Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23530 |
| ensemblid | ENSG00000112992.18 |
| hgncid | 7863 |
| symbol | NNT |
| name | nicotinamide nucleotide transhydrogenase |
| refseq_nuc | NM_182977.3 |
| refseq_prot | NP_892022.2 |
| ensembl_nuc | ENST00000344920.9 |
| ensembl_prot | ENSP00000343873.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 43603180 |
| end | 43707396 |
| strand | + |
| ver | v1.2 |
| region | chr5:43603180-43707396 |
| region5000 | chr5:43598180-43712396 |
| regionname0 | NNT_chr5_43603180_43707396 |
| regionname5000 | NNT_chr5_43598180_43712396 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1086 | 151 | 68 | 29 | 28 | 2 | 22 | 19 | NNT_chr5_43598180_43712396 | NNT | MANLL others(1081): Show |
chr5 | 43598180 | 43712396 |
| a0002 | 0/0 | 1086 | 23 | 0 | 3 | 16 | 0 | 4 | 12 | NNT_chr5_43598180_43712396 | NNT | MANLL others(1081): Show |
chr5 | 43598180 | 43712396 |
| a0003 | 0/0 | 1086 | 6 | 0 | 0 | 3 | 0 | 3 | 3 | NNT_chr5_43598180_43712396 | NNT | MANLL others(1081): Show |
chr5 | 43598180 | 43712396 |
| a0004 | 0/0 | 1086 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | MANLL others(1081): Show |
chr5 | 43598180 | 43712396 |
| a0005 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | MANLL others(1081): Show |
chr5 | 43598180 | 43712396 |
| a0006 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | MANLL others(1081): Show |
chr5 | 43598180 | 43712396 |
| a0007 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | MANLL others(1081): Show |
chr5 | 43598180 | 43712396 |
| a0008 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | MANLL others(1081): Show |
chr5 | 43598180 | 43712396 |
| a0009 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NNT_chr5_43598180_43712396 | NNT | MANLL others(1081): Show |
chr5 | 43598180 | 43712396 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3258 | 81 | 45 | 19 | 4 | 1 | 12 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0001c0002 | 1/1 | 3258 | 47 | 5 | 8 | 24 | 1 | 7 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0001c0004 | 0/0 | 3258 | 17 | 13 | 1 | 0 | 0 | 3 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0001c0005 | 0/0 | 3258 | 5 | 4 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0001c0011 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0002c0003 | 0/0 | 3258 | 22 | 0 | 3 | 15 | 0 | 4 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0002c0015 | 0/0 | 3258 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0003c0006 | 0/0 | 3258 | 5 | 0 | 0 | 3 | 0 | 2 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0003c0010 | 0/0 | 3258 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0004c0007 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0004c0009 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0005c0008 | 0/0 | 3258 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0006c0013 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0007c0012 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0008c0014 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 | ||
| a0009c0016 | 0/0 | 3258 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | ATGGC others(3253): Show |
chr5 | 43598180 | 43712396 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6421 | 33 | 30 | 2 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0003 | 0/0 | 6421 | 18 | 1 | 7 | 4 | 0 | 6 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0005 | 0/0 | 6421 | 7 | 5 | 2 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0006 | 0/0 | 6426 | 9 | 5 | 3 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0009 | 0/0 | 6422 | 4 | 0 | 1 | 0 | 0 | 3 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6417): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0014 | 0/0 | 6426 | 2 | 2 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0015 | 0/0 | 6423 | 2 | 1 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6418): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0016 | 0/0 | 6426 | 2 | 1 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0017 | 0/0 | 6421 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0024 | 0/0 | 6421 | 1 | 0 | 0 | 0 | 1 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0027 | 0/0 | 6421 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0001c0001t0028 | 0/0 | 6423 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6418): Show |
chr5 | 43598180 | 43712396 |
| a0001c0002t0001 | 1/1 | 6421 | 37 | 3 | 6 | 21 | 0 | 5 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0001c0002t0002 | 0/0 | 6427 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6422): Show |
chr5 | 43598180 | 43712396 |
| a0001c0002t0008 | 0/0 | 6421 | 5 | 0 | 2 | 0 | 1 | 2 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0001c0002t0010 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0001c0002t0013 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6424): Show |
chr5 | 43598180 | 43712396 |
| a0001c0002t0022 | 0/0 | 6420 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6415): Show |
chr5 | 43598180 | 43712396 |
| a0001c0002t0025 | 0/0 | 6425 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6420): Show |
chr5 | 43598180 | 43712396 |
| a0001c0004t0004 | 0/0 | 6426 | 9 | 6 | 0 | 0 | 0 | 3 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0001c0004t0007 | 0/0 | 6427 | 4 | 3 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6422): Show |
chr5 | 43598180 | 43712396 |
| a0001c0004t0018 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6422): Show |
chr5 | 43598180 | 43712396 |
| a0001c0004t0020 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6415): Show |
chr5 | 43598180 | 43712396 |
| a0001c0004t0021 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6415): Show |
chr5 | 43598180 | 43712396 |
| a0001c0004t0026 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6422): Show |
chr5 | 43598180 | 43712396 |
| a0001c0005t0004 | 0/0 | 6426 | 4 | 3 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0001c0005t0023 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0001c0011t0004 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0002c0003t0002 | 0/0 | 6427 | 17 | 0 | 3 | 10 | 0 | 4 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6422): Show |
chr5 | 43598180 | 43712396 |
| a0002c0003t0011 | 0/0 | 6427 | 2 | 0 | 0 | 2 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6422): Show |
chr5 | 43598180 | 43712396 |
| a0002c0003t0012 | 0/0 | 6427 | 2 | 0 | 0 | 2 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6422): Show |
chr5 | 43598180 | 43712396 |
| a0002c0003t0019 | 0/0 | 6423 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6418): Show |
chr5 | 43598180 | 43712396 |
| a0002c0015t0002 | 0/0 | 6427 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6422): Show |
chr5 | 43598180 | 43712396 |
| a0003c0006t0005 | 0/0 | 6421 | 5 | 0 | 0 | 3 | 0 | 2 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0003c0010t0005 | 0/0 | 6421 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0004c0007t0010 | 0/0 | 6426 | 2 | 2 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0004c0009t0007 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6422): Show |
chr5 | 43598180 | 43712396 |
| a0005c0008t0013 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6424): Show |
chr5 | 43598180 | 43712396 |
| a0006c0013t0001 | 0/0 | 6421 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| a0007c0012t0010 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0008c0014t0004 | 0/0 | 6426 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6421): Show |
chr5 | 43598180 | 43712396 |
| a0009c0016t0005 | 0/0 | 6421 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | GCTGT others(6416): Show |
chr5 | 43598180 | 43712396 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0009g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0009g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0014g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0015g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0015g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0016g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0016g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0017g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0024g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0027g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0001t0028g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0008g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0008g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0008g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0008g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0013g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0022g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0002t0025g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0020g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0021g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0004t0026g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0005t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0005t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0005t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0005t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0005t0023g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0001c0011t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0011g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0012g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0003t0019g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0002c0015t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0003c0006t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0003c0006t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0003c0006t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0003c0006t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0003c0006t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0003c0010t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0004c0007t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0004c0007t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0004c0009t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0005c0008t0013g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0006c0013t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0007c0012t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0008c0014t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| a0009c0016t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00544 | hp1 | a0002 | c0003 | t0002 | g0103 | EAS | CHS | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | CHS | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | CHS | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | CHS | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG00741 | hp1 | a0001 | c0001 | t0009 | g0077 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG00741 | hp2 | a0001 | c0002 | t0008 | g0168 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01069 | hp1 | a0002 | c0003 | t0002 | g0109 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01070 | hp1 | a0002 | c0003 | t0002 | g0105 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01074 | hp2 | a0001 | c0001 | t0027 | g0055 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01109 | hp1 | a0001 | c0004 | t0007 | g0125 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0116 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01167 | hp2 | a0001 | c0005 | t0004 | g0133 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0117 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0067 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01175 | hp2 | a0001 | c0001 | t0028 | g0017 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01243 | hp1 | a0001 | c0001 | t0016 | g0111 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | CLM | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01346 | hp1 | a0001 | c0002 | t0008 | g0171 | AMR | CLM | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | CLM | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01516 | hp1 | a0001 | c0001 | t0024 | g0018 | EUR | IBS | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01516 | hp2 | a0001 | c0002 | t0008 | g0178 | EUR | IBS | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01891 | hp1 | a0001 | c0004 | t0021 | g0132 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01981 | hp1 | a0002 | c0003 | t0002 | g0092 | AMR | PEL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PEL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PEL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG01993 | hp2 | a0001 | c0001 | t0017 | g0038 | AMR | PEL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02071 | hp1 | a0002 | c0003 | t0011 | g0097 | EAS | KHV | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02074 | hp2 | a0005 | c0008 | t0013 | g0174 | EAS | KHV | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02129 | hp1 | a0002 | c0003 | t0002 | g0102 | EAS | KHV | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | KHV | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | CDX | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02165 | hp2 | a0002 | c0003 | t0002 | g0099 | EAS | CDX | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0002 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02257 | hp2 | a0001 | c0004 | t0004 | g0118 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0034 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0072 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | KHV | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02572 | hp2 | a0001 | c0005 | t0023 | g0137 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0021 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02602 | hp2 | a0001 | c0002 | t0008 | g0167 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02615 | hp2 | a0001 | c0004 | t0004 | g0123 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02622 | hp1 | a0001 | c0004 | t0007 | g0082 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02683 | hp1 | a0001 | c0001 | t0009 | g0037 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02683 | hp2 | a0003 | c0010 | t0005 | g0036 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02717 | hp2 | a0001 | c0004 | t0007 | g0081 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02735 | hp1 | a0001 | c0004 | t0004 | g0120 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02809 | hp2 | a0004 | c0007 | t0010 | g0004 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02818 | hp2 | a0006 | c0013 | t0001 | g0059 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0138 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02897 | hp1 | a0001 | c0004 | t0018 | g0127 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02970 | hp2 | a0004 | c0007 | t0010 | g0005 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02976 | hp1 | a0001 | c0005 | t0004 | g0136 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0164 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0110 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0112 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03130 | hp2 | a0001 | c0004 | t0004 | g0130 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03195 | hp1 | a0001 | c0002 | t0010 | g0183 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03209 | hp1 | a0001 | c0004 | t0004 | g0128 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0113 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03225 | hp2 | a0004 | c0009 | t0007 | g0003 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03486 | hp1 | a0001 | c0005 | t0004 | g0135 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03490 | hp1 | a0001 | c0001 | t0009 | g0025 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03490 | hp2 | a0001 | c0004 | t0004 | g0121 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03516 | hp1 | a0008 | c0014 | t0004 | g0119 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03540 | hp2 | a0001 | c0004 | t0004 | g0129 | AFR | GWD | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0104 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03831 | hp1 | a0009 | c0016 | t0005 | g0045 | SAS | BEB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03831 | hp2 | a0001 | c0002 | t0008 | g0170 | SAS | BEB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | BEB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03834 | hp2 | a0002 | c0003 | t0002 | g0093 | SAS | BEB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | BEB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03927 | hp2 | a0002 | c0003 | t0002 | g0106 | SAS | BEB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG04115 | hp1 | a0001 | c0001 | t0015 | g0008 | SAS | STU | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG04115 | hp2 | a0003 | c0006 | t0005 | g0044 | SAS | STU | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | BEB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | BEB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0166 | SAS | STU | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG04199 | hp2 | a0002 | c0003 | t0002 | g0091 | SAS | STU | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG04228 | hp1 | a0001 | c0004 | t0004 | g0122 | SAS | STU | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | STU | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18522 | hp2 | a0001 | c0004 | t0004 | g0131 | AFR | YRI | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18906 | hp2 | a0001 | c0011 | t0004 | g0124 | AFR | YRI | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18941 | hp1 | a0002 | c0003 | t0002 | g0094 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18943 | hp1 | a0002 | c0003 | t0002 | g0088 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18947 | hp1 | a0002 | c0003 | t0012 | g0108 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18947 | hp2 | a0001 | c0002 | t0022 | g0150 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18949 | hp1 | a0003 | c0006 | t0005 | g0075 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18970 | hp1 | a0002 | c0003 | t0012 | g0101 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18971 | hp2 | a0003 | c0006 | t0005 | g0083 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18981 | hp1 | a0002 | c0003 | t0019 | g0090 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19003 | hp2 | a0002 | c0003 | t0002 | g0096 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19006 | hp1 | a0002 | c0015 | t0002 | g0087 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19030 | hp1 | a0001 | c0004 | t0020 | g0020 | AFR | LWK | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19030 | hp2 | a0001 | c0004 | t0007 | g0126 | AFR | LWK | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | LWK | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19043 | hp2 | a0001 | c0005 | t0004 | g0134 | AFR | LWK | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19065 | hp2 | a0002 | c0003 | t0002 | g0089 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19068 | hp1 | a0002 | c0003 | t0011 | g0100 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19068 | hp2 | a0002 | c0003 | t0002 | g0107 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19072 | hp2 | a0002 | c0003 | t0002 | g0095 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19075 | hp1 | a0001 | c0002 | t0013 | g0180 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19075 | hp2 | a0003 | c0006 | t0005 | g0078 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19086 | hp2 | a0002 | c0003 | t0002 | g0098 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ASW | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ASW | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA20905 | hp1 | a0003 | c0006 | t0005 | g0086 | SAS | GIH | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0149 | SAS | GIH | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02109 | hp1 | a0001 | c0001 | t0014 | g0002 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03471 | hp1 | a0007 | c0012 | t0010 | g0046 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | MSL | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG06807 | hp1 | a0001 | c0004 | t0026 | g0186 | AFR | USA | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | USA | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA20300 | hp2 | a0001 | c0002 | t0025 | g0139 | AFR | USA | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | LWK | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0179 | REF | REF | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0162 | REF | REF | NNT_chr5_43598180_43712396 | NNT | chr5 | 43598180 | 43712396 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:43609275 | G | A | 1 | a0004 | 3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.80G>A | p.Arg27His | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/22 | 248/6421 | 80/3261 | 27/1086 | chr5 | 43609275 | |||
| chr5:43612917 | A | G | 1 | a0009 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.161A>G | p.Tyr54Cys | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/22 | 329/6421 | 161/3261 | 54/1086 | chr5 | 43612917 | |||
| chr5:43612944 | A | G | 1 | a0002 | 23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
missense_variant | MODERATE | c.188A>G | p.Lys63Arg | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/22 | 356/6421 | 188/3261 | 63/1086 | chr5 | 43612944 | |||
| chr5:43644216 | A | G | 1 | a0008 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.989A>G | p.Asn330Ser | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 8/22 | 1157/6421 | 989/3261 | 330/1086 | chr5 | 43644216 | |||
| chr5:43653141 | C | T | 2 | a0002 a0005 |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
missense_variant | MODERATE | c.1987C>T | p.Leu663Phe | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/22 | 2155/6421 | 1987/3261 | 663/1086 | chr5 | 43653141 | |||
| chr5:43656764 | C | T | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.2405C>T | p.Thr802Ile | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/22 | 2573/6421 | 2405/3261 | 802/1086 | chr5 | 43656764 | |||
| chr5:43675616 | C | T | 1 | a0007 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.2740C>T | p.Leu914Phe | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/22 | 2908/6421 | 2740/3261 | 914/1086 | chr5 | 43675616 | |||
| chr5:43700219 | A | G | 1 | a0003 | 6 | HG02683.hp2 HG04115.hp2 NA18949.hp1 others(3): Show |
missense_variant | MODERATE | c.2977A>G | p.Ile993Val | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/22 | 3145/6421 | 2977/3261 | 993/1086 | chr5 | 43700219 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:43609241 | C | T | 14 | a0001c0001 a0001c0004 a0001c0005 others(11): Show |
140 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(137): Show |
synonymous_variant | LOW | c.46C>T | p.Leu16Leu | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/22 | 214/6421 | 46/3261 | 16/1086 | chr5 | 43609241 | |||
| chr5:43651866 | T | C | 1 | a0003c0010 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.1845T>C | p.Ser615Ser | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/22 | 2013/6421 | 1845/3261 | 615/1086 | chr5 | 43651866 | |||
| chr5:43655922 | T | C | 4 | a0001c0004 a0001c0005 a0004c0009 others(1): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
synonymous_variant | LOW | c.2142T>C | p.Ala714Ala | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 15/22 | 2310/6421 | 2142/3261 | 714/1086 | chr5 | 43655922 | |||
| chr5:43659212 | C | G | 1 | a0002c0015 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.2496C>G | p.Pro832Pro | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/22 | 2664/6421 | 2496/3261 | 832/1086 | chr5 | 43659212 | |||
| chr5:43700140 | A | G | 3 | a0001c0005 a0001c0011 a0008c0014 |
7 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(4): Show |
synonymous_variant | LOW | c.2898A>G | p.Ala966Ala | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/22 | 3066/6421 | 2898/3261 | 966/1086 | chr5 | 43700140 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:43609170 | T | C | 3 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0017 |
23 | HG00597.hp1 HG00639.hp2 HG00741.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-26T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/22 | 26 | chr5 | 43609170 | ||||||
| chr5:43609173 | G | A | 1 | a0001c0004t0018 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/22 | 23 | chr5 | 43609173 | ||||||
| chr5:43704440 | C | G | 2 | a0001c0001t0017 a0001c0002t0008 |
6 | HG00741.hp2 HG01346.hp1 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*36C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 36 | chr5 | 43704440 | ||||||
| chr5:43704454 | G | A | 8 | a0001c0002t0002 a0001c0002t0013 a0002c0003t0002 others(5): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*50G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 50 | chr5 | 43704454 | ||||||
| chr5:43704489 | G | A | 1 | a0001c0004t0020 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 85 | chr5 | 43704489 | ||||||
| chr5:43704587 | T | TA | 8 | a0001c0002t0002 a0001c0002t0013 a0002c0003t0002 others(5): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*189dupA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 190 | INFO_REALIGN_3_PRIME | chr5 | 43704587 | |||||
| chr5:43704828 | GT | G | 11 | a0001c0002t0022 a0001c0004t0004 a0001c0004t0007 others(8): Show |
25 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*434delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 434 | INFO_REALIGN_3_PRIME | chr5 | 43704828 | |||||
| chr5:43704901 | G | A | 1 | a0001c0001t0014 | 2 | HG02109.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*497G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 497 | chr5 | 43704901 | ||||||
| chr5:43704903 | A | G | 1 | a0001c0001t0028 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 499 | chr5 | 43704903 | ||||||
| chr5:43705366 | A | AT | 1 | a0001c0001t0009 | 4 | HG00741.hp1 HG02602.hp1 HG02683.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*970dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 971 | INFO_REALIGN_3_PRIME | chr5 | 43705366 | |||||
| chr5:43705422 | A | G | 1 | a0001c0001t0027 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1018 | chr5 | 43705422 | ||||||
| chr5:43705689 | G | A | 8 | a0001c0002t0002 a0001c0002t0013 a0002c0003t0002 others(5): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1285G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1285 | chr5 | 43705689 | ||||||
| chr5:43705771 | A | ATG | 2 | a0001c0001t0015 a0001c0001t0028 |
3 | HG01175.hp2 HG02280.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1386_*1387dupTG | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1388 | INFO_REALIGN_3_PRIME | chr5 | 43705771 | |||||
| chr5:43705771 | A | ATGTG | 11 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0016 others(8): Show |
39 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1384_*1387dupTGTG | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1388 | INFO_REALIGN_3_PRIME | chr5 | 43705771 | |||||
| chr5:43705771 | A | ATGTGTG | 11 | a0001c0002t0013 a0001c0004t0004 a0001c0004t0007 others(8): Show |
25 | HG01109.hp1 HG01167.hp2 HG02074.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1382_*1387dupTGTG others(2): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1388 | INFO_REALIGN_3_PRIME | chr5 | 43705771 | |||||
| chr5:43705771 | A | G | 1 | a0002c0003t0019 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1367A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1367 | chr5 | 43705771 | ||||||
| chr5:43705790 | T | TGTGC | 1 | a0002c0003t0011 | 2 | HG02071.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1387_*1388insTGCG | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1388 | INFO_REALIGN_3_PRIME | chr5 | 43705790 | |||||
| chr5:43705873 | G | A | 1 | a0001c0005t0023 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1469G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1469 | chr5 | 43705873 | ||||||
| chr5:43705948 | T | C | 32 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(29): Show |
85 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1544T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1544 | chr5 | 43705948 | ||||||
| chr5:43706033 | A | G | 1 | a0001c0004t0026 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1629A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1629 | chr5 | 43706033 | ||||||
| chr5:43706252 | C | T | 8 | a0001c0002t0002 a0001c0002t0013 a0002c0003t0002 others(5): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1848C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1848 | chr5 | 43706252 | ||||||
| chr5:43706339 | C | T | 3 | a0001c0002t0010 a0004c0007t0010 a0007c0012t0010 |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1935C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1935 | chr5 | 43706339 | ||||||
| chr5:43706402 | A | G | 8 | a0001c0002t0002 a0001c0002t0013 a0002c0003t0002 others(5): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1998A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 1998 | chr5 | 43706402 | ||||||
| chr5:43706811 | T | C | 1 | a0001c0001t0016 | 2 | HG01243.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2407T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 2407 | chr5 | 43706811 | ||||||
| chr5:43707120 | T | TA | 17 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0016 others(14): Show |
49 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2727dupA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 2728 | INFO_REALIGN_3_PRIME | chr5 | 43707120 | |||||
| chr5:43707195 | A | T | 1 | a0001c0001t0024 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2791A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 2791 | chr5 | 43707195 | ||||||
| chr5:43707385 | A | G | 1 | a0002c0003t0012 | 2 | NA18947.hp1 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2981A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 22/22 | 2981 | chr5 | 43707385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:43603373 | T | C | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-54+79T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43603373 | |||||||
| chr5:43603601 | T | C | 1 | a0001c0002t0001g0006 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-54+307T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43603601 | |||||||
| chr5:43603839 | G | T | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-54+545G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43603839 | |||||||
| chr5:43604106 | C | G | 1 | a0001c0002t0001g0185 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-54+812C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43604106 | |||||||
| chr5:43604156 | T | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(78): Show |
82 | HG00597.hp1 HG00639.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.-54+862T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43604156 | |||||||
| chr5:43604164 | G | A | 1 | a0002c0015t0002g0087 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-54+870G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43604164 | |||||||
| chr5:43604316 | A | G | 1 | a0003c0006t0005g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-54+1022A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43604316 | |||||||
| chr5:43604395 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
140 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.-54+1101T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43604395 | |||||||
| chr5:43604415 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-54+1121C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43604415 | |||||||
| chr5:43604996 | G | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
13 | HG01175.hp2 HG01255.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.-54+1702G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43604996 | |||||||
| chr5:43605143 | C | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-54+1849C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605143 | |||||||
| chr5:43605160 | C | G | 1 | a0001c0002t0001g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-54+1866C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605160 | |||||||
| chr5:43605243 | G | A | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-54+1949G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605243 | |||||||
| chr5:43605288 | G | A | 8 | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+1994G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605288 | |||||||
| chr5:43605312 | C | T | 1 | a0001c0002t0010g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-54+2018C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605312 | |||||||
| chr5:43605348 | C | T | 8 | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+2054C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605348 | |||||||
| chr5:43605353 | A | G | 1 | a0001c0001t0006g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54+2059A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605353 | |||||||
| chr5:43605492 | C | T | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-54+2198C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605492 | |||||||
| chr5:43605522 | C | CA | 62 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
62 | HG00544.hp1 HG00639.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.-54+2257dupA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43605522 | ||||||
| chr5:43605522 | C | CAA | 45 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(42): Show |
47 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.-54+2256_-54+2257d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43605522 | ||||||
| chr5:43605522 | C | CAAA | 5 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0024 others(2): Show |
5 | HG01109.hp2 HG01175.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+2255_-54+2257d others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43605522 | ||||||
| chr5:43605522 | C | CAAAAAAA others(3): Show |
1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-54+2248_-54+2257d others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43605522 | ||||||
| chr5:43605522 | CA | C | 5 | a0001c0001t0006g0110 a0001c0001t0016g0111 a0001c0002t0001g0181 others(2): Show |
5 | HG01069.hp2 HG01243.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+2257delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43605522 | ||||||
| chr5:43605522 | CAA | C | 6 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+2256_-54+2257d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43605522 | ||||||
| chr5:43605852 | A | G | 1 | a0001c0004t0021g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-54+2558A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605852 | |||||||
| chr5:43605924 | A | G | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-54+2630A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605924 | |||||||
| chr5:43605935 | T | A | 2 | a0001c0004t0004g0118 a0001c0004t0004g0123 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-54+2641T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43605935 | |||||||
| chr5:43606130 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-54+2836A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43606130 | |||||||
| chr5:43606168 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0006g0072 |
2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-54+2874G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43606168 | |||||||
| chr5:43606312 | C | T | 2 | a0001c0001t0006g0116 a0001c0001t0006g0117 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-53-2831C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43606312 | |||||||
| chr5:43606517 | A | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0069 others(2): Show |
5 | HG02809.hp1 HG03195.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-2626A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43606517 | |||||||
| chr5:43606661 | C | T | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-53-2482C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43606661 | |||||||
| chr5:43606726 | ACT | A | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-53-2414_-53-2413d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43606726 | ||||||
| chr5:43606801 | C | G | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-53-2342C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43606801 | |||||||
| chr5:43606919 | A | G | 1 | a0003c0006t0005g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-53-2224A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43606919 | |||||||
| chr5:43606958 | G | A | 7 | a0001c0005t0004g0133 a0001c0005t0004g0134 a0001c0005t0004g0135 others(4): Show |
7 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-2185G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43606958 | |||||||
| chr5:43606995 | GT | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(72): Show |
76 | HG00597.hp1 HG00639.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.-53-2138delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43606995 | ||||||
| chr5:43607029 | C | CCAGGCTG others(1): Show |
4 | a0001c0001t0001g0073 a0001c0001t0006g0072 a0001c0004t0007g0081 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-2097_-53-2090d others(10): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43607029 | ||||||
| chr5:43607078 | A | G | 1 | a0001c0001t0003g0079 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-53-2065A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607078 | |||||||
| chr5:43607085 | C | G | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-53-2058C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607085 | |||||||
| chr5:43607150 | C | T | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-53-1993C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607150 | |||||||
| chr5:43607215 | G | A | 2 | a0001c0001t0009g0021 a0001c0001t0009g0025 |
2 | HG02602.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-53-1928G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607215 | |||||||
| chr5:43607315 | T | C | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-53-1828T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607315 | |||||||
| chr5:43607608 | C | A | 1 | a0001c0002t0001g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-53-1535C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607608 | |||||||
| chr5:43607704 | G | A | 1 | a0001c0001t0006g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-53-1439G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607704 | |||||||
| chr5:43607798 | A | T | 2 | a0001c0001t0003g0024 a0001c0001t0003g0048 |
2 | HG01074.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-53-1345A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607798 | |||||||
| chr5:43607839 | C | T | 2 | a0001c0001t0006g0116 a0001c0001t0006g0117 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-53-1304C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607839 | |||||||
| chr5:43607882 | G | A | 1 | a0001c0002t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-53-1261G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607882 | |||||||
| chr5:43607913 | C | G | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-53-1230C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607913 | |||||||
| chr5:43607937 | C | CT | 126 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(123): Show |
128 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.-53-1195dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43607937 | ||||||
| chr5:43607947 | T | C | 1 | a0001c0001t0006g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-53-1196T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607947 | |||||||
| chr5:43607953 | C | T | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-53-1190C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43607953 | |||||||
| chr5:43608029 | CA | C | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-53-1112delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | 43608029 | ||||||
| chr5:43608182 | G | C | 1 | a0001c0002t0001g0006 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-53-961G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608182 | |||||||
| chr5:43608221 | G | A | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-53-922G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608221 | |||||||
| chr5:43608276 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-53-867G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608276 | |||||||
| chr5:43608309 | C | T | 2 | a0001c0001t0006g0080 a0001c0004t0020g0020 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-53-834C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608309 | |||||||
| chr5:43608453 | T | C | 2 | a0001c0001t0003g0024 a0001c0001t0003g0048 |
2 | HG01074.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-53-690T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608453 | |||||||
| chr5:43608541 | G | A | 1 | a0001c0005t0004g0133 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-53-602G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608541 | |||||||
| chr5:43608582 | A | G | 1 | a0001c0004t0004g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-53-561A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608582 | |||||||
| chr5:43608742 | T | C | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-53-401T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608742 | |||||||
| chr5:43608750 | T | C | 1 | a0001c0002t0001g0140 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-53-393T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608750 | |||||||
| chr5:43608911 | A | C | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-53-232A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 1/21 | chr5 | 43608911 | |||||||
| chr5:43609818 | A | T | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.151+472A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43609818 | |||||||
| chr5:43610153 | G | A | 13 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(10): Show |
13 | HG01109.hp1 HG01891.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+807G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43610153 | |||||||
| chr5:43610201 | CT | C | 49 | a0001c0001t0001g0073 a0001c0001t0006g0072 a0001c0001t0006g0080 others(46): Show |
49 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.151+877delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 43610201 | ||||||
| chr5:43610201 | CTT | C | 71 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(68): Show |
73 | HG00597.hp1 HG00741.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.151+876_151+877del others(2): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 43610201 | ||||||
| chr5:43610201 | CTTT | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0003g0048 others(2): Show |
5 | HG00639.hp2 HG01074.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+875_151+877del others(3): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 43610201 | ||||||
| chr5:43610249 | G | C | 8 | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+903G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43610249 | |||||||
| chr5:43610288 | C | T | 1 | a0004c0007t0010g0005 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.151+942C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43610288 | |||||||
| chr5:43610299 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
140 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.151+953T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43610299 | |||||||
| chr5:43610330 | G | T | 4 | a0001c0001t0001g0073 a0001c0001t0006g0072 a0001c0004t0007g0081 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+984G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43610330 | |||||||
| chr5:43610350 | C | T | 1 | a0002c0003t0002g0107 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.151+1004C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43610350 | |||||||
| chr5:43610586 | G | C | 139 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
141 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.151+1240G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43610586 | |||||||
| chr5:43611114 | CTT | C | 3 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0122 |
3 | HG02735.hp1 HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.151+1772_151+1773d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 43611114 | ||||||
| chr5:43611447 | A | G | 1 | a0001c0002t0001g0143 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.152-1461A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43611447 | |||||||
| chr5:43611579 | C | A | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152-1329C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43611579 | |||||||
| chr5:43611596 | C | T | 1 | a0002c0015t0002g0087 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.152-1312C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43611596 | |||||||
| chr5:43611844 | A | C | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.152-1064A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43611844 | |||||||
| chr5:43611859 | G | T | 7 | a0001c0001t0006g0110 a0001c0001t0006g0114 a0001c0001t0006g0115 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-1049G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43611859 | |||||||
| chr5:43612093 | A | G | 7 | a0002c0003t0002g0091 a0002c0003t0002g0092 a0002c0003t0002g0104 others(4): Show |
7 | HG01069.hp1 HG01070.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-815A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43612093 | |||||||
| chr5:43612178 | A | G | 1 | a0001c0001t0003g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.152-730A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43612178 | |||||||
| chr5:43612266 | G | A | 1 | a0008c0014t0004g0119 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.152-642G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43612266 | |||||||
| chr5:43612279 | G | T | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152-629G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43612279 | |||||||
| chr5:43612339 | T | A | 77 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
78 | HG00597.hp1 HG00639.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.152-569T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43612339 | |||||||
| chr5:43612526 | A | T | 26 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.152-382A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43612526 | |||||||
| chr5:43612880 | TA | T | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.152-27delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43612880 | |||||||
| chr5:43612882 | T | TA | 81 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(78): Show |
82 | HG00597.hp1 HG00639.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.152-26_152-25insA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43612882 | |||||||
| chr5:43612883 | T | A | 12 | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0114 others(9): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-25T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 2/21 | chr5 | 43612883 | |||||||
| chr5:43613197 | A | G | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.381+60A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43613197 | |||||||
| chr5:43613230 | C | A | 1 | a0001c0001t0027g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.381+93C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43613230 | |||||||
| chr5:43613417 | T | G | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.381+280T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43613417 | |||||||
| chr5:43613558 | G | A | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 |
3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.381+421G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43613558 | |||||||
| chr5:43613662 | C | A | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.381+525C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43613662 | |||||||
| chr5:43613710 | A | T | 3 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0122 |
3 | HG02735.hp1 HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.381+573A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43613710 | |||||||
| chr5:43613736 | T | C | 2 | a0001c0001t0005g0027 a0001c0001t0005g0056 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.381+599T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43613736 | |||||||
| chr5:43613883 | CA | C | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.381+747delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43613883 | |||||||
| chr5:43614068 | C | T | 1 | a0001c0002t0008g0178 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.381+931C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614068 | |||||||
| chr5:43614074 | G | A | 1 | a0001c0002t0001g0006 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.381+937G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614074 | |||||||
| chr5:43614487 | A | G | 1 | a0001c0002t0001g0177 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.381+1350A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614487 | |||||||
| chr5:43614821 | A | G | 2 | a0001c0004t0004g0130 a0001c0004t0004g0131 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.382-1027A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614821 | |||||||
| chr5:43614857 | G | T | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.382-991G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614857 | |||||||
| chr5:43614866 | A | G | 139 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
141 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.382-982A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614866 | |||||||
| chr5:43614873 | C | T | 1 | a0001c0001t0006g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.382-975C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614873 | |||||||
| chr5:43614876 | G | A | 3 | a0001c0001t0005g0028 a0001c0001t0005g0054 a0001c0001t0005g0057 |
3 | HG02922.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.382-972G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614876 | |||||||
| chr5:43614883 | A | G | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.382-965A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614883 | |||||||
| chr5:43614909 | G | A | 73 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
74 | HG00597.hp1 HG00639.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.382-939G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614909 | |||||||
| chr5:43614934 | G | A | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.382-914G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43614934 | |||||||
| chr5:43615150 | CA | C | 27 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(24): Show |
27 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.382-689delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr5 | 43615150 | ||||||
| chr5:43615494 | A | G | 1 | a0001c0002t0001g0176 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.382-354A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43615494 | |||||||
| chr5:43615706 | G | A | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-142G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 3/21 | chr5 | 43615706 | |||||||
| chr5:43616544 | A | G | 1 | a0001c0001t0005g0067 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.599+479A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43616544 | |||||||
| chr5:43616547 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.599+482G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43616547 | |||||||
| chr5:43616600 | G | T | 49 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(46): Show |
49 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.599+535G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43616600 | |||||||
| chr5:43616658 | A | C | 27 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(24): Show |
27 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.599+593A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43616658 | |||||||
| chr5:43616774 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0005g0011 a0001c0001t0024g0018 |
3 | HG01361.hp2 HG01516.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.599+709A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43616774 | |||||||
| chr5:43617018 | G | A | 22 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(19): Show |
22 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.599+953G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617018 | |||||||
| chr5:43617167 | A | G | 4 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+1102A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617167 | |||||||
| chr5:43617221 | A | C | 1 | a0002c0003t0002g0107 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.599+1156A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617221 | |||||||
| chr5:43617236 | G | A | 5 | a0001c0001t0003g0051 a0004c0007t0010g0004 a0004c0007t0010g0005 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.599+1171G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617236 | |||||||
| chr5:43617311 | G | A | 65 | a0001c0001t0001g0073 a0001c0001t0006g0072 a0001c0001t0006g0080 others(62): Show |
66 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.599+1246G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617311 | |||||||
| chr5:43617366 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.599+1301T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617366 | |||||||
| chr5:43617545 | T | C | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.599+1480T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617545 | |||||||
| chr5:43617809 | A | G | 1 | a0001c0004t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.600-1223A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617809 | |||||||
| chr5:43617988 | G | A | 14 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0029 others(11): Show |
14 | HG01361.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.600-1044G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617988 | |||||||
| chr5:43617999 | A | G | 1 | a0001c0001t0028g0017 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.600-1033A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43617999 | |||||||
| chr5:43618061 | A | T | 2 | a0001c0001t0001g0073 a0001c0001t0006g0072 |
2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.600-971A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618061 | |||||||
| chr5:43618217 | C | T | 4 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.600-815C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618217 | |||||||
| chr5:43618254 | C | T | 3 | a0001c0001t0005g0028 a0001c0001t0005g0054 a0001c0001t0005g0057 |
3 | HG02922.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.600-778C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618254 | |||||||
| chr5:43618446 | C | T | 1 | a0001c0001t0006g0080 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.600-586C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618446 | |||||||
| chr5:43618461 | A | G | 15 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0094 others(12): Show |
15 | HG00544.hp1 HG02071.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.600-571A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618461 | |||||||
| chr5:43618488 | A | T | 1 | a0001c0002t0001g0175 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.600-544A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618488 | |||||||
| chr5:43618515 | C | T | 1 | a0005c0008t0013g0174 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.600-517C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618515 | |||||||
| chr5:43618612 | T | C | 1 | a0001c0005t0004g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.600-420T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618612 | |||||||
| chr5:43618615 | T | C | 1 | a0001c0004t0007g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.600-417T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618615 | |||||||
| chr5:43618633 | C | A | 10 | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0114 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.600-399C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | chr5 | 43618633 | |||||||
| chr5:43618999 | A | ATTAT | 7 | a0001c0001t0001g0073 a0001c0001t0006g0072 a0004c0007t0010g0004 others(4): Show |
7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.600-10_600-7dupATT others(1): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 43618999 | ||||||
| chr5:43619154 | C | G | 1 | a0003c0006t0005g0078 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.687+35C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619154 | |||||||
| chr5:43619239 | G | A | 1 | a0001c0002t0001g0006 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.687+120G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619239 | |||||||
| chr5:43619257 | C | T | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.687+138C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619257 | |||||||
| chr5:43619286 | G | T | 22 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(19): Show |
22 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.687+167G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619286 | |||||||
| chr5:43619287 | C | T | 22 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(19): Show |
22 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.687+168C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619287 | |||||||
| chr5:43619412 | T | A | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.687+293T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619412 | |||||||
| chr5:43619413 | A | T | 27 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(24): Show |
27 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.687+294A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619413 | |||||||
| chr5:43619444 | T | A | 3 | a0001c0004t0004g0129 a0001c0004t0004g0130 a0001c0004t0004g0131 |
3 | HG03130.hp2 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.687+325T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619444 | |||||||
| chr5:43619489 | T | C | 2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.687+370T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619489 | |||||||
| chr5:43619514 | C | T | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.687+395C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619514 | |||||||
| chr5:43619594 | T | C | 1 | a0001c0001t0005g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.687+475T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619594 | |||||||
| chr5:43619759 | T | C | 11 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0094 others(8): Show |
11 | HG02071.hp1 HG02165.hp2 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.687+640T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619759 | |||||||
| chr5:43619859 | A | C | 65 | a0001c0001t0001g0073 a0001c0001t0006g0072 a0001c0001t0006g0080 others(62): Show |
66 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.687+740A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619859 | |||||||
| chr5:43619946 | G | T | 4 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+827G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43619946 | |||||||
| chr5:43620242 | C | T | 15 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0029 others(12): Show |
15 | HG01361.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.687+1123C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620242 | |||||||
| chr5:43620264 | G | T | 1 | a0001c0002t0001g0176 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.687+1145G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620264 | |||||||
| chr5:43620365 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.687+1246G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620365 | |||||||
| chr5:43620380 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01175.hp2 HG01255.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.687+1261C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620380 | |||||||
| chr5:43620479 | C | T | 2 | a0001c0001t0005g0067 a0009c0016t0005g0045 |
2 | HG01169.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.687+1360C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620479 | |||||||
| chr5:43620480 | G | A | 49 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(46): Show |
49 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.687+1361G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620480 | |||||||
| chr5:43620584 | G | GAAAAAAA others(316): Show |
1 | a0001c0001t0006g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.687+1480_687+1481i others(325): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 43620584 | ||||||
| chr5:43620668 | T | G | 4 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1549T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620668 | |||||||
| chr5:43620722 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.687+1603C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620722 | |||||||
| chr5:43620933 | A | C | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.687+1814A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620933 | |||||||
| chr5:43620959 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.687+1840C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43620959 | |||||||
| chr5:43621007 | A | G | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.687+1888A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621007 | |||||||
| chr5:43621077 | G | A | 4 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0004c0009t0007g0003 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1958G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621077 | |||||||
| chr5:43621162 | G | A | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.687+2043G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621162 | |||||||
| chr5:43621184 | C | T | 13 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0006g0110 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.687+2065C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621184 | |||||||
| chr5:43621193 | G | T | 1 | a0003c0006t0005g0044 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.687+2074G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621193 | |||||||
| chr5:43621311 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0006g0072 |
2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.687+2192T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621311 | |||||||
| chr5:43621539 | T | TTTA | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.687+2435_687+2437d others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 43621539 | ||||||
| chr5:43621560 | G | A | 1 | a0001c0001t0006g0080 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.687+2441G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621560 | |||||||
| chr5:43621711 | T | C | 1 | a0001c0002t0001g0141 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.688-2321T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621711 | |||||||
| chr5:43621765 | G | A | 2 | a0001c0004t0004g0118 a0001c0004t0004g0123 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.688-2267G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621765 | |||||||
| chr5:43621773 | A | G | 13 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0006g0110 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.688-2259A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43621773 | |||||||
| chr5:43622114 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.688-1918T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43622114 | |||||||
| chr5:43622166 | G | C | 13 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0006g0080 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.688-1866G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43622166 | |||||||
| chr5:43622190 | G | T | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02809.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.688-1842G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43622190 | |||||||
| chr5:43622342 | A | C | 65 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0006g0080 others(62): Show |
66 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.688-1690A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43622342 | |||||||
| chr5:43622442 | T | C | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.688-1590T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43622442 | |||||||
| chr5:43622621 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.688-1411C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43622621 | |||||||
| chr5:43622839 | G | T | 1 | a0001c0002t0001g0173 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.688-1193G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43622839 | |||||||
| chr5:43622865 | G | GT | 7 | a0001c0001t0001g0033 a0001c0001t0006g0117 a0001c0001t0006g0138 others(4): Show |
7 | HG00597.hp2 HG01169.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-1152dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 43622865 | ||||||
| chr5:43622865 | G | T | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02809.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.688-1167G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43622865 | |||||||
| chr5:43622865 | GT | G | 22 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(19): Show |
22 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.688-1152delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 43622865 | ||||||
| chr5:43623127 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.688-905C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43623127 | |||||||
| chr5:43623351 | A | ATGT | 51 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(48): Show |
51 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.688-679_688-677dup others(3): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 43623351 | ||||||
| chr5:43623360 | C | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.688-672C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43623360 | |||||||
| chr5:43623410 | T | C | 26 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.688-622T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43623410 | |||||||
| chr5:43623492 | G | T | 2 | a0001c0004t0004g0130 a0001c0004t0004g0131 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.688-540G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43623492 | |||||||
| chr5:43623563 | G | C | 25 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(22): Show |
25 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.688-469G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43623563 | |||||||
| chr5:43623689 | C | A | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.688-343C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43623689 | |||||||
| chr5:43623733 | A | G | 1 | a0003c0006t0005g0044 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.688-299A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43623733 | |||||||
| chr5:43623924 | G | A | 10 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.688-108G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 5/21 | chr5 | 43623924 | |||||||
| chr5:43624399 | A | G | 25 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(22): Show |
25 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.776+279A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43624399 | |||||||
| chr5:43624589 | T | C | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.776+469T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43624589 | |||||||
| chr5:43624657 | T | A | 1 | a0001c0001t0003g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.776+537T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43624657 | |||||||
| chr5:43624706 | T | G | 3 | a0001c0004t0007g0126 a0001c0004t0018g0127 a0004c0009t0007g0003 |
3 | HG02897.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.776+586T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43624706 | |||||||
| chr5:43624784 | C | T | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.776+664C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43624784 | |||||||
| chr5:43625128 | T | G | 1 | a0007c0012t0010g0046 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.776+1008T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43625128 | |||||||
| chr5:43625359 | A | G | 1 | a0003c0006t0005g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.776+1239A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43625359 | |||||||
| chr5:43625612 | A | C | 15 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0094 others(12): Show |
15 | HG00544.hp1 HG02071.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.776+1492A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43625612 | |||||||
| chr5:43625622 | C | G | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02809.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.776+1502C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43625622 | |||||||
| chr5:43625687 | A | G | 10 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.776+1567A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43625687 | |||||||
| chr5:43625725 | T | C | 66 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0006g0072 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.776+1605T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43625725 | |||||||
| chr5:43625727 | G | A | 25 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(22): Show |
25 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.776+1607G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43625727 | |||||||
| chr5:43625804 | G | A | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02809.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.776+1684G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43625804 | |||||||
| chr5:43625850 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.776+1730G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43625850 | |||||||
| chr5:43626009 | A | G | 1 | a0001c0001t0003g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.776+1889A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43626009 | |||||||
| chr5:43626148 | C | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG06807.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.776+2028C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43626148 | |||||||
| chr5:43626227 | A | G | 12 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(9): Show |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.777-1973A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43626227 | |||||||
| chr5:43626232 | G | A | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.777-1968G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43626232 | |||||||
| chr5:43626264 | A | C | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.777-1936A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43626264 | |||||||
| chr5:43626517 | A | G | 2 | a0001c0004t0004g0130 a0001c0004t0004g0131 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.777-1683A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43626517 | |||||||
| chr5:43626690 | C | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.777-1510C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43626690 | |||||||
| chr5:43626806 | A | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.777-1394A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43626806 | |||||||
| chr5:43626854 | C | T | 1 | a0001c0002t0001g0172 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.777-1346C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43626854 | |||||||
| chr5:43626869 | G | GTA | 8 | a0001c0004t0004g0128 a0001c0004t0007g0081 a0001c0004t0007g0082 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.777-1322_777-1321d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr5 | 43626869 | ||||||
| chr5:43627067 | T | C | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.777-1133T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627067 | |||||||
| chr5:43627097 | T | C | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02809.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.777-1103T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627097 | |||||||
| chr5:43627111 | T | G | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.777-1089T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627111 | |||||||
| chr5:43627189 | C | T | 6 | a0001c0002t0001g0169 a0001c0002t0008g0167 a0001c0002t0008g0168 others(3): Show |
6 | HG00741.hp2 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.777-1011C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627189 | |||||||
| chr5:43627328 | C | T | 1 | a0003c0006t0005g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.777-872C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627328 | |||||||
| chr5:43627346 | T | C | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.777-854T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627346 | |||||||
| chr5:43627584 | A | G | 1 | a0001c0001t0003g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.777-616A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627584 | |||||||
| chr5:43627666 | T | C | 46 | a0001c0004t0004g0118 a0001c0004t0004g0123 a0001c0004t0004g0128 others(43): Show |
46 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.777-534T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627666 | |||||||
| chr5:43627763 | A | G | 6 | a0001c0005t0004g0133 a0001c0005t0004g0134 a0001c0005t0004g0135 others(3): Show |
6 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777-437A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627763 | |||||||
| chr5:43627864 | A | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.777-336A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627864 | |||||||
| chr5:43627950 | T | G | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.777-250T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43627950 | |||||||
| chr5:43628149 | C | G | 1 | a0001c0001t0006g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.777-51C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 6/21 | chr5 | 43628149 | |||||||
| chr5:43628439 | T | A | 26 | a0001c0001t0006g0138 a0001c0004t0020g0020 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.964+52T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43628439 | |||||||
| chr5:43628535 | T | C | 4 | a0001c0011t0004g0124 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+148T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43628535 | |||||||
| chr5:43628567 | C | T | 65 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(62): Show |
66 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.964+180C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43628567 | |||||||
| chr5:43628594 | T | A | 2 | a0001c0001t0015g0008 a0001c0001t0028g0017 |
2 | HG01175.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.964+207T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43628594 | |||||||
| chr5:43628642 | G | A | 2 | a0001c0004t0004g0118 a0001c0004t0004g0123 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.964+255G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43628642 | |||||||
| chr5:43628689 | C | A | 1 | a0001c0004t0004g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.964+302C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43628689 | |||||||
| chr5:43628690 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.964+303G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43628690 | |||||||
| chr5:43628834 | G | A | 2 | a0001c0001t0005g0011 a0001c0001t0024g0018 |
2 | HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.964+447G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43628834 | |||||||
| chr5:43628924 | G | T | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.964+537G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43628924 | |||||||
| chr5:43628935 | G | GT | 53 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(50): Show |
53 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.964+561dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43628935 | ||||||
| chr5:43629145 | C | T | 5 | a0001c0002t0001g0169 a0001c0002t0008g0168 a0001c0002t0008g0170 others(2): Show |
5 | HG00741.hp2 HG01346.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+758C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629145 | |||||||
| chr5:43629154 | C | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+767C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629154 | |||||||
| chr5:43629154 | C | G | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964+767C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629154 | |||||||
| chr5:43629156 | C | G | 1 | a0001c0002t0001g0166 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.964+769C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629156 | |||||||
| chr5:43629248 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.964+861C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629248 | |||||||
| chr5:43629283 | G | C | 1 | a0003c0006t0005g0078 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.964+896G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629283 | |||||||
| chr5:43629372 | C | T | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+985C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629372 | |||||||
| chr5:43629397 | G | T | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.964+1010G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629397 | |||||||
| chr5:43629664 | C | T | 1 | a0001c0001t0005g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.964+1277C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629664 | |||||||
| chr5:43629688 | A | G | 2 | a0002c0003t0002g0099 a0002c0003t0011g0100 |
2 | HG02165.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.964+1301A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43629688 | |||||||
| chr5:43630102 | T | C | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+1715T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43630102 | |||||||
| chr5:43630241 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.964+1854A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43630241 | |||||||
| chr5:43630383 | A | G | 23 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(20): Show |
23 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.964+1996A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43630383 | |||||||
| chr5:43630423 | T | C | 2 | a0001c0001t0003g0022 a0001c0001t0003g0035 |
2 | HG01175.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.964+2036T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43630423 | |||||||
| chr5:43630640 | A | G | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+2253A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43630640 | |||||||
| chr5:43630720 | C | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+2333C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43630720 | |||||||
| chr5:43630784 | C | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+2397C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43630784 | |||||||
| chr5:43630901 | G | A | 28 | a0001c0011t0004g0124 a0002c0003t0002g0088 a0002c0003t0002g0089 others(25): Show |
28 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.964+2514G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43630901 | |||||||
| chr5:43631012 | G | T | 17 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0093 others(14): Show |
17 | HG00544.hp1 HG02071.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.964+2625G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43631012 | |||||||
| chr5:43631040 | T | C | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.964+2653T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43631040 | |||||||
| chr5:43631288 | T | A | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+2901T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43631288 | |||||||
| chr5:43631469 | C | T | 3 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0122 |
3 | HG02735.hp1 HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.964+3082C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43631469 | |||||||
| chr5:43631581 | T | G | 4 | a0001c0011t0004g0124 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3194T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43631581 | |||||||
| chr5:43631686 | A | G | 1 | a0001c0001t0027g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.964+3299A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43631686 | |||||||
| chr5:43631969 | G | GA | 21 | a0001c0001t0003g0051 a0001c0001t0006g0138 a0001c0001t0014g0002 others(18): Show |
22 | HG00597.hp2 HG01109.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.964+3601dupA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43631969 | ||||||
| chr5:43631969 | G | GAA | 7 | a0001c0002t0001g0142 a0001c0005t0004g0133 a0001c0005t0004g0134 others(4): Show |
7 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+3600_964+3601d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43631969 | ||||||
| chr5:43631969 | G | GAAA | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.964+3599_964+3601d others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43631969 | ||||||
| chr5:43631969 | GA | G | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(4): Show |
7 | HG02809.hp2 HG02970.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+3601delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43631969 | ||||||
| chr5:43631997 | A | G | 2 | a0004c0007t0010g0005 a0007c0012t0010g0046 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.964+3610A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43631997 | |||||||
| chr5:43632322 | C | CT | 2 | a0002c0003t0002g0107 a0002c0003t0019g0090 |
2 | NA18981.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.964+3936dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43632322 | ||||||
| chr5:43632323 | T | G | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+3936T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43632323 | |||||||
| chr5:43632418 | G | A | 1 | a0001c0004t0007g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.964+4031G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43632418 | |||||||
| chr5:43632421 | G | A | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+4034G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43632421 | |||||||
| chr5:43632651 | C | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+4264C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43632651 | |||||||
| chr5:43632788 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.964+4401G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43632788 | |||||||
| chr5:43632830 | A | T | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.964+4443A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43632830 | |||||||
| chr5:43632942 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+4555G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43632942 | |||||||
| chr5:43633004 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0065 |
2 | HG03453.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.964+4617A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43633004 | |||||||
| chr5:43633207 | C | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+4820C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43633207 | |||||||
| chr5:43633360 | A | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+4973A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43633360 | |||||||
| chr5:43633495 | C | T | 3 | a0001c0004t0007g0126 a0001c0004t0018g0127 a0004c0009t0007g0003 |
3 | HG02897.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.964+5108C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43633495 | |||||||
| chr5:43633624 | A | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+5237A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43633624 | |||||||
| chr5:43633767 | C | A | 1 | a0001c0002t0001g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.964+5380C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43633767 | |||||||
| chr5:43633821 | A | G | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.964+5434A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43633821 | |||||||
| chr5:43633882 | A | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+5495A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43633882 | |||||||
| chr5:43633892 | AGTCTGC | A | 5 | a0001c0005t0004g0133 a0001c0005t0004g0134 a0001c0005t0004g0135 others(2): Show |
5 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+5506_964+5511d others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43633892 | |||||||
| chr5:43634055 | C | T | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.964+5668C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43634055 | |||||||
| chr5:43634208 | T | A | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.964+5821T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43634208 | |||||||
| chr5:43634301 | G | A | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.964+5914G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43634301 | |||||||
| chr5:43634566 | C | T | 1 | a0001c0002t0001g0165 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.964+6179C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43634566 | |||||||
| chr5:43635054 | A | G | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.964+6667A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43635054 | |||||||
| chr5:43635135 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.964+6748A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43635135 | |||||||
| chr5:43635421 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+7034T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43635421 | |||||||
| chr5:43635547 | A | G | 1 | a0001c0002t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.964+7160A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43635547 | |||||||
| chr5:43635572 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.964+7185G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43635572 | |||||||
| chr5:43635580 | A | G | 3 | a0001c0001t0006g0080 a0001c0001t0006g0116 a0001c0001t0006g0117 |
3 | HG01167.hp1 HG01169.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.964+7193A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43635580 | |||||||
| chr5:43635730 | T | C | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7343T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43635730 | |||||||
| chr5:43635993 | G | A | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+7606G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43635993 | |||||||
| chr5:43636081 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964+7694A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43636081 | |||||||
| chr5:43636228 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.964+7841T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43636228 | |||||||
| chr5:43636244 | C | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.964+7857C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43636244 | |||||||
| chr5:43636336 | G | C | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7856G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43636336 | |||||||
| chr5:43636418 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.965-7774A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43636418 | |||||||
| chr5:43636783 | AT | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.965-7405delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43636783 | ||||||
| chr5:43637131 | G | A | 66 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.965-7061G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43637131 | |||||||
| chr5:43637277 | C | A | 1 | a0001c0002t0022g0150 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.965-6915C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43637277 | |||||||
| chr5:43637354 | C | A | 6 | a0001c0004t0007g0081 a0001c0004t0007g0082 a0001c0004t0007g0125 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.965-6838C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43637354 | |||||||
| chr5:43637355 | C | G | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.965-6837C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43637355 | |||||||
| chr5:43637367 | T | C | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-6825T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43637367 | |||||||
| chr5:43637370 | G | C | 1 | a0001c0002t0001g0151 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.965-6822G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43637370 | |||||||
| chr5:43637601 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.965-6591T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43637601 | |||||||
| chr5:43637954 | C | T | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.965-6238C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43637954 | |||||||
| chr5:43638043 | C | T | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.965-6149C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43638043 | |||||||
| chr5:43638089 | T | C | 1 | a0004c0007t0010g0005 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.965-6103T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43638089 | |||||||
| chr5:43638111 | C | G | 1 | a0001c0002t0001g0151 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.965-6081C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43638111 | |||||||
| chr5:43638462 | G | A | 1 | a0001c0002t0001g0165 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.965-5730G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43638462 | |||||||
| chr5:43638488 | C | T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.965-5704C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43638488 | |||||||
| chr5:43638633 | A | G | 1 | a0001c0002t0002g0163 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.965-5559A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43638633 | |||||||
| chr5:43638664 | G | GT | 34 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0050 others(31): Show |
35 | HG00597.hp1 HG00741.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.965-5513dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43638664 | ||||||
| chr5:43638683 | C | A | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-5509C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43638683 | |||||||
| chr5:43638949 | G | C | 3 | a0001c0002t0010g0183 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02970.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.965-5243G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43638949 | |||||||
| chr5:43639312 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.965-4880C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43639312 | |||||||
| chr5:43639538 | A | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.965-4654A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43639538 | |||||||
| chr5:43639542 | A | G | 1 | a0001c0004t0007g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.965-4650A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43639542 | |||||||
| chr5:43639590 | C | G | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.965-4602C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43639590 | |||||||
| chr5:43639649 | A | C | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4543A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43639649 | |||||||
| chr5:43639719 | C | A | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-4473C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43639719 | |||||||
| chr5:43639921 | A | AT | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.965-4261dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43639921 | ||||||
| chr5:43639936 | G | A | 29 | a0001c0002t0010g0183 a0001c0004t0004g0118 a0001c0004t0004g0120 others(26): Show |
29 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.965-4256G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43639936 | |||||||
| chr5:43639969 | G | A | 2 | a0001c0004t0004g0118 a0001c0004t0004g0123 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.965-4223G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43639969 | |||||||
| chr5:43640631 | T | A | 1 | a0001c0004t0004g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.965-3561T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43640631 | |||||||
| chr5:43640632 | C | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.965-3560C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43640632 | |||||||
| chr5:43640647 | TAA | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.965-3544_965-3543d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43640647 | |||||||
| chr5:43640840 | T | C | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-3352T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43640840 | |||||||
| chr5:43641049 | T | G | 29 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0002c0003t0002g0088 others(26): Show |
29 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.965-3143T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43641049 | |||||||
| chr5:43641386 | C | T | 1 | a0005c0008t0013g0174 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.965-2806C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43641386 | |||||||
| chr5:43641483 | C | T | 7 | a0002c0003t0002g0091 a0002c0003t0002g0092 a0002c0003t0002g0104 others(4): Show |
7 | HG01069.hp1 HG01070.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-2709C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43641483 | |||||||
| chr5:43641490 | C | A | 6 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0122 others(3): Show |
6 | HG02735.hp1 HG03130.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.965-2702C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43641490 | |||||||
| chr5:43641748 | C | T | 1 | a0001c0002t0001g0166 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.965-2444C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43641748 | |||||||
| chr5:43641792 | G | A | 1 | a0001c0002t0001g0172 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.965-2400G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43641792 | |||||||
| chr5:43641933 | G | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.965-2259G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43641933 | |||||||
| chr5:43641997 | C | T | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2195C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43641997 | |||||||
| chr5:43642079 | G | C | 1 | a0001c0001t0015g0008 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.965-2113G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43642079 | |||||||
| chr5:43642267 | G | A | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1925G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43642267 | |||||||
| chr5:43642321 | C | T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.965-1871C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43642321 | |||||||
| chr5:43642630 | G | T | 1 | a0001c0005t0004g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.965-1562G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43642630 | |||||||
| chr5:43642701 | A | G | 1 | a0001c0001t0006g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.965-1491A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43642701 | |||||||
| chr5:43642873 | C | CAGA | 29 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0002c0003t0002g0088 others(26): Show |
29 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.965-1314_965-1312d others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 43642873 | ||||||
| chr5:43642924 | A | G | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.965-1268A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43642924 | |||||||
| chr5:43642934 | T | C | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-1258T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43642934 | |||||||
| chr5:43643002 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.965-1190G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43643002 | |||||||
| chr5:43643044 | A | C | 29 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0002c0003t0002g0088 others(26): Show |
29 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.965-1148A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43643044 | |||||||
| chr5:43643123 | C | G | 1 | a0001c0001t0006g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.965-1069C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43643123 | |||||||
| chr5:43643316 | G | A | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.965-876G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43643316 | |||||||
| chr5:43643370 | C | T | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-822C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43643370 | |||||||
| chr5:43643738 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.965-454C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43643738 | |||||||
| chr5:43643781 | C | G | 1 | a0001c0001t0006g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.965-411C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43643781 | |||||||
| chr5:43644133 | G | A | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.965-59G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 7/21 | chr5 | 43644133 | |||||||
| chr5:43644340 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1098+15G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 8/21 | chr5 | 43644340 | |||||||
| chr5:43644342 | T | C | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+17T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 8/21 | chr5 | 43644342 | |||||||
| chr5:43644379 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1098+54G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 8/21 | chr5 | 43644379 | |||||||
| chr5:43644386 | G | GT | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1098+64dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 43644386 | ||||||
| chr5:43644460 | T | C | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1098+135T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 8/21 | chr5 | 43644460 | |||||||
| chr5:43644849 | T | C | 1 | a0008c0014t0004g0119 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1290+47T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 9/21 | chr5 | 43644849 | |||||||
| chr5:43644869 | G | T | 3 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0122 |
3 | HG02735.hp1 HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1290+67G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 9/21 | chr5 | 43644869 | |||||||
| chr5:43645002 | A | C | 1 | a0001c0004t0004g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1290+200A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 9/21 | chr5 | 43645002 | |||||||
| chr5:43645050 | T | A | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1290+248T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 9/21 | chr5 | 43645050 | |||||||
| chr5:43645181 | A | G | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291-176A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 9/21 | chr5 | 43645181 | |||||||
| chr5:43645190 | T | C | 66 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1291-167T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 9/21 | chr5 | 43645190 | |||||||
| chr5:43645206 | A | G | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291-151A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 9/21 | chr5 | 43645206 | |||||||
| chr5:43645561 | T | TTA | 16 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(13): Show |
16 | HG01069.hp1 HG01070.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1444+65_1444+66dup others(2): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645561 | ||||||
| chr5:43645565 | A | G | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+55A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645565 | |||||||
| chr5:43645584 | T | A | 1 | a0003c0006t0005g0078 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1444+74T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645584 | |||||||
| chr5:43645608 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1444+98T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645608 | |||||||
| chr5:43645640 | CATCT | C | 2 | a0001c0001t0003g0024 a0001c0001t0003g0048 |
2 | HG01074.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1444+143_1444+146d others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645640 | ||||||
| chr5:43645642 | T | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1444+132T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645642 | |||||||
| chr5:43645647 | CTA | C | 4 | a0001c0001t0005g0027 a0001c0001t0005g0056 a0001c0001t0006g0114 others(1): Show |
4 | HG01346.hp2 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444+139_1444+140d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645647 | ||||||
| chr5:43645649 | A | C | 7 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1444+139A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645649 | |||||||
| chr5:43645649 | ATCTATC | A | 3 | a0001c0002t0010g0183 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02970.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1444+143_1444+148d others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645649 | ||||||
| chr5:43645649 | ATCTATCT others(3): Show |
A | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1444+143_1444+152d others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645649 | ||||||
| chr5:43645653 | A | ATC | 4 | a0001c0002t0001g0006 a0001c0002t0001g0176 a0001c0002t0008g0170 others(1): Show |
4 | HG00597.hp2 HG02523.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+173_1444+174d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645653 | ||||||
| chr5:43645653 | A | ATCTATCT others(3): Show |
1 | a0001c0004t0021g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1444+146_1444+147i others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645653 | ||||||
| chr5:43645653 | A | ATCTATCT others(5): Show |
1 | a0001c0001t0014g0002 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1444+146_1444+147i others(14): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645653 | ||||||
| chr5:43645653 | A | ATCTATCT others(7): Show |
1 | a0001c0001t0014g0002 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1444+146_1444+147i others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645653 | ||||||
| chr5:43645653 | A | ATCTCTCT others(3): Show |
1 | a0002c0003t0019g0090 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1444+165_1444+174d others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645653 | ||||||
| chr5:43645653 | A | ATCTCTCT others(5): Show |
1 | a0001c0001t0006g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1444+163_1444+174d others(14): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645653 | ||||||
| chr5:43645653 | A | C | 13 | a0001c0001t0005g0027 a0001c0001t0005g0056 a0001c0001t0006g0080 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1444+143A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645653 | |||||||
| chr5:43645653 | ATC | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0030 others(6): Show |
9 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1444+173_1444+174d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645653 | ||||||
| chr5:43645653 | ATCTC | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0003g0001 others(15): Show |
19 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1444+171_1444+174d others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645653 | ||||||
| chr5:43645653 | ATCTCTCT others(3): Show |
A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0008c0014t0004g0119 |
3 | HG01361.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1444+165_1444+174d others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645653 | ||||||
| chr5:43645657 | C | A | 19 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(16): Show |
19 | HG01167.hp2 HG02257.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.1444+147C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645657 | |||||||
| chr5:43645659 | C | A | 1 | a0001c0004t0007g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1444+149C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645659 | |||||||
| chr5:43645661 | C | A | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1444+151C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645661 | |||||||
| chr5:43645673 | C | A | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1444+163C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645673 | |||||||
| chr5:43645675 | C | A | 2 | a0001c0001t0003g0043 a0004c0007t0010g0004 |
2 | HG02809.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1444+165C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645675 | |||||||
| chr5:43645677 | C | A | 4 | a0001c0001t0003g0043 a0001c0001t0003g0051 a0001c0004t0004g0118 others(1): Show |
4 | HG02257.hp2 HG02809.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+167C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645677 | |||||||
| chr5:43645679 | C | A | 20 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0003g0035 others(17): Show |
20 | HG00544.hp2 HG02257.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.1444+169C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645679 | |||||||
| chr5:43645679 | CTCTCTA | C | 4 | a0001c0001t0005g0028 a0001c0001t0005g0054 a0001c0001t0005g0057 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+171_1444+176d others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645679 | ||||||
| chr5:43645681 | C | A | 46 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0053 others(43): Show |
46 | HG00544.hp2 HG00639.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.1444+171C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645681 | |||||||
| chr5:43645681 | C | CTA | 3 | a0001c0002t0001g0155 a0001c0002t0001g0156 a0001c0002t0001g0185 |
3 | NA18953.hp1 NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1444+172_1444+173i others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645681 | ||||||
| chr5:43645683 | C | A | 81 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(78): Show |
82 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1444+173C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645683 | |||||||
| chr5:43645683 | C | CTA | 2 | a0001c0001t0006g0080 a0001c0002t0001g0141 |
2 | HG02451.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1444+199_1444+200d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTATA | 2 | a0001c0002t0001g0159 a0001c0002t0001g0181 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1444+197_1444+200d others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTAT others(7): Show |
1 | a0002c0003t0012g0101 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1444+174_1444+175i others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTAT others(9): Show |
1 | a0002c0003t0011g0100 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1444+174_1444+175i others(18): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTCT others(5): Show |
1 | a0002c0003t0002g0102 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1444+174_1444+175i others(14): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTCT others(5): Show |
3 | a0002c0003t0002g0093 a0002c0003t0002g0095 a0002c0003t0002g0096 |
3 | HG03834.hp2 NA19003.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1444+174_1444+175i others(14): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTCT others(7): Show |
3 | a0002c0003t0002g0094 a0002c0003t0002g0103 a0002c0003t0012g0108 |
3 | HG00544.hp1 NA18941.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1444+174_1444+175i others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTCT others(6): Show |
1 | a0005c0008t0013g0174 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1444+174_1444+175i others(15): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTCT others(7): Show |
2 | a0002c0003t0002g0088 a0002c0003t0011g0097 |
2 | HG02071.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1444+174_1444+175i others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTCT others(7): Show |
3 | a0002c0003t0002g0089 a0002c0003t0002g0098 a0002c0003t0002g0109 |
3 | HG01069.hp1 NA19065.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1444+174_1444+175i others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTCT others(9): Show |
1 | a0002c0003t0002g0104 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1444+174_1444+175i others(18): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTCT others(9): Show |
3 | a0002c0003t0002g0091 a0002c0003t0002g0092 a0002c0003t0002g0106 |
3 | HG01981.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1444+174_1444+175i others(18): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | C | CTCTCTCT others(11): Show |
2 | a0002c0003t0002g0105 a0002c0015t0002g0087 |
2 | HG01070.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1444+174_1444+175i others(20): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645683 | CTA | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0026 others(7): Show |
10 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1444+199_1444+200d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645683 | ||||||
| chr5:43645685 | A | C | 18 | a0001c0001t0001g0032 a0001c0001t0001g0073 a0001c0001t0003g0024 others(15): Show |
18 | HG01074.hp1 HG01109.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1444+175A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645685 | |||||||
| chr5:43645687 | A | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0006g0116 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1444+177A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645687 | |||||||
| chr5:43645702 | TA | T | 2 | a0004c0007t0010g0005 a0007c0012t0010g0046 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1444+193delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645702 | |||||||
| chr5:43645702 | TATATATA | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0009 |
2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1444+193_1444+199d others(9): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645702 | |||||||
| chr5:43645704 | TATA | T | 2 | a0001c0001t0001g0012 a0001c0001t0003g0051 |
2 | HG03486.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1444+195_1444+197d others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645704 | |||||||
| chr5:43645705 | A | T | 2 | a0004c0007t0010g0005 a0007c0012t0010g0046 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1444+195A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645705 | |||||||
| chr5:43645705 | ATATAT | A | 8 | a0001c0001t0001g0085 a0001c0004t0004g0121 a0001c0004t0004g0122 others(5): Show |
8 | HG01167.hp2 HG02572.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1444+197_1444+201d others(7): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645705 | ||||||
| chr5:43645706 | TA | T | 4 | a0001c0001t0005g0057 a0001c0001t0006g0114 a0001c0001t0006g0115 others(1): Show |
4 | HG01346.hp2 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+197delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645706 | |||||||
| chr5:43645706 | TATA | T | 8 | a0001c0001t0001g0010 a0001c0001t0005g0011 a0001c0001t0027g0055 others(5): Show |
8 | HG01074.hp2 HG01175.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1444+197_1444+199d others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645706 | |||||||
| chr5:43645707 | A | AT | 2 | a0001c0001t0006g0112 a0001c0002t0022g0150 |
2 | HG03098.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1444+198dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645707 | ||||||
| chr5:43645707 | A | T | 6 | a0001c0001t0001g0015 a0001c0001t0006g0110 a0001c0011t0004g0124 others(3): Show |
6 | HG01255.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1444+197A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645707 | |||||||
| chr5:43645707 | ATAT | A | 7 | a0001c0001t0005g0067 a0001c0004t0004g0130 a0001c0004t0004g0131 others(4): Show |
7 | HG01169.hp2 HG02717.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1444+199_1444+201d others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645707 | ||||||
| chr5:43645708 | TA | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0069 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1444+199delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645708 | |||||||
| chr5:43645709 | A | AT | 20 | a0001c0001t0014g0002 a0001c0002t0001g0152 a0001c0002t0008g0167 others(17): Show |
20 | HG00544.hp1 HG00544.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1444+222dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645709 | ||||||
| chr5:43645709 | A | ATATATAT others(7): Show |
1 | a0002c0003t0002g0099 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1444+200_1444+201i others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645709 | ||||||
| chr5:43645709 | A | T | 45 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0032 others(42): Show |
46 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1444+199A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645709 | |||||||
| chr5:43645709 | AT | A | 11 | a0001c0001t0006g0072 a0001c0001t0024g0018 a0001c0002t0001g0140 others(8): Show |
11 | HG01516.hp1 HG01516.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1444+222delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43645709 | ||||||
| chr5:43645710 | T | TA | 2 | a0001c0001t0006g0138 a0001c0002t0001g0173 |
2 | HG02886.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1444+200_1444+201i others(3): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645710 | |||||||
| chr5:43645710 | T | TATA | 2 | a0001c0004t0004g0118 a0001c0004t0004g0123 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1444+200_1444+201i others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645710 | |||||||
| chr5:43645711 | T | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0002t0001g0141 others(7): Show |
10 | HG01069.hp2 HG01071.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1444+201T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645711 | |||||||
| chr5:43645712 | T | A | 3 | a0001c0001t0006g0072 a0001c0002t0001g0146 a0001c0004t0004g0129 |
3 | HG02451.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1444+202T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645712 | |||||||
| chr5:43645713 | T | A | 1 | a0001c0002t0001g0155 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1444+203T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645713 | |||||||
| chr5:43645912 | A | T | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1444+402A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645912 | |||||||
| chr5:43645945 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1444+435C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43645945 | |||||||
| chr5:43646171 | G | A | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1444+661G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43646171 | |||||||
| chr5:43646320 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1444+810T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43646320 | |||||||
| chr5:43646343 | T | A | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+833T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43646343 | |||||||
| chr5:43646354 | C | T | 66 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1444+844C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43646354 | |||||||
| chr5:43646446 | C | T | 5 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(2): Show |
5 | HG02809.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1444+936C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43646446 | |||||||
| chr5:43646464 | A | AT | 13 | a0001c0001t0001g0012 a0001c0001t0006g0080 a0001c0001t0006g0110 others(10): Show |
14 | HG00597.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1444+969dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43646464 | ||||||
| chr5:43646530 | C | T | 1 | a0001c0002t0001g0176 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1444+1020C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43646530 | |||||||
| chr5:43646537 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1444+1027G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43646537 | |||||||
| chr5:43646960 | A | T | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1444+1450A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43646960 | |||||||
| chr5:43646966 | G | T | 1 | a0002c0003t0002g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1444+1456G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43646966 | |||||||
| chr5:43647067 | G | T | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1444+1557G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647067 | |||||||
| chr5:43647105 | G | A | 1 | a0001c0001t0006g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1444+1595G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647105 | |||||||
| chr5:43647118 | C | T | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1444+1608C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647118 | |||||||
| chr5:43647142 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1444+1632G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647142 | |||||||
| chr5:43647299 | T | C | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+1789T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647299 | |||||||
| chr5:43647483 | A | G | 3 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0122 |
3 | HG02735.hp1 HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1445-1664A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647483 | |||||||
| chr5:43647607 | T | C | 66 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1445-1540T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647607 | |||||||
| chr5:43647661 | G | A | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1445-1486G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647661 | |||||||
| chr5:43647677 | T | A | 1 | a0001c0001t0027g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1445-1470T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647677 | |||||||
| chr5:43647698 | G | A | 29 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0002c0003t0002g0088 others(26): Show |
29 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1445-1449G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647698 | |||||||
| chr5:43647862 | T | C | 66 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1445-1285T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647862 | |||||||
| chr5:43647894 | C | CAA | 64 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(61): Show |
65 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.1445-1252_1445-125 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 43647894 | ||||||
| chr5:43647992 | C | A | 1 | a0001c0001t0006g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1445-1155C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647992 | |||||||
| chr5:43647993 | C | T | 1 | a0001c0004t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1445-1154C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43647993 | |||||||
| chr5:43648019 | A | C | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1445-1128A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648019 | |||||||
| chr5:43648073 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1445-1074C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648073 | |||||||
| chr5:43648257 | A | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1445-890A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648257 | |||||||
| chr5:43648414 | C | T | 1 | a0001c0002t0001g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1445-733C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648414 | |||||||
| chr5:43648470 | A | G | 1 | a0001c0005t0023g0137 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1445-677A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648470 | |||||||
| chr5:43648595 | T | C | 66 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1445-552T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648595 | |||||||
| chr5:43648604 | C | T | 1 | a0003c0006t0005g0075 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1445-543C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648604 | |||||||
| chr5:43648724 | G | A | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1445-423G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648724 | |||||||
| chr5:43648759 | G | C | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1445-388G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648759 | |||||||
| chr5:43648802 | A | G | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1445-345A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648802 | |||||||
| chr5:43648808 | G | T | 2 | a0002c0003t0002g0088 a0002c0003t0002g0089 |
2 | NA18943.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1445-339G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648808 | |||||||
| chr5:43648812 | A | G | 64 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(61): Show |
65 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.1445-335A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648812 | |||||||
| chr5:43648939 | G | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1445-208G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 10/21 | chr5 | 43648939 | |||||||
| chr5:43649458 | C | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1606+150C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43649458 | |||||||
| chr5:43649465 | AG | A | 23 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(20): Show |
23 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1606+160delG | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr5 | 43649465 | ||||||
| chr5:43649499 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1606+191C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43649499 | |||||||
| chr5:43649503 | G | A | 1 | a0001c0001t0006g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1606+195G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43649503 | |||||||
| chr5:43649571 | T | G | 1 | a0001c0001t0006g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1606+263T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43649571 | |||||||
| chr5:43649577 | C | CT | 6 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0002c0003t0002g0105 others(3): Show |
6 | HG01069.hp1 HG01070.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1606+284dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr5 | 43649577 | ||||||
| chr5:43649577 | C | CTT | 22 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(19): Show |
22 | HG00544.hp1 HG01981.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1606+283_1606+284d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr5 | 43649577 | ||||||
| chr5:43649671 | C | T | 2 | a0001c0005t0004g0134 a0001c0005t0004g0136 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1606+363C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43649671 | |||||||
| chr5:43649681 | A | G | 1 | a0002c0003t0002g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1606+373A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43649681 | |||||||
| chr5:43649775 | G | A | 1 | a0005c0008t0013g0174 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1606+467G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43649775 | |||||||
| chr5:43649804 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1606+496G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43649804 | |||||||
| chr5:43650158 | G | A | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1607-319G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43650158 | |||||||
| chr5:43650187 | C | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1607-290C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43650187 | |||||||
| chr5:43650212 | A | G | 2 | a0002c0003t0002g0099 a0002c0003t0011g0100 |
2 | HG02165.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1607-265A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43650212 | |||||||
| chr5:43650391 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1607-86A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 11/21 | chr5 | 43650391 | |||||||
| chr5:43650633 | T | C | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1717+46T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43650633 | |||||||
| chr5:43650688 | T | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1717+101T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43650688 | |||||||
| chr5:43650714 | T | G | 40 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(37): Show |
41 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1717+127T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43650714 | |||||||
| chr5:43650843 | T | C | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1717+256T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43650843 | |||||||
| chr5:43650876 | C | T | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1717+289C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43650876 | |||||||
| chr5:43651266 | G | A | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1718-473G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43651266 | |||||||
| chr5:43651296 | G | T | 1 | a0001c0001t0005g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1718-443G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43651296 | |||||||
| chr5:43651321 | G | C | 1 | a0001c0004t0004g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1718-418G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43651321 | |||||||
| chr5:43651395 | G | T | 3 | a0001c0001t0003g0001 a0001c0001t0003g0024 a0001c0001t0003g0048 |
4 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1718-344G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43651395 | |||||||
| chr5:43651401 | A | AC | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1718-332dupC | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | 43651401 | ||||||
| chr5:43651407 | C | A | 1 | a0001c0001t0015g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1718-332C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43651407 | |||||||
| chr5:43651423 | C | A | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1718-316C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43651423 | |||||||
| chr5:43651446 | C | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1718-293C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43651446 | |||||||
| chr5:43651542 | C | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1718-197C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43651542 | |||||||
| chr5:43651726 | T | G | 1 | a0001c0004t0004g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1718-13T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 12/21 | chr5 | 43651726 | |||||||
| chr5:43651942 | T | TAATC | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1863+58_1863+59ins others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | chr5 | 43651942 | |||||||
| chr5:43651970 | G | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1863+86G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | chr5 | 43651970 | |||||||
| chr5:43652330 | A | G | 2 | a0004c0007t0010g0005 a0007c0012t0010g0046 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1863+446A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | chr5 | 43652330 | |||||||
| chr5:43652493 | A | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1864-525A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | chr5 | 43652493 | |||||||
| chr5:43652527 | AT | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(17): Show |
21 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.1864-475delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 43652527 | ||||||
| chr5:43652714 | A | T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1864-304A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | chr5 | 43652714 | |||||||
| chr5:43652739 | C | A | 1 | a0001c0001t0003g0023 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1864-279C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | chr5 | 43652739 | |||||||
| chr5:43652851 | A | G | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1864-167A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | chr5 | 43652851 | |||||||
| chr5:43652941 | C | T | 1 | a0001c0001t0009g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1864-77C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | chr5 | 43652941 | |||||||
| chr5:43652962 | C | T | 16 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0094 others(13): Show |
16 | HG00544.hp1 HG02071.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1864-56C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 13/21 | chr5 | 43652962 | |||||||
| chr5:43653580 | G | GA | 39 | a0001c0001t0003g0042 a0001c0001t0006g0072 a0001c0001t0006g0080 others(36): Show |
39 | HG00597.hp1 HG00597.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2059+384dupA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr5 | 43653580 | ||||||
| chr5:43653580 | GA | G | 28 | a0001c0001t0003g0079 a0001c0001t0005g0027 a0001c0002t0013g0180 others(25): Show |
28 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.2059+384delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr5 | 43653580 | ||||||
| chr5:43653936 | C | A | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2059+723C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43653936 | |||||||
| chr5:43653970 | A | T | 42 | a0001c0001t0001g0058 a0001c0001t0001g0084 a0001c0001t0006g0080 others(39): Show |
43 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.2059+757A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43653970 | |||||||
| chr5:43654713 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2060-1127T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43654713 | |||||||
| chr5:43654825 | C | T | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2060-1015C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43654825 | |||||||
| chr5:43654874 | T | C | 9 | a0001c0001t0005g0011 a0001c0001t0024g0018 a0001c0001t0027g0055 others(6): Show |
9 | HG01074.hp2 HG01361.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.2060-966T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43654874 | |||||||
| chr5:43655126 | T | C | 1 | a0001c0002t0002g0163 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2060-714T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43655126 | |||||||
| chr5:43655139 | G | A | 9 | a0001c0001t0005g0011 a0001c0001t0024g0018 a0001c0001t0027g0055 others(6): Show |
9 | HG01074.hp2 HG01361.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.2060-701G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43655139 | |||||||
| chr5:43655267 | G | A | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2060-573G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43655267 | |||||||
| chr5:43655583 | T | C | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2060-257T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43655583 | |||||||
| chr5:43655605 | A | G | 1 | a0001c0001t0009g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2060-235A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43655605 | |||||||
| chr5:43655719 | G | A | 25 | a0001c0001t0003g0079 a0002c0003t0002g0088 a0002c0003t0002g0089 others(22): Show |
25 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.2060-121G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 14/21 | chr5 | 43655719 | |||||||
| chr5:43656223 | C | T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2293+150C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 15/21 | chr5 | 43656223 | |||||||
| chr5:43656228 | C | G | 1 | a0001c0002t0008g0178 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2293+155C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 15/21 | chr5 | 43656228 | |||||||
| chr5:43656475 | G | C | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2294-178G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 15/21 | chr5 | 43656475 | |||||||
| chr5:43656550 | A | G | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2294-103A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 15/21 | chr5 | 43656550 | |||||||
| chr5:43656863 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2454+50A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43656863 | |||||||
| chr5:43657145 | A | G | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2454+332A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657145 | |||||||
| chr5:43657277 | C | G | 3 | a0001c0001t0006g0080 a0001c0001t0006g0116 a0001c0001t0006g0117 |
3 | HG01167.hp1 HG01169.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2454+464C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657277 | |||||||
| chr5:43657335 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2454+522T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657335 | |||||||
| chr5:43657336 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2454+523T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657336 | |||||||
| chr5:43657442 | C | G | 1 | a0001c0002t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2454+629C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657442 | |||||||
| chr5:43657513 | TA | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2454+707delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 43657513 | ||||||
| chr5:43657551 | A | G | 7 | a0001c0004t0004g0128 a0001c0004t0007g0081 a0001c0004t0007g0082 others(4): Show |
7 | HG01109.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2454+738A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657551 | |||||||
| chr5:43657722 | T | A | 1 | a0001c0002t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2454+909T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657722 | |||||||
| chr5:43657792 | T | C | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2454+979T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657792 | |||||||
| chr5:43657929 | G | A | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2454+1116G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657929 | |||||||
| chr5:43657949 | G | A | 64 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(61): Show |
65 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.2454+1136G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657949 | |||||||
| chr5:43657964 | G | A | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2454+1151G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657964 | |||||||
| chr5:43657966 | C | T | 1 | a0001c0002t0001g0172 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2454+1153C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657966 | |||||||
| chr5:43657997 | T | A | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2455-1174T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43657997 | |||||||
| chr5:43658102 | T | G | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2455-1069T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43658102 | |||||||
| chr5:43658161 | A | G | 1 | a0001c0002t0008g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2455-1010A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43658161 | |||||||
| chr5:43658205 | C | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2455-966C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43658205 | |||||||
| chr5:43658355 | TA | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2455-811delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr5 | 43658355 | ||||||
| chr5:43658381 | A | C | 64 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(61): Show |
65 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.2455-790A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43658381 | |||||||
| chr5:43658409 | C | T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2455-762C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43658409 | |||||||
| chr5:43658651 | G | A | 1 | a0009c0016t0005g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2455-520G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43658651 | |||||||
| chr5:43658962 | T | G | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2455-209T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43658962 | |||||||
| chr5:43659034 | C | A | 1 | a0001c0001t0003g0023 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2455-137C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 16/21 | chr5 | 43659034 | |||||||
| chr5:43659468 | C | T | 4 | a0002c0003t0002g0091 a0002c0003t0002g0092 a0002c0003t0002g0106 others(1): Show |
4 | HG01069.hp1 HG01981.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2634+118C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43659468 | |||||||
| chr5:43659469 | A | G | 53 | a0001c0002t0010g0183 a0001c0004t0004g0118 a0001c0004t0004g0120 others(50): Show |
53 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.2634+119A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43659469 | |||||||
| chr5:43659561 | T | TC | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+212dupC | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43659561 | ||||||
| chr5:43659681 | C | G | 1 | a0001c0002t0001g0165 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2634+331C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43659681 | |||||||
| chr5:43660314 | T | TAAA | 48 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(45): Show |
48 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.2634+966_2634+968d others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43660314 | ||||||
| chr5:43660381 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+1031T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43660381 | |||||||
| chr5:43660433 | CT | C | 48 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(45): Show |
48 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.2634+1092delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43660433 | ||||||
| chr5:43660540 | A | G | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2634+1190A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43660540 | |||||||
| chr5:43660611 | T | A | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2634+1261T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43660611 | |||||||
| chr5:43660712 | T | C | 1 | a0001c0002t0001g0153 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2634+1362T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43660712 | |||||||
| chr5:43660756 | T | G | 2 | a0003c0006t0005g0078 a0003c0006t0005g0083 |
2 | NA18971.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2634+1406T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43660756 | |||||||
| chr5:43660764 | C | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+1414C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43660764 | |||||||
| chr5:43660871 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2634+1521C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43660871 | |||||||
| chr5:43661109 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2634+1759C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43661109 | |||||||
| chr5:43661116 | AG | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+1770delG | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43661116 | ||||||
| chr5:43661389 | T | TTTTA | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(5): Show |
8 | HG01070.hp1 HG01993.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.2634+2067_2634+207 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43661389 | ||||||
| chr5:43661389 | T | TTTTATTT others(1): Show |
8 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(5): Show |
8 | HG01069.hp1 HG01981.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.2634+2063_2634+207 others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43661389 | ||||||
| chr5:43661389 | T | TTTTATTT others(5): Show |
11 | a0002c0003t0002g0093 a0002c0003t0002g0094 a0002c0003t0002g0095 others(8): Show |
11 | HG02071.hp1 HG02074.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.2634+2059_2634+207 others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43661389 | ||||||
| chr5:43661389 | T | TTTTATTT others(9): Show |
2 | a0002c0003t0002g0103 a0002c0003t0012g0108 |
2 | HG00544.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.2634+2055_2634+207 others(20): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43661389 | ||||||
| chr5:43661389 | TTTTA | T | 17 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(14): Show |
18 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2634+2067_2634+207 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43661389 | ||||||
| chr5:43661389 | TTTTATTT others(1): Show |
T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+2063_2634+207 others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43661389 | ||||||
| chr5:43661652 | C | T | 40 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(37): Show |
41 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.2634+2302C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43661652 | |||||||
| chr5:43661655 | T | G | 40 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(37): Show |
41 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.2634+2305T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43661655 | |||||||
| chr5:43661656 | C | T | 40 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(37): Show |
41 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.2634+2306C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43661656 | |||||||
| chr5:43661726 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
10 | HG01175.hp2 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2634+2376C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43661726 | |||||||
| chr5:43661813 | G | T | 1 | a0001c0002t0001g0177 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2634+2463G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43661813 | |||||||
| chr5:43661872 | T | C | 25 | a0001c0001t0006g0138 a0002c0003t0002g0088 a0002c0003t0002g0089 others(22): Show |
25 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.2634+2522T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43661872 | |||||||
| chr5:43661928 | G | C | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634+2578G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43661928 | |||||||
| chr5:43662132 | T | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+2782T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43662132 | |||||||
| chr5:43662339 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2634+2989G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43662339 | |||||||
| chr5:43662566 | T | A | 1 | a0003c0006t0005g0075 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2634+3216T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43662566 | |||||||
| chr5:43662893 | C | CA | 9 | a0001c0002t0001g0160 a0001c0002t0002g0163 a0001c0002t0010g0183 others(6): Show |
9 | HG02071.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2634+3560dupA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43662893 | ||||||
| chr5:43662893 | C | CAA | 23 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.2634+3559_2634+356 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43662893 | ||||||
| chr5:43662893 | CA | C | 8 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0114 others(5): Show |
9 | HG01243.hp1 HG01346.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634+3560delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43662893 | ||||||
| chr5:43663352 | C | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2634+4002C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663352 | |||||||
| chr5:43663479 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+4129G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663479 | |||||||
| chr5:43663538 | G | A | 66 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.2634+4188G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663538 | |||||||
| chr5:43663569 | T | C | 1 | a0001c0002t0010g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2634+4219T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663569 | |||||||
| chr5:43663616 | C | T | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634+4266C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663616 | |||||||
| chr5:43663617 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2634+4267G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663617 | |||||||
| chr5:43663629 | A | C | 1 | a0001c0004t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2634+4279A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663629 | |||||||
| chr5:43663711 | A | C | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2634+4361A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663711 | |||||||
| chr5:43663781 | G | A | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2634+4431G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663781 | |||||||
| chr5:43663900 | T | C | 23 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(20): Show |
23 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.2634+4550T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43663900 | |||||||
| chr5:43664045 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2634+4695T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43664045 | |||||||
| chr5:43664061 | A | AC | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+4715dupC | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43664061 | ||||||
| chr5:43664294 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2634+4944G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43664294 | |||||||
| chr5:43664314 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+4964G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43664314 | |||||||
| chr5:43664519 | C | T | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2634+5169C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43664519 | |||||||
| chr5:43664549 | A | G | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2634+5199A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43664549 | |||||||
| chr5:43664676 | CTGT | C | 3 | a0001c0002t0010g0183 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02970.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2634+5328_2634+533 others(7): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43664676 | ||||||
| chr5:43664729 | C | A | 4 | a0001c0001t0009g0021 a0001c0001t0009g0025 a0001c0001t0009g0037 others(1): Show |
4 | HG00741.hp1 HG02602.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2634+5379C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43664729 | |||||||
| chr5:43664760 | A | G | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2634+5410A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43664760 | |||||||
| chr5:43664764 | C | G | 6 | a0001c0001t0017g0038 a0001c0002t0008g0167 a0001c0002t0008g0168 others(3): Show |
6 | HG00741.hp2 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2634+5414C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43664764 | |||||||
| chr5:43664908 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2634+5558C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43664908 | |||||||
| chr5:43665136 | G | A | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+5786G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665136 | |||||||
| chr5:43665183 | T | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+5833T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665183 | |||||||
| chr5:43665214 | ATTTAT | A | 2 | a0001c0001t0014g0002 a0001c0001t0016g0113 |
3 | HG02109.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2634+5867_2634+587 others(9): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43665214 | ||||||
| chr5:43665215 | T | TTATTATT others(1): Show |
2 | a0004c0007t0010g0005 a0007c0012t0010g0046 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2634+5866_2634+586 others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43665215 | ||||||
| chr5:43665216 | T | TA | 4 | a0001c0001t0006g0110 a0001c0001t0006g0138 a0001c0011t0004g0124 others(1): Show |
4 | HG02809.hp2 HG02886.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2634+5866_2634+586 others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665216 | |||||||
| chr5:43665216 | TTA | T | 57 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0112 others(54): Show |
57 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2634+5868_2634+586 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43665216 | ||||||
| chr5:43665218 | A | T | 4 | a0001c0001t0006g0110 a0001c0001t0006g0138 a0001c0011t0004g0124 others(1): Show |
4 | HG02809.hp2 HG02886.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2634+5868A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665218 | |||||||
| chr5:43665219 | T | A | 61 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(58): Show |
61 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.2634+5869T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665219 | |||||||
| chr5:43665219 | T | TTA | 3 | a0001c0002t0010g0183 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02970.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2634+5870_2634+587 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43665219 | ||||||
| chr5:43665221 | T | A | 1 | a0001c0002t0001g0177 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2634+5871T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665221 | |||||||
| chr5:43665234 | A | T | 15 | a0001c0004t0004g0128 a0001c0004t0007g0081 a0001c0004t0007g0082 others(12): Show |
15 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2634+5884A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665234 | |||||||
| chr5:43665237 | A | T | 15 | a0001c0004t0004g0128 a0001c0004t0007g0081 a0001c0004t0007g0082 others(12): Show |
15 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2634+5887A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665237 | |||||||
| chr5:43665240 | A | T | 46 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0122 others(43): Show |
46 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.2634+5890A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665240 | |||||||
| chr5:43665491 | C | T | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2634+6141C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665491 | |||||||
| chr5:43665686 | T | C | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6336T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665686 | |||||||
| chr5:43665705 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6355G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665705 | |||||||
| chr5:43665710 | C | T | 24 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(21): Show |
25 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.2634+6360C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665710 | |||||||
| chr5:43665711 | G | A | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2634+6361G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665711 | |||||||
| chr5:43665718 | TGGCCC | T | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6370_2634+637 others(9): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43665718 | ||||||
| chr5:43665732 | G | T | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6382G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665732 | |||||||
| chr5:43665738 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6388G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665738 | |||||||
| chr5:43665757 | C | T | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6407C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665757 | |||||||
| chr5:43665765 | T | C | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6415T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665765 | |||||||
| chr5:43665780 | G | GCTC | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6431_2634+643 others(7): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43665780 | ||||||
| chr5:43665794 | C | T | 24 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(21): Show |
25 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.2634+6444C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665794 | |||||||
| chr5:43665804 | A | G | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6454A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665804 | |||||||
| chr5:43665813 | C | CA | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6463_2634+646 others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665813 | |||||||
| chr5:43665814 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6464G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665814 | |||||||
| chr5:43665816 | A | C | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6466A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665816 | |||||||
| chr5:43665819 | C | T | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6469C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665819 | |||||||
| chr5:43665827 | T | C | 89 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(86): Show |
91 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.2634+6477T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665827 | |||||||
| chr5:43665828 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6478G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665828 | |||||||
| chr5:43665831 | C | G | 23 | a0001c0001t0001g0015 a0001c0001t0003g0001 a0001c0001t0003g0022 others(20): Show |
24 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6481C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665831 | |||||||
| chr5:43665874 | G | A | 1 | a0001c0001t0005g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2634+6524G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665874 | |||||||
| chr5:43665885 | C | T | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2634+6535C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665885 | |||||||
| chr5:43665913 | C | CG | 18 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0003g0022 others(15): Show |
18 | HG00597.hp1 HG00741.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2634+6567dupG | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43665913 | ||||||
| chr5:43665959 | C | T | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2634+6609C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665959 | |||||||
| chr5:43665962 | G | A | 25 | a0001c0011t0004g0124 a0002c0003t0002g0088 a0002c0003t0002g0089 others(22): Show |
25 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.2634+6612G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665962 | |||||||
| chr5:43665963 | C | G | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2634+6613C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665963 | |||||||
| chr5:43665993 | C | T | 5 | a0001c0005t0004g0133 a0001c0005t0004g0134 a0001c0005t0004g0135 others(2): Show |
5 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2634+6643C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665993 | |||||||
| chr5:43665996 | G | T | 1 | a0001c0001t0005g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2634+6646G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43665996 | |||||||
| chr5:43666004 | G | A | 1 | a0001c0004t0021g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2634+6654G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666004 | |||||||
| chr5:43666030 | C | T | 33 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(30): Show |
33 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2634+6680C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666030 | |||||||
| chr5:43666038 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6688G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666038 | |||||||
| chr5:43666076 | ACGGCCGG others(30): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2634+6735_2634+677 others(41): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43666076 | ||||||
| chr5:43666163 | G | C | 2 | a0001c0002t0001g0157 a0001c0002t0001g0173 |
2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2634+6813G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666163 | |||||||
| chr5:43666217 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6867G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666217 | |||||||
| chr5:43666251 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+6901G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666251 | |||||||
| chr5:43666320 | C | T | 1 | a0002c0003t0002g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2634+6970C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666320 | |||||||
| chr5:43666363 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG06807.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2634+7013G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666363 | |||||||
| chr5:43666561 | C | T | 1 | a0003c0010t0005g0036 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2634+7211C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666561 | |||||||
| chr5:43666570 | G | A | 109 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
110 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(107): Show |
intron_variant | MODIFIER | c.2634+7220G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666570 | |||||||
| chr5:43666614 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+7264G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666614 | |||||||
| chr5:43666633 | A | AT | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634+7294dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43666633 | ||||||
| chr5:43666720 | TG | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2634+7376delG | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43666720 | ||||||
| chr5:43666786 | G | A | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2634+7436G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666786 | |||||||
| chr5:43666908 | A | G | 68 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(65): Show |
69 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2634+7558A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666908 | |||||||
| chr5:43666961 | C | T | 1 | a0001c0001t0009g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2634+7611C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43666961 | |||||||
| chr5:43667031 | G | A | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2634+7681G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667031 | |||||||
| chr5:43667157 | A | AT | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2634+7808dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43667157 | ||||||
| chr5:43667192 | C | T | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2634+7842C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667192 | |||||||
| chr5:43667205 | G | A | 23 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(20): Show |
23 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.2634+7855G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667205 | |||||||
| chr5:43667312 | T | G | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2634+7962T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667312 | |||||||
| chr5:43667602 | C | A | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2635-7909C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667602 | |||||||
| chr5:43667682 | G | T | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2635-7829G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667682 | |||||||
| chr5:43667768 | C | T | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-7743C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667768 | |||||||
| chr5:43667810 | T | TA | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-7700dupA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43667810 | ||||||
| chr5:43667838 | C | T | 1 | a0001c0002t0008g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2635-7673C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667838 | |||||||
| chr5:43667889 | T | G | 2 | a0003c0006t0005g0078 a0003c0006t0005g0083 |
2 | NA18971.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2635-7622T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667889 | |||||||
| chr5:43667920 | A | T | 27 | a0001c0002t0001g0151 a0001c0002t0002g0163 a0001c0002t0013g0180 others(24): Show |
27 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.2635-7591A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667920 | |||||||
| chr5:43667922 | C | T | 1 | a0001c0002t0001g0151 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2635-7589C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667922 | |||||||
| chr5:43667958 | A | G | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2635-7553A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667958 | |||||||
| chr5:43667995 | C | T | 178 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(175): Show |
180 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(177): Show |
intron_variant | MODIFIER | c.2635-7516C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43667995 | |||||||
| chr5:43668244 | G | GT | 22 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(19): Show |
22 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2635-7252dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43668244 | ||||||
| chr5:43668244 | G | GTT | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0005 others(2): Show |
5 | HG02970.hp2 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-7253_2635-725 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43668244 | ||||||
| chr5:43668244 | G | T | 1 | a0001c0004t0004g0130 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2635-7267G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668244 | |||||||
| chr5:43668244 | GT | G | 124 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(121): Show |
126 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.2635-7252delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43668244 | ||||||
| chr5:43668270 | A | G | 1 | a0001c0002t0001g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2635-7241A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668270 | |||||||
| chr5:43668313 | T | A | 1 | a0002c0003t0002g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2635-7198T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668313 | |||||||
| chr5:43668397 | G | A | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2635-7114G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668397 | |||||||
| chr5:43668547 | C | T | 7 | a0001c0004t0004g0128 a0001c0004t0007g0081 a0001c0004t0007g0082 others(4): Show |
7 | HG01109.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2635-6964C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668547 | |||||||
| chr5:43668551 | T | G | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-6960T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668551 | |||||||
| chr5:43668654 | C | G | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2635-6857C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668654 | |||||||
| chr5:43668773 | G | C | 1 | a0001c0001t0005g0067 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2635-6738G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668773 | |||||||
| chr5:43668830 | A | G | 1 | a0005c0008t0013g0174 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2635-6681A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668830 | |||||||
| chr5:43668849 | G | C | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2635-6662G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668849 | |||||||
| chr5:43668962 | C | G | 42 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(39): Show |
43 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.2635-6549C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43668962 | |||||||
| chr5:43669034 | T | C | 2 | a0001c0001t0006g0116 a0001c0001t0006g0117 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2635-6477T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43669034 | |||||||
| chr5:43669060 | G | C | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2635-6451G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43669060 | |||||||
| chr5:43669275 | T | C | 1 | a0001c0002t0022g0150 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2635-6236T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43669275 | |||||||
| chr5:43669417 | T | C | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2635-6094T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43669417 | |||||||
| chr5:43669599 | G | A | 1 | a0002c0015t0002g0087 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2635-5912G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43669599 | |||||||
| chr5:43669600 | T | C | 1 | a0001c0001t0005g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2635-5911T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43669600 | |||||||
| chr5:43669720 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2635-5791G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43669720 | |||||||
| chr5:43669874 | A | G | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2635-5637A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43669874 | |||||||
| chr5:43669973 | TATTCAGG others(1): Show |
T | 3 | a0001c0001t0001g0030 a0001c0002t0001g0146 a0001c0002t0001g0147 |
3 | NA19043.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2635-5531_2635-552 others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43669973 | ||||||
| chr5:43670086 | T | G | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2635-5425T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670086 | |||||||
| chr5:43670272 | A | T | 66 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.2635-5239A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670272 | |||||||
| chr5:43670288 | C | T | 1 | a0001c0001t0006g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2635-5223C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670288 | |||||||
| chr5:43670396 | T | C | 31 | a0001c0002t0002g0163 a0001c0002t0010g0183 a0001c0002t0013g0180 others(28): Show |
31 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.2635-5115T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670396 | |||||||
| chr5:43670400 | C | G | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2635-5111C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670400 | |||||||
| chr5:43670412 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0009 |
2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2635-5099G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670412 | |||||||
| chr5:43670427 | A | G | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2635-5084A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670427 | |||||||
| chr5:43670485 | T | C | 7 | a0002c0003t0002g0091 a0002c0003t0002g0092 a0002c0003t0002g0104 others(4): Show |
7 | HG01069.hp1 HG01070.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2635-5026T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670485 | |||||||
| chr5:43670576 | A | G | 1 | a0008c0014t0004g0119 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2635-4935A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670576 | |||||||
| chr5:43670647 | G | C | 64 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(61): Show |
65 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.2635-4864G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670647 | |||||||
| chr5:43670656 | A | G | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-4855A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670656 | |||||||
| chr5:43670740 | G | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-4771G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670740 | |||||||
| chr5:43670816 | G | A | 5 | a0001c0002t0001g0141 a0001c0002t0001g0144 a0001c0002t0001g0155 others(2): Show |
5 | HG01981.hp2 NA18953.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2635-4695G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670816 | |||||||
| chr5:43670906 | G | T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-4605G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670906 | |||||||
| chr5:43670927 | TG | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01891.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2635-4583delG | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670927 | |||||||
| chr5:43670964 | C | G | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-4547C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43670964 | |||||||
| chr5:43671022 | C | G | 6 | a0001c0002t0001g0157 a0001c0002t0001g0173 a0001c0002t0010g0183 others(3): Show |
6 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2635-4489C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671022 | |||||||
| chr5:43671304 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2635-4207G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671304 | |||||||
| chr5:43671335 | G | A | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2635-4176G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671335 | |||||||
| chr5:43671342 | A | C | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-4169A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671342 | |||||||
| chr5:43671350 | C | G | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-4161C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671350 | |||||||
| chr5:43671415 | C | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-4096C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671415 | |||||||
| chr5:43671480 | C | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-4031C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671480 | |||||||
| chr5:43671509 | T | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-4002T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671509 | |||||||
| chr5:43671534 | G | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-3977G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671534 | |||||||
| chr5:43671618 | C | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-3893C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671618 | |||||||
| chr5:43671665 | A | C | 2 | a0001c0001t0006g0116 a0001c0001t0006g0117 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2635-3846A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671665 | |||||||
| chr5:43671741 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-3770T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671741 | |||||||
| chr5:43671857 | C | T | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-3654C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671857 | |||||||
| chr5:43671923 | A | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-3588A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671923 | |||||||
| chr5:43671929 | C | T | 3 | a0001c0001t0005g0011 a0001c0001t0024g0018 a0001c0001t0027g0055 |
3 | HG01074.hp2 HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2635-3582C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671929 | |||||||
| chr5:43671957 | A | G | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2635-3554A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671957 | |||||||
| chr5:43671978 | C | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-3533C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671978 | |||||||
| chr5:43671979 | A | G | 66 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.2635-3532A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43671979 | |||||||
| chr5:43672013 | T | C | 3 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0122 |
3 | HG02735.hp1 HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2635-3498T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672013 | |||||||
| chr5:43672066 | T | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-3445T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672066 | |||||||
| chr5:43672091 | G | T | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2635-3420G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672091 | |||||||
| chr5:43672209 | G | T | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2635-3302G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672209 | |||||||
| chr5:43672221 | G | A | 1 | a0009c0016t0005g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2635-3290G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672221 | |||||||
| chr5:43672228 | A | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-3283A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672228 | |||||||
| chr5:43672325 | G | A | 2 | a0001c0002t0001g0157 a0001c0002t0001g0173 |
2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2635-3186G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672325 | |||||||
| chr5:43672334 | C | T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-3177C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672334 | |||||||
| chr5:43672395 | A | G | 1 | a0001c0002t0001g0156 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2635-3116A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672395 | |||||||
| chr5:43672559 | G | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-2952G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672559 | |||||||
| chr5:43672565 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2635-2946G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672565 | |||||||
| chr5:43672576 | A | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-2935A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672576 | |||||||
| chr5:43672724 | A | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-2787A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672724 | |||||||
| chr5:43672861 | G | A | 2 | a0001c0001t0006g0138 a0001c0002t0001g0006 |
2 | HG02523.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2635-2650G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672861 | |||||||
| chr5:43672938 | C | T | 1 | a0001c0001t0016g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2635-2573C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43672938 | |||||||
| chr5:43673045 | C | T | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2635-2466C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673045 | |||||||
| chr5:43673168 | C | T | 2 | a0001c0001t0005g0067 a0009c0016t0005g0045 |
2 | HG01169.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2635-2343C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673168 | |||||||
| chr5:43673250 | G | A | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2635-2261G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673250 | |||||||
| chr5:43673366 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2635-2145C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673366 | |||||||
| chr5:43673377 | A | T | 1 | a0001c0004t0020g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2635-2134A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673377 | |||||||
| chr5:43673486 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-2025T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673486 | |||||||
| chr5:43673487 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-2024G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673487 | |||||||
| chr5:43673495 | C | T | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2635-2016C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673495 | |||||||
| chr5:43673564 | A | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0069 others(2): Show |
5 | HG02809.hp1 HG03195.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2635-1947A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673564 | |||||||
| chr5:43673673 | T | A | 1 | a0001c0001t0003g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2635-1838T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673673 | |||||||
| chr5:43673822 | T | C | 68 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(65): Show |
69 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2635-1689T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673822 | |||||||
| chr5:43673942 | C | T | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2635-1569C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43673942 | |||||||
| chr5:43674019 | C | CA | 30 | a0001c0001t0003g0023 a0001c0001t0006g0080 a0001c0002t0001g0006 others(27): Show |
30 | HG00544.hp1 HG01070.hp1 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.2635-1476dupA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 43674019 | ||||||
| chr5:43674110 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2635-1401G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43674110 | |||||||
| chr5:43674165 | T | C | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2635-1346T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43674165 | |||||||
| chr5:43674345 | C | G | 1 | a0002c0003t0002g0105 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2635-1166C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43674345 | |||||||
| chr5:43674535 | A | G | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2635-976A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43674535 | |||||||
| chr5:43674554 | A | T | 1 | a0001c0002t0001g0160 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2635-957A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43674554 | |||||||
| chr5:43674683 | T | C | 2 | a0001c0001t0001g0012 a0001c0002t0001g0161 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2635-828T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43674683 | |||||||
| chr5:43674684 | C | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2635-827C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43674684 | |||||||
| chr5:43674718 | A | G | 1 | a0001c0004t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2635-793A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43674718 | |||||||
| chr5:43674744 | C | T | 140 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
142 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.2635-767C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43674744 | |||||||
| chr5:43675090 | T | G | 1 | a0001c0004t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2635-421T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43675090 | |||||||
| chr5:43675215 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2635-296C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43675215 | |||||||
| chr5:43675355 | A | G | 1 | a0001c0004t0021g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2635-156A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43675355 | |||||||
| chr5:43675390 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0060 |
3 | HG02109.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2635-121G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43675390 | |||||||
| chr5:43675417 | T | A | 1 | a0001c0001t0016g0111 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2635-94T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 17/21 | chr5 | 43675417 | |||||||
| chr5:43675821 | A | G | 1 | a0001c0004t0007g0126 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2794+151A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43675821 | |||||||
| chr5:43675902 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2794+232G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43675902 | |||||||
| chr5:43676149 | C | T | 1 | a0002c0003t0019g0090 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2794+479C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43676149 | |||||||
| chr5:43676269 | C | T | 1 | a0003c0006t0005g0075 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2794+599C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43676269 | |||||||
| chr5:43676369 | C | T | 1 | a0001c0002t0001g0152 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2794+699C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43676369 | |||||||
| chr5:43676488 | T | A | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2794+818T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43676488 | |||||||
| chr5:43676527 | G | A | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2794+857G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43676527 | |||||||
| chr5:43676541 | A | C | 31 | a0001c0002t0002g0163 a0001c0002t0010g0183 a0001c0002t0013g0180 others(28): Show |
31 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.2794+871A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43676541 | |||||||
| chr5:43676794 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2795-931T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43676794 | |||||||
| chr5:43676830 | G | T | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2795-895G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43676830 | |||||||
| chr5:43677131 | C | A | 1 | a0008c0014t0004g0119 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2795-594C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43677131 | |||||||
| chr5:43677164 | G | A | 1 | a0001c0001t0016g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2795-561G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43677164 | |||||||
| chr5:43677237 | A | G | 1 | a0001c0004t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2795-488A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43677237 | |||||||
| chr5:43677282 | C | T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0019 others(11): Show |
14 | HG01361.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2795-443C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43677282 | |||||||
| chr5:43677309 | A | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2795-416A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43677309 | |||||||
| chr5:43677399 | T | TGA | 2 | a0001c0001t0001g0073 a0001c0002t0001g0157 |
2 | HG02717.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.2795-299_2795-298d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr5 | 43677399 | ||||||
| chr5:43677399 | TGAGA | T | 39 | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0114 others(36): Show |
40 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.2795-301_2795-298d others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr5 | 43677399 | ||||||
| chr5:43677467 | G | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2795-258G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43677467 | |||||||
| chr5:43677651 | C | A | 1 | a0001c0001t0006g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2795-74C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 18/21 | chr5 | 43677651 | |||||||
| chr5:43677874 | G | A | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2876+68G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43677874 | |||||||
| chr5:43677903 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2876+97G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43677903 | |||||||
| chr5:43677915 | C | T | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2876+109C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43677915 | |||||||
| chr5:43678679 | C | T | 12 | a0001c0002t0001g0141 a0001c0002t0001g0142 a0001c0002t0001g0144 others(9): Show |
12 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2876+873C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43678679 | |||||||
| chr5:43679063 | A | G | 6 | a0001c0005t0004g0133 a0001c0005t0004g0134 a0001c0005t0004g0135 others(3): Show |
6 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2876+1257A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43679063 | |||||||
| chr5:43679094 | T | C | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2876+1288T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43679094 | |||||||
| chr5:43679140 | A | AT | 2 | a0001c0002t0001g0159 a0001c0002t0001g0181 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2876+1335dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43679140 | ||||||
| chr5:43679208 | T | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2876+1402T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43679208 | |||||||
| chr5:43679583 | C | G | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2876+1777C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43679583 | |||||||
| chr5:43679609 | G | T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2876+1803G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43679609 | |||||||
| chr5:43679708 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2876+1902G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43679708 | |||||||
| chr5:43679832 | C | G | 8 | a0001c0004t0004g0128 a0001c0004t0007g0081 a0001c0004t0007g0082 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2876+2026C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43679832 | |||||||
| chr5:43679838 | A | G | 1 | a0001c0002t0001g0153 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2876+2032A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43679838 | |||||||
| chr5:43679860 | A | G | 1 | a0001c0001t0003g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2876+2054A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43679860 | |||||||
| chr5:43680094 | C | G | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2876+2288C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680094 | |||||||
| chr5:43680113 | G | T | 2 | a0001c0001t0006g0116 a0001c0001t0006g0117 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2876+2307G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680113 | |||||||
| chr5:43680118 | C | A | 1 | a0001c0004t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2876+2312C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680118 | |||||||
| chr5:43680118 | C | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2876+2312C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680118 | |||||||
| chr5:43680129 | A | AT | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2876+2328dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43680129 | ||||||
| chr5:43680141 | G | A | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2876+2335G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680141 | |||||||
| chr5:43680160 | A | C | 1 | a0001c0002t0008g0167 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2876+2354A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680160 | |||||||
| chr5:43680314 | G | A | 6 | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0114 others(3): Show |
6 | HG01243.hp1 HG01346.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2876+2508G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680314 | |||||||
| chr5:43680388 | A | G | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2876+2582A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680388 | |||||||
| chr5:43680565 | A | G | 66 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.2876+2759A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680565 | |||||||
| chr5:43680589 | G | A | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2876+2783G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680589 | |||||||
| chr5:43680820 | A | G | 1 | a0001c0004t0007g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2876+3014A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680820 | |||||||
| chr5:43680842 | G | A | 17 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(14): Show |
17 | HG01109.hp1 HG01891.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2876+3036G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680842 | |||||||
| chr5:43680871 | C | T | 15 | a0001c0001t0005g0011 a0001c0001t0005g0027 a0001c0001t0005g0028 others(12): Show |
15 | HG01074.hp2 HG01169.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.2876+3065C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680871 | |||||||
| chr5:43680875 | C | T | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2876+3069C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680875 | |||||||
| chr5:43680878 | C | T | 1 | a0001c0002t0001g0145 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2876+3072C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680878 | |||||||
| chr5:43680963 | A | G | 31 | a0001c0002t0002g0163 a0001c0002t0010g0183 a0001c0002t0013g0180 others(28): Show |
31 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.2876+3157A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680963 | |||||||
| chr5:43680968 | C | G | 1 | a0001c0001t0015g0008 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2876+3162C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43680968 | |||||||
| chr5:43681077 | G | T | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+3271G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43681077 | |||||||
| chr5:43681176 | C | T | 1 | a0001c0001t0016g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2876+3370C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43681176 | |||||||
| chr5:43681191 | T | C | 66 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(63): Show |
67 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.2876+3385T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43681191 | |||||||
| chr5:43681214 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2876+3408C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43681214 | |||||||
| chr5:43681259 | C | CA | 16 | a0001c0001t0003g0023 a0001c0001t0006g0110 a0001c0001t0006g0116 others(13): Show |
16 | HG01069.hp1 HG01070.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2876+3474dupA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43681259 | ||||||
| chr5:43681259 | C | CAA | 11 | a0001c0001t0006g0080 a0001c0001t0006g0112 a0001c0001t0006g0114 others(8): Show |
12 | HG01243.hp1 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2876+3473_2876+347 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43681259 | ||||||
| chr5:43681259 | CA | C | 29 | a0001c0001t0001g0030 a0001c0001t0001g0061 a0001c0001t0001g0062 others(26): Show |
29 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.2876+3474delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43681259 | ||||||
| chr5:43681294 | T | G | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2876+3488T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43681294 | |||||||
| chr5:43681606 | G | C | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2876+3800G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43681606 | |||||||
| chr5:43681680 | G | A | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2876+3874G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43681680 | |||||||
| chr5:43681779 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2876+3973A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43681779 | |||||||
| chr5:43682027 | A | AT | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+4227dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43682027 | ||||||
| chr5:43682105 | A | G | 6 | a0001c0001t0017g0038 a0001c0002t0008g0167 a0001c0002t0008g0168 others(3): Show |
6 | HG00741.hp2 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2876+4299A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43682105 | |||||||
| chr5:43682208 | C | CT | 6 | a0001c0001t0001g0071 a0001c0001t0003g0035 a0001c0001t0003g0079 others(3): Show |
6 | HG02451.hp2 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2876+4424dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43682208 | ||||||
| chr5:43682208 | C | CTTT | 17 | a0001c0002t0002g0163 a0002c0003t0002g0088 a0002c0003t0002g0089 others(14): Show |
17 | HG00544.hp1 HG01069.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.2876+4422_2876+442 others(7): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43682208 | ||||||
| chr5:43682208 | CT | C | 29 | a0001c0001t0003g0040 a0001c0001t0005g0067 a0001c0001t0006g0110 others(26): Show |
30 | HG01109.hp1 HG01169.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.2876+4424delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43682208 | ||||||
| chr5:43682208 | CTT | C | 13 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0002t0010g0183 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2876+4423_2876+442 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43682208 | ||||||
| chr5:43682280 | G | A | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2876+4474G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43682280 | |||||||
| chr5:43682369 | CCTGA | C | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+4566_2876+456 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43682369 | ||||||
| chr5:43683124 | G | T | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2876+5318G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43683124 | |||||||
| chr5:43683149 | C | G | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2876+5343C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43683149 | |||||||
| chr5:43683243 | A | G | 1 | a0001c0001t0009g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2876+5437A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43683243 | |||||||
| chr5:43683381 | C | G | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2876+5575C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43683381 | |||||||
| chr5:43683678 | G | T | 24 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0002g0091 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2876+5872G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43683678 | |||||||
| chr5:43683823 | A | G | 1 | a0001c0002t0001g0165 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2876+6017A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43683823 | |||||||
| chr5:43683916 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01891.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2876+6110C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43683916 | |||||||
| chr5:43683964 | A | T | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2876+6158A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43683964 | |||||||
| chr5:43684006 | G | A | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2876+6200G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43684006 | |||||||
| chr5:43684184 | C | A | 1 | a0001c0001t0003g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2876+6378C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43684184 | |||||||
| chr5:43684217 | AT | A | 6 | a0001c0001t0006g0072 a0001c0002t0010g0183 a0001c0011t0004g0124 others(3): Show |
6 | HG02451.hp2 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2876+6427delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43684217 | ||||||
| chr5:43684217 | ATT | A | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+6426_2876+642 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43684217 | ||||||
| chr5:43684218 | T | A | 1 | a0001c0001t0009g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2876+6412T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43684218 | |||||||
| chr5:43684380 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2876+6574T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43684380 | |||||||
| chr5:43684508 | C | A | 1 | a0005c0008t0013g0174 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2876+6702C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43684508 | |||||||
| chr5:43684728 | TA | T | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+6932delA | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43684728 | ||||||
| chr5:43684816 | A | G | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+7010A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43684816 | |||||||
| chr5:43684975 | A | G | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2876+7169A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43684975 | |||||||
| chr5:43684979 | A | G | 3 | a0001c0002t0010g0183 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02970.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2876+7173A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43684979 | |||||||
| chr5:43685010 | C | T | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2876+7204C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43685010 | |||||||
| chr5:43685259 | C | G | 6 | a0001c0001t0017g0038 a0001c0002t0008g0167 a0001c0002t0008g0168 others(3): Show |
6 | HG00741.hp2 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2876+7453C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43685259 | |||||||
| chr5:43685478 | A | G | 1 | a0001c0004t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2876+7672A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43685478 | |||||||
| chr5:43685486 | T | G | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+7680T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43685486 | |||||||
| chr5:43685493 | T | A | 37 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(34): Show |
38 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.2876+7687T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43685493 | |||||||
| chr5:43685494 | A | T | 7 | a0001c0002t0001g0148 a0001c0002t0001g0160 a0001c0002t0010g0183 others(4): Show |
7 | HG02071.hp2 HG02523.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2876+7688A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43685494 | |||||||
| chr5:43685919 | A | G | 1 | a0009c0016t0005g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2876+8113A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43685919 | |||||||
| chr5:43685974 | T | G | 2 | a0001c0004t0004g0130 a0001c0004t0004g0131 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2876+8168T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43685974 | |||||||
| chr5:43685978 | C | T | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+8172C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43685978 | |||||||
| chr5:43686031 | T | C | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+8225T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43686031 | |||||||
| chr5:43686093 | T | G | 5 | a0001c0005t0004g0133 a0001c0005t0004g0134 a0001c0005t0004g0135 others(2): Show |
5 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2876+8287T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43686093 | |||||||
| chr5:43686171 | A | G | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+8365A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43686171 | |||||||
| chr5:43686234 | T | C | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2876+8428T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43686234 | |||||||
| chr5:43686238 | A | AT | 27 | a0001c0001t0006g0138 a0001c0001t0014g0002 a0001c0002t0002g0163 others(24): Show |
28 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.2876+8446dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43686238 | ||||||
| chr5:43686521 | CT | C | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2876+8719delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43686521 | ||||||
| chr5:43686662 | G | A | 1 | a0002c0003t0002g0105 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2876+8856G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43686662 | |||||||
| chr5:43686746 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2876+8940A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43686746 | |||||||
| chr5:43686827 | G | C | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2876+9021G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43686827 | |||||||
| chr5:43686958 | T | G | 2 | a0001c0001t0005g0027 a0001c0001t0005g0056 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2876+9152T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43686958 | |||||||
| chr5:43687157 | G | A | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2876+9351G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43687157 | |||||||
| chr5:43687372 | T | C | 5 | a0001c0002t0010g0183 a0001c0011t0004g0124 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2876+9566T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43687372 | |||||||
| chr5:43687446 | A | G | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2876+9640A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43687446 | |||||||
| chr5:43687608 | G | A | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2876+9802G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43687608 | |||||||
| chr5:43687736 | G | T | 1 | a0004c0007t0010g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2876+9930G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43687736 | |||||||
| chr5:43687838 | C | T | 31 | a0001c0002t0002g0163 a0001c0002t0010g0183 a0001c0002t0013g0180 others(28): Show |
31 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.2876+10032C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43687838 | |||||||
| chr5:43688011 | G | A | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2876+10205G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43688011 | |||||||
| chr5:43688097 | C | T | 62 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(59): Show |
63 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.2876+10291C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43688097 | |||||||
| chr5:43688179 | T | C | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2876+10373T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43688179 | |||||||
| chr5:43688218 | C | T | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2876+10412C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43688218 | |||||||
| chr5:43688294 | G | A | 6 | a0001c0005t0004g0133 a0001c0005t0004g0134 a0001c0005t0004g0135 others(3): Show |
6 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2876+10488G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43688294 | |||||||
| chr5:43688415 | A | T | 1 | a0001c0002t0025g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2876+10609A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43688415 | |||||||
| chr5:43688812 | T | C | 7 | a0002c0003t0002g0091 a0002c0003t0002g0092 a0002c0003t0002g0104 others(4): Show |
7 | HG01069.hp1 HG01070.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2876+11006T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43688812 | |||||||
| chr5:43688821 | A | G | 1 | a0001c0001t0006g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2876+11015A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43688821 | |||||||
| chr5:43689074 | T | A | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2877-11045T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43689074 | |||||||
| chr5:43689355 | T | A | 1 | a0001c0001t0006g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2877-10764T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43689355 | |||||||
| chr5:43689494 | C | T | 42 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(39): Show |
43 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.2877-10625C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43689494 | |||||||
| chr5:43689554 | C | T | 3 | a0001c0001t0015g0008 a0001c0001t0015g0034 a0001c0001t0028g0017 |
3 | HG01175.hp2 HG02280.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2877-10565C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43689554 | |||||||
| chr5:43689786 | A | G | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2877-10333A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43689786 | |||||||
| chr5:43689895 | G | A | 1 | a0001c0005t0004g0136 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2877-10224G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43689895 | |||||||
| chr5:43690438 | G | A | 1 | a0001c0011t0004g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2877-9681G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43690438 | |||||||
| chr5:43690457 | A | G | 2 | a0001c0001t0006g0116 a0001c0001t0006g0117 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2877-9662A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43690457 | |||||||
| chr5:43690687 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2877-9432C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43690687 | |||||||
| chr5:43690862 | A | C | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2877-9257A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43690862 | |||||||
| chr5:43691064 | T | TGA | 6 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0129 others(3): Show |
6 | HG02735.hp1 HG03130.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2877-9049_2877-904 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691064 | ||||||
| chr5:43691064 | T | TGAGA | 2 | a0001c0004t0004g0123 a0002c0003t0002g0092 |
2 | HG01981.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2877-9051_2877-904 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691064 | ||||||
| chr5:43691064 | T | TGAGAGAG others(1): Show |
2 | a0002c0003t0002g0091 a0002c0003t0002g0105 |
2 | HG01070.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2877-9048_2877-904 others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691064 | ||||||
| chr5:43691068 | A | AGT | 2 | a0001c0001t0001g0084 a0001c0004t0021g0132 |
2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2877-9050_2877-904 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691068 | ||||||
| chr5:43691070 | A | AGAGAGAG others(5): Show |
6 | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0114 others(3): Show |
6 | HG01243.hp1 HG01346.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2877-9048_2877-904 others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | A | AGAGAGAG others(7): Show |
1 | a0001c0001t0006g0080 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2877-9048_2877-904 others(18): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | A | AGAGAGAG others(9): Show |
2 | a0001c0001t0006g0116 a0001c0001t0006g0117 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2877-9048_2877-904 others(20): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | A | AGAGAGAG others(1): Show |
3 | a0002c0003t0002g0104 a0002c0003t0002g0109 a0002c0015t0002g0087 |
3 | HG01069.hp1 HG03669.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2877-9048_2877-904 others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | A | AGAGAGAG others(3): Show |
1 | a0002c0003t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2877-9048_2877-904 others(14): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | A | AGAGT | 4 | a0001c0001t0014g0002 a0001c0004t0004g0118 a0001c0004t0004g0122 others(1): Show |
5 | HG02071.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2877-9048_2877-904 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | A | AGT | 32 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0049 others(29): Show |
32 | HG01074.hp2 HG01361.hp2 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.2877-9006_2877-900 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | A | AGTGT | 16 | a0001c0001t0003g0035 a0001c0001t0005g0027 a0001c0001t0005g0056 others(13): Show |
16 | HG01167.hp2 HG01169.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2877-9008_2877-900 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | A | AGTGTGTG others(3): Show |
2 | a0001c0004t0007g0126 a0001c0004t0018g0127 |
2 | HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2877-9014_2877-900 others(14): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | A | T | 5 | a0001c0001t0001g0084 a0001c0004t0007g0081 a0001c0004t0007g0082 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2877-9049A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691070 | |||||||
| chr5:43691070 | AGT | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0003g0068 others(24): Show |
27 | HG00544.hp1 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.2877-9006_2877-900 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691070 | AGTGT | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0006g0138 others(1): Show |
4 | HG01891.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2877-9008_2877-900 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43691070 | ||||||
| chr5:43691072 | T | A | 5 | a0001c0001t0003g0040 a0001c0002t0022g0150 a0001c0004t0020g0020 others(2): Show |
5 | HG01981.hp1 HG03834.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.2877-9047T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691072 | |||||||
| chr5:43691074 | T | A | 3 | a0004c0007t0010g0004 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02809.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2877-9045T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691074 | |||||||
| chr5:43691076 | T | A | 5 | a0001c0001t0006g0138 a0001c0002t0010g0183 a0004c0007t0010g0004 others(2): Show |
5 | HG02809.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2877-9043T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691076 | |||||||
| chr5:43691078 | T | A | 1 | a0001c0002t0010g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2877-9041T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691078 | |||||||
| chr5:43691114 | T | TGTG | 2 | a0001c0004t0004g0128 a0001c0011t0004g0124 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2877-9005_2877-900 others(7): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691114 | |||||||
| chr5:43691115 | T | G | 2 | a0001c0002t0008g0178 a0003c0006t0005g0086 |
2 | HG01516.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2877-9004T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691115 | |||||||
| chr5:43691161 | G | A | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2877-8958G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691161 | |||||||
| chr5:43691273 | G | T | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2877-8846G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691273 | |||||||
| chr5:43691461 | A | T | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2877-8658A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691461 | |||||||
| chr5:43691753 | A | G | 2 | a0001c0001t0003g0066 a0001c0001t0003g0068 |
2 | HG01243.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2877-8366A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43691753 | |||||||
| chr5:43692193 | AT | A | 68 | a0001c0001t0006g0072 a0001c0001t0006g0080 a0001c0001t0006g0110 others(65): Show |
69 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2877-7916delT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43692193 | ||||||
| chr5:43692292 | A | G | 2 | a0001c0004t0004g0130 a0001c0004t0004g0131 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2877-7827A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43692292 | |||||||
| chr5:43692387 | G | A | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2877-7732G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43692387 | |||||||
| chr5:43692496 | G | C | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2877-7623G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43692496 | |||||||
| chr5:43692640 | C | T | 1 | a0001c0001t0014g0002 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2877-7479C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43692640 | |||||||
| chr5:43692641 | G | A | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2877-7478G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43692641 | |||||||
| chr5:43692749 | T | C | 3 | a0001c0002t0010g0183 a0004c0007t0010g0005 a0007c0012t0010g0046 |
3 | HG02970.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2877-7370T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43692749 | |||||||
| chr5:43693042 | A | AT | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2877-7067dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43693042 | ||||||
| chr5:43693045 | T | TA | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2877-7074_2877-707 others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43693045 | |||||||
| chr5:43693138 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2877-6981G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43693138 | |||||||
| chr5:43693324 | G | T | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2877-6795G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43693324 | |||||||
| chr5:43693402 | T | A | 1 | a0001c0001t0006g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2877-6717T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43693402 | |||||||
| chr5:43693795 | T | C | 2 | a0001c0004t0004g0118 a0001c0004t0004g0123 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2877-6324T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43693795 | |||||||
| chr5:43693799 | G | T | 1 | a0002c0003t0011g0100 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2877-6320G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43693799 | |||||||
| chr5:43693914 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2877-6205A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43693914 | |||||||
| chr5:43693998 | G | C | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2877-6121G>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43693998 | |||||||
| chr5:43694431 | C | T | 1 | a0001c0004t0021g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2877-5688C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43694431 | |||||||
| chr5:43694704 | G | A | 2 | a0001c0001t0003g0042 a0001c0002t0001g0169 |
2 | HG00597.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2877-5415G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43694704 | |||||||
| chr5:43694735 | A | AGT | 2 | a0001c0001t0001g0032 a0001c0001t0001g0085 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2877-5383_2877-538 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694735 | ||||||
| chr5:43694738 | T | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0085 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2877-5381T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43694738 | |||||||
| chr5:43694738 | T | TG | 2 | a0001c0001t0001g0030 a0001c0002t0001g0146 |
2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2877-5381_2877-538 others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43694738 | |||||||
| chr5:43694738 | T | TGTG | 2 | a0001c0001t0005g0054 a0001c0002t0001g0159 |
2 | HG01071.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2877-5381_2877-538 others(7): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43694738 | |||||||
| chr5:43694738 | T | TTG | 32 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0014 others(29): Show |
33 | HG01361.hp1 HG01993.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.2877-5339_2877-533 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694738 | T | TTGTG | 23 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0060 others(20): Show |
24 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.2877-5341_2877-533 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694738 | T | TTGTGTG | 10 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0005g0011 others(7): Show |
10 | HG01109.hp1 HG01175.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.2877-5343_2877-533 others(10): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694738 | T | TTGTGTGT others(1): Show |
12 | a0001c0001t0005g0027 a0001c0001t0006g0138 a0001c0002t0025g0139 others(9): Show |
12 | HG02071.hp1 HG02165.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.2877-5345_2877-533 others(12): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694738 | T | TTGTGTGT others(3): Show |
12 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0002t0002g0163 others(9): Show |
12 | HG00544.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.2877-5347_2877-533 others(14): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694738 | T | TTGTGTGT others(5): Show |
1 | a0002c0003t0012g0108 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2877-5349_2877-533 others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694738 | T | TTGTGTGT others(7): Show |
3 | a0002c0003t0002g0088 a0002c0003t0002g0089 a0002c0003t0012g0101 |
3 | NA18943.hp1 NA18970.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2877-5351_2877-533 others(18): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694738 | TTG | T | 8 | a0001c0002t0001g0153 a0001c0002t0001g0155 a0001c0004t0004g0129 others(5): Show |
8 | HG01167.hp2 HG02976.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2877-5339_2877-533 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694738 | TTGTG | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0070 a0001c0001t0001g0071 others(1): Show |
4 | HG02809.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2877-5341_2877-533 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694738 | TTGTGTGT others(5): Show |
T | 6 | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0114 others(3): Show |
6 | HG01243.hp1 HG01346.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2877-5349_2877-533 others(16): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43694738 | ||||||
| chr5:43694859 | G | A | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2877-5260G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43694859 | |||||||
| chr5:43694961 | T | A | 1 | a0001c0002t0001g0006 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2877-5158T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43694961 | |||||||
| chr5:43695029 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2877-5090C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43695029 | |||||||
| chr5:43695191 | C | A | 178 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(175): Show |
180 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(177): Show |
intron_variant | MODIFIER | c.2877-4928C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43695191 | |||||||
| chr5:43695309 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG06807.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2877-4810T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43695309 | |||||||
| chr5:43695339 | C | A | 26 | a0001c0001t0006g0138 a0001c0004t0004g0118 a0001c0004t0004g0120 others(23): Show |
26 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.2877-4780C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43695339 | |||||||
| chr5:43695525 | G | T | 1 | a0001c0002t0008g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2877-4594G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43695525 | |||||||
| chr5:43695809 | A | T | 1 | a0002c0003t0002g0102 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2877-4310A>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43695809 | |||||||
| chr5:43696185 | T | C | 1 | a0001c0002t0001g0006 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2877-3934T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43696185 | |||||||
| chr5:43696233 | A | G | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2877-3886A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43696233 | |||||||
| chr5:43696455 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2877-3664G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43696455 | |||||||
| chr5:43696696 | G | A | 1 | a0001c0004t0021g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2877-3423G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43696696 | |||||||
| chr5:43696753 | T | C | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2877-3366T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43696753 | |||||||
| chr5:43696946 | G | A | 3 | a0002c0003t0002g0094 a0002c0003t0002g0096 a0002c0003t0011g0097 |
3 | HG02071.hp1 NA18941.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2877-3173G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43696946 | |||||||
| chr5:43697229 | T | C | 1 | a0001c0002t0001g0156 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2877-2890T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43697229 | |||||||
| chr5:43697466 | C | G | 1 | a0001c0004t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2877-2653C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43697466 | |||||||
| chr5:43697530 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2877-2589T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43697530 | |||||||
| chr5:43697632 | G | A | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2877-2487G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43697632 | |||||||
| chr5:43697805 | C | A | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2877-2314C>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43697805 | |||||||
| chr5:43697842 | C | G | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2877-2277C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43697842 | |||||||
| chr5:43697884 | T | C | 3 | a0001c0001t0005g0011 a0001c0001t0024g0018 a0001c0001t0027g0055 |
3 | HG01074.hp2 HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2877-2235T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43697884 | |||||||
| chr5:43697972 | A | G | 7 | a0001c0005t0004g0133 a0001c0005t0004g0134 a0001c0005t0004g0135 others(4): Show |
7 | HG01167.hp2 HG02572.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2877-2147A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43697972 | |||||||
| chr5:43698061 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0002t0001g0161 |
3 | HG02723.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2877-2058G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43698061 | |||||||
| chr5:43698081 | T | C | 1 | a0001c0002t0001g0153 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2877-2038T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43698081 | |||||||
| chr5:43698081 | T | TAC | 13 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(10): Show |
14 | HG00544.hp2 HG01243.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.2877-2020_2877-201 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43698081 | ||||||
| chr5:43698081 | T | TACAC | 2 | a0001c0001t0006g0116 a0001c0001t0006g0117 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2877-2022_2877-201 others(8): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43698081 | ||||||
| chr5:43698083 | C | T | 3 | a0001c0001t0005g0027 a0001c0001t0005g0056 a0001c0004t0004g0123 |
3 | HG02615.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2877-2036C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43698083 | |||||||
| chr5:43698101 | T | C | 1 | a0001c0001t0006g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2877-2018T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43698101 | |||||||
| chr5:43698141 | T | C | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2877-1978T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43698141 | |||||||
| chr5:43698237 | C | T | 1 | a0001c0004t0004g0130 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2877-1882C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43698237 | |||||||
| chr5:43698391 | T | C | 1 | a0002c0003t0002g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2877-1728T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43698391 | |||||||
| chr5:43698512 | ATTATC | A | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2877-1602_2877-159 others(9): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43698512 | ||||||
| chr5:43698761 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2877-1358A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43698761 | |||||||
| chr5:43698897 | C | CAT | 23 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0006g0080 others(20): Show |
23 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.2877-1205_2877-120 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43698897 | ||||||
| chr5:43698897 | CAT | C | 15 | a0001c0001t0005g0011 a0001c0001t0005g0028 a0001c0001t0005g0054 others(12): Show |
16 | HG01074.hp2 HG01169.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.2877-1205_2877-120 others(6): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43698897 | ||||||
| chr5:43698983 | T | G | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2877-1136T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43698983 | |||||||
| chr5:43699191 | C | G | 7 | a0001c0004t0004g0128 a0001c0004t0007g0081 a0001c0004t0007g0082 others(4): Show |
7 | HG01109.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2877-928C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43699191 | |||||||
| chr5:43699282 | G | T | 6 | a0001c0001t0017g0038 a0001c0002t0008g0167 a0001c0002t0008g0168 others(3): Show |
6 | HG00741.hp2 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2877-837G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43699282 | |||||||
| chr5:43699353 | C | CT | 110 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
111 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.2877-748dupT | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43699353 | ||||||
| chr5:43699353 | C | CTT | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG01069.hp1 HG01070.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.2877-749_2877-748d others(4): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43699353 | ||||||
| chr5:43699353 | C | CTTT | 34 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(31): Show |
34 | HG00544.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.2877-750_2877-748d others(5): Show |
NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 43699353 | ||||||
| chr5:43699442 | C | G | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2877-677C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43699442 | |||||||
| chr5:43699452 | C | T | 2 | a0001c0001t0006g0116 a0001c0001t0006g0117 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2877-667C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43699452 | |||||||
| chr5:43699720 | G | T | 1 | a0001c0004t0026g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2877-399G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43699720 | |||||||
| chr5:43699728 | G | A | 26 | a0001c0002t0002g0163 a0001c0002t0013g0180 a0002c0003t0002g0088 others(23): Show |
26 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2877-391G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43699728 | |||||||
| chr5:43699809 | A | C | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2877-310A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 19/21 | chr5 | 43699809 | |||||||
| chr5:43700442 | T | G | 7 | a0001c0004t0004g0128 a0001c0004t0007g0081 a0001c0004t0007g0082 others(4): Show |
7 | HG01109.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2995+205T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43700442 | |||||||
| chr5:43700493 | T | A | 1 | a0001c0004t0007g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2995+256T>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43700493 | |||||||
| chr5:43700794 | C | G | 2 | a0001c0004t0004g0118 a0001c0004t0004g0123 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2995+557C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43700794 | |||||||
| chr5:43700828 | C | G | 2 | a0001c0004t0004g0118 a0001c0004t0004g0123 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2995+591C>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43700828 | |||||||
| chr5:43701019 | G | T | 24 | a0001c0004t0004g0118 a0001c0004t0004g0120 a0001c0004t0004g0121 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2995+782G>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43701019 | |||||||
| chr5:43701188 | T | C | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2995+951T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43701188 | |||||||
| chr5:43701194 | G | A | 1 | a0001c0001t0006g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2995+957G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43701194 | |||||||
| chr5:43701284 | T | C | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2995+1047T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43701284 | |||||||
| chr5:43701494 | T | C | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2996-1127T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43701494 | |||||||
| chr5:43701719 | C | T | 4 | a0001c0002t0010g0183 a0004c0007t0010g0004 a0004c0007t0010g0005 others(1): Show |
4 | HG02809.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2996-902C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43701719 | |||||||
| chr5:43702465 | T | G | 1 | a0001c0002t0001g0006 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2996-156T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43702465 | |||||||
| chr5:43702539 | A | C | 1 | a0001c0001t0003g0023 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2996-82A>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 20/21 | chr5 | 43702539 | |||||||
| chr5:43702782 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3111+46T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43702782 | |||||||
| chr5:43702785 | A | G | 30 | a0001c0002t0002g0163 a0001c0002t0010g0183 a0001c0002t0013g0180 others(27): Show |
30 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.3111+49A>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43702785 | |||||||
| chr5:43702991 | G | A | 2 | a0001c0001t0006g0138 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3111+255G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43702991 | |||||||
| chr5:43703379 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3111+643G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43703379 | |||||||
| chr5:43703512 | T | C | 9 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3112-743T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43703512 | |||||||
| chr5:43703779 | G | A | 1 | a0001c0002t0008g0168 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3112-476G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43703779 | |||||||
| chr5:43703782 | T | G | 1 | a0002c0003t0002g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3112-473T>G | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43703782 | |||||||
| chr5:43703805 | T | C | 2 | a0001c0001t0006g0072 a0001c0002t0025g0139 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3112-450T>C | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43703805 | |||||||
| chr5:43703970 | G | A | 41 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(38): Show |
42 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.3112-285G>A | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43703970 | |||||||
| chr5:43704129 | C | T | 11 | a0001c0001t0006g0080 a0001c0001t0006g0110 a0001c0001t0006g0112 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.3112-126C>T | NNT | ENSG00000112992.18 | transcript | ENST00000344920.9 | protein_coding | 21/21 | chr5 | 43704129 |