 HG03834.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-900_345-899ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631244 | |||||||
| chr15:92631245 | T | C | 8 | a0001c0001t0002g0022 a0001c0001t0008g0137 a0001c0001t0010g0015 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-900A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631245 | |||||||
| chr15:92631245 | TATTATAT others(64): Show |
T | 83 | a0001c0001t0001g0039 a0001c0001t0001g0161 a0001c0001t0001g0164 others(80): Show |
84 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.345-971_345-901del others(71): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631245 | |||||||
| chr15:92631246 | AT | A | 3 | a0001c0001t0002g0116 a0001c0001t0006g0268 a0001c0001t0006g0269 |
3 | NA19002.hp1 NA19079.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.345-902delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631246 | |||||||
| chr15:92631247 | T | TATAATA | 37 | a0001c0001t0001g0052 a0001c0001t0001g0144 a0001c0001t0001g0283 others(34): Show |
37 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.345-903_345-902ins others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631247 | |||||||
| chr15:92631248 | T | A | 13 | a0001c0001t0002g0022 a0001c0001t0003g0042 a0001c0001t0003g0105 others(10): Show |
13 | HG00741.hp2 HG01109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-903A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631248 | |||||||
| chr15:92631249 | A | AT | 37 | a0001c0001t0001g0052 a0001c0001t0001g0144 a0001c0001t0001g0283 others(34): Show |
37 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.345-905dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631249 | |||||||
| chr15:92631249 | A | T | 10 | a0001c0001t0002g0022 a0001c0001t0008g0014 a0001c0001t0008g0137 others(7): Show |
10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-904T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631249 | |||||||
| chr15:92631250 | T | C | 3 | a0001c0001t0004g0131 a0001c0001t0004g0133 a0001c0001t0018g0262 |
3 | HG00741.hp1 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.345-905A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631250 | |||||||
| chr15:92631252 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-907A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631252 | |||||||
| chr15:92631253 | A | T | 11 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0002g0116 others(8): Show |
12 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-908T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631253 | |||||||
| chr15:92631254 | T | A | 11 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0002g0116 others(8): Show |
12 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-909A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631254 | |||||||
| chr15:92631254 | TA | T | 5 | a0001c0001t0007g0348 a0001c0001t0016g0341 a0001c0001t0016g0351 others(2): Show |
5 | HG00099.hp1 HG00544.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-910delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631254 | |||||||
| chr15:92631255 | A | C | 3 | a0001c0001t0002g0116 a0001c0001t0006g0268 a0001c0001t0006g0269 |
3 | NA19002.hp1 NA19079.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.345-910T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631255 | |||||||
| chr15:92631255 | A | T | 42 | a0001c0001t0001g0134 a0001c0001t0001g0231 a0001c0001t0001g0285 others(39): Show |
43 | HG00140.hp2 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.345-910T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631255 | |||||||
| chr15:92631256 | A | T | 39 | a0001c0001t0001g0052 a0001c0001t0001g0124 a0001c0001t0001g0144 others(36): Show |
39 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.345-911T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631256 | |||||||
| chr15:92631257 | T | C | 5 | a0001c0001t0004g0131 a0001c0001t0004g0133 a0001c0001t0008g0012 others(2): Show |
5 | HG00741.hp1 HG03225.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-912A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631257 | |||||||
| chr15:92631258 | A | G | 2 | a0001c0001t0008g0012 a0001c0001t0033g0028 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-913T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631258 | |||||||
| chr15:92631260 | A | T | 1 | a0001c0001t0006g0272 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.345-915T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631260 | |||||||
| chr15:92631261 | T | A | 2 | a0001c0001t0001g0204 a0001c0001t0006g0272 |
2 | HG03942.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.345-916A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631261 | |||||||
| chr15:92631262 | T | A | 3 | a0001c0001t0002g0074 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02135.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.345-917A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631262 | |||||||
| chr15:92631264 | T | C | 7 | a0001c0001t0001g0326 a0001c0001t0002g0155 a0001c0001t0002g0291 others(4): Show |
7 | HG02056.hp2 HG03225.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-919A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631264 | |||||||
| chr15:92631265 | A | G | 4 | a0001c0001t0001g0326 a0001c0001t0002g0291 a0001c0001t0008g0012 others(1): Show |
4 | HG02056.hp2 HG03225.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-920T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631265 | |||||||
| chr15:92631265 | ATAT | A | 3 | a0001c0001t0002g0155 a0001c0001t0056g0207 a0007c0011t0025g0365 |
3 | NA18947.hp1 NA19006.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.345-923_345-921del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631265 | |||||||
| chr15:92631267 | A | T | 6 | a0001c0001t0003g0105 a0001c0001t0003g0167 a0001c0001t0003g0274 others(3): Show |
6 | HG00741.hp1 HG01346.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-922T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631267 | |||||||
| chr15:92631268 | T | A | 16 | a0001c0001t0001g0204 a0001c0001t0002g0022 a0001c0001t0003g0105 others(13): Show |
16 | HG00741.hp1 HG01109.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.345-923A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | |||||||
| chr15:92631268 | T | TAATA | 6 | a0001c0001t0004g0069 a0001c0001t0004g0081 a0001c0001t0004g0103 others(3): Show |
6 | HG00735.hp1 HG01074.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-924_345-923ins others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | |||||||
| chr15:92631268 | T | TAATATAT others(2): Show |
31 | a0001c0001t0001g0052 a0001c0001t0001g0144 a0001c0001t0001g0283 others(28): Show |
31 | HG00408.hp1 HG00558.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.345-924_345-923ins others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | |||||||
| chr15:92631268 | T | TTATATAT others(9): Show |
1 | a0001c0001t0002g0074 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.345-924_345-923ins others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | |||||||
| chr15:92631268 | T | TTATATAT others(28): Show |
2 | a0001c0001t0001g0093 a0006c0007t0001g0008 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.345-924_345-923ins others(35): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | |||||||
| chr15:92631268 | T | TTATATAT others(35): Show |
5 | a0001c0001t0015g0107 a0001c0001t0015g0109 a0001c0001t0020g0110 others(2): Show |
5 | HG01243.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-924_345-923ins others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | |||||||
| chr15:92631268 | TTATATTA others(61): Show |
T | 9 | a0001c0001t0001g0032 a0001c0001t0001g0330 a0001c0001t0006g0247 others(6): Show |
9 | HG02055.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-991_345-924del others(68): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | |||||||
| chr15:92631269 | T | A | 3 | a0001c0001t0010g0362 a0001c0001t0046g0364 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.345-924A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631269 | |||||||
| chr15:92631271 | T | A | 8 | a0001c0001t0002g0022 a0001c0001t0008g0137 a0001c0001t0010g0015 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-926A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631271 | |||||||
| chr15:92631271 | T | C | 4 | a0001c0001t0001g0326 a0001c0001t0002g0291 a0001c0001t0008g0012 others(1): Show |
4 | HG02056.hp2 HG03225.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-926A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631271 | |||||||
| chr15:92631271 | TATTATAT others(38): Show |
T | 3 | a0001c0001t0007g0254 a0001c0001t0007g0260 a0001c0001t0057g0261 |
3 | HG01496.hp2 HG01993.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.345-971_345-927del others(45): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631271 | |||||||
| chr15:92631272 | A | T | 8 | a0001c0001t0002g0022 a0001c0001t0008g0137 a0001c0001t0010g0015 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-927T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631272 | |||||||
| chr15:92631273 | T | A | 1 | a0001c0001t0006g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-928A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631273 | |||||||
| chr15:92631274 | T | A | 13 | a0001c0001t0001g0326 a0001c0001t0002g0080 a0001c0001t0002g0153 others(10): Show |
13 | HG00544.hp1 HG02056.hp2 HG03130.hp1 others(10): Show |
intron_variant | MODIFIER | c.345-929A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631274 | |||||||
| chr15:92631274 | T | C | 1 | a0001c0001t0021g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.345-929A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631274 | |||||||
| chr15:92631274 | TATATATA others(68): Show |
T | 1 | a0001c0001t0021g0361 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.345-1004_345-930de others(76): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631274 | |||||||
| chr15:92631275 | A | T | 14 | a0001c0001t0001g0124 a0001c0001t0001g0326 a0001c0001t0002g0080 others(11): Show |
14 | HG00544.hp1 HG01361.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-930T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631275 | |||||||
| chr15:92631275 | ATATATAA others(113): Show |
A | 2 | a0001c0001t0003g0167 a0001c0001t0003g0274 |
2 | HG01346.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.345-1050_345-931de others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631275 | |||||||
| chr15:92631276 | T | A | 2 | a0001c0001t0002g0080 a0001c0001t0009g0106 |
2 | HG00544.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.345-931A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631276 | |||||||
| chr15:92631276 | TATATAAT others(53): Show |
T | 1 | a0001c0001t0009g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.345-991_345-932del others(60): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631276 | |||||||
| chr15:92631276 | TATATAAT others(66): Show |
T | 1 | a0001c0001t0001g0134 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.345-1004_345-932de others(74): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631276 | |||||||
| chr15:92631277 | A | ATAT | 8 | a0001c0001t0002g0022 a0001c0001t0008g0137 a0001c0001t0010g0015 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-935_345-933dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631277 | |||||||
| chr15:92631278 | T | C | 2 | a0001c0001t0001g0326 a0001c0001t0002g0291 |
2 | HG02056.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.345-933A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631278 | |||||||
| chr15:92631280 | TAATATAT others(2): Show |
T | 3 | a0001c0001t0002g0153 a0001c0001t0003g0146 a0001c0001t0007g0152 |
3 | NA18973.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.345-944_345-936del others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631280 | |||||||
| chr15:92631281 | A | ATTAC | 3 | a0001c0001t0004g0131 a0001c0001t0004g0133 a0001c0001t0018g0262 |
3 | HG00741.hp1 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.345-937_345-936ins others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631281 | |||||||
| chr15:92631281 | A | T | 8 | a0001c0001t0001g0211 a0001c0001t0003g0105 a0001c0001t0006g0272 others(5): Show |
8 | HG01261.hp1 HG02735.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-936T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631281 | |||||||
| chr15:92631282 | A | T | 16 | a0001c0001t0001g0124 a0001c0001t0001g0326 a0001c0001t0002g0022 others(13): Show |
16 | HG00544.hp1 HG01109.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-937T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631282 | |||||||
| chr15:92631286 | ATTATATA others(2): Show |
A | 3 | a0001c0001t0002g0155 a0001c0001t0056g0207 a0007c0011t0025g0365 |
3 | NA18947.hp1 NA19006.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.345-950_345-942del others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631286 | |||||||
| chr15:92631286 | ATTATATA others(113): Show |
A | 1 | a0001c0001t0001g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.345-1061_345-942de others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631286 | |||||||
| chr15:92631288 | T | A | 12 | a0001c0001t0002g0022 a0001c0001t0002g0080 a0001c0001t0008g0137 others(9): Show |
12 | HG00544.hp1 HG01109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-943A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631288 | |||||||
| chr15:92631289 | A | ATATAT | 54 | a0001c0001t0001g0040 a0001c0001t0001g0071 a0001c0001t0001g0083 others(51): Show |
54 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.345-949_345-945dup others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631289 | |||||||
| chr15:92631289 | A | T | 10 | a0001c0001t0002g0022 a0001c0001t0002g0080 a0001c0001t0008g0137 others(7): Show |
10 | HG00544.hp1 HG01109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-944T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631289 | |||||||
| chr15:92631290 | T | A | 2 | a0001c0001t0002g0175 a0001c0001t0005g0217 |
2 | NA19001.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.345-945A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631290 | |||||||
| chr15:92631290 | T | C | 2 | a0001c0001t0010g0339 a0001c0001t0033g0336 |
2 | HG00140.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.345-945A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631290 | |||||||
| chr15:92631292 | TATTATAT others(46): Show |
T | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-1000_345-948de others(54): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631292 | |||||||
| chr15:92631294 | T | A | 2 | a0001c0001t0008g0012 a0001c0001t0033g0028 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-949A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631294 | |||||||
| chr15:92631294 | TTA | T | 3 | a0001c0001t0001g0072 a0001c0001t0002g0089 a0001c0001t0006g0078 |
3 | HG02074.hp2 NA18983.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.345-951_345-950del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631294 | |||||||
| chr15:92631294 | TTATATAT others(35): Show |
T | 2 | a0001c0001t0007g0215 a0001c0001t0024g0209 |
2 | HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.345-991_345-950del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631294 | |||||||
| chr15:92631295 | T | A | 8 | a0001c0001t0002g0175 a0001c0001t0003g0115 a0001c0001t0005g0217 others(5): Show |
8 | HG03579.hp1 NA18522.hp2 NA18990.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-950A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631295 | |||||||
| chr15:92631296 | A | ATAT | 4 | a0001c0001t0003g0042 a0001c0001t0004g0113 a0001c0001t0004g0114 others(1): Show |
4 | HG00741.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-954_345-952dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631296 | |||||||
| chr15:92631299 | TATAATAT others(65): Show |
T | 1 | a0001c0001t0001g0285 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.345-1026_345-955de others(73): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631299 | |||||||
| chr15:92631300 | A | T | 1 | a0001c0001t0002g0318 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.345-955T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631300 | |||||||
| chr15:92631300 | ATAATATA others(14): Show |
A | 1 | a0001c0001t0009g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.345-976_345-956del others(21): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631300 | |||||||
| chr15:92631300 | ATAATATA others(61): Show |
A | 1 | a0001c0001t0039g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.345-1023_345-956de others(69): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631300 | |||||||
| chr15:92631301 | T | A | 1 | a0001c0001t0002g0318 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.345-956A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631301 | |||||||
| chr15:92631302 | A | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0211 a0001c0001t0002g0089 others(14): Show |
17 | HG01099.hp2 HG01261.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-957T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631302 | |||||||
| chr15:92631303 | A | T | 3 | a0001c0001t0006g0250 a0001c0001t0008g0012 a0001c0001t0033g0028 |
3 | HG01361.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-958T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631303 | |||||||
| chr15:92631306 | T | C | 1 | a0001c0001t0006g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-961A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631306 | |||||||
| chr15:92631308 | T | A | 1 | a0001c0001t0002g0318 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.345-963A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631308 | |||||||
| chr15:92631309 | T | A | 3 | a0001c0001t0001g0072 a0001c0001t0002g0089 a0001c0001t0006g0078 |
3 | HG02074.hp2 NA18983.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.345-964A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631309 | |||||||
| chr15:92631313 | TATAA | T | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-972_345-969del others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631313 | |||||||
| chr15:92631314 | A | T | 1 | a0001c0001t0006g0272 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.345-969T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631314 | |||||||
| chr15:92631315 | T | A | 2 | a0001c0001t0002g0318 a0001c0001t0006g0272 |
2 | NA18940.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.345-970A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631315 | |||||||
| chr15:92631315 | TAATATTA others(14): Show |
T | 4 | a0001c0001t0002g0116 a0001c0001t0003g0121 a0001c0001t0006g0268 others(1): Show |
4 | HG01099.hp2 NA19002.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-991_345-971del others(21): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631315 | |||||||
| chr15:92631315 | TAATATTA others(21): Show |
T | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-998_345-971del others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631315 | |||||||
| chr15:92631316 | A | T | 143 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(140): Show |
144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.345-971T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631316 | |||||||
| chr15:92631316 | AATATT | A | 3 | a0001c0001t0007g0129 a0001c0001t0021g0127 a0001c0001t0031g0130 |
3 | HG03491.hp2 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.345-976_345-972del others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631316 | |||||||
| chr15:92631316 | AATATTAT others(47): Show |
A | 3 | a0001c0001t0002g0153 a0001c0001t0003g0146 a0001c0001t0007g0152 |
3 | NA18973.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.345-1025_345-972de others(55): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631316 | |||||||
| chr15:92631319 | AT | A | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-975delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631319 | |||||||
| chr15:92631321 | T | A | 15 | a0001c0001t0001g0072 a0001c0001t0001g0087 a0001c0001t0002g0089 others(12): Show |
15 | HG00741.hp1 HG01978.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-976A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631321 | |||||||
| chr15:92631322 | A | T | 11 | a0001c0001t0001g0072 a0001c0001t0001g0087 a0001c0001t0002g0089 others(8): Show |
11 | HG00741.hp1 HG01978.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-977T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631322 | |||||||
| chr15:92631328 | A | T | 108 | a0001c0001t0001g0039 a0001c0001t0001g0161 a0001c0001t0001g0164 others(105): Show |
109 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.345-983T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631328 | |||||||
| chr15:92631329 | A | T | 9 | a0001c0001t0001g0072 a0001c0001t0002g0089 a0001c0001t0003g0105 others(6): Show |
9 | HG00741.hp1 HG02074.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-984T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631329 | |||||||
| chr15:92631333 | A | T | 4 | a0001c0001t0004g0122 a0001c0001t0006g0250 a0001c0001t0011g0123 others(1): Show |
4 | HG00642.hp1 HG01361.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-988T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631333 | |||||||
| chr15:92631334 | T | A | 4 | a0001c0001t0004g0122 a0001c0001t0006g0250 a0001c0001t0011g0123 others(1): Show |
4 | HG00642.hp1 HG01361.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-989A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631334 | |||||||
| chr15:92631334 | TTA | T | 105 | a0001c0001t0001g0039 a0001c0001t0001g0072 a0001c0001t0001g0161 others(102): Show |
106 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.345-991_345-990del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631334 | |||||||
| chr15:92631335 | T | A | 7 | a0001c0001t0002g0005 a0001c0001t0003g0115 a0001c0001t0004g0133 others(4): Show |
8 | HG00741.hp1 HG02559.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-990A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631335 | |||||||
| chr15:92631336 | A | ATATAT | 64 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0083 others(61): Show |
64 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.345-996_345-992dup others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631336 | |||||||
| chr15:92631336 | A | T | 3 | a0001c0001t0004g0133 a0001c0001t0018g0262 a0001c0001t0021g0192 |
3 | HG00741.hp1 HG02735.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.345-991T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631336 | |||||||
| chr15:92631338 | A | G | 11 | a0001c0001t0001g0161 a0001c0001t0001g0230 a0001c0001t0005g0214 others(8): Show |
12 | HG01346.hp2 HG01496.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-993T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631338 | |||||||
| chr15:92631342 | T | A | 7 | a0001c0001t0001g0087 a0001c0001t0003g0105 a0001c0001t0007g0100 others(4): Show |
7 | HG00733.hp1 HG01975.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-997A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631342 | |||||||
| chr15:92631345 | A | ATAT | 4 | a0001c0001t0001g0071 a0001c0001t0003g0156 a0001c0001t0006g0062 others(1): Show |
4 | HG02071.hp1 HG03130.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1003_345-1001d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631345 | |||||||
| chr15:92631348 | TAATATAT others(2): Show |
T | 37 | a0001c0001t0001g0088 a0001c0001t0001g0095 a0001c0001t0001g0096 others(34): Show |
37 | HG00423.hp1 HG00673.hp2 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.345-1012_345-1004d others(11): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631348 | |||||||
| chr15:92631349 | A | T | 89 | a0001c0001t0001g0087 a0001c0001t0001g0119 a0001c0001t0001g0157 others(86): Show |
91 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.345-1004T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631349 | |||||||
| chr15:92631349 | AATATATT others(59): Show |
A | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-1070_345-1005d others(68): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631349 | |||||||
| chr15:92631350 | A | T | 5 | a0001c0001t0001g0071 a0001c0001t0002g0140 a0001c0001t0003g0156 others(2): Show |
5 | HG02071.hp1 HG03130.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-1005T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631350 | |||||||
| chr15:92631355 | TTA | T | 3 | a0001c0001t0001g0072 a0001c0001t0002g0089 a0001c0001t0006g0078 |
3 | HG02074.hp2 NA18983.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.345-1012_345-1011d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631355 | |||||||
| chr15:92631356 | T | A | 6 | a0001c0001t0002g0140 a0001c0001t0004g0122 a0001c0001t0011g0123 others(3): Show |
6 | HG00642.hp1 HG02630.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1011A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631356 | |||||||
| chr15:92631357 | A | ATATAT | 5 | a0001c0001t0001g0087 a0001c0001t0003g0105 a0001c0001t0007g0100 others(2): Show |
5 | HG01978.hp1 HG03017.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-1017_345-1013d others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | |||||||
| chr15:92631357 | A | ATATATAA others(5): Show |
3 | a0001c0001t0001g0071 a0001c0001t0003g0156 a0001c0001t0006g0062 |
3 | HG02071.hp1 NA18747.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.345-1013_345-1012i others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | |||||||
| chr15:92631357 | A | ATATATAA others(19): Show |
1 | a0001c0001t0009g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.345-1013_345-1012i others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | |||||||
| chr15:92631357 | A | ATATATTA others(5): Show |
31 | a0001c0001t0001g0040 a0001c0001t0001g0083 a0001c0001t0001g0084 others(28): Show |
31 | HG00558.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.345-1013_345-1012i others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | |||||||
| chr15:92631357 | A | ATATATTA others(29): Show |
1 | a0001c0001t0002g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.345-1013_345-1012i others(38): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | |||||||
| chr15:92631357 | A | ATATATTA others(31): Show |
26 | a0001c0001t0001g0052 a0001c0001t0001g0283 a0001c0001t0001g0288 others(23): Show |
26 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.345-1050_345-1013d others(40): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | |||||||
| chr15:92631357 | A | ATATATTA others(83): Show |
1 | a0001c0001t0002g0318 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.345-1013_345-1012i others(92): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | |||||||
| chr15:92631357 | A | ATATATTA others(123): Show |
1 | a0001c0001t0003g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.345-1013_345-1012i others(132): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | |||||||
| chr15:92631357 | A | T | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1012T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | |||||||
| chr15:92631361 | A | T | 3 | a0001c0001t0009g0194 a0001c0001t0015g0197 a0001c0001t0063g0385 |
3 | HG02970.hp1 NA18961.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.345-1016T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631361 | |||||||
| chr15:92631362 | T | A | 12 | a0001c0001t0002g0022 a0001c0001t0008g0014 a0001c0001t0008g0137 others(9): Show |
12 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-1017A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631362 | |||||||
| chr15:92631363 | T | A | 6 | a0001c0001t0001g0346 a0001c0001t0002g0140 a0001c0001t0004g0347 others(3): Show |
6 | HG00733.hp1 HG01175.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1018A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631363 | |||||||
| chr15:92631368 | T | A | 11 | a0001c0001t0001g0346 a0001c0001t0002g0005 a0001c0001t0004g0347 others(8): Show |
12 | HG00423.hp2 HG00733.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-1023A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631368 | |||||||
| chr15:92631369 | A | T | 4 | a0001c0001t0005g0068 a0001c0001t0005g0218 a0001c0001t0008g0012 others(1): Show |
4 | HG00423.hp2 HG03225.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1024T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631369 | |||||||
| chr15:92631370 | T | A | 2 | a0001c0001t0008g0012 a0001c0001t0033g0028 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-1025A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631370 | |||||||
| chr15:92631374 | TAA | T | 4 | a0001c0001t0005g0068 a0001c0001t0009g0194 a0001c0001t0015g0197 others(1): Show |
4 | HG02970.hp1 HG04204.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1031_345-1030d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631374 | |||||||
| chr15:92631375 | A | ATT | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1031_345-1030i others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631375 | |||||||
| chr15:92631375 | A | T | 77 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(74): Show |
79 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.345-1030T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631375 | |||||||
| chr15:92631375 | AATATATT others(52): Show |
A | 5 | a0001c0001t0001g0346 a0001c0001t0004g0347 a0001c0001t0010g0349 others(2): Show |
5 | HG00733.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-1089_345-1031d others(61): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631375 | |||||||
| chr15:92631376 | A | T | 3 | a0001c0001t0005g0218 a0001c0001t0008g0012 a0001c0001t0033g0028 |
3 | HG00423.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-1031T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631376 | |||||||
| chr15:92631381 | T | A | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-1036A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631381 | |||||||
| chr15:92631382 | T | A | 7 | a0001c0001t0004g0122 a0001c0001t0008g0012 a0001c0001t0011g0123 others(4): Show |
7 | HG00642.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-1037A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631382 | |||||||
| chr15:92631382 | T | C | 1 | a0001c0001t0058g0329 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.345-1037A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631382 | |||||||
| chr15:92631383 | ATATATTA others(10): Show |
A | 1 | a0001c0001t0035g0027 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.345-1055_345-1039d others(19): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631383 | |||||||
| chr15:92631387 | A | T | 75 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(72): Show |
77 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.345-1042T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631387 | |||||||
| chr15:92631388 | T | A | 77 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(74): Show |
79 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.345-1043A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631388 | |||||||
| chr15:92631388 | TTA | T | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1045_345-1044d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631388 | |||||||
| chr15:92631389 | T | A | 2 | a0001c0001t0005g0068 a0001c0001t0021g0361 |
2 | HG04204.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.345-1044A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631389 | |||||||
| chr15:92631390 | ATATAT | A | 8 | a0001c0001t0001g0134 a0001c0001t0003g0067 a0001c0001t0003g0079 others(5): Show |
8 | HG00423.hp2 HG00735.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-1050_345-1046d others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631390 | |||||||
| chr15:92631390 | ATATATTA others(3): Show |
A | 8 | a0001c0001t0002g0022 a0001c0001t0008g0014 a0001c0001t0008g0137 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-1055_345-1046d others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631390 | |||||||
| chr15:92631391 | T | C | 1 | a0001c0001t0005g0059 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.345-1046A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631391 | |||||||
| chr15:92631392 | ATAT | A | 14 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0003g0334 others(11): Show |
15 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-1050_345-1048d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631392 | |||||||
| chr15:92631393 | T | A | 1 | a0001c0001t0003g0327 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.345-1048A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631393 | |||||||
| chr15:92631394 | A | T | 74 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(71): Show |
76 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.345-1049T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631394 | |||||||
| chr15:92631395 | T | A | 80 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(77): Show |
82 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.345-1050A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631395 | |||||||
| chr15:92631396 | T | A | 2 | a0001c0001t0021g0361 a0001c0001t0033g0028 |
2 | NA18954.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-1051A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631396 | |||||||
| chr15:92631400 | T | A | 15 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0002g0005 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-1055A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631400 | |||||||
| chr15:92631400 | T | TTA | 5 | a0001c0001t0008g0012 a0001c0001t0009g0112 a0001c0001t0009g0194 others(2): Show |
5 | HG01109.hp2 HG02970.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-1057_345-1056d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631400 | |||||||
| chr15:92631401 | T | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-1056A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631401 | |||||||
| chr15:92631406 | T | A | 13 | a0001c0001t0002g0022 a0001c0001t0002g0140 a0001c0001t0004g0113 others(10): Show |
13 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-1061A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631406 | |||||||
| chr15:92631407 | A | T | 3 | a0001c0001t0002g0140 a0001c0001t0004g0113 a0001c0001t0004g0114 |
3 | HG02145.hp2 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.345-1062T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631407 | |||||||
| chr15:92631408 | T | A | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-1063A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631408 | |||||||
| chr15:92631410 | T | C | 1 | a0001c0001t0021g0361 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.345-1065A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631410 | |||||||
| chr15:92631413 | A | T | 3 | a0001c0001t0027g0335 a0001c0001t0058g0329 a0003c0004t0038g0367 |
3 | HG02280.hp1 HG03130.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.345-1068T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631413 | |||||||
| chr15:92631413 | AAT | A | 19 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0002g0080 others(16): Show |
20 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.345-1070_345-1069d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631413 | |||||||
| chr15:92631414 | A | T | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-1069T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631414 | |||||||
| chr15:92631415 | T | A | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-1070A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631415 | |||||||
| chr15:92631415 | T | C | 2 | a0001c0001t0046g0364 a0001c0001t0049g0363 |
2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.345-1070A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631415 | |||||||
| chr15:92631420 | A | T | 11 | a0001c0001t0002g0153 a0001c0001t0003g0051 a0001c0001t0003g0146 others(8): Show |
11 | HG01258.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-1075T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631420 | |||||||
| chr15:92631420 | AAT | A | 12 | a0001c0001t0002g0022 a0001c0001t0003g0170 a0001c0001t0008g0014 others(9): Show |
12 | HG00323.hp1 HG01109.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-1077_345-1076d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631420 | |||||||
| chr15:92631421 | A | T | 1 | a0001c0001t0021g0361 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.345-1076T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631421 | |||||||
| chr15:92631422 | TA | T | 7 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0021 others(4): Show |
9 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-1078delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631422 | |||||||
| chr15:92631427 | A | AAT | 7 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0008g0198 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-1084_345-1083d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631427 | |||||||
| chr15:92631427 | A | T | 3 | a0001c0001t0010g0038 a0001c0001t0037g0381 a0001c0001t0037g0382 |
3 | HG02280.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-1082T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631427 | |||||||
| chr15:92631427 | AAT | A | 4 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(1): Show |
5 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-1084_345-1083d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631427 | |||||||
| chr15:92631427 | AATATAAT | A | 15 | a0001c0001t0001g0344 a0001c0001t0002g0005 a0001c0001t0002g0140 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-1089_345-1083d others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631427 | |||||||
| chr15:92631428 | A | AT | 3 | a0001c0003t0002g0001 a0001c0003t0002g0016 a0001c0003t0002g0018 |
4 | HG02809.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1084dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631428 | |||||||
| chr15:92631432 | A | G | 2 | a0001c0001t0004g0122 a0001c0001t0011g0123 |
2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1087T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631432 | |||||||
| chr15:92631432 | A | T | 7 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-1087T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631432 | |||||||
| chr15:92631433 | A | AT | 3 | a0001c0003t0002g0001 a0001c0003t0002g0016 a0001c0003t0002g0018 |
4 | HG02809.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1089dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631433 | |||||||
| chr15:92631433 | A | T | 88 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(85): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.345-1088T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631433 | |||||||
| chr15:92631434 | T | A | 88 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(85): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.345-1089A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631434 | |||||||
| chr15:92631434 | T | TATATA | 4 | a0001c0001t0001g0124 a0001c0001t0008g0012 a0001c0001t0024g0037 others(1): Show |
4 | HG02615.hp1 HG03225.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-1090_345-1089i others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631434 | |||||||
| chr15:92631435 | A | T | 1 | a0001c0001t0021g0361 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.345-1090T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631435 | |||||||
| chr15:92631435 | AT | A | 5 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(2): Show |
6 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1091delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631435 | |||||||
| chr15:92631436 | T | TA | 3 | a0001c0003t0002g0001 a0001c0003t0002g0016 a0001c0003t0002g0018 |
4 | HG02809.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1092dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631436 | |||||||
| chr15:92631437 | A | T | 6 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0008g0198 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1092T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631437 | |||||||
| chr15:92631438 | T | A | 6 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0008g0198 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1093A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631438 | |||||||
| chr15:92631439 | T | A | 2 | a0001c0001t0001g0303 a0001c0001t0021g0361 |
2 | HG01981.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.345-1094A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631439 | |||||||
| chr15:92631443 | T | A | 8 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1098A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631443 | |||||||
| chr15:92631444 | A | T | 8 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1099T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631444 | |||||||
| chr15:92631448 | AACAT | A | 8 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1107_345-1104d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631448 | |||||||
| chr15:92631450 | C | T | 2 | a0001c0001t0016g0101 a0001c0006t0024g0102 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.345-1105G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631450 | |||||||
| chr15:92631454 | A | T | 10 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(7): Show |
12 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-1109T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631454 | |||||||
| chr15:92631459 | T | A | 8 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1114A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631459 | |||||||
| chr15:92631465 | A | AAT | 8 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1121_345-1120i others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631465 | |||||||
| chr15:92631469 | A | T | 107 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(104): Show |
107 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.345-1124T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631469 | |||||||
| chr15:92631482 | T | TTA | 338 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(335): Show |
343 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.345-1139_345-1138d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631482 | |||||||
| chr15:92631482 | T | TTATA | 7 | a0001c0001t0004g0122 a0001c0001t0004g0171 a0001c0001t0011g0123 others(4): Show |
7 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-1141_345-1138d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631482 | |||||||
| chr15:92631482 | T | TTGTA | 30 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.345-1138_345-1137i others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631482 | |||||||
| chr15:92631500 | C | CT | 7 | a0001c0001t0001g0308 a0001c0001t0001g0315 a0001c0001t0002g0320 others(4): Show |
7 | HG00673.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-1156dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631500 | |||||||
| chr15:92631500 | CT | C | 12 | a0001c0001t0001g0032 a0001c0001t0001g0216 a0001c0001t0001g0294 others(9): Show |
12 | HG01975.hp2 HG02451.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-1156delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631500 | |||||||
| chr15:92631552 | T | C | 238 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(235): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.345-1207A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631552 | |||||||
| chr15:92631564 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-1219C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631564 | |||||||
| chr15:92631590 | G | A | 7 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0008g0198 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-1245C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631590 | |||||||
| chr15:92631591 | T | C | 2 | a0001c0001t0009g0112 a0001c0001t0024g0037 |
2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.345-1246A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631591 | |||||||
| chr15:92631596 | A | G | 4 | a0001c0001t0010g0333 a0001c0001t0011g0044 a0001c0001t0011g0045 others(1): Show |
4 | HG02055.hp1 HG02886.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-1251T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631596 | |||||||
| chr15:92631656 | G | A | 1 | a0001c0001t0026g0225 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.345-1311C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631656 | |||||||
| chr15:92631678 | T | C | 1 | a0001c0001t0016g0341 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.345-1333A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631678 | |||||||
| chr15:92631791 | C | T | 1 | a0001c0001t0039g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.345-1446G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631791 | |||||||
| chr15:92631801 | C | T | 225 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(222): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.345-1456G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631801 | |||||||
| chr15:92631833 | TA | T | 373 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(370): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.345-1489delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631833 | |||||||
| chr15:92631836 | A | G | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-1491T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631836 | |||||||
| chr15:92631873 | C | T | 2 | a0001c0001t0009g0112 a0001c0001t0024g0037 |
2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.345-1528G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631873 | |||||||
| chr15:92631874 | G | C | 1 | a0001c0001t0048g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.345-1529C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631874 | |||||||
| chr15:92632013 | C | CCAAATTG others(20): Show |
3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1669_345-1668i others(29): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632013 | |||||||
| chr15:92632027 | A | G | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-1682T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632027 | |||||||
| chr15:92632093 | G | T | 1 | a0001c0001t0003g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.345-1748C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632093 | |||||||
| chr15:92632283 | G | A | 2 | a0001c0001t0009g0112 a0001c0001t0024g0037 |
2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.345-1938C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632283 | |||||||
| chr15:92632340 | A | C | 4 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0001c0001t0047g0111 others(1): Show |
4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1995T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632340 | |||||||
| chr15:92632487 | A | T | 3 | a0001c0001t0001g0303 a0001c0001t0002g0304 a0001c0001t0006g0305 |
3 | HG01934.hp1 HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.345-2142T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632487 | |||||||
| chr15:92632584 | G | A | 2 | a0001c0001t0001g0344 a0001c0001t0012g0343 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.345-2239C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632584 | |||||||
| chr15:92632680 | T | G | 1 | a0001c0001t0001g0303 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345-2335A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632680 | |||||||
| chr15:92632681 | G | T | 1 | a0001c0001t0001g0303 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345-2336C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632681 | |||||||
| chr15:92632681 | GT | G | 89 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(86): Show |
91 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.345-2337delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632681 | |||||||
| chr15:92632684 | T | G | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-2339A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632684 | |||||||
| chr15:92632717 | T | C | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-2372A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632717 | |||||||
| chr15:92632723 | T | C | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-2378A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632723 | |||||||
| chr15:92632759 | C | T | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-2414G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632759 | |||||||
| chr15:92632796 | G | A | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-2451C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632796 | |||||||
| chr15:92632858 | T | A | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.345-2513A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632858 | |||||||
| chr15:92632914 | ACT | A | 116 | a0001c0001t0001g0039 a0001c0001t0001g0134 a0001c0001t0001g0161 others(113): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.345-2571_345-2570d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632914 | |||||||
| chr15:92632934 | G | A | 1 | a0001c0001t0013g0149 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.345-2589C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632934 | |||||||
| chr15:92632968 | C | T | 101 | a0001c0001t0001g0039 a0001c0001t0001g0161 a0001c0001t0001g0164 others(98): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.345-2623G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632968 | |||||||
| chr15:92633009 | TTTG | T | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-2667_345-2665d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633009 | |||||||
| chr15:92633051 | C | CTT | 3 | a0001c0001t0006g0268 a0001c0001t0006g0269 a0001c0001t0006g0272 |
3 | NA18940.hp2 NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-2708_345-2707d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633051 | |||||||
| chr15:92633100 | A | T | 2 | a0001c0001t0002g0279 a0001c0001t0002g0280 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.345-2755T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633100 | |||||||
| chr15:92633181 | C | A | 4 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0001c0001t0047g0111 others(1): Show |
4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-2836G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633181 | |||||||
| chr15:92633203 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.345-2858G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633203 | |||||||
| chr15:92633263 | G | A | 34 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(31): Show |
35 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.345-2918C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633263 | |||||||
| chr15:92633319 | C | T | 88 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(85): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.345-2974G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633319 | |||||||
| chr15:92633334 | C | G | 10 | a0001c0001t0002g0153 a0001c0001t0003g0051 a0001c0001t0003g0146 others(7): Show |
10 | HG00642.hp1 HG01109.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-2989G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633334 | |||||||
| chr15:92633385 | A | T | 1 | a0002c0002t0015g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.345-3040T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633385 | |||||||
| chr15:92633498 | T | C | 9 | a0001c0001t0002g0140 a0001c0001t0003g0002 a0001c0001t0003g0020 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-3153A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633498 | |||||||
| chr15:92633576 | G | A | 1 | a0001c0001t0053g0138 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.345-3231C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633576 | |||||||
| chr15:92633753 | C | A | 4 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0001c0001t0047g0111 others(1): Show |
4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-3408G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633753 | |||||||
| chr15:92633786 | C | T | 1 | a0001c0001t0024g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.345-3441G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633786 | |||||||
| chr15:92633795 | A | T | 48 | a0001c0001t0001g0032 a0001c0001t0001g0124 a0001c0001t0001g0344 others(45): Show |
49 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.345-3450T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633795 | |||||||
| chr15:92633998 | C | T | 1 | a0001c0006t0002g0013 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.345-3653G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633998 | |||||||
| chr15:92634000 | A | T | 1 | a0001c0001t0002g0319 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.345-3655T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634000 | |||||||
| chr15:92634134 | C | G | 4 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0001c0001t0047g0111 others(1): Show |
4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-3789G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634134 | |||||||
| chr15:92634141 | G | A | 1 | a0001c0006t0024g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.345-3796C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634141 | |||||||
| chr15:92634158 | C | T | 7 | a0001c0001t0001g0093 a0001c0001t0009g0106 a0001c0001t0015g0107 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-3813G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634158 | |||||||
| chr15:92634341 | A | T | 1 | a0001c0001t0048g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.345-3996T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634341 | |||||||
| chr15:92634369 | A | G | 220 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(217): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.345-4024T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634369 | |||||||
| chr15:92634377 | A | T | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-4032T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634377 | |||||||
| chr15:92634420 | T | C | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-4075A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634420 | |||||||
| chr15:92634563 | A | G | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-4218T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634563 | |||||||
| chr15:92634568 | C | T | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-4223G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634568 | |||||||
| chr15:92634598 | T | C | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-4253A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634598 | |||||||
| chr15:92634712 | G | A | 9 | a0001c0001t0002g0140 a0001c0001t0003g0002 a0001c0001t0003g0020 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-4367C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634712 | |||||||
| chr15:92634738 | C | T | 2 | a0001c0001t0004g0122 a0001c0001t0011g0123 |
2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-4393G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634738 | |||||||
| chr15:92634873 | A | G | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-4528T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634873 | |||||||
| chr15:92634878 | T | C | 1 | a0001c0001t0006g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-4533A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634878 | |||||||
| chr15:92634922 | G | GT | 18 | a0001c0001t0002g0195 a0001c0001t0002g0353 a0001c0001t0002g0354 others(15): Show |
19 | HG01346.hp1 HG01515.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.345-4578dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634922 | |||||||
| chr15:92634952 | C | A | 4 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0001c0001t0047g0111 others(1): Show |
4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-4607G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634952 | |||||||
| chr15:92634985 | G | C | 32 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.345-4640C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634985 | |||||||
| chr15:92635047 | T | C | 371 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(368): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.345-4702A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635047 | |||||||
| chr15:92635077 | A | G | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-4732T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635077 | |||||||
| chr15:92635096 | G | GCC | 32 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.345-4753_345-4752d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635096 | |||||||
| chr15:92635120 | GTC | G | 224 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(221): Show |
225 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.345-4777_345-4776d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635120 | |||||||
| chr15:92635136 | CCT | C | 4 | a0001c0003t0002g0001 a0001c0003t0002g0016 a0001c0003t0002g0017 others(1): Show |
5 | HG02630.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-4793_345-4792d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635136 | |||||||
| chr15:92635158 | TCCACACA others(3): Show |
T | 93 | a0001c0001t0001g0088 a0001c0001t0001g0093 a0001c0001t0001g0098 others(90): Show |
95 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.345-4823_345-4814d others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635158 | |||||||
| chr15:92635159 | CCACACAC others(5): Show |
C | 62 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(59): Show |
64 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.345-4826_345-4815d others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635159 | |||||||
| chr15:92635159 | CCACACAC others(7): Show |
C | 6 | a0001c0001t0001g0032 a0001c0001t0005g0265 a0001c0001t0009g0034 others(3): Show |
6 | HG01258.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-4828_345-4815d others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635159 | |||||||
| chr15:92635161 | ACACACAC others(1): Show |
A | 29 | a0001c0001t0001g0124 a0001c0001t0001g0282 a0001c0001t0001g0283 others(26): Show |
29 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.345-4824_345-4817d others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635161 | |||||||
| chr15:92635163 | ACACACC | A | 175 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0134 others(172): Show |
177 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.345-4824_345-4819d others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635163 | |||||||
| chr15:92635165 | ACACC | A | 5 | a0001c0001t0003g0121 a0001c0001t0004g0133 a0001c0001t0005g0221 others(2): Show |
5 | HG01099.hp2 HG02622.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-4824_345-4821d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635165 | |||||||
| chr15:92635169 | C | A | 1 | a0001c0001t0022g0267 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.345-4824G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635169 | |||||||
| chr15:92635169 | C | CCACA | 7 | a0001c0001t0010g0362 a0002c0002t0004g0372 a0002c0002t0004g0375 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-4828_345-4825d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635169 | |||||||
| chr15:92635180 | C | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-4835G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635180 | |||||||
| chr15:92635199 | C | A | 1 | a0001c0001t0003g0325 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.345-4854G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635199 | |||||||
| chr15:92635359 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0032g0033 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-5014A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635359 | |||||||
| chr15:92635579 | C | CT | 26 | a0001c0001t0001g0039 a0001c0001t0001g0093 a0001c0001t0001g0119 others(23): Show |
27 | HG00438.hp2 HG01074.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.345-5235dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635579 | |||||||
| chr15:92635579 | CT | C | 45 | a0001c0001t0001g0032 a0001c0001t0001g0124 a0001c0001t0001g0248 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.345-5235delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635579 | |||||||
| chr15:92635772 | G | T | 7 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0161 others(4): Show |
7 | HG01346.hp2 HG01928.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-5427C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635772 | |||||||
| chr15:92635862 | T | C | 3 | a0001c0001t0010g0038 a0001c0001t0037g0381 a0001c0001t0037g0382 |
3 | HG02280.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-5517A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635862 | |||||||
| chr15:92635870 | C | T | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-5525G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635870 | |||||||
| chr15:92635871 | G | A | 1 | a0001c0001t0005g0073 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.345-5526C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635871 | |||||||
| chr15:92635923 | G | T | 1 | a0001c0001t0009g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345-5578C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635923 | |||||||
| chr15:92635924 | C | T | 1 | a0001c0001t0009g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345-5579G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635924 | |||||||
| chr15:92635945 | T | C | 33 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.345-5600A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635945 | |||||||
| chr15:92636035 | C | G | 1 | a0001c0001t0007g0117 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.345-5690G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636035 | |||||||
| chr15:92636150 | A | T | 112 | a0001c0001t0001g0032 a0001c0001t0001g0119 a0001c0001t0001g0157 others(109): Show |
116 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.345-5805T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636150 | |||||||
| chr15:92636271 | G | A | 3 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0003c0004t0004g0368 |
3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-5926C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636271 | |||||||
| chr15:92636315 | AAAT | A | 5 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0032g0033 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-5973_345-5971d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636315 | |||||||
| chr15:92636338 | A | G | 2 | a0001c0001t0007g0065 a0001c0001t0013g0099 |
2 | NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.345-5993T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636338 | |||||||
| chr15:92636354 | C | T | 33 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.345-6009G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636354 | |||||||
| chr15:92636369 | G | A | 1 | a0001c0001t0003g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.345-6024C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636369 | |||||||
| chr15:92636572 | G | A | 1 | a0001c0001t0005g0232 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.345-6227C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636572 | |||||||
| chr15:92636628 | A | AGGCT | 33 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.345-6287_345-6284d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636628 | |||||||
| chr15:92636632 | T | C | 19 | a0001c0001t0001g0040 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
19 | HG00558.hp1 HG01106.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.345-6287A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636632 | |||||||
| chr15:92636749 | C | T | 14 | a0001c0001t0001g0248 a0001c0001t0006g0004 a0001c0001t0006g0190 others(11): Show |
15 | HG01099.hp1 HG01255.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-6404G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636749 | |||||||
| chr15:92636750 | G | A | 1 | a0001c0001t0016g0351 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345-6405C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636750 | |||||||
| chr15:92637000 | A | G | 8 | a0001c0001t0002g0140 a0001c0001t0004g0122 a0001c0001t0011g0123 others(5): Show |
8 | HG00642.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-6655T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637000 | |||||||
| chr15:92637012 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.345-6667G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637012 | |||||||
| chr15:92637268 | G | A | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-6923C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637268 | |||||||
| chr15:92637484 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.345-7139C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637484 | |||||||
| chr15:92637684 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.345-7339G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637684 | |||||||
| chr15:92637688 | G | A | 7 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0001c0001t0016g0101 others(4): Show |
7 | HG00642.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-7343C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637688 | |||||||
| chr15:92637727 | C | T | 4 | a0001c0001t0002g0153 a0001c0001t0003g0051 a0001c0001t0003g0146 others(1): Show |
4 | HG01258.hp1 NA18973.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-7382G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637727 | |||||||
| chr15:92637730 | C | A | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-7385G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637730 | |||||||
| chr15:92637735 | G | A | 5 | a0001c0001t0009g0106 a0001c0001t0015g0107 a0001c0001t0015g0109 others(2): Show |
5 | HG01243.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-7390C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637735 | |||||||
| chr15:92637881 | G | C | 1 | a0006c0007t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.345-7536C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637881 | |||||||
| chr15:92637890 | A | G | 378 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(375): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.345-7545T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637890 | |||||||
| chr15:92637993 | G | A | 3 | a0001c0001t0002g0080 a0001c0001t0006g0062 a0001c0001t0006g0078 |
3 | HG00544.hp1 NA18983.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.345-7648C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637993 | |||||||
| chr15:92638139 | C | T | 1 | a0001c0001t0016g0352 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.345-7794G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638139 | |||||||
| chr15:92638254 | C | T | 2 | a0001c0001t0037g0381 a0001c0001t0037g0382 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-7909G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638254 | |||||||
| chr15:92638265 | G | A | 244 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0124 others(241): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.345-7920C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638265 | |||||||
| chr15:92638433 | C | T | 1 | a0001c0001t0013g0149 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.345-8088G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638433 | |||||||
| chr15:92638467 | G | C | 1 | a0001c0001t0003g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.345-8122C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638467 | |||||||
| chr15:92638471 | G | A | 1 | a0001c0001t0003g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.345-8126C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638471 | |||||||
| chr15:92638471 | G | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0233 a0001c0001t0025g0234 |
3 | HG00438.hp2 HG02523.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.345-8126C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638471 | |||||||
| chr15:92638475 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.345-8130G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638475 | |||||||
| chr15:92638498 | C | T | 7 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0001c0001t0016g0101 others(4): Show |
7 | HG00642.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-8153G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638498 | |||||||
| chr15:92638582 | G | A | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-8237C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638582 | |||||||
| chr15:92638654 | C | T | 134 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0052 others(131): Show |
136 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.345-8309G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638654 | |||||||
| chr15:92638706 | G | A | 1 | a0001c0001t0004g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.345-8361C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638706 | |||||||
| chr15:92638819 | G | A | 12 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0122 others(9): Show |
12 | HG00642.hp1 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-8474C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638819 | |||||||
| chr15:92638874 | A | G | 124 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(121): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.345-8529T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638874 | |||||||
| chr15:92638904 | G | A | 5 | a0001c0001t0001g0344 a0001c0001t0010g0038 a0001c0001t0012g0343 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-8559C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638904 | |||||||
| chr15:92638918 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.345-8573A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638918 | |||||||
| chr15:92638955 | C | T | 4 | a0001c0001t0002g0153 a0001c0001t0003g0051 a0001c0001t0003g0146 others(1): Show |
4 | HG01258.hp1 NA18973.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-8610G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638955 | |||||||
| chr15:92639099 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.345-8754C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639099 | |||||||
| chr15:92639192 | C | T | 214 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0157 others(211): Show |
217 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.345-8847G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639192 | |||||||
| chr15:92639233 | G | C | 1 | a0001c0001t0002g0063 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.345-8888C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639233 | |||||||
| chr15:92639235 | AAGTT | A | 11 | a0001c0001t0002g0022 a0001c0001t0008g0012 a0001c0001t0008g0014 others(8): Show |
11 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-8894_345-8891d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639235 | |||||||
| chr15:92639241 | T | C | 11 | a0001c0001t0002g0022 a0001c0001t0008g0012 a0001c0001t0008g0014 others(8): Show |
11 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-8896A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639241 | |||||||
| chr15:92639243 | T | C | 11 | a0001c0001t0002g0022 a0001c0001t0008g0012 a0001c0001t0008g0014 others(8): Show |
11 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-8898A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639243 | |||||||
| chr15:92639263 | G | T | 1 | a0001c0001t0002g0354 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.345-8918C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639263 | |||||||
| chr15:92639319 | G | A | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-8974C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639319 | |||||||
| chr15:92639329 | AG | A | 5 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0032g0033 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-8985delC | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639329 | |||||||
| chr15:92639398 | G | C | 1 | a0001c0001t0051g0324 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.345-9053C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639398 | |||||||
| chr15:92639485 | G | T | 1 | a0001c0001t0004g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.345-9140C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639485 | |||||||
| chr15:92639715 | T | A | 75 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(72): Show |
75 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.345-9370A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639715 | |||||||
| chr15:92639829 | A | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-9484T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639829 | |||||||
| chr15:92639889 | C | G | 5 | a0001c0001t0011g0029 a0001c0001t0011g0031 a0001c0001t0033g0028 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-9544G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639889 | |||||||
| chr15:92639908 | C | T | 1 | a0001c0001t0005g0218 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.345-9563G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639908 | |||||||
| chr15:92639992 | G | C | 1 | a0001c0001t0003g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.345-9647C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639992 | |||||||
| chr15:92640200 | C | A | 1 | a0006c0007t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.345-9855G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640200 | |||||||
| chr15:92640268 | T | C | 357 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(354): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.345-9923A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640268 | |||||||
| chr15:92640285 | C | T | 5 | a0001c0001t0011g0029 a0001c0001t0011g0031 a0001c0001t0033g0028 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-9940G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640285 | |||||||
| chr15:92640444 | C | T | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-10099G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640444 | |||||||
| chr15:92640539 | G | A | 2 | a0001c0001t0046g0364 a0001c0001t0049g0363 |
2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.345-10194C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640539 | |||||||
| chr15:92640551 | CAA | C | 9 | a0001c0001t0001g0124 a0001c0001t0001g0301 a0001c0001t0001g0344 others(6): Show |
9 | HG01258.hp1 HG02145.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-10208_345-1020 others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | |||||||
| chr15:92640551 | CAAA | C | 30 | a0001c0001t0001g0162 a0001c0001t0001g0236 a0001c0001t0001g0299 others(27): Show |
31 | HG01109.hp1 HG01175.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.345-10209_345-1020 others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | |||||||
| chr15:92640551 | CAAAA | C | 101 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0087 others(98): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.345-10210_345-1020 others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | |||||||
| chr15:92640551 | CAAAAA | C | 129 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0086 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.345-10211_345-1020 others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | |||||||
| chr15:92640551 | CAAAAAA | C | 87 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0071 others(84): Show |
88 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.345-10212_345-1020 others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | |||||||
| chr15:92640551 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0004g0323 a0001c0001t0051g0324 |
2 | HG00642.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.345-10220_345-1020 others(18): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | |||||||
| chr15:92640551 | CAAAAAAA others(11): Show |
C | 9 | a0001c0001t0002g0140 a0001c0001t0003g0002 a0001c0001t0003g0020 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-10224_345-1020 others(22): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | |||||||
| chr15:92640551 | CAAAAAAA others(13): Show |
C | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-10226_345-1020 others(24): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | |||||||
| chr15:92640656 | T | A | 9 | a0001c0001t0002g0140 a0001c0001t0003g0002 a0001c0001t0003g0020 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-10311A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640656 | |||||||
| chr15:92640674 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.345-10329T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640674 | |||||||
| chr15:92640731 | G | T | 9 | a0001c0001t0002g0140 a0001c0001t0003g0002 a0001c0001t0003g0020 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-10386C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640731 | |||||||
| chr15:92640760 | T | G | 5 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0032g0033 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-10415A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640760 | |||||||
| chr15:92640780 | G | A | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-10435C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640780 | |||||||
| chr15:92640892 | G | A | 1 | a0003c0004t0038g0367 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.345-10547C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640892 | |||||||
| chr15:92640934 | C | T | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-10589G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640934 | |||||||
| chr15:92641062 | T | TCA | 126 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(123): Show |
126 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.345-10719_345-1071 others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641062 | |||||||
| chr15:92641201 | A | C | 1 | a0006c0007t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.345-10856T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641201 | |||||||
| chr15:92641394 | G | A | 5 | a0001c0001t0002g0153 a0001c0001t0003g0051 a0001c0001t0003g0146 others(2): Show |
5 | HG01258.hp1 NA18973.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-11049C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641394 | |||||||
| chr15:92641439 | A | C | 7 | a0001c0001t0002g0005 a0001c0001t0003g0334 a0001c0001t0009g0338 others(4): Show |
8 | HG00099.hp1 HG00140.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-11094T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641439 | |||||||
| chr15:92641514 | A | G | 361 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(358): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.345-11169T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641514 | |||||||
| chr15:92641518 | A | G | 362 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(359): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.345-11173T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641518 | |||||||
| chr15:92641547 | A | C | 364 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(361): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.345-11202T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641547 | |||||||
| chr15:92641558 | T | C | 17 | a0001c0001t0001g0134 a0001c0001t0001g0330 a0001c0001t0004g0131 others(14): Show |
17 | HG01884.hp1 HG02965.hp2 HG03041.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-11213A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641558 | |||||||
| chr15:92641560 | T | G | 2 | a0001c0001t0004g0122 a0001c0001t0011g0123 |
2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-11215A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641560 | |||||||
| chr15:92641578 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.345-11233C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641578 | |||||||
| chr15:92641658 | C | T | 1 | a0001c0003t0002g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.345-11313G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641658 | |||||||
| chr15:92641702 | G | A | 1 | a0001c0001t0018g0154 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.345-11357C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641702 | |||||||
| chr15:92641716 | G | T | 1 | a0001c0001t0004g0131 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.345-11371C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641716 | |||||||
| chr15:92641760 | C | A | 1 | a0001c0001t0007g0117 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.345-11415G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641760 | |||||||
| chr15:92641776 | C | G | 5 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0032g0033 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-11431G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641776 | |||||||
| chr15:92641816 | G | T | 7 | a0001c0001t0004g0122 a0001c0001t0011g0123 a0001c0001t0016g0101 others(4): Show |
7 | HG00642.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-11471C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641816 | |||||||
| chr15:92641850 | G | T | 4 | a0001c0001t0002g0153 a0001c0001t0003g0051 a0001c0001t0003g0146 others(1): Show |
4 | HG01258.hp1 NA18973.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-11505C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641850 | |||||||
| chr15:92641867 | T | G | 8 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-11522A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641867 | |||||||
| chr15:92642083 | A | G | 1 | a0001c0001t0021g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.345-11738T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642083 | |||||||
| chr15:92642283 | C | G | 1 | a0001c0001t0005g0251 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.345-11938G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642283 | |||||||
| chr15:92642417 | C | G | 356 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(353): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.345-12072G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642417 | |||||||
| chr15:92642548 | T | C | 1 | a0001c0001t0010g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.345-12203A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642548 | |||||||
| chr15:92642654 | C | T | 180 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0157 others(177): Show |
183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.345-12309G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642654 | |||||||
| chr15:92642683 | T | C | 4 | a0001c0001t0003g0115 a0001c0001t0009g0112 a0001c0001t0024g0037 others(1): Show |
4 | HG01109.hp2 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-12338A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642683 | |||||||
| chr15:92642798 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0032g0033 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-12453T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642798 | |||||||
| chr15:92642867 | C | T | 375 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(372): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.344+12449G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642867 | |||||||
| chr15:92642899 | C | T | 55 | a0001c0001t0001g0032 a0001c0001t0001g0124 a0001c0001t0001g0344 others(52): Show |
58 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.344+12417G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642899 | |||||||
| chr15:92642939 | T | G | 2 | a0001c0001t0001g0344 a0001c0001t0012g0343 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.344+12377A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642939 | |||||||
| chr15:92642981 | T | C | 2 | a0001c0001t0003g0189 a0001c0001t0004g0188 |
2 | HG00733.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.344+12335A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642981 | |||||||
| chr15:92642995 | A | G | 2 | a0001c0001t0047g0111 a0002c0002t0015g0379 |
2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.344+12321T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642995 | |||||||
| chr15:92643001 | A | G | 360 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(357): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.344+12315T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643001 | |||||||
| chr15:92643136 | GT | G | 368 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(365): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.344+12179delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643136 | |||||||
| chr15:92643141 | T | A | 14 | a0001c0001t0001g0248 a0001c0001t0006g0004 a0001c0001t0006g0190 others(11): Show |
15 | HG01099.hp1 HG01255.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.344+12175A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643141 | |||||||
| chr15:92643157 | TG | T | 186 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0157 others(183): Show |
189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.344+12158delC | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643157 | |||||||
| chr15:92643167 | C | G | 1 | a0001c0001t0042g0191 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.344+12149G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643167 | |||||||
| chr15:92643285 | G | A | 2 | a0001c0001t0002g0155 a0001c0001t0002g0175 |
2 | NA18947.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.344+12031C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643285 | |||||||
| chr15:92643304 | G | C | 1 | a0001c0001t0020g0345 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.344+12012C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643304 | |||||||
| chr15:92643343 | A | AGTGTGTG others(3): Show |
7 | a0001c0001t0001g0040 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG00558.hp1 HG01106.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+11972_344+1197 others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643343 | |||||||
| chr15:92643344 | A | ATATGTGT others(5): Show |
1 | a0001c0001t0024g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.344+11971_344+1197 others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | A | ATGTG | 23 | a0001c0001t0001g0093 a0001c0001t0001g0124 a0001c0001t0003g0274 others(20): Show |
23 | HG00642.hp1 HG00733.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.344+11968_344+1197 others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | A | ATGTGTG | 11 | a0001c0001t0001g0134 a0001c0001t0003g0325 a0001c0001t0004g0323 others(8): Show |
11 | HG00639.hp2 HG00642.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.344+11966_344+1197 others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | A | ATGTGTGT others(1): Show |
34 | a0001c0001t0001g0032 a0001c0001t0001g0284 a0001c0001t0001g0317 others(31): Show |
34 | HG01109.hp1 HG01168.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.344+11964_344+1197 others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | A | ATGTGTGT others(3): Show |
40 | a0001c0001t0001g0088 a0001c0001t0001g0119 a0001c0001t0001g0253 others(37): Show |
41 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.344+11962_344+1197 others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | A | ATGTGTGT others(5): Show |
167 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0095 others(164): Show |
170 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.344+11960_344+1197 others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | A | ATGTGTGT others(7): Show |
51 | a0001c0001t0001g0039 a0001c0001t0001g0177 a0001c0001t0001g0295 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.344+11958_344+1197 others(18): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | A | ATGTGTGT others(9): Show |
21 | a0001c0001t0001g0052 a0001c0001t0001g0285 a0001c0001t0001g0309 others(18): Show |
21 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.344+11956_344+1197 others(20): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | A | ATGTGTGT others(11): Show |
2 | a0001c0001t0002g0166 a0001c0001t0016g0351 |
2 | HG01934.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.344+11954_344+1197 others(22): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | A | G | 8 | a0001c0001t0001g0040 a0001c0001t0001g0083 a0001c0001t0001g0084 others(5): Show |
8 | HG00558.hp1 HG01106.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+11972T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643344 | ATGTG | A | 8 | a0001c0001t0002g0140 a0001c0001t0003g0002 a0001c0001t0003g0020 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+11968_344+1197 others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | |||||||
| chr15:92643378 | A | G | 1 | a0001c0001t0008g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.344+11938T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643378 | |||||||
| chr15:92643447 | T | C | 3 | a0001c0001t0010g0362 a0001c0001t0046g0364 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+11869A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643447 | |||||||
| chr15:92643499 | T | A | 32 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.344+11817A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643499 | |||||||
| chr15:92643543 | T | C | 364 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(361): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.344+11773A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643543 | |||||||
| chr15:92643569 | T | A | 4 | a0001c0001t0003g0115 a0001c0001t0009g0112 a0001c0001t0024g0037 others(1): Show |
4 | HG01109.hp2 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+11747A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643569 | |||||||
| chr15:92643572 | A | G | 2 | a0001c0001t0009g0112 a0001c0001t0024g0037 |
2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.344+11744T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643572 | |||||||
| chr15:92643652 | C | T | 1 | a0001c0001t0007g0275 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.344+11664G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643652 | |||||||
| chr15:92643758 | G | A | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.344+11558C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643758 | |||||||
| chr15:92643798 | A | G | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+11518T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643798 | |||||||
| chr15:92643826 | G | A | 96 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(93): Show |
96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.344+11490C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643826 | |||||||
| chr15:92643955 | G | A | 16 | a0001c0001t0001g0134 a0001c0001t0001g0330 a0001c0001t0004g0131 others(13): Show |
16 | HG01884.hp1 HG02602.hp2 HG02965.hp2 others(13): Show |
intron_variant | MODIFIER | c.344+11361C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643955 | |||||||
| chr15:92643989 | G | A | 2 | a0001c0001t0037g0381 a0001c0001t0037g0382 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.344+11327C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643989 | |||||||
| chr15:92643999 | A | G | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+11317T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643999 | |||||||
| chr15:92644023 | T | C | 1 | a0001c0001t0005g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.344+11293A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644023 | |||||||
| chr15:92644046 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0032g0033 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+11270G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644046 | |||||||
| chr15:92644105 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.344+11211G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644105 | |||||||
| chr15:92644125 | A | G | 1 | a0001c0001t0030g0165 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.344+11191T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644125 | |||||||
| chr15:92644363 | G | C | 2 | a0001c0001t0011g0135 a0001c0001t0061g0136 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.344+10953C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644363 | |||||||
| chr15:92644367 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.344+10949A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644367 | |||||||
| chr15:92644413 | T | C | 2 | a0001c0001t0009g0112 a0001c0001t0024g0037 |
2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.344+10903A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644413 | |||||||
| chr15:92644482 | C | T | 1 | a0001c0001t0019g0307 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.344+10834G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644482 | |||||||
| chr15:92644499 | C | T | 5 | a0001c0001t0002g0153 a0001c0001t0003g0051 a0001c0001t0003g0146 others(2): Show |
5 | HG01258.hp1 NA18970.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+10817G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644499 | |||||||
| chr15:92644573 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.344+10743G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644573 | |||||||
| chr15:92644587 | G | A | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+10729C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644587 | |||||||
| chr15:92644712 | T | C | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+10604A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644712 | |||||||
| chr15:92644769 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.344+10547G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644769 | |||||||
| chr15:92644803 | G | A | 1 | a0002c0002t0031g0373 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.344+10513C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644803 | |||||||
| chr15:92644890 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.344+10426G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644890 | |||||||
| chr15:92645121 | C | G | 7 | a0001c0001t0001g0124 a0001c0001t0002g0022 a0001c0001t0008g0012 others(4): Show |
7 | HG02257.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.344+10195G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645121 | |||||||
| chr15:92645152 | G | A | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.344+10164C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645152 | |||||||
| chr15:92645211 | T | C | 363 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(360): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.344+10105A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645211 | |||||||
| chr15:92645281 | T | C | 8 | a0001c0001t0001g0303 a0001c0001t0002g0304 a0001c0001t0002g0318 others(5): Show |
8 | HG00558.hp2 HG01934.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+10035A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645281 | |||||||
| chr15:92645368 | T | C | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+9948A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645368 | |||||||
| chr15:92645473 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.344+9843A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645473 | |||||||
| chr15:92645482 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.344+9834G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645482 | |||||||
| chr15:92645506 | A | G | 7 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0161 others(4): Show |
7 | HG01346.hp2 HG01928.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.344+9810T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645506 | |||||||
| chr15:92645641 | A | G | 108 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(105): Show |
108 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.344+9675T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645641 | |||||||
| chr15:92645653 | T | C | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+9663A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645653 | |||||||
| chr15:92645726 | C | A | 186 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0157 others(183): Show |
188 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.344+9590G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645726 | |||||||
| chr15:92645747 | C | T | 186 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0157 others(183): Show |
188 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.344+9569G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645747 | |||||||
| chr15:92645797 | G | A | 254 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0119 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.344+9519C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645797 | |||||||
| chr15:92645869 | C | A | 1 | a0001c0001t0003g0278 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.344+9447G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645869 | |||||||
| chr15:92645992 | C | T | 2 | a0002c0002t0004g0372 a0002c0002t0031g0373 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.344+9324G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645992 | |||||||
| chr15:92645995 | T | C | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.344+9321A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645995 | |||||||
| chr15:92646168 | G | A | 2 | a0001c0001t0002g0279 a0001c0001t0002g0280 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.344+9148C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646168 | |||||||
| chr15:92646188 | G | C | 1 | a0001c0001t0039g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.344+9128C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646188 | |||||||
| chr15:92646222 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.344+9094T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646222 | |||||||
| chr15:92646298 | T | C | 174 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0052 others(171): Show |
175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.344+9018A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646298 | |||||||
| chr15:92646299 | C | T | 29 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0001g0346 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.344+9017G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646299 | |||||||
| chr15:92646301 | T | C | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.344+9015A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646301 | |||||||
| chr15:92646318 | T | A | 194 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0157 others(191): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.344+8998A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646318 | |||||||
| chr15:92646323 | T | G | 107 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(104): Show |
107 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.344+8993A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646323 | |||||||
| chr15:92646459 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.344+8857T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646459 | |||||||
| chr15:92646670 | A | C | 90 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(87): Show |
90 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.344+8646T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646670 | |||||||
| chr15:92646688 | C | T | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+8628G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646688 | |||||||
| chr15:92646714 | A | T | 6 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0032g0033 others(3): Show |
6 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.344+8602T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646714 | |||||||
| chr15:92646889 | A | G | 1 | a0001c0001t0018g0154 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.344+8427T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646889 | |||||||
| chr15:92647062 | G | A | 13 | a0001c0001t0001g0098 a0001c0001t0001g0124 a0001c0001t0002g0022 others(10): Show |
13 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.344+8254C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647062 | |||||||
| chr15:92647106 | T | C | 3 | a0001c0001t0002g0140 a0001c0001t0004g0113 a0001c0001t0004g0114 |
3 | HG02145.hp2 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.344+8210A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647106 | |||||||
| chr15:92647174 | C | G | 1 | a0001c0001t0048g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.344+8142G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647174 | |||||||
| chr15:92647227 | T | C | 2 | a0001c0001t0016g0351 a0001c0001t0016g0352 |
2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.344+8089A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647227 | |||||||
| chr15:92647271 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.344+8045C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647271 | |||||||
| chr15:92647285 | G | A | 2 | a0001c0001t0003g0115 a0002c0002t0015g0377 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+8031C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647285 | |||||||
| chr15:92647299 | C | T | 73 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(70): Show |
73 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.344+8017G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647299 | |||||||
| chr15:92647445 | C | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | NA18963.hp1 NA18968.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+7871G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647445 | |||||||
| chr15:92647586 | C | A | 80 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0071 others(77): Show |
80 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.344+7730G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647586 | |||||||
| chr15:92647619 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.344+7697C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647619 | |||||||
| chr15:92647691 | C | T | 375 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(372): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.344+7625G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647691 | |||||||
| chr15:92647833 | A | C | 235 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0134 others(232): Show |
238 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.344+7483T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647833 | |||||||
| chr15:92647834 | G | C | 1 | a0001c0001t0013g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.344+7482C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647834 | |||||||
| chr15:92648005 | A | G | 1 | a0001c0001t0007g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.344+7311T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648005 | |||||||
| chr15:92648099 | T | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.344+7217A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648099 | |||||||
| chr15:92648439 | G | A | 1 | a0001c0001t0007g0100 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.344+6877C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648439 | |||||||
| chr15:92648463 | C | T | 1 | a0001c0001t0048g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.344+6853G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648463 | |||||||
| chr15:92648489 | G | C | 4 | a0001c0001t0016g0101 a0001c0006t0024g0102 a0003c0004t0004g0368 others(1): Show |
4 | HG00642.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+6827C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648489 | |||||||
| chr15:92648520 | T | C | 47 | a0001c0001t0001g0032 a0001c0001t0001g0124 a0001c0001t0001g0344 others(44): Show |
50 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.344+6796A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648520 | |||||||
| chr15:92648529 | G | A | 193 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0157 others(190): Show |
196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.344+6787C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648529 | |||||||
| chr15:92648531 | C | A | 8 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0009g0019 others(5): Show |
10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+6785G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648531 | |||||||
| chr15:92648597 | C | A | 227 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0157 others(224): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.344+6719G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648597 | |||||||
| chr15:92648633 | T | A | 1 | a0001c0001t0009g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.344+6683A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648633 | |||||||
| chr15:92648786 | G | A | 194 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0119 others(191): Show |
196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.344+6530C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648786 | |||||||
| chr15:92648809 | C | T | 326 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(323): Show |
329 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.344+6507G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648809 | |||||||
| chr15:92648810 | G | A | 1 | a0001c0001t0004g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.344+6506C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648810 | |||||||
| chr15:92648880 | T | G | 1 | a0001c0001t0009g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.344+6436A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648880 | |||||||
| chr15:92648943 | G | A | 1 | a0001c0001t0062g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.344+6373C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648943 | |||||||
| chr15:92649118 | C | G | 104 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0052 others(101): Show |
104 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.344+6198G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649118 | |||||||
| chr15:92649121 | A | G | 4 | a0001c0001t0010g0333 a0001c0001t0011g0044 a0001c0001t0011g0045 others(1): Show |
4 | HG02055.hp1 HG02886.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+6195T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649121 | |||||||
| chr15:92649255 | G | A | 1 | a0001c0001t0025g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.344+6061C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649255 | |||||||
| chr15:92649267 | G | A | 2 | a0002c0002t0010g0378 a0002c0002t0015g0379 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.344+6049C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649267 | |||||||
| chr15:92649293 | G | A | 180 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(177): Show |
183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.344+6023C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649293 | |||||||
| chr15:92649527 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0009g0034 a0001c0001t0032g0033 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+5789A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649527 | |||||||
| chr15:92649586 | T | C | 3 | a0001c0001t0010g0362 a0001c0001t0046g0364 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+5730A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649586 | |||||||
| chr15:92649615 | T | C | 1 | a0001c0001t0013g0297 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.344+5701A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649615 | |||||||
| chr15:92649646 | A | C | 14 | a0001c0001t0002g0022 a0001c0001t0007g0023 a0001c0001t0007g0025 others(11): Show |
14 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.344+5670T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649646 | |||||||
| chr15:92649678 | G | A | 3 | a0001c0001t0010g0362 a0001c0001t0046g0364 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+5638C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649678 | |||||||
| chr15:92649733 | C | T | 22 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0330 others(19): Show |
22 | HG01884.hp1 HG02280.hp2 HG02896.hp1 others(19): Show |
intron_variant | MODIFIER | c.344+5583G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649733 | |||||||
| chr15:92649757 | C | G | 1 | a0001c0001t0048g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.344+5559G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649757 | |||||||
| chr15:92649782 | A | G | 323 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(320): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.344+5534T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649782 | |||||||
| chr15:92649836 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.344+5480C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649836 | |||||||
| chr15:92650037 | C | A | 1 | a0001c0001t0004g0298 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.344+5279G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650037 | |||||||
| chr15:92650201 | G | A | 1 | a0001c0001t0024g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.344+5115C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650201 | |||||||
| chr15:92650336 | G | C | 99 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(96): Show |
99 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.344+4980C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650336 | |||||||
| chr15:92650337 | G | A | 3 | a0001c0001t0001g0299 a0001c0001t0001g0301 a0001c0001t0004g0300 |
3 | NA18965.hp2 NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.344+4979C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650337 | |||||||
| chr15:92650509 | C | T | 3 | a0001c0001t0002g0116 a0001c0001t0003g0146 a0001c0001t0007g0117 |
3 | NA18970.hp2 NA18973.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.344+4807G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650509 | |||||||
| chr15:92650544 | C | A | 1 | a0001c0001t0044g0302 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.344+4772G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650544 | |||||||
| chr15:92650696 | G | A | 121 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(118): Show |
121 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.344+4620C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650696 | |||||||
| chr15:92650750 | C | CA | 8 | a0001c0001t0003g0115 a0001c0001t0004g0113 a0001c0001t0004g0114 others(5): Show |
8 | HG01109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+4565dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650750 | |||||||
| chr15:92650949 | T | C | 3 | a0001c0001t0010g0362 a0001c0001t0046g0364 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+4367A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650949 | |||||||
| chr15:92651025 | A | T | 1 | a0001c0001t0010g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.344+4291T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651025 | |||||||
| chr15:92651049 | T | C | 1 | a0001c0001t0002g0321 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.344+4267A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651049 | |||||||
| chr15:92651065 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+4251C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651065 | |||||||
| chr15:92651171 | A | C | 2 | a0001c0001t0004g0122 a0001c0001t0011g0123 |
2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.344+4145T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651171 | |||||||
| chr15:92651186 | C | A | 4 | a0001c0001t0003g0325 a0001c0001t0004g0323 a0001c0001t0022g0322 others(1): Show |
4 | HG00639.hp2 HG00642.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+4130G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651186 | |||||||
| chr15:92651439 | C | A | 1 | a0001c0001t0003g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.344+3877G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651439 | |||||||
| chr15:92651441 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.344+3875A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651441 | |||||||
| chr15:92651450 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.344+3866T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651450 | |||||||
| chr15:92651458 | T | C | 323 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(320): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.344+3858A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651458 | |||||||
| chr15:92651524 | T | C | 8 | a0001c0001t0003g0115 a0001c0001t0004g0113 a0001c0001t0004g0114 others(5): Show |
8 | HG01109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+3792A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651524 | |||||||
| chr15:92651565 | G | C | 5 | a0001c0001t0009g0106 a0001c0001t0015g0107 a0001c0001t0015g0109 others(2): Show |
5 | HG01243.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+3751C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651565 | |||||||
| chr15:92651692 | A | C | 1 | a0001c0001t0002g0116 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.344+3624T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651692 | |||||||
| chr15:92651713 | A | C | 1 | a0001c0001t0007g0145 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.344+3603T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651713 | |||||||
| chr15:92651749 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.344+3567A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651749 | |||||||
| chr15:92651777 | G | A | 3 | a0002c0002t0010g0378 a0002c0002t0015g0377 a0002c0002t0015g0379 |
3 | HG01243.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.344+3539C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651777 | |||||||
| chr15:92651865 | GAC | G | 319 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(316): Show |
322 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.344+3449_344+3450d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651865 | |||||||
| chr15:92651958 | A | C | 24 | a0001c0001t0001g0039 a0001c0001t0001g0124 a0001c0001t0001g0134 others(21): Show |
24 | HG01884.hp1 HG02280.hp2 HG02896.hp1 others(21): Show |
intron_variant | MODIFIER | c.344+3358T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651958 | |||||||
| chr15:92651972 | C | T | 10 | a0001c0001t0003g0115 a0001c0001t0004g0113 a0001c0001t0004g0114 others(7): Show |
10 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+3344G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651972 | |||||||
| chr15:92652232 | A | T | 321 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(318): Show |
324 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.344+3084T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652232 | |||||||
| chr15:92652572 | A | G | 58 | a0001c0001t0001g0032 a0001c0001t0001g0344 a0001c0001t0001g0346 others(55): Show |
61 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.344+2744T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652572 | |||||||
| chr15:92652575 | G | A | 1 | a0001c0001t0003g0327 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.344+2741C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652575 | |||||||
| chr15:92652605 | G | A | 316 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(313): Show |
319 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.344+2711C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652605 | |||||||
| chr15:92652655 | A | T | 1 | a0001c0001t0047g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.344+2661T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652655 | |||||||
| chr15:92652713 | T | C | 376 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(373): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.344+2603A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652713 | |||||||
| chr15:92652855 | T | G | 236 | a0001c0001t0001g0119 a0001c0001t0001g0124 a0001c0001t0001g0134 others(233): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.344+2461A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652855 | |||||||
| chr15:92653048 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.344+2268T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653048 | |||||||
| chr15:92653081 | C | T | 1 | a0001c0001t0064g0387 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.344+2235G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653081 | |||||||
| chr15:92653115 | G | A | 8 | a0001c0001t0002g0354 a0001c0001t0002g0355 a0001c0001t0005g0356 others(5): Show |
8 | HG02071.hp2 HG02135.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+2201C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653115 | |||||||
| chr15:92653291 | C | T | 1 | a0001c0001t0020g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.344+2025G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653291 | |||||||
| chr15:92653295 | C | A | 1 | a0001c0001t0011g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.344+2021G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653295 | |||||||
| chr15:92653374 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0007g0023 a0001c0001t0007g0025 others(6): Show |
9 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.344+1942G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653374 | |||||||
| chr15:92653587 | A | C | 326 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(323): Show |
329 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.344+1729T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653587 | |||||||
| chr15:92653832 | G | A | 23 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0330 others(20): Show |
23 | HG01884.hp1 HG02280.hp2 HG02896.hp1 others(20): Show |
intron_variant | MODIFIER | c.344+1484C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653832 | |||||||
| chr15:92654069 | A | G | 373 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(370): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.344+1247T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654069 | |||||||
| chr15:92654194 | T | C | 325 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(322): Show |
328 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.344+1122A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654194 | |||||||
| chr15:92654352 | C | A | 1 | a0001c0001t0027g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.344+964G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654352 | |||||||
| chr15:92654378 | C | T | 1 | a0001c0001t0005g0142 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.344+938G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654378 | |||||||
| chr15:92654400 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.344+916A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654400 | |||||||
| chr15:92654446 | A | G | 1 | a0001c0001t0010g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.344+870T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654446 | |||||||
| chr15:92654485 | G | T | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.344+831C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654485 | |||||||
| chr15:92654499 | A | C | 1 | a0001c0001t0059g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.344+817T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654499 | |||||||
| chr15:92654544 | G | A | 1 | a0001c0001t0010g0339 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.344+772C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654544 | |||||||
| chr15:92654546 | G | T | 1 | a0001c0001t0059g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.344+770C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654546 | |||||||
| chr15:92654567 | C | T | 7 | a0001c0001t0002g0005 a0001c0001t0003g0334 a0001c0001t0009g0338 others(4): Show |
8 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+749G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654567 | |||||||
| chr15:92654653 | A | T | 1 | a0001c0001t0024g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.344+663T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654653 | |||||||
| chr15:92654719 | C | T | 3 | a0003c0004t0004g0368 a0003c0004t0016g0366 a0003c0004t0038g0367 |
3 | HG00642.hp1 HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.344+597G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654719 | |||||||
| chr15:92654731 | G | A | 1 | a0001c0001t0058g0329 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.344+585C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654731 | |||||||
| chr15:92654787 | C | CA | 201 | a0001c0001t0001g0144 a0001c0001t0001g0157 a0001c0001t0001g0158 others(198): Show |
204 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.344+528dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654787 | |||||||
| chr15:92654787 | CA | C | 43 | a0001c0001t0001g0344 a0001c0001t0001g0346 a0001c0001t0002g0005 others(40): Show |
46 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.344+528delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654787 | |||||||
| chr15:92654799 | A | AAAG | 26 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0330 others(23): Show |
26 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.344+514_344+516dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654799 | |||||||
| chr15:92654799 | AAAG | A | 12 | a0001c0001t0003g0067 a0001c0001t0003g0079 a0001c0001t0004g0113 others(9): Show |
12 | HG01109.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.344+514_344+516del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654799 | |||||||
| chr15:92655066 | G | A | 316 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(313): Show |
319 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.344+250C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655066 | |||||||
| chr15:92655067 | G | A | 3 | a0001c0001t0001g0330 a0001c0001t0006g0331 a0001c0001t0006g0332 |
3 | NA18944.hp2 NA18977.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.344+249C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655067 | |||||||
| chr15:92655089 | T | C | 1 | a0001c0001t0010g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.344+227A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655089 | |||||||
| chr15:92655283 | C | A | 29 | a0001c0001t0001g0344 a0001c0001t0001g0346 a0001c0001t0002g0005 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.344+33G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655283 | |||||||
| chr15:92655304 | G | A | 3 | a0001c0001t0010g0362 a0001c0001t0046g0364 a0001c0001t0049g0363 |
3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+12C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655304 |