Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8439 |
| ensemblid | ENSG00000035681.9 |
| hgncid | 8017 |
| symbol | NSMAF |
| name | neutral sphingomyelinase activation associated factor |
| refseq_nuc | NM_003580.4 |
| refseq_prot | NP_003571.2 |
| ensembl_nuc | ENST00000038176.8 |
| ensembl_prot | ENSP00000038176.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 58583508 |
| end | 58659853 |
| strand | - |
| ver | v1.2 |
| region | chr8:58583508-58659853 |
| region5000 | chr8:58578508-58664853 |
| regionname0 | NSMAF_chr8_58583508_58659853 |
| regionname5000 | NSMAF_chr8_58578508_58664853 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 917 | 290 | 74 | 50 | 121 | 14 | 29 | 98 | NSMAF_chr8_58578508_58664853 | NSMAF | MAFIR others(912): Show |
chr8 | 58578508 | 58664853 |
| a0002 | 0/0 | 917 | 64 | 8 | 2 | 52 | 0 | 2 | 43 | NSMAF_chr8_58578508_58664853 | NSMAF | MAFIR others(912): Show |
chr8 | 58578508 | 58664853 |
| a0003 | 0/0 | 917 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | MAFIR others(912): Show |
chr8 | 58578508 | 58664853 |
| a0004 | 0/0 | 917 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | MAFIR others(912): Show |
chr8 | 58578508 | 58664853 |
| a0005 | 0/0 | 917 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | MAFIR others(912): Show |
chr8 | 58578508 | 58664853 |
| a0006 | 0/0 | 917 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | MAFIR others(912): Show |
chr8 | 58578508 | 58664853 |
| a0007 | 0/0 | 917 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | MAFIR others(912): Show |
chr8 | 58578508 | 58664853 |
| a0008 | 0/0 | 917 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | MAFIR others(912): Show |
chr8 | 58578508 | 58664853 |
| a0009 | 0/0 | 917 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | MAFIR others(912): Show |
chr8 | 58578508 | 58664853 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2751 | 251 | 53 | 41 | 118 | 12 | 26 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0001c0003 | 1/0 | 2751 | 28 | 15 | 6 | 2 | 2 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0001c0004 | 0/0 | 2751 | 4 | 4 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0001c0008 | 0/0 | 2751 | 2 | 0 | 1 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0001c0009 | 0/0 | 2751 | 2 | 0 | 2 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0001c0010 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0001c0011 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0001c0017 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0002c0002 | 0/0 | 2751 | 63 | 7 | 2 | 52 | 0 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0002c0013 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0003c0005 | 0/0 | 2751 | 4 | 4 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0004c0006 | 0/0 | 2751 | 3 | 0 | 0 | 3 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0005c0015 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0005c0016 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0006c0007 | 0/0 | 2751 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0007c0012 | 0/0 | 2751 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0008c0014 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 | ||
| a0009c0018 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ATGGC others(2746): Show |
chr8 | 58578508 | 58664853 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3574 | 150 | 29 | 28 | 72 | 6 | 15 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0002 | 0/1 | 3574 | 69 | 6 | 11 | 34 | 6 | 11 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0003 | 0/0 | 3574 | 11 | 10 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0004 | 0/0 | 3574 | 6 | 0 | 0 | 6 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0006 | 0/0 | 3574 | 2 | 1 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0007 | 0/0 | 3574 | 3 | 0 | 0 | 3 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0008 | 0/0 | 3574 | 3 | 3 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0010 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0011 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0012 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0013 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0014 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0015 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0001t0016 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0003t0001 | 1/0 | 3574 | 27 | 14 | 6 | 2 | 2 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0003t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0004t0001 | 0/0 | 3574 | 4 | 4 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0008t0002 | 0/0 | 3574 | 2 | 0 | 1 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0009t0001 | 0/0 | 3574 | 2 | 0 | 2 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0010t0006 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0011t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0001c0017t0001 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0002c0002t0001 | 0/0 | 3574 | 50 | 6 | 2 | 40 | 0 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0002c0002t0002 | 0/0 | 3574 | 2 | 1 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0002c0002t0004 | 0/0 | 3574 | 6 | 0 | 0 | 6 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0002c0002t0005 | 0/0 | 3574 | 5 | 0 | 0 | 5 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0002c0013t0001 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0003c0005t0001 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0003c0005t0002 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0003c0005t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0003c0005t0009 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0004c0006t0001 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0004c0006t0002 | 0/0 | 3574 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0005c0015t0009 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0005c0016t0006 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0006c0007t0001 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0006c0007t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0007c0012t0001 | 0/0 | 3574 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0008c0014t0001 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| a0009c0018t0002 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | ACGGT others(3569): Show |
chr8 | 58578508 | 58664853 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0319 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0012g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0013g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0014g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0016g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0008t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0008t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0009t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0009t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0010t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0011t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0017t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0005g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0013t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0003c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0003c0005t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0003c0005t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0003c0005t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0004c0006t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0004c0006t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0004c0006t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0005c0015t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0005c0016t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0006c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0006c0007t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0007c0012t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0008c0014t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0009c0018t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0012 | EUR | GBR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0322 | EUR | GBR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0306 | EUR | GBR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | FIN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00408 | hp1 | a0004 | c0006 | t0002 | g0346 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00597 | hp2 | a0001 | c0017 | t0001 | g0128 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0086 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01070 | hp2 | a0001 | c0009 | t0001 | g0251 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01071 | hp1 | a0001 | c0009 | t0001 | g0252 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0259 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0333 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0174 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | IBS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0317 | EUR | IBS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0305 | EUR | IBS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0135 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0258 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0300 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01993 | hp1 | a0001 | c0008 | t0002 | g0316 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02071 | hp2 | a0001 | c0001 | t0013 | g0158 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02074 | hp1 | a0004 | c0006 | t0001 | g0344 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02080 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0341 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0271 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02572 | hp1 | a0005 | c0016 | t0006 | g0102 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0051 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02622 | hp1 | a0002 | c0013 | t0001 | g0197 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0202 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0193 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0113 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0299 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02738 | hp1 | a0001 | c0008 | t0002 | g0315 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0085 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02818 | hp2 | a0001 | c0011 | t0003 | g0050 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0210 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0039 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02976 | hp2 | a0001 | c0001 | t0014 | g0260 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0339 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0218 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0106 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03130 | hp1 | a0001 | c0010 | t0006 | g0112 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03130 | hp2 | a0003 | c0005 | t0009 | g0035 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0110 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0042 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0211 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0116 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03540 | hp1 | a0006 | c0007 | t0001 | g0103 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0111 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03579 | hp2 | a0003 | c0005 | t0003 | g0044 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0338 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04204 | hp1 | a0007 | c0012 | t0001 | g0294 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18747 | hp1 | a0002 | c0002 | t0004 | g0026 | EAS | CHB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | CHB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18906 | hp2 | a0003 | c0005 | t0001 | g0212 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18945 | hp2 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18952 | hp1 | a0004 | c0006 | t0002 | g0345 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0020 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18961 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18973 | hp1 | a0001 | c0001 | t0015 | g0131 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18985 | hp1 | a0008 | c0014 | t0001 | g0140 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18987 | hp1 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18990 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18992 | hp2 | a0002 | c0002 | t0004 | g0023 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18995 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | LWK | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19055 | hp1 | a0002 | c0002 | t0005 | g0018 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19057 | hp1 | a0009 | c0018 | t0002 | g0120 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19072 | hp1 | a0002 | c0002 | t0005 | g0019 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19083 | hp2 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19086 | hp1 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ASW | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ASW | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0309 | EUR | TSI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | TSI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | TSI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | GIH | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | GIH | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0298 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0037 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0264 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03471 | hp1 | a0005 | c0015 | t0009 | g0034 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20300 | hp1 | a0003 | c0005 | t0002 | g0207 | AFR | USA | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | USA | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA21309 | hp2 | a0006 | c0007 | t0003 | g0038 | AFR | LWK | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0319 | REF | REF | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0293 | REF | REF | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58587638 | C | T | 1 | a0007 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2275G>A | p.Glu759Lys | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/31 | 2497/3574 | 2275/2754 | 759/917 | chr8 | 58587638 | |||
| chr8:58589547 | G | A | 1 | a0008 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.2116C>T | p.Arg706Cys | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/31 | 2338/3574 | 2116/2754 | 706/917 | chr8 | 58589547 | |||
| chr8:58595575 | T | C | 2 | a0002 a0008 |
65 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
missense_variant | MODERATE | c.1877A>G | p.Tyr626Cys | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/31 | 2099/3574 | 1877/2754 | 626/917 | chr8 | 58595575 | |||
| chr8:58599358 | C | T | 1 | a0006 | 2 | HG03540.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1459G>A | p.Glu487Lys | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/31 | 1681/3574 | 1459/2754 | 487/917 | chr8 | 58599358 | |||
| chr8:58599762 | G | C | 1 | a0005 | 2 | HG02572.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.1441C>G | p.Pro481Ala | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/31 | 1663/3574 | 1441/2754 | 481/917 | chr8 | 58599762 | |||
| chr8:58603374 | G | A | 1 | a0003 | 4 | HG03130.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
missense_variant | MODERATE | c.881C>T | p.Ala294Val | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/31 | 1103/3574 | 881/2754 | 294/917 | chr8 | 58603374 | |||
| chr8:58631527 | T | C | 1 | a0009 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.353A>G | p.His118Arg | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/31 | 575/3574 | 353/2754 | 118/917 | chr8 | 58631527 | |||
| chr8:58659589 | G | C | 1 | a0004 | 3 | HG00408.hp1 HG02074.hp1 NA18952.hp1 |
missense_variant | MODERATE | c.43C>G | p.Leu15Val | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 265/3574 | 43/2754 | 15/917 | chr8 | 58659589 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58589470 | C | T | 2 | a0001c0004 a0005c0015 |
5 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.2193G>A | p.Ser731Ser | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/31 | 2415/3574 | 2193/2754 | 731/917 | chr8 | 58589470 | |||
| chr8:58589518 | A | G | 1 | a0002c0013 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.2145T>C | p.Asp715Asp | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/31 | 2367/3574 | 2145/2754 | 715/917 | chr8 | 58589518 | |||
| chr8:58595607 | A | G | 1 | a0001c0008 | 2 | HG01993.hp1 HG02738.hp1 |
synonymous_variant | LOW | c.1845T>C | p.Asn615Asn | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/31 | 2067/3574 | 1845/2754 | 615/917 | chr8 | 58595607 | |||
| chr8:58597505 | C | T | 2 | a0001c0010 a0001c0011 |
2 | HG02818.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.1674G>A | p.Leu558Leu | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/31 | 1896/3574 | 1674/2754 | 558/917 | chr8 | 58597505 | |||
| chr8:58599775 | G | A | 16 | a0001c0001 a0001c0004 a0001c0008 others(13): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
synonymous_variant | LOW | c.1428C>T | p.Asp476Asp | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/31 | 1650/3574 | 1428/2754 | 476/917 | chr8 | 58599775 | |||
| chr8:58606005 | G | A | 1 | a0001c0017 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.790C>T | p.Leu264Leu | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/31 | 1012/3574 | 790/2754 | 264/917 | chr8 | 58606005 | |||
| chr8:58609655 | G | A | 1 | a0001c0009 | 2 | HG01070.hp2 HG01071.hp1 |
synonymous_variant | LOW | c.636C>T | p.His212His | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/31 | 858/3574 | 636/2754 | 212/917 | chr8 | 58609655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58583565 | C | G | 1 | a0001c0001t0014 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 541 | chr8 | 58583565 | ||||||
| chr8:58583817 | A | C | 3 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0016 |
5 | HG02615.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*289T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 289 | chr8 | 58583817 | ||||||
| chr8:58583857 | C | T | 11 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(8): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*249G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 249 | chr8 | 58583857 | ||||||
| chr8:58583927 | G | A | 1 | a0001c0001t0015 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*179C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 179 | chr8 | 58583927 | ||||||
| chr8:58583931 | A | G | 14 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(11): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*175T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 175 | chr8 | 58583931 | ||||||
| chr8:58584004 | C | T | 1 | a0001c0001t0013 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 102 | chr8 | 58584004 | ||||||
| chr8:58659752 | G | T | 2 | a0003c0005t0009 a0005c0015t0009 |
2 | HG03130.hp2 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-121C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 121 | chr8 | 58659752 | ||||||
| chr8:58659781 | G | T | 10 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0011 others(7): Show |
22 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-150C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 150 | chr8 | 58659781 | ||||||
| chr8:58659797 | C | T | 3 | a0001c0001t0004 a0001c0001t0007 a0002c0002t0004 |
15 | HG02080.hp1 NA18747.hp1 NA18747.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-166G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 166 | chr8 | 58659797 | ||||||
| chr8:58659821 | A | G | 2 | a0001c0001t0010 a0002c0002t0005 |
6 | NA18960.hp1 NA18961.hp1 NA18990.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-190T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 190 | chr8 | 58659821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58584375 | C | T | 78 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0001c0001t0001g0104 others(75): Show |
85 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.2660-175G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584375 | |||||||
| chr8:58584510 | C | CAAAAGTT others(346): Show |
1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2660-311_2660-310i others(355): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584510 | |||||||
| chr8:58584782 | G | A | 1 | a0002c0002t0001g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2660-582C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584782 | |||||||
| chr8:58584812 | G | A | 88 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(85): Show |
89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2660-612C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584812 | |||||||
| chr8:58584836 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2660-636C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584836 | |||||||
| chr8:58584838 | T | C | 1 | a0001c0001t0002g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2660-638A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584838 | |||||||
| chr8:58584940 | G | T | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2659+712C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584940 | |||||||
| chr8:58585185 | T | G | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2659+467A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585185 | |||||||
| chr8:58585266 | G | A | 3 | a0001c0001t0001g0136 a0003c0005t0001g0212 a0003c0005t0009g0035 |
3 | HG02451.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2659+386C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585266 | |||||||
| chr8:58585302 | T | C | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2659+350A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585302 | |||||||
| chr8:58585317 | G | GT | 31 | a0001c0001t0001g0014 a0001c0001t0001g0069 a0001c0001t0001g0121 others(28): Show |
32 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.2659+334dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | |||||||
| chr8:58585317 | G | GTTATTTT others(7): Show |
1 | a0001c0003t0001g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2659+334_2659+335i others(16): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | |||||||
| chr8:58585317 | G | GTTATTTT others(8): Show |
9 | a0001c0001t0001g0138 a0001c0003t0001g0010 a0001c0003t0001g0105 others(6): Show |
10 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2659+334_2659+335i others(17): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | |||||||
| chr8:58585317 | G | GTTATTTT others(9): Show |
1 | a0001c0003t0001g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2659+334_2659+335i others(18): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | |||||||
| chr8:58585317 | G | GTTTTTTT others(3): Show |
3 | a0001c0004t0001g0135 a0001c0004t0001g0202 a0001c0004t0001g0210 |
3 | HG01884.hp2 HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2659+325_2659+334d others(12): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | |||||||
| chr8:58585317 | G | GTTTTTTT others(5): Show |
1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2659+323_2659+334d others(14): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | |||||||
| chr8:58585317 | G | GTTTTTTT others(6): Show |
1 | a0005c0015t0009g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2659+334_2659+335i others(15): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | |||||||
| chr8:58585347 | T | C | 1 | a0001c0008t0002g0316 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2659+305A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585347 | |||||||
| chr8:58585564 | CAA | C | 11 | a0001c0001t0001g0138 a0001c0003t0001g0010 a0001c0003t0001g0105 others(8): Show |
12 | HG01884.hp1 HG02145.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2659+86_2659+87del others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585564 | |||||||
| chr8:58585631 | G | A | 193 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0093 others(190): Show |
202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.2659+21C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585631 | |||||||
| chr8:58585855 | A | T | 78 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0001c0001t0001g0104 others(75): Show |
85 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.2549+43T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 29/30 | chr8 | 58585855 | |||||||
| chr8:58585861 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2549+37C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 29/30 | chr8 | 58585861 | |||||||
| chr8:58585874 | C | T | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2549+24G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 29/30 | chr8 | 58585874 | |||||||
| chr8:58586035 | A | G | 11 | a0001c0001t0001g0138 a0001c0003t0001g0010 a0001c0003t0001g0105 others(8): Show |
12 | HG01884.hp1 HG02145.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2447-35T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586035 | |||||||
| chr8:58586049 | G | T | 5 | a0001c0001t0008g0036 a0001c0001t0008g0041 a0001c0001t0008g0051 others(2): Show |
5 | HG02615.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2447-49C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586049 | |||||||
| chr8:58586055 | A | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0093 others(187): Show |
199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2447-55T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586055 | |||||||
| chr8:58586115 | A | T | 1 | a0001c0003t0001g0258 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2447-115T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586115 | |||||||
| chr8:58586126 | T | G | 68 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(65): Show |
69 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.2447-126A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586126 | |||||||
| chr8:58586156 | T | A | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2447-156A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586156 | |||||||
| chr8:58586181 | A | C | 5 | a0001c0004t0001g0116 a0001c0004t0001g0135 a0001c0004t0001g0202 others(2): Show |
5 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2447-181T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586181 | |||||||
| chr8:58586209 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 |
3 | HG01109.hp1 HG02886.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2447-209A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586209 | |||||||
| chr8:58586215 | T | C | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2447-215A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586215 | |||||||
| chr8:58586439 | T | TAAAAAGG others(311): Show |
5 | a0001c0004t0001g0116 a0001c0004t0001g0135 a0001c0004t0001g0202 others(2): Show |
5 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2446+18_2446+19ins others(318): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586439 | |||||||
| chr8:58586439 | T | TAAAAAGG others(314): Show |
10 | a0001c0001t0001g0138 a0001c0003t0001g0010 a0001c0003t0001g0106 others(7): Show |
11 | HG01884.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2446+18_2446+19ins others(321): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586439 | |||||||
| chr8:58586439 | T | TAAAAAGG others(315): Show |
1 | a0001c0003t0001g0105 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2446+18_2446+19ins others(322): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586439 | |||||||
| chr8:58586678 | G | A | 85 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(82): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2296-70C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58586678 | |||||||
| chr8:58586731 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2296-123C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58586731 | |||||||
| chr8:58586830 | T | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
127 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2296-222A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58586830 | |||||||
| chr8:58587204 | C | G | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2295+414G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58587204 | |||||||
| chr8:58587558 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2295+60G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58587558 | |||||||
| chr8:58587564 | G | A | 1 | a0002c0002t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2295+54C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58587564 | |||||||
| chr8:58587574 | A | T | 1 | a0002c0002t0004g0024 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2295+44T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58587574 | |||||||
| chr8:58588160 | C | T | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2212-459G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588160 | |||||||
| chr8:58588228 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2212-527C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588228 | |||||||
| chr8:58588334 | CT | C | 83 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0001c0001t0001g0104 others(80): Show |
90 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.2212-634delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588334 | |||||||
| chr8:58588367 | A | T | 84 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(81): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2212-666T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588367 | |||||||
| chr8:58588466 | T | C | 84 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(81): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2212-765A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588466 | |||||||
| chr8:58588578 | A | C | 84 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(81): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2211+874T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588578 | |||||||
| chr8:58588588 | A | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0093 others(187): Show |
199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2211+864T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588588 | |||||||
| chr8:58588634 | A | G | 2 | a0006c0007t0001g0103 a0006c0007t0003g0038 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2211+818T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588634 | |||||||
| chr8:58588677 | T | G | 1 | a0001c0003t0001g0341 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2211+775A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588677 | |||||||
| chr8:58588700 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2211+752G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588700 | |||||||
| chr8:58588713 | C | A | 1 | a0009c0018t0002g0120 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2211+739G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588713 | |||||||
| chr8:58588714 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01167.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2211+738C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588714 | |||||||
| chr8:58588724 | C | A | 83 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(80): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.2211+728G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588724 | |||||||
| chr8:58588725 | C | A | 1 | a0001c0001t0002g0337 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2211+727G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588725 | |||||||
| chr8:58588755 | T | C | 11 | a0001c0001t0001g0138 a0001c0003t0001g0010 a0001c0003t0001g0105 others(8): Show |
12 | HG01884.hp1 HG02145.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2211+697A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588755 | |||||||
| chr8:58588824 | A | G | 6 | a0001c0001t0001g0069 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02074.hp2 NA18963.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2211+628T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588824 | |||||||
| chr8:58588903 | C | T | 1 | a0001c0003t0001g0105 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2211+549G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588903 | |||||||
| chr8:58589028 | A | T | 4 | a0002c0002t0001g0011 a0002c0002t0001g0222 a0002c0002t0004g0006 others(1): Show |
6 | NA18943.hp1 NA18945.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.2211+424T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589028 | |||||||
| chr8:58589208 | T | A | 84 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(81): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2211+244A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589208 | |||||||
| chr8:58589256 | G | A | 190 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0093 others(187): Show |
199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2211+196C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589256 | |||||||
| chr8:58589304 | G | A | 84 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(81): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2211+148C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589304 | |||||||
| chr8:58589403 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0273 |
2 | HG00621.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2211+49A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589403 | |||||||
| chr8:58589414 | A | G | 1 | a0005c0015t0009g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2211+38T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589414 | |||||||
| chr8:58589722 | C | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 |
3 | HG01109.hp1 HG02886.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2088-147G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589722 | |||||||
| chr8:58589745 | A | T | 1 | a0001c0001t0002g0275 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2088-170T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589745 | |||||||
| chr8:58589808 | C | G | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2087+199G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589808 | |||||||
| chr8:58589908 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2087+99C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589908 | |||||||
| chr8:58589976 | G | A | 12 | a0001c0001t0002g0052 a0001c0001t0002g0099 a0001c0001t0002g0100 others(9): Show |
12 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2087+31C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589976 | |||||||
| chr8:58590107 | A | C | 1 | a0001c0001t0002g0275 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2020-33T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590107 | |||||||
| chr8:58590202 | A | G | 3 | a0001c0001t0001g0136 a0003c0005t0001g0212 a0003c0005t0009g0035 |
3 | HG02451.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2020-128T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590202 | |||||||
| chr8:58590366 | T | C | 84 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0015 others(81): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2020-292A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590366 | |||||||
| chr8:58590657 | C | A | 3 | a0001c0001t0006g0053 a0001c0001t0006g0086 a0001c0010t0006g0112 |
3 | HG00741.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2019+210G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590657 | |||||||
| chr8:58590766 | A | G | 1 | a0002c0002t0001g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2019+101T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590766 | |||||||
| chr8:58590783 | G | A | 5 | a0001c0004t0001g0116 a0001c0004t0001g0135 a0001c0004t0001g0202 others(2): Show |
5 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019+84C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590783 | |||||||
| chr8:58591082 | G | T | 1 | a0001c0001t0001g0267 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1952-148C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591082 | |||||||
| chr8:58591150 | A | G | 1 | a0002c0002t0001g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1952-216T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591150 | |||||||
| chr8:58591210 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1952-276G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591210 | |||||||
| chr8:58591248 | G | A | 3 | a0001c0001t0006g0053 a0001c0001t0006g0086 a0001c0010t0006g0112 |
3 | HG00741.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1952-314C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591248 | |||||||
| chr8:58591268 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1952-334A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591268 | |||||||
| chr8:58591279 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1952-345T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591279 | |||||||
| chr8:58591430 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1952-496C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591430 | |||||||
| chr8:58591471 | A | T | 4 | a0001c0004t0001g0116 a0001c0004t0001g0135 a0001c0004t0001g0202 others(1): Show |
4 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1952-537T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591471 | |||||||
| chr8:58591481 | C | CT | 102 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0081 others(99): Show |
113 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.1952-548dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591481 | |||||||
| chr8:58591481 | C | CTT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0101 others(16): Show |
20 | HG00423.hp1 HG00558.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1952-549_1952-548d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591481 | |||||||
| chr8:58591481 | CT | C | 21 | a0001c0001t0001g0171 a0001c0001t0001g0208 a0001c0001t0001g0233 others(18): Show |
21 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1952-548delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591481 | |||||||
| chr8:58591788 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1952-854G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591788 | |||||||
| chr8:58591893 | C | T | 59 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(56): Show |
65 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1952-959G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591893 | |||||||
| chr8:58592350 | G | A | 1 | a0002c0002t0004g0024 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1952-1416C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592350 | |||||||
| chr8:58592352 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0273 |
2 | HG00621.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1952-1418G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592352 | |||||||
| chr8:58592466 | T | C | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1952-1532A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592466 | |||||||
| chr8:58592565 | GA | G | 330 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(327): Show |
351 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.1952-1632delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592565 | |||||||
| chr8:58592707 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1951+1525C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592707 | |||||||
| chr8:58592746 | G | C | 1 | a0001c0001t0011g0039 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1951+1486C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592746 | |||||||
| chr8:58592763 | T | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0306 |
2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1951+1469A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592763 | |||||||
| chr8:58592805 | T | C | 1 | a0001c0001t0002g0180 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1951+1427A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592805 | |||||||
| chr8:58592819 | G | A | 188 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(185): Show |
198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1951+1413C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592819 | |||||||
| chr8:58592902 | C | CA | 9 | a0001c0001t0002g0052 a0001c0001t0002g0099 a0001c0001t0002g0199 others(6): Show |
9 | HG00408.hp1 HG01891.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1951+1329dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592902 | |||||||
| chr8:58592906 | AAC | A | 3 | a0003c0005t0001g0212 a0003c0005t0002g0207 a0003c0005t0009g0035 |
3 | HG03130.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1951+1324_1951+132 others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592906 | |||||||
| chr8:58592908 | C | A | 16 | a0001c0001t0001g0138 a0001c0001t0002g0052 a0001c0001t0002g0099 others(13): Show |
16 | HG00408.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1951+1324G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592908 | |||||||
| chr8:58592909 | AAC | A | 139 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(136): Show |
147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1951+1321_1951+132 others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592909 | |||||||
| chr8:58592910 | AC | A | 42 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0104 others(39): Show |
44 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1951+1321delG | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592910 | |||||||
| chr8:58592911 | C | A | 25 | a0001c0001t0001g0138 a0001c0001t0002g0052 a0001c0001t0002g0099 others(22): Show |
25 | HG00408.hp1 HG00735.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1951+1321G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592911 | |||||||
| chr8:58592913 | A | C | 2 | a0006c0007t0001g0103 a0006c0007t0003g0038 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1951+1319T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592913 | |||||||
| chr8:58592914 | C | A | 75 | a0001c0001t0001g0138 a0001c0001t0002g0052 a0001c0001t0002g0099 others(72): Show |
81 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1951+1318G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592914 | |||||||
| chr8:58592915 | AAC | A | 38 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0104 others(35): Show |
40 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1951+1315_1951+131 others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592915 | |||||||
| chr8:58592916 | AC | A | 88 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(85): Show |
90 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1951+1315delG | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592916 | |||||||
| chr8:58592917 | C | A | 80 | a0001c0001t0001g0138 a0001c0001t0002g0052 a0001c0001t0002g0099 others(77): Show |
86 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1951+1315G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592917 | |||||||
| chr8:58592919 | A | C | 85 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(82): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1951+1313T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592919 | |||||||
| chr8:58592923 | A | C | 1 | a0002c0002t0001g0222 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1951+1309T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592923 | |||||||
| chr8:58592940 | T | G | 3 | a0001c0001t0001g0104 a0001c0001t0003g0007 a0001c0001t0003g0043 |
4 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1951+1292A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592940 | |||||||
| chr8:58593092 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1951+1140T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593092 | |||||||
| chr8:58593123 | T | C | 11 | a0001c0001t0002g0052 a0001c0001t0002g0099 a0001c0001t0002g0100 others(8): Show |
11 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1951+1109A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593123 | |||||||
| chr8:58593453 | C | A | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1951+779G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593453 | |||||||
| chr8:58593473 | T | G | 206 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(203): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1951+759A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593473 | |||||||
| chr8:58593544 | C | T | 5 | a0001c0001t0001g0138 a0001c0004t0001g0116 a0001c0004t0001g0135 others(2): Show |
5 | HG01884.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1951+688G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593544 | |||||||
| chr8:58593570 | A | G | 206 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(203): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1951+662T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593570 | |||||||
| chr8:58593592 | T | C | 5 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0256 others(2): Show |
5 | NA18747.hp2 NA18954.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951+640A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593592 | |||||||
| chr8:58593624 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1951+608A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593624 | |||||||
| chr8:58593628 | G | A | 206 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(203): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1951+604C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593628 | |||||||
| chr8:58593675 | A | G | 17 | a0001c0001t0002g0052 a0001c0001t0002g0099 a0001c0001t0002g0100 others(14): Show |
17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1951+557T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593675 | |||||||
| chr8:58593936 | C | G | 17 | a0001c0001t0002g0052 a0001c0001t0002g0099 a0001c0001t0002g0100 others(14): Show |
17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1951+296G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593936 | |||||||
| chr8:58594114 | A | G | 2 | a0006c0007t0001g0103 a0006c0007t0003g0038 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1951+118T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58594114 | |||||||
| chr8:58594142 | C | A | 1 | a0001c0001t0002g0250 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1951+90G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58594142 | |||||||
| chr8:58594209 | G | A | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1951+23C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58594209 | |||||||
| chr8:58594215 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1951+17G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58594215 | |||||||
| chr8:58594355 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1893-65A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594355 | |||||||
| chr8:58594412 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0001t0003g0007 others(2): Show |
6 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1893-122G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594412 | |||||||
| chr8:58594566 | G | A | 17 | a0001c0001t0002g0052 a0001c0001t0002g0099 a0001c0001t0002g0100 others(14): Show |
17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1893-276C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594566 | |||||||
| chr8:58594595 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0003g0007 a0001c0001t0003g0043 |
4 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-305C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594595 | |||||||
| chr8:58594636 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1893-346G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594636 | |||||||
| chr8:58594680 | AATG | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0126 a0001c0001t0001g0302 |
3 | NA19060.hp1 NA19080.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1893-393_1893-391d others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594680 | |||||||
| chr8:58594796 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0104 a0001c0001t0001g0173 others(26): Show |
34 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.1893-506A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594796 | |||||||
| chr8:58594912 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(54): Show |
63 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1893-622C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594912 | |||||||
| chr8:58595114 | A | ATTG | 17 | a0001c0001t0002g0052 a0001c0001t0002g0099 a0001c0001t0002g0100 others(14): Show |
17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1892+445_1892+446i others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595114 | |||||||
| chr8:58595226 | C | T | 1 | a0001c0001t0002g0306 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1892+334G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595226 | |||||||
| chr8:58595313 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1892+247A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595313 | |||||||
| chr8:58595391 | A | C | 186 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(183): Show |
196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1892+169T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595391 | |||||||
| chr8:58595517 | A | G | 201 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(198): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1892+43T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595517 | |||||||
| chr8:58595685 | CT | C | 85 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(82): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1793-27delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58595685 | |||||||
| chr8:58595781 | T | C | 2 | a0001c0001t0002g0256 a0001c0001t0007g0030 |
2 | NA18747.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1793-122A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58595781 | |||||||
| chr8:58595816 | C | T | 186 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(183): Show |
196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1793-157G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58595816 | |||||||
| chr8:58595874 | G | C | 59 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0055 others(56): Show |
65 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1793-215C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58595874 | |||||||
| chr8:58596021 | C | T | 17 | a0001c0001t0002g0052 a0001c0001t0002g0099 a0001c0001t0002g0100 others(14): Show |
17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1793-362G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596021 | |||||||
| chr8:58596185 | A | T | 1 | a0001c0001t0007g0029 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1793-526T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596185 | |||||||
| chr8:58596288 | T | C | 59 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0055 others(56): Show |
65 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1793-629A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596288 | |||||||
| chr8:58596404 | A | G | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1793-745T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596404 | |||||||
| chr8:58596428 | T | C | 13 | a0001c0001t0002g0052 a0001c0001t0002g0099 a0001c0001t0002g0100 others(10): Show |
13 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1793-769A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596428 | |||||||
| chr8:58596430 | G | C | 6 | a0001c0001t0001g0253 a0001c0001t0008g0036 a0001c0001t0008g0041 others(3): Show |
6 | HG02615.hp2 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1793-771C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596430 | |||||||
| chr8:58596564 | G | C | 2 | a0006c0007t0001g0103 a0006c0007t0003g0038 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1792+823C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596564 | |||||||
| chr8:58596796 | C | T | 55 | a0001c0001t0001g0240 a0002c0002t0001g0001 a0002c0002t0001g0011 others(52): Show |
61 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1792+591G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596796 | |||||||
| chr8:58596844 | C | T | 1 | a0001c0001t0006g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1792+543G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596844 | |||||||
| chr8:58596868 | T | C | 1 | a0001c0001t0002g0336 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1792+519A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596868 | |||||||
| chr8:58596925 | C | A | 1 | a0005c0015t0009g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1792+462G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596925 | |||||||
| chr8:58596930 | C | CA | 6 | a0001c0001t0002g0181 a0001c0001t0002g0255 a0001c0001t0002g0306 others(3): Show |
6 | HG00140.hp2 HG00642.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+456dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596930 | |||||||
| chr8:58596930 | CA | C | 19 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(16): Show |
19 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1792+456delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596930 | |||||||
| chr8:58597034 | G | T | 6 | a0001c0001t0001g0253 a0001c0001t0008g0036 a0001c0001t0008g0041 others(3): Show |
6 | HG02615.hp2 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792+353C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597034 | |||||||
| chr8:58597128 | C | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0278 a0001c0001t0013g0158 |
3 | HG00673.hp2 HG02071.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1792+259G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597128 | |||||||
| chr8:58597141 | G | T | 1 | a0001c0001t0007g0029 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1792+246C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597141 | |||||||
| chr8:58597156 | T | C | 15 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(12): Show |
15 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1792+231A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597156 | |||||||
| chr8:58597261 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1792+126A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597261 | |||||||
| chr8:58597305 | C | T | 2 | a0001c0003t0001g0299 a0001c0003t0001g0339 |
2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1792+82G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597305 | |||||||
| chr8:58597326 | A | T | 3 | a0001c0001t0002g0088 a0001c0001t0002g0090 a0001c0001t0002g0092 |
3 | NA18969.hp2 NA18970.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1792+61T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597326 | |||||||
| chr8:58597553 | T | A | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.1629-3A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597553 | |||||||
| chr8:58597575 | C | T | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1629-25G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597575 | |||||||
| chr8:58597646 | C | T | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1629-96G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597646 | |||||||
| chr8:58597701 | C | A | 2 | a0006c0007t0001g0103 a0006c0007t0003g0038 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1629-151G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597701 | |||||||
| chr8:58597785 | A | G | 1 | a0002c0002t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1628+75T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597785 | |||||||
| chr8:58597917 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1586-15G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58597917 | |||||||
| chr8:58598102 | T | G | 2 | a0002c0002t0001g0065 a0002c0002t0005g0018 |
2 | NA18955.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1586-200A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598102 | |||||||
| chr8:58598309 | T | C | 146 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(143): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1586-407A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598309 | |||||||
| chr8:58598353 | T | A | 2 | a0006c0007t0001g0103 a0006c0007t0003g0038 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1586-451A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598353 | |||||||
| chr8:58598490 | CA | C | 63 | a0001c0001t0001g0089 a0001c0001t0001g0129 a0001c0001t0001g0130 others(60): Show |
64 | HG00408.hp2 HG00673.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1586-589delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | |||||||
| chr8:58598490 | CAAA | C | 13 | a0001c0001t0001g0138 a0001c0001t0001g0253 a0001c0001t0006g0053 others(10): Show |
13 | HG00741.hp2 HG01884.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1586-591_1586-589d others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | |||||||
| chr8:58598490 | CAAAA | C | 8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(5): Show |
8 | HG01069.hp1 HG01192.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1586-592_1586-589d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | |||||||
| chr8:58598490 | CAAAAAAA others(1): Show |
C | 59 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0055 others(56): Show |
65 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1586-596_1586-589d others(10): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | |||||||
| chr8:58598490 | CAAAAAAA others(7): Show |
C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
147 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1586-602_1586-589d others(16): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | |||||||
| chr8:58598506 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1586-604T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598506 | |||||||
| chr8:58598567 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0142 others(12): Show |
17 | HG00438.hp2 HG00609.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.1585+665C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598567 | |||||||
| chr8:58598570 | C | T | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1585+662G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598570 | |||||||
| chr8:58598591 | T | C | 1 | a0001c0001t0006g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1585+641A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598591 | |||||||
| chr8:58598687 | A | G | 314 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(311): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1585+545T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598687 | |||||||
| chr8:58598751 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1585+481T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598751 | |||||||
| chr8:58598824 | A | G | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1585+408T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598824 | |||||||
| chr8:58598849 | C | CCT | 314 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(311): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1585+382_1585+383i others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598849 | |||||||
| chr8:58598854 | C | T | 15 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(12): Show |
15 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1585+378G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598854 | |||||||
| chr8:58598861 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1585+371T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598861 | |||||||
| chr8:58598987 | C | T | 15 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(12): Show |
15 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1585+245G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598987 | |||||||
| chr8:58599075 | G | A | 1 | a0001c0003t0001g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1585+157C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58599075 | |||||||
| chr8:58599178 | A | G | 1 | a0002c0002t0001g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1585+54T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58599178 | |||||||
| chr8:58599197 | C | T | 146 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(143): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1585+35G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58599197 | |||||||
| chr8:58599535 | G | T | 1 | a0001c0001t0002g0180 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1454-172C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/30 | chr8 | 58599535 | |||||||
| chr8:58599684 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1453+66T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/30 | chr8 | 58599684 | |||||||
| chr8:58599685 | A | T | 11 | a0001c0001t0001g0138 a0001c0001t0001g0253 a0001c0001t0008g0036 others(8): Show |
11 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1453+65T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/30 | chr8 | 58599685 | |||||||
| chr8:58599881 | C | T | 13 | a0001c0003t0001g0010 a0001c0003t0001g0105 a0001c0003t0001g0106 others(10): Show |
14 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1333-11G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 17/30 | chr8 | 58599881 | |||||||
| chr8:58600085 | T | A | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1281-64A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600085 | |||||||
| chr8:58600241 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1281-220C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600241 | |||||||
| chr8:58600253 | G | A | 2 | a0006c0007t0001g0103 a0006c0007t0003g0038 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1281-232C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600253 | |||||||
| chr8:58600396 | G | A | 159 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(156): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1281-375C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600396 | |||||||
| chr8:58600442 | G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1281-421C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600442 | |||||||
| chr8:58600452 | A | G | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1281-431T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600452 | |||||||
| chr8:58600484 | G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1281-463C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600484 | |||||||
| chr8:58600585 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0001t0003g0007 others(2): Show |
6 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281-564C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600585 | |||||||
| chr8:58600621 | C | CA | 23 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0134 others(20): Show |
24 | HG00323.hp1 HG00609.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1281-601dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | |||||||
| chr8:58600621 | C | CAA | 92 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(89): Show |
94 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1281-602_1281-601d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | |||||||
| chr8:58600621 | C | CAAA | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(20): Show |
23 | HG00423.hp2 HG01069.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1281-603_1281-601d others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | |||||||
| chr8:58600621 | C | CAAAA | 36 | a0001c0001t0001g0176 a0001c0001t0001g0226 a0001c0001t0002g0337 others(33): Show |
42 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1281-604_1281-601d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | |||||||
| chr8:58600621 | C | CAAAAA | 16 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(13): Show |
16 | HG00558.hp2 HG00741.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1281-605_1281-601d others(7): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | |||||||
| chr8:58600621 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1281-611_1281-601d others(13): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | |||||||
| chr8:58600633 | A | T | 4 | a0003c0005t0001g0212 a0003c0005t0002g0207 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281-612T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600633 | |||||||
| chr8:58600639 | A | AAAAAAAA others(6): Show |
4 | a0003c0005t0001g0212 a0003c0005t0002g0207 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281-619_1281-618i others(15): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600639 | |||||||
| chr8:58600768 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1280+517C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600768 | |||||||
| chr8:58600770 | G | GTAA | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
147 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1280+514_1280+515i others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600770 | |||||||
| chr8:58601154 | A | T | 1 | a0004c0006t0001g0344 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1280+131T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58601154 | |||||||
| chr8:58601234 | A | C | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1280+51T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58601234 | |||||||
| chr8:58601546 | G | GA | 17 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0182 others(14): Show |
17 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1126-12dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601546 | |||||||
| chr8:58601546 | G | GAA | 30 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0104 others(27): Show |
32 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1126-13_1126-12dup others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601546 | |||||||
| chr8:58601546 | G | GAAA | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1126-14_1126-12dup others(3): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601546 | |||||||
| chr8:58601546 | G | GAAAA | 7 | a0001c0001t0001g0139 a0001c0001t0001g0185 a0001c0001t0001g0230 others(4): Show |
7 | HG00735.hp1 HG03688.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126-15_1126-12dup others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601546 | |||||||
| chr8:58601626 | A | C | 2 | a0002c0002t0001g0196 a0002c0002t0002g0264 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1126-91T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601626 | |||||||
| chr8:58601799 | T | C | 2 | a0006c0007t0001g0103 a0006c0007t0003g0038 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1125+259A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601799 | |||||||
| chr8:58601961 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1125+97A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601961 | |||||||
| chr8:58601976 | G | A | 58 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0055 others(55): Show |
64 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1125+82C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601976 | |||||||
| chr8:58602214 | A | G | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1046-77T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602214 | |||||||
| chr8:58602410 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0278 a0001c0001t0013g0158 |
3 | HG00673.hp2 HG02071.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1046-273A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602410 | |||||||
| chr8:58602433 | C | G | 7 | a0001c0001t0002g0076 a0001c0001t0002g0156 a0001c0001t0002g0215 others(4): Show |
7 | NA18951.hp2 NA18952.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1046-296G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602433 | |||||||
| chr8:58602515 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
142 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1046-378G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602515 | |||||||
| chr8:58602520 | A | G | 22 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0104 others(19): Show |
23 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1046-383T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602520 | |||||||
| chr8:58602569 | T | A | 315 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(312): Show |
335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.1046-432A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602569 | |||||||
| chr8:58602804 | G | C | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1045+406C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602804 | |||||||
| chr8:58602843 | T | A | 1 | a0002c0002t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1045+367A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602843 | |||||||
| chr8:58602855 | A | G | 1 | a0001c0010t0006g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1045+355T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602855 | |||||||
| chr8:58602953 | G | A | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1045+257C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602953 | |||||||
| chr8:58603110 | C | A | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1045+100G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58603110 | |||||||
| chr8:58603197 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
148 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1045+13C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58603197 | |||||||
| chr8:58603470 | C | T | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.869-84G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603470 | |||||||
| chr8:58603551 | A | G | 67 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0253 others(64): Show |
73 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.869-165T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603551 | |||||||
| chr8:58603551 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.869-165T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603551 | |||||||
| chr8:58603597 | C | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
148 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.869-211G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603597 | |||||||
| chr8:58603650 | G | A | 1 | a0002c0002t0001g0222 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.869-264C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603650 | |||||||
| chr8:58603657 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.869-271C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603657 | |||||||
| chr8:58603725 | C | CTG | 24 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0104 others(21): Show |
25 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.869-341_869-340dup others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603725 | |||||||
| chr8:58603816 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.869-430A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603816 | |||||||
| chr8:58603831 | T | G | 6 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0077 others(3): Show |
6 | HG01168.hp1 HG02300.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-445A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603831 | |||||||
| chr8:58603849 | T | G | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.869-463A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603849 | |||||||
| chr8:58603922 | G | A | 314 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(311): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.869-536C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603922 | |||||||
| chr8:58604379 | C | A | 66 | a0001c0001t0001g0138 a0001c0001t0001g0253 a0001c0001t0008g0036 others(63): Show |
72 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.869-993G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604379 | |||||||
| chr8:58604499 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
170 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.869-1113A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604499 | |||||||
| chr8:58604557 | A | AAT | 22 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(19): Show |
23 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.869-1173_869-1172d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604557 | |||||||
| chr8:58604557 | A | AATAT | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
147 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.869-1175_869-1172d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604557 | |||||||
| chr8:58604758 | T | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0214 |
2 | HG03098.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.868+1169A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604758 | |||||||
| chr8:58604952 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.868+975G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604952 | |||||||
| chr8:58605003 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.868+924G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605003 | |||||||
| chr8:58605139 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.868+788G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605139 | |||||||
| chr8:58605161 | A | G | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(6): Show |
9 | HG01069.hp1 HG01192.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.868+766T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605161 | |||||||
| chr8:58605399 | A | G | 69 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0253 others(66): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.868+528T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605399 | |||||||
| chr8:58605621 | C | T | 1 | a0002c0002t0001g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.868+306G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605621 | |||||||
| chr8:58605629 | C | G | 89 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(86): Show |
96 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.868+298G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605629 | |||||||
| chr8:58605784 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+143C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605784 | |||||||
| chr8:58605847 | T | C | 1 | a0001c0001t0011g0039 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.868+80A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605847 | |||||||
| chr8:58605857 | G | T | 5 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.868+70C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605857 | |||||||
| chr8:58605880 | C | CA | 25 | a0001c0001t0001g0081 a0001c0001t0001g0132 a0001c0001t0001g0139 others(22): Show |
26 | HG00621.hp1 HG01167.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.868+46dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605880 | |||||||
| chr8:58605893 | A | AG | 4 | a0002c0002t0001g0011 a0002c0002t0001g0222 a0002c0002t0004g0006 others(1): Show |
6 | NA18943.hp1 NA18945.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.868+33_868+34insC | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605893 | |||||||
| chr8:58605893 | A | G | 85 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(82): Show |
90 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.868+34T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605893 | |||||||
| chr8:58606052 | A | AAAATAAT others(5): Show |
86 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(83): Show |
88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.760-29_760-18dupAT others(10): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606052 | |||||||
| chr8:58606205 | T | G | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.760-170A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606205 | |||||||
| chr8:58606214 | G | GTA | 3 | a0001c0001t0001g0290 a0001c0001t0002g0015 a0001c0001t0002g0215 |
4 | HG00738.hp2 HG03704.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-181_760-180dup others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606214 | |||||||
| chr8:58606250 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.760-215C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606250 | |||||||
| chr8:58606398 | C | G | 3 | a0001c0001t0002g0214 a0006c0007t0001g0103 a0006c0007t0003g0038 |
3 | HG03098.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.760-363G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606398 | |||||||
| chr8:58606769 | T | A | 89 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(86): Show |
96 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.760-734A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606769 | |||||||
| chr8:58606842 | T | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0287 a0007c0012t0001g0294 |
3 | HG02735.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.760-807A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606842 | |||||||
| chr8:58606862 | G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.760-827C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606862 | |||||||
| chr8:58606899 | T | C | 1 | a0001c0003t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.760-864A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606899 | |||||||
| chr8:58606917 | T | C | 92 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(89): Show |
94 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.759+852A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606917 | |||||||
| chr8:58606960 | A | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.759+809T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606960 | |||||||
| chr8:58606985 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.759+784A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606985 | |||||||
| chr8:58607040 | G | A | 1 | a0002c0002t0001g0220 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.759+729C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607040 | |||||||
| chr8:58607078 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
144 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.759+691T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607078 | |||||||
| chr8:58607108 | T | C | 3 | a0001c0001t0001g0208 a0003c0005t0001g0212 a0003c0005t0009g0035 |
3 | HG03130.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.759+661A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607108 | |||||||
| chr8:58607161 | A | G | 69 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0253 others(66): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.759+608T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607161 | |||||||
| chr8:58607168 | T | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.759+601A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607168 | |||||||
| chr8:58607169 | C | G | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.759+600G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607169 | |||||||
| chr8:58607232 | G | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.759+537C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607232 | |||||||
| chr8:58607415 | C | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+354G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607415 | |||||||
| chr8:58607640 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.759+129T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607640 | |||||||
| chr8:58607688 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.759+81T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607688 | |||||||
| chr8:58607701 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | NA18955.hp1 NA18971.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.759+68C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607701 | |||||||
| chr8:58607751 | A | C | 18 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(15): Show |
19 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.759+18T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607751 | |||||||
| chr8:58607992 | T | C | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.688-152A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58607992 | |||||||
| chr8:58608152 | G | A | 82 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(79): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.688-312C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58608152 | |||||||
| chr8:58608524 | G | T | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.688-684C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58608524 | |||||||
| chr8:58608698 | G | A | 1 | a0001c0003t0001g0258 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.688-858C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58608698 | |||||||
| chr8:58608753 | A | G | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.687+851T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58608753 | |||||||
| chr8:58609151 | T | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0145 a0001c0001t0001g0340 others(2): Show |
5 | HG00408.hp2 NA18955.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+453A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609151 | |||||||
| chr8:58609296 | C | G | 3 | a0001c0001t0001g0208 a0003c0005t0001g0212 a0003c0005t0009g0035 |
3 | HG03130.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.687+308G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609296 | |||||||
| chr8:58609322 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.687+282C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609322 | |||||||
| chr8:58609328 | T | C | 2 | a0001c0001t0002g0256 a0001c0001t0007g0030 |
2 | NA18747.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.687+276A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609328 | |||||||
| chr8:58609387 | C | T | 5 | a0001c0001t0002g0181 a0001c0001t0002g0255 a0001c0001t0002g0301 others(2): Show |
5 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+217G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609387 | |||||||
| chr8:58609412 | C | G | 66 | a0001c0001t0001g0138 a0001c0001t0001g0253 a0001c0001t0008g0036 others(63): Show |
72 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.687+192G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609412 | |||||||
| chr8:58609426 | A | C | 1 | a0001c0001t0001g0323 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.687+178T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609426 | |||||||
| chr8:58609434 | T | C | 1 | a0001c0003t0001g0300 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.687+170A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609434 | |||||||
| chr8:58609475 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
145 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.687+129G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609475 | |||||||
| chr8:58609875 | T | G | 1 | a0002c0002t0001g0327 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.558-142A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58609875 | |||||||
| chr8:58609918 | A | T | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558-185T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58609918 | |||||||
| chr8:58609976 | G | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.558-243C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58609976 | |||||||
| chr8:58610191 | C | T | 88 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(85): Show |
95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-458G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610191 | |||||||
| chr8:58610347 | A | G | 89 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(86): Show |
96 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.558-614T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610347 | |||||||
| chr8:58610578 | C | T | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.558-845G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610578 | |||||||
| chr8:58610640 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.558-907C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610640 | |||||||
| chr8:58610673 | C | A | 92 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(89): Show |
94 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.558-940G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610673 | |||||||
| chr8:58610707 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.558-974G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610707 | |||||||
| chr8:58610769 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0164 |
2 | NA18953.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.558-1036C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610769 | |||||||
| chr8:58610807 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.558-1074C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610807 | |||||||
| chr8:58610835 | T | C | 88 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(85): Show |
95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-1102A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610835 | |||||||
| chr8:58610885 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
145 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.558-1152A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610885 | |||||||
| chr8:58610893 | A | T | 1 | a0001c0003t0001g0300 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.558-1160T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610893 | |||||||
| chr8:58611031 | C | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0324 a0001c0001t0001g0325 |
3 | HG01257.hp1 HG01258.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.558-1298G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611031 | |||||||
| chr8:58611232 | T | C | 10 | a0001c0001t0001g0138 a0001c0001t0001g0253 a0001c0001t0008g0036 others(7): Show |
10 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.558-1499A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611232 | |||||||
| chr8:58611489 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.558-1756A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611489 | |||||||
| chr8:58611565 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.558-1832A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611565 | |||||||
| chr8:58611577 | T | C | 88 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(85): Show |
95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-1844A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611577 | |||||||
| chr8:58611772 | G | A | 5 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.558-2039C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611772 | |||||||
| chr8:58611871 | G | A | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.558-2138C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611871 | |||||||
| chr8:58611978 | T | C | 183 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(180): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.558-2245A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611978 | |||||||
| chr8:58612325 | G | T | 82 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(79): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.558-2592C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612325 | |||||||
| chr8:58612326 | A | T | 82 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(79): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.558-2593T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612326 | |||||||
| chr8:58612355 | G | A | 11 | a0002c0002t0001g0011 a0002c0002t0001g0072 a0002c0002t0001g0073 others(8): Show |
13 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.558-2622C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612355 | |||||||
| chr8:58612386 | G | C | 1 | a0002c0002t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.558-2653C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612386 | |||||||
| chr8:58612395 | C | G | 1 | a0001c0001t0001g0328 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.558-2662G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612395 | |||||||
| chr8:58612566 | T | C | 88 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(85): Show |
95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-2833A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612566 | |||||||
| chr8:58612641 | G | C | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.558-2908C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612641 | |||||||
| chr8:58612894 | A | G | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558-3161T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612894 | |||||||
| chr8:58612963 | T | G | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.558-3230A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612963 | |||||||
| chr8:58613151 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.558-3418T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613151 | |||||||
| chr8:58613180 | T | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
146 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.558-3447A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613180 | |||||||
| chr8:58613210 | C | T | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.558-3477G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613210 | |||||||
| chr8:58613287 | G | T | 2 | a0001c0001t0001g0192 a0001c0003t0001g0211 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.558-3554C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613287 | |||||||
| chr8:58613520 | G | T | 88 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(85): Show |
95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-3787C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613520 | |||||||
| chr8:58613847 | A | T | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.558-4114T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613847 | |||||||
| chr8:58614106 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.558-4373A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614106 | |||||||
| chr8:58614140 | C | T | 84 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0089 others(81): Show |
86 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.558-4407G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614140 | |||||||
| chr8:58614479 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.558-4746G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614479 | |||||||
| chr8:58614513 | G | C | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.558-4780C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614513 | |||||||
| chr8:58614577 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.558-4844G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614577 | |||||||
| chr8:58614640 | C | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558-4907G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614640 | |||||||
| chr8:58614653 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.558-4920C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614653 | |||||||
| chr8:58614701 | C | T | 1 | a0002c0002t0002g0264 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.558-4968G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614701 | |||||||
| chr8:58614769 | G | A | 2 | a0001c0001t0008g0036 a0001c0003t0001g0110 |
2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.558-5036C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614769 | |||||||
| chr8:58614782 | C | T | 1 | a0001c0003t0001g0339 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.558-5049G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614782 | |||||||
| chr8:58615150 | G | A | 13 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(10): Show |
13 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.558-5417C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615150 | |||||||
| chr8:58615254 | C | A | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.558-5521G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615254 | |||||||
| chr8:58615347 | C | T | 1 | a0001c0001t0002g0338 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.558-5614G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615347 | |||||||
| chr8:58615482 | ACATATTC others(4): Show |
A | 2 | a0002c0002t0005g0005 a0002c0002t0005g0019 |
3 | NA18961.hp1 NA18990.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.558-5760_558-5750d others(13): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615482 | |||||||
| chr8:58615588 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.558-5855G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615588 | |||||||
| chr8:58615686 | A | T | 1 | a0001c0001t0002g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.558-5953T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615686 | |||||||
| chr8:58615753 | C | G | 20 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(17): Show |
21 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.558-6020G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615753 | |||||||
| chr8:58615974 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.558-6241C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615974 | |||||||
| chr8:58615976 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.558-6243T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615976 | |||||||
| chr8:58616047 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.558-6314C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616047 | |||||||
| chr8:58616224 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0003g0007 a0001c0001t0003g0043 others(1): Show |
5 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.558-6491G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616224 | |||||||
| chr8:58616452 | G | GA | 5 | a0001c0001t0002g0191 a0001c0001t0002g0329 a0001c0001t0002g0330 others(2): Show |
5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.558-6720dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616452 | |||||||
| chr8:58616701 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+6519T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616701 | |||||||
| chr8:58616704 | T | A | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.557+6516A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616704 | |||||||
| chr8:58616874 | A | G | 5 | a0001c0001t0002g0191 a0001c0001t0002g0329 a0001c0001t0002g0330 others(2): Show |
5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.557+6346T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616874 | |||||||
| chr8:58616876 | G | A | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.557+6344C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616876 | |||||||
| chr8:58616880 | C | T | 5 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.557+6340G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616880 | |||||||
| chr8:58616985 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.557+6235T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616985 | |||||||
| chr8:58616988 | T | C | 96 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(93): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.557+6232A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616988 | |||||||
| chr8:58617087 | T | C | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(9): Show |
12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.557+6133A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617087 | |||||||
| chr8:58617379 | C | A | 11 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0199 others(8): Show |
11 | HG00408.hp1 HG00735.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.557+5841G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617379 | |||||||
| chr8:58617494 | A | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.557+5726T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617494 | |||||||
| chr8:58617518 | A | C | 2 | a0001c0001t0002g0214 a0001c0004t0001g0116 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.557+5702T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617518 | |||||||
| chr8:58617608 | A | G | 2 | a0001c0001t0002g0214 a0001c0004t0001g0116 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.557+5612T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617608 | |||||||
| chr8:58617647 | A | G | 2 | a0003c0005t0002g0207 a0003c0005t0003g0044 |
2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.557+5573T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617647 | |||||||
| chr8:58617994 | A | T | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+5226T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617994 | |||||||
| chr8:58618003 | CCTTTGCA others(30): Show |
C | 1 | a0001c0001t0001g0083 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.557+5180_557+5216d others(39): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618003 | |||||||
| chr8:58618008 | G | T | 2 | a0003c0005t0002g0207 a0003c0005t0003g0044 |
2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.557+5212C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618008 | |||||||
| chr8:58618021 | C | T | 4 | a0002c0002t0001g0011 a0002c0002t0001g0222 a0002c0002t0004g0006 others(1): Show |
6 | NA18943.hp1 NA18945.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.557+5199G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618021 | |||||||
| chr8:58618216 | T | G | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.557+5004A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618216 | |||||||
| chr8:58618348 | A | G | 96 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(93): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.557+4872T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618348 | |||||||
| chr8:58618401 | A | C | 1 | a0001c0001t0002g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.557+4819T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618401 | |||||||
| chr8:58618570 | T | C | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.557+4650A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618570 | |||||||
| chr8:58618624 | C | G | 98 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(95): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.557+4596G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618624 | |||||||
| chr8:58618815 | C | T | 19 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(16): Show |
20 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.557+4405G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618815 | |||||||
| chr8:58618826 | C | T | 2 | a0001c0001t0002g0214 a0001c0004t0001g0116 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.557+4394G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618826 | |||||||
| chr8:58618846 | G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.557+4374C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618846 | |||||||
| chr8:58618909 | C | T | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.557+4311G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618909 | |||||||
| chr8:58618972 | C | G | 96 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(93): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.557+4248G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618972 | |||||||
| chr8:58619061 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0194 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.557+4159C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619061 | |||||||
| chr8:58619082 | C | A | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.557+4138G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619082 | |||||||
| chr8:58619308 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+3912C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619308 | |||||||
| chr8:58619335 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+3885A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619335 | |||||||
| chr8:58619389 | G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.557+3831C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619389 | |||||||
| chr8:58619641 | C | A | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.557+3579G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619641 | |||||||
| chr8:58619691 | T | A | 1 | a0001c0003t0001g0298 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.557+3529A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619691 | |||||||
| chr8:58619709 | A | G | 1 | a0006c0007t0001g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.557+3511T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619709 | |||||||
| chr8:58619858 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+3362T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619858 | |||||||
| chr8:58619922 | G | A | 1 | a0001c0001t0006g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.557+3298C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619922 | |||||||
| chr8:58619927 | T | C | 2 | a0001c0009t0001g0251 a0001c0009t0001g0252 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.557+3293A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619927 | |||||||
| chr8:58619986 | G | A | 98 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(95): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.557+3234C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619986 | |||||||
| chr8:58620022 | G | A | 1 | a0001c0001t0006g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.557+3198C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620022 | |||||||
| chr8:58620079 | A | C | 1 | a0001c0001t0003g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.557+3141T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620079 | |||||||
| chr8:58620148 | G | T | 96 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(93): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.557+3072C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620148 | |||||||
| chr8:58620228 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0173 a0001c0001t0001g0241 others(2): Show |
8 | NA18943.hp2 NA18947.hp2 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.557+2992T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620228 | |||||||
| chr8:58620410 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.557+2810G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620410 | |||||||
| chr8:58620467 | T | C | 3 | a0001c0001t0001g0232 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG00642.hp1 HG01123.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.557+2753A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620467 | |||||||
| chr8:58620486 | A | T | 2 | a0001c0003t0001g0107 a0001c0003t0001g0117 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.557+2734T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620486 | |||||||
| chr8:58620501 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0155 a0001c0001t0001g0283 |
3 | NA18951.hp1 NA19070.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.557+2719C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620501 | |||||||
| chr8:58620958 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.557+2262A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620958 | |||||||
| chr8:58621147 | C | T | 2 | a0001c0004t0001g0202 a0001c0004t0001g0210 |
2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.557+2073G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621147 | |||||||
| chr8:58621148 | G | A | 3 | a0001c0001t0011g0039 a0006c0007t0001g0103 a0006c0007t0003g0038 |
3 | HG02970.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.557+2072C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621148 | |||||||
| chr8:58621237 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.557+1983T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621237 | |||||||
| chr8:58621501 | A | G | 98 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(95): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.557+1719T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621501 | |||||||
| chr8:58621783 | T | C | 97 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(94): Show |
102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.557+1437A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621783 | |||||||
| chr8:58621844 | T | C | 1 | a0001c0001t0006g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.557+1376A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621844 | |||||||
| chr8:58621978 | T | G | 99 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(96): Show |
104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.557+1242A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621978 | |||||||
| chr8:58622231 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.557+989G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58622231 | |||||||
| chr8:58622636 | G | T | 5 | a0001c0001t0002g0191 a0001c0001t0002g0329 a0001c0001t0002g0330 others(2): Show |
5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.557+584C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58622636 | |||||||
| chr8:58622843 | A | G | 1 | a0001c0003t0001g0056 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.557+377T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58622843 | |||||||
| chr8:58622915 | G | T | 1 | a0001c0001t0008g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.557+305C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58622915 | |||||||
| chr8:58623063 | G | C | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.557+157C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58623063 | |||||||
| chr8:58623300 | A | ACG | 102 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(99): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.505-29_505-28insCG | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 8/30 | chr8 | 58623300 | |||||||
| chr8:58623301 | T | A | 102 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(99): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.505-29A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 8/30 | chr8 | 58623301 | |||||||
| chr8:58623302 | T | A | 102 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(99): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.505-30A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 8/30 | chr8 | 58623302 | |||||||
| chr8:58623467 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.457-43T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 7/30 | chr8 | 58623467 | |||||||
| chr8:58623552 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.457-128A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 7/30 | chr8 | 58623552 | |||||||
| chr8:58623563 | T | C | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.457-139A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 7/30 | chr8 | 58623563 | |||||||
| chr8:58623613 | A | G | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.456+96T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 7/30 | chr8 | 58623613 | |||||||
| chr8:58624035 | A | AT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.385-256dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | |||||||
| chr8:58624035 | A | ATT | 18 | a0001c0001t0001g0080 a0001c0001t0001g0123 a0001c0001t0001g0166 others(15): Show |
18 | HG00673.hp2 HG00738.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.385-257_385-256dup others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | |||||||
| chr8:58624035 | AT | A | 74 | a0001c0001t0001g0069 a0001c0001t0001g0093 a0001c0001t0001g0136 others(71): Show |
77 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.385-256delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | |||||||
| chr8:58624035 | ATT | A | 86 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(83): Show |
91 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.385-257_385-256del others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | |||||||
| chr8:58624035 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0328 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.385-269_385-256del others(14): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | |||||||
| chr8:58624222 | A | G | 6 | a0002c0002t0001g0072 a0002c0002t0001g0073 a0002c0002t0001g0075 others(3): Show |
6 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.385-442T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624222 | |||||||
| chr8:58624235 | C | T | 1 | a0002c0002t0001g0075 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.385-455G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624235 | |||||||
| chr8:58624299 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-519C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624299 | |||||||
| chr8:58624316 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.385-536C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624316 | |||||||
| chr8:58624483 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.385-703A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624483 | |||||||
| chr8:58624738 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.385-958G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624738 | |||||||
| chr8:58624859 | T | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-1079A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624859 | |||||||
| chr8:58624873 | T | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0046 a0001c0001t0003g0047 others(1): Show |
5 | HG02258.hp2 HG02451.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-1093A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624873 | |||||||
| chr8:58624893 | T | C | 1 | a0001c0001t0008g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.385-1113A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624893 | |||||||
| chr8:58624895 | T | C | 2 | a0001c0001t0002g0088 a0001c0001t0002g0092 |
2 | NA18970.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.385-1115A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624895 | |||||||
| chr8:58624903 | C | T | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385-1123G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624903 | |||||||
| chr8:58625088 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-1308G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625088 | |||||||
| chr8:58625277 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.385-1497G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625277 | |||||||
| chr8:58625386 | G | T | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(9): Show |
12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.385-1606C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625386 | |||||||
| chr8:58625393 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.385-1613G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625393 | |||||||
| chr8:58625394 | A | ATATATAT others(9): Show |
1 | a0004c0006t0002g0345 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.385-1615_385-1614i others(18): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | |||||||
| chr8:58625394 | A | ATATATAT others(13): Show |
14 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.385-1615_385-1614i others(22): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | |||||||
| chr8:58625394 | A | ATATATAT others(17): Show |
70 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0093 others(67): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.385-1615_385-1614i others(26): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | |||||||
| chr8:58625394 | A | ATATATAT others(21): Show |
11 | a0001c0001t0001g0089 a0001c0001t0001g0188 a0001c0001t0001g0189 others(8): Show |
11 | HG00423.hp2 HG00558.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-1615_385-1614i others(30): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | |||||||
| chr8:58625394 | A | ATATGTAT others(9): Show |
1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-1630_385-1615d others(18): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | |||||||
| chr8:58625394 | A | ATATGTAT others(13): Show |
1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.385-1634_385-1615d others(22): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | |||||||
| chr8:58625394 | A | ATATGTAT others(17): Show |
1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.385-1615_385-1614i others(26): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | |||||||
| chr8:58625394 | A | ATGTATGT others(11): Show |
1 | a0001c0001t0002g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.385-1615_385-1614i others(20): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | |||||||
| chr8:58625394 | ATATG | A | 10 | a0001c0001t0001g0138 a0001c0001t0001g0253 a0001c0001t0008g0036 others(7): Show |
10 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-1618_385-1615d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | |||||||
| chr8:58625415 | T | C | 1 | a0002c0002t0001g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.385-1635A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625415 | |||||||
| chr8:58625418 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01167.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.385-1638T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625418 | |||||||
| chr8:58625423 | T | C | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-1643A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625423 | |||||||
| chr8:58625448 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.385-1668G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625448 | |||||||
| chr8:58625511 | T | C | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.385-1731A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625511 | |||||||
| chr8:58625519 | C | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-1739G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625519 | |||||||
| chr8:58625519 | C | T | 2 | a0001c0001t0002g0133 a0001c0001t0002g0206 |
2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.385-1739G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625519 | |||||||
| chr8:58625614 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.385-1834C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625614 | |||||||
| chr8:58625636 | T | C | 2 | a0002c0002t0004g0025 a0002c0002t0004g0026 |
2 | HG02080.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.385-1856A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625636 | |||||||
| chr8:58625677 | C | T | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-1897G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625677 | |||||||
| chr8:58625691 | T | C | 100 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(97): Show |
105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.385-1911A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625691 | |||||||
| chr8:58625755 | G | T | 3 | a0001c0001t0001g0104 a0001c0001t0003g0007 a0001c0001t0003g0043 |
4 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-1975C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625755 | |||||||
| chr8:58625802 | G | T | 1 | a0001c0003t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.385-2022C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625802 | |||||||
| chr8:58625813 | A | G | 27 | a0001c0001t0001g0192 a0001c0003t0001g0010 a0001c0003t0001g0012 others(24): Show |
29 | HG00099.hp2 HG00609.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.385-2033T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625813 | |||||||
| chr8:58625916 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.385-2136T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625916 | |||||||
| chr8:58625930 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-2150A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625930 | |||||||
| chr8:58625986 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.385-2206C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625986 | |||||||
| chr8:58626041 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.385-2261T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626041 | |||||||
| chr8:58626091 | C | CT | 17 | a0001c0001t0001g0153 a0001c0001t0001g0157 a0001c0001t0001g0208 others(14): Show |
17 | HG01934.hp1 HG02071.hp1 HG03453.hp1 others(14): Show |
intron_variant | MODIFIER | c.385-2312dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626091 | |||||||
| chr8:58626091 | C | CTT | 27 | a0001c0001t0001g0192 a0001c0003t0001g0010 a0001c0003t0001g0012 others(24): Show |
29 | HG00099.hp2 HG00609.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.385-2313_385-2312d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626091 | |||||||
| chr8:58626091 | CT | C | 86 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(83): Show |
91 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.385-2312delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626091 | |||||||
| chr8:58626092 | T | G | 17 | a0001c0001t0001g0057 a0001c0001t0001g0093 a0001c0001t0001g0134 others(14): Show |
17 | HG02486.hp1 HG02572.hp2 HG02683.hp1 others(14): Show |
intron_variant | MODIFIER | c.385-2312A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626092 | |||||||
| chr8:58626093 | T | G | 80 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(77): Show |
85 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.385-2313A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626093 | |||||||
| chr8:58626094 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.385-2314A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626094 | |||||||
| chr8:58626159 | C | T | 2 | a0001c0001t0002g0330 a0001c0001t0002g0332 |
2 | NA18994.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.385-2379G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626159 | |||||||
| chr8:58626160 | G | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-2380C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626160 | |||||||
| chr8:58626161 | C | T | 101 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(98): Show |
106 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.385-2381G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626161 | |||||||
| chr8:58626256 | C | T | 67 | a0001c0001t0001g0069 a0001c0001t0001g0138 a0001c0001t0001g0149 others(64): Show |
70 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.385-2476G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626256 | |||||||
| chr8:58626286 | A | AG | 5 | a0001c0001t0001g0208 a0001c0004t0001g0116 a0003c0005t0003g0044 others(2): Show |
5 | HG02572.hp1 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-2507dupC | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626286 | |||||||
| chr8:58626287 | G | GC | 99 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(96): Show |
104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.385-2508_385-2507i others(3): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626287 | |||||||
| chr8:58626374 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-2594T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626374 | |||||||
| chr8:58626583 | T | C | 101 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(98): Show |
106 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.385-2803A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626583 | |||||||
| chr8:58626600 | A | T | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-2820T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626600 | |||||||
| chr8:58626645 | T | A | 17 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0124 others(14): Show |
18 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.385-2865A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626645 | |||||||
| chr8:58626673 | T | A | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(9): Show |
12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.385-2893A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626673 | |||||||
| chr8:58626837 | T | C | 1 | a0001c0001t0002g0332 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.385-3057A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626837 | |||||||
| chr8:58626866 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0321 a0002c0002t0001g0151 |
4 | HG00099.hp1 HG00741.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-3086C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626866 | |||||||
| chr8:58627059 | G | C | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(6): Show |
9 | HG01069.hp1 HG01192.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.385-3279C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627059 | |||||||
| chr8:58627173 | G | T | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.385-3393C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627173 | |||||||
| chr8:58627287 | G | A | 1 | a0001c0004t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.385-3507C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627287 | |||||||
| chr8:58627321 | C | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.385-3541G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627321 | |||||||
| chr8:58627324 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.385-3544A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627324 | |||||||
| chr8:58627555 | T | C | 99 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(96): Show |
104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.385-3775A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627555 | |||||||
| chr8:58627592 | A | G | 1 | a0001c0003t0001g0341 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.385-3812T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627592 | |||||||
| chr8:58627610 | C | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.385-3830G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627610 | |||||||
| chr8:58627635 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385-3855A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627635 | |||||||
| chr8:58627687 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.384+3809T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627687 | |||||||
| chr8:58627884 | A | G | 1 | a0001c0001t0011g0039 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.384+3612T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627884 | |||||||
| chr8:58628020 | G | A | 216 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(213): Show |
227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.384+3476C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628020 | |||||||
| chr8:58628090 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.384+3406A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628090 | |||||||
| chr8:58628200 | T | C | 3 | a0001c0001t0011g0039 a0006c0007t0001g0103 a0006c0007t0003g0038 |
3 | HG02970.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.384+3296A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628200 | |||||||
| chr8:58628272 | C | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.384+3224G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628272 | |||||||
| chr8:58628431 | C | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0171 a0001c0001t0001g0286 others(4): Show |
8 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.384+3065G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628431 | |||||||
| chr8:58628499 | A | G | 2 | a0002c0002t0001g0061 a0002c0002t0001g0062 |
2 | NA18963.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.384+2997T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628499 | |||||||
| chr8:58628827 | A | G | 219 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(216): Show |
230 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.384+2669T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628827 | |||||||
| chr8:58628995 | G | A | 1 | a0001c0003t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.384+2501C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628995 | |||||||
| chr8:58629409 | CTCTT | C | 85 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0089 others(82): Show |
90 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.384+2083_384+2086d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58629409 | |||||||
| chr8:58629457 | A | G | 53 | a0001c0001t0001g0069 a0001c0001t0001g0149 a0001c0001t0001g0150 others(50): Show |
56 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.384+2039T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58629457 | |||||||
| chr8:58629558 | A | G | 2 | a0002c0002t0001g0058 a0002c0002t0001g0060 |
2 | NA18959.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.384+1938T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58629558 | |||||||
| chr8:58630014 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.384+1482G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630014 | |||||||
| chr8:58630098 | G | A | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(9): Show |
12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.384+1398C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630098 | |||||||
| chr8:58630142 | C | T | 94 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(91): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.384+1354G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630142 | |||||||
| chr8:58630173 | G | A | 3 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.384+1323C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630173 | |||||||
| chr8:58630321 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+1175A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630321 | |||||||
| chr8:58630363 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0233 |
2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.384+1133A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630363 | |||||||
| chr8:58630380 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+1116A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630380 | |||||||
| chr8:58630398 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.384+1098A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630398 | |||||||
| chr8:58630600 | G | T | 1 | a0001c0001t0001g0343 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.384+896C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630600 | |||||||
| chr8:58630741 | A | G | 96 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(93): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.384+755T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630741 | |||||||
| chr8:58630839 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+657C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630839 | |||||||
| chr8:58630970 | G | C | 5 | a0001c0001t0001g0208 a0001c0004t0001g0116 a0003c0005t0003g0044 others(2): Show |
5 | HG02572.hp1 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+526C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630970 | |||||||
| chr8:58631031 | G | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.384+465C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58631031 | |||||||
| chr8:58631273 | G | GT | 6 | a0001c0001t0001g0104 a0001c0001t0001g0171 a0001c0001t0001g0262 others(3): Show |
7 | HG00735.hp2 HG02109.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+222dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58631273 | |||||||
| chr8:58631313 | A | C | 1 | a0002c0002t0001g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.384+183T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58631313 | |||||||
| chr8:58631347 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0246 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.384+149G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58631347 | |||||||
| chr8:58631628 | A | C | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(9): Show |
12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.334-82T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631628 | |||||||
| chr8:58631693 | A | T | 85 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0089 others(82): Show |
90 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.334-147T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631693 | |||||||
| chr8:58631777 | T | A | 1 | a0001c0003t0003g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-231A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631777 | |||||||
| chr8:58631852 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.334-306C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631852 | |||||||
| chr8:58631854 | G | A | 85 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0089 others(82): Show |
90 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.334-308C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631854 | |||||||
| chr8:58631870 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0233 |
2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.334-324C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631870 | |||||||
| chr8:58631995 | T | C | 3 | a0001c0001t0011g0039 a0006c0007t0001g0103 a0006c0007t0003g0038 |
3 | HG02970.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.334-449A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631995 | |||||||
| chr8:58632001 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.334-455T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632001 | |||||||
| chr8:58632450 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.334-904G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632450 | |||||||
| chr8:58632503 | A | T | 95 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(92): Show |
100 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.334-957T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632503 | |||||||
| chr8:58632569 | G | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1023C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632569 | |||||||
| chr8:58632795 | A | G | 102 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(99): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.334-1249T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632795 | |||||||
| chr8:58632819 | T | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(2): Show |
5 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-1273A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632819 | |||||||
| chr8:58633008 | T | C | 1 | a0002c0002t0001g0058 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.334-1462A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633008 | |||||||
| chr8:58633019 | C | T | 94 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(91): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.334-1473G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633019 | |||||||
| chr8:58633187 | C | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.334-1641G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633187 | |||||||
| chr8:58633189 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0208 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.334-1643G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633189 | |||||||
| chr8:58633190 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.334-1644C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633190 | |||||||
| chr8:58633199 | G | T | 1 | a0002c0002t0001g0195 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.334-1653C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633199 | |||||||
| chr8:58633202 | C | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.334-1656G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633202 | |||||||
| chr8:58633622 | G | A | 1 | a0002c0013t0001g0197 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.333+1567C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633622 | |||||||
| chr8:58633906 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0208 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.333+1283T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633906 | |||||||
| chr8:58633985 | A | T | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+1204T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633985 | |||||||
| chr8:58633987 | A | G | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+1202T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633987 | |||||||
| chr8:58634011 | T | C | 216 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(213): Show |
227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.333+1178A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634011 | |||||||
| chr8:58634031 | T | C | 1 | a0001c0003t0001g0300 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.333+1158A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634031 | |||||||
| chr8:58634076 | T | C | 1 | a0006c0007t0001g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.333+1113A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634076 | |||||||
| chr8:58634124 | C | T | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+1065G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634124 | |||||||
| chr8:58634226 | A | G | 1 | a0001c0003t0001g0298 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.333+963T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634226 | |||||||
| chr8:58634367 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0173 a0001c0001t0001g0241 others(3): Show |
9 | NA18943.hp2 NA18947.hp2 NA18974.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+822G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634367 | |||||||
| chr8:58634379 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.333+810G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634379 | |||||||
| chr8:58634516 | A | G | 27 | a0001c0001t0001g0192 a0001c0003t0001g0010 a0001c0003t0001g0012 others(24): Show |
29 | HG00099.hp2 HG00609.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.333+673T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634516 | |||||||
| chr8:58634601 | C | A | 1 | a0001c0001t0002g0146 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.333+588G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634601 | |||||||
| chr8:58634658 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.333+531T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634658 | |||||||
| chr8:58634941 | G | A | 7 | a0001c0001t0001g0312 a0001c0001t0002g0156 a0001c0001t0002g0215 others(4): Show |
7 | NA18951.hp2 NA18952.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+248C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634941 | |||||||
| chr8:58635240 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.297-15T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 4/30 | chr8 | 58635240 | |||||||
| chr8:58635243 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0287 a0007c0012t0001g0294 |
3 | HG02735.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.297-18C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 4/30 | chr8 | 58635243 | |||||||
| chr8:58635245 | C | A | 84 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0089 others(81): Show |
89 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.297-20G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 4/30 | chr8 | 58635245 | |||||||
| chr8:58635551 | G | A | 26 | a0001c0001t0001g0192 a0001c0003t0001g0010 a0001c0003t0001g0012 others(23): Show |
28 | HG00099.hp2 HG00609.hp1 HG01123.hp1 others(25): Show |
splice_region_variant&intron_variant | LOW | c.150-5C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635551 | |||||||
| chr8:58635709 | A | G | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(13): Show |
17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-163T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635709 | |||||||
| chr8:58635742 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.150-196G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635742 | |||||||
| chr8:58635875 | G | A | 26 | a0001c0001t0001g0192 a0001c0003t0001g0010 a0001c0003t0001g0012 others(23): Show |
28 | HG00099.hp2 HG00609.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.150-329C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635875 | |||||||
| chr8:58635930 | A | G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0119 others(23): Show |
28 | HG00438.hp2 HG00609.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.150-384T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635930 | |||||||
| chr8:58635943 | T | C | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.150-397A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635943 | |||||||
| chr8:58635973 | C | T | 5 | a0001c0001t0002g0249 a0001c0001t0002g0303 a0001c0001t0002g0304 others(2): Show |
5 | HG00323.hp1 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-427G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635973 | |||||||
| chr8:58636085 | T | C | 4 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0005c0015t0009g0034 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-539A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636085 | |||||||
| chr8:58636209 | A | G | 1 | a0002c0002t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.150-663T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636209 | |||||||
| chr8:58636246 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.150-700G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636246 | |||||||
| chr8:58636257 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.150-711G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636257 | |||||||
| chr8:58636353 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-807T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636353 | |||||||
| chr8:58636386 | T | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-840A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636386 | |||||||
| chr8:58636433 | G | C | 85 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0089 others(82): Show |
90 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.150-887C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636433 | |||||||
| chr8:58636694 | T | G | 58 | a0001c0001t0001g0069 a0001c0001t0001g0149 a0001c0001t0001g0150 others(55): Show |
61 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.150-1148A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636694 | |||||||
| chr8:58636712 | C | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-1166G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636712 | |||||||
| chr8:58636736 | A | G | 3 | a0001c0001t0002g0098 a0001c0001t0002g0114 a0001c0001t0002g0186 |
3 | HG02559.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.150-1190T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636736 | |||||||
| chr8:58636740 | C | G | 1 | a0001c0001t0002g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.150-1194G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636740 | |||||||
| chr8:58636784 | C | G | 98 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(95): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.150-1238G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636784 | |||||||
| chr8:58636945 | A | G | 1 | a0001c0001t0006g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.150-1399T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636945 | |||||||
| chr8:58637017 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.150-1485_150-1472d others(16): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637017 | |||||||
| chr8:58637017 | TACAC | T | 202 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0069 others(199): Show |
213 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.150-1475_150-1472d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637017 | |||||||
| chr8:58637038 | ACACC | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(3): Show |
6 | HG01109.hp1 HG01192.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-1496_150-1493d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637038 | |||||||
| chr8:58637040 | A | C | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.150-1494T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637040 | |||||||
| chr8:58637042 | C | A | 7 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0001t0001g0274 others(4): Show |
7 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-1496G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637042 | |||||||
| chr8:58637102 | C | T | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.150-1556G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637102 | |||||||
| chr8:58637233 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0171 a0001c0001t0001g0286 others(2): Show |
6 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-1687G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637233 | |||||||
| chr8:58637288 | T | C | 1 | a0006c0007t0003g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150-1742A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637288 | |||||||
| chr8:58637373 | C | A | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.150-1827G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637373 | |||||||
| chr8:58637528 | C | G | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.150-1982G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637528 | |||||||
| chr8:58637608 | T | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-2062A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637608 | |||||||
| chr8:58637718 | A | C | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.150-2172T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637718 | |||||||
| chr8:58637836 | G | A | 1 | a0001c0003t0001g0137 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.150-2290C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637836 | |||||||
| chr8:58637962 | AATCCCAA others(4): Show |
A | 7 | a0002c0002t0001g0072 a0002c0002t0001g0073 a0002c0002t0001g0075 others(4): Show |
7 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-2427_150-2417d others(13): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637962 | |||||||
| chr8:58638012 | T | C | 99 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(96): Show |
104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.150-2466A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638012 | |||||||
| chr8:58638057 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0208 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.150-2511A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638057 | |||||||
| chr8:58638307 | G | A | 1 | a0001c0008t0002g0316 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.150-2761C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638307 | |||||||
| chr8:58638341 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.150-2795C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638341 | |||||||
| chr8:58638457 | TG | T | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(13): Show |
17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-2912delC | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638457 | |||||||
| chr8:58638508 | G | A | 68 | a0001c0001t0001g0069 a0001c0001t0001g0138 a0001c0001t0001g0149 others(65): Show |
71 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.150-2962C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638508 | |||||||
| chr8:58638575 | C | T | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(13): Show |
17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-3029G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638575 | |||||||
| chr8:58638620 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-3074T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638620 | |||||||
| chr8:58638702 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-3156G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638702 | |||||||
| chr8:58638910 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.150-3364C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638910 | |||||||
| chr8:58639083 | C | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-3537G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639083 | |||||||
| chr8:58639152 | G | T | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.150-3606C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639152 | |||||||
| chr8:58639227 | T | C | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.150-3681A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639227 | |||||||
| chr8:58639248 | C | T | 1 | a0001c0001t0003g0008 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.150-3702G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639248 | |||||||
| chr8:58639278 | C | T | 26 | a0001c0001t0001g0192 a0001c0003t0001g0010 a0001c0003t0001g0012 others(23): Show |
28 | HG00099.hp2 HG00609.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.149+3706G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639278 | |||||||
| chr8:58639286 | TA | T | 10 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(7): Show |
10 | HG01069.hp1 HG01192.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+3697delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639286 | |||||||
| chr8:58639297 | A | G | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.149+3687T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639297 | |||||||
| chr8:58639297 | AAAG | A | 112 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0054 others(109): Show |
119 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.149+3684_149+3686d others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639297 | |||||||
| chr8:58639300 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0208 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.149+3684C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639300 | |||||||
| chr8:58639325 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.149+3659A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639325 | |||||||
| chr8:58639355 | C | A | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.149+3629G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639355 | |||||||
| chr8:58639722 | T | G | 229 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(226): Show |
240 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.149+3262A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639722 | |||||||
| chr8:58639810 | C | T | 1 | a0001c0001t0002g0329 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.149+3174G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639810 | |||||||
| chr8:58639875 | A | G | 1 | a0002c0002t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.149+3109T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639875 | |||||||
| chr8:58639917 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+3067G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639917 | |||||||
| chr8:58639918 | G | A | 5 | a0001c0001t0002g0191 a0001c0001t0002g0329 a0001c0001t0002g0330 others(2): Show |
5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+3066C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639918 | |||||||
| chr8:58639958 | T | C | 1 | a0001c0010t0006g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.149+3026A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639958 | |||||||
| chr8:58640236 | A | T | 3 | a0001c0001t0002g0214 a0001c0001t0003g0007 a0001c0001t0003g0043 |
4 | HG02109.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+2748T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640236 | |||||||
| chr8:58640336 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.149+2648A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640336 | |||||||
| chr8:58640555 | GA | G | 101 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(98): Show |
106 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.149+2428delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640555 | |||||||
| chr8:58640592 | C | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+2392G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640592 | |||||||
| chr8:58640671 | G | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.149+2313C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640671 | |||||||
| chr8:58640868 | G | T | 58 | a0001c0001t0001g0069 a0001c0001t0001g0149 a0001c0001t0001g0150 others(55): Show |
61 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.149+2116C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640868 | |||||||
| chr8:58640930 | A | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0194 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+2054T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640930 | |||||||
| chr8:58641109 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0246 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+1875G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641109 | |||||||
| chr8:58641387 | A | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+1597T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641387 | |||||||
| chr8:58641415 | C | T | 2 | a0001c0009t0001g0251 a0001c0009t0001g0252 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.149+1569G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641415 | |||||||
| chr8:58641470 | CAT | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+1512_149+1513d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641470 | |||||||
| chr8:58641533 | G | A | 2 | a0001c0008t0002g0315 a0001c0008t0002g0316 |
2 | HG01993.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.149+1451C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641533 | |||||||
| chr8:58641534 | C | A | 2 | a0001c0008t0002g0315 a0001c0008t0002g0316 |
2 | HG01993.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.149+1450G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641534 | |||||||
| chr8:58641616 | T | C | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.149+1368A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641616 | |||||||
| chr8:58641665 | G | C | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(9): Show |
12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.149+1319C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641665 | |||||||
| chr8:58641849 | C | T | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.149+1135G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641849 | |||||||
| chr8:58641894 | C | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.149+1090G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641894 | |||||||
| chr8:58642147 | A | G | 93 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(90): Show |
98 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.149+837T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642147 | |||||||
| chr8:58642210 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+774C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642210 | |||||||
| chr8:58642217 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149+767A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642217 | |||||||
| chr8:58642442 | T | C | 1 | a0001c0001t0002g0318 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.149+542A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642442 | |||||||
| chr8:58642482 | G | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.149+502C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642482 | |||||||
| chr8:58642571 | C | A | 68 | a0001c0001t0001g0069 a0001c0001t0001g0138 a0001c0001t0001g0149 others(65): Show |
71 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.149+413G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642571 | |||||||
| chr8:58642708 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+276T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642708 | |||||||
| chr8:58642766 | A | G | 1 | a0001c0001t0002g0199 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.149+218T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642766 | |||||||
| chr8:58643086 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.60-13G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643086 | |||||||
| chr8:58643087 | G | A | 1 | a0001c0001t0002g0338 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.60-14C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643087 | |||||||
| chr8:58643097 | C | T | 73 | a0001c0001t0001g0069 a0001c0001t0001g0138 a0001c0001t0001g0149 others(70): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.60-24G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643097 | |||||||
| chr8:58643172 | T | A | 102 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(99): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.60-99A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643172 | |||||||
| chr8:58643232 | T | C | 1 | a0001c0001t0002g0320 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.60-159A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643232 | |||||||
| chr8:58643306 | T | G | 4 | a0001c0001t0001g0205 a0001c0001t0001g0324 a0001c0001t0001g0325 others(1): Show |
4 | HG00642.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-233A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643306 | |||||||
| chr8:58643435 | G | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-362C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643435 | |||||||
| chr8:58643481 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-408G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643481 | |||||||
| chr8:58643486 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.60-413A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643486 | |||||||
| chr8:58643534 | CT | C | 196 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(193): Show |
206 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.60-462delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643534 | |||||||
| chr8:58643549 | T | G | 4 | a0001c0001t0001g0182 a0001c0009t0001g0251 a0001c0009t0001g0252 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-476A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643549 | |||||||
| chr8:58643554 | C | T | 1 | a0001c0001t0002g0256 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.60-481G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643554 | |||||||
| chr8:58643597 | G | A | 100 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(97): Show |
105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.60-524C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643597 | |||||||
| chr8:58643625 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.60-552C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643625 | |||||||
| chr8:58643725 | T | A | 1 | a0002c0002t0001g0073 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.60-652A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643725 | |||||||
| chr8:58643767 | G | A | 11 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0199 others(8): Show |
11 | HG00408.hp1 HG00735.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.60-694C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643767 | |||||||
| chr8:58643820 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-747G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643820 | |||||||
| chr8:58643851 | T | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-778A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643851 | |||||||
| chr8:58643921 | G | T | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.60-848C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643921 | |||||||
| chr8:58643923 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.60-850C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643923 | |||||||
| chr8:58644434 | C | T | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.60-1361G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644434 | |||||||
| chr8:58644474 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1401T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644474 | |||||||
| chr8:58644479 | C | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1406G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644479 | |||||||
| chr8:58644655 | A | C | 104 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(101): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.60-1582T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644655 | |||||||
| chr8:58644670 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1597C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644670 | |||||||
| chr8:58644677 | G | A | 3 | a0001c0001t0011g0039 a0006c0007t0001g0103 a0006c0007t0003g0038 |
3 | HG02970.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.60-1604C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644677 | |||||||
| chr8:58644703 | T | C | 54 | a0001c0001t0001g0069 a0001c0001t0001g0149 a0001c0001t0001g0150 others(51): Show |
57 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.60-1630A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644703 | |||||||
| chr8:58644820 | A | G | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-1747T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644820 | |||||||
| chr8:58644936 | T | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1863A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644936 | |||||||
| chr8:58644964 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0069 a0001c0001t0001g0097 others(75): Show |
84 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.60-1891C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644964 | |||||||
| chr8:58644979 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1906T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644979 | |||||||
| chr8:58645004 | C | T | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(13): Show |
17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.60-1931G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645004 | |||||||
| chr8:58645112 | T | C | 1 | a0006c0007t0001g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.60-2039A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645112 | |||||||
| chr8:58645113 | TA | T | 15 | a0001c0001t0001g0097 a0001c0001t0001g0104 a0001c0001t0001g0125 others(12): Show |
16 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-2041delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645113 | |||||||
| chr8:58645204 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2131T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645204 | |||||||
| chr8:58645266 | T | TA | 98 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(95): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.60-2194dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645266 | |||||||
| chr8:58645367 | T | A | 1 | a0001c0001t0002g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.60-2294A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645367 | |||||||
| chr8:58645380 | G | A | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.60-2307C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645380 | |||||||
| chr8:58645460 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2387G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645460 | |||||||
| chr8:58645468 | G | C | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-2395C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645468 | |||||||
| chr8:58645696 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.60-2623A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645696 | |||||||
| chr8:58645697 | C | G | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-2624G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645697 | |||||||
| chr8:58645766 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2693G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645766 | |||||||
| chr8:58645788 | C | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0001c0001t0001g0125 others(6): Show |
10 | HG00597.hp2 NA18977.hp2 NA19000.hp2 others(7): Show |
intron_variant | MODIFIER | c.60-2715G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645788 | |||||||
| chr8:58645838 | C | T | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60-2765G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645838 | |||||||
| chr8:58645859 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.60-2786C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645859 | |||||||
| chr8:58645910 | G | A | 69 | a0001c0001t0001g0069 a0001c0001t0001g0138 a0001c0001t0001g0149 others(66): Show |
72 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.60-2837C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645910 | |||||||
| chr8:58645972 | T | C | 12 | a0001c0001t0001g0104 a0001c0001t0001g0182 a0001c0001t0001g0208 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.60-2899A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645972 | |||||||
| chr8:58645985 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.60-2912C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645985 | |||||||
| chr8:58646001 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2928T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646001 | |||||||
| chr8:58646016 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2943T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646016 | |||||||
| chr8:58646035 | C | G | 60 | a0001c0001t0001g0069 a0001c0001t0001g0149 a0001c0001t0001g0150 others(57): Show |
63 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.60-2962G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646035 | |||||||
| chr8:58646044 | A | AATC | 8 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0001t0001g0295 others(5): Show |
8 | HG01433.hp2 HG01515.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-2974_60-2972dup others(3): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646044 | |||||||
| chr8:58646390 | T | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-3317A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646390 | |||||||
| chr8:58646531 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0208 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.60-3458A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646531 | |||||||
| chr8:58646561 | A | T | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.60-3488T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646561 | |||||||
| chr8:58646670 | T | C | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-3597A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646670 | |||||||
| chr8:58646803 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.60-3730C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646803 | |||||||
| chr8:58646840 | C | T | 17 | a0001c0001t0001g0089 a0001c0001t0001g0145 a0001c0001t0001g0340 others(14): Show |
17 | HG00408.hp2 HG00673.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.60-3767G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646840 | |||||||
| chr8:58646993 | T | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-3920A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646993 | |||||||
| chr8:58647359 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-4286T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647359 | |||||||
| chr8:58647440 | G | C | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(13): Show |
17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.60-4367C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647440 | |||||||
| chr8:58647501 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.60-4428T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647501 | |||||||
| chr8:58647503 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.60-4430C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647503 | |||||||
| chr8:58647524 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.60-4451C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647524 | |||||||
| chr8:58647534 | G | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0005c0015t0009g0034 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-4461C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647534 | |||||||
| chr8:58647542 | G | C | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(13): Show |
17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.60-4469C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647542 | |||||||
| chr8:58647556 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-4483T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647556 | |||||||
| chr8:58647594 | CA | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-4522delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647594 | |||||||
| chr8:58647738 | A | G | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-4665T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647738 | |||||||
| chr8:58647789 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-4716G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647789 | |||||||
| chr8:58648391 | T | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-5318A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648391 | |||||||
| chr8:58648574 | C | T | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-5501G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648574 | |||||||
| chr8:58648772 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-5699C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648772 | |||||||
| chr8:58648793 | A | G | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.60-5720T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648793 | |||||||
| chr8:58648908 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-5835T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648908 | |||||||
| chr8:58648940 | T | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-5867A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648940 | |||||||
| chr8:58648979 | C | T | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.60-5906G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648979 | |||||||
| chr8:58649079 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0208 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.60-6006C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649079 | |||||||
| chr8:58649181 | T | C | 1 | a0002c0002t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.60-6108A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649181 | |||||||
| chr8:58649186 | G | T | 199 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(196): Show |
209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.60-6113C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649186 | |||||||
| chr8:58649233 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-6160C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649233 | |||||||
| chr8:58649350 | C | T | 1 | a0001c0001t0002g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.60-6277G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649350 | |||||||
| chr8:58649528 | G | A | 199 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(196): Show |
209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.60-6455C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649528 | |||||||
| chr8:58649546 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.60-6473C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649546 | |||||||
| chr8:58649628 | C | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-6555G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649628 | |||||||
| chr8:58649634 | G | T | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.60-6561C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649634 | |||||||
| chr8:58649700 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-6627T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649700 | |||||||
| chr8:58649926 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0208 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.60-6853A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649926 | |||||||
| chr8:58650097 | A | C | 217 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(214): Show |
228 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.60-7024T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650097 | |||||||
| chr8:58650256 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-7183C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650256 | |||||||
| chr8:58650442 | ATTTTCT | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-7375_60-7370del others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650442 | |||||||
| chr8:58650450 | T | C | 1 | a0001c0001t0002g0146 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.60-7377A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650450 | |||||||
| chr8:58650866 | T | A | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.60-7793A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650866 | |||||||
| chr8:58650934 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0004t0001g0116 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-7861G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650934 | |||||||
| chr8:58651005 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.60-7932A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651005 | |||||||
| chr8:58651070 | C | T | 1 | a0002c0002t0001g0195 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.60-7997G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651070 | |||||||
| chr8:58651228 | A | G | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-8155T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651228 | |||||||
| chr8:58651336 | G | C | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.59+8237C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651336 | |||||||
| chr8:58651438 | A | G | 2 | a0005c0015t0009g0034 a0005c0016t0006g0102 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.59+8135T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651438 | |||||||
| chr8:58651441 | A | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(53): Show |
62 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.59+8132T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651441 | |||||||
| chr8:58651537 | C | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+8036G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651537 | |||||||
| chr8:58651556 | C | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+8017G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651556 | |||||||
| chr8:58651572 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.59+8001C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651572 | |||||||
| chr8:58651573 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.59+8000T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651573 | |||||||
| chr8:58651757 | C | A | 4 | a0001c0004t0001g0116 a0003c0005t0003g0044 a0005c0015t0009g0034 others(1): Show |
4 | HG02572.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+7816G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651757 | |||||||
| chr8:58651763 | G | A | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.59+7810C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651763 | |||||||
| chr8:58651797 | G | A | 4 | a0001c0004t0001g0116 a0003c0005t0003g0044 a0005c0015t0009g0034 others(1): Show |
4 | HG02572.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+7776C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651797 | |||||||
| chr8:58651886 | G | A | 1 | a0001c0003t0001g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59+7687C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651886 | |||||||
| chr8:58652157 | G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.59+7416C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652157 | |||||||
| chr8:58652244 | A | G | 7 | a0001c0001t0001g0119 a0001c0001t0001g0152 a0001c0001t0001g0270 others(4): Show |
7 | NA18949.hp2 NA18978.hp2 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.59+7329T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652244 | |||||||
| chr8:58652401 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59+7172G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652401 | |||||||
| chr8:58652429 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59+7144T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652429 | |||||||
| chr8:58652485 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59+7088A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652485 | |||||||
| chr8:58652514 | G | A | 70 | a0001c0001t0001g0069 a0001c0001t0001g0138 a0001c0001t0001g0149 others(67): Show |
73 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.59+7059C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652514 | |||||||
| chr8:58652692 | C | A | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.59+6881G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652692 | |||||||
| chr8:58652922 | G | A | 14 | a0001c0001t0001g0208 a0001c0001t0002g0099 a0001c0001t0002g0100 others(11): Show |
14 | HG00408.hp1 HG02572.hp1 HG03130.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+6651C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652922 | |||||||
| chr8:58652958 | C | T | 13 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0256 others(10): Show |
13 | HG00408.hp1 HG02572.hp1 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+6615G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652958 | |||||||
| chr8:58652959 | A | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0275 |
2 | NA19075.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.59+6614T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652959 | |||||||
| chr8:58653084 | G | A | 9 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0256 others(6): Show |
9 | HG00408.hp1 HG02572.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+6489C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653084 | |||||||
| chr8:58653093 | C | G | 24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0176 others(21): Show |
24 | HG00408.hp1 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+6480G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653093 | |||||||
| chr8:58653106 | C | T | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+6467G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653106 | |||||||
| chr8:58653130 | GAGAGT | G | 13 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0256 others(10): Show |
13 | HG00408.hp1 HG02572.hp1 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+6438_59+6442del others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653130 | |||||||
| chr8:58653159 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.59+6414G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653159 | |||||||
| chr8:58653186 | G | A | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0176 others(13): Show |
17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.59+6387C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653186 | |||||||
| chr8:58653273 | C | T | 1 | a0005c0015t0009g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59+6300G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653273 | |||||||
| chr8:58653286 | G | T | 8 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0256 others(5): Show |
8 | HG00408.hp1 NA18747.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.59+6287C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653286 | |||||||
| chr8:58653307 | A | C | 1 | a0001c0001t0002g0156 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.59+6266T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653307 | |||||||
| chr8:58653461 | AC | A | 64 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0149 others(61): Show |
67 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.59+6111delG | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653461 | |||||||
| chr8:58653498 | A | T | 10 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0256 others(7): Show |
10 | HG00408.hp1 HG02572.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.59+6075T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653498 | |||||||
| chr8:58653571 | GAAGTA | G | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5997_59+6001del others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653571 | |||||||
| chr8:58653609 | C | T | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.59+5964G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653609 | |||||||
| chr8:58653635 | T | G | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5938A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653635 | |||||||
| chr8:58653780 | C | A | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.59+5793G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653780 | |||||||
| chr8:58653799 | T | A | 1 | a0002c0002t0002g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.59+5774A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653799 | |||||||
| chr8:58653831 | T | A | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5742A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653831 | |||||||
| chr8:58653850 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.59+5723A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653850 | |||||||
| chr8:58653944 | C | T | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5629G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653944 | |||||||
| chr8:58653956 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59+5617A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653956 | |||||||
| chr8:58654016 | T | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+5557A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654016 | |||||||
| chr8:58654278 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.59+5295A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654278 | |||||||
| chr8:58654321 | G | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+5252C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654321 | |||||||
| chr8:58654340 | C | A | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.59+5233G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654340 | |||||||
| chr8:58654433 | T | C | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5140A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654433 | |||||||
| chr8:58654491 | G | A | 2 | a0001c0004t0001g0116 a0003c0005t0003g0044 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+5082C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654491 | |||||||
| chr8:58654555 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.59+5018T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654555 | |||||||
| chr8:58654580 | C | T | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+4993G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654580 | |||||||
| chr8:58654609 | T | C | 32 | a0001c0001t0001g0139 a0001c0001t0001g0192 a0001c0001t0001g0263 others(29): Show |
34 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.59+4964A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654609 | |||||||
| chr8:58654787 | C | A | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.59+4786G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654787 | |||||||
| chr8:58654830 | C | T | 228 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0057 others(225): Show |
239 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.59+4743G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654830 | |||||||
| chr8:58654959 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0139 a0001c0001t0001g0169 others(2): Show |
5 | HG00621.hp1 HG02135.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+4614G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654959 | |||||||
| chr8:58655036 | A | C | 1 | a0001c0001t0003g0047 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.59+4537T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655036 | |||||||
| chr8:58655088 | C | A | 107 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(104): Show |
113 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.59+4485G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655088 | |||||||
| chr8:58655164 | G | A | 2 | a0002c0002t0001g0272 a0002c0002t0001g0296 |
2 | NA18949.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.59+4409C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655164 | |||||||
| chr8:58655236 | G | T | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+4337C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655236 | |||||||
| chr8:58655252 | G | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59+4321C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655252 | |||||||
| chr8:58655288 | A | G | 1 | a0002c0002t0001g0272 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.59+4285T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655288 | |||||||
| chr8:58655303 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+4270A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655303 | |||||||
| chr8:58655326 | G | T | 75 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0093 others(72): Show |
80 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.59+4247C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655326 | |||||||
| chr8:58655329 | G | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59+4244C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655329 | |||||||
| chr8:58655358 | T | C | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+4215A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655358 | |||||||
| chr8:58655399 | CT | C | 104 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0149 others(101): Show |
109 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.59+4173delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655399 | |||||||
| chr8:58655477 | G | GT | 32 | a0001c0001t0001g0139 a0001c0001t0001g0192 a0001c0001t0001g0263 others(29): Show |
34 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.59+4095dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655477 | |||||||
| chr8:58655616 | T | C | 27 | a0001c0001t0001g0192 a0001c0001t0001g0263 a0001c0001t0001g0340 others(24): Show |
29 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.59+3957A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655616 | |||||||
| chr8:58655708 | C | G | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.59+3865G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655708 | |||||||
| chr8:58655732 | T | C | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3841A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655732 | |||||||
| chr8:58655824 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.59+3749C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655824 | |||||||
| chr8:58655840 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3733C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655840 | |||||||
| chr8:58655851 | G | T | 32 | a0001c0001t0001g0139 a0001c0001t0001g0192 a0001c0001t0001g0263 others(29): Show |
34 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.59+3722C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655851 | |||||||
| chr8:58655852 | G | A | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3721C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655852 | |||||||
| chr8:58655855 | T | C | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3718A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655855 | |||||||
| chr8:58655885 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0011g0039 a0005c0015t0009g0034 others(2): Show |
5 | HG02970.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+3688G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655885 | |||||||
| chr8:58655895 | A | C | 63 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0149 others(60): Show |
66 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.59+3678T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655895 | |||||||
| chr8:58655907 | T | TA | 27 | a0001c0001t0001g0192 a0001c0001t0001g0263 a0001c0001t0001g0340 others(24): Show |
29 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.59+3665dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655907 | |||||||
| chr8:58655917 | C | A | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3656G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655917 | |||||||
| chr8:58655966 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.59+3607T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655966 | |||||||
| chr8:58656007 | T | C | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3566A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656007 | |||||||
| chr8:58656016 | CT | C | 32 | a0001c0001t0001g0139 a0001c0001t0001g0192 a0001c0001t0001g0263 others(29): Show |
34 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.59+3556delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656016 | |||||||
| chr8:58656023 | TTG | T | 63 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0149 others(60): Show |
66 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.59+3548_59+3549del others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656023 | |||||||
| chr8:58656025 | G | T | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3548C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656025 | |||||||
| chr8:58656029 | G | T | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3544C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656029 | |||||||
| chr8:58656033 | G | T | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3540C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656033 | |||||||
| chr8:58656121 | C | G | 13 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0175 others(10): Show |
13 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.59+3452G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656121 | |||||||
| chr8:58656156 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.59+3417G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656156 | |||||||
| chr8:58656211 | C | A | 5 | a0001c0001t0002g0191 a0001c0001t0002g0329 a0001c0001t0002g0330 others(2): Show |
5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+3362G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656211 | |||||||
| chr8:58656282 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3291C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656282 | |||||||
| chr8:58656404 | A | C | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3169T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656404 | |||||||
| chr8:58656488 | G | C | 5 | a0001c0001t0001g0139 a0001c0001t0011g0039 a0005c0015t0009g0034 others(2): Show |
5 | HG02970.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+3085C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656488 | |||||||
| chr8:58656597 | CGGGT | C | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2972_59+2975del others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656597 | |||||||
| chr8:58656612 | C | T | 1 | a0001c0003t0003g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.59+2961G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656612 | |||||||
| chr8:58656697 | A | G | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2876T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656697 | |||||||
| chr8:58656779 | A | G | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2794T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656779 | |||||||
| chr8:58656788 | C | A | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2785G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656788 | |||||||
| chr8:58656857 | A | G | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2716T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656857 | |||||||
| chr8:58657099 | G | A | 2 | a0003c0005t0001g0212 a0003c0005t0009g0035 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.59+2474C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657099 | |||||||
| chr8:58657331 | C | T | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2242G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657331 | |||||||
| chr8:58657341 | C | A | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.59+2232G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657341 | |||||||
| chr8:58657397 | A | AAGTTTTC others(13): Show |
10 | a0001c0001t0001g0138 a0001c0001t0008g0036 a0001c0001t0008g0041 others(7): Show |
10 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2156_59+2175dup others(20): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657397 | |||||||
| chr8:58657464 | C | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59+2109G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657464 | |||||||
| chr8:58657494 | A | G | 10 | a0001c0001t0001g0138 a0001c0001t0008g0036 a0001c0001t0008g0041 others(7): Show |
10 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2079T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657494 | |||||||
| chr8:58657531 | G | C | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2042C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657531 | |||||||
| chr8:58657549 | A | G | 1 | a0001c0001t0002g0334 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.59+2024T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657549 | |||||||
| chr8:58657569 | A | G | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.59+2004T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657569 | |||||||
| chr8:58657617 | C | A | 151 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(148): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.59+1956G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657617 | |||||||
| chr8:58657650 | A | G | 4 | a0001c0004t0001g0116 a0003c0005t0001g0212 a0003c0005t0003g0044 others(1): Show |
4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+1923T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657650 | |||||||
| chr8:58657714 | T | G | 3 | a0001c0001t0001g0136 a0001c0004t0001g0116 a0003c0005t0003g0044 |
3 | HG02451.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+1859A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657714 | |||||||
| chr8:58657768 | C | T | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59+1805G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657768 | |||||||
| chr8:58657828 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.59+1745T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657828 | |||||||
| chr8:58657869 | T | C | 3 | a0002c0002t0001g0077 a0002c0002t0001g0141 a0002c0002t0001g0333 |
3 | HG01168.hp1 NA18954.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.59+1704A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657869 | |||||||
| chr8:58657915 | A | G | 66 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0149 others(63): Show |
69 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.59+1658T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657915 | |||||||
| chr8:58657924 | A | G | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.59+1649T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657924 | |||||||
| chr8:58657937 | T | C | 6 | a0001c0001t0002g0257 a0001c0001t0002g0334 a0001c0001t0002g0335 others(3): Show |
6 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.59+1636A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657937 | |||||||
| chr8:58657952 | T | C | 28 | a0001c0001t0001g0136 a0001c0001t0001g0166 a0001c0001t0001g0192 others(25): Show |
29 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.59+1621A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657952 | |||||||
| chr8:58658060 | C | T | 4 | a0001c0001t0001g0166 a0001c0001t0001g0194 a0001c0001t0001g0209 others(1): Show |
4 | HG02280.hp1 HG02602.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+1513G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658060 | |||||||
| chr8:58658116 | T | G | 1 | a0001c0001t0001g0343 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.59+1457A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658116 | |||||||
| chr8:58658208 | T | A | 25 | a0001c0001t0001g0104 a0001c0001t0001g0136 a0001c0001t0001g0139 others(22): Show |
26 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.59+1365A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658208 | |||||||
| chr8:58658572 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0261 a0001c0001t0002g0114 |
3 | HG01978.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.59+1001A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658572 | |||||||
| chr8:58658624 | G | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0115 a0001c0001t0001g0138 others(9): Show |
12 | HG01109.hp1 HG02280.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.59+949C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658624 | |||||||
| chr8:58658632 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.59+941G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658632 | |||||||
| chr8:58658667 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.59+906G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658667 | |||||||
| chr8:58658675 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.59+898G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658675 | |||||||
| chr8:58658728 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0054 others(192): Show |
208 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.59+845G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658728 | |||||||
| chr8:58658969 | C | T | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59+604G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658969 | |||||||
| chr8:58658988 | C | T | 6 | a0001c0001t0001g0139 a0001c0001t0001g0213 a0001c0001t0002g0214 others(3): Show |
6 | HG02615.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.59+585G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658988 | |||||||
| chr8:58658989 | G | T | 166 | a0001c0001t0001g0009 a0001c0001t0001g0054 a0001c0001t0001g0057 others(163): Show |
175 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(172): Show |
intron_variant | MODIFIER | c.59+584C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658989 | |||||||
| chr8:58659128 | G | A | 1 | a0001c0001t0008g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.59+445C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58659128 | |||||||
| chr8:58659236 | C | T | 7 | a0001c0001t0002g0052 a0001c0001t0006g0053 a0001c0001t0008g0036 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.59+337G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58659236 | |||||||
| chr8:58659270 | C | T | 8 | a0001c0001t0003g0007 a0001c0001t0003g0040 a0001c0001t0008g0036 others(5): Show |
9 | HG01243.hp2 HG02486.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+303G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58659270 | |||||||
| chr8:58659297 | A | C | 145 | a0001c0001t0001g0009 a0001c0001t0001g0054 a0001c0001t0001g0057 others(142): Show |
154 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.59+276T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58659297 |