Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83891 |
| ensemblid | ENSG00000109762.17 |
| hgncid | 21883 |
| symbol | SNX25 |
| name | sorting nexin 25 |
| refseq_nuc | NM_001378034.2 |
| refseq_prot | NP_001364963.1 |
| ensembl_nuc | ENST00000652585.2 |
| ensembl_prot | ENSP00000498676.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 185209598 |
| end | 185363966 |
| strand | + |
| ver | v1.2 |
| region | chr4:185209598-185363966 |
| region5000 | chr4:185204598-185368966 |
| regionname0 | SNX25_chr4_185209598_185363966 |
| regionname5000 | SNX25_chr4_185204598_185368966 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1004 | 235 | 56 | 51 | 92 | 11 | 23 | 75 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0002 | 0/0 | 1004 | 22 | 21 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0003 | 0/0 | 1004 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0004 | 0/0 | 1004 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0005 | 0/0 | 1004 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0006 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0007 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0008 | 0/0 | 1004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0009 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0010 | 0/0 | 1004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0011 | 0/0 | 1004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0012 | 0/0 | 1004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0013 | 0/0 | 1004 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| a0014 | 0/0 | 1004 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | MHPDA others(999): Show |
chr4 | 185204598 | 185368966 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3012 | 212 | 54 | 50 | 75 | 11 | 20 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0001c0003 | 0/0 | 3012 | 19 | 0 | 1 | 15 | 0 | 3 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0001c0006 | 0/0 | 3012 | 2 | 2 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0001c0009 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0001c0014 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0002c0002 | 0/0 | 3012 | 22 | 21 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0003c0004 | 0/0 | 3012 | 3 | 3 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0003c0007 | 0/0 | 3012 | 2 | 2 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0004c0005 | 0/0 | 3012 | 3 | 0 | 0 | 3 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0005c0008 | 0/0 | 3012 | 2 | 0 | 1 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0006c0013 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0007c0016 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0008c0018 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0009c0012 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0010c0019 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0011c0010 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0012c0017 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0013c0015 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 | ||
| a0014c0011 | 0/0 | 3012 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | ATGCA others(3007): Show |
chr4 | 185204598 | 185368966 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3745 | 201 | 54 | 45 | 69 | 11 | 20 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0001c0001t0002 | 0/0 | 3745 | 9 | 0 | 3 | 6 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0001c0001t0003 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0001c0001t0006 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0001c0003t0001 | 0/0 | 3745 | 19 | 0 | 1 | 15 | 0 | 3 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0001c0006t0001 | 0/0 | 3745 | 2 | 2 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0001c0009t0001 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0001c0014t0001 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0002c0002t0001 | 0/0 | 3745 | 21 | 20 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0002c0002t0004 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0003c0004t0001 | 0/0 | 3745 | 3 | 3 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0003c0007t0001 | 0/0 | 3745 | 2 | 2 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0004c0005t0001 | 0/0 | 3745 | 3 | 0 | 0 | 3 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0005c0008t0001 | 0/0 | 3745 | 2 | 0 | 1 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0006c0013t0001 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0007c0016t0001 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0008c0018t0001 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0009c0012t0001 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0010c0019t0005 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0011c0010t0001 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0012c0017t0001 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0013c0015t0001 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| a0014c0011t0001 | 0/0 | 3745 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | AGTCA others(3740): Show |
chr4 | 185204598 | 185368966 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0006t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0006t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0009t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0001c0014t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0002c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0003c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0003c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0003c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0003c0007t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0003c0007t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0004c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0004c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0004c0005t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0005c0008t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0005c0008t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0006c0013t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0007c0016t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0008c0018t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0009c0012t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0010c0019t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0011c0010t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0012c0017t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0013c0015t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| a0014c0011t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | GBR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | FIN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00408 | hp2 | a0004 | c0005 | t0001 | g0047 | EAS | CHS | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0090 | EAS | CHS | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01081 | hp2 | a0005 | c0008 | t0001 | g0230 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01099 | hp2 | a0006 | c0013 | t0001 | g0123 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0274 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01433 | hp1 | a0007 | c0016 | t0001 | g0037 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0152 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02258 | hp1 | a0003 | c0007 | t0001 | g0184 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02280 | hp1 | a0008 | c0018 | t0001 | g0061 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02300 | hp1 | a0009 | c0012 | t0001 | g0122 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02451 | hp1 | a0002 | c0002 | t0004 | g0258 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0254 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02572 | hp2 | a0001 | c0006 | t0001 | g0068 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02615 | hp1 | a0001 | c0006 | t0001 | g0069 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0272 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0268 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0269 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0209 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03130 | hp1 | a0003 | c0007 | t0001 | g0070 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03139 | hp1 | a0010 | c0019 | t0005 | g0267 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0257 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0270 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0063 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03688 | hp2 | a0005 | c0008 | t0001 | g0231 | SAS | STU | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0273 | SAS | BEB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | YRI | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18906 | hp2 | a0012 | c0017 | t0001 | g0049 | AFR | YRI | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0067 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18985 | hp1 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18993 | hp2 | a0001 | c0014 | t0001 | g0151 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19002 | hp1 | a0004 | c0005 | t0001 | g0046 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19010 | hp1 | a0001 | c0009 | t0001 | g0233 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | LWK | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19064 | hp2 | a0004 | c0005 | t0001 | g0045 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19074 | hp2 | a0013 | c0015 | t0001 | g0010 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0256 | AFR | ASW | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA20129 | hp2 | a0003 | c0004 | t0001 | g0249 | AFR | ASW | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA20752 | hp1 | a0014 | c0011 | t0001 | g0110 | EUR | TSI | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03471 | hp1 | a0003 | c0004 | t0001 | g0204 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG06807 | hp1 | a0011 | c0010 | t0001 | g0207 | AFR | USA | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18955 | hp1 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | LWK | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0153 | REF | REF | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0022 | REF | REF | SNX25_chr4_185204598_185368966 | SNX25 | chr4 | 185204598 | 185368966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185210188 | A | C | 2 | a0002 a0010 |
23 | HG00733.hp2 HG01891.hp2 HG02257.hp2 others(20): Show |
missense_variant | MODERATE | c.362A>C | p.Gln121Pro | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/19 | 591/3745 | 362/3015 | 121/1004 | chr4 | 185210188 | |||
| chr4:185210241 | C | T | 1 | a0008 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.415C>T | p.Arg139Cys | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/19 | 644/3745 | 415/3015 | 139/1004 | chr4 | 185210241 | |||
| chr4:185247310 | A | G | 1 | a0005 | 2 | HG01081.hp2 HG03688.hp2 |
missense_variant | MODERATE | c.446A>G | p.Asn149Ser | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/19 | 675/3745 | 446/3015 | 149/1004 | chr4 | 185247310 | |||
| chr4:185258853 | G | A | 1 | a0011 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.520G>A | p.Asp174Asn | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/19 | 749/3745 | 520/3015 | 174/1004 | chr4 | 185258853 | |||
| chr4:185266978 | C | T | 1 | a0012 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.914C>T | p.Pro305Leu | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/19 | 1143/3745 | 914/3015 | 305/1004 | chr4 | 185266978 | |||
| chr4:185320832 | G | A | 1 | a0014 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1444G>A | p.Glu482Lys | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/19 | 1673/3745 | 1444/3015 | 482/1004 | chr4 | 185320832 | |||
| chr4:185332751 | G | A | 1 | a0009 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1906G>A | p.Asp636Asn | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/19 | 2135/3745 | 1906/3015 | 636/1004 | chr4 | 185332751 | |||
| chr4:185339415 | G | A | 1 | a0006 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1951G>A | p.Glu651Lys | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/19 | 2180/3745 | 1951/3015 | 651/1004 | chr4 | 185339415 | |||
| chr4:185342064 | C | T | 1 | a0004 | 3 | HG00408.hp2 NA19002.hp1 NA19064.hp2 |
missense_variant | MODERATE | c.2135C>T | p.Thr712Met | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/19 | 2364/3745 | 2135/3015 | 712/1004 | chr4 | 185342064 | |||
| chr4:185346597 | A | G | 1 | a0013 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.2248A>G | p.Ile750Val | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/19 | 2477/3745 | 2248/3015 | 750/1004 | chr4 | 185346597 | |||
| chr4:185351462 | A | C | 2 | a0003 a0010 |
6 | HG02258.hp1 HG02970.hp2 HG03130.hp1 others(3): Show |
missense_variant | MODERATE | c.2319A>C | p.Glu773Asp | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/19 | 2548/3745 | 2319/3015 | 773/1004 | chr4 | 185351462 | |||
| chr4:185351538 | G | A | 1 | a0007 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.2395G>A | p.Gly799Arg | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/19 | 2624/3745 | 2395/3015 | 799/1004 | chr4 | 185351538 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185209982 | G | C | 1 | a0001c0009 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.156G>C | p.Pro52Pro | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/19 | 385/3745 | 156/3015 | 52/1004 | chr4 | 185209982 | |||
| chr4:185267105 | C | T | 1 | a0007c0016 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1041C>T | p.Phe347Phe | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/19 | 1270/3745 | 1041/3015 | 347/1004 | chr4 | 185267105 | |||
| chr4:185323575 | G | A | 2 | a0001c0006 a0003c0007 |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
synonymous_variant | LOW | c.1524G>A | p.Val508Val | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/19 | 1753/3745 | 1524/3015 | 508/1004 | chr4 | 185323575 | |||
| chr4:185351567 | A | G | 2 | a0001c0003 a0014c0011 |
20 | HG00544.hp2 HG01168.hp2 HG02735.hp2 others(17): Show |
synonymous_variant | LOW | c.2424A>G | p.Ser808Ser | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/19 | 2653/3745 | 2424/3015 | 808/1004 | chr4 | 185351567 | |||
| chr4:185361936 | C | T | 1 | a0001c0014 | 1 | NA18993.hp2 | synonymous_variant | LOW | c.2664C>T | p.Asp888Asp | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 17/19 | 2893/3745 | 2664/3015 | 888/1004 | chr4 | 185361936 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185209683 | A | G | 1 | a0001c0001t0002 | 9 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-144A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/19 | 144 | chr4 | 185209683 | ||||||
| chr4:185363541 | G | A | 1 | a0001c0001t0003 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*76G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 19/19 | 76 | chr4 | 185363541 | ||||||
| chr4:185363702 | G | A | 1 | a0002c0002t0004 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*237G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 19/19 | 237 | chr4 | 185363702 | ||||||
| chr4:185363815 | G | A | 1 | a0010c0019t0005 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 19/19 | 350 | chr4 | 185363815 | ||||||
| chr4:185363931 | G | A | 1 | a0001c0001t0006 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*466G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 19/19 | 466 | chr4 | 185363931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185210390 | GCGGGCCC others(45): Show |
G | 2 | a0001c0003t0001g0273 a0001c0003t0001g0274 |
2 | HG01168.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.429+141_429+192del others(52): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185210390 | ||||||
| chr4:185210435 | GCGGGCTC | G | 14 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(11): Show |
14 | HG00621.hp2 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.429+197_429+203del others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185210435 | ||||||
| chr4:185210452 | G | GGCTCCGC | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG02040.hp2 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.429+206_429+212dup others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185210452 | ||||||
| chr4:185210494 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(37): Show |
41 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.429+239C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185210494 | |||||||
| chr4:185210780 | G | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.429+525G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185210780 | |||||||
| chr4:185210878 | G | A | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+623G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185210878 | |||||||
| chr4:185210895 | A | G | 1 | a0001c0009t0001g0233 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.429+640A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185210895 | |||||||
| chr4:185210941 | C | T | 6 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+686C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185210941 | |||||||
| chr4:185210981 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.429+726C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185210981 | |||||||
| chr4:185211397 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.429+1142C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185211397 | |||||||
| chr4:185211460 | GTC | G | 6 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(3): Show |
6 | HG01081.hp2 HG01243.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+1210_429+1211d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185211460 | ||||||
| chr4:185211901 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
148 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(145): Show |
intron_variant | MODIFIER | c.429+1646C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185211901 | |||||||
| chr4:185211941 | T | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(14): Show |
18 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+1686T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185211941 | |||||||
| chr4:185212042 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01975.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.429+1787C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212042 | |||||||
| chr4:185212157 | G | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG00639.hp1 HG01106.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.429+1902G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212157 | |||||||
| chr4:185212214 | A | G | 1 | a0003c0004t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.429+1959A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212214 | |||||||
| chr4:185212219 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0004c0005t0001g0045 others(2): Show |
5 | HG00408.hp1 HG00408.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+1964C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212219 | |||||||
| chr4:185212235 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.429+1980C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212235 | |||||||
| chr4:185212291 | T | TA | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
187 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(184): Show |
intron_variant | MODIFIER | c.429+2049dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212291 | ||||||
| chr4:185212304 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.429+2049A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212304 | |||||||
| chr4:185212305 | T | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
161 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(158): Show |
intron_variant | MODIFIER | c.429+2050T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212305 | |||||||
| chr4:185212306 | T | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | NA19056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.429+2051T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212306 | |||||||
| chr4:185212313 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.429+2058T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212313 | |||||||
| chr4:185212329 | A | T | 8 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG00733.hp1 HG01074.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+2074A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212329 | |||||||
| chr4:185212397 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.429+2142A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212397 | |||||||
| chr4:185212463 | ATG | A | 12 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(9): Show |
12 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+2236_429+2237d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212463 | ||||||
| chr4:185212463 | ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01975.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.429+2226_429+2237d others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212463 | ||||||
| chr4:185212465 | G | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
195 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.429+2210G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212465 | |||||||
| chr4:185212471 | G | C | 12 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(9): Show |
12 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+2216G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212471 | |||||||
| chr4:185212485 | G | GT | 14 | a0001c0001t0001g0002 a0001c0001t0001g0235 a0001c0001t0001g0236 others(11): Show |
15 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.429+2231dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212485 | ||||||
| chr4:185212485 | G | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02559.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.429+2230G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212485 | |||||||
| chr4:185212487 | G | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0235 a0001c0001t0001g0236 others(13): Show |
17 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.429+2232G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212487 | |||||||
| chr4:185212489 | G | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0235 a0001c0001t0001g0236 others(13): Show |
17 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.429+2234G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212489 | |||||||
| chr4:185212491 | G | GTGTGTGT others(14): Show |
1 | a0001c0001t0001g0053 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.429+2237_429+2238i others(23): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTGT others(10): Show |
1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.429+2237_429+2238i others(19): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTGT others(12): Show |
4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | NA18942.hp2 NA18994.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+2237_429+2238i others(21): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTGT others(13): Show |
3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0154 |
3 | HG00621.hp2 HG02738.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.429+2237_429+2238i others(22): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTGT others(10): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0065 others(24): Show |
28 | HG01192.hp2 HG02040.hp1 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.429+2237_429+2238i others(19): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTGT others(11): Show |
2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18961.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.429+2237_429+2238i others(20): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTGT others(8): Show |
8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG02055.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+2237_429+2238i others(17): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTTT others(6): Show |
2 | a0002c0002t0001g0250 a0002c0002t0001g0262 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.429+2237_429+2238i others(15): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTTT others(7): Show |
1 | a0002c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.429+2237_429+2238i others(16): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTTT others(4): Show |
7 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
7 | HG01123.hp1 HG01123.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+2237_429+2238i others(13): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTTT others(6): Show |
1 | a0001c0001t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.429+2237_429+2238i others(15): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTTT others(6): Show |
2 | a0001c0001t0001g0088 a0001c0001t0001g0178 |
2 | HG01257.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.429+2237_429+2238i others(15): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTGTTT others(7): Show |
3 | a0001c0001t0001g0091 a0001c0001t0003g0089 a0001c0003t0001g0090 |
3 | HG00544.hp2 HG01952.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.429+2237_429+2238i others(16): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTTTCT others(4): Show |
20 | a0001c0001t0001g0185 a0002c0002t0001g0251 a0002c0002t0001g0252 others(17): Show |
20 | HG00733.hp2 HG01891.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.429+2237_429+2238i others(13): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTTTCT others(5): Show |
2 | a0002c0002t0001g0271 a0002c0002t0001g0272 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.429+2237_429+2238i others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTTTTT others(4): Show |
70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
70 | HG00621.hp1 HG00639.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.429+2237_429+2238i others(13): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTGTTTTT others(5): Show |
13 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0052 others(10): Show |
13 | HG02055.hp1 HG02080.hp1 HG03688.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+2237_429+2238i others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | GTTTTTGT others(2): Show |
10 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0186 others(7): Show |
10 | HG02145.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.429+2241_429+2242i others(11): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185212491 | ||||||
| chr4:185212491 | G | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0216 others(17): Show |
21 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.429+2236G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212491 | |||||||
| chr4:185212492 | T | TGTGTTTG others(6): Show |
1 | a0001c0001t0001g0079 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.429+2237_429+2238i others(15): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212492 | |||||||
| chr4:185212493 | T | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.429+2238T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212493 | |||||||
| chr4:185212685 | A | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+2430A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212685 | |||||||
| chr4:185212686 | G | T | 11 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0253 others(8): Show |
11 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+2431G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212686 | |||||||
| chr4:185212777 | G | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(14): Show |
18 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+2522G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185212777 | |||||||
| chr4:185213050 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
180 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(177): Show |
intron_variant | MODIFIER | c.429+2795A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213050 | |||||||
| chr4:185213092 | A | C | 1 | a0001c0001t0001g0227 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.429+2837A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213092 | |||||||
| chr4:185213280 | CA | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
180 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(177): Show |
intron_variant | MODIFIER | c.429+3026delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213280 | |||||||
| chr4:185213385 | G | A | 1 | a0002c0002t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.429+3130G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213385 | |||||||
| chr4:185213508 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+3253C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213508 | |||||||
| chr4:185213509 | G | A | 1 | a0013c0015t0001g0010 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.429+3254G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213509 | |||||||
| chr4:185213666 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.429+3411G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213666 | |||||||
| chr4:185213666 | G | C | 1 | a0002c0002t0001g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.429+3411G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213666 | |||||||
| chr4:185213819 | A | G | 7 | a0001c0001t0001g0185 a0002c0002t0001g0262 a0002c0002t0001g0263 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+3564A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213819 | |||||||
| chr4:185213887 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02109.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.429+3632A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185213887 | |||||||
| chr4:185213938 | C | CT | 6 | a0001c0001t0001g0144 a0001c0003t0001g0067 a0001c0003t0001g0161 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+3697dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185213938 | ||||||
| chr4:185214060 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
168 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(165): Show |
intron_variant | MODIFIER | c.429+3805T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185214060 | |||||||
| chr4:185214394 | C | CA | 22 | a0001c0001t0001g0012 a0001c0001t0001g0199 a0001c0001t0001g0200 others(19): Show |
22 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.429+4157dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185214394 | ||||||
| chr4:185214394 | C | CAA | 6 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(3): Show |
6 | HG01081.hp1 HG01099.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+4156_429+4157d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185214394 | ||||||
| chr4:185214394 | CA | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0185 others(29): Show |
33 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.429+4157delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185214394 | ||||||
| chr4:185214394 | CAA | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
142 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.429+4156_429+4157d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185214394 | ||||||
| chr4:185214414 | A | G | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+4159A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185214414 | |||||||
| chr4:185214447 | T | G | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.429+4192T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185214447 | |||||||
| chr4:185214616 | G | A | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02738.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+4361G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185214616 | |||||||
| chr4:185214704 | T | C | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02738.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+4449T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185214704 | |||||||
| chr4:185214746 | A | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(14): Show |
18 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+4491A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185214746 | |||||||
| chr4:185214782 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.429+4527A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185214782 | |||||||
| chr4:185214864 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
174 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.429+4609T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185214864 | |||||||
| chr4:185214969 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.429+4714G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185214969 | |||||||
| chr4:185215000 | G | A | 1 | a0002c0002t0001g0253 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429+4745G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215000 | |||||||
| chr4:185215095 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.429+4840T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215095 | |||||||
| chr4:185215146 | G | A | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02738.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+4891G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215146 | |||||||
| chr4:185215184 | G | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
96 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.429+4929G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215184 | |||||||
| chr4:185215185 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
96 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.429+4930T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215185 | |||||||
| chr4:185215187 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.429+4932C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215187 | |||||||
| chr4:185215190 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(14): Show |
18 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+4935C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215190 | |||||||
| chr4:185215198 | C | T | 8 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(5): Show |
8 | HG00621.hp2 HG02738.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+4943C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215198 | |||||||
| chr4:185215199 | A | G | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02738.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+4944A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215199 | |||||||
| chr4:185215215 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
143 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.429+4960C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215215 | |||||||
| chr4:185215224 | G | A | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02738.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+4969G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215224 | |||||||
| chr4:185215228 | CA | C | 8 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(5): Show |
8 | HG00621.hp2 HG02738.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+4986delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185215228 | ||||||
| chr4:185215357 | A | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0237 others(12): Show |
16 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.429+5102A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215357 | |||||||
| chr4:185215674 | G | A | 1 | a0002c0002t0001g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.429+5419G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215674 | |||||||
| chr4:185215708 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02109.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.429+5453A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215708 | |||||||
| chr4:185215792 | C | CT | 8 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0087 others(5): Show |
8 | HG01433.hp1 HG01934.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+5552dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185215792 | ||||||
| chr4:185215792 | CT | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0075 others(18): Show |
22 | HG01192.hp2 HG01981.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.429+5552delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185215792 | ||||||
| chr4:185215857 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.429+5602T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215857 | |||||||
| chr4:185215897 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.429+5642C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215897 | |||||||
| chr4:185215921 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.429+5666C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215921 | |||||||
| chr4:185215948 | C | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(14): Show |
18 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+5693C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185215948 | |||||||
| chr4:185216044 | G | A | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02738.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+5789G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216044 | |||||||
| chr4:185216129 | A | G | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02738.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+5874A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216129 | |||||||
| chr4:185216257 | G | A | 1 | a0007c0016t0001g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.429+6002G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216257 | |||||||
| chr4:185216304 | T | C | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02738.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+6049T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216304 | |||||||
| chr4:185216513 | G | GT | 17 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(14): Show |
17 | HG00733.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.429+6281dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185216513 | ||||||
| chr4:185216513 | G | T | 2 | a0002c0002t0001g0272 a0010c0019t0005g0267 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.429+6258G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216513 | |||||||
| chr4:185216513 | GT | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
139 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.429+6281delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185216513 | ||||||
| chr4:185216513 | GTT | G | 10 | a0001c0001t0001g0088 a0001c0001t0001g0098 a0001c0001t0001g0099 others(7): Show |
10 | HG01168.hp2 HG01192.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.429+6280_429+6281d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185216513 | ||||||
| chr4:185216523 | T | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(15): Show |
19 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+6268T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216523 | |||||||
| chr4:185216648 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.429+6393T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216648 | |||||||
| chr4:185216658 | G | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.429+6403G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216658 | |||||||
| chr4:185216762 | C | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
182 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.429+6507C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216762 | |||||||
| chr4:185216799 | C | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+6544C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216799 | |||||||
| chr4:185216806 | C | T | 19 | a0001c0001t0001g0044 a0001c0001t0001g0131 a0001c0001t0001g0132 others(16): Show |
19 | HG00408.hp1 HG00544.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.429+6551C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185216806 | |||||||
| chr4:185217096 | T | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(15): Show |
19 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+6841T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217096 | |||||||
| chr4:185217126 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.429+6871G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217126 | |||||||
| chr4:185217204 | G | T | 1 | a0008c0018t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.429+6949G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217204 | |||||||
| chr4:185217205 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
147 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.429+6950G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217205 | |||||||
| chr4:185217226 | C | A | 1 | a0001c0001t0001g0033 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.429+6971C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217226 | |||||||
| chr4:185217252 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.429+6997T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217252 | |||||||
| chr4:185217255 | G | GA | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.429+7010dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185217255 | ||||||
| chr4:185217384 | T | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.429+7129T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217384 | |||||||
| chr4:185217384 | T | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(98): Show |
103 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.429+7129T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217384 | |||||||
| chr4:185217533 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.429+7278A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217533 | |||||||
| chr4:185217618 | A | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
79 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.429+7363A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217618 | |||||||
| chr4:185217622 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.429+7367T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217622 | |||||||
| chr4:185217724 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
173 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.429+7469A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217724 | |||||||
| chr4:185217769 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.429+7514G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217769 | |||||||
| chr4:185217791 | G | A | 3 | a0002c0002t0001g0255 a0002c0002t0001g0256 a0002c0002t0001g0257 |
3 | HG03209.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.429+7536G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217791 | |||||||
| chr4:185217923 | C | A | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+7668C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217923 | |||||||
| chr4:185217969 | T | C | 3 | a0002c0002t0001g0268 a0002c0002t0001g0269 a0002c0002t0001g0270 |
3 | HG02896.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.429+7714T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185217969 | |||||||
| chr4:185218063 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.429+7808C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218063 | |||||||
| chr4:185218123 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+7868C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218123 | |||||||
| chr4:185218177 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+7922C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218177 | |||||||
| chr4:185218187 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+7932T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218187 | |||||||
| chr4:185218247 | G | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+7992G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218247 | |||||||
| chr4:185218495 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.429+8240G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218495 | |||||||
| chr4:185218650 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.429+8395G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218650 | |||||||
| chr4:185218752 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+8497C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218752 | |||||||
| chr4:185218817 | C | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+8562C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218817 | |||||||
| chr4:185218885 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.429+8630T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218885 | |||||||
| chr4:185218892 | GT | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+8645delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185218892 | ||||||
| chr4:185218900 | T | A | 2 | a0004c0005t0001g0045 a0004c0005t0001g0046 |
2 | NA19002.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.429+8645T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185218900 | |||||||
| chr4:185219288 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.429+9033A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219288 | |||||||
| chr4:185219312 | A | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+9057A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219312 | |||||||
| chr4:185219350 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.429+9095G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219350 | |||||||
| chr4:185219356 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0205 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.429+9101A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219356 | |||||||
| chr4:185219416 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.429+9161A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219416 | |||||||
| chr4:185219427 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+9172T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219427 | |||||||
| chr4:185219432 | G | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+9177G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219432 | |||||||
| chr4:185219491 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+9236G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219491 | |||||||
| chr4:185219753 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+9498C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219753 | |||||||
| chr4:185219868 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.429+9613A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185219868 | |||||||
| chr4:185219908 | C | CT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(67): Show |
71 | HG00621.hp2 HG00733.hp2 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.429+9667dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185219908 | ||||||
| chr4:185219908 | C | CTT | 9 | a0001c0001t0001g0091 a0001c0001t0001g0177 a0001c0003t0001g0060 others(6): Show |
9 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+9666_429+9667d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185219908 | ||||||
| chr4:185219908 | C | CTTT | 27 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(24): Show |
28 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.429+9665_429+9667d others(5): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185219908 | ||||||
| chr4:185220030 | G | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(27): Show |
31 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.429+9775G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220030 | |||||||
| chr4:185220268 | CT | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
183 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.429+10022delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185220268 | ||||||
| chr4:185220302 | T | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(27): Show |
31 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.429+10047T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220302 | |||||||
| chr4:185220484 | C | CT | 7 | a0001c0001t0001g0088 a0001c0001t0001g0211 a0001c0001t0001g0212 others(4): Show |
7 | HG00140.hp2 HG00741.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+10245dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185220484 | ||||||
| chr4:185220484 | C | CTT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
146 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(143): Show |
intron_variant | MODIFIER | c.429+10244_429+1024 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185220484 | ||||||
| chr4:185220484 | CTT | C | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02738.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+10244_429+1024 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185220484 | ||||||
| chr4:185220587 | T | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(14): Show |
18 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.429+10332T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220587 | |||||||
| chr4:185220634 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.429+10379C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220634 | |||||||
| chr4:185220682 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.429+10427A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220682 | |||||||
| chr4:185220702 | G | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+10447G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220702 | |||||||
| chr4:185220727 | A | G | 8 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(5): Show |
8 | HG00621.hp2 HG02738.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+10472A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220727 | |||||||
| chr4:185220738 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.429+10483C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220738 | |||||||
| chr4:185220857 | T | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+10602T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220857 | |||||||
| chr4:185220906 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+10651T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220906 | |||||||
| chr4:185220941 | G | T | 1 | a0002c0002t0001g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.429+10686G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185220941 | |||||||
| chr4:185221055 | C | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+10800C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221055 | |||||||
| chr4:185221064 | G | A | 1 | a0001c0003t0001g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.429+10809G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221064 | |||||||
| chr4:185221220 | A | G | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+10965A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221220 | |||||||
| chr4:185221336 | G | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(15): Show |
19 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+11081G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221336 | |||||||
| chr4:185221366 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+11111A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221366 | |||||||
| chr4:185221761 | T | C | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+11506T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221761 | |||||||
| chr4:185221790 | G | GT | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+11537dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185221790 | ||||||
| chr4:185221825 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+11570T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221825 | |||||||
| chr4:185221842 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+11587T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221842 | |||||||
| chr4:185221852 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+11597A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221852 | |||||||
| chr4:185221884 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.429+11629A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221884 | |||||||
| chr4:185221971 | A | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+11716A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221971 | |||||||
| chr4:185221998 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+11743T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185221998 | |||||||
| chr4:185222004 | A | G | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+11749A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222004 | |||||||
| chr4:185222013 | A | G | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+11758A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222013 | |||||||
| chr4:185222021 | T | C | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+11766T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222021 | |||||||
| chr4:185222027 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+11772G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222027 | |||||||
| chr4:185222030 | CACTGTAG others(72): Show |
C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.429+11777_429+1185 others(83): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185222030 | ||||||
| chr4:185222033 | T | G | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+11778T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222033 | |||||||
| chr4:185222038 | G | A | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+11783G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222038 | |||||||
| chr4:185222043 | C | T | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+11788C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222043 | |||||||
| chr4:185222055 | C | T | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+11800C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222055 | |||||||
| chr4:185222069 | TAGGTATA others(38): Show |
T | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+11817_429+1186 others(49): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185222069 | ||||||
| chr4:185222112 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.429+11857A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222112 | |||||||
| chr4:185222114 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.429+11859C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222114 | |||||||
| chr4:185222179 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+11924T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222179 | |||||||
| chr4:185222194 | TCCATATA others(129): Show |
T | 8 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(5): Show |
8 | HG00621.hp2 HG02738.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+11972_429+1210 others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185222194 | ||||||
| chr4:185222208 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(28): Show |
32 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.429+11953C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222208 | |||||||
| chr4:185222228 | GCCATATA others(27): Show |
G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
182 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.429+12016_429+1204 others(38): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185222228 | ||||||
| chr4:185222246 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+11991G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222246 | |||||||
| chr4:185222248 | G | T | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+11993G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222248 | |||||||
| chr4:185222271 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12016C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222271 | |||||||
| chr4:185222276 | C | G | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12021C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222276 | |||||||
| chr4:185222280 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+12025G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222280 | |||||||
| chr4:185222282 | G | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.429+12027G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222282 | |||||||
| chr4:185222304 | C | A | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12049C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222304 | |||||||
| chr4:185222305 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12050T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222305 | |||||||
| chr4:185222310 | G | C | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12055G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222310 | |||||||
| chr4:185222315 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12060C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222315 | |||||||
| chr4:185222316 | T | G | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12061T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222316 | |||||||
| chr4:185222318 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12063T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222318 | |||||||
| chr4:185222325 | A | T | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12070A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222325 | |||||||
| chr4:185222329 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12074C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222329 | |||||||
| chr4:185222330 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12075A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222330 | |||||||
| chr4:185222338 | A | C | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12083A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222338 | |||||||
| chr4:185222345 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12090T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222345 | |||||||
| chr4:185222349 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12094T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222349 | |||||||
| chr4:185222352 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12097C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222352 | |||||||
| chr4:185222359 | T | A | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12104T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222359 | |||||||
| chr4:185222363 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12108T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222363 | |||||||
| chr4:185222367 | A | C | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12112A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222367 | |||||||
| chr4:185222367 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(31): Show |
35 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.429+12112A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222367 | |||||||
| chr4:185222382 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12127A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222382 | |||||||
| chr4:185222393 | A | T | 2 | a0001c0001t0001g0180 a0001c0001t0003g0089 |
2 | HG01952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.429+12138A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222393 | |||||||
| chr4:185222393 | ACAGCGCC others(27): Show |
A | 1 | a0001c0001t0001g0208 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.429+12161_429+1219 others(38): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185222393 | ||||||
| chr4:185222398 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.429+12143G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222398 | |||||||
| chr4:185222415 | C | T | 1 | a0001c0001t0003g0089 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.429+12160C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222415 | |||||||
| chr4:185222416 | T | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
183 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.429+12161T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222416 | |||||||
| chr4:185222432 | GCCCTATA others(27): Show |
G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.429+12195_429+1222 others(38): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185222432 | ||||||
| chr4:185222449 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
182 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.429+12194C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222449 | |||||||
| chr4:185222450 | G | T | 1 | a0001c0001t0003g0089 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.429+12195G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222450 | |||||||
| chr4:185222459 | A | T | 1 | a0001c0001t0003g0089 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.429+12204A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222459 | |||||||
| chr4:185222461 | T | A | 1 | a0001c0001t0003g0089 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.429+12206T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222461 | |||||||
| chr4:185222466 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+12211A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222466 | |||||||
| chr4:185222485 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+12230C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222485 | |||||||
| chr4:185222486 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0105 |
3 | NA19056.hp2 NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.429+12231G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222486 | |||||||
| chr4:185222519 | C | T | 21 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(18): Show |
21 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.429+12264C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222519 | |||||||
| chr4:185222524 | G | A | 2 | a0001c0001t0001g0208 a0003c0004t0001g0209 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.429+12269G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222524 | |||||||
| chr4:185222542 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
194 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.429+12287T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222542 | |||||||
| chr4:185222549 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+12294C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222549 | |||||||
| chr4:185222653 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.429+12398T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222653 | |||||||
| chr4:185222728 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+12473A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222728 | |||||||
| chr4:185222750 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0065 others(32): Show |
36 | HG01192.hp2 HG01981.hp1 HG02040.hp1 others(33): Show |
intron_variant | MODIFIER | c.429+12495C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222750 | |||||||
| chr4:185222837 | C | A | 8 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(5): Show |
8 | HG01081.hp1 HG01099.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+12582C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222837 | |||||||
| chr4:185222873 | C | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+12618C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222873 | |||||||
| chr4:185222895 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+12640A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222895 | |||||||
| chr4:185222908 | A | G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(5): Show |
8 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+12653A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222908 | |||||||
| chr4:185222983 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.429+12728G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185222983 | |||||||
| chr4:185223139 | C | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0175 |
2 | HG02040.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.429+12884C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223139 | |||||||
| chr4:185223177 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+12922A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223177 | |||||||
| chr4:185223309 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+13054C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223309 | |||||||
| chr4:185223397 | C | G | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+13142C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223397 | |||||||
| chr4:185223475 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+13220C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223475 | |||||||
| chr4:185223573 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.429+13318G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223573 | |||||||
| chr4:185223574 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.429+13319G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223574 | |||||||
| chr4:185223588 | G | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0009c0012t0001g0122 |
3 | HG01346.hp1 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.429+13333G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223588 | |||||||
| chr4:185223650 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
157 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(154): Show |
intron_variant | MODIFIER | c.429+13395G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223650 | |||||||
| chr4:185223720 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0065 others(36): Show |
40 | HG01192.hp2 HG01981.hp1 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.429+13465G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223720 | |||||||
| chr4:185223741 | GA | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0079 others(33): Show |
37 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.429+13500delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185223741 | ||||||
| chr4:185223741 | GAA | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
156 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(153): Show |
intron_variant | MODIFIER | c.429+13499_429+1350 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185223741 | ||||||
| chr4:185223907 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+13652C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223907 | |||||||
| chr4:185223917 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+13662C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185223917 | |||||||
| chr4:185224044 | T | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
157 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(154): Show |
intron_variant | MODIFIER | c.429+13789T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224044 | |||||||
| chr4:185224280 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+14025A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224280 | |||||||
| chr4:185224368 | A | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02145.hp1 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+14113A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224368 | |||||||
| chr4:185224410 | GATATATA others(3): Show |
G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.429+14173_429+1418 others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224410 | ||||||
| chr4:185224430 | AATATATA others(13): Show |
A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG00639.hp1 HG01106.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+14199_429+1421 others(24): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224430 | ||||||
| chr4:185224438 | G | GATATATA others(21): Show |
2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.429+14199_429+1422 others(32): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224438 | ||||||
| chr4:185224445 | A | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(28): Show |
32 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.429+14190A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224445 | |||||||
| chr4:185224446 | AATATATA others(5): Show |
A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
169 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.429+14199_429+1421 others(16): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224446 | ||||||
| chr4:185224450 | T | TATAA | 22 | a0001c0001t0001g0150 a0001c0001t0001g0159 a0001c0001t0001g0162 others(19): Show |
22 | HG02257.hp2 HG02258.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.429+14198_429+1419 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224450 | ||||||
| chr4:185224458 | G | A | 1 | a0002c0002t0001g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.429+14203G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224458 | |||||||
| chr4:185224466 | A | G | 1 | a0002c0002t0001g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.429+14211A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224466 | |||||||
| chr4:185224474 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
169 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.429+14219A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224474 | |||||||
| chr4:185224482 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
172 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.429+14227G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224482 | |||||||
| chr4:185224486 | TATAA | T | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.429+14235_429+1423 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224486 | ||||||
| chr4:185224489 | A | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(15): Show |
19 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+14234A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224489 | |||||||
| chr4:185224490 | AATAG | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
172 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.429+14239_429+1424 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224490 | ||||||
| chr4:185224494 | GATATATA others(29): Show |
G | 18 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0185 others(15): Show |
18 | HG02257.hp2 HG02258.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+14255_429+1429 others(40): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224494 | ||||||
| chr4:185224508 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.429+14253T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224508 | |||||||
| chr4:185224510 | G | A | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.429+14255G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224510 | |||||||
| chr4:185224510 | G | GATATATA others(13): Show |
1 | a0001c0001t0001g0017 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.429+14293_429+1431 others(24): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224510 | ||||||
| chr4:185224510 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.429+14255G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224510 | |||||||
| chr4:185224510 | GATATATA others(13): Show |
G | 8 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(5): Show |
8 | HG01081.hp1 HG01099.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+14293_429+1431 others(24): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224510 | ||||||
| chr4:185224520 | TATATATA others(1): Show |
T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(90): Show |
95 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.429+14273_429+1428 others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224520 | ||||||
| chr4:185224521 | ATATATAC others(43): Show |
A | 1 | a0001c0001t0001g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.429+14273_429+1432 others(54): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224521 | ||||||
| chr4:185224522 | T | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
75 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.429+14267T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224522 | |||||||
| chr4:185224524 | TATAC | T | 5 | a0001c0001t0001g0091 a0001c0001t0001g0205 a0001c0003t0001g0104 others(2): Show |
5 | HG03139.hp2 HG03225.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+14273_429+1427 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224524 | ||||||
| chr4:185224526 | TACATATA others(5): Show |
T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
75 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.429+14273_429+1428 others(16): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224526 | ||||||
| chr4:185224528 | CAT | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0011c0010t0001g0207 |
3 | HG02145.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.429+14281_429+1428 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224528 | ||||||
| chr4:185224530 | T | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(95): Show |
100 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.429+14275T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224530 | |||||||
| chr4:185224542 | T | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
75 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.429+14287T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224542 | |||||||
| chr4:185224542 | T | G | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.429+14287T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224542 | |||||||
| chr4:185224546 | TAC | T | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.429+14293_429+1429 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224546 | ||||||
| chr4:185224548 | C | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(15): Show |
19 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+14293C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224548 | |||||||
| chr4:185224548 | CAT | C | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+14301_429+1430 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224548 | ||||||
| chr4:185224548 | CATATATA others(3): Show |
C | 2 | a0001c0001t0001g0203 a0003c0004t0001g0204 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.429+14304_429+1431 others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224548 | ||||||
| chr4:185224549 | A | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(15): Show |
19 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+14294A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224549 | |||||||
| chr4:185224551 | A | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(15): Show |
19 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+14296A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224551 | |||||||
| chr4:185224552 | T | A | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.429+14297T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224552 | |||||||
| chr4:185224558 | A | C | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.429+14303A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224558 | |||||||
| chr4:185224569 | G | A | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.429+14314G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224569 | |||||||
| chr4:185224569 | GTGTATAT others(3): Show |
G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
75 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.429+14316_429+1432 others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185224569 | ||||||
| chr4:185224571 | G | A | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.429+14316G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224571 | |||||||
| chr4:185224579 | A | G | 5 | a0001c0001t0001g0159 a0001c0003t0001g0104 a0001c0003t0001g0106 others(2): Show |
5 | HG01168.hp2 NA18942.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+14324A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224579 | |||||||
| chr4:185224633 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+14378A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224633 | |||||||
| chr4:185224637 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.429+14382A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224637 | |||||||
| chr4:185224761 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.429+14506C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224761 | |||||||
| chr4:185224847 | A | G | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+14592A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224847 | |||||||
| chr4:185224854 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.429+14599A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224854 | |||||||
| chr4:185224946 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.429+14691G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185224946 | |||||||
| chr4:185225118 | C | CT | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(8): Show |
11 | HG01123.hp1 HG01123.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+14881dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185225118 | ||||||
| chr4:185225118 | CT | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0108 a0001c0001t0001g0150 others(3): Show |
6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+14881delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185225118 | ||||||
| chr4:185225204 | C | T | 1 | a0002c0002t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.429+14949C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185225204 | |||||||
| chr4:185225282 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.429+15027C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185225282 | |||||||
| chr4:185225416 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.429+15161A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185225416 | |||||||
| chr4:185225419 | C | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | NA18942.hp2 NA18964.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+15164C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185225419 | |||||||
| chr4:185225599 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0205 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.429+15344A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185225599 | |||||||
| chr4:185225661 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+15406G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185225661 | |||||||
| chr4:185225702 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+15447A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185225702 | |||||||
| chr4:185225844 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.429+15589A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185225844 | |||||||
| chr4:185226035 | A | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+15780A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226035 | |||||||
| chr4:185226131 | C | A | 1 | a0002c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.429+15876C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226131 | |||||||
| chr4:185226154 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.429+15899C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226154 | |||||||
| chr4:185226170 | G | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG02922.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+15915G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226170 | |||||||
| chr4:185226193 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+15938G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226193 | |||||||
| chr4:185226452 | TTTG | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(4): Show |
7 | HG02040.hp2 NA18612.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+16206_429+1620 others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185226452 | ||||||
| chr4:185226458 | GTTGT | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.429+16211_429+1621 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185226458 | ||||||
| chr4:185226490 | G | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+16235G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226490 | |||||||
| chr4:185226569 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+16314A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226569 | |||||||
| chr4:185226579 | T | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(27): Show |
31 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.429+16324T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226579 | |||||||
| chr4:185226662 | G | T | 1 | a0002c0002t0001g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.429+16407G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226662 | |||||||
| chr4:185226747 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+16492T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226747 | |||||||
| chr4:185226855 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+16600G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226855 | |||||||
| chr4:185226895 | T | TA | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+16642dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185226895 | ||||||
| chr4:185226986 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.429+16731T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185226986 | |||||||
| chr4:185227043 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429+16788C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185227043 | |||||||
| chr4:185227090 | G | A | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG00733.hp1 HG01074.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.429+16835G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185227090 | |||||||
| chr4:185227301 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+17046G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185227301 | |||||||
| chr4:185227479 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0073 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.429+17224G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185227479 | |||||||
| chr4:185227490 | T | G | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
6 | HG00639.hp1 HG01106.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+17235T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185227490 | |||||||
| chr4:185227501 | T | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+17246T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185227501 | |||||||
| chr4:185227946 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0242 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.429+17691A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185227946 | |||||||
| chr4:185228017 | C | T | 9 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0254 others(6): Show |
9 | HG00733.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+17762C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185228017 | |||||||
| chr4:185228047 | C | T | 1 | a0003c0004t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.429+17792C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185228047 | |||||||
| chr4:185228060 | C | T | 1 | a0005c0008t0001g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.429+17805C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185228060 | |||||||
| chr4:185228183 | A | G | 2 | a0001c0001t0002g0137 a0001c0001t0002g0160 |
2 | NA18941.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.429+17928A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185228183 | |||||||
| chr4:185228361 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.429+18106G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185228361 | |||||||
| chr4:185228512 | TA | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
194 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.429+18259delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185228512 | ||||||
| chr4:185229100 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(26): Show |
30 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.430-18194C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229100 | |||||||
| chr4:185229137 | AACACTC | A | 7 | a0001c0001t0001g0185 a0002c0002t0001g0262 a0002c0002t0001g0263 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-18156_430-1815 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229137 | |||||||
| chr4:185229177 | C | T | 1 | a0002c0002t0004g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.430-18117C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229177 | |||||||
| chr4:185229269 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-18025C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229269 | |||||||
| chr4:185229306 | C | T | 1 | a0001c0003t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.430-17988C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229306 | |||||||
| chr4:185229413 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.430-17881C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229413 | |||||||
| chr4:185229599 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-17695C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229599 | |||||||
| chr4:185229603 | T | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(14): Show |
18 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.430-17691T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229603 | |||||||
| chr4:185229634 | A | G | 1 | a0006c0013t0001g0123 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.430-17660A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229634 | |||||||
| chr4:185229677 | G | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.430-17617G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229677 | |||||||
| chr4:185229741 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.430-17553G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229741 | |||||||
| chr4:185229790 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430-17504C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229790 | |||||||
| chr4:185229854 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.430-17440G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229854 | |||||||
| chr4:185229943 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(27): Show |
31 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.430-17351C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229943 | |||||||
| chr4:185229945 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(27): Show |
31 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.430-17349C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185229945 | |||||||
| chr4:185230014 | G | A | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG02559.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-17280G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230014 | |||||||
| chr4:185230029 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.430-17265C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230029 | |||||||
| chr4:185230184 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(158): Show |
intron_variant | MODIFIER | c.430-17110T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230184 | |||||||
| chr4:185230364 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.430-16930C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230364 | |||||||
| chr4:185230385 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.430-16909A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230385 | |||||||
| chr4:185230392 | A | AT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(158): Show |
intron_variant | MODIFIER | c.430-16886dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185230392 | ||||||
| chr4:185230460 | A | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.430-16834A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230460 | |||||||
| chr4:185230470 | G | T | 13 | a0001c0001t0001g0185 a0002c0002t0001g0262 a0002c0002t0001g0263 others(10): Show |
13 | HG02257.hp2 HG02258.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.430-16824G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230470 | |||||||
| chr4:185230495 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0205 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.430-16799C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230495 | |||||||
| chr4:185230549 | C | T | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-16745C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230549 | |||||||
| chr4:185230550 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.430-16744A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230550 | |||||||
| chr4:185230580 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.430-16714A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230580 | |||||||
| chr4:185230626 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.430-16668C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230626 | |||||||
| chr4:185230651 | G | A | 8 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG00733.hp1 HG01074.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-16643G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230651 | |||||||
| chr4:185230710 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(1): Show |
4 | HG01243.hp1 HG01361.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-16584A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185230710 | |||||||
| chr4:185231102 | G | T | 1 | a0001c0001t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.430-16192G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231102 | |||||||
| chr4:185231102 | GT | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0091 others(32): Show |
36 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.430-16178delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185231102 | ||||||
| chr4:185231102 | GTT | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
158 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(155): Show |
intron_variant | MODIFIER | c.430-16179_430-1617 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185231102 | ||||||
| chr4:185231124 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
196 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.430-16170T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231124 | |||||||
| chr4:185231191 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430-16103T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231191 | |||||||
| chr4:185231232 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.430-16062G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231232 | |||||||
| chr4:185231259 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.430-16035C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231259 | |||||||
| chr4:185231282 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
158 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(155): Show |
intron_variant | MODIFIER | c.430-16012G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231282 | |||||||
| chr4:185231452 | G | A | 6 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-15842G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231452 | |||||||
| chr4:185231579 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
122 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.430-15715T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231579 | |||||||
| chr4:185231690 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
2 | HG00621.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.430-15604G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231690 | |||||||
| chr4:185231711 | CA | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
188 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.430-15568delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185231711 | ||||||
| chr4:185231728 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.430-15566C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231728 | |||||||
| chr4:185231765 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-15529G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231765 | |||||||
| chr4:185231835 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
87 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.430-15459C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231835 | |||||||
| chr4:185231999 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430-15295T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185231999 | |||||||
| chr4:185232045 | T | C | 9 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0186 others(6): Show |
9 | HG02145.hp2 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.430-15249T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185232045 | |||||||
| chr4:185232217 | C | G | 7 | a0001c0001t0001g0185 a0002c0002t0001g0262 a0002c0002t0001g0263 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-15077C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185232217 | |||||||
| chr4:185232371 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-14923C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185232371 | |||||||
| chr4:185232372 | G | A | 1 | a0002c0002t0001g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.430-14922G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185232372 | |||||||
| chr4:185232534 | A | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
80 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.430-14760A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185232534 | |||||||
| chr4:185232592 | G | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0203 |
2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.430-14702G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185232592 | |||||||
| chr4:185232962 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
80 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.430-14332T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185232962 | |||||||
| chr4:185233055 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.430-14239G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185233055 | |||||||
| chr4:185233251 | C | T | 10 | a0001c0001t0001g0185 a0002c0002t0001g0262 a0002c0002t0001g0263 others(7): Show |
10 | HG02257.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-14043C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185233251 | |||||||
| chr4:185233283 | TA | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.430-13998delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185233283 | ||||||
| chr4:185233290 | A | G | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-14004A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185233290 | |||||||
| chr4:185233554 | A | G | 3 | a0002c0002t0001g0265 a0002c0002t0001g0266 a0002c0002t0001g0271 |
3 | HG02717.hp2 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.430-13740A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185233554 | |||||||
| chr4:185233631 | T | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.430-13663T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185233631 | |||||||
| chr4:185233856 | G | GTTA | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
89 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.430-13423_430-1342 others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185233856 | ||||||
| chr4:185233950 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0125 a0001c0001t0001g0126 others(15): Show |
19 | HG01192.hp2 HG01981.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.430-13344C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185233950 | |||||||
| chr4:185234262 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-13032A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185234262 | |||||||
| chr4:185234386 | TAAAAAGT others(304): Show |
T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
190 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.430-12893_430-1258 others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185234386 | ||||||
| chr4:185234386 | TAAAAAGT others(305): Show |
T | 1 | a0001c0001t0002g0137 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.430-12903_430-1259 others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185234386 | ||||||
| chr4:185234401 | G | A | 7 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG01081.hp1 HG01099.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-12893G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185234401 | |||||||
| chr4:185234406 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430-12888G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185234406 | |||||||
| chr4:185234681 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.430-12592_430-1259 others(26): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185234681 | ||||||
| chr4:185234681 | C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02055.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.430-12592_430-1259 others(27): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185234681 | ||||||
| chr4:185234766 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.430-12528T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185234766 | |||||||
| chr4:185234787 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.430-12507T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185234787 | |||||||
| chr4:185234828 | G | A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(16): Show |
20 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.430-12466G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185234828 | |||||||
| chr4:185234905 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.430-12389G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185234905 | |||||||
| chr4:185234990 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.430-12304G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185234990 | |||||||
| chr4:185235283 | G | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
88 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.430-12011G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185235283 | |||||||
| chr4:185235451 | G | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
88 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.430-11843G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185235451 | |||||||
| chr4:185235576 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.430-11718G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185235576 | |||||||
| chr4:185235590 | C | T | 1 | a0005c0008t0001g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.430-11704C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185235590 | |||||||
| chr4:185235672 | G | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
6 | HG00639.hp1 HG01106.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-11622G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185235672 | |||||||
| chr4:185235762 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.430-11532T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185235762 | |||||||
| chr4:185235831 | A | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.430-11463A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185235831 | |||||||
| chr4:185235861 | A | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
88 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.430-11433A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185235861 | |||||||
| chr4:185236024 | C | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
79 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.430-11270C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185236024 | |||||||
| chr4:185236140 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.430-11154C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185236140 | |||||||
| chr4:185236150 | G | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
79 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.430-11144G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185236150 | |||||||
| chr4:185236163 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
79 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.430-11131C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185236163 | |||||||
| chr4:185236234 | CCTATAA | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02055.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.430-11057_430-1105 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185236234 | ||||||
| chr4:185236369 | G | GA | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
88 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.430-10917dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185236369 | ||||||
| chr4:185236384 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.430-10910C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185236384 | |||||||
| chr4:185236385 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430-10909C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185236385 | |||||||
| chr4:185236539 | G | GA | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
88 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.430-10747dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185236539 | ||||||
| chr4:185236642 | A | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(11): Show |
15 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.430-10652A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185236642 | |||||||
| chr4:185236684 | T | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(26): Show |
29 | HG00733.hp2 HG01081.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.430-10610T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185236684 | |||||||
| chr4:185236825 | A | ATC | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.430-10467_430-1046 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185236825 | ||||||
| chr4:185236835 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-10459C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185236835 | |||||||
| chr4:185236984 | T | TA | 8 | a0001c0001t0001g0044 a0001c0001t0001g0131 a0001c0001t0001g0132 others(5): Show |
8 | HG00408.hp1 HG00544.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-10309dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185236984 | ||||||
| chr4:185237150 | A | AG | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
188 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.430-10141dupG | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185237150 | ||||||
| chr4:185237153 | G | GA | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG02055.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-10134dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185237153 | ||||||
| chr4:185237419 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.430-9875T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237419 | |||||||
| chr4:185237599 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.430-9695C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237599 | |||||||
| chr4:185237635 | C | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
89 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.430-9659C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237635 | |||||||
| chr4:185237741 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
195 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.430-9553T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237741 | |||||||
| chr4:185237753 | T | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(67): Show |
71 | HG00733.hp2 HG01081.hp2 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.430-9541T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237753 | |||||||
| chr4:185237838 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.430-9456G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237838 | |||||||
| chr4:185237860 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.430-9434C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237860 | |||||||
| chr4:185237919 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG02040.hp2 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.430-9375C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237919 | |||||||
| chr4:185237933 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430-9361C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237933 | |||||||
| chr4:185237934 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.430-9360G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237934 | |||||||
| chr4:185237943 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-9351G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185237943 | |||||||
| chr4:185238062 | C | CA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0118 others(5): Show |
8 | HG00639.hp2 HG01099.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-9209dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185238062 | ||||||
| chr4:185238062 | C | CAA | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(74): Show |
77 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.430-9210_430-9209d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185238062 | ||||||
| chr4:185238062 | C | CAAA | 6 | a0001c0001t0001g0057 a0001c0001t0001g0120 a0001c0001t0001g0133 others(3): Show |
6 | HG01346.hp1 NA18954.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-9211_430-9209d others(5): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185238062 | ||||||
| chr4:185238062 | CA | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0043 others(34): Show |
38 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.430-9209delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185238062 | ||||||
| chr4:185238062 | CAA | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
32 | HG01192.hp2 HG01981.hp1 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.430-9210_430-9209d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185238062 | ||||||
| chr4:185238063 | A | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0150 others(25): Show |
28 | HG00733.hp2 HG01081.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.430-9231A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238063 | |||||||
| chr4:185238064 | A | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0173 |
2 | NA18992.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.430-9230A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238064 | |||||||
| chr4:185238065 | A | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
32 | HG01192.hp2 HG01981.hp1 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.430-9229A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238065 | |||||||
| chr4:185238066 | A | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | NA18951.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.430-9228A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238066 | |||||||
| chr4:185238089 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02109.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.430-9205A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238089 | |||||||
| chr4:185238103 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.430-9191C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238103 | |||||||
| chr4:185238275 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-9019A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238275 | |||||||
| chr4:185238291 | C | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
89 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.430-9003C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238291 | |||||||
| chr4:185238300 | C | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02055.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.430-8994C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238300 | |||||||
| chr4:185238320 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.430-8974C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238320 | |||||||
| chr4:185238412 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
195 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.430-8882G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238412 | |||||||
| chr4:185238523 | G | A | 2 | a0001c0001t0001g0140 a0014c0011t0001g0110 |
2 | HG01167.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.430-8771G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238523 | |||||||
| chr4:185238601 | G | C | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-8693G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238601 | |||||||
| chr4:185238628 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430-8666A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238628 | |||||||
| chr4:185238771 | C | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(75): Show |
80 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.430-8523C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238771 | |||||||
| chr4:185238866 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(17): Show |
21 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.430-8428G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238866 | |||||||
| chr4:185238867 | T | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(17): Show |
21 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.430-8427T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238867 | |||||||
| chr4:185238877 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0065 others(32): Show |
36 | HG01192.hp2 HG01981.hp1 HG02040.hp1 others(33): Show |
intron_variant | MODIFIER | c.430-8417G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185238877 | |||||||
| chr4:185239083 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.430-8211C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239083 | |||||||
| chr4:185239093 | T | G | 16 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(13): Show |
16 | HG00733.hp2 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.430-8201T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239093 | |||||||
| chr4:185239140 | A | G | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0003t0001g0060 others(4): Show |
7 | NA18954.hp1 NA18985.hp1 NA19009.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-8154A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239140 | |||||||
| chr4:185239164 | C | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.430-8130C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239164 | |||||||
| chr4:185239170 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0065 others(38): Show |
42 | HG01192.hp2 HG01258.hp2 HG01981.hp1 others(39): Show |
intron_variant | MODIFIER | c.430-8124A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239170 | |||||||
| chr4:185239182 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(66): Show |
71 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.430-8112T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239182 | |||||||
| chr4:185239204 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.430-8090A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239204 | |||||||
| chr4:185239209 | C | T | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-8085C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239209 | |||||||
| chr4:185239215 | C | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-8079C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239215 | |||||||
| chr4:185239220 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0149 |
2 | HG03942.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.430-8074A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239220 | |||||||
| chr4:185239239 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(108): Show |
113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.430-8055T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239239 | |||||||
| chr4:185239241 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0009c0012t0001g0122 |
3 | HG01346.hp1 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.430-8053G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239241 | |||||||
| chr4:185239241 | G | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0162 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.430-8053G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239241 | |||||||
| chr4:185239247 | C | T | 3 | a0001c0003t0001g0273 a0001c0003t0001g0274 a0014c0011t0001g0110 |
3 | HG01168.hp2 HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.430-8047C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239247 | |||||||
| chr4:185239248 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
134 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.430-8046A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239248 | |||||||
| chr4:185239252 | C | T | 12 | a0001c0001t0001g0159 a0001c0001t0001g0192 a0002c0002t0001g0250 others(9): Show |
12 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.430-8042C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239252 | |||||||
| chr4:185239256 | C | T | 10 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0254 others(7): Show |
10 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.430-8038C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239256 | |||||||
| chr4:185239257 | A | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0050 others(41): Show |
45 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.430-8037A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239257 | |||||||
| chr4:185239263 | CTT | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
188 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.430-8030_430-8029d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239263 | |||||||
| chr4:185239266 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
136 | HG00544.hp2 HG00621.hp2 HG01081.hp2 others(133): Show |
intron_variant | MODIFIER | c.430-8028G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239266 | |||||||
| chr4:185239268 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
136 | HG00544.hp2 HG00621.hp2 HG01081.hp2 others(133): Show |
intron_variant | MODIFIER | c.430-8026G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239268 | |||||||
| chr4:185239272 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.430-8022A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239272 | |||||||
| chr4:185239279 | C | G | 16 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(13): Show |
16 | HG00621.hp2 HG01099.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-8015C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239279 | |||||||
| chr4:185239279 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(5): Show |
8 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-8015C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239279 | |||||||
| chr4:185239280 | G | A | 1 | a0001c0003t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.430-8014G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239280 | |||||||
| chr4:185239294 | C | T | 20 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0139 others(17): Show |
20 | HG00733.hp2 HG01081.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.430-8000C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239294 | |||||||
| chr4:185239297 | C | T | 10 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0254 others(7): Show |
10 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.430-7997C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239297 | |||||||
| chr4:185239299 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.430-7995C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239299 | |||||||
| chr4:185239308 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
118 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.430-7986T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239308 | |||||||
| chr4:185239311 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.430-7983G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239311 | |||||||
| chr4:185239326 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0052 others(12): Show |
15 | HG01346.hp1 HG01433.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.430-7968G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239326 | |||||||
| chr4:185239334 | T | A | 2 | a0001c0001t0001g0112 a0001c0001t0006g0152 |
2 | HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.430-7960T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239334 | |||||||
| chr4:185239340 | G | A | 1 | a0001c0001t0002g0137 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.430-7954G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239340 | |||||||
| chr4:185239343 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(23): Show |
27 | HG01123.hp1 HG01192.hp2 HG01981.hp1 others(24): Show |
intron_variant | MODIFIER | c.430-7951C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239343 | |||||||
| chr4:185239351 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0100 a0001c0001t0001g0180 others(7): Show |
10 | HG01192.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.430-7943T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239351 | |||||||
| chr4:185239356 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0180 a0001c0001t0006g0152 |
3 | HG01433.hp2 HG01516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.430-7938A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239356 | |||||||
| chr4:185239400 | T | G | 10 | a0001c0001t0001g0100 a0001c0001t0001g0112 a0001c0001t0001g0115 others(7): Show |
10 | HG01192.hp1 HG01346.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-7894T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239400 | |||||||
| chr4:185239408 | A | G | 6 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
6 | HG01346.hp1 HG02293.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-7886A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239408 | |||||||
| chr4:185239412 | C | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0141 others(1): Show |
4 | HG01346.hp1 HG02293.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-7882C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239412 | |||||||
| chr4:185239412 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430-7882C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239412 | |||||||
| chr4:185239413 | G | A | 1 | a0002c0002t0001g0255 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.430-7881G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239413 | |||||||
| chr4:185239431 | T | C | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
23 | HG00733.hp2 HG01081.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.430-7863T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239431 | |||||||
| chr4:185239438 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.430-7856G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239438 | |||||||
| chr4:185239440 | A | G | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-7854A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239440 | |||||||
| chr4:185239443 | G | A | 6 | a0001c0001t0001g0112 a0001c0001t0001g0190 a0001c0001t0006g0152 others(3): Show |
6 | HG01433.hp2 HG01516.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-7851G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239443 | |||||||
| chr4:185239457 | T | TG | 16 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(13): Show |
16 | HG01433.hp2 HG01516.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.430-7835dupG | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185239457 | ||||||
| chr4:185239461 | A | G | 14 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(11): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.430-7833A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239461 | |||||||
| chr4:185239468 | T | C | 12 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(9): Show |
12 | HG02145.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.430-7826T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239468 | |||||||
| chr4:185239469 | G | C | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.430-7825G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239469 | |||||||
| chr4:185239487 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG02922.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430-7807G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239487 | |||||||
| chr4:185239639 | A | G | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0248 |
3 | HG00099.hp2 HG00280.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.430-7655A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239639 | |||||||
| chr4:185239713 | G | A | 5 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-7581G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239713 | |||||||
| chr4:185239714 | G | GT | 7 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0164 others(4): Show |
7 | HG02622.hp1 HG06807.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-7571dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185239714 | ||||||
| chr4:185239714 | GTTTT | G | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02630.hp2 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-7574_430-7571d others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185239714 | ||||||
| chr4:185239722 | T | G | 10 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG00621.hp1 HG02132.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-7572T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239722 | |||||||
| chr4:185239754 | AT | A | 5 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-7539delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239754 | |||||||
| chr4:185239763 | AT | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(18): Show |
22 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.430-7521delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185239763 | ||||||
| chr4:185239772 | TTC | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
83 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.430-7520_430-7519d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185239772 | ||||||
| chr4:185239774 | C | CT | 9 | a0001c0001t0001g0210 a0001c0006t0001g0068 a0001c0006t0001g0069 others(6): Show |
9 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.430-7505dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185239774 | ||||||
| chr4:185239775 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
83 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.430-7519T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239775 | |||||||
| chr4:185239776 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.430-7518T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239776 | |||||||
| chr4:185239782 | T | G | 6 | a0002c0002t0001g0262 a0002c0002t0001g0263 a0002c0002t0001g0268 others(3): Show |
6 | HG02258.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-7512T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239782 | |||||||
| chr4:185239789 | T | A | 1 | a0001c0001t0001g0018 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.430-7505T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239789 | |||||||
| chr4:185239838 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.430-7456C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239838 | |||||||
| chr4:185239870 | A | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01975.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.430-7424A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239870 | |||||||
| chr4:185239890 | T | A | 3 | a0001c0003t0001g0090 a0001c0003t0001g0128 a0001c0003t0001g0129 |
3 | HG00544.hp2 NA18955.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.430-7404T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239890 | |||||||
| chr4:185239904 | G | C | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-7390G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239904 | |||||||
| chr4:185239915 | C | T | 5 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0190 others(2): Show |
5 | HG02145.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-7379C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239915 | |||||||
| chr4:185239920 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.430-7374G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239920 | |||||||
| chr4:185239920 | G | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.430-7374G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239920 | |||||||
| chr4:185239963 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.430-7331T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239963 | |||||||
| chr4:185239973 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.430-7321C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239973 | |||||||
| chr4:185239983 | T | G | 37 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
37 | HG00280.hp1 HG00621.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.430-7311T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239983 | |||||||
| chr4:185239984 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.430-7310C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185239984 | |||||||
| chr4:185240021 | A | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.430-7273A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240021 | |||||||
| chr4:185240035 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-7259C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240035 | |||||||
| chr4:185240055 | A | G | 12 | a0001c0001t0001g0180 a0002c0002t0001g0250 a0002c0002t0001g0251 others(9): Show |
12 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.430-7239A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240055 | |||||||
| chr4:185240081 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.430-7213G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240081 | |||||||
| chr4:185240092 | T | C | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00099.hp2 HG00621.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.430-7202T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240092 | |||||||
| chr4:185240142 | A | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG03209.hp2 HG03225.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-7152A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240142 | |||||||
| chr4:185240164 | C | T | 2 | a0001c0001t0001g0044 a0001c0014t0001g0151 |
2 | HG00408.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.430-7130C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240164 | |||||||
| chr4:185240181 | T | C | 12 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0199 others(9): Show |
12 | HG00408.hp1 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.430-7113T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240181 | |||||||
| chr4:185240202 | G | A | 10 | a0001c0001t0001g0044 a0001c0001t0001g0127 a0001c0001t0001g0130 others(7): Show |
10 | HG00408.hp1 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.430-7092G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240202 | |||||||
| chr4:185240222 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.430-7072C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240222 | |||||||
| chr4:185240248 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.430-7046T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240248 | |||||||
| chr4:185240280 | A | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
27 | HG00408.hp1 HG01081.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.430-7014A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240280 | |||||||
| chr4:185240282 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0115 a0001c0001t0001g0132 others(4): Show |
7 | HG00408.hp1 NA18983.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-7012T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240282 | |||||||
| chr4:185240325 | A | ACTTCCCA others(120): Show |
2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.430-6936_430-6810d others(129): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185240325 | ||||||
| chr4:185240341 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-6953G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240341 | |||||||
| chr4:185240354 | C | T | 9 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0254 others(6): Show |
9 | HG00733.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.430-6940C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240354 | |||||||
| chr4:185240368 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.430-6926C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240368 | |||||||
| chr4:185240372 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(26): Show |
29 | HG00621.hp2 HG01081.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.430-6922C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240372 | |||||||
| chr4:185240404 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-6890C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240404 | |||||||
| chr4:185240421 | T | TGGGGCGG others(47): Show |
1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.430-6856_430-6855i others(56): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185240421 | ||||||
| chr4:185240427 | G | A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(14): Show |
17 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.430-6867G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240427 | |||||||
| chr4:185240444 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.430-6850G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240444 | |||||||
| chr4:185240469 | G | A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(14): Show |
17 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.430-6825G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240469 | |||||||
| chr4:185240505 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0065 others(42): Show |
46 | HG01123.hp1 HG01168.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.430-6789G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240505 | |||||||
| chr4:185240517 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-6777G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240517 | |||||||
| chr4:185240643 | C | CG | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(18): Show |
22 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.430-6645dupG | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185240643 | ||||||
| chr4:185240652 | A | G | 1 | a0001c0014t0001g0151 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.430-6642A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240652 | |||||||
| chr4:185240658 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.430-6636C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240658 | |||||||
| chr4:185240671 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-6623C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240671 | |||||||
| chr4:185240675 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.430-6619C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240675 | |||||||
| chr4:185240681 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.430-6613G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240681 | |||||||
| chr4:185240701 | A | AC | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-6588dupC | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185240701 | ||||||
| chr4:185240774 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.430-6520G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240774 | |||||||
| chr4:185240784 | G | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.430-6510G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240784 | |||||||
| chr4:185240790 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0126 others(16): Show |
20 | HG01123.hp1 HG01192.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.430-6504C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240790 | |||||||
| chr4:185240807 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.430-6487G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240807 | |||||||
| chr4:185240830 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-6464C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240830 | |||||||
| chr4:185240877 | A | G | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-6417A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240877 | |||||||
| chr4:185240878 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.430-6416C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240878 | |||||||
| chr4:185240883 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-6411C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240883 | |||||||
| chr4:185240884 | G | A | 3 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0138 |
3 | HG01496.hp1 HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.430-6410G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240884 | |||||||
| chr4:185240940 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.430-6354T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185240940 | |||||||
| chr4:185241027 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02109.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.430-6267C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241027 | |||||||
| chr4:185241052 | C | T | 1 | a0002c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-6242C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241052 | |||||||
| chr4:185241053 | G | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0126 others(16): Show |
20 | HG01123.hp1 HG01192.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.430-6241G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241053 | |||||||
| chr4:185241070 | C | CG | 10 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0148 others(7): Show |
10 | HG00544.hp2 HG01192.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.430-6220dupG | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241070 | ||||||
| chr4:185241163 | G | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-6131G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241163 | |||||||
| chr4:185241213 | C | T | 12 | a0001c0001t0001g0180 a0002c0002t0001g0250 a0002c0002t0001g0251 others(9): Show |
12 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.430-6081C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241213 | |||||||
| chr4:185241260 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.430-6034G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241260 | |||||||
| chr4:185241285 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.430-6009G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241285 | |||||||
| chr4:185241348 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0127 others(1): Show |
4 | NA18984.hp1 NA18985.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-5946C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241348 | |||||||
| chr4:185241349 | G | A | 2 | a0002c0002t0001g0268 a0002c0002t0001g0269 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.430-5945G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241349 | |||||||
| chr4:185241361 | G | T | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-5933G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241361 | |||||||
| chr4:185241395 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.430-5899G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241395 | |||||||
| chr4:185241399 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-5895G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241399 | |||||||
| chr4:185241415 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-5879T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241415 | |||||||
| chr4:185241447 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.430-5847C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241447 | |||||||
| chr4:185241453 | C | CAG | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.430-5841_430-5840i others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241453 | |||||||
| chr4:185241453 | C | CGG | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-5838_430-5837d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241453 | ||||||
| chr4:185241463 | G | A | 1 | a0002c0002t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.430-5831G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241463 | |||||||
| chr4:185241487 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.430-5807T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241487 | |||||||
| chr4:185241502 | ACC | A | 5 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0135 others(2): Show |
5 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-5791_430-5790d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241502 | |||||||
| chr4:185241503 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430-5791C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241503 | |||||||
| chr4:185241504 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430-5790C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241504 | |||||||
| chr4:185241504 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-5790C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241504 | |||||||
| chr4:185241506 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430-5788T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241506 | |||||||
| chr4:185241506 | T | G | 5 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0135 others(2): Show |
5 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-5788T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241506 | |||||||
| chr4:185241508 | G | A | 6 | a0001c0001t0001g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(3): Show |
6 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-5786G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241508 | |||||||
| chr4:185241510 | G | A | 5 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0135 others(2): Show |
5 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-5784G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241510 | |||||||
| chr4:185241511 | A | AGAGGGAG others(8): Show |
96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(93): Show |
98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.430-5718_430-5704d others(17): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241511 | ||||||
| chr4:185241511 | A | AGAGGGAG others(23): Show |
31 | a0001c0001t0001g0053 a0001c0001t0001g0065 a0001c0001t0001g0177 others(28): Show |
31 | HG00733.hp1 HG01074.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.430-5733_430-5704d others(32): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241511 | ||||||
| chr4:185241511 | A | AGAGGGAG others(38): Show |
12 | a0001c0001t0001g0100 a0001c0001t0001g0186 a0001c0001t0001g0187 others(9): Show |
12 | HG01192.hp1 HG01975.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.430-5748_430-5704d others(47): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241511 | ||||||
| chr4:185241511 | A | AGAGGGAG others(53): Show |
2 | a0001c0001t0001g0224 a0001c0003t0001g0063 |
2 | HG02723.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.430-5763_430-5704d others(62): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241511 | ||||||
| chr4:185241511 | A | AGAGGGAG others(29): Show |
3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.430-5767_430-5766i others(38): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241511 | ||||||
| chr4:185241511 | A | AGGGAGAG others(6): Show |
1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430-5782_430-5781i others(15): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241511 | ||||||
| chr4:185241511 | A | G | 5 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0135 others(2): Show |
5 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-5783A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241511 | |||||||
| chr4:185241511 | AGAGGGAG others(23): Show |
A | 1 | a0001c0001t0001g0201 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.430-5733_430-5704d others(32): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241511 | ||||||
| chr4:185241517 | AGAGGGAG others(2): Show |
A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.430-5766_430-5758d others(11): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185241517 | ||||||
| chr4:185241535 | G | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.430-5759G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185241535 | |||||||
| chr4:185242077 | TA | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.430-5215delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185242077 | ||||||
| chr4:185242141 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(18): Show |
22 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.430-5153G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242141 | |||||||
| chr4:185242168 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.430-5126G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242168 | |||||||
| chr4:185242189 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-5105A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242189 | |||||||
| chr4:185242191 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.430-5103T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242191 | |||||||
| chr4:185242309 | G | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.430-4985G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242309 | |||||||
| chr4:185242388 | G | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.430-4906G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242388 | |||||||
| chr4:185242464 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.430-4830G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242464 | |||||||
| chr4:185242570 | A | G | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.430-4724A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242570 | |||||||
| chr4:185242571 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.430-4723C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242571 | |||||||
| chr4:185242594 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.430-4700C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185242594 | |||||||
| chr4:185243126 | T | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.430-4168T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185243126 | |||||||
| chr4:185243137 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.430-4157T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185243137 | |||||||
| chr4:185243203 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.430-4091T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185243203 | |||||||
| chr4:185243214 | G | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
91 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.430-4080G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185243214 | |||||||
| chr4:185243462 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-3832A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185243462 | |||||||
| chr4:185243471 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0003g0089 |
3 | HG01243.hp2 HG01952.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.430-3823C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185243471 | |||||||
| chr4:185243613 | A | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.430-3681A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185243613 | |||||||
| chr4:185244239 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430-3055C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185244239 | |||||||
| chr4:185244240 | G | A | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-3054G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185244240 | |||||||
| chr4:185244253 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG02040.hp2 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.430-3041G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185244253 | |||||||
| chr4:185244282 | C | T | 2 | a0001c0001t0001g0064 a0001c0003t0001g0179 |
2 | NA19062.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.430-3012C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185244282 | |||||||
| chr4:185244737 | A | C | 1 | a0003c0007t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.430-2557A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185244737 | |||||||
| chr4:185244850 | C | T | 10 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0254 others(7): Show |
10 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.430-2444C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185244850 | |||||||
| chr4:185245008 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(18): Show |
22 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.430-2286G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245008 | |||||||
| chr4:185245069 | G | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-2225G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245069 | |||||||
| chr4:185245079 | C | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
6 | HG00639.hp1 HG01106.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-2215C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245079 | |||||||
| chr4:185245087 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.430-2207C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245087 | |||||||
| chr4:185245248 | T | TA | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.430-2037dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185245248 | ||||||
| chr4:185245248 | TA | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): Show |
142 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(139): Show |
intron_variant | MODIFIER | c.430-2037delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185245248 | ||||||
| chr4:185245294 | G | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-2000G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245294 | |||||||
| chr4:185245391 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-1903G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245391 | |||||||
| chr4:185245397 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.430-1897G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245397 | |||||||
| chr4:185245494 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(22): Show |
26 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.430-1800C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245494 | |||||||
| chr4:185245590 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.430-1704C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245590 | |||||||
| chr4:185245613 | A | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-1681A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245613 | |||||||
| chr4:185245938 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(22): Show |
26 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.430-1356A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185245938 | |||||||
| chr4:185246010 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430-1284G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246010 | |||||||
| chr4:185246010 | G | C | 1 | a0002c0002t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.430-1284G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246010 | |||||||
| chr4:185246015 | G | A | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.430-1279G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246015 | |||||||
| chr4:185246084 | G | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.430-1210G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246084 | |||||||
| chr4:185246106 | G | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.430-1188G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246106 | |||||||
| chr4:185246161 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.430-1133T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246161 | |||||||
| chr4:185246197 | A | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG00639.hp1 HG01106.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.430-1097A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246197 | |||||||
| chr4:185246283 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.430-1011A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246283 | |||||||
| chr4:185246349 | T | C | 1 | a0008c0018t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.430-945T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246349 | |||||||
| chr4:185246381 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.430-913C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246381 | |||||||
| chr4:185246449 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.430-845A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246449 | |||||||
| chr4:185246643 | T | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(22): Show |
26 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.430-651T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246643 | |||||||
| chr4:185246741 | C | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-553C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246741 | |||||||
| chr4:185246945 | T | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.430-349T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185246945 | |||||||
| chr4:185247023 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.430-271C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185247023 | |||||||
| chr4:185247035 | T | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.430-259T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185247035 | |||||||
| chr4:185247228 | AT | A | 16 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(13): Show |
16 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.430-54delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 185247228 | ||||||
| chr4:185247233 | T | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.430-61T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185247233 | |||||||
| chr4:185247253 | C | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0011c0010t0001g0207 |
3 | HG02145.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.430-41C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | chr4 | 185247253 | |||||||
| chr4:185247855 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0117 |
3 | HG00741.hp2 HG01258.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.514+477A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185247855 | |||||||
| chr4:185247903 | T | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.514+525T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185247903 | |||||||
| chr4:185248031 | G | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.514+653G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185248031 | |||||||
| chr4:185248036 | A | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.514+658A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185248036 | |||||||
| chr4:185248294 | A | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0185 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.514+916A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185248294 | |||||||
| chr4:185248382 | A | T | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.514+1004A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185248382 | |||||||
| chr4:185248464 | C | CA | 12 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(9): Show |
13 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.514+1088dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185248464 | ||||||
| chr4:185248584 | A | G | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.514+1206A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185248584 | |||||||
| chr4:185248643 | A | T | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.514+1265A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185248643 | |||||||
| chr4:185248742 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.514+1364A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185248742 | |||||||
| chr4:185248967 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.514+1589A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185248967 | |||||||
| chr4:185249018 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.514+1640A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185249018 | |||||||
| chr4:185249204 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.514+1826G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185249204 | |||||||
| chr4:185249481 | G | GT | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(1): Show |
4 | HG01243.hp1 HG01361.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+2108dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185249481 | ||||||
| chr4:185249619 | A | G | 5 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0135 others(2): Show |
5 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.514+2241A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185249619 | |||||||
| chr4:185249683 | A | AT | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.514+2313dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185249683 | ||||||
| chr4:185249755 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.514+2377T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185249755 | |||||||
| chr4:185249976 | G | A | 1 | a0003c0004t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.514+2598G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185249976 | |||||||
| chr4:185250033 | T | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0003c0004t0001g0209 |
3 | HG02280.hp2 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.514+2655T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185250033 | |||||||
| chr4:185250135 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(22): Show |
26 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.514+2757T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185250135 | |||||||
| chr4:185250173 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.514+2795G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185250173 | |||||||
| chr4:185250267 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.514+2889C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185250267 | |||||||
| chr4:185250608 | T | C | 12 | a0001c0001t0001g0180 a0002c0002t0001g0250 a0002c0002t0001g0251 others(9): Show |
12 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.514+3230T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185250608 | |||||||
| chr4:185250722 | GT | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
83 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.514+3358delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185250722 | ||||||
| chr4:185250930 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.514+3552A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185250930 | |||||||
| chr4:185251031 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.514+3653G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185251031 | |||||||
| chr4:185251033 | C | T | 1 | a0008c0018t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.514+3655C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185251033 | |||||||
| chr4:185251521 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.514+4143A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185251521 | |||||||
| chr4:185251598 | C | CGT | 52 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(49): Show |
52 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.514+4258_514+4259d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | C | CGTGT | 7 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0032 others(4): Show |
7 | HG00140.hp1 HG01167.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.514+4256_514+4259d others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | C | CGTGTGT | 5 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0040 others(2): Show |
5 | HG01106.hp2 HG02109.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.514+4254_514+4259d others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | CGT | C | 48 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0064 others(45): Show |
48 | HG00733.hp2 HG01168.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.514+4258_514+4259d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | CGTGT | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(12): Show |
16 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.514+4256_514+4259d others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | CGTGTGT | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.514+4254_514+4259d others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | CGTGTGTG others(1): Show |
C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0056 others(18): Show |
22 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.514+4252_514+4259d others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | CGTGTGTG others(3): Show |
C | 8 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0246 others(5): Show |
8 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.514+4250_514+4259d others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0240 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.514+4248_514+4259d others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | CGTGTGTG others(9): Show |
C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0088 a0001c0001t0001g0098 others(1): Show |
4 | HG01257.hp1 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+4244_514+4259d others(18): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251598 | CGTGTGTG others(11): Show |
C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.514+4242_514+4259d others(20): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185251598 | ||||||
| chr4:185251602 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.514+4224T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185251602 | |||||||
| chr4:185251636 | T | C | 5 | a0001c0003t0001g0060 a0001c0003t0001g0066 a0001c0003t0001g0067 others(2): Show |
5 | NA18954.hp1 NA18985.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.514+4258T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185251636 | |||||||
| chr4:185251639 | C | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.514+4261C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185251639 | |||||||
| chr4:185251937 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.514+4559C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185251937 | |||||||
| chr4:185252068 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.514+4690A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185252068 | |||||||
| chr4:185252217 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.514+4839A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185252217 | |||||||
| chr4:185252474 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.514+5096C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185252474 | |||||||
| chr4:185252600 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.514+5222A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185252600 | |||||||
| chr4:185252606 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.514+5228A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185252606 | |||||||
| chr4:185252892 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.514+5514C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185252892 | |||||||
| chr4:185252971 | C | T | 4 | a0002c0002t0001g0252 a0002c0002t0001g0255 a0002c0002t0001g0256 others(1): Show |
4 | HG01891.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+5593C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185252971 | |||||||
| chr4:185253048 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.514+5670A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185253048 | |||||||
| chr4:185253073 | AGAC | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.514+5699_514+5701d others(5): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185253073 | ||||||
| chr4:185253190 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0088 a0001c0001t0001g0099 |
3 | HG01257.hp1 HG01981.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.515-5658T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185253190 | |||||||
| chr4:185253369 | A | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG00099.hp1 HG01074.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.515-5479A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185253369 | |||||||
| chr4:185253451 | C | CTT | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-5390_515-5389d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185253451 | ||||||
| chr4:185253492 | G | T | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.515-5356G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185253492 | |||||||
| chr4:185253697 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-5151G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185253697 | |||||||
| chr4:185253927 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-4921G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185253927 | |||||||
| chr4:185254043 | A | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
91 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.515-4805A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185254043 | |||||||
| chr4:185254110 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0105 |
3 | NA19056.hp2 NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.515-4738G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185254110 | |||||||
| chr4:185254111 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.515-4737C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185254111 | |||||||
| chr4:185254397 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.515-4451C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185254397 | |||||||
| chr4:185254412 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(22): Show |
26 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.515-4436G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185254412 | |||||||
| chr4:185254561 | G | C | 1 | a0011c0010t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.515-4287G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185254561 | |||||||
| chr4:185254850 | GA | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0071 others(43): Show |
47 | HG01123.hp1 HG01168.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.515-3995delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185254850 | ||||||
| chr4:185254868 | G | A | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.515-3980G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185254868 | |||||||
| chr4:185255040 | G | A | 2 | a0001c0003t0001g0128 a0001c0003t0001g0129 |
2 | NA18955.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.515-3808G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255040 | |||||||
| chr4:185255070 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.515-3778T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255070 | |||||||
| chr4:185255117 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-3731A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255117 | |||||||
| chr4:185255162 | C | T | 1 | a0003c0004t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.515-3686C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255162 | |||||||
| chr4:185255210 | T | C | 8 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG00733.hp1 HG01074.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.515-3638T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255210 | |||||||
| chr4:185255227 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.515-3621G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255227 | |||||||
| chr4:185255277 | G | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG02145.hp2 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.515-3571G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255277 | |||||||
| chr4:185255279 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-3569G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255279 | |||||||
| chr4:185255294 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.515-3554C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255294 | |||||||
| chr4:185255300 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.515-3548A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255300 | |||||||
| chr4:185255362 | G | C | 1 | a0011c0010t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.515-3486G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255362 | |||||||
| chr4:185255459 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.515-3389A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255459 | |||||||
| chr4:185255628 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.515-3220A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255628 | |||||||
| chr4:185255640 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.515-3208C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255640 | |||||||
| chr4:185255830 | A | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0176 |
3 | NA18961.hp1 NA18988.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.515-3018A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255830 | |||||||
| chr4:185255929 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-2919C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255929 | |||||||
| chr4:185255998 | A | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0071 others(43): Show |
47 | HG01123.hp1 HG01168.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.515-2850A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185255998 | |||||||
| chr4:185256061 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-2787G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185256061 | |||||||
| chr4:185256072 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-2776T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185256072 | |||||||
| chr4:185256086 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-2762T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185256086 | |||||||
| chr4:185256125 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
5 | HG01123.hp2 HG01928.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.515-2723G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185256125 | |||||||
| chr4:185256146 | G | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-2702G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185256146 | |||||||
| chr4:185256224 | A | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(2): Show |
5 | HG02630.hp2 HG03486.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.515-2624A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185256224 | |||||||
| chr4:185256624 | C | CT | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.515-2205dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185256624 | ||||||
| chr4:185256624 | CT | C | 5 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0166 others(2): Show |
5 | HG00639.hp1 HG02165.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.515-2205delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185256624 | ||||||
| chr4:185256802 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-2046T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185256802 | |||||||
| chr4:185256934 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.515-1914C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185256934 | |||||||
| chr4:185256968 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-1880A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185256968 | |||||||
| chr4:185257124 | T | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.515-1724T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185257124 | |||||||
| chr4:185257176 | G | GA | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.515-1653dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185257176 | ||||||
| chr4:185257176 | GA | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.515-1653delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185257176 | ||||||
| chr4:185257176 | GAA | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(22): Show |
26 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.515-1654_515-1653d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185257176 | ||||||
| chr4:185257333 | G | A | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.515-1515G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185257333 | |||||||
| chr4:185257460 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.515-1388T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185257460 | |||||||
| chr4:185257509 | C | T | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.515-1339C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185257509 | |||||||
| chr4:185257582 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.515-1266C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185257582 | |||||||
| chr4:185257593 | T | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.515-1255T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185257593 | |||||||
| chr4:185258081 | G | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.515-767G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185258081 | |||||||
| chr4:185258096 | A | G | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.515-752A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185258096 | |||||||
| chr4:185258161 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.515-687C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185258161 | |||||||
| chr4:185258633 | A | AAAATTTA others(32): Show |
1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.515-213_515-175dup others(39): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | 185258633 | ||||||
| chr4:185258688 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.515-160G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | chr4 | 185258688 | |||||||
| chr4:185259345 | A | G | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG00621.hp2 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.731+281A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185259345 | |||||||
| chr4:185259656 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.731+592G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185259656 | |||||||
| chr4:185259777 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.731+713A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185259777 | |||||||
| chr4:185259912 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.731+848T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185259912 | |||||||
| chr4:185259991 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.731+927A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185259991 | |||||||
| chr4:185260173 | A | ATTTTATT others(29): Show |
2 | a0002c0002t0001g0256 a0002c0002t0001g0257 |
2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.731+1142_731+1177d others(38): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185260173 | ||||||
| chr4:185260173 | ATTTTATT others(29): Show |
A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0088 a0001c0001t0001g0098 others(1): Show |
4 | HG01257.hp1 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+1142_731+1177d others(38): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185260173 | ||||||
| chr4:185260207 | T | C | 4 | a0001c0001t0001g0205 a0001c0006t0001g0068 a0001c0006t0001g0069 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+1143T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185260207 | |||||||
| chr4:185260381 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0039 others(1): Show |
4 | HG01975.hp1 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.731+1317G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185260381 | |||||||
| chr4:185260414 | CT | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.731+1352delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185260414 | ||||||
| chr4:185260509 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.731+1445G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185260509 | |||||||
| chr4:185260636 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.731+1572T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185260636 | |||||||
| chr4:185261114 | C | CTG | 25 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0032 others(22): Show |
26 | HG00140.hp1 HG01123.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.731+2092_731+2093d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261114 | C | CTGTG | 14 | a0001c0001t0001g0059 a0001c0001t0001g0170 a0001c0001t0001g0195 others(11): Show |
14 | HG00621.hp2 HG01099.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.731+2090_731+2093d others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261114 | C | CTGTGTG | 14 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(11): Show |
15 | HG00621.hp1 HG01081.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.731+2088_731+2093d others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261114 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0215 others(1): Show |
4 | HG02155.hp2 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+2086_731+2093d others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261114 | C | CTGTGTGT others(3): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.731+2084_731+2093d others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261114 | CTG | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.731+2092_731+2093d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261114 | CTGTG | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0064 others(12): Show |
15 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.731+2090_731+2093d others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261114 | CTGTGTG | C | 41 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0074 others(38): Show |
41 | HG00408.hp1 HG00544.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.731+2088_731+2093d others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261114 | CTGTGTGT others(1): Show |
C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0111 a0001c0001t0001g0144 others(4): Show |
7 | HG01106.hp2 HG02145.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.731+2086_731+2093d others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261114 | CTGTGTGT others(3): Show |
C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0041 others(2): Show |
5 | HG02109.hp2 HG02723.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.731+2084_731+2093d others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261114 | ||||||
| chr4:185261122 | G | GTGTGTGT others(1): Show |
13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.731+2065_731+2066i others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 185261122 | ||||||
| chr4:185261133 | T | G | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.731+2069T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185261133 | |||||||
| chr4:185261140 | G | C | 1 | a0002c0002t0001g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.731+2076G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185261140 | |||||||
| chr4:185261185 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.731+2121T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185261185 | |||||||
| chr4:185261209 | C | G | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.731+2145C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185261209 | |||||||
| chr4:185261349 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.731+2285G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185261349 | |||||||
| chr4:185261468 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.731+2404C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185261468 | |||||||
| chr4:185261670 | G | A | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.731+2606G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185261670 | |||||||
| chr4:185261788 | C | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
209 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.732-2650C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185261788 | |||||||
| chr4:185261936 | A | T | 1 | a0001c0003t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.732-2502A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185261936 | |||||||
| chr4:185262049 | C | T | 5 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.732-2389C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185262049 | |||||||
| chr4:185262138 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.732-2300A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185262138 | |||||||
| chr4:185262220 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.732-2218C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185262220 | |||||||
| chr4:185262349 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.732-2089A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185262349 | |||||||
| chr4:185262425 | C | G | 1 | a0004c0005t0001g0046 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.732-2013C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185262425 | |||||||
| chr4:185262515 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.732-1923T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185262515 | |||||||
| chr4:185262900 | A | C | 2 | a0001c0001t0001g0131 a0001c0001t0002g0134 |
2 | HG02165.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.732-1538A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185262900 | |||||||
| chr4:185262955 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.732-1483G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185262955 | |||||||
| chr4:185262994 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.732-1444A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185262994 | |||||||
| chr4:185263009 | C | G | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.732-1429C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263009 | |||||||
| chr4:185263068 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.732-1370G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263068 | |||||||
| chr4:185263148 | G | A | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.732-1290G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263148 | |||||||
| chr4:185263215 | G | A | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.732-1223G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263215 | |||||||
| chr4:185263242 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.732-1196T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263242 | |||||||
| chr4:185263329 | T | G | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.732-1109T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263329 | |||||||
| chr4:185263461 | A | G | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.732-977A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263461 | |||||||
| chr4:185263603 | T | C | 19 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(16): Show |
19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.732-835T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263603 | |||||||
| chr4:185263691 | T | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.732-747T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263691 | |||||||
| chr4:185263738 | A | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.732-700A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263738 | |||||||
| chr4:185263769 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.732-669A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263769 | |||||||
| chr4:185263822 | C | T | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.732-616C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263822 | |||||||
| chr4:185263868 | G | T | 1 | a0001c0001t0001g0019 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.732-570G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263868 | |||||||
| chr4:185263956 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.732-482A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263956 | |||||||
| chr4:185263961 | A | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
90 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.732-477A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263961 | |||||||
| chr4:185263976 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.732-462G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185263976 | |||||||
| chr4:185264139 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.732-299A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185264139 | |||||||
| chr4:185264214 | G | A | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.732-224G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185264214 | |||||||
| chr4:185264262 | C | G | 1 | a0002c0002t0001g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.732-176C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185264262 | |||||||
| chr4:185264397 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.732-41T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | chr4 | 185264397 | |||||||
| chr4:185264738 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.904+128A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185264738 | |||||||
| chr4:185264760 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.904+150A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185264760 | |||||||
| chr4:185264803 | T | C | 4 | a0001c0001t0001g0205 a0001c0006t0001g0068 a0001c0006t0001g0069 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+193T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185264803 | |||||||
| chr4:185264832 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.904+222A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185264832 | |||||||
| chr4:185264837 | T | G | 1 | a0007c0016t0001g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.904+227T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185264837 | |||||||
| chr4:185264973 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.904+363C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185264973 | |||||||
| chr4:185265005 | TC | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.904+396delC | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265005 | |||||||
| chr4:185265006 | C | T | 9 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(6): Show |
9 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.904+396C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265006 | |||||||
| chr4:185265235 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.904+625G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265235 | |||||||
| chr4:185265260 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.904+650C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265260 | |||||||
| chr4:185265331 | G | A | 1 | a0006c0013t0001g0123 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.904+721G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265331 | |||||||
| chr4:185265388 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.904+778G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265388 | |||||||
| chr4:185265477 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.904+867C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265477 | |||||||
| chr4:185265566 | CTG | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.904+959_904+960del others(2): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 185265566 | ||||||
| chr4:185265715 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.904+1105T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265715 | |||||||
| chr4:185265791 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0036 |
2 | HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.905-1178G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265791 | |||||||
| chr4:185265918 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.905-1051G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185265918 | |||||||
| chr4:185266278 | G | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.905-691G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185266278 | |||||||
| chr4:185266312 | T | C | 10 | a0001c0001t0001g0193 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01081.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-657T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185266312 | |||||||
| chr4:185266775 | C | T | 4 | a0001c0001t0001g0205 a0001c0006t0001g0068 a0001c0006t0001g0069 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-194C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185266775 | |||||||
| chr4:185266808 | A | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.905-161A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185266808 | |||||||
| chr4:185266854 | CCT | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.905-114_905-113del others(2): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | 185266854 | |||||||
| chr4:185267219 | TA | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0108 others(4): Show |
7 | HG01167.hp2 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1091+78delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185267219 | ||||||
| chr4:185267251 | A | C | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG00621.hp2 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1091+96A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185267251 | |||||||
| chr4:185267306 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1091+151C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185267306 | |||||||
| chr4:185267464 | A | G | 2 | a0001c0001t0002g0137 a0001c0001t0002g0160 |
2 | NA18941.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1091+309A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185267464 | |||||||
| chr4:185267557 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1091+402C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185267557 | |||||||
| chr4:185267592 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0185 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1091+437G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185267592 | |||||||
| chr4:185267729 | TA | T | 9 | a0001c0001t0001g0162 a0001c0001t0001g0215 a0001c0001t0001g0216 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1091+590delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185267729 | ||||||
| chr4:185267752 | C | T | 1 | a0001c0003t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1091+597C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185267752 | |||||||
| chr4:185267812 | C | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(10): Show |
13 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1091+657C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185267812 | |||||||
| chr4:185268074 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1091+919T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185268074 | |||||||
| chr4:185268088 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1091+933A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185268088 | |||||||
| chr4:185268349 | A | G | 2 | a0002c0002t0001g0264 a0002c0002t0001g0272 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1091+1194A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185268349 | |||||||
| chr4:185268357 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0064 others(58): Show |
62 | HG00733.hp2 HG01123.hp1 HG01168.hp2 others(59): Show |
intron_variant | MODIFIER | c.1091+1202T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185268357 | |||||||
| chr4:185268495 | C | G | 1 | a0001c0003t0001g0062 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1091+1340C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185268495 | |||||||
| chr4:185268529 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
131 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1091+1374T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185268529 | |||||||
| chr4:185268958 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1091+1803G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185268958 | |||||||
| chr4:185269069 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1091+1914C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185269069 | |||||||
| chr4:185269140 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1091+1985C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185269140 | |||||||
| chr4:185269207 | AAAGAGCT others(9): Show |
A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1091+2055_1091+207 others(20): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185269207 | ||||||
| chr4:185269315 | C | T | 1 | a0011c0010t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1091+2160C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185269315 | |||||||
| chr4:185269408 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
117 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1091+2253G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185269408 | |||||||
| chr4:185269803 | A | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1091+2648A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185269803 | |||||||
| chr4:185269848 | T | C | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+2693T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185269848 | |||||||
| chr4:185270079 | CA | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
118 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1091+2942delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185270079 | ||||||
| chr4:185270267 | T | C | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+3112T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185270267 | |||||||
| chr4:185270334 | G | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
199 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1091+3179G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185270334 | |||||||
| chr4:185270399 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1091+3244A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185270399 | |||||||
| chr4:185270626 | CAGAAT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1091+3473_1091+347 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185270626 | ||||||
| chr4:185270975 | C | T | 1 | a0006c0013t0001g0123 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1091+3820C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185270975 | |||||||
| chr4:185271090 | G | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1091+3935G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185271090 | |||||||
| chr4:185271100 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1091+3945G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185271100 | |||||||
| chr4:185271370 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1091+4215C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185271370 | |||||||
| chr4:185271373 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1091+4218G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185271373 | |||||||
| chr4:185271506 | C | T | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1091+4351C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185271506 | |||||||
| chr4:185271639 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1091+4484T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185271639 | |||||||
| chr4:185271642 | A | G | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1091+4487A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185271642 | |||||||
| chr4:185271883 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1091+4728C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185271883 | |||||||
| chr4:185271887 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1091+4732A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185271887 | |||||||
| chr4:185272244 | C | T | 1 | a0002c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1091+5089C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185272244 | |||||||
| chr4:185272265 | A | G | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+5110A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185272265 | |||||||
| chr4:185272288 | T | C | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1091+5133T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185272288 | |||||||
| chr4:185272319 | A | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(2): Show |
5 | HG02630.hp2 HG03486.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+5164A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185272319 | |||||||
| chr4:185272429 | A | G | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1091+5274A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185272429 | |||||||
| chr4:185272481 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1091+5326G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185272481 | |||||||
| chr4:185272912 | C | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0148 |
2 | HG02080.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1091+5757C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185272912 | |||||||
| chr4:185272943 | G | A | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1091+5788G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185272943 | |||||||
| chr4:185273022 | T | C | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1091+5867T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273022 | |||||||
| chr4:185273027 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1091+5872G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273027 | |||||||
| chr4:185273068 | T | G | 3 | a0004c0005t0001g0045 a0004c0005t0001g0046 a0004c0005t0001g0047 |
3 | HG00408.hp2 NA19002.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1091+5913T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273068 | |||||||
| chr4:185273173 | A | T | 1 | a0001c0003t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1091+6018A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273173 | |||||||
| chr4:185273236 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0003g0089 |
3 | HG01243.hp2 HG01952.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1091+6081C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273236 | |||||||
| chr4:185273471 | T | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0011c0010t0001g0207 |
3 | HG02145.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1091+6316T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273471 | |||||||
| chr4:185273562 | G | A | 1 | a0007c0016t0001g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1091+6407G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273562 | |||||||
| chr4:185273611 | C | T | 12 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(9): Show |
12 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1091+6456C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273611 | |||||||
| chr4:185273648 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1091+6493C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273648 | |||||||
| chr4:185273752 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1091+6597C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273752 | |||||||
| chr4:185273841 | T | C | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+6686T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273841 | |||||||
| chr4:185273919 | C | T | 1 | a0008c0018t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1091+6764C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273919 | |||||||
| chr4:185273993 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1091+6838C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185273993 | |||||||
| chr4:185274064 | T | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(5): Show |
8 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1091+6909T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185274064 | |||||||
| chr4:185274353 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1091+7198C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185274353 | |||||||
| chr4:185274360 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1091+7205A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185274360 | |||||||
| chr4:185274999 | A | G | 3 | a0001c0003t0001g0104 a0001c0003t0001g0106 a0001c0003t0001g0107 |
3 | NA18942.hp1 NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1091+7844A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185274999 | |||||||
| chr4:185275004 | G | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1091+7849G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185275004 | |||||||
| chr4:185275029 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1091+7874G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185275029 | |||||||
| chr4:185275201 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | HG00621.hp1 HG02132.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1091+8046G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185275201 | |||||||
| chr4:185275278 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0064 others(45): Show |
49 | HG01123.hp1 HG01168.hp2 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.1091+8123A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185275278 | |||||||
| chr4:185275299 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1091+8144G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185275299 | |||||||
| chr4:185275443 | TTAATG | T | 4 | a0001c0001t0001g0205 a0001c0006t0001g0068 a0001c0006t0001g0069 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091+8292_1091+829 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185275443 | ||||||
| chr4:185275566 | C | T | 1 | a0001c0003t0001g0090 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1091+8411C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185275566 | |||||||
| chr4:185275745 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1091+8590C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185275745 | |||||||
| chr4:185275889 | A | G | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+8734A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185275889 | |||||||
| chr4:185275916 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.1091+8761C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185275916 | |||||||
| chr4:185276026 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02109.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1091+8871C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185276026 | |||||||
| chr4:185276089 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(5): Show |
8 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1091+8934G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185276089 | |||||||
| chr4:185276195 | A | G | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1091+9040A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185276195 | |||||||
| chr4:185276250 | A | C | 1 | a0002c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1091+9095A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185276250 | |||||||
| chr4:185276371 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(9): Show |
13 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1091+9216A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185276371 | |||||||
| chr4:185276763 | C | G | 6 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0083 others(3): Show |
6 | HG01123.hp2 HG01928.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+9608C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185276763 | |||||||
| chr4:185276920 | T | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1091+9765T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185276920 | |||||||
| chr4:185277069 | G | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
2 | NA18943.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1091+9914G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185277069 | |||||||
| chr4:185277170 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1091+10015G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185277170 | |||||||
| chr4:185277588 | G | A | 2 | a0001c0001t0001g0201 a0003c0004t0001g0204 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1092-10424G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185277588 | |||||||
| chr4:185277606 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1092-10406T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185277606 | |||||||
| chr4:185277610 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0032 |
2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1092-10402G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185277610 | |||||||
| chr4:185277711 | ACTTATTA others(312): Show |
A | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1092-10287_1092-99 others(5): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185277711 | ||||||
| chr4:185277715 | ATTACCTT others(6): Show |
A | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1092-10294_1092-10 others(19): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185277715 | ||||||
| chr4:185277720 | C | CT | 21 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0027 others(18): Show |
21 | HG00408.hp2 HG00544.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1092-10262dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185277720 | ||||||
| chr4:185277720 | C | CTTTT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0071 others(13): Show |
17 | HG02622.hp2 NA18612.hp1 NA18941.hp2 others(14): Show |
intron_variant | MODIFIER | c.1092-10265_1092-10 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185277720 | ||||||
| chr4:185277720 | C | CTTTTT | 14 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0157 others(11): Show |
14 | HG02040.hp1 HG02055.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1092-10266_1092-10 others(11): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185277720 | ||||||
| chr4:185277720 | C | CTTTTTT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0165 a0001c0001t0001g0174 others(4): Show |
7 | HG01192.hp1 HG01192.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092-10267_1092-10 others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185277720 | ||||||
| chr4:185277720 | CT | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0028 others(4): Show |
7 | HG00099.hp1 HG00621.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092-10262delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185277720 | ||||||
| chr4:185277720 | CTTTTTTT | C | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG02922.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092-10268_1092-10 others(13): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185277720 | ||||||
| chr4:185277720 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1092-10272_1092-10 others(17): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185277720 | ||||||
| chr4:185277729 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1092-10283T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185277729 | |||||||
| chr4:185277882 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1092-10130G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185277882 | |||||||
| chr4:185277974 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1092-10038C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185277974 | |||||||
| chr4:185277998 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1092-10014C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185277998 | |||||||
| chr4:185278035 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1092-9977T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278035 | |||||||
| chr4:185278179 | C | T | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1092-9833C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278179 | |||||||
| chr4:185278251 | G | A | 1 | a0011c0010t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1092-9761G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278251 | |||||||
| chr4:185278271 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1092-9741T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278271 | |||||||
| chr4:185278406 | A | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0108 |
3 | HG02155.hp1 NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1092-9606A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278406 | |||||||
| chr4:185278467 | A | C | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02630.hp2 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-9545A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278467 | |||||||
| chr4:185278498 | GGAAT | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1092-9492_1092-948 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185278498 | ||||||
| chr4:185278743 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1092-9269T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278743 | |||||||
| chr4:185278801 | A | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(5): Show |
8 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1092-9211A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278801 | |||||||
| chr4:185278837 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG01361.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1092-9175A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278837 | |||||||
| chr4:185278968 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1092-9044G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185278968 | |||||||
| chr4:185279318 | G | A | 1 | a0003c0004t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1092-8694G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185279318 | |||||||
| chr4:185279518 | A | ACTTCCC | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1092-8492_1092-849 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185279518 | ||||||
| chr4:185279762 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092-8250A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185279762 | |||||||
| chr4:185279803 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1092-8209T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185279803 | |||||||
| chr4:185279836 | C | CTT | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092-8176_1092-817 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185279836 | |||||||
| chr4:185279894 | T | C | 1 | a0002c0002t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1092-8118T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185279894 | |||||||
| chr4:185279949 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1092-8063C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185279949 | |||||||
| chr4:185279983 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1092-8029C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185279983 | |||||||
| chr4:185280437 | A | G | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-7575A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185280437 | |||||||
| chr4:185280459 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1092-7553G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185280459 | |||||||
| chr4:185280710 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1092-7302T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185280710 | |||||||
| chr4:185280720 | C | T | 6 | a0001c0001t0001g0239 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-7292C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185280720 | |||||||
| chr4:185280781 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1092-7231T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185280781 | |||||||
| chr4:185281003 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1092-7009A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185281003 | |||||||
| chr4:185281061 | C | T | 1 | a0002c0002t0001g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1092-6951C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185281061 | |||||||
| chr4:185281073 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1092-6939C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185281073 | |||||||
| chr4:185281343 | CTG | C | 5 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092-6665_1092-666 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185281343 | ||||||
| chr4:185281437 | T | C | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1092-6575T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185281437 | |||||||
| chr4:185281677 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1092-6335T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185281677 | |||||||
| chr4:185281843 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
199 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1092-6169T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185281843 | |||||||
| chr4:185281868 | T | C | 5 | a0002c0002t0001g0262 a0002c0002t0001g0268 a0002c0002t0001g0269 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092-6144T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185281868 | |||||||
| chr4:185281938 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1092-6074C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185281938 | |||||||
| chr4:185282033 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0108 |
3 | HG02155.hp1 NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1092-5979A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282033 | |||||||
| chr4:185282110 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1092-5902A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282110 | |||||||
| chr4:185282111 | G | C | 6 | a0002c0002t0001g0262 a0002c0002t0001g0268 a0002c0002t0001g0269 others(3): Show |
6 | HG02258.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-5901G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282111 | |||||||
| chr4:185282190 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1092-5822T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282190 | |||||||
| chr4:185282265 | G | A | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1092-5747G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282265 | |||||||
| chr4:185282393 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0162 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1092-5619T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282393 | |||||||
| chr4:185282509 | G | A | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-5503G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282509 | |||||||
| chr4:185282514 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1092-5498G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282514 | |||||||
| chr4:185282654 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0064 others(45): Show |
49 | HG01123.hp1 HG01168.hp2 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.1092-5358C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282654 | |||||||
| chr4:185282818 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1092-5194C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282818 | |||||||
| chr4:185282936 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
192 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1092-5076T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185282936 | |||||||
| chr4:185283390 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1092-4622T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185283390 | |||||||
| chr4:185283599 | ATTAACCT others(10): Show |
A | 1 | a0001c0001t0001g0031 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1092-4409_1092-439 others(21): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185283599 | ||||||
| chr4:185284027 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1092-3985A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284027 | |||||||
| chr4:185284054 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092-3958A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284054 | |||||||
| chr4:185284150 | C | G | 9 | a0001c0001t0001g0195 a0001c0001t0001g0217 a0001c0001t0001g0218 others(6): Show |
9 | HG00733.hp1 HG01074.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1092-3862C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284150 | |||||||
| chr4:185284191 | G | A | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1092-3821G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284191 | |||||||
| chr4:185284197 | T | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092-3815T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284197 | |||||||
| chr4:185284423 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1092-3589G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284423 | |||||||
| chr4:185284571 | A | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0011c0010t0001g0207 |
3 | HG02145.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1092-3441A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284571 | |||||||
| chr4:185284637 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1092-3375T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284637 | |||||||
| chr4:185284712 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1092-3300T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284712 | |||||||
| chr4:185284780 | G | T | 1 | a0001c0003t0001g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1092-3232G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284780 | |||||||
| chr4:185284924 | A | G | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02630.hp2 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-3088A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284924 | |||||||
| chr4:185284983 | G | A | 1 | a0002c0002t0001g0262 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1092-3029G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185284983 | |||||||
| chr4:185285318 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1092-2694G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185285318 | |||||||
| chr4:185285537 | T | C | 4 | a0001c0001t0001g0205 a0001c0006t0001g0068 a0001c0006t0001g0069 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-2475T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185285537 | |||||||
| chr4:185285795 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0241 |
2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.1092-2217C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185285795 | |||||||
| chr4:185285903 | G | A | 7 | a0001c0001t0001g0194 a0002c0002t0001g0262 a0002c0002t0001g0268 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092-2109G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185285903 | |||||||
| chr4:185285917 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1092-2095T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185285917 | |||||||
| chr4:185285936 | C | CTAATTTT others(7): Show |
14 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1092-2073_1092-206 others(18): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185285936 | ||||||
| chr4:185285939 | A | AT | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1092-2061dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185285939 | ||||||
| chr4:185285962 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0248 |
2 | HG00280.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1092-2050G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185285962 | |||||||
| chr4:185286093 | G | GTTTGT | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-1897_1092-189 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 185286093 | ||||||
| chr4:185286213 | T | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1092-1799T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185286213 | |||||||
| chr4:185286270 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1092-1742C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185286270 | |||||||
| chr4:185286296 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1092-1716T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185286296 | |||||||
| chr4:185286474 | T | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0064 others(26): Show |
30 | HG01123.hp1 HG01192.hp1 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.1092-1538T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185286474 | |||||||
| chr4:185286475 | G | A | 9 | a0001c0001t0001g0195 a0001c0001t0001g0217 a0001c0001t0001g0218 others(6): Show |
9 | HG00733.hp1 HG01074.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1092-1537G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185286475 | |||||||
| chr4:185286598 | A | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0138 |
3 | HG01496.hp1 HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1092-1414A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185286598 | |||||||
| chr4:185286617 | A | G | 4 | a0001c0001t0001g0205 a0001c0006t0001g0068 a0001c0006t0001g0069 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-1395A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185286617 | |||||||
| chr4:185286718 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
2 | HG00621.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1092-1294G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185286718 | |||||||
| chr4:185287211 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0148 |
2 | HG02080.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1092-801A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287211 | |||||||
| chr4:185287281 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1092-731C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287281 | |||||||
| chr4:185287390 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1092-622G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287390 | |||||||
| chr4:185287478 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1092-534C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287478 | |||||||
| chr4:185287511 | A | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0203 a0002c0002t0001g0264 others(4): Show |
7 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092-501A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287511 | |||||||
| chr4:185287553 | A | G | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-459A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287553 | |||||||
| chr4:185287561 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1092-451C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287561 | |||||||
| chr4:185287737 | G | C | 3 | a0002c0002t0001g0265 a0002c0002t0001g0266 a0002c0002t0001g0271 |
3 | HG02717.hp2 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1092-275G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287737 | |||||||
| chr4:185287807 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1092-205G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287807 | |||||||
| chr4:185287821 | A | AG | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1092-191_1092-190i others(3): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287821 | |||||||
| chr4:185287831 | C | T | 6 | a0001c0001t0001g0203 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-181C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287831 | |||||||
| chr4:185287886 | G | T | 20 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(17): Show |
20 | HG00621.hp2 HG02258.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1092-126G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287886 | |||||||
| chr4:185287989 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1092-23T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | chr4 | 185287989 | |||||||
| chr4:185288119 | A | G | 12 | a0001c0001t0001g0195 a0001c0001t0001g0199 a0001c0001t0001g0200 others(9): Show |
12 | HG00733.hp1 HG01074.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162+37A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288119 | |||||||
| chr4:185288157 | G | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02055.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1162+75G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288157 | |||||||
| chr4:185288161 | T | C | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1162+79T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288161 | |||||||
| chr4:185288460 | A | G | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1162+378A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288460 | |||||||
| chr4:185288614 | G | C | 1 | a0001c0003t0001g0161 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1162+532G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288614 | |||||||
| chr4:185288614 | G | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
22 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.1162+532G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288614 | |||||||
| chr4:185288622 | G | A | 1 | a0001c0003t0001g0106 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1162+540G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288622 | |||||||
| chr4:185288703 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0002c0002t0001g0264 others(4): Show |
7 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1162+621C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288703 | |||||||
| chr4:185288798 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1162+716G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288798 | |||||||
| chr4:185288828 | G | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
187 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1162+746G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288828 | |||||||
| chr4:185288899 | C | A | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1162+817C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185288899 | |||||||
| chr4:185289021 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
11 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162+939G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289021 | |||||||
| chr4:185289165 | G | A | 2 | a0001c0003t0001g0143 a0001c0003t0001g0163 |
2 | NA18993.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1162+1083G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289165 | |||||||
| chr4:185289202 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1162+1120C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289202 | |||||||
| chr4:185289203 | A | C | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1162+1121A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289203 | |||||||
| chr4:185289307 | T | G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1162+1225T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289307 | |||||||
| chr4:185289364 | C | T | 1 | a0002c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1162+1282C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289364 | |||||||
| chr4:185289393 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1162+1311T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289393 | |||||||
| chr4:185289561 | G | A | 21 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(18): Show |
21 | HG01168.hp2 HG02280.hp2 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.1162+1479G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289561 | |||||||
| chr4:185289565 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162+1483C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289565 | |||||||
| chr4:185289566 | A | G | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+1484A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289566 | |||||||
| chr4:185289653 | T | A | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+1571T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289653 | |||||||
| chr4:185289657 | T | C | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+1575T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289657 | |||||||
| chr4:185289674 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1162+1592T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289674 | |||||||
| chr4:185289896 | A | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1162+1814A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289896 | |||||||
| chr4:185289976 | G | A | 1 | a0002c0002t0001g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1162+1894G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185289976 | |||||||
| chr4:185290035 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1162+1953G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290035 | |||||||
| chr4:185290089 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1162+2007A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290089 | |||||||
| chr4:185290096 | C | G | 1 | a0001c0003t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1162+2014C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290096 | |||||||
| chr4:185290108 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1162+2026T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290108 | |||||||
| chr4:185290200 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162+2118C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290200 | |||||||
| chr4:185290206 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1162+2124G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290206 | |||||||
| chr4:185290417 | G | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(5): Show |
8 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162+2335G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290417 | |||||||
| chr4:185290434 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1162+2352C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290434 | |||||||
| chr4:185290650 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1162+2568A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290650 | |||||||
| chr4:185290718 | C | CTTAATTA others(51): Show |
11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+2637_1162+263 others(62): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185290718 | ||||||
| chr4:185290720 | G | A | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+2638G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290720 | |||||||
| chr4:185290764 | A | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0002c0002t0001g0264 others(4): Show |
7 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1162+2682A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290764 | |||||||
| chr4:185290812 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
180 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.1162+2730G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290812 | |||||||
| chr4:185290827 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
135 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1162+2745T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290827 | |||||||
| chr4:185290931 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
124 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1162+2849G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185290931 | |||||||
| chr4:185291073 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162+2991A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291073 | |||||||
| chr4:185291161 | C | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162+3079C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291161 | |||||||
| chr4:185291166 | GA | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
124 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1162+3091delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185291166 | ||||||
| chr4:185291254 | G | C | 1 | a0001c0001t0001g0029 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1162+3172G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291254 | |||||||
| chr4:185291340 | A | G | 6 | a0002c0002t0001g0262 a0002c0002t0001g0268 a0002c0002t0001g0269 others(3): Show |
6 | HG02258.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162+3258A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291340 | |||||||
| chr4:185291481 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1162+3399C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291481 | |||||||
| chr4:185291583 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1162+3501C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291583 | |||||||
| chr4:185291598 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1162+3516G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291598 | |||||||
| chr4:185291631 | A | T | 15 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0187 others(12): Show |
15 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1162+3549A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291631 | |||||||
| chr4:185291657 | G | A | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1162+3575G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291657 | |||||||
| chr4:185291701 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1162+3619A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291701 | |||||||
| chr4:185291789 | C | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0130 |
2 | NA18984.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1162+3707C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291789 | |||||||
| chr4:185291828 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1162+3746C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185291828 | |||||||
| chr4:185292112 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0002g0092 |
2 | NA18990.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1162+4030T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185292112 | |||||||
| chr4:185292173 | T | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(5): Show |
8 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162+4091T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185292173 | |||||||
| chr4:185292185 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0113 a0001c0001t0001g0181 others(3): Show |
6 | HG00639.hp1 HG01106.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162+4103G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185292185 | |||||||
| chr4:185292281 | TA | T | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02630.hp2 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+4202delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185292281 | ||||||
| chr4:185292441 | C | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG02145.hp2 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1162+4359C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185292441 | |||||||
| chr4:185292681 | G | A | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1162+4599G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185292681 | |||||||
| chr4:185292763 | A | T | 23 | a0001c0001t0001g0194 a0001c0001t0001g0208 a0001c0001t0001g0236 others(20): Show |
23 | HG01168.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1162+4681A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185292763 | |||||||
| chr4:185292854 | G | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1162+4772G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185292854 | |||||||
| chr4:185293028 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1162+4946G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185293028 | |||||||
| chr4:185293032 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1162+4950T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185293032 | |||||||
| chr4:185293052 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1162+4970C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185293052 | |||||||
| chr4:185293117 | G | A | 20 | a0001c0001t0001g0117 a0001c0001t0001g0150 a0001c0001t0001g0162 others(17): Show |
20 | HG00733.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1162+5035G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185293117 | |||||||
| chr4:185293347 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1162+5265A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185293347 | |||||||
| chr4:185293500 | G | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0043 |
2 | HG01168.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1162+5418G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185293500 | |||||||
| chr4:185293604 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1162+5522A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185293604 | |||||||
| chr4:185293647 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1162+5565T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185293647 | |||||||
| chr4:185293715 | T | TTAAA | 13 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0054 others(10): Show |
13 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1162+5636_1162+563 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185293715 | ||||||
| chr4:185293866 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1162+5784C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185293866 | |||||||
| chr4:185294024 | G | A | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+5942G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294024 | |||||||
| chr4:185294111 | C | T | 1 | a0008c0018t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1162+6029C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294111 | |||||||
| chr4:185294224 | C | T | 1 | a0002c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1162+6142C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294224 | |||||||
| chr4:185294365 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1162+6283G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294365 | |||||||
| chr4:185294744 | C | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1162+6662C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294744 | |||||||
| chr4:185294844 | G | C | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1162+6762G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294844 | |||||||
| chr4:185294853 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1162+6771T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294853 | |||||||
| chr4:185294924 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1162+6842C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294924 | |||||||
| chr4:185294939 | G | A | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+6857G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294939 | |||||||
| chr4:185294982 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1162+6900A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185294982 | |||||||
| chr4:185295158 | T | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1162+7076T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185295158 | |||||||
| chr4:185295391 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1162+7309T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185295391 | |||||||
| chr4:185295451 | C | CTT | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02145.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1162+7384_1162+738 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185295451 | ||||||
| chr4:185295451 | CT | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
110 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1162+7385delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185295451 | ||||||
| chr4:185295494 | C | T | 24 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(21): Show |
24 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.1162+7412C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185295494 | |||||||
| chr4:185295715 | G | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162+7633G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185295715 | |||||||
| chr4:185295853 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1162+7771A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185295853 | |||||||
| chr4:185295956 | T | C | 3 | a0004c0005t0001g0045 a0004c0005t0001g0046 a0004c0005t0001g0047 |
3 | HG00408.hp2 NA19002.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1162+7874T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185295956 | |||||||
| chr4:185296055 | A | G | 5 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162+7973A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185296055 | |||||||
| chr4:185296215 | A | ATAC | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+8135_1162+813 others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185296215 | ||||||
| chr4:185296256 | C | T | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+8174C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185296256 | |||||||
| chr4:185296412 | C | T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(13): Show |
16 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1162+8330C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185296412 | |||||||
| chr4:185296443 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1162+8361T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185296443 | |||||||
| chr4:185296456 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0142 |
2 | HG00544.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1162+8374A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185296456 | |||||||
| chr4:185296458 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1162+8376T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185296458 | |||||||
| chr4:185296660 | A | C | 1 | a0001c0001t0001g0055 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1162+8578A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185296660 | |||||||
| chr4:185296677 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1162+8595A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185296677 | |||||||
| chr4:185296897 | T | C | 1 | a0002c0002t0001g0262 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1162+8815T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185296897 | |||||||
| chr4:185297047 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1162+8965T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185297047 | |||||||
| chr4:185297089 | CTT | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1162+9010_1162+901 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185297089 | ||||||
| chr4:185297275 | C | T | 3 | a0003c0004t0001g0249 a0003c0007t0001g0184 a0010c0019t0005g0267 |
3 | HG02258.hp1 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1162+9193C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185297275 | |||||||
| chr4:185297306 | A | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162+9224A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185297306 | |||||||
| chr4:185297421 | C | T | 20 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(17): Show |
20 | HG01168.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162+9339C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185297421 | |||||||
| chr4:185297669 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1162+9587G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185297669 | |||||||
| chr4:185297747 | A | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
80 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1162+9665A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185297747 | |||||||
| chr4:185297819 | ATCTAAAT others(3): Show |
A | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1162+9740_1162+974 others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185297819 | ||||||
| chr4:185297830 | TCA | T | 17 | a0001c0001t0001g0117 a0001c0001t0001g0195 a0001c0001t0001g0199 others(14): Show |
17 | HG00733.hp1 HG01074.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1162+9749_1162+975 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185297830 | |||||||
| chr4:185297963 | T | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162+9881T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185297963 | |||||||
| chr4:185298067 | C | T | 1 | a0001c0001t0006g0152 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1162+9985C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298067 | |||||||
| chr4:185298093 | C | CTTTTTTT | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
100 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1162+10018_1162+10 others(13): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185298093 | ||||||
| chr4:185298093 | C | CTTTTTTT others(1): Show |
17 | a0001c0001t0001g0082 a0001c0001t0001g0099 a0001c0001t0001g0193 others(14): Show |
17 | HG01081.hp1 HG02148.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1162+10017_1162+10 others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185298093 | ||||||
| chr4:185298130 | C | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
80 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1162+10048C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298130 | |||||||
| chr4:185298248 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1162+10166C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298248 | |||||||
| chr4:185298249 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1162+10167G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298249 | |||||||
| chr4:185298332 | A | G | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+10250A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298332 | |||||||
| chr4:185298340 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1162+10258C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298340 | |||||||
| chr4:185298341 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0048 others(38): Show |
42 | HG00733.hp2 HG01123.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.1162+10259G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298341 | |||||||
| chr4:185298364 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1162+10282C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298364 | |||||||
| chr4:185298381 | A | T | 1 | a0001c0001t0001g0225 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1162+10299A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298381 | |||||||
| chr4:185298481 | T | TA | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+10399_1162+10 others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298481 | |||||||
| chr4:185298482 | T | A | 17 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(14): Show |
17 | HG00621.hp2 HG00733.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1162+10400T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298482 | |||||||
| chr4:185298483 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1162+10401A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298483 | |||||||
| chr4:185298495 | A | C | 1 | a0001c0003t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1162+10413A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298495 | |||||||
| chr4:185298557 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1162+10475C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298557 | |||||||
| chr4:185298711 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1162+10629G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298711 | |||||||
| chr4:185298784 | T | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
88 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1162+10702T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298784 | |||||||
| chr4:185298813 | C | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0173 |
2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1162+10731C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298813 | |||||||
| chr4:185298881 | G | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
119 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1162+10799G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298881 | |||||||
| chr4:185298903 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1162+10821T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298903 | |||||||
| chr4:185298909 | G | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG02145.hp2 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1162+10827G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298909 | |||||||
| chr4:185298948 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1162+10866A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185298948 | |||||||
| chr4:185299103 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG02145.hp2 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1162+11021T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185299103 | |||||||
| chr4:185299224 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
187 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.1162+11142C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185299224 | |||||||
| chr4:185299257 | T | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0094 others(7): Show |
11 | HG00280.hp1 HG00621.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162+11175T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185299257 | |||||||
| chr4:185299484 | A | C | 1 | a0001c0001t0001g0005 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1163-11151A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185299484 | |||||||
| chr4:185300163 | A | AT | 13 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0126 others(10): Show |
13 | HG03942.hp1 NA18612.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.1163-10458dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300163 | ||||||
| chr4:185300163 | AT | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
117 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1163-10458delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300163 | ||||||
| chr4:185300163 | ATT | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1163-10459_1163-10 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300163 | ||||||
| chr4:185300170 | T | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1163-10465T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300170 | |||||||
| chr4:185300199 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0002g0093 |
2 | HG02647.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1163-10436G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300199 | |||||||
| chr4:185300215 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
121 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1163-10420G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300215 | |||||||
| chr4:185300221 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1163-10414A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300221 | |||||||
| chr4:185300259 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0042 others(30): Show |
34 | HG00639.hp1 HG00733.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1163-10376A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300259 | |||||||
| chr4:185300324 | A | AT | 17 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0054 others(14): Show |
17 | HG00621.hp2 HG00639.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1163-10295dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300324 | ||||||
| chr4:185300330 | T | G | 9 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0254 others(6): Show |
9 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-10305T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300330 | |||||||
| chr4:185300341 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0042 others(30): Show |
34 | HG00639.hp1 HG00733.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1163-10294G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300341 | |||||||
| chr4:185300415 | C | T | 5 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1163-10220C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300415 | |||||||
| chr4:185300459 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1163-10176C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300459 | |||||||
| chr4:185300527 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1163-10108G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300527 | |||||||
| chr4:185300650 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1163-9985C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300650 | |||||||
| chr4:185300655 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1163-9980A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300655 | |||||||
| chr4:185300696 | ATATT | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0042 others(30): Show |
34 | HG00639.hp1 HG00733.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1163-9935_1163-993 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300696 | ||||||
| chr4:185300720 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1163-9915A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300720 | |||||||
| chr4:185300738 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0032 |
2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1163-9897C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300738 | |||||||
| chr4:185300779 | T | G | 1 | a0001c0001t0001g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1163-9856T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300779 | |||||||
| chr4:185300785 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0147 |
2 | NA18963.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1163-9850A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300785 | |||||||
| chr4:185300839 | T | TCACACAC others(17): Show |
1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1163-9796_1163-979 others(28): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300839 | |||||||
| chr4:185300839 | T | TCACACAC others(19): Show |
1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1163-9796_1163-979 others(30): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300839 | |||||||
| chr4:185300840 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1163-9795G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300840 | |||||||
| chr4:185300840 | G | GAC | 16 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
16 | HG00408.hp2 HG00621.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.1163-9761_1163-976 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACAC | 4 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
4 | HG02257.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-9763_1163-976 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(1): Show |
10 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0165 others(7): Show |
10 | HG01981.hp1 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1163-9767_1163-976 others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(3): Show |
30 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0103 others(27): Show |
30 | HG01099.hp2 HG01167.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1163-9769_1163-976 others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(5): Show |
49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(46): Show |
50 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1163-9771_1163-976 others(16): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(7): Show |
29 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(26): Show |
29 | HG00741.hp2 HG01257.hp1 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1163-9773_1163-976 others(18): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(9): Show |
24 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0111 others(21): Show |
24 | HG01081.hp1 HG01081.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1163-9775_1163-976 others(20): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(11): Show |
5 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0229 others(2): Show |
5 | HG00408.hp1 HG01934.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-9777_1163-976 others(22): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(13): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0133 |
2 | NA19030.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1163-9779_1163-976 others(24): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(15): Show |
1 | a0001c0001t0001g0007 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1163-9781_1163-976 others(26): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(17): Show |
1 | a0001c0001t0001g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1163-9783_1163-976 others(28): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(21): Show |
1 | a0001c0001t0001g0083 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1163-9787_1163-976 others(32): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | G | GACACACA others(25): Show |
1 | a0001c0001t0001g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1163-9791_1163-976 others(36): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | GAC | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(29): Show |
33 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1163-9761_1163-976 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | GACACAC | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0108 |
3 | HG02155.hp1 NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1163-9765_1163-976 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300840 | GACACACA others(3): Show |
G | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02145.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163-9769_1163-976 others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185300840 | ||||||
| chr4:185300927 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1163-9708G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300927 | |||||||
| chr4:185300972 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1163-9663C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185300972 | |||||||
| chr4:185301025 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1163-9610A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301025 | |||||||
| chr4:185301047 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | HG00621.hp1 HG02132.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1163-9588A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301047 | |||||||
| chr4:185301203 | ACATTTCA others(17): Show |
A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0003c0004t0001g0249 |
3 | HG02922.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1163-9428_1163-940 others(28): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185301203 | ||||||
| chr4:185301322 | C | T | 1 | a0002c0002t0001g0260 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1163-9313C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301322 | |||||||
| chr4:185301361 | A | T | 1 | a0001c0003t0001g0090 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1163-9274A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301361 | |||||||
| chr4:185301390 | A | G | 1 | a0001c0003t0001g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1163-9245A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301390 | |||||||
| chr4:185301410 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1163-9225G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301410 | |||||||
| chr4:185301484 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1163-9151C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301484 | |||||||
| chr4:185301712 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
187 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.1163-8923A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301712 | |||||||
| chr4:185301736 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1163-8899G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301736 | |||||||
| chr4:185301800 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1163-8835T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301800 | |||||||
| chr4:185301835 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0043 |
2 | HG01168.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1163-8800C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301835 | |||||||
| chr4:185301871 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1163-8764C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301871 | |||||||
| chr4:185301895 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1163-8740C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185301895 | |||||||
| chr4:185302093 | T | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG01346.hp1 HG02293.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-8542T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302093 | |||||||
| chr4:185302095 | T | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1163-8540T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302095 | |||||||
| chr4:185302100 | G | GT | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
130 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1163-8520dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185302100 | ||||||
| chr4:185302100 | G | T | 14 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(11): Show |
14 | HG00621.hp2 HG02572.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1163-8535G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302100 | |||||||
| chr4:185302135 | T | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1163-8500T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302135 | |||||||
| chr4:185302141 | G | T | 1 | a0005c0008t0001g0230 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1163-8494G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302141 | |||||||
| chr4:185302182 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1163-8453C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302182 | |||||||
| chr4:185302300 | AAG | A | 15 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0187 others(12): Show |
15 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1163-8332_1163-833 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185302300 | ||||||
| chr4:185302384 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1163-8251G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302384 | |||||||
| chr4:185302493 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1163-8142A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302493 | |||||||
| chr4:185302621 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1163-8014C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302621 | |||||||
| chr4:185302654 | G | A | 17 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(14): Show |
17 | HG01168.hp2 HG02280.hp2 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1163-7981G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302654 | |||||||
| chr4:185302808 | C | T | 1 | a0008c0018t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1163-7827C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185302808 | |||||||
| chr4:185303056 | T | C | 6 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1163-7579T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303056 | |||||||
| chr4:185303116 | C | T | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1163-7519C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303116 | |||||||
| chr4:185303381 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
119 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1163-7254A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303381 | |||||||
| chr4:185303386 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1163-7249G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303386 | |||||||
| chr4:185303425 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1163-7210C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303425 | |||||||
| chr4:185303581 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1163-7054C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303581 | |||||||
| chr4:185303658 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1163-6977C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303658 | |||||||
| chr4:185303658 | C | CA | 43 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0027 others(40): Show |
43 | HG00621.hp1 HG00621.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1163-6954dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185303658 | ||||||
| chr4:185303658 | C | CAA | 10 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1163-6955_1163-695 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185303658 | ||||||
| chr4:185303773 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1163-6862C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303773 | |||||||
| chr4:185303834 | G | A | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1163-6801G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303834 | |||||||
| chr4:185303911 | C | G | 10 | a0001c0001t0001g0193 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01081.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1163-6724C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185303911 | |||||||
| chr4:185304033 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1163-6602T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304033 | |||||||
| chr4:185304092 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1163-6543A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304092 | |||||||
| chr4:185304327 | G | A | 17 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(14): Show |
17 | HG01168.hp2 HG02280.hp2 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1163-6308G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304327 | |||||||
| chr4:185304420 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1163-6215G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304420 | |||||||
| chr4:185304427 | G | A | 1 | a0001c0003t0001g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1163-6208G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304427 | |||||||
| chr4:185304434 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1163-6201C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304434 | |||||||
| chr4:185304437 | A | C | 5 | a0001c0001t0001g0081 a0001c0001t0001g0100 a0001c0001t0001g0157 others(2): Show |
5 | HG01123.hp1 HG01192.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-6198A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304437 | |||||||
| chr4:185304518 | C | T | 6 | a0002c0002t0001g0262 a0002c0002t0001g0268 a0002c0002t0001g0269 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1163-6117C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304518 | |||||||
| chr4:185304691 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1163-5944G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304691 | |||||||
| chr4:185304700 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1163-5935G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304700 | |||||||
| chr4:185304870 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01975.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1163-5765C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304870 | |||||||
| chr4:185304904 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1163-5731C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304904 | |||||||
| chr4:185304915 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01975.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1163-5720A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185304915 | |||||||
| chr4:185305202 | G | A | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1163-5433G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185305202 | |||||||
| chr4:185305224 | A | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1163-5411A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185305224 | |||||||
| chr4:185305481 | T | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1163-5154T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185305481 | |||||||
| chr4:185305693 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1163-4942A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185305693 | |||||||
| chr4:185306270 | A | G | 2 | a0001c0001t0001g0201 a0003c0004t0001g0204 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1163-4365A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185306270 | |||||||
| chr4:185306325 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1163-4310C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185306325 | |||||||
| chr4:185306378 | T | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
119 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1163-4257T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185306378 | |||||||
| chr4:185306420 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0002g0134 |
2 | HG02165.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1163-4215A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185306420 | |||||||
| chr4:185306890 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1163-3745T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185306890 | |||||||
| chr4:185306989 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1163-3646A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185306989 | |||||||
| chr4:185307355 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(5): Show |
8 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1163-3280G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185307355 | |||||||
| chr4:185307386 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
117 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1163-3249T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185307386 | |||||||
| chr4:185307613 | T | C | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1163-3022T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185307613 | |||||||
| chr4:185307723 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1163-2912C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185307723 | |||||||
| chr4:185307974 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1163-2661G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185307974 | |||||||
| chr4:185308114 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
125 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.1163-2521G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185308114 | |||||||
| chr4:185308227 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0036 |
2 | HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1163-2408A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185308227 | |||||||
| chr4:185308460 | A | C | 7 | a0001c0001t0001g0194 a0002c0002t0001g0262 a0002c0002t0001g0268 others(4): Show |
7 | HG02109.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1163-2175A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185308460 | |||||||
| chr4:185308467 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0189 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1163-2168G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185308467 | |||||||
| chr4:185308497 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1163-2138T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185308497 | |||||||
| chr4:185308587 | C | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
188 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.1163-2048C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185308587 | |||||||
| chr4:185308860 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1163-1775C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185308860 | |||||||
| chr4:185308954 | C | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0139 |
2 | NA18988.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1163-1681C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185308954 | |||||||
| chr4:185309047 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1163-1588C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309047 | |||||||
| chr4:185309084 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1163-1551G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309084 | |||||||
| chr4:185309122 | T | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
114 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.1163-1513T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309122 | |||||||
| chr4:185309140 | T | C | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1163-1495T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309140 | |||||||
| chr4:185309173 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1163-1462C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309173 | |||||||
| chr4:185309177 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1163-1458G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309177 | |||||||
| chr4:185309211 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1163-1424T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309211 | |||||||
| chr4:185309599 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1163-1036T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309599 | |||||||
| chr4:185309634 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1163-1001C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309634 | |||||||
| chr4:185309668 | C | T | 1 | a0001c0003t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1163-967C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309668 | |||||||
| chr4:185309881 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1163-754C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185309881 | |||||||
| chr4:185310040 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1163-595A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185310040 | |||||||
| chr4:185310053 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0162 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1163-582G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185310053 | |||||||
| chr4:185310168 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1163-467T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185310168 | |||||||
| chr4:185310203 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1163-432A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185310203 | |||||||
| chr4:185310430 | G | GCT | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1163-205_1163-204i others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185310430 | |||||||
| chr4:185310431 | G | GTT | 30 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0194 others(27): Show |
30 | HG00544.hp2 HG01168.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1163-203_1163-202i others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 185310431 | ||||||
| chr4:185310431 | G | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1163-204G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | 185310431 | |||||||
| chr4:185310927 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
98 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.1344+111A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185310927 | |||||||
| chr4:185310968 | C | T | 3 | a0001c0001t0001g0194 a0003c0004t0001g0249 a0010c0019t0005g0267 |
3 | HG02109.hp1 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+152C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185310968 | |||||||
| chr4:185310988 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1344+172C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185310988 | |||||||
| chr4:185311346 | C | G | 6 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344+530C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185311346 | |||||||
| chr4:185311424 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1344+608G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185311424 | |||||||
| chr4:185311532 | G | A | 7 | a0001c0001t0001g0194 a0002c0002t0001g0262 a0002c0002t0001g0268 others(4): Show |
7 | HG02109.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+716G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185311532 | |||||||
| chr4:185311560 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1344+744G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185311560 | |||||||
| chr4:185311560 | G | T | 1 | a0001c0001t0002g0134 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1344+744G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185311560 | |||||||
| chr4:185311711 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0105 |
3 | NA19056.hp2 NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1344+895T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185311711 | |||||||
| chr4:185311915 | T | A | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1344+1099T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185311915 | |||||||
| chr4:185312482 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1344+1666G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185312482 | |||||||
| chr4:185312525 | C | CT | 8 | a0001c0001t0001g0246 a0002c0002t0001g0262 a0002c0002t0001g0268 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1344+1724dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185312525 | ||||||
| chr4:185312583 | C | T | 48 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
48 | HG00544.hp2 HG00621.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1344+1767C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185312583 | |||||||
| chr4:185312661 | TAC | T | 23 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(20): Show |
23 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1344+1847_1344+184 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185312661 | ||||||
| chr4:185312746 | C | T | 1 | a0002c0002t0001g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1344+1930C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185312746 | |||||||
| chr4:185312871 | G | C | 6 | a0002c0002t0001g0262 a0002c0002t0001g0268 a0002c0002t0001g0269 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344+2055G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185312871 | |||||||
| chr4:185313035 | T | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1344+2219T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185313035 | |||||||
| chr4:185313037 | G | A | 23 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(20): Show |
23 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1344+2221G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185313037 | |||||||
| chr4:185313432 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1344+2616A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185313432 | |||||||
| chr4:185313495 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0105 |
3 | NA19056.hp2 NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1344+2679A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185313495 | |||||||
| chr4:185313610 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1344+2794A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185313610 | |||||||
| chr4:185313646 | G | GTATATTG others(5): Show |
1 | a0001c0001t0001g0023 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1344+2840_1344+285 others(16): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185313646 | ||||||
| chr4:185313826 | A | G | 18 | a0001c0001t0001g0117 a0001c0001t0001g0195 a0001c0001t0001g0199 others(15): Show |
18 | HG00733.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.1344+3010A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185313826 | |||||||
| chr4:185313878 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1344+3062T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185313878 | |||||||
| chr4:185314194 | A | G | 9 | a0001c0001t0001g0091 a0001c0001t0001g0210 a0001c0001t0001g0215 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1344+3378A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314194 | |||||||
| chr4:185314237 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
182 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.1344+3421T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314237 | |||||||
| chr4:185314250 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1344+3434G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314250 | |||||||
| chr4:185314324 | C | CA | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.1344+3528dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185314324 | ||||||
| chr4:185314324 | C | CAA | 15 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0164 others(12): Show |
16 | HG00544.hp2 HG00639.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1344+3527_1344+352 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185314324 | ||||||
| chr4:185314324 | CAAAAA | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1344+3524_1344+352 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185314324 | ||||||
| chr4:185314345 | T | A | 1 | a0002c0002t0001g0264 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1344+3529T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314345 | |||||||
| chr4:185314394 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1344+3578A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314394 | |||||||
| chr4:185314716 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1344+3900G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314716 | |||||||
| chr4:185314735 | A | G | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0002c0002t0001g0264 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+3919A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314735 | |||||||
| chr4:185314751 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1344+3935G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314751 | |||||||
| chr4:185314765 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0036 |
2 | HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1344+3949G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314765 | |||||||
| chr4:185314770 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1344+3954A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314770 | |||||||
| chr4:185314835 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1344+4019C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314835 | |||||||
| chr4:185314856 | C | CA | 31 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(28): Show |
31 | HG00621.hp2 HG01123.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1344+4058dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185314856 | ||||||
| chr4:185314856 | CA | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1344+4058delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185314856 | ||||||
| chr4:185314946 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
18 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1344+4130C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314946 | |||||||
| chr4:185314957 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1344+4141G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185314957 | |||||||
| chr4:185315045 | A | G | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1344+4229A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315045 | |||||||
| chr4:185315054 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0048 others(39): Show |
43 | HG00733.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.1344+4238C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315054 | |||||||
| chr4:185315085 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1344+4269G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315085 | |||||||
| chr4:185315088 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1344+4272C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315088 | |||||||
| chr4:185315101 | G | A | 1 | a0011c0010t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1344+4285G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315101 | |||||||
| chr4:185315152 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
139 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.1344+4336T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315152 | |||||||
| chr4:185315194 | C | T | 1 | a0009c0012t0001g0122 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1344+4378C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315194 | |||||||
| chr4:185315209 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1344+4393C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315209 | |||||||
| chr4:185315236 | AG | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
81 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1344+4421delG | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315236 | |||||||
| chr4:185315237 | G | A | 58 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
58 | HG00544.hp2 HG00621.hp2 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.1344+4421G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315237 | |||||||
| chr4:185315292 | AT | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0042 others(69): Show |
73 | HG00639.hp1 HG00733.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.1344+4495delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185315292 | ||||||
| chr4:185315292 | ATT | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
119 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1344+4494_1344+449 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185315292 | ||||||
| chr4:185315292 | ATTT | A | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1344+4493_1344+449 others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185315292 | ||||||
| chr4:185315450 | C | A | 1 | a0001c0003t0001g0161 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1344+4634C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315450 | |||||||
| chr4:185315494 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1344+4678A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315494 | |||||||
| chr4:185315509 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1344+4693G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315509 | |||||||
| chr4:185315728 | G | GA | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0002c0002t0001g0264 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+4921dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185315728 | ||||||
| chr4:185315763 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1344+4947C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315763 | |||||||
| chr4:185315784 | A | G | 1 | a0002c0002t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1345-4949A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315784 | |||||||
| chr4:185315994 | A | T | 1 | a0003c0004t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1345-4739A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185315994 | |||||||
| chr4:185316240 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(2): Show |
5 | HG01975.hp1 HG01993.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345-4493T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185316240 | |||||||
| chr4:185316292 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1345-4441A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185316292 | |||||||
| chr4:185316345 | G | A | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0002c0002t0001g0264 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-4388G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185316345 | |||||||
| chr4:185316689 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1345-4044G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185316689 | |||||||
| chr4:185317079 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1345-3654C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185317079 | |||||||
| chr4:185317276 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
139 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.1345-3457G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185317276 | |||||||
| chr4:185317584 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1345-3149A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185317584 | |||||||
| chr4:185317744 | A | G | 4 | a0002c0002t0001g0252 a0002c0002t0001g0255 a0002c0002t0001g0256 others(1): Show |
4 | HG01891.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-2989A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185317744 | |||||||
| chr4:185317786 | G | A | 1 | a0001c0001t0006g0152 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1345-2947G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185317786 | |||||||
| chr4:185317789 | G | C | 7 | a0001c0001t0001g0145 a0001c0001t0001g0198 a0001c0001t0001g0235 others(4): Show |
7 | HG02055.hp1 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345-2944G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185317789 | |||||||
| chr4:185317859 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0048 others(59): Show |
63 | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.1345-2874G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185317859 | |||||||
| chr4:185318129 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1345-2604T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318129 | |||||||
| chr4:185318153 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1345-2580A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318153 | |||||||
| chr4:185318196 | A | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1345-2537A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318196 | |||||||
| chr4:185318491 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1345-2242C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318491 | |||||||
| chr4:185318569 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345-2164A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318569 | |||||||
| chr4:185318588 | C | T | 20 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(17): Show |
20 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1345-2145C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318588 | |||||||
| chr4:185318609 | A | G | 5 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0001g0169 others(2): Show |
5 | NA18612.hp1 NA18941.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345-2124A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318609 | |||||||
| chr4:185318639 | G | A | 23 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(20): Show |
23 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1345-2094G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318639 | |||||||
| chr4:185318779 | C | T | 2 | a0003c0004t0001g0249 a0010c0019t0005g0267 |
2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345-1954C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318779 | |||||||
| chr4:185318889 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1345-1844C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318889 | |||||||
| chr4:185318899 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1345-1834C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318899 | |||||||
| chr4:185318971 | A | G | 1 | a0001c0001t0006g0152 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1345-1762A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185318971 | |||||||
| chr4:185319081 | ATTTTATT others(7): Show |
A | 8 | a0001c0001t0001g0048 a0001c0001t0001g0166 a0001c0001t0001g0167 others(5): Show |
8 | HG02145.hp2 HG03471.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345-1642_1345-162 others(18): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185319081 | ||||||
| chr4:185319090 | TA | T | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
51 | HG00733.hp1 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1345-1642delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319090 | |||||||
| chr4:185319091 | A | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
111 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.1345-1642A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319091 | |||||||
| chr4:185319091 | AT | A | 21 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(18): Show |
21 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1345-1634delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185319091 | ||||||
| chr4:185319098 | T | A | 1 | a0002c0002t0001g0253 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1345-1635T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319098 | |||||||
| chr4:185319098 | TTA | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1345-1633_1345-163 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185319098 | ||||||
| chr4:185319099 | T | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
85 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1345-1634T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319099 | |||||||
| chr4:185319100 | A | AT | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
80 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.1345-1620dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185319100 | ||||||
| chr4:185319100 | A | T | 1 | a0002c0002t0001g0253 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1345-1633A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319100 | |||||||
| chr4:185319101 | T | A | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1345-1632T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319101 | |||||||
| chr4:185319105 | T | A | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG02922.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345-1628T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319105 | |||||||
| chr4:185319106 | T | A | 20 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(17): Show |
20 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1345-1627T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319106 | |||||||
| chr4:185319108 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0162 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1345-1625T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319108 | |||||||
| chr4:185319183 | T | G | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1345-1550T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319183 | |||||||
| chr4:185319193 | CT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
84 | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(81): Show |
intron_variant | MODIFIER | c.1345-1517delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185319193 | ||||||
| chr4:185319193 | CTT | C | 26 | a0001c0001t0001g0157 a0001c0001t0001g0208 a0001c0001t0001g0219 others(23): Show |
26 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.1345-1518_1345-151 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185319193 | ||||||
| chr4:185319193 | CTTTTTTT others(4): Show |
C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
84 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1345-1527_1345-151 others(15): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185319193 | ||||||
| chr4:185319446 | G | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
2 | NA18943.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1345-1287G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319446 | |||||||
| chr4:185319462 | G | A | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0002c0002t0001g0264 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-1271G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319462 | |||||||
| chr4:185319464 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1345-1269G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319464 | |||||||
| chr4:185319513 | C | CT | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
25 | HG01081.hp2 HG01361.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.1345-1206dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185319513 | ||||||
| chr4:185319513 | C | CTT | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
75 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1345-1207_1345-120 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185319513 | ||||||
| chr4:185319819 | C | T | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0002c0002t0001g0264 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-914C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319819 | |||||||
| chr4:185319983 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1345-750C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185319983 | |||||||
| chr4:185320156 | G | A | 23 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(20): Show |
23 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1345-577G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185320156 | |||||||
| chr4:185320188 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0203 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1345-545G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185320188 | |||||||
| chr4:185320224 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
79 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1345-509C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185320224 | |||||||
| chr4:185320315 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1345-418T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185320315 | |||||||
| chr4:185320380 | A | C | 6 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345-353A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185320380 | |||||||
| chr4:185320406 | C | T | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1345-327C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185320406 | |||||||
| chr4:185320452 | A | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0048 others(25): Show |
29 | HG00733.hp2 HG01123.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1345-281A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | 185320452 | |||||||
| chr4:185320574 | TTAAA | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1345-148_1345-145d others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 185320574 | ||||||
| chr4:185320897 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0035 others(34): Show |
38 | HG00621.hp2 HG00733.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.1476+33A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185320897 | |||||||
| chr4:185320996 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1476+132T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185320996 | |||||||
| chr4:185321079 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0035 others(62): Show |
66 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1476+215T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185321079 | |||||||
| chr4:185321132 | T | A | 1 | a0001c0001t0001g0004 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1476+268T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185321132 | |||||||
| chr4:185321222 | TATC | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0117 a0001c0001t0001g0140 others(17): Show |
20 | HG00733.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1476+361_1476+363d others(5): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 185321222 | ||||||
| chr4:185321262 | A | AT | 9 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0162 others(6): Show |
9 | HG02145.hp2 HG02818.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1476+416dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 185321262 | ||||||
| chr4:185321262 | AT | A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0173 a0001c0001t0002g0137 others(2): Show |
5 | HG02896.hp2 HG03225.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.1476+416delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 185321262 | ||||||
| chr4:185321262 | ATTT | A | 5 | a0001c0001t0001g0203 a0001c0006t0001g0068 a0001c0006t0001g0069 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1476+414_1476+416d others(5): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 185321262 | ||||||
| chr4:185321290 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1476+426C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185321290 | |||||||
| chr4:185321604 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0173 |
2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1476+740T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185321604 | |||||||
| chr4:185321650 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1476+786T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185321650 | |||||||
| chr4:185321718 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1476+854C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185321718 | |||||||
| chr4:185321808 | T | C | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1476+944T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185321808 | |||||||
| chr4:185321828 | T | C | 6 | a0002c0002t0001g0262 a0002c0002t0001g0268 a0002c0002t0001g0269 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1476+964T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185321828 | |||||||
| chr4:185321904 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1476+1040G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185321904 | |||||||
| chr4:185322132 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1476+1268A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322132 | |||||||
| chr4:185322160 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0002c0002t0001g0253 |
3 | HG01081.hp1 HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1476+1296C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322160 | |||||||
| chr4:185322171 | G | A | 2 | a0004c0005t0001g0045 a0004c0005t0001g0046 |
2 | NA19002.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1476+1307G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322171 | |||||||
| chr4:185322298 | A | G | 5 | a0001c0001t0001g0203 a0001c0006t0001g0068 a0001c0006t0001g0069 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477-1230A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322298 | |||||||
| chr4:185322376 | A | G | 5 | a0001c0001t0001g0203 a0001c0006t0001g0068 a0001c0006t0001g0069 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477-1152A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322376 | |||||||
| chr4:185322380 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1477-1148C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322380 | |||||||
| chr4:185322410 | C | T | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1477-1118C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322410 | |||||||
| chr4:185322439 | G | C | 6 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1477-1089G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322439 | |||||||
| chr4:185322575 | T | A | 1 | a0002c0002t0001g0260 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1477-953T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322575 | |||||||
| chr4:185322941 | C | G | 1 | a0001c0001t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1477-587C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322941 | |||||||
| chr4:185322990 | C | T | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477-538C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185322990 | |||||||
| chr4:185323168 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1477-360C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185323168 | |||||||
| chr4:185323346 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01975.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1477-182A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | chr4 | 185323346 | |||||||
| chr4:185323882 | A | C | 1 | a0002c0002t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1749+82A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185323882 | |||||||
| chr4:185324154 | A | G | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1749+354A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185324154 | |||||||
| chr4:185324384 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1749+584C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185324384 | |||||||
| chr4:185324409 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1749+609C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185324409 | |||||||
| chr4:185324437 | A | C | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1749+637A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185324437 | |||||||
| chr4:185324825 | C | T | 5 | a0001c0001t0001g0203 a0001c0006t0001g0068 a0001c0006t0001g0069 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1749+1025C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185324825 | |||||||
| chr4:185324911 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1749+1111T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185324911 | |||||||
| chr4:185324920 | G | A | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1749+1120G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185324920 | |||||||
| chr4:185325091 | T | C | 1 | a0002c0002t0001g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1749+1291T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325091 | |||||||
| chr4:185325158 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1749+1358G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325158 | |||||||
| chr4:185325176 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1749+1376C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325176 | |||||||
| chr4:185325211 | A | G | 1 | a0002c0002t0001g0262 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1749+1411A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325211 | |||||||
| chr4:185325270 | A | G | 6 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1749+1470A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325270 | |||||||
| chr4:185325274 | C | G | 1 | a0003c0004t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1749+1474C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325274 | |||||||
| chr4:185325282 | C | T | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1749+1482C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325282 | |||||||
| chr4:185325532 | C | CA | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1749+1751dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 185325532 | ||||||
| chr4:185325532 | C | CAA | 32 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0086 others(29): Show |
33 | HG00544.hp2 HG01168.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.1749+1750_1749+175 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 185325532 | ||||||
| chr4:185325708 | A | C | 1 | a0001c0001t0006g0152 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1749+1908A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325708 | |||||||
| chr4:185325804 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(162): Show |
167 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(164): Show |
intron_variant | MODIFIER | c.1749+2004A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325804 | |||||||
| chr4:185325935 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1749+2135C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325935 | |||||||
| chr4:185325945 | C | T | 1 | a0011c0010t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1749+2145C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185325945 | |||||||
| chr4:185326334 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1749+2534C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185326334 | |||||||
| chr4:185326336 | A | G | 1 | a0004c0005t0001g0046 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1749+2536A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185326336 | |||||||
| chr4:185326612 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1749+2812C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185326612 | |||||||
| chr4:185326685 | C | T | 1 | a0003c0004t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1749+2885C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185326685 | |||||||
| chr4:185326875 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1749+3075C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185326875 | |||||||
| chr4:185327205 | T | C | 9 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0254 others(6): Show |
9 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1749+3405T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185327205 | |||||||
| chr4:185327311 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1749+3511C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185327311 | |||||||
| chr4:185327398 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1749+3598G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185327398 | |||||||
| chr4:185327415 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1749+3615A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185327415 | |||||||
| chr4:185327618 | T | C | 1 | a0008c0018t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1749+3818T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185327618 | |||||||
| chr4:185327623 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1749+3823T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185327623 | |||||||
| chr4:185327740 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1749+3940A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185327740 | |||||||
| chr4:185327741 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1749+3941G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185327741 | |||||||
| chr4:185328331 | G | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0035 others(58): Show |
62 | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.1750-4264G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328331 | |||||||
| chr4:185328340 | A | AT | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1750-4249dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 185328340 | ||||||
| chr4:185328392 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1750-4203C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328392 | |||||||
| chr4:185328536 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1750-4059G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328536 | |||||||
| chr4:185328545 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0035 others(58): Show |
62 | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.1750-4050C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328545 | |||||||
| chr4:185328720 | T | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0035 others(58): Show |
62 | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.1750-3875T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328720 | |||||||
| chr4:185328756 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1750-3839C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328756 | |||||||
| chr4:185328784 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1750-3811C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328784 | |||||||
| chr4:185328869 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1750-3726G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328869 | |||||||
| chr4:185328902 | A | G | 6 | a0001c0001t0001g0203 a0001c0001t0001g0215 a0001c0006t0001g0068 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1750-3693A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328902 | |||||||
| chr4:185328920 | C | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0099 a0001c0001t0001g0101 others(5): Show |
8 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.1750-3675C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185328920 | |||||||
| chr4:185329427 | CAG | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1750-3164_1750-316 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 185329427 | ||||||
| chr4:185329431 | G | GACCCAGC others(13): Show |
1 | a0001c0001t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1750-3162_1750-314 others(24): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 185329431 | ||||||
| chr4:185329438 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1750-3157C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185329438 | |||||||
| chr4:185329484 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1750-3111A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185329484 | |||||||
| chr4:185329484 | A | T | 11 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(8): Show |
11 | HG01081.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1750-3111A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185329484 | |||||||
| chr4:185329551 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1750-3044C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185329551 | |||||||
| chr4:185329681 | C | CAG | 19 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
19 | HG00544.hp1 HG01361.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.1750-2894_1750-289 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 185329681 | ||||||
| chr4:185329681 | C | CAGAG | 9 | a0001c0001t0001g0042 a0001c0001t0001g0203 a0001c0006t0001g0068 others(6): Show |
9 | HG01081.hp2 HG01433.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1750-2896_1750-289 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 185329681 | ||||||
| chr4:185329979 | C | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | NA18961.hp2 NA18988.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.1750-2616C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185329979 | |||||||
| chr4:185330068 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1750-2527C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330068 | |||||||
| chr4:185330085 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1750-2510A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330085 | |||||||
| chr4:185330180 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1750-2415T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330180 | |||||||
| chr4:185330210 | A | T | 1 | a0001c0001t0001g0065 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1750-2385A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330210 | |||||||
| chr4:185330227 | T | G | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1750-2368T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330227 | |||||||
| chr4:185330252 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1750-2343G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330252 | |||||||
| chr4:185330608 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02055.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1750-1987C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330608 | |||||||
| chr4:185330614 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1750-1981G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330614 | |||||||
| chr4:185330663 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1750-1932G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330663 | |||||||
| chr4:185330947 | C | G | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1750-1648C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330947 | |||||||
| chr4:185330984 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(145): Show |
149 | HG00140.hp2 HG00544.hp2 HG00621.hp2 others(146): Show |
intron_variant | MODIFIER | c.1750-1611T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185330984 | |||||||
| chr4:185331202 | C | A | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1750-1393C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185331202 | |||||||
| chr4:185331246 | A | G | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1750-1349A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185331246 | |||||||
| chr4:185331395 | C | T | 1 | a0003c0004t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1750-1200C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185331395 | |||||||
| chr4:185331503 | G | A | 7 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0265 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1750-1092G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185331503 | |||||||
| chr4:185331511 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1750-1084T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185331511 | |||||||
| chr4:185331673 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0035 others(58): Show |
62 | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.1750-922C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185331673 | |||||||
| chr4:185331708 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0035 others(58): Show |
62 | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.1750-887G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185331708 | |||||||
| chr4:185331807 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1750-788C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185331807 | |||||||
| chr4:185331884 | C | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1750-711C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185331884 | |||||||
| chr4:185332046 | T | C | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1750-549T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185332046 | |||||||
| chr4:185332103 | T | C | 40 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(37): Show |
40 | HG00544.hp2 HG01081.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1750-492T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185332103 | |||||||
| chr4:185332105 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1750-490G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185332105 | |||||||
| chr4:185332271 | A | G | 3 | a0001c0003t0001g0273 a0001c0003t0001g0274 a0014c0011t0001g0110 |
3 | HG01168.hp2 HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1750-324A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185332271 | |||||||
| chr4:185332316 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1750-279C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185332316 | |||||||
| chr4:185332463 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1750-132C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185332463 | |||||||
| chr4:185332556 | A | C | 1 | a0001c0003t0001g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1750-39A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 9/18 | chr4 | 185332556 | |||||||
| chr4:185332835 | A | G | 10 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(7): Show |
10 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1914+76A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185332835 | |||||||
| chr4:185332957 | G | A | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1914+198G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185332957 | |||||||
| chr4:185332972 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0035 others(63): Show |
67 | HG00639.hp1 HG00733.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.1914+213A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185332972 | |||||||
| chr4:185333013 | A | G | 5 | a0001c0001t0001g0203 a0001c0006t0001g0068 a0001c0006t0001g0069 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1914+254A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333013 | |||||||
| chr4:185333072 | A | C | 1 | a0001c0003t0001g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1914+313A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333072 | |||||||
| chr4:185333334 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1914+575G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333334 | |||||||
| chr4:185333379 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1914+620C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333379 | |||||||
| chr4:185333408 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1914+649G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333408 | |||||||
| chr4:185333465 | C | G | 1 | a0002c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1914+706C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333465 | |||||||
| chr4:185333503 | T | G | 1 | a0001c0001t0001g0028 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1914+744T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333503 | |||||||
| chr4:185333517 | A | G | 35 | a0001c0001t0001g0013 a0001c0001t0001g0117 a0001c0001t0001g0140 others(32): Show |
35 | HG00733.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1914+758A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333517 | |||||||
| chr4:185333541 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1914+782A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333541 | |||||||
| chr4:185333811 | A | G | 1 | a0002c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1914+1052A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333811 | |||||||
| chr4:185333873 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1914+1114A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185333873 | |||||||
| chr4:185334036 | C | CA | 12 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0127 others(9): Show |
12 | HG00621.hp1 HG00639.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1914+1295dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185334036 | ||||||
| chr4:185334036 | C | CAA | 11 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(8): Show |
11 | HG01081.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1914+1294_1914+129 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185334036 | ||||||
| chr4:185334036 | CA | C | 16 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(13): Show |
16 | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1914+1295delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185334036 | ||||||
| chr4:185334126 | G | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG02922.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+1367G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185334126 | |||||||
| chr4:185334173 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1914+1414T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185334173 | |||||||
| chr4:185334192 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1914+1433A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185334192 | |||||||
| chr4:185334534 | C | T | 1 | a0008c0018t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1914+1775C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185334534 | |||||||
| chr4:185334652 | A | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1914+1893A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185334652 | |||||||
| chr4:185334692 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1914+1933G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185334692 | |||||||
| chr4:185334707 | C | T | 1 | a0002c0002t0001g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1914+1948C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185334707 | |||||||
| chr4:185334946 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1914+2187C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185334946 | |||||||
| chr4:185335027 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1914+2268A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335027 | |||||||
| chr4:185335244 | C | T | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1914+2485C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335244 | |||||||
| chr4:185335313 | G | GTC | 8 | a0001c0001t0001g0236 a0001c0003t0001g0062 a0001c0003t0001g0063 others(5): Show |
8 | HG01168.hp2 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1914+2557_1914+255 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335313 | ||||||
| chr4:185335313 | GTC | G | 4 | a0001c0001t0001g0216 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
4 | HG02145.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1914+2557_1914+255 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335313 | ||||||
| chr4:185335316 | T | TCA | 36 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0001c0001t0001g0088 others(33): Show |
36 | HG00733.hp1 HG01074.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1914+2598_1914+259 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | T | TCACA | 8 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0181 others(5): Show |
8 | HG00408.hp1 HG00639.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1914+2596_1914+259 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | T | TCTCA | 5 | a0001c0001t0001g0208 a0001c0003t0001g0128 a0001c0003t0001g0129 others(2): Show |
5 | HG02809.hp2 NA18955.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1914+2558_1914+255 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | T | TCTCACA | 4 | a0001c0003t0001g0090 a0001c0003t0001g0106 a0001c0003t0001g0107 others(1): Show |
4 | HG00544.hp2 NA18964.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+2558_1914+255 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | T | TCTCACAC others(3): Show |
4 | a0001c0003t0001g0060 a0001c0003t0001g0066 a0001c0003t0001g0155 others(1): Show |
4 | NA18985.hp1 NA19000.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+2558_1914+255 others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | TCA | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1914+2598_1914+259 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | TCACA | T | 13 | a0001c0001t0001g0018 a0001c0001t0001g0087 a0001c0001t0001g0091 others(10): Show |
13 | HG00544.hp1 HG00741.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1914+2596_1914+259 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | TCACACA | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0041 a0001c0001t0001g0103 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1914+2594_1914+259 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | TCACACAC others(1): Show |
T | 6 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(3): Show |
6 | HG02258.hp1 HG02630.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1914+2592_1914+259 others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | TCACACAC others(3): Show |
T | 4 | a0001c0001t0001g0040 a0001c0006t0001g0068 a0001c0006t0001g0069 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+2590_1914+259 others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335316 | TCACACAC others(9): Show |
T | 1 | a0003c0004t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1914+2584_1914+259 others(20): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185335316 | ||||||
| chr4:185335318 | A | T | 1 | a0002c0002t0001g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1914+2559A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335318 | |||||||
| chr4:185335320 | A | T | 1 | a0001c0003t0001g0273 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1914+2561A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335320 | |||||||
| chr4:185335322 | A | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0210 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1914+2563A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335322 | |||||||
| chr4:185335359 | A | C | 6 | a0001c0003t0001g0060 a0001c0003t0001g0066 a0001c0003t0001g0067 others(3): Show |
6 | NA18954.hp1 NA18985.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.1914+2600A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335359 | |||||||
| chr4:185335477 | T | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0242 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1914+2718T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335477 | |||||||
| chr4:185335820 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1914+3061T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335820 | |||||||
| chr4:185335822 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1914+3063G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335822 | |||||||
| chr4:185335903 | T | C | 1 | a0003c0004t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1914+3144T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335903 | |||||||
| chr4:185335968 | A | C | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1914+3209A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185335968 | |||||||
| chr4:185336167 | T | TA | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1915-3207dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185336167 | ||||||
| chr4:185336218 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1915-3161G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336218 | |||||||
| chr4:185336230 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1915-3149A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336230 | |||||||
| chr4:185336284 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1915-3095A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336284 | |||||||
| chr4:185336320 | C | A | 11 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(8): Show |
11 | HG01081.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1915-3059C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336320 | |||||||
| chr4:185336483 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1915-2896C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336483 | |||||||
| chr4:185336637 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1915-2742A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336637 | |||||||
| chr4:185336665 | T | C | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1915-2714T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336665 | |||||||
| chr4:185336666 | C | T | 3 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 |
3 | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1915-2713C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336666 | |||||||
| chr4:185336779 | C | T | 1 | a0002c0002t0001g0262 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1915-2600C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336779 | |||||||
| chr4:185336793 | T | G | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1915-2586T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185336793 | |||||||
| chr4:185337236 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1915-2143C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185337236 | |||||||
| chr4:185337411 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1915-1968G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185337411 | |||||||
| chr4:185337484 | CTATT | C | 13 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(10): Show |
13 | HG01081.hp1 HG02055.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1915-1891_1915-188 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185337484 | ||||||
| chr4:185337694 | A | G | 1 | a0003c0004t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1915-1685A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185337694 | |||||||
| chr4:185337741 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0042 others(28): Show |
32 | HG00639.hp1 HG00733.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1915-1638A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185337741 | |||||||
| chr4:185337787 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1915-1592A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185337787 | |||||||
| chr4:185337888 | T | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(58): Show |
61 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1915-1491T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185337888 | |||||||
| chr4:185337924 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0035 others(93): Show |
97 | HG00621.hp2 HG00733.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.1915-1455G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185337924 | |||||||
| chr4:185338025 | G | A | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1915-1354G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338025 | |||||||
| chr4:185338109 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1915-1270G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338109 | |||||||
| chr4:185338276 | G | GT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(7): Show |
10 | HG00733.hp1 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1915-1102dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185338276 | ||||||
| chr4:185338276 | G | GTT | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(10): Show |
13 | HG00621.hp2 HG02257.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1915-1102_1915-110 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185338276 | ||||||
| chr4:185338277 | TG | T | 16 | a0001c0001t0001g0145 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG01081.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1915-1101delG | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338277 | |||||||
| chr4:185338278 | G | GT | 5 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0098 others(2): Show |
5 | HG01257.hp1 HG01993.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1915-1086dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 185338278 | ||||||
| chr4:185338278 | G | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(146): Show |
151 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(148): Show |
intron_variant | MODIFIER | c.1915-1101G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338278 | |||||||
| chr4:185338308 | C | T | 11 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(8): Show |
11 | HG01081.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1915-1071C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338308 | |||||||
| chr4:185338379 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1915-1000G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338379 | |||||||
| chr4:185338466 | T | C | 6 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1915-913T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338466 | |||||||
| chr4:185338535 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1915-844G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338535 | |||||||
| chr4:185338583 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0048 others(23): Show |
27 | HG00733.hp2 HG01123.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.1915-796C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338583 | |||||||
| chr4:185338584 | G | A | 2 | a0001c0001t0001g0201 a0003c0004t0001g0204 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1915-795G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338584 | |||||||
| chr4:185338652 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1915-727G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338652 | |||||||
| chr4:185338694 | C | T | 22 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(19): Show |
22 | HG00621.hp2 HG02109.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1915-685C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338694 | |||||||
| chr4:185338765 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1915-614G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338765 | |||||||
| chr4:185338878 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1915-501G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185338878 | |||||||
| chr4:185339055 | T | C | 20 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(17): Show |
20 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1915-324T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185339055 | |||||||
| chr4:185339077 | A | T | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1915-302A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185339077 | |||||||
| chr4:185339120 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1915-259G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185339120 | |||||||
| chr4:185339129 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1915-250A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185339129 | |||||||
| chr4:185339174 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1915-205C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185339174 | |||||||
| chr4:185339175 | G | A | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1915-204G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185339175 | |||||||
| chr4:185339270 | G | C | 1 | a0001c0001t0001g0031 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1915-109G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185339270 | |||||||
| chr4:185339286 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1915-93G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | 185339286 | |||||||
| chr4:185339560 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2046+50T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185339560 | |||||||
| chr4:185339579 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2046+69G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185339579 | |||||||
| chr4:185339939 | T | C | 1 | a0002c0002t0001g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2046+429T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185339939 | |||||||
| chr4:185340377 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2046+867A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340377 | |||||||
| chr4:185340495 | G | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0064 others(15): Show |
19 | HG01123.hp1 HG01192.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.2046+985G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340495 | |||||||
| chr4:185340543 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2046+1033A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340543 | |||||||
| chr4:185340566 | T | G | 40 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(37): Show |
40 | HG00544.hp2 HG01081.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.2046+1056T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340566 | |||||||
| chr4:185340607 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2046+1097A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340607 | |||||||
| chr4:185340791 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2047-1185C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340791 | |||||||
| chr4:185340792 | G | A | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2047-1184G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340792 | |||||||
| chr4:185340822 | T | C | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2047-1154T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340822 | |||||||
| chr4:185340873 | C | T | 13 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(10): Show |
13 | HG01081.hp1 HG02055.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2047-1103C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340873 | |||||||
| chr4:185340921 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2047-1055C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340921 | |||||||
| chr4:185340978 | G | A | 1 | a0001c0003t0001g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2047-998G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185340978 | |||||||
| chr4:185341105 | A | C | 1 | a0001c0001t0001g0018 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2047-871A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185341105 | |||||||
| chr4:185341219 | G | A | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2047-757G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185341219 | |||||||
| chr4:185341226 | C | CGCATGCA others(5): Show |
20 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(17): Show |
20 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2047-740_2047-739i others(14): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr4 | 185341226 | ||||||
| chr4:185341242 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2047-734A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185341242 | |||||||
| chr4:185341314 | G | A | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2047-662G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185341314 | |||||||
| chr4:185341825 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2047-151C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 11/18 | chr4 | 185341825 | |||||||
| chr4:185342357 | G | C | 1 | a0001c0003t0001g0090 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2187+241G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342357 | |||||||
| chr4:185342491 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01975.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2187+375C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342491 | |||||||
| chr4:185342558 | A | G | 1 | a0001c0003t0001g0128 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2187+442A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342558 | |||||||
| chr4:185342562 | T | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0215 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2187+446T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342562 | |||||||
| chr4:185342613 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2187+497A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342613 | |||||||
| chr4:185342621 | T | TACAAGGG others(40): Show |
15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2187+544_2187+590d others(49): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 185342621 | ||||||
| chr4:185342754 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2187+638A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342754 | |||||||
| chr4:185342783 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2187+667C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342783 | |||||||
| chr4:185342904 | T | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02630.hp2 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2187+788T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342904 | |||||||
| chr4:185342952 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2187+836G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342952 | |||||||
| chr4:185342998 | C | G | 40 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(37): Show |
40 | HG00544.hp2 HG01081.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.2187+882C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185342998 | |||||||
| chr4:185343089 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2187+973C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343089 | |||||||
| chr4:185343124 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2187+1008C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343124 | |||||||
| chr4:185343136 | C | G | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2187+1020C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343136 | |||||||
| chr4:185343255 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2187+1139G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343255 | |||||||
| chr4:185343274 | G | A | 6 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2187+1158G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343274 | |||||||
| chr4:185343329 | C | T | 3 | a0002c0002t0001g0268 a0002c0002t0001g0269 a0002c0002t0001g0270 |
3 | HG02896.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2187+1213C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343329 | |||||||
| chr4:185343374 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2187+1258G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343374 | |||||||
| chr4:185343478 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2187+1362G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343478 | |||||||
| chr4:185343842 | C | T | 1 | a0009c0012t0001g0122 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2187+1726C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343842 | |||||||
| chr4:185343890 | A | C | 40 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(37): Show |
40 | HG00544.hp2 HG01081.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.2187+1774A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343890 | |||||||
| chr4:185343996 | G | A | 20 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(17): Show |
20 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2187+1880G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185343996 | |||||||
| chr4:185344115 | A | G | 40 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(37): Show |
40 | HG00544.hp2 HG01081.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.2187+1999A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185344115 | |||||||
| chr4:185344199 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2187+2083C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185344199 | |||||||
| chr4:185344282 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0241 |
2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.2187+2166A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185344282 | |||||||
| chr4:185344401 | C | T | 2 | a0002c0002t0001g0251 a0002c0002t0004g0258 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2188-2136C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185344401 | |||||||
| chr4:185344455 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2188-2082A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185344455 | |||||||
| chr4:185344480 | C | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0117 a0001c0001t0001g0140 others(17): Show |
20 | HG00733.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2188-2057C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185344480 | |||||||
| chr4:185344543 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2188-1994A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185344543 | |||||||
| chr4:185344635 | T | TAAGGAGG | 40 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0001g0196 others(37): Show |
40 | HG00544.hp2 HG01081.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.2188-1889_2188-188 others(11): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 185344635 | ||||||
| chr4:185345140 | T | C | 1 | a0002c0002t0004g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2188-1397T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345140 | |||||||
| chr4:185345155 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2188-1382G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345155 | |||||||
| chr4:185345447 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2188-1090C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345447 | |||||||
| chr4:185345453 | A | G | 4 | a0001c0006t0001g0068 a0001c0006t0001g0069 a0003c0007t0001g0070 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2188-1084A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345453 | |||||||
| chr4:185345620 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2188-917G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345620 | |||||||
| chr4:185345662 | A | G | 20 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(17): Show |
20 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2188-875A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345662 | |||||||
| chr4:185345699 | G | T | 1 | a0001c0001t0001g0026 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2188-838G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345699 | |||||||
| chr4:185345742 | G | C | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00621.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2188-795G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345742 | |||||||
| chr4:185345789 | CA | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
19 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.2188-737delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 185345789 | ||||||
| chr4:185345817 | A | G | 27 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(24): Show |
27 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.2188-720A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345817 | |||||||
| chr4:185345923 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
122 | HG00140.hp2 HG00544.hp2 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.2188-614C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345923 | |||||||
| chr4:185345983 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2188-554C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185345983 | |||||||
| chr4:185346046 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
127 | HG00544.hp2 HG00621.hp2 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.2188-491G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185346046 | |||||||
| chr4:185346107 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
2 | HG00621.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2188-430C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185346107 | |||||||
| chr4:185346236 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2188-301C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185346236 | |||||||
| chr4:185346384 | A | G | 1 | a0008c0018t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2188-153A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185346384 | |||||||
| chr4:185346427 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2188-110G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185346427 | |||||||
| chr4:185346495 | T | C | 4 | a0001c0001t0001g0109 a0001c0001t0002g0093 a0001c0001t0002g0135 others(1): Show |
4 | HG01243.hp2 HG01928.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.2188-42T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | chr4 | 185346495 | |||||||
| chr4:185346938 | C | G | 2 | a0002c0002t0001g0268 a0002c0002t0001g0269 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2301+288C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185346938 | |||||||
| chr4:185346975 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0033 others(81): Show |
86 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.2301+325A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185346975 | |||||||
| chr4:185347000 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2301+350A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347000 | |||||||
| chr4:185347080 | A | G | 1 | a0001c0003t0001g0062 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2301+430A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347080 | |||||||
| chr4:185347136 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0215 a0001c0006t0001g0068 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301+486G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347136 | |||||||
| chr4:185347246 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2301+596T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347246 | |||||||
| chr4:185347321 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0148 |
2 | HG02080.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2301+671C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347321 | |||||||
| chr4:185347419 | C | T | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2301+769C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347419 | |||||||
| chr4:185347422 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(124): Show |
129 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.2301+772A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347422 | |||||||
| chr4:185347458 | C | CTTTTG | 3 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0010c0019t0005g0267 |
3 | HG03139.hp1 NA19010.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2301+834_2301+838d others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185347458 | ||||||
| chr4:185347458 | C | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG03669.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2301+808C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347458 | |||||||
| chr4:185347458 | CTTTTG | C | 4 | a0001c0001t0002g0136 a0002c0002t0001g0260 a0003c0004t0001g0249 others(1): Show |
4 | HG00733.hp2 HG01496.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301+834_2301+838d others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185347458 | ||||||
| chr4:185347458 | CTTTTGTT others(3): Show |
C | 3 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0001g0232 |
3 | HG01243.hp1 HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2301+829_2301+838d others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185347458 | ||||||
| chr4:185347468 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2301+818G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347468 | |||||||
| chr4:185347492 | C | T | 3 | a0003c0004t0001g0249 a0003c0007t0001g0184 a0010c0019t0005g0267 |
3 | HG02258.hp1 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2301+842C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347492 | |||||||
| chr4:185347500 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2301+850C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347500 | |||||||
| chr4:185347528 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2301+878T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347528 | |||||||
| chr4:185347661 | G | A | 1 | a0002c0002t0001g0260 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2301+1011G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347661 | |||||||
| chr4:185347671 | G | A | 10 | a0001c0001t0001g0193 a0001c0001t0001g0215 a0001c0001t0001g0216 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2301+1021G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347671 | |||||||
| chr4:185347852 | A | G | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2301+1202A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347852 | |||||||
| chr4:185347856 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2301+1206C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347856 | |||||||
| chr4:185347858 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2301+1208T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347858 | |||||||
| chr4:185347871 | CGTGCTAC others(7): Show |
C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2301+1224_2301+123 others(18): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185347871 | ||||||
| chr4:185347922 | T | G | 1 | a0001c0001t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2301+1272T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347922 | |||||||
| chr4:185347981 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(122): Show |
127 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(124): Show |
intron_variant | MODIFIER | c.2301+1331C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185347981 | |||||||
| chr4:185348078 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2301+1428C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185348078 | |||||||
| chr4:185348115 | A | G | 6 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2301+1465A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185348115 | |||||||
| chr4:185348399 | A | AT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(72): Show |
77 | HG00621.hp1 HG01123.hp1 HG01192.hp1 others(74): Show |
intron_variant | MODIFIER | c.2301+1760dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185348399 | ||||||
| chr4:185348399 | A | ATT | 52 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0117 others(49): Show |
52 | HG00140.hp2 HG00544.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.2301+1759_2301+176 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185348399 | ||||||
| chr4:185348543 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(60): Show |
65 | HG00621.hp1 HG01123.hp1 HG01192.hp1 others(62): Show |
intron_variant | MODIFIER | c.2301+1893C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185348543 | |||||||
| chr4:185348545 | T | C | 4 | a0001c0001t0002g0093 a0001c0001t0002g0135 a0001c0001t0002g0138 others(1): Show |
4 | HG01928.hp2 HG01952.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301+1895T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185348545 | |||||||
| chr4:185348559 | G | T | 27 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0117 others(24): Show |
27 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2301+1909G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185348559 | |||||||
| chr4:185348645 | C | T | 2 | a0005c0008t0001g0230 a0005c0008t0001g0231 |
2 | HG01081.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2301+1995C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185348645 | |||||||
| chr4:185348891 | C | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.2301+2241C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185348891 | |||||||
| chr4:185348899 | TGTACCTC others(5): Show |
T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2301+2250_2301+226 others(16): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185348899 | |||||||
| chr4:185348900 | G | C | 55 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0117 others(52): Show |
55 | HG00140.hp2 HG00544.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2301+2250G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185348900 | |||||||
| chr4:185348942 | G | GT | 55 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0117 others(52): Show |
55 | HG00140.hp2 HG00544.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2301+2293dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185348942 | ||||||
| chr4:185349254 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2302-2191G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185349254 | |||||||
| chr4:185349384 | A | T | 1 | a0001c0001t0001g0020 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2302-2061A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185349384 | |||||||
| chr4:185349487 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(146): Show |
151 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(148): Show |
intron_variant | MODIFIER | c.2302-1958A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185349487 | |||||||
| chr4:185349548 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2302-1897C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185349548 | |||||||
| chr4:185349795 | G | A | 1 | a0003c0004t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2302-1650G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185349795 | |||||||
| chr4:185350000 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(117): Show |
122 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(119): Show |
intron_variant | MODIFIER | c.2302-1445G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350000 | |||||||
| chr4:185350015 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0210 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2302-1430G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350015 | |||||||
| chr4:185350015 | G | C | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2302-1430G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350015 | |||||||
| chr4:185350142 | CGTG | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.2302-1301_2302-129 others(7): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185350142 | ||||||
| chr4:185350163 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2302-1282G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350163 | |||||||
| chr4:185350396 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(146): Show |
151 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(148): Show |
intron_variant | MODIFIER | c.2302-1049G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350396 | |||||||
| chr4:185350453 | C | T | 2 | a0003c0004t0001g0204 a0003c0007t0001g0070 |
2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2302-992C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350453 | |||||||
| chr4:185350515 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(150): Show |
155 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(152): Show |
intron_variant | MODIFIER | c.2302-930T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350515 | |||||||
| chr4:185350628 | T | C | 1 | a0012c0017t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2302-817T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350628 | |||||||
| chr4:185350658 | C | T | 1 | a0009c0012t0001g0122 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2302-787C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350658 | |||||||
| chr4:185350707 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2302-738C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350707 | |||||||
| chr4:185350730 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(155): Show |
160 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2302-715T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350730 | |||||||
| chr4:185350802 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2302-643C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350802 | |||||||
| chr4:185350828 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2302-617C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350828 | |||||||
| chr4:185350856 | C | T | 1 | a0003c0004t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2302-589C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350856 | |||||||
| chr4:185350867 | A | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(142): Show |
147 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.2302-578A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350867 | |||||||
| chr4:185350967 | C | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2302-478C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185350967 | |||||||
| chr4:185350980 | C | CA | 3 | a0002c0002t0001g0250 a0002c0002t0001g0259 a0002c0002t0001g0261 |
3 | HG02717.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2302-462dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185350980 | ||||||
| chr4:185351024 | A | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2302-421A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185351024 | |||||||
| chr4:185351029 | A | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.2302-416A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185351029 | |||||||
| chr4:185351051 | GTGTAATT others(10): Show |
G | 4 | a0001c0001t0001g0203 a0003c0004t0001g0249 a0003c0007t0001g0184 others(1): Show |
4 | HG02258.hp1 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2302-392_2302-376d others(19): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 185351051 | ||||||
| chr4:185351055 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2302-390A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185351055 | |||||||
| chr4:185351114 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2302-331G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185351114 | |||||||
| chr4:185351171 | C | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0242 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2302-274C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185351171 | |||||||
| chr4:185351325 | G | A | 1 | a0002c0002t0001g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2302-120G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185351325 | |||||||
| chr4:185351389 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0215 a0001c0006t0001g0068 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2302-56C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185351389 | |||||||
| chr4:185351410 | C | T | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2302-35C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 13/18 | chr4 | 185351410 | |||||||
| chr4:185351619 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(157): Show |
162 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.2466+10T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185351619 | |||||||
| chr4:185351641 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2466+32A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185351641 | |||||||
| chr4:185351708 | A | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.2466+99A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185351708 | |||||||
| chr4:185351804 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(151): Show |
156 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(153): Show |
intron_variant | MODIFIER | c.2466+195G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185351804 | |||||||
| chr4:185351906 | C | CGGGGTGG others(1): Show |
12 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0028 others(9): Show |
12 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.2466+303_2466+310d others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr4 | 185351906 | ||||||
| chr4:185351912 | G | GGGGGGGT | 9 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
9 | HG00733.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2466+304_2466+310d others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr4 | 185351912 | ||||||
| chr4:185351986 | C | G | 5 | a0002c0002t0001g0254 a0002c0002t0001g0255 a0002c0002t0001g0256 others(2): Show |
5 | HG02572.hp1 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2466+377C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185351986 | |||||||
| chr4:185352224 | C | T | 3 | a0001c0001t0001g0193 a0001c0006t0001g0068 a0001c0006t0001g0069 |
3 | HG02257.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2466+615C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185352224 | |||||||
| chr4:185352334 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(148): Show |
153 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(150): Show |
intron_variant | MODIFIER | c.2466+725A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185352334 | |||||||
| chr4:185352411 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2466+802G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185352411 | |||||||
| chr4:185352657 | G | A | 30 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(27): Show |
30 | HG00621.hp2 HG00733.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.2467-828G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185352657 | |||||||
| chr4:185352741 | C | T | 2 | a0001c0001t0001g0041 a0002c0002t0001g0263 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2467-744C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185352741 | |||||||
| chr4:185352819 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(57): Show |
62 | HG00621.hp1 HG00639.hp1 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.2467-666C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185352819 | |||||||
| chr4:185352829 | C | A | 25 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(22): Show |
25 | HG00621.hp2 HG00733.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.2467-656C>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185352829 | |||||||
| chr4:185352976 | T | G | 87 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0054 others(84): Show |
87 | HG00140.hp2 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.2467-509T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185352976 | |||||||
| chr4:185352981 | TG | T | 30 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(27): Show |
30 | HG00621.hp2 HG00733.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.2467-502delG | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr4 | 185352981 | ||||||
| chr4:185353016 | T | C | 53 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0117 others(50): Show |
53 | HG00140.hp2 HG00544.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.2467-469T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185353016 | |||||||
| chr4:185353112 | A | G | 5 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0266 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2467-373A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185353112 | |||||||
| chr4:185353217 | C | T | 1 | a0007c0016t0001g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2467-268C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185353217 | |||||||
| chr4:185353256 | G | A | 3 | a0001c0001t0001g0108 a0003c0004t0001g0204 a0003c0007t0001g0070 |
3 | HG03130.hp1 HG03471.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2467-229G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185353256 | |||||||
| chr4:185353270 | T | A | 2 | a0003c0004t0001g0204 a0003c0007t0001g0070 |
2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2467-215T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185353270 | |||||||
| chr4:185353387 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(52): Show |
57 | HG00621.hp1 HG01123.hp1 HG01192.hp1 others(54): Show |
intron_variant | MODIFIER | c.2467-98G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | chr4 | 185353387 | |||||||
| chr4:185353709 | T | C | 1 | a0004c0005t0001g0047 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2584+107T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185353709 | |||||||
| chr4:185353730 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0196 |
2 | HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2584+128A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185353730 | |||||||
| chr4:185353768 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(52): Show |
57 | HG00621.hp1 HG01123.hp1 HG01192.hp1 others(54): Show |
intron_variant | MODIFIER | c.2584+166G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185353768 | |||||||
| chr4:185353772 | A | G | 3 | a0002c0002t0001g0250 a0002c0002t0001g0259 a0002c0002t0001g0261 |
3 | HG02717.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2584+170A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185353772 | |||||||
| chr4:185353872 | C | T | 16 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0216 others(13): Show |
16 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2584+270C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185353872 | |||||||
| chr4:185354041 | C | CA | 6 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0203 others(3): Show |
6 | HG02258.hp1 HG03139.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2584+456dupA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 185354041 | ||||||
| chr4:185354041 | CA | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(64): Show |
69 | HG00621.hp1 HG00639.hp1 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.2584+456delA | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 185354041 | ||||||
| chr4:185354060 | A | G | 3 | a0003c0004t0001g0249 a0003c0007t0001g0184 a0010c0019t0005g0267 |
3 | HG02258.hp1 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2584+458A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185354060 | |||||||
| chr4:185354123 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(159): Show |
164 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(161): Show |
intron_variant | MODIFIER | c.2584+521A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185354123 | |||||||
| chr4:185354239 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0148 |
2 | HG02080.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2584+637T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185354239 | |||||||
| chr4:185354404 | T | A | 30 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(27): Show |
30 | HG00621.hp2 HG00733.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.2584+802T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185354404 | |||||||
| chr4:185354753 | G | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(15): Show |
18 | HG01952.hp2 HG01975.hp1 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.2584+1151G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185354753 | |||||||
| chr4:185354815 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2584+1213G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185354815 | |||||||
| chr4:185354944 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2584+1342C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185354944 | |||||||
| chr4:185355024 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2584+1422A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185355024 | |||||||
| chr4:185355146 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2584+1544C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185355146 | |||||||
| chr4:185355357 | A | G | 5 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0266 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2584+1755A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185355357 | |||||||
| chr4:185355469 | G | C | 1 | a0002c0002t0001g0255 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2584+1867G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185355469 | |||||||
| chr4:185355497 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2584+1895A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185355497 | |||||||
| chr4:185355574 | G | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(80): Show |
85 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.2584+1972G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185355574 | |||||||
| chr4:185356051 | T | C | 6 | a0002c0002t0001g0251 a0002c0002t0001g0254 a0002c0002t0001g0255 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2585-1620T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185356051 | |||||||
| chr4:185356114 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0164 |
3 | NA18943.hp1 NA18951.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2585-1557G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185356114 | |||||||
| chr4:185356146 | C | CGT | 26 | a0001c0001t0001g0187 a0001c0001t0001g0208 a0001c0001t0001g0236 others(23): Show |
26 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.2585-1510_2585-150 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 185356146 | ||||||
| chr4:185356146 | CGT | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2585-1510_2585-150 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 185356146 | ||||||
| chr4:185356363 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0148 |
2 | HG02080.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2585-1308A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185356363 | |||||||
| chr4:185356384 | T | A | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2585-1287T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185356384 | |||||||
| chr4:185356786 | G | A | 1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2585-885G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185356786 | |||||||
| chr4:185356980 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2585-691C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185356980 | |||||||
| chr4:185357091 | T | C | 1 | a0002c0002t0001g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2585-580T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185357091 | |||||||
| chr4:185357137 | G | A | 3 | a0001c0001t0001g0193 a0001c0006t0001g0068 a0001c0006t0001g0069 |
3 | HG02257.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2585-534G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185357137 | |||||||
| chr4:185357168 | C | T | 3 | a0001c0001t0001g0193 a0001c0006t0001g0068 a0001c0006t0001g0069 |
3 | HG02257.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2585-503C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185357168 | |||||||
| chr4:185357581 | A | C | 28 | a0001c0001t0001g0193 a0001c0001t0001g0208 a0001c0001t0001g0236 others(25): Show |
28 | HG00544.hp2 HG01168.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2585-90A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185357581 | |||||||
| chr4:185357623 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0164 |
3 | NA18943.hp1 NA18951.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2585-48A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | chr4 | 185357623 | |||||||
| chr4:185357800 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0238 |
3 | HG02258.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2651+63A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185357800 | |||||||
| chr4:185357866 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2651+129A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185357866 | |||||||
| chr4:185358094 | T | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(30): Show |
34 | HG00621.hp1 HG01123.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.2651+357T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185358094 | |||||||
| chr4:185358159 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2651+422A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185358159 | |||||||
| chr4:185358669 | G | C | 1 | a0001c0001t0002g0146 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2651+932G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185358669 | |||||||
| chr4:185358860 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG00099.hp1 HG01074.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2651+1123T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185358860 | |||||||
| chr4:185358931 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2651+1194T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185358931 | |||||||
| chr4:185359152 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2651+1415C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185359152 | |||||||
| chr4:185359368 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(148): Show |
153 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(150): Show |
intron_variant | MODIFIER | c.2651+1631G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185359368 | |||||||
| chr4:185359447 | T | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0210 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2651+1710T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185359447 | |||||||
| chr4:185359650 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(146): Show |
151 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(148): Show |
intron_variant | MODIFIER | c.2651+1913T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185359650 | |||||||
| chr4:185359854 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
2 | HG00621.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2652-2070T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185359854 | |||||||
| chr4:185359940 | G | A | 7 | a0002c0002t0001g0251 a0002c0002t0001g0254 a0002c0002t0001g0255 others(4): Show |
7 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2652-1984G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185359940 | |||||||
| chr4:185360038 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2652-1886A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360038 | |||||||
| chr4:185360238 | A | G | 1 | a0002c0002t0001g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2652-1686A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360238 | |||||||
| chr4:185360337 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2652-1587T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360337 | |||||||
| chr4:185360439 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2652-1485G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360439 | |||||||
| chr4:185360462 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2652-1462G>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360462 | |||||||
| chr4:185360502 | T | A | 1 | a0002c0002t0001g0260 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2652-1422T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360502 | |||||||
| chr4:185360565 | T | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2652-1359T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360565 | |||||||
| chr4:185360601 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(151): Show |
156 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(153): Show |
intron_variant | MODIFIER | c.2652-1323T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360601 | |||||||
| chr4:185360715 | G | A | 2 | a0004c0005t0001g0045 a0004c0005t0001g0046 |
2 | NA19002.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2652-1209G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360715 | |||||||
| chr4:185360725 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(158): Show |
163 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(160): Show |
intron_variant | MODIFIER | c.2652-1199A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360725 | |||||||
| chr4:185360796 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2652-1128G>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360796 | |||||||
| chr4:185360929 | T | TTATA | 8 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0002c0002t0001g0254 others(5): Show |
8 | HG02280.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2652-995_2652-994i others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360929 | |||||||
| chr4:185360929 | T | TTATATAT others(3): Show |
2 | a0002c0002t0001g0251 a0003c0007t0001g0070 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2652-995_2652-994i others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360929 | |||||||
| chr4:185360929 | T | TTATATAT others(7): Show |
1 | a0003c0004t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2652-995_2652-994i others(16): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360929 | |||||||
| chr4:185360929 | TAA | T | 3 | a0001c0001t0001g0193 a0001c0006t0001g0068 a0001c0006t0001g0069 |
3 | HG02257.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2652-994_2652-993d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360929 | |||||||
| chr4:185360929 | TAATATAT others(1): Show |
T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2652-994_2652-987d others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360929 | |||||||
| chr4:185360930 | A | AAT | 6 | a0001c0001t0001g0159 a0001c0001t0001g0216 a0002c0002t0001g0264 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2652-972_2652-971d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360930 | ||||||
| chr4:185360930 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2652-980_2652-971d others(12): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360930 | ||||||
| chr4:185360930 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2652-986_2652-971d others(18): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360930 | ||||||
| chr4:185360930 | A | AATATATA others(11): Show |
2 | a0001c0001t0001g0191 a0001c0001t0001g0215 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2652-988_2652-971d others(20): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360930 | ||||||
| chr4:185360930 | A | AATATATA others(15): Show |
3 | a0001c0001t0001g0190 a0003c0004t0001g0249 a0010c0019t0005g0267 |
3 | HG03139.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2652-992_2652-971d others(24): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360930 | ||||||
| chr4:185360930 | A | AATATATA others(17): Show |
1 | a0003c0007t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2652-971_2652-970i others(26): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360930 | ||||||
| chr4:185360930 | A | T | 13 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0002c0002t0001g0251 others(10): Show |
13 | HG00733.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.2652-994A>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185360930 | |||||||
| chr4:185360930 | AAT | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.2652-972_2652-971d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360930 | ||||||
| chr4:185360930 | AATATAT | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(80): Show |
85 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.2652-976_2652-971d others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360930 | ||||||
| chr4:185360950 | T | TATATATA others(13): Show |
15 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(12): Show |
15 | HG00544.hp2 HG02280.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.2652-971_2652-970i others(22): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360950 | ||||||
| chr4:185360950 | T | TATATATA others(15): Show |
6 | a0001c0003t0001g0104 a0001c0003t0001g0161 a0001c0003t0001g0163 others(3): Show |
6 | HG01168.hp2 HG03834.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2652-971_2652-970i others(24): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360950 | ||||||
| chr4:185360950 | T | TATATATA others(17): Show |
1 | a0001c0003t0001g0107 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2652-971_2652-970i others(26): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360950 | ||||||
| chr4:185360950 | T | TATATATA others(19): Show |
3 | a0001c0003t0001g0062 a0001c0003t0001g0106 a0001c0003t0001g0143 |
3 | HG02735.hp2 NA18964.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2652-971_2652-970i others(28): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 185360950 | ||||||
| chr4:185361021 | C | T | 1 | a0002c0002t0001g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2652-903C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185361021 | |||||||
| chr4:185361042 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02055.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2652-882C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185361042 | |||||||
| chr4:185361069 | T | C | 25 | a0001c0001t0001g0208 a0001c0001t0001g0236 a0001c0003t0001g0060 others(22): Show |
25 | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.2652-855T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185361069 | |||||||
| chr4:185361187 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2652-737A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185361187 | |||||||
| chr4:185361192 | A | G | 5 | a0001c0001t0001g0216 a0002c0002t0001g0264 a0002c0002t0001g0266 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2652-732A>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185361192 | |||||||
| chr4:185361204 | C | T | 1 | a0003c0004t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2652-720C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185361204 | |||||||
| chr4:185361205 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(80): Show |
85 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.2652-719G>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185361205 | |||||||
| chr4:185361217 | C | G | 1 | a0010c0019t0005g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2652-707C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185361217 | |||||||
| chr4:185361581 | T | C | 1 | a0007c0016t0001g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2652-343T>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | chr4 | 185361581 | |||||||
| chr4:185362228 | C | G | 2 | a0002c0002t0001g0266 a0002c0002t0001g0271 |
2 | HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2833+123C>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 17/18 | chr4 | 185362228 | |||||||
| chr4:185362355 | A | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2833+250A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 17/18 | chr4 | 185362355 | |||||||
| chr4:185362363 | T | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0237 a0001c0001t0001g0239 others(1): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.2834-248T>A | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 17/18 | chr4 | 185362363 | |||||||
| chr4:185362587 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2834-24T>G | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 17/18 | chr4 | 185362587 | |||||||
| chr4:185362837 | C | CT | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(71): Show |
74 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.2934+148dupT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 185362837 | ||||||
| chr4:185362837 | C | CTT | 8 | a0001c0001t0001g0193 a0001c0001t0002g0160 a0001c0003t0001g0062 others(5): Show |
8 | HG02257.hp1 HG02257.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2934+147_2934+148d others(4): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 185362837 | ||||||
| chr4:185362837 | CT | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(73): Show |
78 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.2934+148delT | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 185362837 | ||||||
| chr4:185363010 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): Show |
152 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(149): Show |
intron_variant | MODIFIER | c.2934+299C>T | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 18/18 | chr4 | 185363010 | |||||||
| chr4:185363082 | A | C | 2 | a0002c0002t0001g0268 a0002c0002t0001g0269 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2935-303A>C | SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 18/18 | chr4 | 185363082 |