Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3684 |
| ensemblid | ENSG00000169896.18 |
| hgncid | 6149 |
| symbol | ITGAM |
| name | integrin subunit alpha M |
| refseq_nuc | NM_000632.4 |
| refseq_prot | NP_000623.2 |
| ensembl_nuc | ENST00000544665.9 |
| ensembl_prot | ENSP00000441691.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 31259975 |
| end | 31332877 |
| strand | + |
| ver | v1.2 |
| region | chr16:31259975-31332877 |
| region5000 | chr16:31254975-31337877 |
| regionname0 | ITGAM_chr16_31259975_31332877 |
| regionname5000 | ITGAM_chr16_31254975_31337877 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1152 | 176 | 53 | 36 | 64 | 6 | 15 | 36 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| a0002 | 0/0 | 1152 | 24 | 10 | 4 | 2 | 0 | 8 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| a0003 | 0/0 | 1152 | 23 | 15 | 4 | 0 | 2 | 2 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| a0004 | 0/0 | 1152 | 14 | 5 | 7 | 0 | 2 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| a0005 | 0/0 | 1152 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| a0006 | 0/0 | 1152 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| a0007 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| a0008 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| a0009 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| a0010 | 0/0 | 1152 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | MALRV others(1147): Show |
chr16 | 31254975 | 31337877 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3456 | 88 | 20 | 18 | 32 | 4 | 12 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0001c0002 | 0/0 | 3456 | 57 | 3 | 17 | 32 | 2 | 3 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0001c0005 | 0/0 | 3456 | 19 | 19 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0001c0007 | 0/0 | 3456 | 9 | 8 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0001c0008 | 0/0 | 3456 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0001c0013 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0002c0003 | 0/0 | 3456 | 24 | 10 | 4 | 2 | 0 | 8 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0003c0004 | 0/0 | 3456 | 23 | 15 | 4 | 0 | 2 | 2 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0004c0006 | 0/0 | 3456 | 14 | 5 | 7 | 0 | 2 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0005c0009 | 0/0 | 3456 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0006c0014 | 0/0 | 3456 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0007c0012 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0008c0010 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0009c0011 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 | ||
| a0010c0015 | 0/0 | 3456 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | ATGGC others(3451): Show |
chr16 | 31254975 | 31337877 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4719 | 74 | 6 | 18 | 32 | 4 | 12 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0001c0001t0002 | 0/0 | 4727 | 11 | 11 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4722): Show |
chr16 | 31254975 | 31337877 |
| a0001c0001t0004 | 0/0 | 4719 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0001c0002t0002 | 0/0 | 4727 | 56 | 3 | 16 | 32 | 2 | 3 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4722): Show |
chr16 | 31254975 | 31337877 |
| a0001c0002t0007 | 0/0 | 4727 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4722): Show |
chr16 | 31254975 | 31337877 |
| a0001c0005t0004 | 0/0 | 4719 | 19 | 19 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0001c0007t0004 | 0/0 | 4719 | 8 | 7 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0001c0007t0009 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0001c0008t0004 | 0/0 | 4719 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0001c0013t0008 | 0/0 | 4727 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4722): Show |
chr16 | 31254975 | 31337877 |
| a0002c0003t0003 | 0/0 | 4719 | 24 | 10 | 4 | 2 | 0 | 8 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0003c0004t0005 | 0/0 | 4732 | 22 | 15 | 3 | 0 | 2 | 2 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4727): Show |
chr16 | 31254975 | 31337877 |
| a0003c0004t0006 | 0/0 | 4732 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4727): Show |
chr16 | 31254975 | 31337877 |
| a0004c0006t0003 | 0/0 | 4719 | 14 | 5 | 7 | 0 | 2 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0005c0009t0002 | 0/0 | 4727 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4722): Show |
chr16 | 31254975 | 31337877 |
| a0006c0014t0001 | 0/0 | 4719 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0007c0012t0004 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0008c0010t0004 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0009c0011t0004 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| a0010c0015t0001 | 0/0 | 4719 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | CCTTC others(4714): Show |
chr16 | 31254975 | 31337877 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0008t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0008t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0013t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0005c0009t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0005c0009t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0006c0014t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0007c0012t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0008c0010t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0009c0011t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0010c0015t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0005 | g0032 | EUR | GBR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00323 | hp1 | a0004 | c0006 | t0003 | g0015 | EUR | FIN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0076 | EUR | FIN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00733 | hp2 | a0004 | c0006 | t0003 | g0017 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00738 | hp1 | a0001 | c0002 | t0007 | g0073 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00738 | hp2 | a0004 | c0006 | t0003 | g0004 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00741 | hp1 | a0004 | c0006 | t0003 | g0007 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00741 | hp2 | a0002 | c0003 | t0003 | g0119 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0106 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01070 | hp2 | a0006 | c0014 | t0001 | g0233 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0104 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01106 | hp1 | a0002 | c0003 | t0003 | g0122 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01106 | hp2 | a0002 | c0003 | t0003 | g0120 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01109 | hp1 | a0004 | c0006 | t0003 | g0018 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01109 | hp2 | a0003 | c0004 | t0006 | g0099 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01175 | hp1 | a0003 | c0004 | t0005 | g0031 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01243 | hp1 | a0002 | c0003 | t0003 | g0078 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01255 | hp2 | a0003 | c0004 | t0005 | g0030 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01256 | hp1 | a0004 | c0006 | t0003 | g0009 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01256 | hp2 | a0003 | c0004 | t0005 | g0020 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01258 | hp1 | a0004 | c0006 | t0003 | g0008 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01433 | hp2 | a0004 | c0006 | t0003 | g0011 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01496 | hp2 | a0001 | c0007 | t0004 | g0024 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01516 | hp1 | a0004 | c0006 | t0003 | g0005 | EUR | IBS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0028 | EUR | IBS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01891 | hp1 | a0002 | c0003 | t0003 | g0125 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01891 | hp2 | a0001 | c0008 | t0004 | g0139 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0081 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02040 | hp2 | a0005 | c0009 | t0002 | g0084 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02055 | hp2 | a0004 | c0006 | t0003 | g0016 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0067 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02129 | hp1 | a0005 | c0009 | t0002 | g0083 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02135 | hp2 | a0002 | c0003 | t0003 | g0070 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02145 | hp1 | a0001 | c0005 | t0004 | g0148 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02145 | hp2 | a0003 | c0004 | t0005 | g0089 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02257 | hp2 | a0003 | c0004 | t0005 | g0061 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02258 | hp2 | a0001 | c0005 | t0004 | g0159 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0021 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02280 | hp2 | a0001 | c0005 | t0004 | g0151 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02451 | hp1 | a0001 | c0013 | t0008 | g0173 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02572 | hp1 | a0002 | c0003 | t0003 | g0006 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02572 | hp2 | a0003 | c0004 | t0005 | g0098 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02615 | hp2 | a0003 | c0004 | t0005 | g0095 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02622 | hp1 | a0002 | c0003 | t0003 | g0126 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02622 | hp2 | a0001 | c0005 | t0004 | g0152 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02630 | hp1 | a0001 | c0005 | t0004 | g0155 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02630 | hp2 | a0002 | c0003 | t0003 | g0110 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02647 | hp1 | a0001 | c0007 | t0004 | g0145 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02647 | hp2 | a0007 | c0012 | t0004 | g0156 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02683 | hp1 | a0002 | c0003 | t0003 | g0038 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02717 | hp1 | a0001 | c0007 | t0004 | g0143 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02723 | hp2 | a0001 | c0005 | t0004 | g0242 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02735 | hp1 | a0003 | c0004 | t0005 | g0079 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02809 | hp2 | a0001 | c0007 | t0004 | g0147 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02818 | hp1 | a0003 | c0004 | t0005 | g0093 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02886 | hp2 | a0003 | c0004 | t0005 | g0097 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02895 | hp1 | a0004 | c0006 | t0003 | g0012 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02895 | hp2 | a0001 | c0005 | t0004 | g0002 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02896 | hp1 | a0008 | c0010 | t0004 | g0019 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02896 | hp2 | a0003 | c0004 | t0005 | g0100 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02897 | hp1 | a0001 | c0005 | t0004 | g0002 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02897 | hp2 | a0003 | c0004 | t0005 | g0103 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02922 | hp1 | a0001 | c0007 | t0004 | g0108 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02922 | hp2 | a0002 | c0003 | t0003 | g0112 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02965 | hp1 | a0001 | c0007 | t0004 | g0144 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02965 | hp2 | a0001 | c0005 | t0004 | g0162 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02970 | hp1 | a0004 | c0006 | t0003 | g0013 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02970 | hp2 | a0001 | c0005 | t0004 | g0163 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02976 | hp2 | a0003 | c0004 | t0005 | g0102 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03017 | hp2 | a0002 | c0003 | t0003 | g0036 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03041 | hp1 | a0003 | c0004 | t0005 | g0023 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03041 | hp2 | a0001 | c0005 | t0004 | g0157 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03098 | hp1 | a0003 | c0004 | t0005 | g0090 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0111 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03195 | hp2 | a0009 | c0011 | t0004 | g0003 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03209 | hp1 | a0001 | c0005 | t0004 | g0149 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0123 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03225 | hp1 | a0001 | c0005 | t0004 | g0158 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0027 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03453 | hp1 | a0003 | c0004 | t0005 | g0101 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03453 | hp2 | a0001 | c0005 | t0004 | g0153 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03486 | hp1 | a0001 | c0005 | t0004 | g0164 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03486 | hp2 | a0002 | c0003 | t0003 | g0109 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03491 | hp1 | a0002 | c0003 | t0003 | g0118 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03491 | hp2 | a0002 | c0003 | t0003 | g0060 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03516 | hp1 | a0001 | c0007 | t0004 | g0025 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03579 | hp1 | a0001 | c0007 | t0004 | g0146 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03579 | hp2 | a0004 | c0006 | t0003 | g0014 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03688 | hp1 | a0002 | c0003 | t0003 | g0039 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0071 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03710 | hp2 | a0003 | c0004 | t0005 | g0080 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03834 | hp2 | a0010 | c0015 | t0001 | g0172 | SAS | BEB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03942 | hp1 | a0002 | c0003 | t0003 | g0037 | SAS | BEB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG04115 | hp2 | a0002 | c0003 | t0003 | g0115 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG04199 | hp1 | a0002 | c0003 | t0003 | g0040 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18522 | hp2 | a0004 | c0006 | t0003 | g0010 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | CHB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18906 | hp2 | a0001 | c0008 | t0004 | g0140 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0121 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA20752 | hp2 | a0003 | c0004 | t0005 | g0029 | EUR | TSI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0105 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02109 | hp1 | a0001 | c0005 | t0004 | g0154 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02109 | hp2 | a0001 | c0005 | t0004 | g0150 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02486 | hp1 | a0002 | c0003 | t0003 | g0124 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02486 | hp2 | a0003 | c0004 | t0005 | g0088 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | USA | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG06807 | hp2 | a0003 | c0004 | t0005 | g0096 | AFR | USA | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA20300 | hp1 | a0001 | c0005 | t0004 | g0161 | AFR | USA | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA20300 | hp2 | a0001 | c0007 | t0009 | g0141 | AFR | USA | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA21309 | hp1 | a0003 | c0004 | t0005 | g0094 | AFR | LWK | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA21309 | hp2 | a0001 | c0005 | t0004 | g0160 | AFR | LWK | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0107 | REF | REF | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0235 | REF | REF | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31265490 | G | A | 3 | a0004 a0008 a0009 |
16 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(13): Show |
missense_variant | MODERATE | c.230G>A | p.Arg77His | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 3/30 | 320/4719 | 230/3459 | 77/1152 | chr16 | 31265490 | |||
| chr16:31277978 | G | A | 1 | a0007 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1225G>A | p.Ala409Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/30 | 1315/4719 | 1225/3459 | 409/1152 | chr16 | 31277978 | |||
| chr16:31278075 | T | C | 1 | a0003 | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
missense_variant | MODERATE | c.1322T>C | p.Met441Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/30 | 1412/4719 | 1322/3459 | 441/1152 | chr16 | 31278075 | |||
| chr16:31297854 | C | T | 1 | a0010 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1607C>T | p.Thr536Met | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/30 | 1697/4719 | 1607/3459 | 536/1152 | chr16 | 31297854 | |||
| chr16:31324464 | G | A | 1 | a0008 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.2068G>A | p.Val690Ile | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 17/30 | 2158/4719 | 2068/3459 | 690/1152 | chr16 | 31324464 | |||
| chr16:31325567 | C | T | 2 | a0002 a0004 |
38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
missense_variant | MODERATE | c.2573C>T | p.Ala858Val | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/30 | 2663/4719 | 2573/3459 | 858/1152 | chr16 | 31325567 | |||
| chr16:31326927 | T | A | 1 | a0005 | 2 | HG02040.hp2 HG02129.hp1 |
missense_variant | MODERATE | c.2700T>A | p.Asn900Lys | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/30 | 2790/4719 | 2700/3459 | 900/1152 | chr16 | 31326927 | |||
| chr16:31331663 | G | A | 1 | a0006 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.3415G>A | p.Asp1139Asn | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 3505/4719 | 3415/3459 | 1139/1152 | chr16 | 31331663 | |||
| chr16:31331684 | C | T | 2 | a0002 a0004 |
38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
missense_variant | MODERATE | c.3436C>T | p.Pro1146Ser | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 3526/4719 | 3436/3459 | 1146/1152 | chr16 | 31331684 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31271969 | G | A | 1 | a0001c0008 | 2 | HG01891.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.681G>A | p.Thr227Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/30 | 771/4719 | 681/3459 | 227/1152 | chr16 | 31271969 | |||
| chr16:31321334 | C | T | 3 | a0001c0005 a0001c0008 a0007c0012 |
22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
synonymous_variant | LOW | c.1801C>T | p.Leu601Leu | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 15/30 | 1891/4719 | 1801/3459 | 601/1152 | chr16 | 31321334 | |||
| chr16:31321569 | C | T | 3 | a0001c0007 a0008c0010 a0009c0011 |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
synonymous_variant | LOW | c.1944C>T | p.Ala648Ala | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/30 | 2034/4719 | 1944/3459 | 648/1152 | chr16 | 31321569 | |||
| chr16:31325398 | G | A | 2 | a0001c0002 a0005c0009 |
59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
synonymous_variant | LOW | c.2499G>A | p.Thr833Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 20/30 | 2589/4719 | 2499/3459 | 833/1152 | chr16 | 31325398 | |||
| chr16:31326873 | G | A | 1 | a0008c0010 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.2646G>A | p.Thr882Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/30 | 2736/4719 | 2646/3459 | 882/1152 | chr16 | 31326873 | |||
| chr16:31326897 | C | G | 1 | a0008c0010 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.2670C>G | p.Ser890Ser | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/30 | 2760/4719 | 2670/3459 | 890/1152 | chr16 | 31326897 | |||
| chr16:31328198 | G | A | 1 | a0001c0013 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.2760G>A | p.Pro920Pro | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/30 | 2850/4719 | 2760/3459 | 920/1152 | chr16 | 31328198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31260027 | C | T | 1 | a0001c0007t0009 | 1 | NA20300.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/30 | chr16 | 31260027 | |||||||
| chr16:31331860 | C | CGTGTGTG others(3): Show |
7 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0007 others(4): Show |
94 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*161_*162insGAGTGT others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 162 | INFO_REALIGN_3_PRIME | chr16 | 31331860 | |||||
| chr16:31331894 | CAT | C | 7 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0007 others(4): Show |
94 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*188_*189delAT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 188 | chr16 | 31331894 | ||||||
| chr16:31331914 | T | C | 2 | a0003c0004t0005 a0003c0004t0006 |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*207T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 207 | chr16 | 31331914 | ||||||
| chr16:31331922 | T | C | 17 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(14): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*215T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 215 | chr16 | 31331922 | ||||||
| chr16:31332065 | A | G | 2 | a0002c0003t0003 a0004c0006t0003 |
38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*358A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 358 | chr16 | 31332065 | ||||||
| chr16:31332332 | A | G | 17 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(14): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*625A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 625 | chr16 | 31332332 | ||||||
| chr16:31332349 | G | C | 1 | a0001c0002t0007 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 642 | chr16 | 31332349 | ||||||
| chr16:31332399 | G | A | 1 | a0001c0013t0008 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*692G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 692 | chr16 | 31332399 | ||||||
| chr16:31332448 | T | C | 17 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(14): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*741T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 741 | chr16 | 31332448 | ||||||
| chr16:31332619 | C | T | 1 | a0003c0004t0006 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*912C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 912 | chr16 | 31332619 | ||||||
| chr16:31332634 | T | TTTTAC | 2 | a0003c0004t0005 a0003c0004t0006 |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*928_*932dupTTTAC | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 933 | INFO_REALIGN_3_PRIME | chr16 | 31332634 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31260224 | G | A | 139 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(136): Show |
140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.28+132G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260224 | |||||||
| chr16:31260344 | G | T | 1 | a0001c0005t0004g0242 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28+252G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260344 | |||||||
| chr16:31260379 | T | C | 25 | a0001c0001t0004g0142 a0001c0005t0004g0002 a0001c0005t0004g0148 others(22): Show |
26 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.28+287T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260379 | |||||||
| chr16:31260549 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.28+457G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260549 | |||||||
| chr16:31260659 | C | T | 1 | a0001c0007t0009g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.28+567C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260659 | |||||||
| chr16:31260670 | C | T | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.28+578C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260670 | |||||||
| chr16:31260796 | C | G | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.28+704C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260796 | |||||||
| chr16:31261032 | G | A | 17 | a0002c0003t0003g0006 a0004c0006t0003g0004 a0004c0006t0003g0005 others(14): Show |
17 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.29-660G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261032 | |||||||
| chr16:31261093 | C | T | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.29-599C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261093 | |||||||
| chr16:31261116 | G | A | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-576G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261116 | |||||||
| chr16:31261198 | C | CT | 21 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(18): Show |
21 | HG01106.hp1 HG01358.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.29-472dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261198 | ||||||
| chr16:31261198 | C | CTTT | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-474_29-472dupTT others(1): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261198 | ||||||
| chr16:31261198 | CT | C | 13 | a0001c0001t0001g0022 a0001c0001t0001g0166 a0001c0001t0001g0167 others(10): Show |
13 | HG01256.hp2 HG01496.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-472delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261198 | ||||||
| chr16:31261198 | CTTTTTTT | C | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.29-478_29-472delTT others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261198 | ||||||
| chr16:31261221 | G | C | 1 | a0002c0003t0003g0121 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.29-471G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261221 | |||||||
| chr16:31261342 | C | T | 3 | a0002c0003t0003g0118 a0002c0003t0003g0119 a0002c0003t0003g0120 |
3 | HG00741.hp2 HG01106.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.29-350C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261342 | |||||||
| chr16:31261513 | G | GT | 6 | a0001c0001t0001g0117 a0001c0001t0001g0237 a0001c0001t0001g0238 others(3): Show |
6 | HG02040.hp1 HG03486.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-169dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261513 | ||||||
| chr16:31261808 | T | C | 148 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(145): Show |
150 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.134+11T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31261808 | |||||||
| chr16:31262209 | T | A | 149 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(146): Show |
151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.134+412T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262209 | |||||||
| chr16:31262234 | C | T | 1 | a0001c0007t0004g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.134+437C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262234 | |||||||
| chr16:31262328 | C | CTCCCTTC others(2): Show |
7 | a0001c0005t0004g0157 a0001c0005t0004g0158 a0001c0005t0004g0159 others(4): Show |
7 | HG02258.hp2 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.134+539_134+540ins others(9): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262328 | ||||||
| chr16:31262330 | C | CCCTTCCT others(6): Show |
1 | a0001c0005t0004g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.134+539_134+540ins others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262330 | ||||||
| chr16:31262330 | CCCTTCCA others(1): Show |
C | 4 | a0001c0007t0004g0144 a0001c0007t0004g0145 a0001c0007t0004g0146 others(1): Show |
4 | HG02647.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+540_134+547del others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262330 | ||||||
| chr16:31262337 | A | ATCCT | 16 | a0001c0001t0001g0043 a0001c0001t0001g0181 a0001c0001t0001g0195 others(13): Show |
16 | HG00544.hp2 HG00609.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.134+603_134+606dup others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | ||||||
| chr16:31262337 | A | T | 24 | a0001c0001t0001g0168 a0001c0001t0001g0176 a0001c0001t0004g0142 others(21): Show |
25 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.134+540A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262337 | |||||||
| chr16:31262337 | ATCCT | A | 55 | a0001c0001t0001g0042 a0001c0001t0001g0075 a0001c0001t0001g0165 others(52): Show |
55 | HG00558.hp2 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.134+603_134+606del others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | ||||||
| chr16:31262337 | ATCCTTCC others(1): Show |
A | 56 | a0001c0001t0001g0022 a0001c0001t0001g0171 a0001c0001t0001g0180 others(53): Show |
56 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.134+599_134+606del others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | ||||||
| chr16:31262337 | ATCCTTCC others(5): Show |
A | 24 | a0001c0001t0001g0062 a0001c0001t0001g0086 a0001c0001t0001g0087 others(21): Show |
24 | HG00323.hp1 HG00673.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.134+595_134+606del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | ||||||
| chr16:31262337 | ATCCTTCC others(9): Show |
A | 7 | a0001c0001t0001g0214 a0001c0001t0001g0237 a0001c0001t0001g0238 others(4): Show |
7 | HG00733.hp2 HG00741.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.134+591_134+606del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | ||||||
| chr16:31262337 | ATCCTTCC others(13): Show |
A | 1 | a0001c0002t0002g0026 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.134+587_134+606del others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | ||||||
| chr16:31262337 | ATCCTTCC others(17): Show |
A | 5 | a0001c0007t0009g0141 a0001c0008t0004g0139 a0001c0008t0004g0140 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.134+583_134+606del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | ||||||
| chr16:31262337 | ATCCTTCC others(21): Show |
A | 2 | a0001c0001t0002g0174 a0004c0006t0003g0018 |
2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.134+579_134+606del others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | ||||||
| chr16:31262341 | T | A | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.134+544T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262341 | |||||||
| chr16:31262345 | T | A | 7 | a0001c0001t0002g0130 a0001c0007t0004g0024 a0001c0007t0004g0025 others(4): Show |
7 | HG01496.hp2 HG02630.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.134+548T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262345 | |||||||
| chr16:31262349 | T | A | 16 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0133 others(13): Show |
16 | HG00738.hp2 HG01106.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.134+552T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262349 | |||||||
| chr16:31262353 | T | A | 12 | a0001c0007t0004g0108 a0002c0003t0003g0126 a0004c0006t0003g0007 others(9): Show |
12 | HG00323.hp1 HG00741.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.134+556T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262353 | |||||||
| chr16:31262357 | T | A | 2 | a0002c0003t0003g0112 a0004c0006t0003g0017 |
2 | HG00733.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.134+560T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262357 | |||||||
| chr16:31262365 | T | A | 4 | a0001c0007t0009g0141 a0001c0008t0004g0139 a0001c0008t0004g0140 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.134+568T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262365 | |||||||
| chr16:31262369 | T | A | 2 | a0001c0001t0002g0174 a0004c0006t0003g0018 |
2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.134+572T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262369 | |||||||
| chr16:31262390 | T | G | 18 | a0001c0001t0004g0142 a0001c0005t0004g0002 a0001c0005t0004g0148 others(15): Show |
19 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.134+593T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262390 | |||||||
| chr16:31262390 | T | TCCTG | 5 | a0001c0005t0004g0151 a0001c0005t0004g0152 a0001c0005t0004g0153 others(2): Show |
5 | HG02109.hp1 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.134+596_134+597ins others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262390 | ||||||
| chr16:31262390 | T | TCCTTCCT others(5): Show |
1 | a0001c0005t0004g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.134+604_134+605ins others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262390 | ||||||
| chr16:31262390 | T | TCCTTCCT others(9): Show |
1 | a0007c0012t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.134+606_134+607ins others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262390 | ||||||
| chr16:31262421 | C | A | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.134+624C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262421 | |||||||
| chr16:31262539 | ACTACAG | A | 25 | a0001c0001t0004g0142 a0001c0005t0004g0002 a0001c0005t0004g0148 others(22): Show |
26 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.134+743_134+748del others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262539 | |||||||
| chr16:31262560 | ACCTGGCT others(5): Show |
A | 3 | a0001c0002t0002g0104 a0001c0002t0002g0105 a0001c0002t0002g0106 |
3 | HG01070.hp1 HG01071.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.134+764_134+775del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262560 | |||||||
| chr16:31262924 | A | G | 14 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(11): Show |
14 | HG01496.hp2 HG02280.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.134+1127A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262924 | |||||||
| chr16:31263230 | C | T | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.134+1433C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263230 | |||||||
| chr16:31263554 | C | T | 19 | a0002c0003t0003g0006 a0002c0003t0003g0119 a0002c0003t0003g0120 others(16): Show |
19 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.134+1757C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263554 | |||||||
| chr16:31263572 | T | C | 1 | a0001c0007t0009g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.134+1775T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263572 | |||||||
| chr16:31263608 | T | A | 14 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(11): Show |
14 | HG01496.hp2 HG02280.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.135-1787T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263608 | |||||||
| chr16:31263665 | CT | C | 29 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0004g0142 others(26): Show |
30 | HG01516.hp2 HG01517.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.135-1715delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263665 | ||||||
| chr16:31263669 | T | C | 1 | a0001c0002t0002g0026 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.135-1726T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263669 | |||||||
| chr16:31263802 | A | AATTT | 12 | a0001c0001t0002g0130 a0001c0001t0002g0135 a0001c0001t0002g0136 others(9): Show |
12 | HG01516.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.135-1545_135-1542d others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | ||||||
| chr16:31263802 | AATTT | A | 115 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0086 others(112): Show |
116 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.135-1545_135-1542d others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | ||||||
| chr16:31263802 | AATTTATT others(1): Show |
A | 36 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(33): Show |
36 | HG00544.hp1 HG00609.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.135-1549_135-1542d others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | ||||||
| chr16:31263802 | AATTTATT others(5): Show |
A | 8 | a0001c0002t0002g0033 a0001c0007t0004g0108 a0003c0004t0005g0020 others(5): Show |
8 | HG00099.hp1 HG00741.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.135-1553_135-1542d others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | ||||||
| chr16:31263802 | AATTTATT others(9): Show |
A | 27 | a0001c0001t0001g0178 a0001c0001t0004g0142 a0001c0005t0004g0002 others(24): Show |
28 | HG01257.hp2 HG01496.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.135-1557_135-1542d others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | ||||||
| chr16:31263802 | AATTTATT others(13): Show |
A | 1 | a0001c0001t0001g0177 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.135-1561_135-1542d others(22): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | ||||||
| chr16:31263905 | G | A | 2 | a0001c0001t0002g0174 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.135-1490G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263905 | |||||||
| chr16:31263993 | G | A | 1 | a0001c0002t0002g0001 | 2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.135-1402G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263993 | |||||||
| chr16:31264053 | T | G | 162 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(159): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.135-1342T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264053 | |||||||
| chr16:31264072 | G | A | 18 | a0002c0003t0003g0006 a0002c0003t0003g0119 a0002c0003t0003g0120 others(15): Show |
18 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.135-1323G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264072 | |||||||
| chr16:31264085 | C | T | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.135-1310C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264085 | |||||||
| chr16:31264088 | G | A | 10 | a0003c0004t0005g0020 a0003c0004t0005g0023 a0003c0004t0005g0029 others(7): Show |
10 | HG00099.hp1 HG01175.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.135-1307G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264088 | |||||||
| chr16:31264302 | C | T | 25 | a0001c0001t0004g0142 a0001c0005t0004g0002 a0001c0005t0004g0148 others(22): Show |
26 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.135-1093C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264302 | |||||||
| chr16:31264542 | A | G | 1 | a0002c0003t0003g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.135-853A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264542 | |||||||
| chr16:31264648 | A | C | 93 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.135-747A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264648 | |||||||
| chr16:31264749 | C | T | 1 | a0001c0002t0002g0231 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.135-646C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264749 | |||||||
| chr16:31264750 | G | A | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.135-645G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264750 | |||||||
| chr16:31265060 | G | A | 1 | a0003c0004t0005g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.135-335G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31265060 | |||||||
| chr16:31265160 | G | A | 25 | a0001c0001t0004g0142 a0001c0005t0004g0002 a0001c0005t0004g0148 others(22): Show |
26 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.135-235G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31265160 | |||||||
| chr16:31265244 | AT | A | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.135-144delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31265244 | ||||||
| chr16:31265570 | G | A | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.238+72G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 3/29 | chr16 | 31265570 | |||||||
| chr16:31265616 | C | T | 138 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(135): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.238+118C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 3/29 | chr16 | 31265616 | |||||||
| chr16:31265916 | G | A | 1 | a0001c0002t0002g0232 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.309+35G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 4/29 | chr16 | 31265916 | |||||||
| chr16:31265981 | C | T | 1 | a0010c0015t0001g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.310-49C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 4/29 | chr16 | 31265981 | |||||||
| chr16:31266219 | T | C | 1 | a0003c0004t0005g0088 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.427+72T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266219 | |||||||
| chr16:31266417 | T | TA | 7 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(4): Show |
7 | HG01175.hp2 HG01243.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.427+290dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266417 | ||||||
| chr16:31266417 | TA | T | 153 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(150): Show |
155 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.427+290delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266417 | ||||||
| chr16:31266417 | TAA | T | 6 | a0001c0001t0001g0022 a0001c0001t0002g0134 a0001c0002t0002g0106 others(3): Show |
6 | HG01070.hp1 HG02809.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+289_427+290del others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266417 | ||||||
| chr16:31266417 | TAAA | T | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+288_427+290del others(3): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266417 | ||||||
| chr16:31266558 | C | CA | 30 | a0001c0001t0001g0186 a0001c0001t0004g0113 a0001c0001t0004g0114 others(27): Show |
31 | HG00741.hp1 HG01106.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.427+426dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266558 | ||||||
| chr16:31266616 | A | C | 1 | a0001c0001t0001g0230 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.427+469A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266616 | |||||||
| chr16:31266738 | A | G | 2 | a0002c0003t0003g0110 a0002c0003t0003g0111 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.427+591A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266738 | |||||||
| chr16:31266741 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.427+594A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266741 | |||||||
| chr16:31266862 | A | AT | 10 | a0001c0001t0001g0185 a0001c0001t0001g0221 a0001c0001t0001g0222 others(7): Show |
10 | HG02055.hp1 HG02451.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.427+738dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266862 | ||||||
| chr16:31266862 | AT | A | 8 | a0001c0001t0001g0166 a0001c0001t0004g0142 a0001c0007t0004g0143 others(5): Show |
8 | HG01070.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.427+738delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266862 | ||||||
| chr16:31266862 | ATTTTTTT others(4): Show |
A | 1 | a0004c0006t0003g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+728_427+738del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266862 | ||||||
| chr16:31266862 | ATTTTTTT others(5): Show |
A | 157 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(154): Show |
159 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.427+727_427+738del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266862 | ||||||
| chr16:31266970 | C | T | 1 | a0004c0006t0003g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.427+823C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266970 | |||||||
| chr16:31267216 | C | G | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+1069C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267216 | |||||||
| chr16:31267435 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0228 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.427+1288C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267435 | |||||||
| chr16:31267491 | G | A | 2 | a0001c0001t0002g0174 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.427+1344G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267491 | |||||||
| chr16:31267507 | C | G | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+1360C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267507 | |||||||
| chr16:31267670 | G | T | 166 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(163): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.427+1523G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267670 | |||||||
| chr16:31267911 | T | G | 2 | a0004c0006t0003g0008 a0004c0006t0003g0009 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.427+1764T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267911 | |||||||
| chr16:31268124 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.427+1977C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268124 | |||||||
| chr16:31268127 | C | A | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+1980C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268127 | |||||||
| chr16:31268215 | T | C | 144 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(141): Show |
146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.427+2068T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268215 | |||||||
| chr16:31268528 | G | A | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+2381G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268528 | |||||||
| chr16:31268756 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.428-2198C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268756 | |||||||
| chr16:31268791 | C | A | 5 | a0001c0005t0004g0148 a0001c0005t0004g0149 a0001c0005t0004g0150 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-2163C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268791 | |||||||
| chr16:31268934 | G | A | 159 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(156): Show |
161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.428-2020G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268934 | |||||||
| chr16:31268936 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0117 a0001c0002t0002g0058 |
3 | HG02083.hp2 NA18960.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.428-2018C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268936 | |||||||
| chr16:31268961 | G | A | 159 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(156): Show |
161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.428-1993G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268961 | |||||||
| chr16:31269081 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.428-1873C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269081 | |||||||
| chr16:31269127 | T | C | 1 | a0001c0007t0004g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.428-1827T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269127 | |||||||
| chr16:31269131 | C | T | 1 | a0001c0007t0004g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.428-1823C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269131 | |||||||
| chr16:31269188 | C | T | 1 | a0001c0005t0004g0161 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.428-1766C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269188 | |||||||
| chr16:31269340 | T | C | 159 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(156): Show |
161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.428-1614T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269340 | |||||||
| chr16:31269349 | T | C | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.428-1605T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269349 | |||||||
| chr16:31269412 | G | A | 1 | a0009c0011t0004g0003 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.428-1542G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269412 | |||||||
| chr16:31269826 | A | G | 95 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(92): Show |
96 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.428-1128A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269826 | |||||||
| chr16:31269849 | G | A | 8 | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0001g0180 others(5): Show |
8 | HG01243.hp2 HG01257.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-1105G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269849 | |||||||
| chr16:31270084 | CCTT | C | 49 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(46): Show |
49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.428-869_428-867del others(3): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270084 | |||||||
| chr16:31270103 | A | ATCCT | 5 | a0001c0001t0001g0177 a0001c0005t0004g0149 a0001c0005t0004g0153 others(2): Show |
5 | HG02165.hp1 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-826_428-823dup others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270103 | ||||||
| chr16:31270103 | A | ATCCTTCC others(5): Show |
1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.428-834_428-823dup others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270103 | ||||||
| chr16:31270103 | A | ATCCTTCC others(9): Show |
4 | a0001c0007t0004g0143 a0001c0007t0004g0144 a0001c0007t0004g0145 others(1): Show |
4 | HG02647.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-838_428-823dup others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270103 | ||||||
| chr16:31270103 | A | ATCCTTCC others(13): Show |
1 | a0001c0007t0004g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.428-842_428-823dup others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270103 | ||||||
| chr16:31270126 | C | CTCCTTTG others(7): Show |
2 | a0001c0008t0004g0139 a0009c0011t0004g0003 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.428-827_428-826ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270126 | C | CTCCTTTG others(12): Show |
2 | a0001c0007t0004g0024 a0001c0007t0009g0141 |
2 | HG01496.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.428-827_428-826ins others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270126 | C | CTCCTTTG others(17): Show |
3 | a0001c0007t0004g0108 a0002c0003t0003g0124 a0002c0003t0003g0125 |
3 | HG01891.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.428-827_428-826ins others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270126 | C | CTCCTTTG others(22): Show |
3 | a0001c0007t0004g0025 a0004c0006t0003g0012 a0008c0010t0004g0019 |
3 | HG02895.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.428-827_428-826ins others(29): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270126 | C | CTCCTTTG others(27): Show |
5 | a0002c0003t0003g0006 a0002c0003t0003g0126 a0004c0006t0003g0013 others(2): Show |
5 | HG00733.hp2 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-827_428-826ins others(34): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270126 | C | CTCCTTTG others(32): Show |
7 | a0002c0003t0003g0121 a0002c0003t0003g0122 a0002c0003t0003g0123 others(4): Show |
7 | HG00323.hp1 HG00738.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-827_428-826ins others(39): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270126 | C | CTCCTTTG others(37): Show |
5 | a0002c0003t0003g0039 a0002c0003t0003g0040 a0002c0003t0003g0115 others(2): Show |
5 | HG03579.hp2 HG03688.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-827_428-826ins others(44): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270126 | C | CTCCTTTG others(42): Show |
4 | a0002c0003t0003g0037 a0002c0003t0003g0038 a0004c0006t0003g0005 others(1): Show |
4 | HG00741.hp1 HG01516.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-827_428-826ins others(49): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270126 | C | CTCCTTTG others(47): Show |
3 | a0002c0003t0003g0036 a0004c0006t0003g0008 a0004c0006t0003g0009 |
3 | HG01256.hp1 HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.428-827_428-826ins others(54): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270126 | C | CTCCTTTG others(57): Show |
1 | a0002c0003t0003g0060 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.428-827_428-826ins others(64): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | ||||||
| chr16:31270130 | C | CTT | 36 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(33): Show |
36 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.428-823_428-822ins others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | ||||||
| chr16:31270130 | C | CTTCCTCC others(7): Show |
8 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG00099.hp2 HG01123.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.428-823_428-822ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | ||||||
| chr16:31270130 | C | CTTCCTCC others(12): Show |
8 | a0001c0001t0001g0216 a0001c0001t0001g0230 a0001c0005t0004g0002 others(5): Show |
9 | HG00642.hp1 HG02258.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.428-823_428-822ins others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | ||||||
| chr16:31270130 | C | CTTCCTCC others(17): Show |
1 | a0001c0005t0004g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.428-823_428-822ins others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | ||||||
| chr16:31270130 | C | CTTCCTCC others(22): Show |
3 | a0001c0005t0004g0154 a0001c0005t0004g0157 a0007c0012t0004g0156 |
3 | HG02109.hp1 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.428-823_428-822ins others(29): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | ||||||
| chr16:31270130 | C | CTTCCTTC others(11): Show |
1 | a0001c0005t0004g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.428-823_428-822ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | ||||||
| chr16:31270130 | C | CTTCCTTC others(16): Show |
1 | a0001c0005t0004g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.428-823_428-822ins others(23): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | ||||||
| chr16:31270130 | C | CTTCCTTC others(47): Show |
1 | a0001c0001t0004g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.428-823_428-822ins others(54): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | ||||||
| chr16:31270130 | C | CTTCCTTC others(52): Show |
1 | a0001c0001t0004g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.428-823_428-822ins others(59): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | ||||||
| chr16:31270137 | G | C | 60 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(57): Show |
61 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.428-817G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270137 | |||||||
| chr16:31270137 | G | GCTTTC | 8 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0210 others(5): Show |
8 | HG02015.hp2 HG02165.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.428-767_428-763dup others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | ||||||
| chr16:31270137 | G | GCTTTCCT others(3): Show |
29 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0165 others(26): Show |
29 | HG00544.hp2 HG00609.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.428-772_428-763dup others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | ||||||
| chr16:31270137 | G | GCTTTCCT others(8): Show |
21 | a0001c0001t0001g0167 a0001c0001t0001g0170 a0001c0001t0001g0181 others(18): Show |
21 | HG00558.hp2 HG00673.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.428-777_428-763dup others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | ||||||
| chr16:31270137 | G | GCTTTCCT others(13): Show |
1 | a0001c0002t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.428-782_428-763dup others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | ||||||
| chr16:31270137 | G | GCTTTCCT others(18): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0192 |
2 | HG01243.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.428-787_428-763dup others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | ||||||
| chr16:31270137 | GCTTTCCT others(3): Show |
G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0227 a0001c0002t0002g0236 |
3 | NA18945.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.428-772_428-763del others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | ||||||
| chr16:31270137 | GCTTTCCT others(18): Show |
G | 12 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(9): Show |
12 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.428-787_428-763del others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | ||||||
| chr16:31270137 | GCTTTCCT others(23): Show |
G | 1 | a0002c0003t0003g0112 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.428-792_428-763del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | ||||||
| chr16:31270160 | TTCCTTTC | T | 87 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(84): Show |
88 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.428-793_428-787del others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270160 | |||||||
| chr16:31270167 | C | CCTT | 7 | a0001c0001t0002g0174 a0001c0001t0004g0142 a0001c0007t0004g0143 others(4): Show |
7 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-786_428-784dup others(3): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270167 | ||||||
| chr16:31270216 | C | T | 87 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(84): Show |
88 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.428-738C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270216 | |||||||
| chr16:31270217 | G | A | 2 | a0001c0007t0004g0024 a0001c0007t0004g0108 |
2 | HG01496.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428-737G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270217 | |||||||
| chr16:31270393 | C | T | 13 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(10): Show |
13 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.428-561C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270393 | |||||||
| chr16:31270430 | T | C | 165 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(162): Show |
167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.428-524T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270430 | |||||||
| chr16:31270688 | C | CGT | 18 | a0001c0001t0001g0087 a0001c0001t0001g0117 a0001c0001t0001g0170 others(15): Show |
19 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.428-255_428-254dup others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270688 | ||||||
| chr16:31270699 | G | GTA | 4 | a0001c0001t0001g0186 a0001c0001t0001g0222 a0004c0006t0003g0010 others(1): Show |
4 | HG00733.hp2 HG03669.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-211_428-210dup others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTATA | 9 | a0001c0001t0001g0213 a0002c0003t0003g0036 a0002c0003t0003g0123 others(6): Show |
9 | HG00738.hp2 HG01070.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.428-213_428-210dup others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTATATA | 7 | a0001c0001t0001g0226 a0001c0007t0004g0024 a0002c0003t0003g0122 others(4): Show |
7 | HG01106.hp1 HG01109.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-215_428-210dup others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTATATAT others(1): Show |
6 | a0001c0001t0001g0210 a0002c0003t0003g0060 a0002c0003t0003g0121 others(3): Show |
6 | HG00323.hp1 HG01258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-217_428-210dup others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTATATAT others(3): Show |
1 | a0004c0006t0003g0011 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.428-219_428-210dup others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTA | 19 | a0001c0001t0001g0075 a0001c0001t0001g0192 a0001c0001t0001g0197 others(16): Show |
19 | HG00609.hp1 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTATA | 25 | a0001c0001t0001g0046 a0001c0001t0001g0086 a0001c0001t0001g0166 others(22): Show |
25 | HG00544.hp1 HG00673.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTATAT others(1): Show |
17 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0185 others(14): Show |
17 | HG01243.hp2 HG01257.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTATAT others(3): Show |
9 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG01123.hp1 HG03239.hp2 HG04115.hp1 others(6): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTATAT others(5): Show |
5 | a0001c0001t0001g0194 a0001c0002t0002g0041 a0001c0002t0002g0064 others(2): Show |
5 | HG00642.hp2 HG01361.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTATAT others(7): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0167 a0001c0001t0001g0223 others(2): Show |
5 | HG00558.hp1 HG01934.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0059 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.428-254_428-253ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTATAT others(23): Show |
2 | a0001c0002t0002g0104 a0001c0002t0002g0106 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.428-254_428-253ins others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTAT others(3): Show |
6 | a0001c0001t0001g0182 a0001c0001t0001g0239 a0001c0001t0002g0130 others(3): Show |
6 | HG01358.hp2 HG01952.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTAT others(5): Show |
6 | a0001c0001t0002g0132 a0001c0001t0002g0137 a0001c0001t0002g0138 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTAT others(7): Show |
4 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0002t0002g0232 others(1): Show |
4 | HG02615.hp1 HG03453.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTAT others(9): Show |
3 | a0001c0002t0002g0057 a0001c0005t0004g0149 a0002c0003t0003g0110 |
3 | HG02523.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.428-254_428-253ins others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTAT others(11): Show |
2 | a0001c0005t0004g0150 a0001c0005t0004g0159 |
2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.428-254_428-253ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTAT others(13): Show |
1 | a0001c0001t0002g0131 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.428-254_428-253ins others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTGT others(3): Show |
1 | a0001c0007t0004g0146 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.428-254_428-253ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0171 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.428-254_428-253ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTGT others(9): Show |
1 | a0001c0007t0004g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.428-254_428-253ins others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTGT others(11): Show |
2 | a0001c0002t0002g0169 a0001c0007t0004g0147 |
2 | HG02809.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.428-254_428-253ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | G | GTGTGTGT others(15): Show |
2 | a0001c0007t0004g0143 a0001c0007t0004g0144 |
2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.428-254_428-253ins others(22): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTA | G | 13 | a0001c0001t0001g0165 a0001c0001t0001g0183 a0001c0001t0001g0225 others(10): Show |
14 | HG01175.hp2 HG01361.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-211_428-210del others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATA | G | 7 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG00544.hp2 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-213_428-210del others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATATA | G | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0002t0002g0021 others(1): Show |
4 | HG00609.hp2 HG02273.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-215_428-210del others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATATAT others(1): Show |
G | 6 | a0001c0001t0001g0228 a0001c0002t0002g0035 a0001c0002t0002g0082 others(3): Show |
6 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-217_428-210del others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATATAT others(3): Show |
G | 2 | a0001c0005t0004g0154 a0001c0007t0009g0141 |
2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.428-219_428-210del others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATATAT others(5): Show |
G | 2 | a0001c0001t0002g0174 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428-221_428-210del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATATAT others(7): Show |
G | 3 | a0001c0001t0001g0209 a0005c0009t0002g0083 a0005c0009t0002g0084 |
3 | HG02040.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.428-223_428-210del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.428-225_428-210del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATATAT others(13): Show |
G | 1 | a0004c0006t0003g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.428-229_428-210del others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATATAT others(17): Show |
G | 2 | a0001c0002t0002g0055 a0001c0002t0002g0056 |
2 | NA18747.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.428-233_428-210del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270699 | GTATATAT others(23): Show |
G | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.428-239_428-210del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | ||||||
| chr16:31270701 | A | G | 32 | a0001c0001t0001g0207 a0001c0001t0001g0215 a0001c0001t0001g0220 others(29): Show |
32 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.428-253A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270701 | |||||||
| chr16:31270703 | A | G | 11 | a0001c0001t0001g0165 a0001c0001t0001g0183 a0001c0001t0001g0225 others(8): Show |
12 | HG00099.hp1 HG01175.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.428-251A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270703 | |||||||
| chr16:31270705 | A | G | 12 | a0001c0001t0001g0175 a0001c0001t0001g0183 a0001c0001t0001g0212 others(9): Show |
13 | HG00544.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.428-249A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270705 | |||||||
| chr16:31270706 | TATATATA others(50): Show |
T | 2 | a0002c0003t0003g0039 a0002c0003t0003g0115 |
2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.428-234_428-178del others(57): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270706 | ||||||
| chr16:31270707 | A | G | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0002t0002g0021 others(1): Show |
4 | HG00609.hp2 HG02273.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-247A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270707 | |||||||
| chr16:31270709 | A | G | 6 | a0001c0001t0001g0228 a0001c0002t0002g0035 a0001c0002t0002g0082 others(3): Show |
6 | HG02055.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-245A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270709 | |||||||
| chr16:31270711 | A | G | 3 | a0001c0005t0004g0154 a0001c0005t0004g0155 a0007c0012t0004g0156 |
3 | HG02109.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.428-243A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270711 | |||||||
| chr16:31270713 | A | G | 3 | a0001c0001t0002g0174 a0001c0005t0004g0154 a0001c0013t0008g0173 |
3 | HG02109.hp1 HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428-241A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270713 | |||||||
| chr16:31270715 | A | G | 5 | a0001c0001t0001g0209 a0001c0001t0002g0174 a0001c0013t0008g0173 others(2): Show |
5 | HG02040.hp2 HG02129.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-239A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270715 | |||||||
| chr16:31270717 | A | G | 2 | a0001c0001t0002g0174 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428-237A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270717 | |||||||
| chr16:31270719 | A | G | 2 | a0001c0001t0002g0174 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428-235A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270719 | |||||||
| chr16:31270721 | A | G | 2 | a0001c0001t0002g0174 a0004c0006t0003g0013 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.428-233A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270721 | |||||||
| chr16:31270725 | A | G | 2 | a0001c0002t0002g0055 a0001c0002t0002g0056 |
2 | NA18747.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.428-229A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270725 | |||||||
| chr16:31270727 | A | T | 1 | a0001c0002t0002g0074 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.428-227A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270727 | |||||||
| chr16:31270731 | A | G | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.428-223A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270731 | |||||||
| chr16:31270734 | TATATATA others(4): Show |
T | 1 | a0003c0004t0005g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.428-219_428-209del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270734 | |||||||
| chr16:31270741 | A | T | 1 | a0003c0004t0005g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.428-213A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270741 | |||||||
| chr16:31270742 | T | TA | 19 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(16): Show |
19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.428-211dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270742 | ||||||
| chr16:31270743 | A | T | 3 | a0003c0004t0005g0030 a0003c0004t0005g0032 a0003c0004t0005g0090 |
3 | HG00099.hp1 HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.428-211A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270743 | |||||||
| chr16:31270744 | T | TA | 3 | a0003c0004t0005g0023 a0003c0004t0005g0079 a0003c0004t0005g0088 |
3 | HG02486.hp2 HG02735.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.428-210_428-209ins others(1): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270744 | |||||||
| chr16:31270744 | T | TATATATA others(4): Show |
1 | a0003c0004t0005g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.428-210_428-209ins others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270744 | |||||||
| chr16:31270744 | TG | T | 4 | a0003c0004t0005g0061 a0003c0004t0005g0094 a0003c0004t0005g0095 others(1): Show |
4 | HG02257.hp2 HG02615.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-209delG | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270744 | |||||||
| chr16:31270745 | G | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0029 a0003c0004t0005g0030 others(13): Show |
16 | HG00099.hp1 HG01109.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.428-209G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270745 | |||||||
| chr16:31270763 | CAT | C | 14 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(11): Show |
14 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.428-179_428-178del others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270763 | ||||||
| chr16:31270777 | C | T | 57 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(54): Show |
58 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.428-177C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270777 | |||||||
| chr16:31271392 | T | G | 165 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(162): Show |
167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.558+308T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271392 | |||||||
| chr16:31271498 | G | A | 19 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(16): Show |
19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.559-349G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271498 | |||||||
| chr16:31271573 | A | G | 19 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(16): Show |
19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.559-274A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271573 | |||||||
| chr16:31271649 | G | A | 35 | a0001c0007t0004g0025 a0001c0007t0004g0108 a0001c0007t0009g0141 others(32): Show |
35 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.559-198G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271649 | |||||||
| chr16:31271659 | C | T | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.559-188C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271659 | |||||||
| chr16:31271843 | G | A | 40 | a0001c0001t0002g0174 a0001c0001t0004g0113 a0001c0001t0004g0114 others(37): Show |
40 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(37): Show |
splice_region_variant&intron_variant | LOW | c.559-4G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271843 | |||||||
| chr16:31272002 | C | G | 28 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(25): Show |
28 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.704+10C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272002 | |||||||
| chr16:31272151 | T | C | 45 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(42): Show |
46 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(43): Show |
intron_variant | MODIFIER | c.704+159T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272151 | |||||||
| chr16:31272233 | A | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0228 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.704+241A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272233 | |||||||
| chr16:31272255 | T | C | 101 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(98): Show |
102 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(99): Show |
intron_variant | MODIFIER | c.704+263T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272255 | |||||||
| chr16:31272423 | C | CCATATAT others(3): Show |
1 | a0001c0002t0002g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.704+431_704+432ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272423 | |||||||
| chr16:31272423 | C | CTATA | 3 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0002t0002g0058 |
3 | HG00673.hp2 HG02083.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.704+469_704+472dup others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | ||||||
| chr16:31272423 | C | G | 76 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(73): Show |
77 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.704+431C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272423 | |||||||
| chr16:31272423 | CTA | C | 5 | a0001c0001t0001g0185 a0001c0001t0001g0228 a0001c0001t0001g0239 others(2): Show |
5 | HG01358.hp2 HG02055.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+471_704+472del others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | ||||||
| chr16:31272423 | CTATA | C | 14 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0178 others(11): Show |
14 | HG01071.hp1 HG01257.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.704+469_704+472del others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | ||||||
| chr16:31272423 | CTATATAT others(1): Show |
C | 3 | a0001c0001t0001g0212 a0001c0001t0001g0218 a0001c0001t0001g0220 |
3 | HG01123.hp2 HG01255.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.704+465_704+472del others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | ||||||
| chr16:31272423 | CTATATAT others(7): Show |
C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0222 |
2 | HG01192.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.704+459_704+472del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | ||||||
| chr16:31272423 | CTATATAT others(9): Show |
C | 1 | a0001c0001t0001g0198 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.704+457_704+472del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | ||||||
| chr16:31272423 | CTATATAT others(11): Show |
C | 1 | a0001c0001t0001g0237 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.704+455_704+472del others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | ||||||
| chr16:31272423 | CTATATAT others(17): Show |
C | 1 | a0001c0001t0001g0241 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.704+449_704+472del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | ||||||
| chr16:31272424 | T | C | 1 | a0001c0002t0002g0081 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.704+432T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272424 | |||||||
| chr16:31272433 | ATATATAT others(32): Show |
A | 1 | a0001c0002t0002g0033 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.704+443_704+481del others(39): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272433 | ||||||
| chr16:31272435 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.704+445_704+475del others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272435 | ||||||
| chr16:31272436 | TATATATA others(18): Show |
T | 1 | a0001c0001t0001g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.704+445_704+469del others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272436 | |||||||
| chr16:31272437 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0001g0202 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.704+447_704+474del others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272437 | ||||||
| chr16:31272440 | TATATATA others(14): Show |
T | 1 | a0001c0001t0001g0219 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.704+449_704+469del others(21): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272440 | |||||||
| chr16:31272441 | ATATATAT others(35): Show |
A | 3 | a0001c0005t0004g0150 a0001c0005t0004g0153 a0001c0005t0004g0162 |
3 | HG02109.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.704+451_704+492del others(42): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272441 | ||||||
| chr16:31272441 | ATATATAT others(36): Show |
A | 3 | a0001c0005t0004g0148 a0001c0005t0004g0149 a0001c0005t0004g0151 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.704+451_704+493del others(43): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272441 | ||||||
| chr16:31272442 | TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.704+451_704+469del others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272442 | |||||||
| chr16:31272443 | ATATATAT others(20): Show |
A | 1 | a0002c0003t0003g0112 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.704+453_704+479del others(27): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | ||||||
| chr16:31272443 | ATATATAT others(22): Show |
A | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.704+453_704+481del others(29): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | ||||||
| chr16:31272443 | ATATATAT others(23): Show |
A | 6 | a0003c0004t0005g0088 a0003c0004t0005g0093 a0003c0004t0005g0096 others(3): Show |
6 | HG01109.hp2 HG02486.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.704+453_704+482del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | ||||||
| chr16:31272443 | ATATATAT others(24): Show |
A | 1 | a0003c0004t0005g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.704+453_704+483del others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | ||||||
| chr16:31272443 | ATATATAT others(35): Show |
A | 12 | a0001c0005t0004g0002 a0001c0005t0004g0152 a0001c0005t0004g0154 others(9): Show |
13 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.704+453_704+494del others(42): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | ||||||
| chr16:31272445 | ATATATAT others(17): Show |
A | 1 | a0001c0002t0002g0129 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.704+455_704+478del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | ||||||
| chr16:31272445 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0004g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704+455_704+481del others(27): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | ||||||
| chr16:31272445 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0004g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.704+455_704+482del others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | ||||||
| chr16:31272445 | ATATATAT others(22): Show |
A | 2 | a0003c0004t0005g0031 a0003c0004t0005g0089 |
2 | HG01175.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.704+455_704+483del others(29): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | ||||||
| chr16:31272445 | ATATATAT others(23): Show |
A | 7 | a0003c0004t0005g0029 a0003c0004t0005g0080 a0003c0004t0005g0090 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+455_704+484del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | ||||||
| chr16:31272445 | ATATATAT others(24): Show |
A | 2 | a0003c0004t0005g0020 a0003c0004t0005g0100 |
2 | HG01256.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.704+455_704+485del others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | ||||||
| chr16:31272445 | ATATATAT others(30): Show |
A | 1 | a0003c0004t0005g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.704+455_704+491del others(37): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | ||||||
| chr16:31272445 | ATATATAT others(35): Show |
A | 1 | a0001c0005t0004g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.704+455_704+496del others(42): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | ||||||
| chr16:31272447 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0002g0085 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.704+457_704+476del others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | ||||||
| chr16:31272447 | ATATATAT others(17): Show |
A | 1 | a0004c0006t0003g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.704+457_704+480del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | ||||||
| chr16:31272447 | ATATATAT others(18): Show |
A | 1 | a0009c0011t0004g0003 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.704+457_704+481del others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | ||||||
| chr16:31272447 | ATATATAT others(19): Show |
A | 2 | a0002c0003t0003g0123 a0002c0003t0003g0125 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.704+457_704+482del others(26): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | ||||||
| chr16:31272447 | ATATATAT others(21): Show |
A | 1 | a0003c0004t0005g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.704+457_704+484del others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | ||||||
| chr16:31272447 | ATATATAT others(23): Show |
A | 2 | a0003c0004t0005g0030 a0003c0004t0005g0061 |
2 | HG01255.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.704+457_704+486del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | ||||||
| chr16:31272447 | ATATATAT others(24): Show |
A | 1 | a0003c0004t0005g0032 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.704+457_704+487del others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | ||||||
| chr16:31272449 | ATATATAT others(9): Show |
A | 1 | a0001c0007t0004g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.704+459_704+474del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272449 | ||||||
| chr16:31272449 | ATATATAT others(17): Show |
A | 5 | a0002c0003t0003g0037 a0004c0006t0003g0008 a0004c0006t0003g0009 others(2): Show |
5 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+459_704+482del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272449 | ||||||
| chr16:31272449 | ATATATAT others(19): Show |
A | 2 | a0002c0003t0003g0122 a0002c0003t0003g0124 |
2 | HG01106.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.704+459_704+484del others(26): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272449 | ||||||
| chr16:31272450 | TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0175 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.704+459_704+469del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272450 | |||||||
| chr16:31272451 | ATATATAT others(7): Show |
A | 1 | a0002c0003t0003g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.704+461_704+474del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272451 | ATATATAT others(10): Show |
A | 2 | a0001c0002t0002g0074 a0001c0007t0004g0108 |
2 | HG02080.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.704+461_704+477del others(17): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272451 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0046 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.704+461_704+478del others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272451 | ATATATAT others(12): Show |
A | 1 | a0001c0002t0002g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.704+461_704+479del others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272451 | ATATATAT others(13): Show |
A | 1 | a0001c0002t0002g0054 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.704+461_704+480del others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272451 | ATATATAT others(15): Show |
A | 3 | a0002c0003t0003g0038 a0002c0003t0003g0115 a0004c0006t0003g0007 |
3 | HG00741.hp1 HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.704+461_704+482del others(22): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272451 | ATATATAT others(16): Show |
A | 1 | a0002c0003t0003g0039 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.704+461_704+483del others(23): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272451 | ATATATAT others(17): Show |
A | 6 | a0002c0003t0003g0036 a0002c0003t0003g0040 a0002c0003t0003g0060 others(3): Show |
6 | HG00733.hp2 HG01109.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.704+461_704+484del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272451 | ATATATAT others(18): Show |
A | 4 | a0001c0007t0009g0141 a0002c0003t0003g0126 a0004c0006t0003g0004 others(1): Show |
4 | HG00738.hp2 HG02622.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+461_704+485del others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272451 | ATATATAT others(19): Show |
A | 4 | a0002c0003t0003g0006 a0002c0003t0003g0121 a0004c0006t0003g0013 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+461_704+486del others(26): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | ||||||
| chr16:31272453 | ATATATAT others(10): Show |
A | 7 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0064 others(4): Show |
7 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.704+463_704+479del others(17): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | ||||||
| chr16:31272453 | ATATATAT others(11): Show |
A | 1 | a0001c0002t0002g0051 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.704+463_704+480del others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | ||||||
| chr16:31272453 | ATATATAT others(14): Show |
A | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.704+463_704+483del others(21): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | ||||||
| chr16:31272453 | ATATATAT others(17): Show |
A | 1 | a0004c0006t0003g0011 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.704+463_704+486del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | ||||||
| chr16:31272453 | ATATATAT others(26): Show |
A | 1 | a0001c0001t0001g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.704+463_704+495del others(33): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | ||||||
| chr16:31272454 | TATATA | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0226 a0001c0002t0002g0187 |
3 | HG02129.hp2 HG03669.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.704+463_704+467del others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272454 | |||||||
| chr16:31272455 | A | T | 1 | a0001c0001t0001g0222 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.704+463A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272455 | |||||||
| chr16:31272455 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0002g0174 a0001c0007t0004g0146 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.704+465_704+476del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | ||||||
| chr16:31272455 | ATATATAT others(6): Show |
A | 1 | a0001c0007t0004g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.704+465_704+477del others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | ||||||
| chr16:31272455 | ATATATAT others(9): Show |
A | 2 | a0001c0002t0002g0041 a0001c0002t0002g0044 |
2 | HG01257.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.704+465_704+480del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | ||||||
| chr16:31272455 | ATATATAT others(10): Show |
A | 1 | a0001c0002t0002g0045 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.704+465_704+481del others(17): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | ||||||
| chr16:31272455 | ATATATAT others(11): Show |
A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0225 |
2 | HG02738.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.704+465_704+482del others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | ||||||
| chr16:31272457 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0210 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.704+466_704+467ins others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272457 | ||||||
| chr16:31272457 | A | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0222 |
2 | HG01952.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.704+465A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272457 | |||||||
| chr16:31272457 | ATATATAT others(4): Show |
A | 1 | a0001c0002t0007g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.704+467_704+477del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272457 | ||||||
| chr16:31272457 | ATATATAT others(6): Show |
A | 4 | a0001c0007t0004g0143 a0001c0007t0004g0145 a0001c0013t0008g0173 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+467_704+479del others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272457 | ||||||
| chr16:31272457 | ATATATAT others(7): Show |
A | 2 | a0001c0002t0002g0053 a0001c0002t0002g0066 |
2 | HG01358.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.704+467_704+480del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272457 | ||||||
| chr16:31272459 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0214 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.704+468_704+469ins others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | ||||||
| chr16:31272459 | A | ATTTTTTT others(12): Show |
1 | a0006c0014t0001g0233 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.704+468_704+469ins others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | ||||||
| chr16:31272459 | A | T | 7 | a0001c0001t0001g0086 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
7 | HG00558.hp2 HG00642.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+467A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272459 | |||||||
| chr16:31272459 | ATATATTT others(4): Show |
A | 1 | a0002c0003t0003g0078 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.704+469_704+479del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | ||||||
| chr16:31272459 | ATATATTT others(6): Show |
A | 3 | a0001c0002t0002g0026 a0001c0002t0002g0048 a0001c0007t0004g0147 |
3 | HG02809.hp2 NA19063.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.704+469_704+481del others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | ||||||
| chr16:31272459 | ATATATTT others(8): Show |
A | 2 | a0001c0002t0002g0193 a0002c0003t0003g0110 |
2 | HG02630.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.704+469_704+483del others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | ||||||
| chr16:31272461 | A | T | 17 | a0001c0001t0001g0086 a0001c0001t0001g0166 a0001c0001t0001g0182 others(14): Show |
17 | HG00558.hp2 HG00642.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.704+469A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272461 | |||||||
| chr16:31272461 | ATATTTTT others(4): Show |
A | 1 | a0001c0002t0002g0081 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.704+471_704+481del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272461 | ||||||
| chr16:31272461 | ATATTTTT others(7): Show |
A | 1 | a0001c0001t0002g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.704+471_704+484del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272461 | ||||||
| chr16:31272463 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0240 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.704+472_704+473ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | ||||||
| chr16:31272463 | A | T | 36 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0166 others(33): Show |
36 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.704+471A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272463 | |||||||
| chr16:31272463 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0002g0133 a0001c0002t0002g0179 |
2 | HG02723.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.704+500_704+509del others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | ||||||
| chr16:31272463 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0022 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.704+499_704+509del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | ||||||
| chr16:31272463 | ATTTTTTT others(5): Show |
A | 7 | a0001c0001t0001g0176 a0001c0001t0001g0213 a0001c0001t0002g0130 others(4): Show |
7 | HG01516.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.704+498_704+509del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | ||||||
| chr16:31272463 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0168 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.704+497_704+509del others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | ||||||
| chr16:31272463 | ATTTTTTT others(9): Show |
A | 1 | a0001c0007t0004g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.704+494_704+509del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | ||||||
| chr16:31272464 | T | TATATATA | 3 | a0001c0002t0002g0065 a0001c0002t0002g0077 a0005c0009t0002g0084 |
3 | HG02040.hp2 NA18963.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.704+472_704+473ins others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272464 | |||||||
| chr16:31272464 | T | TATATATA others(6): Show |
2 | a0001c0002t0002g0063 a0005c0009t0002g0083 |
2 | HG00558.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.704+472_704+473ins others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272464 | |||||||
| chr16:31272465 | T | A | 7 | a0001c0001t0001g0059 a0001c0002t0002g0001 a0001c0002t0002g0058 others(4): Show |
7 | HG02015.hp1 HG02071.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+473T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272465 | |||||||
| chr16:31272466 | T | A | 7 | a0001c0002t0002g0001 a0001c0002t0002g0063 a0001c0002t0002g0065 others(4): Show |
7 | HG00558.hp1 HG00673.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+474T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272466 | |||||||
| chr16:31272467 | T | A | 6 | a0001c0001t0001g0059 a0001c0002t0002g0001 a0001c0002t0002g0058 others(3): Show |
6 | HG02015.hp1 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.704+475T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272467 | |||||||
| chr16:31272468 | T | A | 8 | a0001c0001t0001g0180 a0001c0002t0002g0001 a0001c0002t0002g0063 others(5): Show |
8 | HG00558.hp1 HG00673.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.704+476T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272468 | |||||||
| chr16:31272469 | T | A | 7 | a0001c0001t0001g0059 a0001c0002t0002g0001 a0001c0002t0002g0058 others(4): Show |
7 | HG02015.hp1 HG02056.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+477T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272469 | |||||||
| chr16:31272470 | T | A | 9 | a0001c0001t0001g0180 a0001c0002t0002g0001 a0001c0002t0002g0049 others(6): Show |
9 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.704+478T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272470 | |||||||
| chr16:31272471 | T | A | 7 | a0001c0001t0001g0059 a0001c0002t0002g0055 a0001c0002t0002g0058 others(4): Show |
7 | HG02056.hp1 HG02083.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.704+479T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272471 | |||||||
| chr16:31272472 | T | A | 3 | a0001c0002t0002g0072 a0001c0002t0002g0128 a0002c0003t0003g0120 |
3 | HG01106.hp2 HG03516.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.704+480T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272472 | |||||||
| chr16:31272473 | T | A | 3 | a0001c0001t0002g0134 a0001c0002t0002g0055 a0001c0002t0002g0116 |
3 | HG02809.hp1 NA18994.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.704+481T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272473 | |||||||
| chr16:31272474 | T | A | 5 | a0001c0001t0001g0042 a0001c0001t0002g0137 a0001c0002t0002g0034 others(2): Show |
5 | HG01106.hp2 NA18522.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+482T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272474 | |||||||
| chr16:31272475 | T | A | 5 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0002t0002g0055 others(2): Show |
5 | HG02723.hp1 HG02809.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.704+483T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272475 | |||||||
| chr16:31272476 | T | A | 3 | a0001c0001t0002g0137 a0001c0002t0002g0034 a0001c0002t0002g0056 |
3 | NA18522.hp1 NA18747.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.704+484T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272476 | |||||||
| chr16:31272477 | T | A | 7 | a0001c0001t0001g0176 a0001c0001t0001g0213 a0001c0001t0002g0134 others(4): Show |
7 | HG01516.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.704+485T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272477 | |||||||
| chr16:31272478 | T | A | 2 | a0001c0001t0001g0168 a0001c0001t0002g0137 |
2 | HG01517.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.704+486T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272478 | |||||||
| chr16:31272479 | T | A | 2 | a0001c0001t0002g0135 a0001c0002t0002g0116 |
2 | HG02615.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.704+487T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272479 | |||||||
| chr16:31272535 | A | G | 19 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(16): Show |
19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.704+543A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272535 | |||||||
| chr16:31272675 | G | T | 31 | a0001c0007t0009g0141 a0002c0003t0003g0006 a0002c0003t0003g0036 others(28): Show |
31 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.704+683G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272675 | |||||||
| chr16:31272855 | G | A | 1 | a0004c0006t0003g0017 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.705-510G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272855 | |||||||
| chr16:31273001 | C | T | 19 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(16): Show |
19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.705-364C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273001 | |||||||
| chr16:31273096 | T | C | 19 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(16): Show |
19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.705-269T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273096 | |||||||
| chr16:31273104 | A | G | 19 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(16): Show |
19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.705-261A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273104 | |||||||
| chr16:31273208 | A | C | 19 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(16): Show |
19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.705-157A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273208 | |||||||
| chr16:31273297 | T | TA | 7 | a0001c0001t0001g0062 a0001c0001t0001g0212 a0001c0002t0002g0068 others(4): Show |
7 | HG00323.hp2 HG02015.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.705-53dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31273297 | ||||||
| chr16:31273310 | A | C | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.705-55A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273310 | |||||||
| chr16:31273611 | G | A | 1 | a0001c0002t0002g0001 | 2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.858+93G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31273611 | |||||||
| chr16:31273924 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0226 a0010c0015t0001g0172 |
3 | HG03669.hp2 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.858+406C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31273924 | |||||||
| chr16:31274053 | G | T | 1 | a0001c0002t0002g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.858+535G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274053 | |||||||
| chr16:31274135 | G | C | 1 | a0001c0005t0004g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.858+617G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274135 | |||||||
| chr16:31274410 | C | T | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.858+892C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274410 | |||||||
| chr16:31274478 | C | G | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.858+960C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274478 | |||||||
| chr16:31274572 | G | T | 13 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(10): Show |
13 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.859-977G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274572 | |||||||
| chr16:31274608 | T | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.859-941T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274608 | |||||||
| chr16:31274610 | A | ATATTTAT others(1): Show |
21 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.859-925_859-918dup others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | ||||||
| chr16:31274610 | A | ATTTATT | 30 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0007t0004g0108 others(27): Show |
30 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.859-938_859-937ins others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | ||||||
| chr16:31274610 | A | ATTTATTT others(3): Show |
11 | a0001c0001t0004g0142 a0001c0007t0004g0144 a0001c0007t0004g0145 others(8): Show |
11 | HG02630.hp2 HG02647.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.859-938_859-937ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | ||||||
| chr16:31274610 | A | ATTTATTT others(7): Show |
11 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(8): Show |
11 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.859-938_859-937ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | ||||||
| chr16:31274610 | A | ATTTATTT others(11): Show |
1 | a0001c0001t0002g0137 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.859-938_859-937ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | ||||||
| chr16:31274693 | C | A | 49 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(46): Show |
49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.859-856C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274693 | |||||||
| chr16:31274709 | G | A | 49 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(46): Show |
49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.859-840G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274709 | |||||||
| chr16:31274965 | G | T | 6 | a0001c0001t0004g0142 a0001c0007t0004g0143 a0001c0007t0004g0144 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-584G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274965 | |||||||
| chr16:31275375 | C | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0176 a0001c0001t0001g0213 |
3 | HG01516.hp2 HG01517.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.859-174C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31275375 | |||||||
| chr16:31275827 | A | T | 49 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(46): Show |
49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1009+128A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31275827 | |||||||
| chr16:31276106 | A | T | 99 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(96): Show |
100 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.1009+407A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276106 | |||||||
| chr16:31276148 | A | G | 7 | a0001c0001t0001g0165 a0001c0001t0001g0195 a0001c0001t0001g0204 others(4): Show |
7 | HG02683.hp2 HG02735.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009+449A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276148 | |||||||
| chr16:31276328 | T | C | 47 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(44): Show |
47 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1010-343T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276328 | |||||||
| chr16:31276476 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1010-195C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276476 | |||||||
| chr16:31276486 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1010-185C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276486 | |||||||
| chr16:31276488 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1010-183C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276488 | |||||||
| chr16:31276582 | T | G | 13 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(10): Show |
13 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1010-89T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276582 | |||||||
| chr16:31276800 | A | C | 54 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(51): Show |
54 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1083+56A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 10/29 | chr16 | 31276800 | |||||||
| chr16:31277240 | G | A | 21 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(18): Show |
21 | HG01496.hp2 HG02280.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.1213+191G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277240 | |||||||
| chr16:31277287 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1213+238C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277287 | |||||||
| chr16:31277359 | A | AT | 38 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(35): Show |
38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1213+325dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr16 | 31277359 | ||||||
| chr16:31277359 | A | ATT | 15 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(12): Show |
15 | HG02055.hp2 HG02280.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1213+324_1213+325d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr16 | 31277359 | ||||||
| chr16:31277444 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1213+395C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277444 | |||||||
| chr16:31277460 | G | A | 1 | a0001c0007t0004g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1213+411G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277460 | |||||||
| chr16:31277538 | A | C | 5 | a0001c0007t0004g0143 a0001c0007t0004g0144 a0001c0007t0004g0145 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1214-429A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277538 | |||||||
| chr16:31277593 | G | A | 46 | a0001c0001t0001g0216 a0001c0007t0004g0024 a0001c0007t0004g0025 others(43): Show |
46 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1214-374G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277593 | |||||||
| chr16:31277735 | C | T | 1 | a0001c0002t0002g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1214-232C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277735 | |||||||
| chr16:31277745 | G | A | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1214-222G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277745 | |||||||
| chr16:31277788 | C | T | 21 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1214-179C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277788 | |||||||
| chr16:31277806 | T | C | 23 | a0003c0004t0005g0020 a0003c0004t0005g0023 a0003c0004t0005g0029 others(20): Show |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1214-161T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277806 | |||||||
| chr16:31277943 | C | A | 2 | a0001c0002t0002g0179 a0001c0002t0002g0193 |
2 | NA18960.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1214-24C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277943 | |||||||
| chr16:31278197 | T | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+88T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278197 | |||||||
| chr16:31278207 | G | A | 1 | a0001c0002t0002g0091 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1356+98G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278207 | |||||||
| chr16:31278544 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1356+435G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278544 | |||||||
| chr16:31278623 | T | C | 1 | a0001c0002t0002g0211 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1356+514T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278623 | |||||||
| chr16:31278882 | T | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+773T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278882 | |||||||
| chr16:31278972 | G | A | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+863G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278972 | |||||||
| chr16:31278982 | G | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+873G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278982 | |||||||
| chr16:31278983 | C | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+874C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278983 | |||||||
| chr16:31278984 | A | G | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+875A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278984 | |||||||
| chr16:31279038 | T | G | 1 | a0004c0006t0003g0010 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1356+929T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279038 | |||||||
| chr16:31279129 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+1020G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279129 | |||||||
| chr16:31279141 | T | C | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356+1032T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279141 | |||||||
| chr16:31279199 | T | C | 44 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(41): Show |
44 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1356+1090T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279199 | |||||||
| chr16:31279236 | T | C | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+1127T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279236 | |||||||
| chr16:31279582 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+1473G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279582 | |||||||
| chr16:31279660 | T | G | 1 | a0001c0002t0002g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1356+1551T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279660 | |||||||
| chr16:31279688 | G | T | 1 | a0001c0002t0002g0048 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1356+1579G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279688 | |||||||
| chr16:31279739 | T | G | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1356+1630T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279739 | |||||||
| chr16:31279799 | A | T | 2 | a0001c0002t0002g0179 a0001c0002t0002g0193 |
2 | NA18960.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1356+1690A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279799 | |||||||
| chr16:31280018 | T | TG | 69 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0142 others(66): Show |
70 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.1356+1909_1356+191 others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280018 | |||||||
| chr16:31280169 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0230 |
2 | HG02523.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1356+2060G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280169 | |||||||
| chr16:31280249 | C | T | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1356+2140C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280249 | |||||||
| chr16:31280257 | T | C | 1 | a0004c0006t0003g0018 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1356+2148T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280257 | |||||||
| chr16:31280630 | G | A | 69 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0142 others(66): Show |
70 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.1356+2521G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280630 | |||||||
| chr16:31280675 | G | A | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+2566G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280675 | |||||||
| chr16:31280689 | A | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+2580A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280689 | |||||||
| chr16:31280889 | C | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+2780C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280889 | |||||||
| chr16:31280910 | T | G | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+2801T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280910 | |||||||
| chr16:31281219 | C | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+3110C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281219 | |||||||
| chr16:31281271 | C | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+3162C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281271 | |||||||
| chr16:31281292 | T | C | 1 | a0001c0002t0002g0027 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1356+3183T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281292 | |||||||
| chr16:31281299 | A | G | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356+3190A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281299 | |||||||
| chr16:31281309 | T | C | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356+3200T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281309 | |||||||
| chr16:31281339 | C | T | 2 | a0005c0009t0002g0083 a0005c0009t0002g0084 |
2 | HG02040.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1356+3230C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281339 | |||||||
| chr16:31281452 | G | T | 23 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0005t0004g0002 others(20): Show |
24 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1356+3343G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281452 | |||||||
| chr16:31281635 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1356+3526G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281635 | |||||||
| chr16:31281673 | C | T | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356+3564C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281673 | |||||||
| chr16:31281823 | T | G | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1356+3714T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281823 | |||||||
| chr16:31282236 | C | T | 2 | a0001c0002t0002g0052 a0001c0013t0008g0173 |
2 | HG01192.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1356+4127C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31282236 | |||||||
| chr16:31282362 | G | T | 1 | a0001c0002t0002g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1356+4253G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31282362 | |||||||
| chr16:31282815 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0228 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1356+4706G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31282815 | |||||||
| chr16:31282879 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+4770G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31282879 | |||||||
| chr16:31283012 | A | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01192.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1356+4903A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283012 | |||||||
| chr16:31283150 | C | T | 4 | a0001c0001t0001g0171 a0001c0001t0001g0221 a0001c0002t0002g0169 others(1): Show |
4 | NA18951.hp1 NA18966.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1356+5041C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283150 | |||||||
| chr16:31283196 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1356+5087C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283196 | |||||||
| chr16:31283213 | T | C | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1356+5104T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283213 | |||||||
| chr16:31283303 | C | A | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+5194C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283303 | |||||||
| chr16:31283364 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1356+5255C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283364 | |||||||
| chr16:31283744 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1356+5635C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283744 | |||||||
| chr16:31283837 | G | T | 2 | a0001c0005t0004g0154 a0007c0012t0004g0156 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1356+5728G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283837 | |||||||
| chr16:31283841 | C | T | 2 | a0001c0005t0004g0154 a0007c0012t0004g0156 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1356+5732C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283841 | |||||||
| chr16:31284223 | A | G | 237 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1356+6114A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284223 | |||||||
| chr16:31284279 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1356+6170C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284279 | |||||||
| chr16:31284416 | C | G | 1 | a0001c0002t0002g0035 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1356+6307C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284416 | |||||||
| chr16:31284487 | G | A | 1 | a0003c0004t0005g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1356+6378G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284487 | |||||||
| chr16:31284488 | C | CA | 94 | a0001c0001t0002g0174 a0001c0001t0004g0113 a0001c0001t0004g0114 others(91): Show |
95 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1356+6379_1356+638 others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284488 | |||||||
| chr16:31284577 | G | A | 1 | a0001c0002t0002g0105 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1356+6468G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284577 | |||||||
| chr16:31284697 | G | T | 1 | a0001c0002t0002g0231 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1356+6588G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284697 | |||||||
| chr16:31284798 | G | A | 1 | a0001c0005t0004g0242 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1356+6689G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284798 | |||||||
| chr16:31284811 | G | A | 1 | a0002c0003t0003g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1356+6702G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284811 | |||||||
| chr16:31284840 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+6731G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284840 | |||||||
| chr16:31285014 | C | T | 2 | a0001c0001t0001g0186 a0010c0015t0001g0172 |
2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1356+6905C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285014 | |||||||
| chr16:31285391 | A | G | 1 | a0003c0004t0005g0020 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1356+7282A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285391 | |||||||
| chr16:31285496 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1356+7387G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285496 | |||||||
| chr16:31285504 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+7395G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285504 | |||||||
| chr16:31285815 | T | C | 1 | a0004c0006t0003g0017 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1356+7706T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285815 | |||||||
| chr16:31285825 | G | T | 23 | a0003c0004t0005g0020 a0003c0004t0005g0023 a0003c0004t0005g0029 others(20): Show |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1356+7716G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285825 | |||||||
| chr16:31286180 | AT | A | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+8082delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31286180 | ||||||
| chr16:31286679 | C | T | 2 | a0001c0005t0004g0154 a0007c0012t0004g0156 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1356+8570C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31286679 | |||||||
| chr16:31286693 | GTTAT | G | 3 | a0001c0001t0002g0130 a0001c0001t0002g0134 a0001c0001t0002g0138 |
3 | HG02280.hp1 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1356+8587_1356+859 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31286693 | ||||||
| chr16:31287148 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+9039C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287148 | |||||||
| chr16:31287202 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+9093T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287202 | |||||||
| chr16:31287368 | G | A | 23 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0005t0004g0002 others(20): Show |
24 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1356+9259G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287368 | |||||||
| chr16:31287618 | T | G | 94 | a0001c0001t0002g0174 a0001c0001t0004g0113 a0001c0001t0004g0114 others(91): Show |
95 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1356+9509T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287618 | |||||||
| chr16:31287693 | G | A | 2 | a0002c0003t0003g0110 a0002c0003t0003g0112 |
2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1356+9584G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287693 | |||||||
| chr16:31287833 | GA | G | 23 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0005t0004g0002 others(20): Show |
24 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1357-9675delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31287833 | ||||||
| chr16:31287848 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-9666G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287848 | |||||||
| chr16:31287854 | C | T | 2 | a0001c0001t0002g0174 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1357-9660C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287854 | |||||||
| chr16:31288043 | A | G | 1 | a0003c0004t0005g0032 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1357-9471A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288043 | |||||||
| chr16:31288153 | A | G | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1357-9361A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288153 | |||||||
| chr16:31288159 | T | C | 1 | a0001c0002t0002g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1357-9355T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288159 | |||||||
| chr16:31288305 | C | T | 23 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0005t0004g0002 others(20): Show |
24 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1357-9209C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288305 | |||||||
| chr16:31288355 | AAATGTTT others(3): Show |
A | 2 | a0001c0005t0004g0149 a0001c0005t0004g0151 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1357-9158_1357-914 others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288355 | |||||||
| chr16:31288454 | C | T | 31 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(28): Show |
31 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1357-9060C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288454 | |||||||
| chr16:31288783 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1357-8731C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288783 | |||||||
| chr16:31289045 | T | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1357-8469T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289045 | |||||||
| chr16:31289108 | C | T | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1357-8406C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289108 | |||||||
| chr16:31289268 | T | G | 1 | a0003c0004t0005g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8246T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289268 | |||||||
| chr16:31289269 | G | A | 1 | a0003c0004t0005g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8245G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289269 | |||||||
| chr16:31289271 | C | T | 1 | a0003c0004t0005g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8243C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289271 | |||||||
| chr16:31289299 | T | C | 1 | a0003c0004t0005g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8215T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289299 | |||||||
| chr16:31289305 | C | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-8209C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289305 | |||||||
| chr16:31289306 | G | A | 1 | a0003c0004t0005g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8208G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289306 | |||||||
| chr16:31289307 | A | T | 1 | a0003c0004t0005g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8207A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289307 | |||||||
| chr16:31289318 | C | T | 2 | a0002c0003t0003g0111 a0003c0004t0005g0094 |
2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1357-8196C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289318 | |||||||
| chr16:31289322 | T | A | 2 | a0002c0003t0003g0111 a0003c0004t0005g0094 |
2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1357-8192T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289322 | |||||||
| chr16:31289448 | T | C | 94 | a0001c0001t0002g0174 a0001c0001t0004g0113 a0001c0001t0004g0114 others(91): Show |
95 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1357-8066T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289448 | |||||||
| chr16:31289690 | A | G | 94 | a0001c0001t0002g0174 a0001c0001t0004g0113 a0001c0001t0004g0114 others(91): Show |
95 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1357-7824A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289690 | |||||||
| chr16:31289804 | G | A | 72 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0046 others(69): Show |
73 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1357-7710G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289804 | |||||||
| chr16:31289899 | T | C | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-7615T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289899 | |||||||
| chr16:31289940 | G | A | 1 | a0001c0002t0002g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1357-7574G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289940 | |||||||
| chr16:31289996 | G | A | 2 | a0001c0007t0009g0141 a0009c0011t0004g0003 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1357-7518G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289996 | |||||||
| chr16:31290045 | C | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-7469C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290045 | |||||||
| chr16:31290080 | C | CA | 9 | a0001c0001t0001g0043 a0001c0001t0001g0086 a0001c0001t0001g0215 others(6): Show |
9 | HG00741.hp2 HG01192.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1357-7413dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31290080 | ||||||
| chr16:31290080 | CA | C | 24 | a0001c0001t0001g0178 a0001c0001t0001g0229 a0001c0001t0002g0130 others(21): Show |
24 | HG01257.hp2 HG01891.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.1357-7413delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31290080 | ||||||
| chr16:31290080 | CAA | C | 19 | a0001c0001t0002g0085 a0001c0005t0004g0002 a0001c0005t0004g0148 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1357-7414_1357-741 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31290080 | ||||||
| chr16:31290099 | A | G | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1357-7415A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290099 | |||||||
| chr16:31290157 | G | A | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-7357G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290157 | |||||||
| chr16:31290589 | G | C | 69 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0142 others(66): Show |
70 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.1357-6925G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290589 | |||||||
| chr16:31290822 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1357-6692T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290822 | |||||||
| chr16:31291082 | GGA | G | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1357-6425_1357-642 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31291082 | ||||||
| chr16:31291142 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1357-6372A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291142 | |||||||
| chr16:31291289 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1357-6225C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291289 | |||||||
| chr16:31291513 | C | T | 21 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1357-6001C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291513 | |||||||
| chr16:31291519 | G | A | 2 | a0002c0003t0003g0110 a0002c0003t0003g0112 |
2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1357-5995G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291519 | |||||||
| chr16:31291612 | G | A | 9 | a0002c0003t0003g0006 a0002c0003t0003g0121 a0002c0003t0003g0122 others(6): Show |
9 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1357-5902G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291612 | |||||||
| chr16:31291617 | A | G | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-5897A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291617 | |||||||
| chr16:31291733 | A | C | 1 | a0001c0002t0002g0056 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1357-5781A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291733 | |||||||
| chr16:31291880 | T | C | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1357-5634T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291880 | |||||||
| chr16:31292049 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1357-5465C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292049 | |||||||
| chr16:31292139 | T | C | 1 | a0001c0002t0002g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1357-5375T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292139 | |||||||
| chr16:31292237 | A | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-5277A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292237 | |||||||
| chr16:31292371 | A | AT | 21 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1357-5143_1357-514 others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292371 | |||||||
| chr16:31292372 | G | A | 21 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1357-5142G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292372 | |||||||
| chr16:31292625 | C | T | 68 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0005t0004g0002 others(65): Show |
69 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.1357-4889C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292625 | |||||||
| chr16:31292629 | G | A | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-4885G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292629 | |||||||
| chr16:31292679 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1357-4835G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292679 | |||||||
| chr16:31292839 | T | C | 1 | a0001c0005t0004g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1357-4675T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292839 | |||||||
| chr16:31292968 | T | G | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1357-4546T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292968 | |||||||
| chr16:31293061 | C | T | 28 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(25): Show |
28 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1357-4453C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293061 | |||||||
| chr16:31293137 | T | C | 1 | a0003c0004t0005g0030 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1357-4377T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293137 | |||||||
| chr16:31293353 | TCTTC | T | 33 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(30): Show |
34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1357-4159_1357-415 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31293353 | ||||||
| chr16:31293385 | A | G | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-4129A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293385 | |||||||
| chr16:31293533 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1357-3981A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293533 | |||||||
| chr16:31293572 | T | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG01175.hp2 HG01952.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1357-3942T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293572 | |||||||
| chr16:31293969 | A | G | 78 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(75): Show |
79 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.1357-3545A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293969 | |||||||
| chr16:31294002 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0228 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1357-3512G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294002 | |||||||
| chr16:31294047 | G | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1357-3467G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294047 | |||||||
| chr16:31294272 | A | C | 104 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(101): Show |
105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1357-3242A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294272 | |||||||
| chr16:31294486 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1357-3028T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294486 | |||||||
| chr16:31294570 | C | T | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1357-2944C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294570 | |||||||
| chr16:31294618 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1357-2896G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294618 | |||||||
| chr16:31294857 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1357-2657G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294857 | |||||||
| chr16:31294999 | T | C | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1357-2515T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294999 | |||||||
| chr16:31295143 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-2371G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31295143 | |||||||
| chr16:31295719 | T | C | 3 | a0004c0006t0003g0010 a0004c0006t0003g0012 a0004c0006t0003g0014 |
3 | HG02895.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1357-1795T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31295719 | |||||||
| chr16:31295872 | T | C | 2 | a0001c0002t0002g0034 a0001c0002t0002g0116 |
2 | NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1357-1642T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31295872 | |||||||
| chr16:31295902 | G | A | 2 | a0001c0007t0009g0141 a0009c0011t0004g0003 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1357-1612G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31295902 | |||||||
| chr16:31296063 | C | T | 7 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0064 others(4): Show |
7 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357-1451C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296063 | |||||||
| chr16:31296106 | C | CT | 6 | a0001c0001t0001g0192 a0001c0001t0001g0220 a0001c0007t0004g0143 others(3): Show |
6 | HG01255.hp1 HG02135.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1357-1390dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31296106 | ||||||
| chr16:31296106 | CT | C | 63 | a0001c0001t0001g0075 a0001c0001t0002g0085 a0001c0001t0002g0130 others(60): Show |
64 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.1357-1390delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31296106 | ||||||
| chr16:31296271 | A | AT | 125 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0059 others(122): Show |
126 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1357-1230dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31296271 | ||||||
| chr16:31296301 | T | C | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1357-1213T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296301 | |||||||
| chr16:31296457 | AC | A | 7 | a0001c0007t0004g0024 a0001c0007t0004g0108 a0001c0007t0004g0143 others(4): Show |
7 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357-1056delC | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296457 | |||||||
| chr16:31296516 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1357-998C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296516 | |||||||
| chr16:31296580 | TATGAGGC others(28): Show |
T | 1 | a0001c0001t0001g0022 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1357-930_1357-896d others(37): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31296580 | ||||||
| chr16:31296710 | A | G | 1 | a0002c0003t0003g0040 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1357-804A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296710 | |||||||
| chr16:31296960 | C | T | 33 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(30): Show |
34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1357-554C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296960 | |||||||
| chr16:31297670 | A | C | 1 | a0001c0005t0004g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1497+16A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 13/29 | chr16 | 31297670 | |||||||
| chr16:31297689 | C | T | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1497+35C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 13/29 | chr16 | 31297689 | |||||||
| chr16:31298204 | C | CA | 52 | a0001c0001t0001g0046 a0001c0001t0001g0117 a0001c0001t0001g0166 others(49): Show |
52 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1707+274dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | ||||||
| chr16:31298204 | C | CAA | 25 | a0001c0001t0004g0142 a0001c0005t0004g0002 a0001c0005t0004g0148 others(22): Show |
26 | HG00733.hp2 HG01175.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1707+273_1707+274d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | ||||||
| chr16:31298204 | C | CAAA | 25 | a0001c0005t0004g0152 a0002c0003t0003g0006 a0002c0003t0003g0038 others(22): Show |
25 | HG00323.hp1 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1707+272_1707+274d others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | ||||||
| chr16:31298204 | C | CAAAA | 9 | a0002c0003t0003g0036 a0002c0003t0003g0037 a0002c0003t0003g0109 others(6): Show |
9 | HG00741.hp1 HG01516.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707+271_1707+274d others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | ||||||
| chr16:31298204 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1707+265_1707+274d others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | ||||||
| chr16:31298204 | CAAAAAAA others(4): Show |
C | 9 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(6): Show |
9 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707+264_1707+274d others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | ||||||
| chr16:31298281 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+327G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298281 | |||||||
| chr16:31298343 | A | G | 23 | a0003c0004t0005g0020 a0003c0004t0005g0023 a0003c0004t0005g0029 others(20): Show |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1707+389A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298343 | |||||||
| chr16:31298386 | C | T | 1 | a0003c0004t0005g0032 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1707+432C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298386 | |||||||
| chr16:31298484 | C | T | 15 | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0001g0180 others(12): Show |
15 | HG00099.hp2 HG00642.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1707+530C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298484 | |||||||
| chr16:31298624 | G | C | 3 | a0001c0002t0002g0048 a0001c0002t0002g0054 a0001c0002t0002g0074 |
3 | HG02080.hp1 NA18951.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1707+670G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298624 | |||||||
| chr16:31298795 | T | G | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+841T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298795 | |||||||
| chr16:31298831 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1707+877G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298831 | |||||||
| chr16:31298833 | C | CT | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+881dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298833 | ||||||
| chr16:31298935 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0212 |
2 | HG00609.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1707+981G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298935 | |||||||
| chr16:31298984 | A | G | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+1030A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298984 | |||||||
| chr16:31299051 | T | C | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1707+1097T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299051 | |||||||
| chr16:31299192 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1707+1238C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299192 | |||||||
| chr16:31299293 | A | G | 1 | a0001c0007t0004g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1707+1339A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299293 | |||||||
| chr16:31299321 | G | C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+1367G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299321 | |||||||
| chr16:31299536 | C | T | 2 | a0001c0001t0002g0174 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1707+1582C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299536 | |||||||
| chr16:31299749 | TCTCCTCC others(20): Show |
T | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1707+1803_1707+182 others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31299749 | ||||||
| chr16:31299765 | T | TTCC | 24 | a0001c0001t0002g0174 a0001c0013t0008g0173 a0003c0004t0005g0020 others(21): Show |
24 | HG01109.hp2 HG01175.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1707+1827_1707+182 others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31299765 | ||||||
| chr16:31299775 | T | TCCC | 77 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(74): Show |
78 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1707+1823_1707+182 others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31299775 | ||||||
| chr16:31299836 | C | A | 1 | a0001c0002t0002g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1707+1882C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299836 | |||||||
| chr16:31299844 | T | TCTC | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+1911_1707+191 others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31299844 | ||||||
| chr16:31299865 | C | A | 1 | a0001c0002t0002g0035 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1707+1911C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299865 | |||||||
| chr16:31300018 | C | A | 33 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(30): Show |
34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+2064C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300018 | |||||||
| chr16:31300053 | G | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+2099G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300053 | |||||||
| chr16:31300394 | G | A | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+2440G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300394 | |||||||
| chr16:31300422 | T | C | 1 | a0002c0003t0003g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1707+2468T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300422 | |||||||
| chr16:31300508 | A | T | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+2554A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300508 | |||||||
| chr16:31300676 | C | T | 1 | a0001c0007t0004g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1707+2722C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300676 | |||||||
| chr16:31300677 | G | A | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+2723G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300677 | |||||||
| chr16:31300685 | T | C | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1707+2731T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300685 | |||||||
| chr16:31300732 | A | G | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1707+2778A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300732 | |||||||
| chr16:31300740 | A | G | 3 | a0003c0004t0005g0023 a0003c0004t0005g0061 a0003c0004t0005g0088 |
3 | HG02257.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1707+2786A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300740 | |||||||
| chr16:31300791 | A | G | 1 | a0001c0002t0002g0055 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1707+2837A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300791 | |||||||
| chr16:31300836 | C | T | 21 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1707+2882C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300836 | |||||||
| chr16:31300861 | G | A | 2 | a0001c0005t0004g0150 a0001c0005t0004g0153 |
2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1707+2907G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300861 | |||||||
| chr16:31300911 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+2957C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300911 | |||||||
| chr16:31300965 | A | G | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0194 others(4): Show |
7 | HG00673.hp2 HG01192.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+3011A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300965 | |||||||
| chr16:31301180 | T | G | 25 | a0001c0001t0002g0174 a0001c0013t0008g0173 a0003c0004t0005g0020 others(22): Show |
25 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1707+3226T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31301180 | |||||||
| chr16:31301534 | T | C | 11 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0064 others(8): Show |
11 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+3580T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31301534 | |||||||
| chr16:31301564 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+3610T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31301564 | |||||||
| chr16:31301932 | C | T | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1707+3978C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31301932 | |||||||
| chr16:31302039 | A | C | 2 | a0001c0002t0002g0069 a0002c0003t0003g0037 |
2 | HG00673.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1707+4085A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302039 | |||||||
| chr16:31302376 | T | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+4422T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302376 | |||||||
| chr16:31302378 | CTTTTCTT others(5): Show |
C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+4439_1707+445 others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302378 | ||||||
| chr16:31302396 | T | TTTCTTTC | 6 | a0003c0004t0005g0020 a0003c0004t0005g0080 a0003c0004t0005g0095 others(3): Show |
6 | HG01256.hp2 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | ||||||
| chr16:31302396 | T | TTTCTTTC others(4): Show |
7 | a0003c0004t0005g0030 a0003c0004t0005g0079 a0003c0004t0005g0093 others(4): Show |
7 | HG01109.hp2 HG01255.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | ||||||
| chr16:31302396 | T | TTTCTTTC others(8): Show |
1 | a0003c0004t0005g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1707+4444_1707+444 others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | ||||||
| chr16:31302396 | T | TTTCTTTC others(23): Show |
3 | a0003c0004t0005g0029 a0003c0004t0005g0032 a0003c0004t0005g0090 |
3 | HG00099.hp1 HG03098.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(34): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | ||||||
| chr16:31302396 | T | TTTCTTTC others(27): Show |
1 | a0003c0004t0005g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1707+4444_1707+444 others(38): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | ||||||
| chr16:31302396 | T | TTTCTTTC others(39): Show |
2 | a0003c0004t0005g0088 a0003c0004t0005g0096 |
2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(50): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | ||||||
| chr16:31302396 | T | TTTCTTTC others(43): Show |
2 | a0003c0004t0005g0023 a0003c0004t0005g0089 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(54): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | ||||||
| chr16:31302396 | T | TTTCTTTC others(43): Show |
1 | a0003c0004t0005g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1707+4444_1707+444 others(54): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | ||||||
| chr16:31302398 | TTCTTTTC others(53): Show |
T | 2 | a0001c0005t0004g0154 a0007c0012t0004g0156 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1707+4445_1707+450 others(64): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302398 | |||||||
| chr16:31302401 | T | TTTC | 13 | a0003c0004t0005g0020 a0003c0004t0005g0030 a0003c0004t0005g0079 others(10): Show |
13 | HG01109.hp2 HG01255.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1707+4449_1707+445 others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302401 | ||||||
| chr16:31302404 | T | C | 9 | a0003c0004t0005g0023 a0003c0004t0005g0029 a0003c0004t0005g0031 others(6): Show |
9 | HG00099.hp1 HG01175.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707+4450T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302404 | |||||||
| chr16:31302405 | C | T | 9 | a0003c0004t0005g0023 a0003c0004t0005g0029 a0003c0004t0005g0031 others(6): Show |
9 | HG00099.hp1 HG01175.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707+4451C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302405 | |||||||
| chr16:31302408 | T | C | 18 | a0001c0002t0002g0072 a0003c0004t0005g0023 a0003c0004t0005g0029 others(15): Show |
18 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1707+4454T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302408 | |||||||
| chr16:31302408 | TTTTC | T | 14 | a0001c0007t0004g0025 a0001c0007t0004g0143 a0002c0003t0003g0036 others(11): Show |
14 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1707+4473_1707+447 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302408 | ||||||
| chr16:31302409 | T | C | 6 | a0003c0004t0005g0020 a0003c0004t0005g0080 a0003c0004t0005g0095 others(3): Show |
6 | HG01256.hp2 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707+4455T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302409 | |||||||
| chr16:31302417 | TTTCTTTC others(4): Show |
T | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1707+4477_1707+448 others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302417 | ||||||
| chr16:31302424 | CTTTCTTC others(1): Show |
C | 15 | a0001c0007t0004g0108 a0001c0007t0004g0144 a0001c0007t0004g0145 others(12): Show |
15 | HG01106.hp1 HG01891.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.1707+4473_1707+448 others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302424 | ||||||
| chr16:31302424 | CTTTCTTC others(5): Show |
C | 3 | a0001c0007t0004g0024 a0001c0007t0004g0146 a0001c0007t0004g0147 |
3 | HG01496.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1707+4473_1707+448 others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302424 | ||||||
| chr16:31302424 | CTTTCTTC others(17): Show |
C | 1 | a0002c0003t0003g0111 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1707+4473_1707+449 others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302424 | ||||||
| chr16:31302424 | CTTTCTTC others(55): Show |
C | 12 | a0001c0005t0004g0002 a0001c0005t0004g0152 a0001c0005t0004g0155 others(9): Show |
13 | HG02258.hp2 HG02622.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1707+4477_1707+453 others(66): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302424 | ||||||
| chr16:31302426 | TTCTTCTT others(21): Show |
T | 1 | a0002c0003t0003g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1707+4473_1707+450 others(32): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302426 | |||||||
| chr16:31302426 | TTCTTCTT others(25): Show |
T | 1 | a0004c0006t0003g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1707+4473_1707+450 others(36): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302426 | |||||||
| chr16:31302427 | T | C | 7 | a0002c0003t0003g0067 a0002c0003t0003g0126 a0004c0006t0003g0004 others(4): Show |
7 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+4473T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302427 | |||||||
| chr16:31302428 | C | CT | 17 | a0003c0004t0005g0020 a0003c0004t0005g0029 a0003c0004t0005g0031 others(14): Show |
17 | HG00099.hp1 HG01175.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.1707+4476dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302428 | ||||||
| chr16:31302428 | C | CTTCT | 11 | a0001c0001t0001g0062 a0001c0001t0001g0182 a0001c0001t0001g0216 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1707+4496_1707+449 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302428 | ||||||
| chr16:31302428 | C | CTTTCTTT others(25): Show |
1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4476_1707+447 others(36): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302428 | ||||||
| chr16:31302428 | C | CTTTCTTT others(33): Show |
1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1707+4476_1707+447 others(44): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302428 | ||||||
| chr16:31302428 | C | T | 7 | a0002c0003t0003g0067 a0002c0003t0003g0126 a0004c0006t0003g0004 others(4): Show |
7 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+4474C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302428 | |||||||
| chr16:31302434 | T | C | 3 | a0003c0004t0005g0023 a0003c0004t0005g0088 a0003c0004t0005g0090 |
3 | HG02486.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1707+4480T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302434 | |||||||
| chr16:31302438 | T | C | 1 | a0003c0004t0005g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1707+4484T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302438 | |||||||
| chr16:31302442 | T | C | 1 | a0003c0004t0005g0032 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1707+4488T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302442 | |||||||
| chr16:31302443 | CTTTCTTT others(36): Show |
C | 19 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(16): Show |
19 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1707+4498_1707+454 others(47): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302443 | ||||||
| chr16:31302446 | T | C | 4 | a0003c0004t0005g0029 a0003c0004t0005g0031 a0003c0004t0005g0079 others(1): Show |
4 | HG01175.hp1 HG02735.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+4492T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302446 | |||||||
| chr16:31302450 | TCTTCCTT others(1): Show |
T | 16 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0143 others(13): Show |
16 | HG01256.hp1 HG01258.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1707+4500_1707+450 others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302450 | ||||||
| chr16:31302454 | C | CCTTT | 4 | a0003c0004t0005g0020 a0003c0004t0005g0080 a0003c0004t0005g0093 others(1): Show |
4 | HG01109.hp2 HG01256.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1707+4503_1707+450 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302454 | ||||||
| chr16:31302454 | C | T | 164 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.1707+4500C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302454 | |||||||
| chr16:31302458 | C | T | 53 | a0001c0001t0004g0142 a0001c0007t0004g0108 a0001c0007t0004g0144 others(50): Show |
53 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1707+4504C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302458 | |||||||
| chr16:31302458 | CCTTT | C | 6 | a0001c0001t0001g0168 a0001c0001t0001g0176 a0001c0001t0001g0194 others(3): Show |
6 | HG01358.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707+4529_1707+453 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302458 | ||||||
| chr16:31302462 | T | C | 125 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(122): Show |
126 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1707+4508T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302462 | |||||||
| chr16:31302466 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1707+4512T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302466 | |||||||
| chr16:31302466 | T | TCTTC | 8 | a0003c0004t0005g0094 a0003c0004t0005g0095 a0003c0004t0005g0097 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707+4515_1707+451 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302466 | ||||||
| chr16:31302483 | CT | C | 43 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(40): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1707+4535delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302483 | ||||||
| chr16:31302487 | T | C | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4533T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302487 | |||||||
| chr16:31302490 | C | T | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4536C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302490 | |||||||
| chr16:31302495 | C | T | 2 | a0001c0001t0004g0142 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1707+4541C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302495 | |||||||
| chr16:31302499 | T | C | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4545T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302499 | |||||||
| chr16:31302503 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+4549T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302503 | |||||||
| chr16:31302691 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1707+4737C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302691 | |||||||
| chr16:31302707 | TTC | T | 4 | a0003c0004t0005g0029 a0003c0004t0005g0030 a0003c0004t0005g0031 others(1): Show |
4 | HG00099.hp1 HG01175.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+4757_1707+475 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302707 | ||||||
| chr16:31302714 | T | C | 1 | a0001c0002t0002g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1707+4760T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302714 | |||||||
| chr16:31302749 | C | G | 1 | a0001c0002t0002g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1707+4795C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302749 | |||||||
| chr16:31302872 | C | T | 3 | a0001c0002t0002g0041 a0001c0002t0002g0044 a0001c0002t0002g0045 |
3 | HG01257.hp1 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1707+4918C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302872 | |||||||
| chr16:31302884 | CTCTTTCT others(39): Show |
C | 1 | a0010c0015t0001g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1707+4946_1707+499 others(50): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302884 | ||||||
| chr16:31302918 | C | CTCTT | 10 | a0001c0001t0001g0165 a0001c0001t0001g0209 a0001c0001t0001g0225 others(7): Show |
10 | HG01891.hp1 HG02129.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1707+5042_1707+504 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | C | CTCTTTCT others(1): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0086 a0001c0002t0002g0035 others(1): Show |
4 | HG01192.hp1 HG02647.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+5038_1707+504 others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | C | CTCTTTCT others(5): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0004c0006t0003g0010 |
3 | HG00558.hp2 HG00673.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1707+5034_1707+504 others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | C | CTCTTTCT others(29): Show |
1 | a0001c0002t0002g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1707+5010_1707+504 others(40): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | C | T | 1 | a0001c0007t0004g0146 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1707+4964C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302918 | |||||||
| chr16:31302918 | CTCTT | C | 42 | a0001c0001t0001g0059 a0001c0001t0001g0170 a0001c0001t0001g0175 others(39): Show |
42 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1707+5042_1707+504 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(1): Show |
C | 33 | a0001c0001t0001g0117 a0001c0001t0001g0166 a0001c0001t0001g0182 others(30): Show |
33 | HG00609.hp2 HG00642.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1707+5038_1707+504 others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(5): Show |
C | 24 | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0212 others(21): Show |
24 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1707+5034_1707+504 others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(9): Show |
C | 35 | a0001c0001t0001g0043 a0001c0001t0001g0171 a0001c0001t0001g0178 others(32): Show |
35 | HG00323.hp1 HG00609.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1707+5030_1707+504 others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(13): Show |
C | 20 | a0001c0001t0001g0192 a0001c0001t0001g0205 a0001c0001t0001g0223 others(17): Show |
21 | HG00099.hp1 HG00733.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1707+5026_1707+504 others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(17): Show |
C | 7 | a0001c0001t0001g0167 a0001c0001t0002g0132 a0001c0001t0002g0133 others(4): Show |
7 | HG00323.hp2 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+5022_1707+504 others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(21): Show |
C | 9 | a0001c0001t0001g0216 a0001c0001t0002g0130 a0001c0001t0002g0138 others(6): Show |
9 | HG00642.hp1 HG00673.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707+5018_1707+504 others(32): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(25): Show |
C | 7 | a0001c0001t0001g0075 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | HG01123.hp2 HG01255.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+5014_1707+504 others(36): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(29): Show |
C | 2 | a0001c0002t0002g0001 a0001c0002t0002g0063 |
2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1707+5010_1707+504 others(40): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(33): Show |
C | 1 | a0001c0002t0002g0001 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1707+5006_1707+504 others(44): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302918 | CTCTTTCT others(53): Show |
C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+4986_1707+504 others(64): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | ||||||
| chr16:31302925 | T | TTTCTTTC others(3): Show |
1 | a0001c0002t0002g0187 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1707+4980_1707+498 others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302925 | ||||||
| chr16:31302926 | T | TTCTTTCT others(19): Show |
1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4979_1707+498 others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302926 | ||||||
| chr16:31302933 | T | TCTCTCTC others(11): Show |
1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1707+4979_1707+498 others(22): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302933 | |||||||
| chr16:31302934 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1707+4980T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302934 | |||||||
| chr16:31302972 | CTTTCTTT others(19): Show |
C | 1 | a0003c0004t0005g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+5028_1707+505 others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302972 | ||||||
| chr16:31302984 | CTTTCTTT others(6): Show |
C | 1 | a0004c0006t0003g0018 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1707+5034_1707+504 others(17): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302984 | ||||||
| chr16:31302984 | CTTTCTTT others(7): Show |
C | 1 | a0001c0002t0002g0129 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1707+5040_1707+505 others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302984 | ||||||
| chr16:31302984 | CTTTCTTT others(8): Show |
C | 1 | a0003c0004t0005g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1707+5033_1707+504 others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302984 | ||||||
| chr16:31302988 | CTTTCTTT others(4): Show |
C | 1 | a0003c0004t0005g0020 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1707+5037_1707+504 others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302988 | ||||||
| chr16:31302998 | T | C | 1 | a0002c0003t0003g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1707+5044T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302998 | |||||||
| chr16:31302998 | TTTTCTTT others(9): Show |
T | 1 | a0001c0001t0001g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1707+5050_1707+506 others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302998 | ||||||
| chr16:31303016 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1707+5062T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303016 | |||||||
| chr16:31303016 | TTC | T | 33 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(30): Show |
34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+5068_1707+506 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31303016 | ||||||
| chr16:31303180 | G | A | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+5226G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303180 | |||||||
| chr16:31303216 | A | G | 1 | a0001c0002t0002g0231 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1707+5262A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303216 | |||||||
| chr16:31303278 | T | C | 104 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(101): Show |
105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+5324T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303278 | |||||||
| chr16:31303775 | G | C | 1 | a0004c0006t0003g0017 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1707+5821G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303775 | |||||||
| chr16:31303800 | T | C | 2 | a0001c0002t0002g0034 a0001c0002t0002g0116 |
2 | NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1707+5846T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303800 | |||||||
| chr16:31304089 | A | T | 1 | a0002c0003t0003g0118 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+6135A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304089 | |||||||
| chr16:31304173 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1707+6219G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304173 | |||||||
| chr16:31304260 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+6306C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304260 | |||||||
| chr16:31304363 | T | C | 1 | a0001c0002t0002g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1707+6409T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304363 | |||||||
| chr16:31304693 | C | T | 2 | a0001c0007t0009g0141 a0009c0011t0004g0003 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1707+6739C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304693 | |||||||
| chr16:31304714 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1707+6760G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304714 | |||||||
| chr16:31305313 | C | A | 1 | a0001c0002t0002g0184 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1707+7359C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305313 | |||||||
| chr16:31305489 | C | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+7535C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305489 | |||||||
| chr16:31305574 | T | C | 1 | a0001c0002t0002g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1707+7620T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305574 | |||||||
| chr16:31305679 | C | T | 1 | a0001c0007t0004g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1707+7725C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305679 | |||||||
| chr16:31305704 | G | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+7750G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305704 | |||||||
| chr16:31305751 | G | A | 34 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(31): Show |
35 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1707+7797G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305751 | |||||||
| chr16:31305797 | G | A | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1707+7843G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305797 | |||||||
| chr16:31305917 | T | C | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+7963T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305917 | |||||||
| chr16:31305941 | C | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+7987C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305941 | |||||||
| chr16:31306106 | T | C | 104 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(101): Show |
105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+8152T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306106 | |||||||
| chr16:31306184 | G | A | 104 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(101): Show |
105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+8230G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306184 | |||||||
| chr16:31306376 | A | T | 1 | a0001c0001t0001g0222 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1707+8422A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306376 | |||||||
| chr16:31306508 | CT | C | 16 | a0001c0001t0001g0170 a0001c0007t0009g0141 a0002c0003t0003g0006 others(13): Show |
16 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1707+8569delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31306508 | ||||||
| chr16:31306569 | A | G | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+8615A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306569 | |||||||
| chr16:31306631 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1707+8677C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306631 | |||||||
| chr16:31306656 | A | C | 104 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(101): Show |
105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+8702A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306656 | |||||||
| chr16:31306660 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1707+8706C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306660 | |||||||
| chr16:31306703 | G | A | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+8749G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306703 | |||||||
| chr16:31306757 | G | A | 1 | a0001c0002t0002g0129 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1707+8803G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306757 | |||||||
| chr16:31306936 | A | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+8982A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306936 | |||||||
| chr16:31306969 | CAT | C | 6 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0064 others(3): Show |
6 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707+9017_1707+901 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31306969 | ||||||
| chr16:31306976 | G | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+9022G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306976 | |||||||
| chr16:31306993 | T | C | 104 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(101): Show |
105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+9039T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306993 | |||||||
| chr16:31307027 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+9073C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307027 | |||||||
| chr16:31307078 | C | T | 1 | a0001c0002t0002g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1707+9124C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307078 | |||||||
| chr16:31307127 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+9173C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307127 | |||||||
| chr16:31307128 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0202 others(1): Show |
4 | HG00673.hp2 HG02132.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+9174G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307128 | |||||||
| chr16:31307502 | C | G | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0142 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+9548C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307502 | |||||||
| chr16:31307555 | G | A | 1 | a0001c0002t0002g0021 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1707+9601G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307555 | |||||||
| chr16:31307712 | C | T | 33 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(30): Show |
34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+9758C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307712 | |||||||
| chr16:31307790 | T | C | 7 | a0001c0007t0004g0024 a0001c0007t0004g0108 a0001c0007t0004g0143 others(4): Show |
7 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+9836T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307790 | |||||||
| chr16:31307917 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1707+9963C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307917 | |||||||
| chr16:31307962 | G | A | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+10008G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307962 | |||||||
| chr16:31308042 | C | T | 1 | a0009c0011t0004g0003 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1707+10088C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308042 | |||||||
| chr16:31308044 | G | A | 1 | a0001c0001t0004g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1707+10090G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308044 | |||||||
| chr16:31308076 | A | C | 81 | a0001c0001t0001g0192 a0001c0001t0001g0213 a0001c0001t0002g0085 others(78): Show |
82 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1707+10122A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308076 | |||||||
| chr16:31308115 | T | C | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+10161T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308115 | |||||||
| chr16:31308181 | T | G | 3 | a0002c0003t0003g0118 a0002c0003t0003g0119 a0002c0003t0003g0120 |
3 | HG00741.hp2 HG01106.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1707+10227T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308181 | |||||||
| chr16:31308200 | T | C | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+10246T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308200 | |||||||
| chr16:31308300 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+10346G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308300 | |||||||
| chr16:31308420 | T | G | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+10466T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308420 | |||||||
| chr16:31308435 | G | A | 7 | a0003c0004t0005g0020 a0003c0004t0005g0029 a0003c0004t0005g0030 others(4): Show |
7 | HG00099.hp1 HG01175.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+10481G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308435 | |||||||
| chr16:31308447 | G | A | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+10493G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308447 | |||||||
| chr16:31308454 | C | T | 1 | a0001c0007t0004g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1707+10500C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308454 | |||||||
| chr16:31308459 | G | C | 2 | a0002c0003t0003g0110 a0002c0003t0003g0112 |
2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1707+10505G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308459 | |||||||
| chr16:31308591 | C | CA | 21 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1707+10644dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31308591 | ||||||
| chr16:31308687 | C | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+10733C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308687 | |||||||
| chr16:31308711 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+10757T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308711 | |||||||
| chr16:31308737 | C | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+10783C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308737 | |||||||
| chr16:31308738 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0228 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1707+10784G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308738 | |||||||
| chr16:31308920 | C | A | 2 | a0004c0006t0003g0008 a0004c0006t0003g0009 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1707+10966C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308920 | |||||||
| chr16:31308977 | C | A | 81 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(78): Show |
81 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.1707+11023C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308977 | |||||||
| chr16:31308979 | C | A | 1 | a0003c0004t0005g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+11025C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308979 | |||||||
| chr16:31309083 | G | A | 1 | a0001c0002t0002g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1707+11129G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309083 | |||||||
| chr16:31309100 | G | T | 1 | a0003c0004t0005g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+11146G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309100 | |||||||
| chr16:31309101 | T | G | 1 | a0003c0004t0005g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+11147T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309101 | |||||||
| chr16:31309102 | G | T | 1 | a0003c0004t0005g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+11148G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309102 | |||||||
| chr16:31309169 | C | T | 3 | a0001c0007t0009g0141 a0008c0010t0004g0019 a0009c0011t0004g0003 |
3 | HG02896.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1707+11215C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309169 | |||||||
| chr16:31309455 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+11501C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309455 | |||||||
| chr16:31309554 | T | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0176 a0001c0001t0001g0213 |
3 | HG01516.hp2 HG01517.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1707+11600T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309554 | |||||||
| chr16:31309580 | C | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+11626C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309580 | |||||||
| chr16:31309605 | C | G | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1708-11636C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309605 | |||||||
| chr16:31309616 | T | G | 1 | a0001c0002t0002g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1708-11625T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309616 | |||||||
| chr16:31309668 | T | G | 5 | a0001c0007t0004g0143 a0001c0007t0004g0144 a0001c0007t0004g0145 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1708-11573T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309668 | |||||||
| chr16:31309784 | C | G | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1708-11457C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309784 | |||||||
| chr16:31309793 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-11448G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309793 | |||||||
| chr16:31309794 | C | T | 1 | a0001c0002t0002g0091 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1708-11447C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309794 | |||||||
| chr16:31309874 | T | C | 1 | a0001c0007t0004g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1708-11367T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309874 | |||||||
| chr16:31309935 | A | G | 2 | a0005c0009t0002g0083 a0005c0009t0002g0084 |
2 | HG02040.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1708-11306A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309935 | |||||||
| chr16:31310100 | C | G | 3 | a0002c0003t0003g0109 a0002c0003t0003g0110 a0002c0003t0003g0112 |
3 | HG02630.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1708-11141C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310100 | |||||||
| chr16:31310156 | T | C | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-11085T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310156 | |||||||
| chr16:31310567 | C | T | 1 | a0001c0007t0004g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1708-10674C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310567 | |||||||
| chr16:31310711 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1708-10530C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310711 | |||||||
| chr16:31310712 | G | A | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-10529G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310712 | |||||||
| chr16:31310727 | G | A | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-10514G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310727 | |||||||
| chr16:31310788 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-10453C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310788 | |||||||
| chr16:31310897 | A | G | 23 | a0003c0004t0005g0020 a0003c0004t0005g0023 a0003c0004t0005g0029 others(20): Show |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-10344A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310897 | |||||||
| chr16:31310926 | G | C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-10315G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310926 | |||||||
| chr16:31311013 | G | A | 25 | a0001c0001t0002g0174 a0001c0013t0008g0173 a0003c0004t0005g0020 others(22): Show |
25 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1708-10228G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311013 | |||||||
| chr16:31311183 | A | G | 1 | a0004c0006t0003g0018 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1708-10058A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311183 | |||||||
| chr16:31311204 | C | T | 2 | a0001c0007t0009g0141 a0009c0011t0004g0003 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1708-10037C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311204 | |||||||
| chr16:31311212 | A | G | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1708-10029A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311212 | |||||||
| chr16:31311225 | C | T | 1 | a0002c0003t0003g0060 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1708-10016C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311225 | |||||||
| chr16:31311531 | A | G | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-9710A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311531 | |||||||
| chr16:31311892 | T | C | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1708-9349T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311892 | |||||||
| chr16:31311895 | A | T | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1708-9346A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311895 | |||||||
| chr16:31311899 | T | C | 1 | a0001c0013t0008g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1708-9342T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311899 | |||||||
| chr16:31311948 | C | T | 1 | a0003c0004t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1708-9293C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311948 | |||||||
| chr16:31312029 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1708-9212G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312029 | |||||||
| chr16:31312251 | G | A | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-8990G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312251 | |||||||
| chr16:31312260 | G | T | 1 | a0001c0007t0004g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1708-8981G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312260 | |||||||
| chr16:31312325 | A | G | 1 | a0001c0002t0002g0077 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1708-8916A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312325 | |||||||
| chr16:31312332 | C | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-8909C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312332 | |||||||
| chr16:31312355 | A | G | 23 | a0003c0004t0005g0020 a0003c0004t0005g0023 a0003c0004t0005g0029 others(20): Show |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-8886A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312355 | |||||||
| chr16:31312391 | A | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1708-8850A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312391 | |||||||
| chr16:31312434 | T | C | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1708-8807T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312434 | |||||||
| chr16:31312463 | G | A | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1708-8778G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312463 | |||||||
| chr16:31312464 | T | C | 1 | a0001c0007t0004g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1708-8777T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312464 | |||||||
| chr16:31312595 | A | T | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-8646A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312595 | |||||||
| chr16:31312629 | A | G | 2 | a0002c0003t0003g0110 a0002c0003t0003g0112 |
2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1708-8612A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312629 | |||||||
| chr16:31312873 | C | CT | 16 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(13): Show |
16 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.1708-8351dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31312873 | ||||||
| chr16:31312873 | CT | C | 152 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1708-8351delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31312873 | ||||||
| chr16:31312974 | C | T | 7 | a0001c0007t0004g0024 a0001c0007t0004g0108 a0001c0007t0004g0143 others(4): Show |
7 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1708-8267C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312974 | |||||||
| chr16:31312995 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-8246G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312995 | |||||||
| chr16:31313650 | C | G | 33 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(30): Show |
34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-7591C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31313650 | |||||||
| chr16:31313665 | T | C | 42 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(39): Show |
42 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1708-7576T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31313665 | |||||||
| chr16:31313962 | C | G | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-7279C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31313962 | |||||||
| chr16:31314112 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1708-7129G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314112 | |||||||
| chr16:31314163 | C | A | 2 | a0001c0005t0004g0154 a0007c0012t0004g0156 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1708-7078C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314163 | |||||||
| chr16:31314268 | A | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1708-6973A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314268 | |||||||
| chr16:31314743 | T | A | 1 | a0001c0007t0004g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1708-6498T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314743 | |||||||
| chr16:31314760 | G | A | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-6481G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314760 | |||||||
| chr16:31314821 | G | GT | 42 | a0001c0001t0001g0175 a0001c0001t0001g0185 a0001c0001t0001g0186 others(39): Show |
42 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1708-6401dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31314821 | ||||||
| chr16:31314821 | GT | G | 29 | a0001c0001t0001g0062 a0001c0002t0002g0052 a0001c0005t0004g0002 others(26): Show |
30 | HG01192.hp2 HG01496.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1708-6401delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31314821 | ||||||
| chr16:31314844 | A | G | 5 | a0003c0004t0005g0023 a0003c0004t0005g0061 a0003c0004t0005g0088 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1708-6397A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314844 | |||||||
| chr16:31314883 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1708-6358C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314883 | |||||||
| chr16:31315035 | A | T | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1708-6206A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315035 | |||||||
| chr16:31315102 | C | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-6139C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315102 | |||||||
| chr16:31315103 | G | A | 1 | a0002c0003t0003g0112 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1708-6138G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315103 | |||||||
| chr16:31315108 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-6133C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315108 | |||||||
| chr16:31315266 | T | G | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-5975T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315266 | |||||||
| chr16:31315308 | T | C | 3 | a0001c0002t0002g0041 a0001c0002t0002g0044 a0001c0002t0002g0045 |
3 | HG01257.hp1 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1708-5933T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315308 | |||||||
| chr16:31315385 | C | T | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-5856C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315385 | |||||||
| chr16:31315446 | A | AT | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-5788dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31315446 | ||||||
| chr16:31315605 | C | T | 1 | a0004c0006t0003g0007 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1708-5636C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315605 | |||||||
| chr16:31315607 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-5634G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315607 | |||||||
| chr16:31315724 | G | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG01175.hp2 HG01952.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1708-5517G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315724 | |||||||
| chr16:31315727 | G | A | 21 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1708-5514G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315727 | |||||||
| chr16:31315754 | C | T | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1708-5487C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315754 | |||||||
| chr16:31315858 | T | C | 23 | a0003c0004t0005g0020 a0003c0004t0005g0023 a0003c0004t0005g0029 others(20): Show |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-5383T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315858 | |||||||
| chr16:31315920 | C | T | 1 | a0001c0007t0004g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1708-5321C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315920 | |||||||
| chr16:31315922 | C | T | 1 | a0001c0002t0002g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1708-5319C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315922 | |||||||
| chr16:31315959 | C | T | 3 | a0001c0007t0009g0141 a0008c0010t0004g0019 a0009c0011t0004g0003 |
3 | HG02896.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1708-5282C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315959 | |||||||
| chr16:31316010 | A | T | 231 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1708-5231A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316010 | |||||||
| chr16:31316016 | A | G | 231 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1708-5225A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316016 | |||||||
| chr16:31316021 | C | T | 3 | a0003c0004t0005g0023 a0003c0004t0005g0061 a0003c0004t0005g0088 |
3 | HG02257.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1708-5220C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316021 | |||||||
| chr16:31316038 | CAAAAAAT others(185): Show |
C | 231 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1708-5196_1708-500 others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31316038 | ||||||
| chr16:31316278 | C | T | 19 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1708-4963C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316278 | |||||||
| chr16:31316339 | A | G | 2 | a0001c0001t0002g0174 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1708-4902A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316339 | |||||||
| chr16:31316387 | G | GA | 67 | a0001c0001t0001g0022 a0001c0001t0001g0177 a0001c0001t0001g0238 others(64): Show |
68 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1708-4840dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31316387 | ||||||
| chr16:31316434 | G | T | 1 | a0001c0007t0004g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1708-4807G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316434 | |||||||
| chr16:31316691 | C | T | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-4550C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316691 | |||||||
| chr16:31316939 | T | C | 5 | a0001c0007t0004g0143 a0001c0007t0004g0144 a0001c0007t0004g0145 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1708-4302T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316939 | |||||||
| chr16:31316992 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1708-4249G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316992 | |||||||
| chr16:31317163 | C | T | 7 | a0003c0004t0005g0094 a0003c0004t0005g0095 a0003c0004t0005g0097 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1708-4078C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317163 | |||||||
| chr16:31317341 | C | T | 1 | a0002c0003t0003g0125 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1708-3900C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317341 | |||||||
| chr16:31317379 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1708-3862G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317379 | |||||||
| chr16:31317559 | T | G | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-3682T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317559 | |||||||
| chr16:31317670 | A | T | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-3571A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317670 | |||||||
| chr16:31317949 | C | G | 2 | a0001c0007t0009g0141 a0009c0011t0004g0003 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1708-3292C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317949 | |||||||
| chr16:31317959 | G | A | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-3282G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317959 | |||||||
| chr16:31318344 | C | CT | 18 | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0001g0180 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1708-2880dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31318344 | ||||||
| chr16:31318344 | CT | C | 23 | a0001c0002t0002g0231 a0003c0004t0005g0020 a0003c0004t0005g0023 others(20): Show |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-2880delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31318344 | ||||||
| chr16:31318464 | C | T | 8 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(5): Show |
8 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1708-2777C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318464 | |||||||
| chr16:31318490 | C | T | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1708-2751C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318490 | |||||||
| chr16:31318633 | T | C | 78 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(75): Show |
79 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.1708-2608T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318633 | |||||||
| chr16:31318806 | A | G | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-2435A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318806 | |||||||
| chr16:31318811 | TTGTAATT others(3): Show |
T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-2429_1708-242 others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318811 | |||||||
| chr16:31318840 | A | G | 86 | a0001c0001t0002g0174 a0001c0002t0002g0001 a0001c0002t0002g0021 others(83): Show |
87 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1708-2401A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318840 | |||||||
| chr16:31318857 | C | T | 23 | a0003c0004t0005g0020 a0003c0004t0005g0023 a0003c0004t0005g0029 others(20): Show |
23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-2384C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318857 | |||||||
| chr16:31318949 | A | C | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-2292A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318949 | |||||||
| chr16:31319003 | TG | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-2237delG | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319003 | |||||||
| chr16:31319214 | G | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-2027G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319214 | |||||||
| chr16:31319239 | G | GT | 50 | a0001c0005t0004g0148 a0001c0005t0004g0152 a0001c0005t0004g0155 others(47): Show |
50 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1708-1992dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31319239 | ||||||
| chr16:31319405 | A | G | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-1836A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319405 | |||||||
| chr16:31319686 | G | C | 61 | a0001c0002t0002g0001 a0001c0002t0002g0021 a0001c0002t0002g0026 others(58): Show |
62 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1708-1555G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319686 | |||||||
| chr16:31319816 | T | C | 45 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(42): Show |
45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1708-1425T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319816 | |||||||
| chr16:31319818 | C | CT | 22 | a0001c0005t0004g0002 a0001c0005t0004g0148 a0001c0005t0004g0149 others(19): Show |
23 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1708-1411dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31319818 | ||||||
| chr16:31319836 | G | A | 14 | a0001c0005t0004g0002 a0001c0005t0004g0152 a0001c0005t0004g0154 others(11): Show |
15 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1708-1405G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319836 | |||||||
| chr16:31319839 | A | G | 165 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(162): Show |
167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1708-1402A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319839 | |||||||
| chr16:31319881 | C | T | 34 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(31): Show |
34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-1360C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319881 | |||||||
| chr16:31319898 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1708-1343C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319898 | |||||||
| chr16:31319923 | C | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-1318C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319923 | |||||||
| chr16:31320002 | T | C | 79 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(76): Show |
80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-1239T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31320002 | |||||||
| chr16:31320054 | C | T | 1 | a0001c0007t0004g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1708-1187C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31320054 | |||||||
| chr16:31320189 | A | G | 1 | a0002c0003t0003g0111 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1708-1052A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31320189 | |||||||
| chr16:31320637 | C | T | 61 | a0001c0002t0002g0001 a0001c0002t0002g0021 a0001c0002t0002g0026 others(58): Show |
62 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1708-604C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31320637 | |||||||
| chr16:31321019 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-222T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31321019 | |||||||
| chr16:31321024 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-217T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31321024 | |||||||
| chr16:31321038 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1708-203G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31321038 | |||||||
| chr16:31321123 | G | C | 1 | a0001c0002t0002g0021 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1708-118G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31321123 | |||||||
| chr16:31321677 | A | G | 3 | a0003c0004t0005g0093 a0003c0004t0005g0096 a0003c0004t0006g0099 |
3 | HG01109.hp2 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2002+50A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31321677 | |||||||
| chr16:31321769 | G | C | 5 | a0001c0007t0004g0143 a0001c0007t0004g0144 a0001c0007t0004g0145 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2002+142G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31321769 | |||||||
| chr16:31321822 | G | A | 1 | a0006c0014t0001g0233 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2002+195G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31321822 | |||||||
| chr16:31322311 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2002+684G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322311 | |||||||
| chr16:31322402 | G | A | 6 | a0002c0003t0003g0121 a0002c0003t0003g0122 a0002c0003t0003g0123 others(3): Show |
6 | HG01106.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2002+775G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322402 | |||||||
| chr16:31322440 | C | T | 1 | a0001c0002t0002g0028 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2002+813C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322440 | |||||||
| chr16:31322819 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2002+1192G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322819 | |||||||
| chr16:31322872 | G | A | 1 | a0004c0006t0003g0007 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2002+1245G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322872 | |||||||
| chr16:31322915 | C | A | 60 | a0001c0002t0002g0001 a0001c0002t0002g0021 a0001c0002t0002g0026 others(57): Show |
61 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2002+1288C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322915 | |||||||
| chr16:31323244 | C | A | 1 | a0004c0006t0003g0015 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2003-1155C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323244 | |||||||
| chr16:31323300 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2003-1099T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323300 | |||||||
| chr16:31323361 | T | G | 165 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(162): Show |
167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.2003-1038T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323361 | |||||||
| chr16:31323426 | C | CA | 15 | a0001c0001t0001g0229 a0001c0001t0004g0142 a0001c0005t0004g0002 others(12): Show |
16 | HG01175.hp1 HG02258.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2003-956dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31323426 | ||||||
| chr16:31323426 | CA | C | 10 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0216 others(7): Show |
10 | HG00099.hp2 HG00642.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2003-956delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31323426 | ||||||
| chr16:31323524 | G | A | 1 | a0001c0002t0002g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2003-875G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323524 | |||||||
| chr16:31323544 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2003-855G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323544 | |||||||
| chr16:31323681 | T | G | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2003-718T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323681 | |||||||
| chr16:31323691 | T | G | 2 | a0002c0003t0003g0067 a0002c0003t0003g0070 |
2 | HG02071.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2003-708T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323691 | |||||||
| chr16:31323702 | G | A | 6 | a0002c0003t0003g0121 a0002c0003t0003g0122 a0002c0003t0003g0123 others(3): Show |
6 | HG01106.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2003-697G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323702 | |||||||
| chr16:31323873 | C | T | 1 | a0003c0004t0005g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2003-526C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323873 | |||||||
| chr16:31323896 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2003-503C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323896 | |||||||
| chr16:31323938 | G | C | 1 | a0008c0010t0004g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2003-461G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323938 | |||||||
| chr16:31323939 | G | A | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2003-460G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323939 | |||||||
| chr16:31324013 | A | G | 1 | a0001c0002t0002g0072 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2003-386A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31324013 | |||||||
| chr16:31324148 | A | G | 1 | a0003c0004t0005g0020 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2003-251A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31324148 | |||||||
| chr16:31324192 | AAAGG | A | 7 | a0001c0001t0001g0194 a0001c0001t0001g0229 a0001c0007t0004g0143 others(4): Show |
7 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003-192_2003-189d others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31324192 | ||||||
| chr16:31324585 | T | C | 83 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(80): Show |
84 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.2157+32T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 17/29 | chr16 | 31324585 | |||||||
| chr16:31325067 | GGACCCGT others(5): Show |
G | 21 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0005t0004g0002 others(18): Show |
22 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2363+43_2363+54del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr16 | 31325067 | ||||||
| chr16:31325116 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0226 a0010c0015t0001g0172 |
3 | HG03669.hp2 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2363+85C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | chr16 | 31325116 | |||||||
| chr16:31325180 | T | C | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2364-83T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | chr16 | 31325180 | |||||||
| chr16:31325198 | T | C | 166 | a0001c0001t0001g0175 a0001c0001t0002g0085 a0001c0001t0002g0130 others(163): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.2364-65T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | chr16 | 31325198 | |||||||
| chr16:31325202 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2364-61G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | chr16 | 31325202 | |||||||
| chr16:31325697 | T | C | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2628+75T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31325697 | |||||||
| chr16:31325834 | G | A | 38 | a0002c0003t0003g0006 a0002c0003t0003g0036 a0002c0003t0003g0037 others(35): Show |
38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.2628+212G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31325834 | |||||||
| chr16:31325846 | G | A | 1 | a0001c0002t0002g0129 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2628+224G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31325846 | |||||||
| chr16:31325927 | G | A | 32 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(29): Show |
33 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.2628+305G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31325927 | |||||||
| chr16:31326016 | T | G | 9 | a0002c0003t0003g0006 a0002c0003t0003g0121 a0002c0003t0003g0122 others(6): Show |
9 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2628+394T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326016 | |||||||
| chr16:31326093 | AAT | A | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2628+473_2628+474d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr16 | 31326093 | ||||||
| chr16:31326207 | C | T | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2628+585C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326207 | |||||||
| chr16:31326210 | C | G | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2628+588C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326210 | |||||||
| chr16:31326356 | A | G | 58 | a0001c0002t0002g0001 a0001c0002t0002g0021 a0001c0002t0002g0026 others(55): Show |
59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2629-500A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326356 | |||||||
| chr16:31326707 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2629-149G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326707 | |||||||
| chr16:31327106 | T | G | 1 | a0004c0006t0003g0005 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2708+171T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327106 | |||||||
| chr16:31327326 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2708+391C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327326 | |||||||
| chr16:31327370 | C | G | 8 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(5): Show |
8 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2708+435C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327370 | |||||||
| chr16:31327423 | C | CA | 58 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(55): Show |
58 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.2708+501dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327423 | ||||||
| chr16:31327423 | C | CAA | 40 | a0001c0001t0001g0062 a0001c0001t0001g0087 a0001c0001t0001g0117 others(37): Show |
40 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.2708+500_2708+501d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327423 | ||||||
| chr16:31327423 | C | CAAA | 6 | a0002c0003t0003g0006 a0002c0003t0003g0110 a0002c0003t0003g0112 others(3): Show |
6 | HG00741.hp2 HG01106.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2708+499_2708+501d others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327423 | ||||||
| chr16:31327423 | CA | C | 14 | a0001c0001t0002g0174 a0001c0007t0004g0024 a0001c0007t0004g0025 others(11): Show |
14 | HG01496.hp2 HG01891.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.2708+501delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327423 | ||||||
| chr16:31327617 | A | G | 134 | a0001c0001t0002g0174 a0001c0002t0002g0001 a0001c0002t0002g0021 others(131): Show |
135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.2709-530A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327617 | |||||||
| chr16:31327619 | T | TAATAAA | 14 | a0001c0005t0004g0002 a0001c0005t0004g0152 a0001c0005t0004g0154 others(11): Show |
15 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2709-526_2709-525i others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327619 | ||||||
| chr16:31327619 | T | TAATAATA others(2): Show |
5 | a0001c0005t0004g0148 a0001c0005t0004g0149 a0001c0005t0004g0150 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2709-526_2709-525i others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327619 | ||||||
| chr16:31327622 | A | T | 1 | a0001c0001t0004g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2709-525A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327622 | |||||||
| chr16:31327729 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2709-418A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327729 | |||||||
| chr16:31327793 | A | G | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2709-354A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327793 | |||||||
| chr16:31327952 | A | T | 1 | a0001c0007t0004g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2709-195A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327952 | |||||||
| chr16:31328304 | G | A | 58 | a0001c0002t0002g0001 a0001c0002t0002g0021 a0001c0002t0002g0026 others(55): Show |
59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2792+74G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328304 | |||||||
| chr16:31328383 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2792+153G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328383 | |||||||
| chr16:31328440 | A | C | 2 | a0001c0001t0002g0174 a0001c0013t0008g0173 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2792+210A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328440 | |||||||
| chr16:31328549 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0227 |
2 | NA18945.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2792+319G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328549 | |||||||
| chr16:31328582 | T | C | 65 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(62): Show |
65 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2792+352T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328582 | |||||||
| chr16:31328589 | A | ATG | 11 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(8): Show |
11 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2792+368_2792+369d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31328589 | ||||||
| chr16:31328704 | G | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2792+474G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328704 | |||||||
| chr16:31328756 | A | G | 2 | a0001c0005t0004g0149 a0001c0005t0004g0151 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2793-472A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328756 | |||||||
| chr16:31328765 | C | T | 49 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(46): Show |
49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2793-463C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328765 | |||||||
| chr16:31328766 | G | A | 1 | a0001c0002t0002g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2793-462G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328766 | |||||||
| chr16:31328772 | G | A | 20 | a0001c0001t0004g0142 a0001c0005t0004g0002 a0001c0005t0004g0148 others(17): Show |
21 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2793-456G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328772 | |||||||
| chr16:31328792 | ATG | A | 152 | a0001c0001t0002g0174 a0001c0002t0002g0001 a0001c0002t0002g0021 others(149): Show |
154 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.2793-425_2793-424d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31328792 | ||||||
| chr16:31328895 | C | T | 85 | a0001c0001t0002g0174 a0001c0002t0002g0001 a0001c0002t0002g0021 others(82): Show |
86 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2793-333C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328895 | |||||||
| chr16:31328896 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2793-332G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328896 | |||||||
| chr16:31328957 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2793-271C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328957 | |||||||
| chr16:31329047 | G | A | 83 | a0001c0001t0002g0174 a0001c0002t0002g0001 a0001c0002t0002g0021 others(80): Show |
84 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.2793-181G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31329047 | |||||||
| chr16:31329189 | C | T | 2 | a0001c0008t0004g0139 a0001c0008t0004g0140 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2793-39C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31329189 | |||||||
| chr16:31329199 | C | T | 4 | a0001c0002t0002g0051 a0001c0002t0002g0057 a0001c0002t0002g0184 others(1): Show |
4 | HG00544.hp2 HG01934.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2793-29C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31329199 | |||||||
| chr16:31329392 | C | T | 11 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(8): Show |
11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2868+89C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 24/29 | chr16 | 31329392 | |||||||
| chr16:31329511 | C | T | 2 | a0001c0007t0009g0141 a0009c0011t0004g0003 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2868+208C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 24/29 | chr16 | 31329511 | |||||||
| chr16:31329588 | T | C | 166 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(163): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.2869-210T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 24/29 | chr16 | 31329588 | |||||||
| chr16:31329676 | C | T | 51 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(48): Show |
51 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2869-122C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 24/29 | chr16 | 31329676 | |||||||
| chr16:31330206 | A | T | 1 | a0001c0002t0002g0169 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3060+42A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 26/29 | chr16 | 31330206 | |||||||
| chr16:31330613 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | splice_region_variant&intron_variant | LOW | c.3276+8T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330613 | |||||||
| chr16:31330645 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0176 a0001c0001t0001g0213 |
3 | HG01516.hp2 HG01517.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3276+40G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330645 | |||||||
| chr16:31330772 | A | G | 2 | a0002c0003t0003g0110 a0002c0003t0003g0112 |
2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3276+167A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330772 | |||||||
| chr16:31330799 | C | G | 58 | a0001c0002t0002g0001 a0001c0002t0002g0021 a0001c0002t0002g0026 others(55): Show |
59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3276+194C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330799 | |||||||
| chr16:31330803 | G | C | 58 | a0001c0002t0002g0001 a0001c0002t0002g0021 a0001c0002t0002g0026 others(55): Show |
59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3276+198G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330803 | |||||||
| chr16:31330805 | C | G | 58 | a0001c0002t0002g0001 a0001c0002t0002g0021 a0001c0002t0002g0026 others(55): Show |
59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3276+200C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330805 | |||||||
| chr16:31330807 | G | C | 58 | a0001c0002t0002g0001 a0001c0002t0002g0021 a0001c0002t0002g0026 others(55): Show |
59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3276+202G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330807 | |||||||
| chr16:31330807 | G | GAC | 86 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(83): Show |
86 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.3276+204_3276+205d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr16 | 31330807 | ||||||
| chr16:31330824 | T | G | 1 | a0006c0014t0001g0233 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3276+219T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330824 | |||||||
| chr16:31330874 | T | TAGAG | 163 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(160): Show |
165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3276+272_3276+273i others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr16 | 31330874 | ||||||
| chr16:31330925 | AGACAGT | A | 51 | a0001c0007t0004g0024 a0001c0007t0004g0025 a0001c0007t0004g0108 others(48): Show |
51 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.3277-237_3277-232d others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr16 | 31330925 | ||||||
| chr16:31331017 | G | A | 1 | a0001c0002t0007g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3277-148G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31331017 | |||||||
| chr16:31331096 | C | A | 1 | a0001c0002t0002g0058 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3277-69C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31331096 | |||||||
| chr16:31331287 | T | C | 232 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.3387+12T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331287 | |||||||
| chr16:31331295 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3387+20C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331295 | |||||||
| chr16:31331407 | A | C | 1 | a0001c0007t0004g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3387+132A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331407 | |||||||
| chr16:31331467 | C | CTTG | 93 | a0001c0001t0002g0085 a0001c0001t0002g0130 a0001c0001t0002g0131 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.3388-167_3388-165d others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr16 | 31331467 | ||||||
| chr16:31331584 | G | A | 1 | a0004c0006t0003g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3388-52G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331584 | |||||||
| chr16:31331634 | A | G | 1 | a0002c0003t0003g0060 | 1 | HG03491.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.3388-2A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331634 |