Search by Gene
| Item | Value |
|---|---|
| geneid | 2 |
| ensemblid | ENSG00000175899.15 |
| hgncid | 7 |
| symbol | A2M |
| name | alpha-2-macroglobulin |
| refseq_nuc | NM_000014.6 |
| refseq_prot | NP_000005.3 |
| ensembl_nuc | ENST00000318602.12 |
| ensembl_prot | ENSP00000323929.8 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 9067708 |
| end | 9115919 |
| strand | - |
| ver | v1.2 |
| region | chr12:9067708-9115919 |
| region5000 | chr12:9062708-9120919 |
| regionname0 | A2M_chr12_9067708_9115919 |
| regionname5000 | A2M_chr12_9062708_9120919 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1474 | 242 | 58 | 33 | 110 | 7 | 33 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0002 | 0/0 | 1474 | 63 | 16 | 22 | 14 | 2 | 9 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0003 | 0/0 | 1474 | 8 | 0 | 8 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0004 | 0/0 | 1474 | 4 | 0 | 1 | 0 | 1 | 2 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0005 | 1/0 | 1474 | 3 | 2 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0006 | 0/0 | 1474 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0007 | 0/0 | 1474 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0008 | 0/0 | 1474 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0009 | 0/0 | 1474 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0010 | 0/0 | 1474 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0011 | 0/0 | 1474 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0012 | 0/0 | 1474 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0013 | 0/0 | 1474 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0014 | 0/0 | 1474 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0015 | 0/0 | 1474 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| a0016 | 0/0 | 1474 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | MGKNK others(1469): Show |
chr12 | 9062708 | 9120919 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4422 | 214 | 47 | 27 | 108 | 7 | 24 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0003 | 0/0 | 4422 | 11 | 0 | 4 | 0 | 0 | 7 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0005 | 0/0 | 4422 | 7 | 7 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0009 | 0/0 | 4422 | 2 | 2 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0011 | 0/0 | 4422 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0015 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0017 | 0/0 | 4422 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0018 | 0/0 | 4422 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0021 | 0/0 | 4422 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0022 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0001c0026 | 0/0 | 4422 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0002c0002 | 0/0 | 4422 | 61 | 15 | 21 | 14 | 2 | 9 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0002c0010 | 0/0 | 4422 | 2 | 1 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0003c0004 | 0/0 | 4422 | 8 | 0 | 8 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0004c0006 | 0/0 | 4422 | 4 | 0 | 1 | 0 | 1 | 2 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0005c0007 | 1/0 | 4422 | 3 | 2 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0006c0008 | 0/0 | 4422 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0007c0023 | 0/0 | 4422 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0008c0024 | 0/0 | 4422 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0009c0025 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0010c0019 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0011c0012 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0012c0027 | 0/0 | 4422 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0013c0014 | 0/0 | 4422 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0014c0013 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0015c0020 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 | ||
| a0016c0016 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | ATGGG others(4417): Show |
chr12 | 9062708 | 9120919 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4610 | 159 | 17 | 22 | 94 | 5 | 20 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0001t0002 | 0/0 | 4610 | 54 | 29 | 5 | 14 | 2 | 4 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0001t0003 | 0/0 | 4610 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0003t0002 | 0/0 | 4610 | 11 | 0 | 4 | 0 | 0 | 7 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0005t0002 | 0/0 | 4610 | 7 | 7 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0009t0002 | 0/0 | 4610 | 2 | 2 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0011t0001 | 0/0 | 4610 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0015t0002 | 0/0 | 4610 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0017t0001 | 0/0 | 4610 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0018t0001 | 0/0 | 4610 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0021t0002 | 0/0 | 4610 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0022t0002 | 0/0 | 4610 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0001c0026t0001 | 0/0 | 4610 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0002c0002t0001 | 0/0 | 4610 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0002c0002t0002 | 0/0 | 4610 | 59 | 15 | 21 | 12 | 2 | 9 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0002c0010t0002 | 0/0 | 4610 | 2 | 1 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0003c0004t0001 | 0/0 | 4610 | 8 | 0 | 8 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0004c0006t0001 | 0/0 | 4610 | 4 | 0 | 1 | 0 | 1 | 2 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0005c0007t0001 | 1/0 | 4610 | 3 | 2 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0006c0008t0001 | 0/0 | 4610 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0007c0023t0001 | 0/0 | 4610 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0008c0024t0001 | 0/0 | 4610 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0009c0025t0001 | 0/0 | 4610 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0010c0019t0002 | 0/0 | 4610 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0011c0012t0002 | 0/0 | 4610 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0012c0027t0001 | 0/0 | 4610 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0013c0014t0002 | 0/0 | 4610 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0014c0013t0002 | 0/0 | 4610 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0015c0020t0002 | 0/0 | 4610 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| a0016c0016t0002 | 0/0 | 4610 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | GGGAC others(4605): Show |
chr12 | 9062708 | 9120919 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0003t0002g0003 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0003t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0005t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0005t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0005t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0005t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0005t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0005t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0009t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0009t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0011t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0011t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0015t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0017t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0018t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0021t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0022t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0001c0026t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0007 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0015 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0010t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0002c0010t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0003c0004t0001g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0003c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0004c0006t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0004c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0004c0006t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0004c0006t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0005c0007t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0005c0007t0001g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0005c0007t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0006c0008t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0006c0008t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0007c0023t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0008c0024t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0009c0025t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0010c0019t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0011c0012t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0012c0027t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0013c0014t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0014c0013t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0015c0020t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| a0016c0016t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0085 | EUR | GBR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0120 | EUR | GBR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00639 | hp1 | a0001 | c0021 | t0002 | g0076 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00735 | hp2 | a0004 | c0006 | t0001 | g0187 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0086 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG00741 | hp2 | a0007 | c0023 | t0001 | g0213 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0014 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0014 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01074 | hp2 | a0001 | c0026 | t0001 | g0219 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01106 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0127 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01169 | hp2 | a0002 | c0010 | t0002 | g0138 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0077 | AMR | PUR | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01257 | hp1 | a0003 | c0004 | t0001 | g0001 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0131 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01358 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01433 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0067 | EUR | IBS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01515 | hp2 | a0004 | c0006 | t0001 | g0199 | EUR | IBS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0112 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01928 | hp2 | a0003 | c0004 | t0001 | g0163 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0126 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01952 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01978 | hp1 | a0003 | c0004 | t0001 | g0001 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0098 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0133 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02145 | hp2 | a0001 | c0009 | t0002 | g0083 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CDX | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02273 | hp1 | a0008 | c0024 | t0001 | g0214 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0087 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0130 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0097 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02602 | hp1 | a0004 | c0006 | t0001 | g0204 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02622 | hp1 | a0001 | c0005 | t0002 | g0134 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0075 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02717 | hp1 | a0001 | c0005 | t0002 | g0019 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02723 | hp1 | a0009 | c0025 | t0001 | g0276 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02738 | hp2 | a0001 | c0003 | t0002 | g0073 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02809 | hp2 | a0001 | c0015 | t0002 | g0040 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02895 | hp2 | a0002 | c0010 | t0002 | g0140 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02922 | hp1 | a0001 | c0005 | t0002 | g0136 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02970 | hp2 | a0010 | c0019 | t0002 | g0043 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02976 | hp2 | a0005 | c0007 | t0001 | g0246 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0119 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03130 | hp1 | a0001 | c0022 | t0002 | g0039 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0117 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03209 | hp2 | a0011 | c0012 | t0002 | g0094 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0100 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03486 | hp2 | a0005 | c0007 | t0001 | g0244 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03490 | hp1 | a0004 | c0006 | t0001 | g0205 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0110 | AFR | ESN | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03540 | hp2 | a0001 | c0009 | t0002 | g0082 | AFR | GWD | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03669 | hp1 | a0001 | c0017 | t0001 | g0236 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0118 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03688 | hp2 | a0001 | c0018 | t0001 | g0258 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0124 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0123 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0107 | SAS | PJL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0048 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03942 | hp2 | a0001 | c0003 | t0002 | g0074 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0115 | SAS | BEB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0128 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG04228 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | STU | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | YRI | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18522 | hp2 | a0001 | c0005 | t0002 | g0142 | AFR | YRI | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | YRI | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | YRI | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18962 | hp1 | a0001 | c0011 | t0001 | g0266 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18981 | hp1 | a0012 | c0027 | t0001 | g0277 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18999 | hp2 | a0013 | c0014 | t0002 | g0079 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19030 | hp1 | a0014 | c0013 | t0002 | g0049 | AFR | LWK | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19030 | hp2 | a0015 | c0020 | t0002 | g0080 | AFR | LWK | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19043 | hp1 | a0016 | c0016 | t0002 | g0139 | AFR | LWK | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19081 | hp1 | a0006 | c0008 | t0001 | g0229 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19082 | hp2 | a0006 | c0008 | t0001 | g0217 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19083 | hp1 | a0001 | c0011 | t0001 | g0264 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | YRI | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ASW | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ASW | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | TSI | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0121 | AMR | CLM | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG02559 | hp2 | a0001 | c0005 | t0002 | g0019 | AFR | ACB | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03471 | hp1 | a0001 | c0005 | t0002 | g0135 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | USA | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| HG06807 | hp2 | a0001 | c0005 | t0002 | g0137 | AFR | USA | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0103 | AFR | USA | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | USA | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | LWK | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | LWK | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0202 | REF | REF | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| homoSapiens | grch38p0 | a0005 | c0007 | t0001 | g0245 | REF | REF | A2M_chr12_9062708_9120919 | A2M | chr12 | 9062708 | 9120919 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9069789 | G | A | 1 | a0010 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.4219C>T | p.Arg1407Trp | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/36 | 4289/4610 | 4219/4425 | 1407/1474 | chr12 | 9069789 | |||
| chr12:9077417 | C | T | 1 | a0015 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.3280G>A | p.Gly1094Arg | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 27/36 | 3350/4610 | 3280/4425 | 1094/1474 | chr12 | 9077417 | |||
| chr12:9079305 | G | A | 1 | a0008 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.3058C>T | p.His1020Tyr | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/36 | 3128/4610 | 3058/4425 | 1020/1474 | chr12 | 9079305 | |||
| chr12:9079672 | T | C | 3 | a0002a0011a0015 | 65 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(62): Show |
missense_variant | MODERATE | c.2998A>G | p.Ile1000Val | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 24/36 | 3068/4610 | 2998/4425 | 1000/1474 | chr12 | 9079672 | |||
| chr12:9080136 | T | C | 1 | a0016 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.2812A>G | p.Asn938Asp | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 23/36 | 2882/4610 | 2812/4425 | 938/1474 | chr12 | 9080136 | |||
| chr12:9090421 | G | A | 1 | a0004 | 4 | HG00735.hp2 HG01515.hp2 HG02602.hp1 others(1): Show |
missense_variant | MODERATE | c.2531C>T | p.Ala844Val | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 20/36 | 2601/4610 | 2531/4425 | 844/1474 | chr12 | 9090421 | |||
| chr12:9095637 | T | C | 15 | a0001a0002a0003others(12): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
missense_variant | MODERATE | c.1915A>G | p.Asn639Asp | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 16/36 | 1985/4610 | 1915/4425 | 639/1474 | chr12 | 9095637 | |||
| chr12:9098701 | C | T | 1 | a0006 | 2 | NA19081.hp1 NA19082.hp2 |
missense_variant | MODERATE | c.1757G>A | p.Arg586Gln | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/36 | 1827/4610 | 1757/4425 | 586/1474 | chr12 | 9098701 | |||
| chr12:9101539 | G | T | 1 | a0013 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.1402C>A | p.Leu468Ile | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1472/4610 | 1402/4425 | 468/1474 | chr12 | 9101539 | |||
| chr12:9101557 | C | T | 1 | a0014 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.1384G>A | p.Glu462Lys | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1454/4610 | 1384/4425 | 462/1474 | chr12 | 9101557 | |||
| chr12:9101602 | T | C | 1 | a0012 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1339A>G | p.Thr447Ala | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1409/4610 | 1339/4425 | 447/1474 | chr12 | 9101602 | |||
| chr12:9106261 | C | T | 1 | a0003 | 8 | HG01106.hp2 HG01109.hp2 HG01257.hp1 others(5): Show |
missense_variant | MODERATE | c.1079G>A | p.Arg360Gln | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/36 | 1149/4610 | 1079/4425 | 360/1474 | chr12 | 9106261 | |||
| chr12:9107621 | G | A | 2 | a0007a0008 | 2 | HG00741.hp2 HG02273.hp1 |
missense_variant | MODERATE | c.782C>T | p.Pro261Leu | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 8/36 | 852/4610 | 782/4425 | 261/1474 | chr12 | 9107621 | |||
| chr12:9112202 | C | T | 1 | a0011 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.440G>A | p.Arg147His | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/36 | 510/4610 | 440/4425 | 147/1474 | chr12 | 9112202 | |||
| chr12:9112203 | G | A | 1 | a0009 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.439C>T | p.Arg147Cys | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/36 | 509/4610 | 439/4425 | 147/1474 | chr12 | 9112203 | |||
| chr12:9113460 | G | A | 1 | a0012 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.170C>T | p.Thr57Ile | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 2/36 | 240/4610 | 170/4425 | 57/1474 | chr12 | 9113460 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9074626 | A | G | 2 | a0001c0011a0012c0027 | 3 | NA18962.hp1 NA18981.hp1 NA19083.hp1 |
synonymous_variant | LOW | c.3690T>C | p.Ser1230Ser | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/36 | 3760/4610 | 3690/4425 | 1230/1474 | chr12 | 9074626 | |||
| chr12:9076832 | A | G | 1 | a0001c0022 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.3456T>C | p.Tyr1152Tyr | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/36 | 3526/4610 | 3456/4425 | 1152/1474 | chr12 | 9076832 | |||
| chr12:9079273 | C | T | 1 | a0001c0021 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.3090G>A | p.Glu1030Glu | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/36 | 3160/4610 | 3090/4425 | 1030/1474 | chr12 | 9079273 | |||
| chr12:9080170 | C | T | 1 | a0001c0018 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2778G>A | p.Glu926Glu | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 23/36 | 2848/4610 | 2778/4425 | 926/1474 | chr12 | 9080170 | |||
| chr12:9089962 | C | T | 1 | a0001c0017 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.2658G>A | p.Glu886Glu | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 21/36 | 2728/4610 | 2658/4425 | 886/1474 | chr12 | 9089962 | |||
| chr12:9090420 | C | T | 3 | a0001c0015a0002c0010a0016c0016 | 4 | HG01169.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
synonymous_variant | LOW | c.2532G>A | p.Ala844Ala | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 20/36 | 2602/4610 | 2532/4425 | 844/1474 | chr12 | 9090420 | |||
| chr12:9098613 | C | T | 1 | a0001c0009 | 2 | HG02145.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.1845G>A | p.Ala615Ala | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/36 | 1915/4610 | 1845/4425 | 615/1474 | chr12 | 9098613 | |||
| chr12:9101630 | C | T | 1 | a0001c0005 | 7 | HG02559.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
synonymous_variant | LOW | c.1311G>A | p.Val437Val | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1381/4610 | 1311/4425 | 437/1474 | chr12 | 9101630 | |||
| chr12:9101645 | G | A | 2 | a0001c0003a0001c0021 | 12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
synonymous_variant | LOW | c.1296C>T | p.Tyr432Tyr | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/36 | 1366/4610 | 1296/4425 | 432/1474 | chr12 | 9101645 | |||
| chr12:9104350 | G | A | 1 | a0001c0022 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1155C>T | p.Phe385Phe | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/36 | 1225/4610 | 1155/4425 | 385/1474 | chr12 | 9104350 | |||
| chr12:9112420 | G | C | 1 | a0001c0026 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.387C>G | p.Val129Val | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 3/36 | 457/4610 | 387/4425 | 129/1474 | chr12 | 9112420 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9115858 | A | T | 1 | a0001c0001t0003 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-9T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/36 | 9 | chr12 | 9115858 | ||||||
| chr12:9115877 | A | C | 16 | a0001c0001t0002a0001c0001t0003a0001c0003t0002others(13): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
5_prime_UTR_variant | MODIFIER | c.-28T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/36 | 28 | chr12 | 9115877 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9067905 | C | G | 2 | a0001c0005t0002g0019a0001c0005t0002g0134 | 3 | HG02559.hp2 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4409-66G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 35/35 | chr12 | 9067905 | |||||||
| chr12:9068133 | G | A | 79 | a0001c0001t0001g0207a0001c0001t0002g0005a0001c0001t0002g0041others(76): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.4408+50C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 35/35 | chr12 | 9068133 | |||||||
| chr12:9068603 | G | A | 121 | a0001c0001t0001g0207a0001c0001t0002g0002a0001c0001t0002g0005others(118): Show | 144 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.4366+137C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 34/35 | chr12 | 9068603 | |||||||
| chr12:9068651 | A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0270a0001c0001t0001g0274 | 5 | HG00544.hp2 HG02015.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.4366+89T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 34/35 | chr12 | 9068651 | |||||||
| chr12:9068874 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4264-32G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9068874 | |||||||
| chr12:9069040 | C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4264-198G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9069040 | |||||||
| chr12:9069111 | T | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4264-269A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9069111 | |||||||
| chr12:9069201 | CA | C | 73 | a0001c0001t0001g0207a0001c0001t0002g0005a0001c0001t0002g0088others(70): Show | 87 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.4264-360delT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9069201 | |||||||
| chr12:9069452 | A | G | 2 | a0001c0005t0002g0019a0001c0005t0002g0134 | 3 | HG02559.hp2 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4263+293T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9069452 | |||||||
| chr12:9069467 | C | A | 3 | a0002c0002t0002g0038a0002c0010t0002g0138a0002c0010t0002g0140 | 3 | HG01169.hp2 HG01993.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4263+278G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9069467 | |||||||
| chr12:9069487 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.4263+258A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9069487 | |||||||
| chr12:9069501 | G | C | 79 | a0001c0001t0001g0207a0001c0001t0002g0005a0001c0001t0002g0041others(76): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.4263+244C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9069501 | |||||||
| chr12:9069507 | T | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(36): Show | 48 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.4263+238A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9069507 | |||||||
| chr12:9069690 | C | T | 46 | a0001c0001t0001g0207a0002c0002t0001g0210a0002c0002t0001g0211others(43): Show | 56 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.4263+55G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 33/35 | chr12 | 9069690 | |||||||
| chr12:9069829 | A | G | 1 | a0016c0016t0002g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4195-16T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 32/35 | chr12 | 9069829 | |||||||
| chr12:9069868 | A | G | 1 | a0002c0002t0002g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4195-55T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 32/35 | chr12 | 9069868 | |||||||
| chr12:9069998 | C | A | 1 | a0001c0005t0002g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4195-185G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 32/35 | chr12 | 9069998 | |||||||
| chr12:9070095 | A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0072 | 2 | NA19001.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.4195-282T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 32/35 | chr12 | 9070095 | |||||||
| chr12:9070190 | A | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0078 | 2 | HG00738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.4194+298T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 32/35 | chr12 | 9070190 | |||||||
| chr12:9070306 | A | G | 70 | a0001c0001t0001g0207a0001c0001t0002g0041a0001c0001t0002g0042others(67): Show | 82 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.4194+182T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 32/35 | chr12 | 9070306 | |||||||
| chr12:9070432 | G | A | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4194+56C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 32/35 | chr12 | 9070432 | |||||||
| chr12:9070646 | A | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(36): Show | 48 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.4104-68T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9070646 | |||||||
| chr12:9070679 | G | A | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4104-101C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9070679 | |||||||
| chr12:9070812 | G | A | 8 | a0001c0001t0002g0141a0001c0005t0002g0019a0001c0005t0002g0134others(5): Show | 10 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.4104-234C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9070812 | |||||||
| chr12:9070825 | A | AT | 80 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0207others(77): Show | 94 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.4104-248dupA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9070825 | |||||||
| chr12:9070851 | A | G | 198 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(195): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.4104-273T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9070851 | |||||||
| chr12:9070933 | G | T | 10 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0051others(7): Show | 13 | HG02056.hp1 NA18953.hp2 NA18970.hp1 others(10): Show |
intron_variant | MODIFIER | c.4104-355C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9070933 | |||||||
| chr12:9070978 | G | T | 48 | a0001c0001t0001g0207a0002c0002t0001g0210a0002c0002t0001g0211others(45): Show | 58 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.4104-400C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9070978 | |||||||
| chr12:9071039 | T | C | 79 | a0001c0001t0001g0207a0001c0001t0002g0005a0001c0001t0002g0041others(76): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.4104-461A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9071039 | |||||||
| chr12:9071100 | G | A | 79 | a0001c0001t0001g0207a0001c0001t0002g0005a0001c0001t0002g0041others(76): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.4104-522C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9071100 | |||||||
| chr12:9071272 | A | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0268 | 2 | NA18963.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.4104-694T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9071272 | |||||||
| chr12:9071357 | C | T | 52 | a0001c0001t0001g0207a0002c0002t0001g0210a0002c0002t0001g0211others(49): Show | 62 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.4104-779G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9071357 | |||||||
| chr12:9071433 | T | A | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(95): Show | 122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.4104-855A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9071433 | |||||||
| chr12:9071435 | T | A | 1 | a0001c0001t0002g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4104-857A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9071435 | |||||||
| chr12:9071555 | A | G | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4103+804T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9071555 | |||||||
| chr12:9071595 | T | C | 3 | a0002c0002t0002g0038a0002c0010t0002g0138a0002c0010t0002g0140 | 3 | HG01169.hp2 HG01993.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4103+764A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9071595 | |||||||
| chr12:9072044 | A | T | 3 | a0002c0002t0002g0038a0002c0010t0002g0138a0002c0010t0002g0140 | 3 | HG01169.hp2 HG01993.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4103+315T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9072044 | |||||||
| chr12:9072290 | A | T | 2 | a0001c0001t0001g0183a0007c0023t0001g0213 | 2 | HG00741.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.4103+69T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9072290 | |||||||
| chr12:9072303 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4103+56G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 31/35 | chr12 | 9072303 | |||||||
| chr12:9072537 | T | C | 1 | a0001c0017t0001g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3976-51A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 30/35 | chr12 | 9072537 | |||||||
| chr12:9073326 | C | CA | 38 | a0001c0001t0001g0207a0002c0002t0001g0210a0002c0002t0001g0211others(35): Show | 48 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.3757-456dupT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9073326 | |||||||
| chr12:9073581 | T | G | 1 | a0001c0001t0001g0254 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3757-710A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9073581 | |||||||
| chr12:9073628 | G | A | 51 | a0001c0001t0001g0207a0002c0002t0001g0210a0002c0002t0001g0211others(48): Show | 61 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.3757-757C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9073628 | |||||||
| chr12:9073654 | G | A | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3757-783C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9073654 | |||||||
| chr12:9073813 | C | T | 1 | a0002c0002t0002g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3756+747G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9073813 | |||||||
| chr12:9074087 | T | TA | 53 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0159others(50): Show | 64 | HG00408.hp1 HG00639.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.3756+472dupT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074087 | |||||||
| chr12:9074087 | TA | T | 11 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(8): Show | 11 | HG00558.hp2 HG01081.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3756+472delT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074087 | |||||||
| chr12:9074087 | TAAAA | T | 77 | a0001c0001t0001g0021a0001c0001t0001g0148a0001c0001t0001g0149others(74): Show | 89 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.3756+469_3756+472d others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074087 | |||||||
| chr12:9074087 | TAAAAA | T | 11 | a0001c0001t0001g0249a0001c0001t0002g0005a0001c0001t0002g0088others(8): Show | 13 | HG02280.hp1 HG02486.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.3756+468_3756+472d others(7): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074087 | |||||||
| chr12:9074116 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3756+444C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074116 | |||||||
| chr12:9074165 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3756+395A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074165 | |||||||
| chr12:9074180 | T | C | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3756+380A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074180 | |||||||
| chr12:9074322 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3756+238A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074322 | |||||||
| chr12:9074365 | G | A | 90 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0030others(87): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.3756+195C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074365 | |||||||
| chr12:9074388 | C | T | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3756+172G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074388 | |||||||
| chr12:9074462 | T | A | 71 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(68): Show | 85 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3756+98A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074462 | |||||||
| chr12:9074492 | T | C | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3756+68A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 29/35 | chr12 | 9074492 | |||||||
| chr12:9075191 | C | G | 122 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.3533-408G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075191 | |||||||
| chr12:9075205 | GA | G | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(4): Show | 7 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3533-423delT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075205 | |||||||
| chr12:9075272 | T | A | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3533-489A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075272 | |||||||
| chr12:9075368 | A | G | 1 | a0001c0005t0002g0137 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3533-585T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075368 | |||||||
| chr12:9075403 | G | T | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3533-620C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075403 | |||||||
| chr12:9075428 | T | G | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3533-645A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075428 | |||||||
| chr12:9075435 | A | G | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3533-652T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075435 | |||||||
| chr12:9075471 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3533-688G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075471 | |||||||
| chr12:9075552 | T | G | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3533-769A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075552 | |||||||
| chr12:9075573 | ATAGTGTT others(5): Show |
A | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3533-802_3533-791d others(14): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075573 | |||||||
| chr12:9075646 | C | T | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3533-863G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075646 | |||||||
| chr12:9075659 | T | C | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3533-876A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075659 | |||||||
| chr12:9075702 | T | C | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3533-919A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075702 | |||||||
| chr12:9075773 | G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.3532+983C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075773 | |||||||
| chr12:9075816 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3532+940G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075816 | |||||||
| chr12:9075838 | T | C | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3532+918A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075838 | |||||||
| chr12:9075873 | G | A | 1 | a0002c0002t0002g0121 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3532+883C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075873 | |||||||
| chr12:9075874 | T | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3532+882A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9075874 | |||||||
| chr12:9076035 | C | T | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3532+721G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076035 | |||||||
| chr12:9076048 | T | C | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3532+708A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076048 | |||||||
| chr12:9076167 | G | A | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3532+589C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076167 | |||||||
| chr12:9076227 | A | G | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3532+529T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076227 | |||||||
| chr12:9076290 | G | A | 3 | a0001c0009t0002g0082a0001c0009t0002g0083a0001c0015t0002g0040 | 3 | HG02145.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3532+466C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076290 | |||||||
| chr12:9076308 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3532+448A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076308 | |||||||
| chr12:9076409 | G | A | 1 | a0001c0026t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3532+347C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076409 | |||||||
| chr12:9076441 | C | T | 7 | a0001c0001t0002g0141a0001c0005t0002g0019a0001c0005t0002g0134others(4): Show | 8 | HG02559.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.3532+315G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076441 | |||||||
| chr12:9076561 | G | A | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3532+195C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076561 | |||||||
| chr12:9076574 | C | T | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3532+182G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076574 | |||||||
| chr12:9076739 | C | T | 2 | a0002c0002t0002g0113a0002c0002t0002g0130 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3532+17G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 28/35 | chr12 | 9076739 | |||||||
| chr12:9077033 | C | T | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3352-97G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 27/35 | chr12 | 9077033 | |||||||
| chr12:9077089 | G | T | 1 | a0001c0022t0002g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3352-153C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 27/35 | chr12 | 9077089 | |||||||
| chr12:9077332 | G | T | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3351+14C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 27/35 | chr12 | 9077332 | |||||||
| chr12:9077442 | C | T | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3277-22G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 26/35 | chr12 | 9077442 | |||||||
| chr12:9077502 | G | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3277-82C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 26/35 | chr12 | 9077502 | |||||||
| chr12:9077535 | G | A | 78 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(75): Show | 92 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3277-115C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 26/35 | chr12 | 9077535 | |||||||
| chr12:9077939 | T | C | 1 | a0002c0002t0002g0086 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3120-82A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9077939 | |||||||
| chr12:9077976 | G | T | 78 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(75): Show | 92 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3120-119C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9077976 | |||||||
| chr12:9078066 | T | A | 78 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(75): Show | 92 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3120-209A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078066 | |||||||
| chr12:9078110 | C | T | 78 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(75): Show | 92 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3120-253G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078110 | |||||||
| chr12:9078136 | G | A | 78 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(75): Show | 92 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3120-279C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078136 | |||||||
| chr12:9078188 | C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3120-331G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078188 | |||||||
| chr12:9078282 | A | AC | 119 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(116): Show | 142 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3120-426_3120-425i others(3): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078282 | |||||||
| chr12:9078330 | G | A | 4 | a0002c0002t0002g0115a0002c0002t0002g0118a0002c0002t0002g0124others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.3120-473C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078330 | |||||||
| chr12:9078489 | C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0252 | 2 | NA18975.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.3120-632G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078489 | |||||||
| chr12:9078492 | G | A | 9 | a0002c0002t0002g0007a0002c0002t0002g0085a0002c0002t0002g0115others(6): Show | 11 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.3120-635C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078492 | |||||||
| chr12:9078630 | T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0150a0001c0001t0001g0151 | 4 | HG00642.hp1 HG01081.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.3119+614A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078630 | |||||||
| chr12:9078694 | G | C | 3 | a0002c0002t0002g0110a0002c0002t0002g0112a0002c0002t0002g0122 | 3 | HG01106.hp1 HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3119+550C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9078694 | |||||||
| chr12:9079042 | T | C | 48 | a0002c0002t0001g0210a0002c0002t0001g0211a0002c0002t0002g0004others(45): Show | 59 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.3119+202A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9079042 | |||||||
| chr12:9079129 | C | T | 2 | a0002c0002t0002g0086a0011c0012t0002g0094 | 2 | HG00738.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3119+115G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 25/35 | chr12 | 9079129 | |||||||
| chr12:9079497 | T | C | 1 | a0002c0002t0002g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3031+142A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 24/35 | chr12 | 9079497 | |||||||
| chr12:9080207 | A | C | 1 | a0001c0001t0001g0270 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2771-30T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9080207 | |||||||
| chr12:9080525 | A | G | 2 | a0002c0002t0001g0210a0002c0002t0002g0125 | 2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2771-348T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9080525 | |||||||
| chr12:9080656 | A | G | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2771-479T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9080656 | |||||||
| chr12:9080710 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2771-533C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9080710 | |||||||
| chr12:9080787 | A | G | 2 | a0002c0002t0002g0087a0002c0002t0002g0133 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2771-610T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9080787 | |||||||
| chr12:9080816 | G | A | 122 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2771-639C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9080816 | |||||||
| chr12:9080951 | T | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.2771-774A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9080951 | |||||||
| chr12:9080956 | C | T | 64 | a0001c0001t0002g0141a0001c0005t0002g0019a0001c0005t0002g0134others(61): Show | 76 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.2771-779G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9080956 | |||||||
| chr12:9080961 | G | A | 7 | a0001c0001t0002g0141a0001c0005t0002g0019a0001c0005t0002g0134others(4): Show | 8 | HG02559.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2771-784C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9080961 | |||||||
| chr12:9081066 | A | G | 2 | a0002c0002t0002g0107a0002c0002t0002g0109 | 2 | HG02293.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2771-889T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9081066 | |||||||
| chr12:9081166 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2771-989C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9081166 | |||||||
| chr12:9081413 | G | T | 120 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(117): Show | 143 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.2771-1236C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9081413 | |||||||
| chr12:9081502 | G | A | 73 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(70): Show | 87 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.2771-1325C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9081502 | |||||||
| chr12:9081660 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2771-1483A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9081660 | |||||||
| chr12:9081946 | T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG02055.hp1 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2771-1769A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9081946 | |||||||
| chr12:9081983 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2771-1806T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9081983 | |||||||
| chr12:9082106 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2771-1929A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9082106 | |||||||
| chr12:9082113 | G | T | 14 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(11): Show | 19 | HG01515.hp1 HG01517.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.2771-1936C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9082113 | |||||||
| chr12:9082382 | A | C | 8 | a0001c0001t0002g0141a0001c0005t0002g0019a0001c0005t0002g0134others(5): Show | 10 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2771-2205T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9082382 | |||||||
| chr12:9082449 | A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(39): Show | 51 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.2771-2272T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9082449 | |||||||
| chr12:9082536 | G | A | 1 | a0016c0016t0002g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2771-2359C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9082536 | |||||||
| chr12:9082621 | T | C | 122 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2771-2444A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9082621 | |||||||
| chr12:9082831 | C | G | 79 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(76): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2771-2654G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9082831 | |||||||
| chr12:9082864 | G | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2771-2687C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9082864 | |||||||
| chr12:9082893 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2771-2716A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9082893 | |||||||
| chr12:9083122 | C | A | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2771-2945G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083122 | |||||||
| chr12:9083143 | G | A | 79 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(76): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2771-2966C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083143 | |||||||
| chr12:9083229 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2771-3052C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083229 | |||||||
| chr12:9083295 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2771-3118G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083295 | |||||||
| chr12:9083296 | G | A | 7 | a0001c0001t0002g0141a0001c0005t0002g0019a0001c0005t0002g0134others(4): Show | 8 | HG02559.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2771-3119C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083296 | |||||||
| chr12:9083309 | C | T | 4 | a0002c0002t0002g0115a0002c0002t0002g0118a0002c0002t0002g0124others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2771-3132G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083309 | |||||||
| chr12:9083386 | T | TAA | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2771-3211_2771-321 others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083386 | |||||||
| chr12:9083528 | G | C | 2 | a0002c0002t0002g0086a0011c0012t0002g0094 | 2 | HG00738.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2771-3351C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083528 | |||||||
| chr12:9083651 | T | A | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2771-3474A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083651 | |||||||
| chr12:9083754 | GA | G | 72 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(69): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.2771-3578delT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083754 | |||||||
| chr12:9083994 | T | G | 120 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(117): Show | 143 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.2771-3817A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9083994 | |||||||
| chr12:9084235 | A | G | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2771-4058T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9084235 | |||||||
| chr12:9084312 | G | T | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2771-4135C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9084312 | |||||||
| chr12:9084316 | T | G | 1 | a0012c0027t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2771-4139A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9084316 | |||||||
| chr12:9084506 | C | T | 122 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2771-4329G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9084506 | |||||||
| chr12:9084561 | A | AAG | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2771-4386_2771-438 others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9084561 | |||||||
| chr12:9084646 | A | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.2771-4469T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9084646 | |||||||
| chr12:9084655 | G | A | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2771-4478C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9084655 | |||||||
| chr12:9084697 | A | G | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2770+4503T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9084697 | |||||||
| chr12:9084765 | CAT | C | 3 | a0001c0011t0001g0264a0001c0011t0001g0266a0012c0027t0001g0277 | 3 | NA18962.hp1 NA18981.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2770+4433_2770+443 others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9084765 | |||||||
| chr12:9085140 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2770+4060T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085140 | |||||||
| chr12:9085237 | T | C | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2770+3963A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085237 | |||||||
| chr12:9085293 | G | A | 9 | a0002c0002t0002g0017a0002c0002t0002g0110a0002c0002t0002g0112others(6): Show | 10 | HG01106.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.2770+3907C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085293 | |||||||
| chr12:9085422 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2770+3778T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085422 | |||||||
| chr12:9085616 | G | C | 79 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(76): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2770+3584C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085616 | |||||||
| chr12:9085660 | A | G | 1 | a0016c0016t0002g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2770+3540T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085660 | |||||||
| chr12:9085686 | G | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0208others(1): Show | 4 | HG02683.hp1 HG02735.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2770+3514C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085686 | |||||||
| chr12:9085696 | A | G | 1 | a0001c0003t0002g0014 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2770+3504T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085696 | |||||||
| chr12:9085714 | T | C | 114 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(111): Show | 137 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.2770+3486A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085714 | |||||||
| chr12:9085715 | G | A | 73 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(70): Show | 87 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.2770+3485C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085715 | |||||||
| chr12:9085744 | A | G | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2770+3456T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085744 | |||||||
| chr12:9085900 | A | G | 2 | a0002c0002t0002g0086a0011c0012t0002g0094 | 2 | HG00738.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2770+3300T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085900 | |||||||
| chr12:9085983 | A | G | 114 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(111): Show | 137 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.2770+3217T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085983 | |||||||
| chr12:9085994 | C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0152 | 3 | HG01175.hp2 HG01192.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2770+3206G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9085994 | |||||||
| chr12:9086027 | T | C | 2 | a0001c0003t0002g0077a0001c0021t0002g0076 | 2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2770+3173A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9086027 | |||||||
| chr12:9086188 | CA | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2770+3011delT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9086188 | |||||||
| chr12:9086306 | T | C | 114 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(111): Show | 137 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.2770+2894A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9086306 | |||||||
| chr12:9086426 | G | T | 114 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(111): Show | 137 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.2770+2774C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9086426 | |||||||
| chr12:9086638 | C | T | 114 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(111): Show | 137 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.2770+2562G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9086638 | |||||||
| chr12:9086712 | C | T | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2770+2488G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9086712 | |||||||
| chr12:9086921 | T | C | 1 | a0002c0002t0002g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2770+2279A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9086921 | |||||||
| chr12:9087098 | A | G | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2770+2102T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087098 | |||||||
| chr12:9087138 | GA | G | 114 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(111): Show | 137 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.2770+2061delT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087138 | |||||||
| chr12:9087242 | A | ATGTC | 114 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(111): Show | 137 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.2770+1954_2770+195 others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087242 | |||||||
| chr12:9087301 | A | G | 2 | a0001c0001t0002g0092a0015c0020t0002g0080 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2770+1899T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087301 | |||||||
| chr12:9087319 | A | G | 7 | a0001c0001t0002g0141a0001c0005t0002g0019a0001c0005t0002g0134others(4): Show | 8 | HG02559.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2770+1881T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087319 | |||||||
| chr12:9087639 | C | G | 81 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(78): Show | 103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2770+1561G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087639 | |||||||
| chr12:9087740 | A | C | 6 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0098others(3): Show | 8 | HG00735.hp1 HG01175.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.2770+1460T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087740 | |||||||
| chr12:9087750 | T | G | 1 | a0016c0016t0002g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2770+1450A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087750 | |||||||
| chr12:9087927 | C | A | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2770+1273G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087927 | |||||||
| chr12:9087967 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2770+1233A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087967 | |||||||
| chr12:9087988 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2770+1212G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9087988 | |||||||
| chr12:9088069 | C | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0106 | 2 | NA18944.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.2770+1131G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088069 | |||||||
| chr12:9088151 | T | A | 20 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(17): Show | 23 | HG01993.hp2 HG02258.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.2770+1049A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088151 | |||||||
| chr12:9088255 | G | GT | 51 | a0001c0001t0002g0104a0001c0001t0002g0106a0002c0002t0002g0004others(48): Show | 62 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2770+944dupA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088255 | |||||||
| chr12:9088255 | GT | G | 21 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(18): Show | 24 | HG01993.hp2 HG02258.hp1 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.2770+944delA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088255 | |||||||
| chr12:9088267 | A | G | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2770+933T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088267 | |||||||
| chr12:9088428 | A | G | 20 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(17): Show | 23 | HG01993.hp2 HG02258.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.2770+772T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088428 | |||||||
| chr12:9088532 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2770+668A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088532 | |||||||
| chr12:9088547 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2770+653C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088547 | |||||||
| chr12:9088558 | T | G | 3 | a0002c0002t0002g0017a0002c0002t0002g0117a0002c0002t0002g0131 | 4 | HG01261.hp1 HG02486.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2770+642A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088558 | |||||||
| chr12:9088638 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2770+562C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088638 | |||||||
| chr12:9088688 | T | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0072 | 2 | NA19001.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2770+512A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088688 | |||||||
| chr12:9088721 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2770+479G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088721 | |||||||
| chr12:9088955 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2770+245G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9088955 | |||||||
| chr12:9089023 | G | A | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2770+177C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9089023 | |||||||
| chr12:9089171 | T | G | 2 | a0001c0001t0002g0143a0001c0001t0002g0144 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2770+29A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 22/35 | chr12 | 9089171 | |||||||
| chr12:9089557 | G | A | 3 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062 | 3 | HG02886.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2719-306C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 21/35 | chr12 | 9089557 | |||||||
| chr12:9090027 | A | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
splice_region_variant&intron_variant | LOW | c.2597-4T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 20/35 | chr12 | 9090027 | |||||||
| chr12:9090104 | T | C | 1 | a0002c0002t0002g0131 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2597-81A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 20/35 | chr12 | 9090104 | |||||||
| chr12:9090117 | T | C | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2597-94A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 20/35 | chr12 | 9090117 | |||||||
| chr12:9090167 | T | A | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2597-144A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 20/35 | chr12 | 9090167 | |||||||
| chr12:9090289 | A | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2596+67T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 20/35 | chr12 | 9090289 | |||||||
| chr12:9090328 | G | C | 54 | a0001c0001t0001g0215a0001c0001t0002g0104a0001c0001t0002g0106others(51): Show | 65 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.2596+28C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 20/35 | chr12 | 9090328 | |||||||
| chr12:9090346 | T | G | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2596+10A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 20/35 | chr12 | 9090346 | |||||||
| chr12:9090525 | C | G | 20 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(17): Show | 23 | HG01993.hp2 HG02258.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.2470-43G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 19/35 | chr12 | 9090525 | |||||||
| chr12:9090714 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2470-232T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 19/35 | chr12 | 9090714 | |||||||
| chr12:9090781 | C | T | 1 | a0002c0002t0002g0098 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2470-299G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 19/35 | chr12 | 9090781 | |||||||
| chr12:9090911 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2469+290G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 19/35 | chr12 | 9090911 | |||||||
| chr12:9091018 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2469+183T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 19/35 | chr12 | 9091018 | |||||||
| chr12:9091065 | C | CA | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2469+135dupT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 19/35 | chr12 | 9091065 | |||||||
| chr12:9091457 | A | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2241-28T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9091457 | |||||||
| chr12:9091506 | G | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2241-77C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9091506 | |||||||
| chr12:9091666 | T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0212 | 3 | HG02155.hp2 NA18953.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.2241-237A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9091666 | |||||||
| chr12:9091671 | C | T | 123 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(120): Show | 146 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.2241-242G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9091671 | |||||||
| chr12:9091771 | C | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0189a0001c0001t0001g0193 | 3 | HG00099.hp2 HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2241-342G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9091771 | |||||||
| chr12:9091792 | C | T | 1 | a0001c0003t0002g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2241-363G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9091792 | |||||||
| chr12:9091905 | T | A | 1 | a0001c0001t0001g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2241-476A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9091905 | |||||||
| chr12:9091986 | G | A | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2241-557C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9091986 | |||||||
| chr12:9092047 | G | C | 9 | a0001c0001t0002g0141a0001c0005t0002g0019a0001c0005t0002g0134others(6): Show | 10 | HG02559.hp2 HG02622.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2241-618C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092047 | |||||||
| chr12:9092133 | C | T | 1 | a0002c0002t0002g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2241-704G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092133 | |||||||
| chr12:9092409 | C | T | 19 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(16): Show | 22 | HG01993.hp2 HG02258.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.2241-980G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092409 | |||||||
| chr12:9092471 | C | T | 1 | a0001c0022t0002g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2240+994G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092471 | |||||||
| chr12:9092535 | C | T | 3 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062 | 3 | HG02886.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2240+930G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092535 | |||||||
| chr12:9092605 | C | G | 123 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(120): Show | 146 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.2240+860G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092605 | |||||||
| chr12:9092605 | C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0235 | 3 | NA18971.hp1 NA18973.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2240+860G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092605 | |||||||
| chr12:9092856 | A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0212others(2): Show | 7 | HG02040.hp1 HG02132.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.2240+609T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092856 | |||||||
| chr12:9092873 | G | A | 3 | a0001c0001t0002g0050a0001c0001t0002g0053a0001c0001t0002g0056 | 3 | HG01109.hp1 HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2240+592C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092873 | |||||||
| chr12:9092875 | G | A | 2 | a0002c0010t0002g0138a0002c0010t0002g0140 | 2 | HG01169.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2240+590C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092875 | |||||||
| chr12:9092946 | C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2240+519G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092946 | |||||||
| chr12:9092947 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2240+518A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9092947 | |||||||
| chr12:9093183 | C | T | 69 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(66): Show | 81 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.2240+282G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9093183 | |||||||
| chr12:9093441 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2240+24A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 18/35 | chr12 | 9093441 | |||||||
| chr12:9093580 | CTATGG | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.2126-6_2126-2delCC others(3): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093580 | |||||||
| chr12:9093654 | C | CA | 16 | a0001c0001t0001g0198a0001c0001t0001g0226a0001c0001t0001g0233others(13): Show | 16 | HG01884.hp2 HG02630.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.2126-76dupT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093654 | |||||||
| chr12:9093680 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2126-101C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093680 | |||||||
| chr12:9093712 | C | T | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2126-133G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093712 | |||||||
| chr12:9093758 | T | A | 69 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(66): Show | 81 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.2126-179A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093758 | |||||||
| chr12:9093787 | G | A | 1 | a0002c0002t0002g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2126-208C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093787 | |||||||
| chr12:9093819 | G | C | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2126-240C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093819 | |||||||
| chr12:9093829 | G | GGCGGGTG others(171): Show |
8 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2126-251_2126-250i others(180): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093829 | |||||||
| chr12:9093891 | T | TCAAA | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2126-316_2126-313d others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093891 | |||||||
| chr12:9093891 | TCAAA | T | 42 | a0001c0001t0001g0154a0001c0001t0002g0002a0001c0001t0002g0012others(39): Show | 51 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.2126-316_2126-313d others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093891 | |||||||
| chr12:9093891 | TCAAACAA others(5): Show |
T | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2126-324_2126-313d others(14): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093891 | |||||||
| chr12:9093897 | A | G | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2126-318T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093897 | |||||||
| chr12:9093908 | C | G | 1 | a0001c0018t0001g0258 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2126-329G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093908 | |||||||
| chr12:9093920 | A | G | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2126-341T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9093920 | |||||||
| chr12:9094110 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2126-531G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094110 | |||||||
| chr12:9094124 | T | C | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2126-545A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094124 | |||||||
| chr12:9094340 | C | CAT | 99 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(96): Show | 126 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.2125+631_2125+632d others(4): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094340 | C | CATAT | 28 | a0001c0001t0001g0026a0001c0001t0001g0150a0001c0001t0001g0154others(25): Show | 29 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2125+629_2125+632d others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094340 | C | CATATAT | 14 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0175others(11): Show | 17 | HG00099.hp2 HG00733.hp2 HG02922.hp2 others(14): Show |
intron_variant | MODIFIER | c.2125+627_2125+632d others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094340 | C | CATATATA others(1): Show |
3 | a0001c0001t0001g0179a0001c0001t0001g0195a0001c0001t0001g0261 | 3 | HG02735.hp1 NA18963.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2125+625_2125+632d others(10): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094340 | C | CATATATA others(3): Show |
2 | a0001c0001t0001g0174a0001c0001t0001g0194 | 2 | HG02300.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2125+623_2125+632d others(12): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094340 | CAT | C | 34 | a0001c0001t0001g0146a0001c0001t0001g0183a0001c0001t0001g0192others(31): Show | 37 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.2125+631_2125+632d others(4): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094340 | CATAT | C | 17 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0145others(14): Show | 19 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2125+629_2125+632d others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094340 | CATATAT | C | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0220others(4): Show | 7 | HG00738.hp1 HG02129.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125+627_2125+632d others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094340 | CATATATA others(11): Show |
C | 1 | a0001c0001t0001g0193 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2125+615_2125+632d others(20): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094340 | CATATATA others(13): Show |
C | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2125+613_2125+632d others(22): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094340 | |||||||
| chr12:9094475 | A | T | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2125+498T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094475 | |||||||
| chr12:9094478 | G | A | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2125+495C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094478 | |||||||
| chr12:9094479 | AGCCAACT others(4): Show |
A | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2125+483_2125+493d others(13): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094479 | |||||||
| chr12:9094491 | C | T | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2125+482G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094491 | |||||||
| chr12:9094958 | T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0178 | 3 | NA18957.hp2 NA18967.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2125+15A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 17/35 | chr12 | 9094958 | |||||||
| chr12:9095371 | A | C | 1 | a0002c0002t0002g0126 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2013+168T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 16/35 | chr12 | 9095371 | |||||||
| chr12:9095387 | G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0178 | 3 | NA18957.hp2 NA18967.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2013+152C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 16/35 | chr12 | 9095387 | |||||||
| chr12:9095736 | T | C | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(59): Show | 80 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1852-36A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095736 | |||||||
| chr12:9095737 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1852-37A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095737 | |||||||
| chr12:9095742 | C | CT | 66 | a0001c0001t0001g0024a0001c0001t0001g0146a0001c0001t0001g0147others(63): Show | 79 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1852-43dupA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095742 | |||||||
| chr12:9095742 | C | CTT | 33 | a0001c0001t0001g0145a0001c0001t0001g0215a0001c0001t0002g0012others(30): Show | 42 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.1852-44_1852-43dup others(2): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095742 | |||||||
| chr12:9095742 | C | CTTT | 9 | a0001c0001t0002g0050a0001c0001t0002g0053a0001c0001t0002g0054others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1852-45_1852-43dup others(3): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095742 | |||||||
| chr12:9095742 | CT | C | 122 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1852-43delA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095742 | |||||||
| chr12:9095742 | CTT | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0165others(4): Show | 8 | HG00609.hp1 HG02056.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1852-44_1852-43del others(2): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095742 | |||||||
| chr12:9095752 | T | G | 1 | a0001c0001t0001g0020 | 2 | HG02683.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1852-52A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095752 | |||||||
| chr12:9095800 | C | T | 7 | a0001c0001t0002g0141a0001c0005t0002g0019a0001c0005t0002g0134others(4): Show | 8 | HG02559.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1852-100G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095800 | |||||||
| chr12:9095805 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1852-105G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095805 | |||||||
| chr12:9095867 | C | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1852-167G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095867 | |||||||
| chr12:9095916 | C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG02886.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-216G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095916 | |||||||
| chr12:9095917 | G | A | 2 | a0001c0001t0002g0070a0001c0001t0002g0071 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1852-217C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095917 | |||||||
| chr12:9095977 | T | C | 32 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(29): Show | 41 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1852-277A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9095977 | |||||||
| chr12:9096007 | C | T | 1 | a0002c0002t0002g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1852-307G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096007 | |||||||
| chr12:9096051 | G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1852-351C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096051 | |||||||
| chr12:9096113 | C | A | 2 | a0001c0001t0002g0070a0001c0001t0002g0071 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1852-413G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096113 | |||||||
| chr12:9096124 | C | T | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1852-424G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096124 | |||||||
| chr12:9096302 | A | G | 2 | a0001c0015t0002g0040a0001c0022t0002g0039 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1852-602T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096302 | |||||||
| chr12:9096358 | C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-658G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096358 | |||||||
| chr12:9096432 | A | G | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1852-732T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096432 | |||||||
| chr12:9096434 | C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0178 | 3 | NA18957.hp2 NA18967.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1852-734G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096434 | |||||||
| chr12:9096664 | G | A | 1 | a0001c0022t0002g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1852-964C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096664 | |||||||
| chr12:9096689 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1852-989C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096689 | |||||||
| chr12:9096964 | G | T | 3 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0003g0037 | 3 | HG02647.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1852-1264C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9096964 | |||||||
| chr12:9097157 | T | C | 122 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1851+1450A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097157 | |||||||
| chr12:9097218 | C | T | 5 | a0001c0001t0001g0157a0001c0001t0001g0174a0001c0001t0001g0175others(2): Show | 5 | HG00544.hp1 HG00558.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1851+1389G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097218 | |||||||
| chr12:9097266 | A | G | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1851+1341T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097266 | |||||||
| chr12:9097278 | AC | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1851+1328delG | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097278 | |||||||
| chr12:9097279 | C | T | 82 | a0001c0001t0001g0215a0001c0001t0002g0005a0001c0001t0002g0041others(79): Show | 96 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1851+1328G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097279 | |||||||
| chr12:9097280 | A | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1851+1327T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097280 | |||||||
| chr12:9097327 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1851+1280G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097327 | |||||||
| chr12:9097367 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1851+1240C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097367 | |||||||
| chr12:9097632 | C | CT | 7 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0002g0088others(4): Show | 7 | HG00733.hp2 HG01993.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1851+974dupA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097632 | |||||||
| chr12:9097632 | C | CTTTTTT | 38 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(35): Show | 47 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.1851+969_1851+974d others(8): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097632 | |||||||
| chr12:9097632 | CT | C | 86 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(83): Show | 108 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1851+974delA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097632 | |||||||
| chr12:9097696 | C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18960.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1851+911G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097696 | |||||||
| chr12:9097753 | C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1851+854G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097753 | |||||||
| chr12:9097778 | G | A | 1 | a0001c0026t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1851+829C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097778 | |||||||
| chr12:9097822 | G | A | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1851+785C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097822 | |||||||
| chr12:9097863 | T | C | 123 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(120): Show | 146 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1851+744A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097863 | |||||||
| chr12:9097871 | T | G | 123 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(120): Show | 146 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1851+736A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097871 | |||||||
| chr12:9097982 | C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1851+625G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9097982 | |||||||
| chr12:9098005 | T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1851+602A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098005 | |||||||
| chr12:9098132 | C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1851+475G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098132 | |||||||
| chr12:9098287 | T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1851+320A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098287 | |||||||
| chr12:9098306 | C | T | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1851+301G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098306 | |||||||
| chr12:9098332 | G | C | 2 | a0001c0001t0002g0143a0001c0001t0002g0144 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1851+275C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098332 | |||||||
| chr12:9098359 | C | T | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1851+248G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098359 | |||||||
| chr12:9098430 | T | TTA | 8 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0270others(5): Show | 10 | HG00544.hp2 HG01081.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.1851+175_1851+176d others(4): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098430 | |||||||
| chr12:9098430 | TTA | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(40): Show | 52 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.1851+175_1851+176d others(4): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098430 | |||||||
| chr12:9098449 | T | A | 197 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1851+158A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098449 | |||||||
| chr12:9098449 | T | TATAA | 7 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 9 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1851+157_1851+158i others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098449 | |||||||
| chr12:9098456 | T | G | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1851+151A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098456 | |||||||
| chr12:9098597 | A | G | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1851+10T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 15/35 | chr12 | 9098597 | |||||||
| chr12:9098811 | T | C | 1 | a0002c0002t0002g0126 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1702-55A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 14/35 | chr12 | 9098811 | |||||||
| chr12:9099017 | G | A | 1 | a0002c0002t0002g0126 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1702-261C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 14/35 | chr12 | 9099017 | |||||||
| chr12:9099028 | C | T | 44 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(41): Show | 53 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.1702-272G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 14/35 | chr12 | 9099028 | |||||||
| chr12:9099148 | A | C | 1 | a0002c0002t0002g0110 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1701+233T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 14/35 | chr12 | 9099148 | |||||||
| chr12:9099228 | GCTT | G | 60 | a0001c0001t0002g0104a0001c0001t0002g0106a0001c0001t0002g0141others(57): Show | 72 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1701+150_1701+152d others(5): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 14/35 | chr12 | 9099228 | |||||||
| chr12:9099527 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.1559-4C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9099527 | |||||||
| chr12:9099718 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1559-195A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9099718 | |||||||
| chr12:9100151 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1559-628C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100151 | |||||||
| chr12:9100160 | G | A | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1559-637C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100160 | |||||||
| chr12:9100182 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1559-659G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100182 | |||||||
| chr12:9100197 | C | A | 1 | a0002c0002t0002g0095 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1559-674G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100197 | |||||||
| chr12:9100212 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1559-689T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100212 | |||||||
| chr12:9100213 | A | C | 1 | a0002c0002t0002g0095 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1559-690T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100213 | |||||||
| chr12:9100427 | C | CTTAT | 3 | a0001c0001t0001g0169a0001c0001t0002g0051a0002c0002t0002g0127 | 3 | HG01169.hp1 HG01361.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.1558+713_1558+716d others(6): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100427 | |||||||
| chr12:9100427 | CTTATTTA others(1): Show |
C | 2 | a0001c0001t0001g0032a0001c0001t0001g0212 | 3 | HG02155.hp2 NA18953.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1558+709_1558+716d others(10): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100427 | |||||||
| chr12:9100511 | T | C | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1558+633A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100511 | |||||||
| chr12:9100530 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1558+614G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100530 | |||||||
| chr12:9100659 | C | A | 1 | a0002c0002t0002g0127 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1558+485G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100659 | |||||||
| chr12:9100720 | G | A | 274 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(271): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1558+424C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100720 | |||||||
| chr12:9100905 | G | A | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1558+239C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100905 | |||||||
| chr12:9100964 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1558+180A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9100964 | |||||||
| chr12:9101116 | G | A | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1558+28C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9101116 | |||||||
| chr12:9101124 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1558+20C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 13/35 | chr12 | 9101124 | |||||||
| chr12:9101298 | C | T | 250 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(247): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1495-91G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/35 | chr12 | 9101298 | |||||||
| chr12:9101423 | C | T | 7 | a0001c0001t0002g0104a0001c0001t0002g0106a0002c0002t0002g0103others(4): Show | 7 | HG01069.hp2 HG02273.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1494+24G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 12/35 | chr12 | 9101423 | |||||||
| chr12:9101789 | T | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(39): Show | 51 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.1267-115A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9101789 | |||||||
| chr12:9101826 | G | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(39): Show | 51 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.1267-152C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9101826 | |||||||
| chr12:9102187 | C | G | 60 | a0001c0001t0001g0215a0001c0001t0002g0104a0001c0001t0002g0106others(57): Show | 72 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1267-513G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102187 | |||||||
| chr12:9102235 | A | T | 1 | a0002c0002t0002g0098 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1267-561T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102235 | |||||||
| chr12:9102254 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1267-580G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102254 | |||||||
| chr12:9102287 | C | A | 1 | a0002c0002t0002g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1267-613G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102287 | |||||||
| chr12:9102417 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1267-743G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102417 | |||||||
| chr12:9102418 | G | A | 1 | a0002c0002t0002g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267-744C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102418 | |||||||
| chr12:9102438 | T | A | 123 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(120): Show | 146 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1267-764A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102438 | |||||||
| chr12:9102451 | C | T | 1 | a0001c0022t0002g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1267-777G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102451 | |||||||
| chr12:9102560 | C | T | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1267-886G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102560 | |||||||
| chr12:9102606 | G | A | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1267-932C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102606 | |||||||
| chr12:9102643 | T | G | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1267-969A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102643 | |||||||
| chr12:9102726 | C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1267-1052G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102726 | |||||||
| chr12:9102864 | T | C | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1267-1190A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102864 | |||||||
| chr12:9102985 | G | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0165a0001c0001t0001g0166 | 4 | HG00609.hp1 NA18998.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+1254C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102985 | |||||||
| chr12:9102997 | A | G | 1 | a0002c0002t0002g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1266+1242T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9102997 | |||||||
| chr12:9103235 | G | T | 80 | a0001c0001t0001g0215a0001c0001t0002g0005a0001c0001t0002g0041others(77): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1266+1004C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9103235 | |||||||
| chr12:9103486 | A | G | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1266+753T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9103486 | |||||||
| chr12:9103623 | T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(39): Show | 51 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.1266+616A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9103623 | |||||||
| chr12:9103659 | C | T | 123 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(120): Show | 146 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1266+580G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9103659 | |||||||
| chr12:9103758 | G | A | 121 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(118): Show | 144 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1266+481C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9103758 | |||||||
| chr12:9103820 | A | C | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+419T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9103820 | |||||||
| chr12:9104112 | C | T | 122 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1266+127G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 11/35 | chr12 | 9104112 | |||||||
| chr12:9104492 | T | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1105-92A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9104492 | |||||||
| chr12:9104529 | G | GA | 121 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(118): Show | 144 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1105-130dupT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9104529 | |||||||
| chr12:9104539 | G | A | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1105-139C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9104539 | |||||||
| chr12:9104552 | T | A | 9 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(6): Show | 11 | HG02258.hp1 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1105-152A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9104552 | |||||||
| chr12:9104607 | C | T | 2 | a0001c0001t0002g0143a0001c0001t0002g0144 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1105-207G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9104607 | |||||||
| chr12:9104674 | A | C | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1105-274T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9104674 | |||||||
| chr12:9104952 | A | T | 1 | a0001c0022t0002g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1105-552T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9104952 | |||||||
| chr12:9105118 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1105-718T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9105118 | |||||||
| chr12:9105516 | A | T | 1 | a0001c0003t0002g0048 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1104+720T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9105516 | |||||||
| chr12:9106156 | T | A | 1 | a0001c0001t0002g0078 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1104+80A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9106156 | |||||||
| chr12:9106225 | A | G | 83 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1104+11T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 10/35 | chr12 | 9106225 | |||||||
| chr12:9106480 | A | T | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.994+11T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 9/35 | chr12 | 9106480 | |||||||
| chr12:9106724 | C | T | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.880-119G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 8/35 | chr12 | 9106724 | |||||||
| chr12:9106725 | G | A | 1 | a0002c0002t0002g0130 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.880-120C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 8/35 | chr12 | 9106725 | |||||||
| chr12:9106735 | T | TA | 122 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.880-131dupT | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 8/35 | chr12 | 9106735 | |||||||
| chr12:9106957 | C | T | 83 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.880-352G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 8/35 | chr12 | 9106957 | |||||||
| chr12:9107311 | T | C | 122 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.879+213A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 8/35 | chr12 | 9107311 | |||||||
| chr12:9107316 | A | G | 1 | a0001c0022t0002g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.879+208T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 8/35 | chr12 | 9107316 | |||||||
| chr12:9107332 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.879+192G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 8/35 | chr12 | 9107332 | |||||||
| chr12:9107684 | T | C | 122 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0005others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.759-40A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9107684 | |||||||
| chr12:9107714 | CT | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-71delA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9107714 | |||||||
| chr12:9107718 | C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-74G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9107718 | |||||||
| chr12:9107843 | A | G | 1 | a0002c0002t0002g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.759-199T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9107843 | |||||||
| chr12:9107865 | T | C | 1 | a0002c0002t0002g0131 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.759-221A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9107865 | |||||||
| chr12:9107925 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.759-281G>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9107925 | |||||||
| chr12:9107968 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.759-324T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9107968 | |||||||
| chr12:9108099 | G | GTTTAT | 21 | a0001c0001t0001g0033a0001c0001t0001g0157a0001c0001t0001g0158others(18): Show | 22 | HG00544.hp1 HG00621.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.759-460_759-456dup others(5): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108099 | |||||||
| chr12:9108099 | G | GTTTATTT others(3): Show |
5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.759-465_759-456dup others(10): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108099 | |||||||
| chr12:9108099 | GTTTAT | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0035others(18): Show | 26 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.759-460_759-456del others(5): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108099 | |||||||
| chr12:9108099 | GTTTATTT others(3): Show |
G | 11 | a0001c0001t0001g0226a0002c0002t0002g0015a0002c0002t0002g0016others(8): Show | 13 | HG00733.hp2 HG00735.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.759-465_759-456del others(10): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108099 | |||||||
| chr12:9108099 | GTTTATTT others(8): Show |
G | 112 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(109): Show | 133 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.759-470_759-456del others(15): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108099 | |||||||
| chr12:9108342 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.759-698C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108342 | |||||||
| chr12:9108457 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.759-813G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108457 | |||||||
| chr12:9108473 | A | G | 2 | a0002c0002t0002g0096a0002c0002t0002g0097 | 2 | HG00733.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.759-829T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108473 | |||||||
| chr12:9108537 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.758+784T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108537 | |||||||
| chr12:9108600 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.758+721C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108600 | |||||||
| chr12:9108649 | A | G | 121 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(118): Show | 144 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.758+672T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108649 | |||||||
| chr12:9108775 | C | CA | 122 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.758+545_758+546ins others(1): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108775 | |||||||
| chr12:9108928 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.758+393A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9108928 | |||||||
| chr12:9109034 | T | TTG | 119 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(116): Show | 142 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.758+285_758+286dup others(2): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9109034 | |||||||
| chr12:9109142 | G | T | 1 | a0015c0020t0002g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.758+179C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9109142 | |||||||
| chr12:9109264 | A | T | 8 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.758+57T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 7/35 | chr12 | 9109264 | |||||||
| chr12:9109682 | C | T | 2 | a0001c0022t0002g0039a0015c0020t0002g0080 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.673+185G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 6/35 | chr12 | 9109682 | |||||||
| chr12:9109693 | G | T | 45 | a0001c0001t0002g0104a0001c0001t0002g0106a0002c0002t0002g0004others(42): Show | 56 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.673+174C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 6/35 | chr12 | 9109693 | |||||||
| chr12:9110131 | T | G | 121 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(118): Show | 144 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.505-96A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 5/35 | chr12 | 9110131 | |||||||
| chr12:9110203 | G | C | 2 | a0001c0009t0002g0082a0001c0009t0002g0083 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.504+111C>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 5/35 | chr12 | 9110203 | |||||||
| chr12:9110378 | A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18960.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.484-44T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9110378 | |||||||
| chr12:9110552 | CATGCAAT others(17): Show |
C | 1 | a0001c0001t0001g0275 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.484-242_484-219del others(24): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9110552 | |||||||
| chr12:9110594 | G | T | 3 | a0001c0001t0002g0143a0001c0001t0002g0144a0002c0002t0002g0038 | 3 | HG01993.hp2 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.484-260C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9110594 | |||||||
| chr12:9110635 | A | G | 207 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(204): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.484-301T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9110635 | |||||||
| chr12:9110946 | A | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 50 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.484-612T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9110946 | |||||||
| chr12:9111051 | C | T | 59 | a0001c0001t0002g0104a0001c0001t0002g0106a0001c0001t0002g0141others(56): Show | 71 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.484-717G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9111051 | |||||||
| chr12:9111075 | T | C | 1 | a0013c0014t0002g0079 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.484-741A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9111075 | |||||||
| chr12:9111136 | T | C | 1 | a0001c0015t0002g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.484-802A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9111136 | |||||||
| chr12:9111185 | A | G | 1 | a0002c0002t0002g0095 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.484-851T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9111185 | |||||||
| chr12:9111262 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.483+897C>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9111262 | |||||||
| chr12:9111648 | A | C | 1 | a0001c0001t0001g0153 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.483+511T>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9111648 | |||||||
| chr12:9111812 | A | G | 21 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(18): Show | 23 | HG01993.hp2 HG02145.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.483+347T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 4/35 | chr12 | 9111812 | |||||||
| chr12:9112350 | T | G | 59 | a0001c0001t0002g0104a0001c0001t0002g0106a0001c0001t0002g0141others(56): Show | 71 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.430+27A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 3/35 | chr12 | 9112350 | |||||||
| chr12:9112723 | G | T | 60 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(57): Show | 71 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.271-187C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 2/35 | chr12 | 9112723 | |||||||
| chr12:9112889 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.271-353G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 2/35 | chr12 | 9112889 | |||||||
| chr12:9113105 | C | CT | 83 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.270+254dupA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 2/35 | chr12 | 9113105 | |||||||
| chr12:9113105 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.270+255G>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 2/35 | chr12 | 9113105 | |||||||
| chr12:9113105 | CT | C | 121 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(118): Show | 144 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.270+254delA | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 2/35 | chr12 | 9113105 | |||||||
| chr12:9113200 | G | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0150a0001c0001t0001g0151 | 4 | HG00642.hp1 HG01081.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+160C>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 2/35 | chr12 | 9113200 | |||||||
| chr12:9113658 | T | C | 1 | a0001c0001t0002g0081 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.87-115A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9113658 | |||||||
| chr12:9113681 | C | T | 120 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(117): Show | 143 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.87-138G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9113681 | |||||||
| chr12:9114004 | A | T | 1 | a0002c0002t0002g0086 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.87-461T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114004 | |||||||
| chr12:9114015 | A | G | 3 | a0001c0015t0002g0040a0001c0022t0002g0039a0002c0002t0002g0038 | 3 | HG01993.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.87-472T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114015 | |||||||
| chr12:9114074 | C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG00558.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.87-531G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114074 | |||||||
| chr12:9114429 | T | C | 1 | a0001c0005t0002g0142 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.87-886A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114429 | |||||||
| chr12:9114734 | AATAC | A | 122 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.86+1026_86+1029del others(4): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114734 | |||||||
| chr12:9114863 | A | G | 3 | a0001c0001t0002g0143a0001c0001t0002g0144a0002c0002t0002g0038 | 3 | HG01993.hp2 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.86+901T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114863 | |||||||
| chr12:9114872 | A | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG02055.hp1 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.86+892T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114872 | |||||||
| chr12:9114888 | T | C | 1 | a0001c0001t0002g0084 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.86+876A>G | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114888 | |||||||
| chr12:9114896 | A | T | 1 | a0002c0002t0002g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.86+868T>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114896 | |||||||
| chr12:9114963 | C | T | 122 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(119): Show | 145 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.86+801G>A | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114963 | |||||||
| chr12:9114994 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG02683.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.86+770T>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9114994 | |||||||
| chr12:9115112 | CATT | C | 67 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0089others(64): Show | 81 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.86+649_86+651delAA others(1): Show |
A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9115112 | |||||||
| chr12:9115407 | T | A | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.86+357A>T | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9115407 | |||||||
| chr12:9115519 | T | G | 2 | a0001c0001t0002g0143a0001c0001t0002g0144 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.86+245A>C | A2M | ENSG00000175899.15 | transcript | ENST00000318602.12 | protein_coding | 1/35 | chr12 | 9115519 |