Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3673 |
| ensemblid | ENSG00000164171.11 |
| hgncid | 6137 |
| symbol | ITGA2 |
| name | integrin subunit alpha 2 |
| refseq_nuc | NM_002203.4 |
| refseq_prot | NP_002194.2 |
| ensembl_nuc | ENST00000296585.10 |
| ensembl_prot | ENSP00000296585.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 52989352 |
| end | 53094779 |
| strand | + |
| ver | v1.2 |
| region | chr5:52989352-53094779 |
| region5000 | chr5:52984352-53099779 |
| regionname0 | ITGA2_chr5_52989352_53094779 |
| regionname5000 | ITGA2_chr5_52984352_53099779 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1181 | 330 | 74 | 64 | 144 | 13 | 33 | 112 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0002 | 0/0 | 1181 | 37 | 15 | 6 | 12 | 3 | 1 | 8 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0003 | 0/0 | 1181 | 10 | 0 | 0 | 10 | 0 | 0 | 9 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0004 | 0/0 | 1181 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0005 | 0/0 | 1181 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0006 | 0/0 | 1181 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0007 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0008 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0009 | 0/0 | 1181 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0010 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0011 | 0/0 | 1181 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0012 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0013 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0014 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0015 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| a0016 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | MGPER others(1176): Show |
chr5 | 52984352 | 53099779 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3543 | 173 | 25 | 36 | 85 | 7 | 19 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0002 | 0/1 | 3543 | 120 | 20 | 26 | 56 | 5 | 12 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0004 | 0/0 | 3543 | 23 | 22 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0008 | 0/0 | 3543 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0011 | 0/0 | 3543 | 3 | 1 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0013 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0014 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0016 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0021 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0022 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0001c0028 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0002c0003 | 0/0 | 3543 | 29 | 10 | 6 | 9 | 3 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0002c0007 | 0/0 | 3543 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0002c0009 | 0/0 | 3543 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0003c0005 | 0/0 | 3543 | 10 | 0 | 0 | 10 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0004c0006 | 0/0 | 3543 | 6 | 0 | 0 | 6 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0004c0020 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0005c0010 | 0/0 | 3543 | 3 | 0 | 3 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0006c0029 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0007c0012 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0008c0018 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0009c0026 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0010c0017 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0011c0015 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0012c0024 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0013c0023 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0014c0025 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0015c0027 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 | ||
| a0016c0019 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | ATGGG others(3538): Show |
chr5 | 52984352 | 53099779 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7843 | 74 | 15 | 9 | 44 | 1 | 4 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0002 | 0/0 | 7858 | 45 | 5 | 12 | 19 | 3 | 6 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0005 | 0/0 | 7843 | 28 | 3 | 10 | 8 | 2 | 5 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0013 | 0/0 | 7842 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7837): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0014 | 0/0 | 7840 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7835): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0015 | 0/0 | 7858 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0020 | 0/0 | 7857 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7852): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0022 | 0/0 | 7839 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7834): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0023 | 0/0 | 7858 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0024 | 0/0 | 7843 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0025 | 0/0 | 7858 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0029 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0032 | 0/0 | 7843 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0033 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0036 | 0/0 | 7843 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0038 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0039 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0001t0051 | 0/0 | 7843 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0003 | 0/0 | 7876 | 34 | 1 | 6 | 22 | 2 | 3 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0004 | 0/0 | 7879 | 34 | 12 | 5 | 10 | 1 | 6 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7874): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0006 | 0/0 | 7878 | 25 | 3 | 5 | 17 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7873): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0009 | 0/0 | 7877 | 6 | 0 | 0 | 5 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7872): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0011 | 0/0 | 7876 | 5 | 0 | 5 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0018 | 0/0 | 7874 | 3 | 0 | 2 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7869): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0019 | 0/0 | 7880 | 3 | 0 | 2 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7875): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0028 | 0/1 | 7876 | 2 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0041 | 0/0 | 7874 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7869): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0042 | 0/0 | 7874 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7869): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0043 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0044 | 0/0 | 7880 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7875): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0046 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7870): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0047 | 0/0 | 7879 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7874): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0048 | 0/0 | 7879 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7874): Show |
chr5 | 52984352 | 53099779 |
| a0001c0002t0049 | 0/0 | 7879 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7874): Show |
chr5 | 52984352 | 53099779 |
| a0001c0004t0002 | 0/0 | 7858 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0004t0008 | 0/0 | 7858 | 21 | 20 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0004t0031 | 0/0 | 7858 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0008t0012 | 0/0 | 7857 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7852): Show |
chr5 | 52984352 | 53099779 |
| a0001c0008t0021 | 0/0 | 7857 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7852): Show |
chr5 | 52984352 | 53099779 |
| a0001c0011t0002 | 0/0 | 7858 | 2 | 0 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0011t0034 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0013t0001 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0014t0003 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0001c0016t0005 | 0/0 | 7843 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0001c0021t0050 | 0/0 | 7879 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7874): Show |
chr5 | 52984352 | 53099779 |
| a0001c0022t0002 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0001c0028t0004 | 0/0 | 7879 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7874): Show |
chr5 | 52984352 | 53099779 |
| a0002c0003t0007 | 0/0 | 7860 | 23 | 7 | 4 | 8 | 3 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7855): Show |
chr5 | 52984352 | 53099779 |
| a0002c0003t0017 | 0/0 | 7855 | 3 | 1 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7850): Show |
chr5 | 52984352 | 53099779 |
| a0002c0003t0026 | 0/0 | 7855 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7850): Show |
chr5 | 52984352 | 53099779 |
| a0002c0003t0040 | 0/0 | 7860 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7855): Show |
chr5 | 52984352 | 53099779 |
| a0002c0007t0010 | 0/0 | 7860 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7855): Show |
chr5 | 52984352 | 53099779 |
| a0002c0009t0016 | 0/0 | 7853 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7848): Show |
chr5 | 52984352 | 53099779 |
| a0003c0005t0003 | 0/0 | 7876 | 7 | 0 | 0 | 7 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0003c0005t0027 | 0/0 | 7876 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0003c0005t0045 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7870): Show |
chr5 | 52984352 | 53099779 |
| a0004c0006t0003 | 0/0 | 7876 | 6 | 0 | 0 | 6 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0004c0020t0003 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0005c0010t0002 | 0/0 | 7858 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0005c0010t0053 | 0/0 | 7858 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0006c0029t0001 | 0/0 | 7843 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0007c0012t0003 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0008c0018t0037 | 0/0 | 7858 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0009c0026t0003 | 0/0 | 7876 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0010c0017t0052 | 0/0 | 7858 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0011c0015t0002 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7853): Show |
chr5 | 52984352 | 53099779 |
| a0012c0024t0005 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7838): Show |
chr5 | 52984352 | 53099779 |
| a0013c0023t0035 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7837): Show |
chr5 | 52984352 | 53099779 |
| a0014c0025t0003 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7871): Show |
chr5 | 52984352 | 53099779 |
| a0015c0027t0006 | 0/0 | 7878 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7873): Show |
chr5 | 52984352 | 53099779 |
| a0016c0019t0030 | 0/0 | 7860 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | AGAGA others(7855): Show |
chr5 | 52984352 | 53099779 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0343 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0013g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0013g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0013g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0014g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0014g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0014g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0015g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0015g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0020g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0020g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0022g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0022g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0023g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0023g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0024g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0024g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0025g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0025g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0029g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0032g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0033g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0036g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0038g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0039g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0051g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0018g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0018g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0018g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0019g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0019g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0019g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0028g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0028g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0041g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0042g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0043g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0044g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0046g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0047g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0048g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0049g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0031g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0008t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0008t0012g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0008t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0008t0021g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0011t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0011t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0011t0034g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0013t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0014t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0016t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0021t0050g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0022t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0028t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0017g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0017g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0026g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0026g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0040g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0009t0016g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0009t0016g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0009t0016g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0027g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0027g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0045g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0020t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0005c0010t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0005c0010t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0005c0010t0053g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0006c0029t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0007c0012t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0008c0018t0037g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0009c0026t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0010c0017t0052g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0011c0015t0002g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0012c0024t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0013c0023t0035g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0014c0025t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0015c0027t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0016c0019t0030g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0028 | g0204 | EUR | GBR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | GBR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0309 | EUR | FIN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00280 | hp2 | a0001 | c0002 | t0009 | g0179 | EUR | FIN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00323 | hp1 | a0001 | c0001 | t0029 | g0137 | EUR | FIN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00323 | hp2 | a0002 | c0003 | t0007 | g0320 | EUR | FIN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00408 | hp1 | a0001 | c0002 | t0006 | g0317 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00544 | hp1 | a0001 | c0013 | t0001 | g0312 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00544 | hp2 | a0002 | c0003 | t0007 | g0078 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00597 | hp1 | a0001 | c0001 | t0023 | g0338 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00597 | hp2 | a0001 | c0002 | t0006 | g0038 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00609 | hp2 | a0001 | c0014 | t0003 | g0064 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00621 | hp1 | a0002 | c0003 | t0007 | g0079 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00621 | hp2 | a0001 | c0002 | t0006 | g0036 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00639 | hp1 | a0005 | c0010 | t0053 | g0248 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00642 | hp1 | a0001 | c0002 | t0018 | g0118 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00673 | hp1 | a0002 | c0009 | t0016 | g0215 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00733 | hp1 | a0001 | c0002 | t0006 | g0035 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00733 | hp2 | a0001 | c0011 | t0002 | g0155 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0264 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0277 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0167 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01069 | hp1 | a0001 | c0001 | t0020 | g0138 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01069 | hp2 | a0001 | c0001 | t0024 | g0285 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01070 | hp1 | a0002 | c0003 | t0007 | g0267 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01071 | hp2 | a0001 | c0001 | t0020 | g0129 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01074 | hp1 | a0001 | c0002 | t0019 | g0237 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0032 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01081 | hp2 | a0001 | c0002 | t0019 | g0236 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0274 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01099 | hp2 | a0001 | c0002 | t0004 | g0249 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01109 | hp2 | a0001 | c0004 | t0008 | g0356 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0280 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01167 | hp2 | a0001 | c0002 | t0041 | g0318 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0279 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01175 | hp1 | a0001 | c0002 | t0018 | g0102 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01175 | hp2 | a0001 | c0002 | t0006 | g0054 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01192 | hp1 | a0002 | c0003 | t0007 | g0331 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0308 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01243 | hp2 | a0002 | c0003 | t0017 | g0025 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01256 | hp1 | a0006 | c0029 | t0001 | g0289 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0232 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01257 | hp2 | a0001 | c0002 | t0006 | g0001 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0239 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01261 | hp1 | a0002 | c0003 | t0017 | g0024 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01346 | hp1 | a0001 | c0001 | t0032 | g0010 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01358 | hp1 | a0002 | c0003 | t0007 | g0319 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0271 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0209 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01496 | hp2 | a0001 | c0002 | t0006 | g0001 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0200 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01515 | hp2 | a0001 | c0011 | t0002 | g0113 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01516 | hp1 | a0002 | c0003 | t0007 | g0021 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01517 | hp1 | a0002 | c0003 | t0007 | g0021 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0199 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01884 | hp2 | a0002 | c0003 | t0007 | g0022 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01891 | hp2 | a0001 | c0004 | t0008 | g0361 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01928 | hp1 | a0005 | c0010 | t0002 | g0123 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01928 | hp2 | a0001 | c0002 | t0011 | g0165 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01975 | hp1 | a0002 | c0003 | t0007 | g0328 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01975 | hp2 | a0001 | c0002 | t0011 | g0214 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01978 | hp1 | a0005 | c0010 | t0002 | g0120 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01978 | hp2 | a0001 | c0002 | t0011 | g0202 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0189 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0190 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01993 | hp2 | a0001 | c0001 | t0024 | g0213 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0216 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02004 | hp2 | a0001 | c0002 | t0011 | g0187 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02015 | hp1 | a0007 | c0012 | t0003 | g0203 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02015 | hp2 | a0001 | c0002 | t0006 | g0042 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02027 | hp1 | a0001 | c0002 | t0004 | g0265 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0286 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02055 | hp1 | a0001 | c0004 | t0008 | g0360 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02055 | hp2 | a0002 | c0003 | t0007 | g0211 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02071 | hp2 | a0003 | c0005 | t0003 | g0177 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02074 | hp1 | a0001 | c0028 | t0004 | g0074 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02132 | hp1 | a0002 | c0003 | t0007 | g0080 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02145 | hp2 | a0001 | c0002 | t0044 | g0222 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CDX | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0192 | EAS | CDX | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02257 | hp1 | a0002 | c0003 | t0017 | g0026 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02273 | hp1 | a0001 | c0002 | t0011 | g0191 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0217 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02280 | hp1 | a0002 | c0007 | t0010 | g0259 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02280 | hp2 | a0001 | c0002 | t0042 | g0296 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02293 | hp1 | a0001 | c0002 | t0004 | g0142 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02451 | hp1 | a0001 | c0004 | t0008 | g0294 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02451 | hp2 | a0002 | c0003 | t0026 | g0364 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02572 | hp1 | a0001 | c0004 | t0008 | g0359 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0228 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02602 | hp2 | a0001 | c0022 | t0002 | g0250 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0252 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02615 | hp2 | a0001 | c0004 | t0008 | g0291 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02622 | hp1 | a0001 | c0004 | t0008 | g0352 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02622 | hp2 | a0002 | c0003 | t0007 | g0210 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02630 | hp1 | a0001 | c0001 | t0025 | g0366 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0101 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02647 | hp2 | a0001 | c0021 | t0050 | g0365 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02683 | hp2 | a0001 | c0001 | t0051 | g0072 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0194 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02698 | hp2 | a0001 | c0002 | t0004 | g0105 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0354 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0329 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02723 | hp1 | a0001 | c0008 | t0021 | g0016 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02723 | hp2 | a0002 | c0003 | t0007 | g0345 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02809 | hp1 | a0001 | c0004 | t0008 | g0295 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0258 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02818 | hp1 | a0002 | c0003 | t0007 | g0212 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02818 | hp2 | a0002 | c0007 | t0010 | g0164 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02886 | hp1 | a0001 | c0004 | t0008 | g0349 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0251 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0234 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02896 | hp1 | a0001 | c0004 | t0008 | g0292 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02896 | hp2 | a0002 | c0003 | t0007 | g0342 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02897 | hp1 | a0001 | c0004 | t0008 | g0299 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0246 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02965 | hp2 | a0001 | c0008 | t0012 | g0161 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02970 | hp1 | a0002 | c0003 | t0026 | g0363 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02970 | hp2 | a0002 | c0007 | t0010 | g0162 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02976 | hp1 | a0001 | c0002 | t0047 | g0061 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0235 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03098 | hp1 | a0001 | c0002 | t0049 | g0337 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03130 | hp1 | a0001 | c0008 | t0012 | g0159 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03130 | hp2 | a0001 | c0004 | t0008 | g0290 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03139 | hp1 | a0001 | c0008 | t0012 | g0160 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03139 | hp2 | a0002 | c0003 | t0007 | g0022 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03195 | hp1 | a0001 | c0004 | t0008 | g0297 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0240 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03209 | hp1 | a0001 | c0004 | t0008 | g0293 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03209 | hp2 | a0001 | c0002 | t0006 | g0111 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03225 | hp1 | a0001 | c0004 | t0008 | g0351 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03239 | hp1 | a0001 | c0002 | t0019 | g0229 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03453 | hp2 | a0001 | c0004 | t0008 | g0357 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0362 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03486 | hp2 | a0001 | c0004 | t0031 | g0350 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03490 | hp1 | a0009 | c0026 | t0003 | g0206 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0300 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03492 | hp1 | a0001 | c0002 | t0004 | g0256 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0268 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03579 | hp1 | a0010 | c0017 | t0052 | g0262 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03654 | hp1 | a0001 | c0001 | t0039 | g0119 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03654 | hp2 | a0001 | c0016 | t0005 | g0103 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03688 | hp1 | a0001 | c0002 | t0004 | g0115 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03688 | hp2 | a0001 | c0002 | t0048 | g0238 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03704 | hp2 | a0001 | c0001 | t0036 | g0278 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03710 | hp1 | a0001 | c0002 | t0018 | g0104 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03831 | hp1 | a0002 | c0003 | t0007 | g0334 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03831 | hp2 | a0011 | c0015 | t0002 | g0370 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0114 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0201 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03942 | hp2 | a0001 | c0001 | t0038 | g0127 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0112 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0284 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04199 | hp2 | a0001 | c0002 | t0004 | g0368 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0097 | AFR | YRI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | CHB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18939 | hp2 | a0001 | c0001 | t0014 | g0275 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18942 | hp1 | a0001 | c0001 | t0015 | g0150 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18942 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18947 | hp1 | a0004 | c0006 | t0003 | g0171 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18947 | hp2 | a0001 | c0001 | t0033 | g0339 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0063 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18950 | hp2 | a0002 | c0003 | t0040 | g0327 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18951 | hp1 | a0012 | c0024 | t0005 | g0128 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18951 | hp2 | a0001 | c0001 | t0014 | g0276 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0178 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0243 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18957 | hp2 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18959 | hp1 | a0001 | c0001 | t0013 | g0011 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18959 | hp2 | a0001 | c0002 | t0006 | g0040 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18961 | hp1 | a0002 | c0009 | t0016 | g0316 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18962 | hp1 | a0001 | c0001 | t0013 | g0325 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18962 | hp2 | a0001 | c0002 | t0006 | g0050 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0109 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18964 | hp1 | a0003 | c0005 | t0003 | g0019 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18964 | hp2 | a0001 | c0002 | t0006 | g0041 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18965 | hp1 | a0001 | c0002 | t0006 | g0046 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18965 | hp2 | a0003 | c0005 | t0027 | g0207 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18970 | hp2 | a0004 | c0006 | t0003 | g0017 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0110 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0288 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18972 | hp2 | a0001 | c0002 | t0006 | g0052 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18973 | hp2 | a0003 | c0005 | t0003 | g0018 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18975 | hp2 | a0001 | c0002 | t0006 | g0049 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18979 | hp1 | a0014 | c0025 | t0003 | g0170 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18980 | hp2 | a0001 | c0002 | t0004 | g0241 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18981 | hp2 | a0001 | c0002 | t0006 | g0039 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18983 | hp1 | a0001 | c0001 | t0022 | g0045 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18983 | hp2 | a0003 | c0005 | t0003 | g0270 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18986 | hp1 | a0003 | c0005 | t0045 | g0018 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18988 | hp1 | a0004 | c0006 | t0003 | g0017 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18989 | hp2 | a0002 | c0003 | t0007 | g0323 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18991 | hp2 | a0001 | c0002 | t0006 | g0043 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18993 | hp1 | a0002 | c0003 | t0007 | g0073 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18993 | hp2 | a0001 | c0001 | t0023 | g0340 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18994 | hp1 | a0015 | c0027 | t0006 | g0037 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18995 | hp1 | a0001 | c0002 | t0009 | g0174 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18995 | hp2 | a0002 | c0009 | t0016 | g0315 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18999 | hp1 | a0003 | c0005 | t0003 | g0314 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19000 | hp1 | a0001 | c0002 | t0006 | g0053 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19002 | hp2 | a0004 | c0020 | t0003 | g0130 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19003 | hp1 | a0001 | c0002 | t0004 | g0242 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19003 | hp2 | a0001 | c0002 | t0009 | g0173 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19005 | hp2 | a0001 | c0002 | t0009 | g0175 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19007 | hp1 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19010 | hp2 | a0003 | c0005 | t0027 | g0332 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19030 | hp1 | a0002 | c0007 | t0010 | g0260 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19030 | hp2 | a0001 | c0004 | t0008 | g0298 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19043 | hp1 | a0001 | c0004 | t0008 | g0353 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0231 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19054 | hp1 | a0001 | c0001 | t0022 | g0047 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19055 | hp2 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0147 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19056 | hp2 | a0002 | c0003 | t0007 | g0341 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19057 | hp2 | a0001 | c0001 | t0015 | g0254 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19060 | hp2 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19063 | hp1 | a0001 | c0002 | t0009 | g0029 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19065 | hp1 | a0001 | c0002 | t0046 | g0003 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19065 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19066 | hp2 | a0004 | c0006 | t0003 | g0166 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0245 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19070 | hp2 | a0004 | c0006 | t0003 | g0169 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19075 | hp1 | a0001 | c0001 | t0013 | g0139 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19075 | hp2 | a0001 | c0002 | t0006 | g0044 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19076 | hp1 | a0001 | c0002 | t0009 | g0208 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19076 | hp2 | a0001 | c0001 | t0014 | g0347 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19080 | hp2 | a0004 | c0006 | t0003 | g0172 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0244 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19082 | hp2 | a0002 | c0003 | t0007 | g0333 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19084 | hp2 | a0002 | c0003 | t0007 | g0346 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19085 | hp2 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0205 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19087 | hp2 | a0003 | c0005 | t0003 | g0176 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19088 | hp2 | a0003 | c0005 | t0003 | g0019 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19091 | hp1 | a0001 | c0002 | t0043 | g0108 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0257 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0230 | AFR | YRI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20129 | hp1 | a0001 | c0002 | t0006 | g0001 | AFR | ASW | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20129 | hp2 | a0016 | c0019 | t0030 | g0034 | AFR | ASW | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0310 | EUR | TSI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20805 | hp1 | a0001 | c0002 | t0004 | g0233 | EUR | TSI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0020 | EUR | TSI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | GIH | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01123 | hp1 | a0001 | c0002 | t0006 | g0051 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0180 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02109 | hp1 | a0001 | c0004 | t0008 | g0348 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02109 | hp2 | a0001 | c0008 | t0021 | g0016 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0088 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02486 | hp2 | a0001 | c0004 | t0008 | g0358 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02559 | hp1 | a0001 | c0004 | t0008 | g0355 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0367 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03471 | hp1 | a0008 | c0018 | t0037 | g0369 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03471 | hp2 | a0002 | c0007 | t0010 | g0163 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG06807 | hp1 | a0001 | c0011 | t0034 | g0084 | AFR | USA | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0195 | AFR | USA | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18955 | hp1 | a0013 | c0023 | t0035 | g0272 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | USA | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | USA | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0028 | g0085 | REF | REF | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0343 | REF | REF | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:53045032 | G | A | 1 | a0007 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.327G>A | p.Met109Ile | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/30 | 444/7843 | 327/3546 | 109/1181 | chr5 | 53045032 | |||
| chr5:53048657 | A | G | 1 | a0006 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.517A>G | p.Ile173Val | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/30 | 634/7843 | 517/3546 | 173/1181 | chr5 | 53048657 | |||
| chr5:53051540 | G | A | 1 | a0011 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.760G>A | p.Gly254Arg | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/30 | 877/7843 | 760/3546 | 254/1181 | chr5 | 53051540 | |||
| chr5:53056008 | G | A | 1 | a0005 | 3 | HG00639.hp1 HG01928.hp1 HG01978.hp1 |
missense_variant | MODERATE | c.955G>A | p.Ala319Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/30 | 1072/7843 | 955/3546 | 319/1181 | chr5 | 53056008 | |||
| chr5:53056144 | T | C | 1 | a0014 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.1091T>C | p.Ile364Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/30 | 1208/7843 | 1091/3546 | 364/1181 | chr5 | 53056144 | |||
| chr5:53058045 | A | G | 1 | a0012 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1117A>G | p.Asn373Asp | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/30 | 1234/7843 | 1117/3546 | 373/1181 | chr5 | 53058045 | |||
| chr5:53062927 | G | A | 2 | a0002 a0016 |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
missense_variant&splice_region_variant | MODERATE | c.1600G>A | p.Glu534Lys | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/30 | 1717/7843 | 1600/3546 | 534/1181 | chr5 | 53062927 | |||
| chr5:53070124 | T | C | 1 | a0009 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.2099T>C | p.Ile700Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/30 | 2216/7843 | 2099/3546 | 700/1181 | chr5 | 53070124 | |||
| chr5:53072643 | G | A | 2 | a0004 a0014 |
8 | NA18947.hp1 NA18970.hp2 NA18979.hp1 others(5): Show |
missense_variant | MODERATE | c.2377G>A | p.Gly793Arg | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/30 | 2494/7843 | 2377/3546 | 793/1181 | chr5 | 53072643 | |||
| chr5:53072695 | A | G | 1 | a0013 | 1 | NA18955.hp1 | missense_variant&splice_region_variant | MODERATE | c.2429A>G | p.Gln810Arg | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/30 | 2546/7843 | 2429/3546 | 810/1181 | chr5 | 53072695 | |||
| chr5:53074418 | G | A | 1 | a0016 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.2605G>A | p.Ala869Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/30 | 2722/7843 | 2605/3546 | 869/1181 | chr5 | 53074418 | |||
| chr5:53074449 | G | T | 1 | a0015 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.2636G>T | p.Gly879Val | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/30 | 2753/7843 | 2636/3546 | 879/1181 | chr5 | 53074449 | |||
| chr5:53075070 | A | C | 1 | a0008 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.2674A>C | p.Thr892Pro | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 22/30 | 2791/7843 | 2674/3546 | 892/1181 | chr5 | 53075070 | |||
| chr5:53075259 | A | G | 1 | a0003 | 10 | HG02071.hp2 NA18964.hp1 NA18965.hp2 others(7): Show |
missense_variant | MODERATE | c.2780A>G | p.Asn927Ser | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/30 | 2897/7843 | 2780/3546 | 927/1181 | chr5 | 53075259 | |||
| chr5:53078840 | A | G | 1 | a0007 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2894A>G | p.Glu965Gly | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/30 | 3011/7843 | 2894/3546 | 965/1181 | chr5 | 53078840 | |||
| chr5:53089976 | A | C | 2 | a0008 a0010 |
2 | HG03471.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.3379A>C | p.Lys1127Gln | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/30 | 3496/7843 | 3379/3546 | 1127/1181 | chr5 | 53089976 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:53051413 | G | A | 2 | a0001c0013 a0001c0014 |
2 | HG00544.hp1 HG00609.hp2 |
splice_region_variant&synonymous_variant | LOW | c.633G>A | p.Val211Val | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/30 | 750/7843 | 633/3546 | 211/1181 | chr5 | 53051413 | |||
| chr5:53051539 | C | T | 9 | a0001c0002 a0001c0011 a0001c0028 others(6): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
synonymous_variant | LOW | c.759C>T | p.Phe253Phe | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/30 | 876/7843 | 759/3546 | 253/1181 | chr5 | 53051539 | |||
| chr5:53055547 | T | C | 3 | a0001c0016 a0002c0003 a0002c0009 |
33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
synonymous_variant | LOW | c.789T>C | p.Ala263Ala | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/30 | 906/7843 | 789/3546 | 263/1181 | chr5 | 53055547 | |||
| chr5:53055583 | G | A | 11 | a0001c0002 a0001c0011 a0001c0028 others(8): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
synonymous_variant | LOW | c.825G>A | p.Thr275Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/30 | 942/7843 | 825/3546 | 275/1181 | chr5 | 53055583 | |||
| chr5:53055607 | C | T | 1 | a0001c0004 | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
synonymous_variant | LOW | c.849C>T | p.Asp283Asp | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/30 | 966/7843 | 849/3546 | 283/1181 | chr5 | 53055607 | |||
| chr5:53056046 | A | G | 3 | a0001c0016 a0002c0003 a0002c0009 |
33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
synonymous_variant | LOW | c.993A>G | p.Ala331Ala | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/30 | 1110/7843 | 993/3546 | 331/1181 | chr5 | 53056046 | |||
| chr5:53059927 | C | G | 1 | a0001c0028 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.1227C>G | p.Val409Val | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/30 | 1344/7843 | 1227/3546 | 409/1181 | chr5 | 53059927 | |||
| chr5:53072642 | C | T | 6 | a0002c0003 a0002c0007 a0002c0009 others(3): Show |
40 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(37): Show |
synonymous_variant | LOW | c.2376C>T | p.Asp792Asp | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/30 | 2493/7843 | 2376/3546 | 792/1181 | chr5 | 53072642 | |||
| chr5:53073172 | G | A | 4 | a0002c0003 a0002c0007 a0002c0009 others(1): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
synonymous_variant | LOW | c.2484G>A | p.Thr828Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/30 | 2601/7843 | 2484/3546 | 828/1181 | chr5 | 53073172 | |||
| chr5:53073256 | G | A | 3 | a0002c0003 a0002c0007 a0016c0019 |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
synonymous_variant | LOW | c.2568G>A | p.Leu856Leu | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/30 | 2685/7843 | 2568/3546 | 856/1181 | chr5 | 53073256 | |||
| chr5:53075114 | G | A | 2 | a0001c0008 a0001c0021 |
6 | HG02109.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
synonymous_variant | LOW | c.2718G>A | p.Ala906Ala | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 22/30 | 2835/7843 | 2718/3546 | 906/1181 | chr5 | 53075114 | |||
| chr5:53083447 | C | T | 11 | a0001c0002 a0001c0014 a0001c0021 others(8): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
synonymous_variant | LOW | c.3252C>T | p.Phe1084Phe | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/30 | 3369/7843 | 3252/3546 | 1084/1181 | chr5 | 53083447 | |||
| chr5:53090521 | C | T | 1 | a0001c0022 | 1 | HG02602.hp2 | splice_region_variant&synonymous_variant | LOW | c.3468C>T | p.Leu1156Leu | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3585/7843 | 3468/3546 | 1156/1181 | chr5 | 53090521 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:52989415 | C | T | 1 | a0005c0010t0053 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/30 | 54 | chr5 | 52989415 | ||||||
| chr5:52989456 | G | A | 2 | a0001c0001t0020 a0001c0001t0029 |
3 | HG00323.hp1 HG01069.hp1 HG01071.hp2 |
5_prime_UTR_variant | MODIFIER | c.-13G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/30 | 13 | chr5 | 52989456 | ||||||
| chr5:53090634 | A | C | 1 | a0001c0002t0028 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 35 | chr5 | 53090634 | ||||||
| chr5:53090667 | A | G | 1 | a0010c0017t0052 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 68 | chr5 | 53090667 | ||||||
| chr5:53090686 | A | AT | 1 | a0001c0002t0009 | 6 | HG00280.hp2 NA18995.hp1 NA19003.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*95dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 96 | INFO_REALIGN_3_PRIME | chr5 | 53090686 | |||||
| chr5:53090736 | C | G | 1 | a0001c0001t0051 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 137 | chr5 | 53090736 | ||||||
| chr5:53090807 | G | A | 2 | a0002c0007t0010 a0016c0019t0030 |
6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*208G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 208 | chr5 | 53090807 | ||||||
| chr5:53090830 | TG | T | 2 | a0001c0008t0012 a0001c0008t0021 |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*236delG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 236 | INFO_REALIGN_3_PRIME | chr5 | 53090830 | |||||
| chr5:53091060 | A | C | 1 | a0001c0021t0050 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 461 | chr5 | 53091060 | ||||||
| chr5:53091071 | TAAC | T | 28 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0006 others(25): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*475_*477delCAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 475 | INFO_REALIGN_3_PRIME | chr5 | 53091071 | |||||
| chr5:53091306 | G | C | 1 | a0001c0004t0031 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*707G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 707 | chr5 | 53091306 | ||||||
| chr5:53091320 | A | C | 61 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(58): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*721A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 721 | chr5 | 53091320 | ||||||
| chr5:53091357 | C | CATTT | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*760_*761insTTAT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 761 | INFO_REALIGN_3_PRIME | chr5 | 53091357 | |||||
| chr5:53091408 | G | C | 1 | a0001c0001t0032 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*809G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 809 | chr5 | 53091408 | ||||||
| chr5:53091493 | C | T | 54 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0020 others(51): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*894C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 894 | chr5 | 53091493 | ||||||
| chr5:53091836 | A | G | 1 | a0001c0011t0034 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1237A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1237 | chr5 | 53091836 | ||||||
| chr5:53091851 | G | A | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1252G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1252 | chr5 | 53091851 | ||||||
| chr5:53092240 | C | G | 1 | a0002c0003t0017 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1641C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1641 | chr5 | 53092240 | ||||||
| chr5:53092356 | GA | G | 3 | a0001c0002t0006 a0001c0002t0049 a0015c0027t0006 |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1764delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1764 | INFO_REALIGN_3_PRIME | chr5 | 53092356 | |||||
| chr5:53092481 | G | A | 1 | a0001c0008t0012 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1882G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1882 | chr5 | 53092481 | ||||||
| chr5:53092496 | A | T | 1 | a0001c0001t0033 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1897A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1897 | chr5 | 53092496 | ||||||
| chr5:53092514 | G | A | 1 | a0013c0023t0035 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1915G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1915 | chr5 | 53092514 | ||||||
| chr5:53092520 | G | T | 1 | a0002c0003t0017 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1921G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1921 | chr5 | 53092520 | ||||||
| chr5:53092624 | TA | T | 12 | a0001c0001t0013 a0001c0001t0020 a0001c0002t0004 others(9): Show |
72 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2041delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2041 | INFO_REALIGN_3_PRIME | chr5 | 53092624 | |||||
| chr5:53092624 | TAAA | T | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2039_*2041delAAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2039 | INFO_REALIGN_3_PRIME | chr5 | 53092624 | |||||
| chr5:53092650 | A | G | 1 | a0001c0001t0039 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2051A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2051 | chr5 | 53092650 | ||||||
| chr5:53092687 | A | G | 1 | a0001c0001t0015 | 3 | NA18942.hp1 NA19055.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2088A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2088 | chr5 | 53092687 | ||||||
| chr5:53092750 | A | G | 2 | a0001c0008t0012 a0001c0008t0021 |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2151A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2151 | chr5 | 53092750 | ||||||
| chr5:53092797 | T | C | 1 | a0002c0003t0040 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2198 | chr5 | 53092797 | ||||||
| chr5:53092928 | TGAAACCC others(16): Show |
T | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2330_*2352delGAAA others(19): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2330 | chr5 | 53092928 | ||||||
| chr5:53093103 | TCAAA | T | 19 | a0001c0001t0022 a0001c0002t0003 a0001c0002t0009 others(16): Show |
76 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2517_*2520delCAAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2517 | INFO_REALIGN_3_PRIME | chr5 | 53093103 | |||||
| chr5:53093115 | A | C | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2516A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2516 | chr5 | 53093115 | ||||||
| chr5:53093116 | C | A | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2517C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2517 | chr5 | 53093116 | ||||||
| chr5:53093118 | A | T | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2519A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2519 | chr5 | 53093118 | ||||||
| chr5:53093120 | A | C | 1 | a0001c0002t0044 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2521A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2521 | chr5 | 53093120 | ||||||
| chr5:53093169 | C | A | 1 | a0001c0002t0011 | 5 | HG01928.hp2 HG01975.hp2 HG01978.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2570C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2570 | chr5 | 53093169 | ||||||
| chr5:53093169 | C | T | 13 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0020 others(10): Show |
63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2570C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2570 | chr5 | 53093169 | ||||||
| chr5:53093173 | C | G | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2574C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2574 | chr5 | 53093173 | ||||||
| chr5:53093322 | G | C | 2 | a0003c0005t0027 a0003c0005t0045 |
3 | NA18965.hp2 NA18986.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2723G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2723 | chr5 | 53093322 | ||||||
| chr5:53093381 | C | G | 1 | a0001c0002t0043 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2782C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2782 | chr5 | 53093381 | ||||||
| chr5:53093481 | G | GGTATGTT others(4): Show |
55 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0020 others(52): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*2883_*2893dupGTAT others(7): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2894 | INFO_REALIGN_3_PRIME | chr5 | 53093481 | |||||
| chr5:53093538 | C | T | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2939C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2939 | chr5 | 53093538 | ||||||
| chr5:53093539 | G | A | 28 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0006 others(25): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2940G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2940 | chr5 | 53093539 | ||||||
| chr5:53093598 | A | G | 23 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0009 others(20): Show |
114 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2999A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2999 | chr5 | 53093598 | ||||||
| chr5:53093625 | A | G | 55 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0020 others(52): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3026A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3026 | chr5 | 53093625 | ||||||
| chr5:53093647 | G | A | 2 | a0008c0018t0037 a0010c0017t0052 |
2 | HG03471.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3048G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3048 | chr5 | 53093647 | ||||||
| chr5:53093763 | G | A | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3164G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3164 | chr5 | 53093763 | ||||||
| chr5:53093769 | A | G | 1 | a0001c0001t0025 | 2 | HG02559.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3170A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3170 | chr5 | 53093769 | ||||||
| chr5:53093904 | ACTC | A | 1 | a0001c0001t0014 | 3 | NA18939.hp2 NA18951.hp2 NA19076.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3308_*3310delCCT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3308 | INFO_REALIGN_3_PRIME | chr5 | 53093904 | |||||
| chr5:53093914 | G | T | 1 | a0001c0001t0038 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3315G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3315 | chr5 | 53093914 | ||||||
| chr5:53093930 | A | G | 1 | a0016c0019t0030 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3331A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3331 | chr5 | 53093930 | ||||||
| chr5:53093967 | A | T | 1 | a0001c0002t0042 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3368A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3368 | chr5 | 53093967 | ||||||
| chr5:53093981 | T | TAAAG | 55 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0020 others(52): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3385_*3386insGAAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3386 | INFO_REALIGN_3_PRIME | chr5 | 53093981 | |||||
| chr5:53093997 | T | G | 1 | a0001c0002t0041 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3398T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3398 | chr5 | 53093997 | ||||||
| chr5:53094191 | A | AATTTAT | 2 | a0002c0003t0017 a0002c0003t0026 |
5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3593_*3594insTTTA others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3594 | INFO_REALIGN_3_PRIME | chr5 | 53094191 | |||||
| chr5:53094196 | A | AACTTTGT others(6): Show |
2 | a0002c0003t0017 a0002c0003t0026 |
5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3598_*3599insCTTT others(9): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3599 | INFO_REALIGN_3_PRIME | chr5 | 53094196 | |||||
| chr5:53094196 | A | AATTATAT others(18): Show |
28 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0006 others(25): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3599_*3600insTATA others(21): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3600 | INFO_REALIGN_3_PRIME | chr5 | 53094196 | |||||
| chr5:53094196 | A | AATTTATA others(17): Show |
4 | a0002c0003t0007 a0002c0003t0040 a0002c0007t0010 others(1): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3599_*3600insTTAT others(20): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3600 | INFO_REALIGN_3_PRIME | chr5 | 53094196 | |||||
| chr5:53094196 | A | AATTTATA others(17): Show |
1 | a0002c0009t0016 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3599_*3600insTTAT others(20): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3600 | INFO_REALIGN_3_PRIME | chr5 | 53094196 | |||||
| chr5:53094360 | TAA | T | 3 | a0001c0002t0018 a0001c0002t0041 a0001c0002t0042 |
5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3763_*3764delAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3763 | INFO_REALIGN_3_PRIME | chr5 | 53094360 | |||||
| chr5:53094373 | G | T | 1 | a0001c0001t0036 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3774G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3774 | chr5 | 53094373 | ||||||
| chr5:53094488 | A | G | 1 | a0001c0002t0048 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3889A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3889 | chr5 | 53094488 | ||||||
| chr5:53094517 | G | C | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3918G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3918 | chr5 | 53094517 | ||||||
| chr5:53094585 | A | C | 29 | a0001c0001t0024 a0001c0002t0003 a0001c0002t0004 others(26): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*3986A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3986 | chr5 | 53094585 | ||||||
| chr5:53094639 | CAGTTAGT | C | 1 | a0002c0009t0016 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4045_*4051delAGTA others(3): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 4045 | INFO_REALIGN_3_PRIME | chr5 | 53094639 | |||||
| chr5:53094642 | TTAG | T | 6 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(3): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4048_*4050delAGT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 4048 | INFO_REALIGN_3_PRIME | chr5 | 53094642 | |||||
| chr5:53094697 | C | G | 7 | a0002c0003t0007 a0002c0003t0017 a0002c0003t0026 others(4): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4098C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 4098 | chr5 | 53094697 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:52989557 | C | A | 3 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 |
3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.64+25C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989557 | |||||||
| chr5:52989559 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | HG01952.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.64+27G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989559 | |||||||
| chr5:52989623 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(3): Show |
7 | HG00673.hp2 HG01081.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+91G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989623 | |||||||
| chr5:52989678 | C | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(21): Show |
30 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.64+146C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989678 | |||||||
| chr5:52989680 | T | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(21): Show |
30 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.64+148T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989680 | |||||||
| chr5:52989814 | G | GCA | 115 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(112): Show |
121 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.64+303_64+304dupCA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | ||||||
| chr5:52989814 | G | GCACA | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0086 others(87): Show |
95 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.64+301_64+304dupCA others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | ||||||
| chr5:52989814 | G | GCACACAC others(1): Show |
23 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0066 others(20): Show |
23 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+297_64+304dupCA others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | ||||||
| chr5:52989814 | G | GCACACAC others(3): Show |
8 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
9 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+295_64+304dupCA others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | ||||||
| chr5:52989814 | G | GCACACAC others(5): Show |
1 | a0001c0002t0006g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.64+293_64+304dupCA others(10): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | ||||||
| chr5:52989833 | CACAG | C | 48 | a0001c0001t0001g0269 a0001c0001t0001g0281 a0001c0001t0001g0282 others(45): Show |
52 | HG00280.hp1 HG00735.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.64+309_64+312delGA others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989833 | ||||||
| chr5:52989835 | CAG | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(25): Show |
34 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+305_64+306delGA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989835 | ||||||
| chr5:52989837 | G | C | 248 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(245): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.64+305G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989837 | |||||||
| chr5:52990007 | G | C | 50 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(47): Show |
51 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.64+475G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990007 | |||||||
| chr5:52990079 | C | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(21): Show |
30 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.64+547C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990079 | |||||||
| chr5:52990081 | A | G | 4 | a0001c0011t0034g0084 a0002c0007t0010g0162 a0002c0007t0010g0163 others(1): Show |
4 | HG02818.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+549A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990081 | |||||||
| chr5:52990134 | A | G | 3 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 |
3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+602A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990134 | |||||||
| chr5:52990150 | A | C | 3 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 |
3 | HG02818.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+618A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990150 | |||||||
| chr5:52990180 | C | T | 209 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(206): Show |
223 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(220): Show |
intron_variant | MODIFIER | c.64+648C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990180 | |||||||
| chr5:52990274 | G | T | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+742G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990274 | |||||||
| chr5:52990283 | G | A | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+751G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990283 | |||||||
| chr5:52990291 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64+759C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990291 | |||||||
| chr5:52990503 | A | T | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+971A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990503 | |||||||
| chr5:52990522 | C | A | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+990C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990522 | |||||||
| chr5:52990567 | G | GTGGT | 3 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 |
3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+1035_64+1036ins others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990567 | |||||||
| chr5:52990568 | G | T | 3 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 |
3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+1036G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990568 | |||||||
| chr5:52990568 | GT | G | 127 | a0001c0001t0001g0011 a0001c0001t0001g0083 a0001c0001t0001g0116 others(124): Show |
133 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.64+1054delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52990568 | ||||||
| chr5:52990568 | GTT | G | 185 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(182): Show |
200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.64+1053_64+1054del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52990568 | ||||||
| chr5:52990622 | T | G | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.64+1090T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990622 | |||||||
| chr5:52990701 | C | T | 1 | a0001c0002t0006g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.64+1169C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990701 | |||||||
| chr5:52990702 | T | C | 1 | a0001c0002t0006g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.64+1170T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990702 | |||||||
| chr5:52991025 | A | G | 1 | a0001c0002t0004g0264 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64+1493A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991025 | |||||||
| chr5:52991417 | TAC | T | 15 | a0001c0001t0002g0015 a0001c0001t0002g0143 a0001c0001t0002g0144 others(12): Show |
16 | HG00558.hp2 NA18942.hp1 NA18957.hp1 others(13): Show |
intron_variant | MODIFIER | c.64+1901_64+1902del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52991417 | ||||||
| chr5:52991559 | T | C | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64+2027T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991559 | |||||||
| chr5:52991575 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.64+2043C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991575 | |||||||
| chr5:52991753 | C | T | 14 | a0001c0002t0006g0354 a0001c0004t0008g0348 a0001c0004t0008g0349 others(11): Show |
14 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+2221C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991753 | |||||||
| chr5:52991794 | A | G | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(44): Show |
48 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.64+2262A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991794 | |||||||
| chr5:52991795 | T | C | 1 | a0001c0002t0018g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.64+2263T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991795 | |||||||
| chr5:52991993 | G | A | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64+2461G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991993 | |||||||
| chr5:52991998 | T | TCCACC | 120 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0134 others(117): Show |
129 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.64+2468_64+2472dup others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52991998 | ||||||
| chr5:52992007 | G | C | 1 | a0001c0002t0006g0035 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.64+2475G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992007 | |||||||
| chr5:52992075 | G | A | 57 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(54): Show |
59 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.64+2543G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992075 | |||||||
| chr5:52992086 | C | A | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2554C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992086 | |||||||
| chr5:52992233 | G | A | 3 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02129.hp1 HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.64+2701G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992233 | |||||||
| chr5:52992265 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.64+2733T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992265 | |||||||
| chr5:52992301 | C | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+2769C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992301 | |||||||
| chr5:52992319 | A | G | 3 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 |
3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+2787A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992319 | |||||||
| chr5:52992343 | A | G | 52 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(49): Show |
53 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.64+2811A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992343 | |||||||
| chr5:52992537 | A | G | 4 | a0001c0001t0002g0307 a0001c0001t0002g0309 a0001c0001t0005g0308 others(1): Show |
4 | HG00280.hp1 HG01243.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+3005A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992537 | |||||||
| chr5:52992547 | C | T | 1 | a0010c0017t0052g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+3015C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992547 | |||||||
| chr5:52992641 | C | A | 1 | a0001c0002t0044g0222 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64+3109C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992641 | |||||||
| chr5:52992652 | T | C | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
96 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.64+3120T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992652 | |||||||
| chr5:52992653 | G | A | 1 | a0001c0002t0006g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.64+3121G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992653 | |||||||
| chr5:52992834 | G | GGTAC | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+3303_64+3306dup others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52992834 | ||||||
| chr5:52993094 | A | G | 1 | a0002c0003t0007g0346 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.64+3562A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993094 | |||||||
| chr5:52993160 | T | G | 2 | a0001c0002t0018g0104 a0001c0016t0005g0103 |
2 | HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.64+3628T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993160 | |||||||
| chr5:52993183 | G | A | 45 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(42): Show |
47 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.64+3651G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993183 | |||||||
| chr5:52993241 | G | A | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | NA18978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.64+3709G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993241 | |||||||
| chr5:52993243 | C | T | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+3711C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993243 | |||||||
| chr5:52993362 | G | T | 1 | a0002c0003t0007g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64+3830G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993362 | |||||||
| chr5:52993389 | G | A | 1 | a0001c0002t0011g0165 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.64+3857G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993389 | |||||||
| chr5:52993547 | T | C | 329 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(326): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.64+4015T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993547 | |||||||
| chr5:52993582 | G | A | 5 | a0001c0001t0005g0261 a0002c0007t0010g0259 a0002c0007t0010g0260 others(2): Show |
5 | HG02280.hp1 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+4050G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993582 | |||||||
| chr5:52993601 | C | G | 1 | a0001c0002t0009g0208 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.64+4069C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993601 | |||||||
| chr5:52993636 | A | C | 2 | a0001c0001t0002g0156 a0001c0001t0002g0266 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64+4104A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993636 | |||||||
| chr5:52993690 | G | T | 1 | a0003c0005t0027g0207 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.64+4158G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993690 | |||||||
| chr5:52993880 | CAA | C | 62 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0134 others(59): Show |
66 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.64+4349_64+4350del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993880 | |||||||
| chr5:52993904 | G | A | 2 | a0001c0002t0006g0038 a0015c0027t0006g0037 |
2 | HG00597.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.64+4372G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993904 | |||||||
| chr5:52993924 | G | T | 1 | a0002c0003t0007g0021 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.64+4392G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993924 | |||||||
| chr5:52993936 | T | G | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
218 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.64+4404T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993936 | |||||||
| chr5:52994074 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.64+4542A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994074 | |||||||
| chr5:52994264 | A | T | 52 | a0001c0001t0002g0106 a0001c0001t0002g0219 a0001c0001t0002g0220 others(49): Show |
54 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.64+4732A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994264 | |||||||
| chr5:52994288 | C | G | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+4756C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994288 | |||||||
| chr5:52994430 | G | C | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64+4898G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994430 | |||||||
| chr5:52994447 | C | T | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+4915C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994447 | |||||||
| chr5:52994466 | G | A | 2 | a0002c0003t0007g0021 a0002c0003t0007g0267 |
3 | HG01070.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.64+4934G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994466 | |||||||
| chr5:52994595 | C | T | 1 | a0001c0002t0006g0051 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.64+5063C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994595 | |||||||
| chr5:52994604 | C | T | 61 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0134 others(58): Show |
65 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.64+5072C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994604 | |||||||
| chr5:52994806 | G | T | 63 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
67 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.64+5274G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994806 | |||||||
| chr5:52995040 | A | C | 1 | a0001c0002t0004g0258 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+5508A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995040 | |||||||
| chr5:52995049 | C | T | 5 | a0001c0002t0004g0142 a0001c0008t0012g0159 a0001c0008t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02293.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+5517C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995049 | |||||||
| chr5:52995050 | G | A | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(48): Show |
52 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.64+5518G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995050 | |||||||
| chr5:52995099 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | NA18991.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.64+5567C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995099 | |||||||
| chr5:52995151 | C | T | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+5619C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995151 | |||||||
| chr5:52995228 | C | A | 63 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
67 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.64+5696C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995228 | |||||||
| chr5:52995286 | G | A | 1 | a0001c0002t0004g0228 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64+5754G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995286 | |||||||
| chr5:52995357 | T | C | 50 | a0001c0001t0001g0269 a0001c0001t0001g0281 a0001c0001t0001g0282 others(47): Show |
54 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+5825T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995357 | |||||||
| chr5:52995401 | A | T | 2 | a0001c0001t0025g0367 a0001c0002t0047g0061 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.64+5869A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995401 | |||||||
| chr5:52995449 | G | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(50): Show |
54 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+5917G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995449 | |||||||
| chr5:52995515 | A | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+5983A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995515 | |||||||
| chr5:52995567 | G | A | 89 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
99 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.64+6035G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995567 | |||||||
| chr5:52995661 | G | A | 2 | a0002c0003t0007g0319 a0002c0003t0007g0320 |
2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.64+6129G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995661 | |||||||
| chr5:52995709 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64+6177C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995709 | |||||||
| chr5:52996244 | T | A | 1 | a0001c0001t0001g0076 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.64+6712T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996244 | |||||||
| chr5:52996407 | T | C | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
215 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.64+6875T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996407 | |||||||
| chr5:52996575 | A | T | 119 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0134 others(116): Show |
127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.64+7043A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996575 | |||||||
| chr5:52996624 | T | C | 1 | a0004c0006t0003g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64+7092T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996624 | |||||||
| chr5:52996647 | T | C | 63 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
67 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.64+7115T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996647 | |||||||
| chr5:52996725 | T | G | 232 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
244 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.64+7193T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996725 | |||||||
| chr5:52996893 | G | A | 5 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0142 others(2): Show |
5 | HG00733.hp2 HG01515.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+7361G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996893 | |||||||
| chr5:52997019 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.64+7487G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997019 | |||||||
| chr5:52997153 | T | C | 9 | a0001c0001t0002g0106 a0001c0001t0005g0261 a0001c0002t0004g0101 others(6): Show |
9 | HG01175.hp1 HG01433.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+7621T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997153 | |||||||
| chr5:52997220 | A | G | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+7688A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997220 | |||||||
| chr5:52997257 | T | C | 119 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0134 others(116): Show |
127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.64+7725T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997257 | |||||||
| chr5:52997417 | T | G | 371 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(368): Show |
395 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.64+7885T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997417 | |||||||
| chr5:52997652 | A | G | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | NA18956.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.64+8120A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997652 | |||||||
| chr5:52997779 | A | T | 3 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 |
3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.64+8247A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997779 | |||||||
| chr5:52997788 | C | T | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64+8256C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997788 | |||||||
| chr5:52997891 | A | G | 321 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(318): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.64+8359A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997891 | |||||||
| chr5:52997932 | T | G | 1 | a0001c0002t0019g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.64+8400T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997932 | |||||||
| chr5:52997980 | C | G | 2 | a0001c0002t0004g0228 a0001c0002t0004g0256 |
2 | HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.64+8448C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997980 | |||||||
| chr5:52998212 | G | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(46): Show |
50 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.64+8680G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998212 | |||||||
| chr5:52998266 | AC | A | 3 | a0001c0002t0004g0101 a0002c0007t0010g0259 a0002c0007t0010g0260 |
3 | HG02280.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.64+8735delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998266 | |||||||
| chr5:52998386 | G | A | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64+8854G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998386 | |||||||
| chr5:52998446 | C | T | 3 | a0001c0004t0008g0359 a0001c0004t0008g0360 a0001c0004t0008g0361 |
3 | HG01891.hp2 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.64+8914C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998446 | |||||||
| chr5:52998483 | A | G | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64+8951A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998483 | |||||||
| chr5:52998599 | A | G | 232 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
244 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.64+9067A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998599 | |||||||
| chr5:52998721 | T | G | 54 | a0001c0001t0002g0106 a0001c0001t0002g0219 a0001c0001t0002g0220 others(51): Show |
56 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.64+9189T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998721 | |||||||
| chr5:52998727 | T | C | 2 | a0001c0001t0025g0367 a0001c0002t0047g0061 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.64+9195T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998727 | |||||||
| chr5:52998842 | G | A | 1 | a0001c0002t0004g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+9310G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998842 | |||||||
| chr5:52998940 | T | G | 1 | a0001c0002t0009g0208 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.64+9408T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998940 | |||||||
| chr5:52998996 | G | C | 2 | a0001c0002t0006g0038 a0015c0027t0006g0037 |
2 | HG00597.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.64+9464G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998996 | |||||||
| chr5:52999026 | T | C | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(48): Show |
52 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.64+9494T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999026 | |||||||
| chr5:52999054 | T | TAGTAACA others(10): Show |
1 | a0001c0002t0004g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+9522_64+9523ins others(17): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999054 | |||||||
| chr5:52999101 | T | C | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+9569T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999101 | |||||||
| chr5:52999754 | C | A | 3 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 |
3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.64+10222C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999754 | |||||||
| chr5:52999874 | T | C | 58 | a0001c0001t0002g0106 a0001c0001t0002g0219 a0001c0001t0002g0220 others(55): Show |
61 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.64+10342T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999874 | |||||||
| chr5:53000047 | G | A | 63 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
67 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.64+10515G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000047 | |||||||
| chr5:53000139 | GATT | G | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+10609_64+10611d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000139 | ||||||
| chr5:53000401 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64+10869T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000401 | |||||||
| chr5:53000485 | C | T | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+10953C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000485 | |||||||
| chr5:53000573 | T | A | 1 | a0002c0007t0010g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64+11041T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000573 | |||||||
| chr5:53000654 | G | A | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | NA18980.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.64+11122G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000654 | |||||||
| chr5:53000654 | G | T | 232 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
244 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.64+11122G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000654 | |||||||
| chr5:53000804 | C | A | 1 | a0002c0003t0007g0323 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64+11272C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000804 | |||||||
| chr5:53000896 | TG | T | 6 | a0001c0002t0009g0173 a0001c0002t0009g0174 a0001c0002t0009g0175 others(3): Show |
6 | HG00280.hp2 HG06807.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+11365delG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000896 | |||||||
| chr5:53000897 | G | GT | 57 | a0001c0001t0001g0090 a0001c0001t0001g0269 a0001c0001t0001g0281 others(54): Show |
61 | HG00673.hp1 HG01069.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.64+11386dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000897 | ||||||
| chr5:53000897 | G | GTT | 12 | a0001c0001t0001g0068 a0001c0001t0002g0307 a0001c0001t0002g0309 others(9): Show |
13 | HG00280.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+11385_64+11386d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000897 | ||||||
| chr5:53000897 | G | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0089 a0001c0001t0001g0094 others(11): Show |
14 | HG01099.hp2 HG01891.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+11365G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000897 | |||||||
| chr5:53000897 | GT | G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(59): Show |
65 | HG00140.hp1 HG00609.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.64+11386delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000897 | ||||||
| chr5:53000897 | GTT | G | 5 | a0001c0001t0001g0006 a0001c0008t0012g0159 a0001c0008t0012g0160 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+11385_64+11386d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000897 | ||||||
| chr5:53000978 | T | C | 59 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0134 others(56): Show |
63 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.64+11446T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000978 | |||||||
| chr5:53001057 | A | G | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+11525A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001057 | |||||||
| chr5:53001059 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG00673.hp2 HG01081.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+11527G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001059 | |||||||
| chr5:53001163 | A | G | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+11631A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001163 | |||||||
| chr5:53001290 | C | T | 1 | a0001c0002t0003g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64+11758C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001290 | |||||||
| chr5:53001412 | C | T | 257 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(254): Show |
275 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.64+11880C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001412 | |||||||
| chr5:53001538 | G | A | 1 | a0001c0002t0004g0264 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64+12006G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001538 | |||||||
| chr5:53001558 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64+12026G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001558 | |||||||
| chr5:53001744 | G | A | 53 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(50): Show |
55 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.64+12212G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001744 | |||||||
| chr5:53001813 | T | TA | 45 | a0001c0001t0001g0269 a0001c0001t0001g0281 a0001c0001t0001g0282 others(42): Show |
49 | HG00280.hp1 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.64+12304dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53001813 | ||||||
| chr5:53001813 | TA | T | 108 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(105): Show |
111 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.64+12304delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53001813 | ||||||
| chr5:53001842 | C | G | 1 | a0004c0006t0003g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64+12310C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001842 | |||||||
| chr5:53002053 | A | T | 2 | a0001c0001t0005g0287 a0001c0001t0005g0288 |
2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.64+12521A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002053 | |||||||
| chr5:53002102 | G | T | 1 | a0001c0002t0028g0204 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.64+12570G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002102 | |||||||
| chr5:53002121 | A | G | 42 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(39): Show |
44 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.64+12589A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002121 | |||||||
| chr5:53002126 | A | T | 2 | a0001c0001t0005g0286 a0001c0001t0005g0311 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.64+12594A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002126 | |||||||
| chr5:53002458 | C | A | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+12926C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002458 | |||||||
| chr5:53002784 | C | T | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+13252C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002784 | |||||||
| chr5:53002967 | A | T | 1 | a0010c0017t0052g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+13435A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002967 | |||||||
| chr5:53003059 | A | G | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+13527A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003059 | |||||||
| chr5:53003227 | G | A | 2 | a0001c0001t0025g0367 a0001c0002t0047g0061 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.64+13695G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003227 | |||||||
| chr5:53003348 | T | C | 6 | a0004c0006t0003g0017 a0004c0006t0003g0166 a0004c0006t0003g0169 others(3): Show |
7 | NA18947.hp1 NA18970.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+13816T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003348 | |||||||
| chr5:53003796 | C | T | 4 | a0001c0001t0005g0005 a0001c0001t0005g0284 a0001c0001t0005g0300 others(1): Show |
6 | HG01069.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+14264C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003796 | |||||||
| chr5:53003847 | G | A | 3 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 |
3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+14315G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003847 | |||||||
| chr5:53003884 | G | A | 1 | a0001c0002t0018g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.64+14352G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003884 | |||||||
| chr5:53003941 | C | T | 2 | a0001c0002t0018g0102 a0001c0002t0018g0104 |
2 | HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.64+14409C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003941 | |||||||
| chr5:53004083 | T | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+14551T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004083 | |||||||
| chr5:53004093 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.64+14561A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004093 | |||||||
| chr5:53004188 | A | T | 1 | a0002c0003t0026g0364 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64+14656A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004188 | |||||||
| chr5:53004275 | G | T | 1 | a0001c0002t0004g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64+14743G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004275 | |||||||
| chr5:53004367 | G | A | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+14835G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004367 | |||||||
| chr5:53004416 | T | C | 367 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(364): Show |
390 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.64+14884T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004416 | |||||||
| chr5:53004444 | G | A | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+14912G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004444 | |||||||
| chr5:53004743 | AGCAGTTG others(5): Show |
A | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+15213_64+15224d others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004743 | ||||||
| chr5:53004783 | T | C | 2 | a0002c0003t0007g0319 a0002c0003t0007g0320 |
2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.64+15251T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004783 | |||||||
| chr5:53004894 | G | GT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0033 others(17): Show |
22 | HG00673.hp2 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.64+15401dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | G | GTT | 7 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0023g0340 others(4): Show |
7 | HG01978.hp2 HG02015.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+15400_64+15401d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | G | GTTTTTTT others(3): Show |
1 | a0010c0017t0052g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+15392_64+15401d others(12): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | G | T | 1 | a0001c0001t0001g0023 | 2 | NA18975.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.64+15362G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004894 | |||||||
| chr5:53004894 | GT | G | 32 | a0001c0001t0001g0181 a0001c0001t0005g0261 a0001c0002t0003g0032 others(29): Show |
33 | HG00280.hp2 HG00609.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.64+15401delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTT | G | 8 | a0002c0009t0016g0315 a0003c0005t0003g0018 a0003c0005t0003g0019 others(5): Show |
9 | HG02071.hp2 NA18964.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+15396_64+15401d others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(2): Show |
G | 11 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0083 others(8): Show |
12 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.64+15393_64+15401d others(11): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(3): Show |
G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(40): Show |
44 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.64+15392_64+15401d others(12): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0001g0090 a0001c0001t0001g0223 a0001c0004t0008g0298 others(3): Show |
6 | HG02897.hp1 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+15391_64+15401d others(13): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(5): Show |
G | 14 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0005g0283 others(11): Show |
14 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+15390_64+15401d others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(6): Show |
G | 46 | a0001c0001t0001g0134 a0001c0001t0001g0269 a0001c0001t0001g0305 others(43): Show |
50 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.64+15389_64+15401d others(15): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(7): Show |
G | 64 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0116 others(61): Show |
68 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.64+15388_64+15401d others(16): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(8): Show |
G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0146 others(18): Show |
27 | HG00408.hp1 HG00733.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.64+15387_64+15401d others(17): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(9): Show |
G | 8 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(5): Show |
8 | HG01516.hp2 HG02074.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+15386_64+15401d others(18): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(10): Show |
G | 32 | a0001c0001t0002g0247 a0001c0002t0004g0004 a0001c0002t0004g0105 others(29): Show |
34 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+15385_64+15401d others(19): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004894 | GTTTTTTT others(12): Show |
G | 1 | a0002c0003t0026g0364 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64+15383_64+15401d others(21): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | ||||||
| chr5:53004902 | T | G | 3 | a0002c0003t0007g0210 a0002c0003t0007g0211 a0002c0003t0007g0212 |
3 | HG02055.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.64+15370T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004902 | |||||||
| chr5:53004908 | T | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+15376T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004908 | |||||||
| chr5:53004909 | T | G | 1 | a0002c0003t0007g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64+15377T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004909 | |||||||
| chr5:53004918 | T | G | 1 | a0001c0001t0024g0213 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.64+15386T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004918 | |||||||
| chr5:53004925 | T | C | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+15393T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004925 | |||||||
| chr5:53005021 | T | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0281 a0001c0001t0001g0282 |
3 | NA18963.hp1 NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.64+15489T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005021 | |||||||
| chr5:53005037 | A | T | 56 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(53): Show |
59 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.64+15505A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005037 | |||||||
| chr5:53005060 | T | C | 6 | a0001c0001t0005g0261 a0001c0002t0004g0101 a0002c0007t0010g0259 others(3): Show |
6 | HG02280.hp1 HG02647.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+15528T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005060 | |||||||
| chr5:53005121 | G | C | 1 | a0011c0015t0002g0370 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.64+15589G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005121 | |||||||
| chr5:53005123 | T | C | 3 | a0001c0001t0002g0362 a0002c0003t0026g0363 a0002c0003t0026g0364 |
3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+15591T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005123 | |||||||
| chr5:53005217 | G | A | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | NA18978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.64+15685G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005217 | |||||||
| chr5:53005247 | A | G | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+15715A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005247 | |||||||
| chr5:53005252 | C | T | 1 | a0001c0002t0004g0252 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.64+15720C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005252 | |||||||
| chr5:53005261 | C | T | 41 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(38): Show |
43 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.64+15729C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005261 | |||||||
| chr5:53005580 | C | CA | 6 | a0001c0001t0002g0221 a0001c0008t0012g0159 a0001c0008t0012g0160 others(3): Show |
7 | HG02109.hp2 HG02523.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+16064dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53005580 | ||||||
| chr5:53005580 | C | CAA | 45 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0247 others(42): Show |
47 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.64+16063_64+16064d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53005580 | ||||||
| chr5:53005580 | CA | C | 262 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(259): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.64+16064delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53005580 | ||||||
| chr5:53005625 | C | T | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+16093C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005625 | |||||||
| chr5:53005709 | C | T | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64+16177C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005709 | |||||||
| chr5:53005730 | G | T | 1 | a0001c0001t0002g0141 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64+16198G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005730 | |||||||
| chr5:53005786 | T | C | 3 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 |
3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.64+16254T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005786 | |||||||
| chr5:53005886 | C | T | 91 | a0001c0001t0001g0269 a0001c0001t0001g0281 a0001c0001t0001g0282 others(88): Show |
98 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.64+16354C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005886 | |||||||
| chr5:53005918 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+16386C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005918 | |||||||
| chr5:53005983 | G | T | 4 | a0001c0001t0002g0362 a0001c0001t0025g0367 a0001c0002t0047g0061 others(1): Show |
4 | HG02559.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+16451G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005983 | |||||||
| chr5:53006012 | T | C | 2 | a0001c0002t0003g0178 a0001c0002t0003g0205 |
2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.64+16480T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006012 | |||||||
| chr5:53006029 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64+16497C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006029 | |||||||
| chr5:53006030 | G | A | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.64+16498G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006030 | |||||||
| chr5:53006212 | A | T | 1 | a0001c0002t0004g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64+16680A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006212 | |||||||
| chr5:53006224 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.64+16692A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006224 | |||||||
| chr5:53006497 | A | AAGAGG | 3 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0013g0011 |
3 | NA18959.hp1 NA18981.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.64+16967_64+16971d others(7): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53006497 | ||||||
| chr5:53006598 | AATT | A | 3 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 |
3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+17073_64+17075d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53006598 | ||||||
| chr5:53006663 | C | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0001g0089 others(11): Show |
14 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+17131C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006663 | |||||||
| chr5:53006709 | T | C | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+17177T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006709 | |||||||
| chr5:53006857 | A | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+17325A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006857 | |||||||
| chr5:53006863 | A | C | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+17331A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006863 | |||||||
| chr5:53007385 | G | T | 1 | a0001c0001t0005g0283 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.64+17853G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007385 | |||||||
| chr5:53007456 | G | A | 2 | a0001c0002t0018g0102 a0001c0002t0018g0104 |
2 | HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.64+17924G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007456 | |||||||
| chr5:53007467 | T | C | 2 | a0001c0001t0005g0308 a0001c0001t0005g0310 |
2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.64+17935T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007467 | |||||||
| chr5:53007515 | G | A | 62 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0301 others(59): Show |
66 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.64+17983G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007515 | |||||||
| chr5:53007596 | T | C | 1 | a0001c0001t0001g0301 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.64+18064T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007596 | |||||||
| chr5:53007674 | A | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+18142A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007674 | |||||||
| chr5:53007721 | G | A | 8 | a0003c0005t0003g0018 a0003c0005t0003g0019 a0003c0005t0003g0176 others(5): Show |
9 | HG02071.hp2 NA18964.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+18189G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007721 | |||||||
| chr5:53007733 | A | C | 1 | a0002c0007t0010g0260 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64+18201A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007733 | |||||||
| chr5:53007826 | G | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64+18294G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007826 | |||||||
| chr5:53008087 | G | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64+18555G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008087 | |||||||
| chr5:53008095 | A | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+18563A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008095 | |||||||
| chr5:53008130 | G | C | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+18598G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008130 | |||||||
| chr5:53008248 | C | T | 3 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 |
3 | HG02818.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-18500C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008248 | |||||||
| chr5:53008289 | G | A | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-18459G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008289 | |||||||
| chr5:53008301 | G | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.65-18447G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008301 | |||||||
| chr5:53008423 | G | A | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-18325G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008423 | |||||||
| chr5:53008523 | C | T | 1 | a0001c0002t0004g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.65-18225C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008523 | |||||||
| chr5:53008625 | G | T | 2 | a0001c0001t0005g0279 a0001c0001t0005g0280 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.65-18123G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008625 | |||||||
| chr5:53008642 | GTC | G | 254 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(251): Show |
272 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.65-18094_65-18093d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53008642 | ||||||
| chr5:53009166 | A | G | 115 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(112): Show |
120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.65-17582A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009166 | |||||||
| chr5:53009489 | A | T | 1 | a0004c0020t0003g0130 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.65-17259A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009489 | |||||||
| chr5:53009643 | G | T | 5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(2): Show |
5 | HG02080.hp2 HG02129.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-17105G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009643 | |||||||
| chr5:53009651 | A | G | 1 | a0002c0003t0007g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.65-17097A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009651 | |||||||
| chr5:53009721 | A | C | 3 | a0001c0002t0003g0199 a0001c0002t0003g0200 a0001c0002t0003g0201 |
3 | HG01515.hp1 HG01517.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.65-17027A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009721 | |||||||
| chr5:53009807 | C | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-16941C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009807 | |||||||
| chr5:53009975 | C | T | 1 | a0001c0001t0001g0330 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.65-16773C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009975 | |||||||
| chr5:53009976 | G | A | 3 | a0001c0002t0004g0101 a0002c0007t0010g0259 a0002c0007t0010g0260 |
3 | HG02280.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.65-16772G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009976 | |||||||
| chr5:53010055 | T | C | 1 | a0001c0002t0006g0035 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.65-16693T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010055 | |||||||
| chr5:53010183 | C | A | 62 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0301 others(59): Show |
66 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.65-16565C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010183 | |||||||
| chr5:53010214 | A | T | 49 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(46): Show |
51 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.65-16534A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010214 | |||||||
| chr5:53010549 | C | T | 5 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 others(2): Show |
5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-16199C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010549 | |||||||
| chr5:53010550 | C | G | 1 | a0001c0001t0002g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.65-16198C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010550 | |||||||
| chr5:53010760 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(51): Show |
55 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.65-15988G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010760 | |||||||
| chr5:53010863 | G | C | 2 | a0001c0002t0006g0038 a0015c0027t0006g0037 |
2 | HG00597.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.65-15885G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010863 | |||||||
| chr5:53011007 | C | G | 1 | a0001c0001t0025g0366 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.65-15741C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011007 | |||||||
| chr5:53011316 | A | G | 1 | a0003c0005t0003g0270 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65-15432A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011316 | |||||||
| chr5:53011342 | G | A | 2 | a0001c0001t0002g0156 a0001c0001t0002g0266 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.65-15406G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011342 | |||||||
| chr5:53011454 | C | T | 2 | a0001c0001t0002g0362 a0001c0002t0047g0061 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-15294C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011454 | |||||||
| chr5:53011455 | G | C | 1 | a0001c0001t0013g0139 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.65-15293G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011455 | |||||||
| chr5:53011540 | C | T | 55 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(52): Show |
57 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.65-15208C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011540 | |||||||
| chr5:53011736 | T | TG | 52 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(49): Show |
54 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.65-15005dupG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53011736 | ||||||
| chr5:53011795 | C | T | 1 | a0001c0001t0001g0330 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.65-14953C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011795 | |||||||
| chr5:53012235 | G | A | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-14513G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012235 | |||||||
| chr5:53012544 | T | C | 127 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
133 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.65-14204T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012544 | |||||||
| chr5:53012554 | A | G | 1 | a0002c0003t0007g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.65-14194A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012554 | |||||||
| chr5:53012605 | G | A | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-14143G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012605 | |||||||
| chr5:53012660 | C | A | 3 | a0001c0002t0004g0231 a0001c0002t0004g0235 a0001c0002t0004g0252 |
3 | HG02615.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.65-14088C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012660 | |||||||
| chr5:53012758 | CA | C | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-13989delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012758 | |||||||
| chr5:53012805 | G | A | 4 | a0001c0002t0004g0264 a0001c0002t0019g0229 a0001c0002t0019g0236 others(1): Show |
4 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-13943G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012805 | |||||||
| chr5:53013024 | C | T | 1 | a0001c0001t0015g0157 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.65-13724C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013024 | |||||||
| chr5:53013097 | T | C | 2 | a0001c0001t0005g0005 a0001c0001t0005g0300 |
4 | HG03490.hp2 HG03492.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-13651T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013097 | |||||||
| chr5:53013185 | C | T | 127 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
133 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.65-13563C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013185 | |||||||
| chr5:53013190 | T | C | 1 | a0001c0002t0004g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-13558T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013190 | |||||||
| chr5:53013374 | C | CT | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(58): Show |
63 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.65-13361dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53013374 | ||||||
| chr5:53013397 | G | T | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-13351G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013397 | |||||||
| chr5:53013459 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.65-13289T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013459 | |||||||
| chr5:53013491 | T | C | 1 | a0001c0004t0008g0290 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.65-13257T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013491 | |||||||
| chr5:53013557 | G | C | 2 | a0001c0013t0001g0312 a0001c0014t0003g0064 |
2 | HG00544.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.65-13191G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013557 | |||||||
| chr5:53013663 | G | C | 38 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(35): Show |
40 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.65-13085G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013663 | |||||||
| chr5:53013808 | A | T | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.65-12940A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013808 | |||||||
| chr5:53013812 | C | A | 1 | a0001c0001t0002g0158 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.65-12936C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013812 | |||||||
| chr5:53013841 | A | G | 2 | a0002c0003t0026g0363 a0002c0003t0026g0364 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-12907A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013841 | |||||||
| chr5:53013845 | A | G | 61 | a0001c0001t0001g0269 a0001c0001t0001g0281 a0001c0001t0001g0282 others(58): Show |
65 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.65-12903A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013845 | |||||||
| chr5:53013909 | G | A | 64 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(61): Show |
68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.65-12839G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013909 | |||||||
| chr5:53014041 | T | C | 5 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 others(2): Show |
5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-12707T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014041 | |||||||
| chr5:53014103 | T | C | 5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(2): Show |
5 | HG02080.hp2 HG02129.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-12645T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014103 | |||||||
| chr5:53014147 | C | G | 8 | a0001c0011t0034g0084 a0002c0003t0017g0024 a0002c0003t0017g0025 others(5): Show |
8 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-12601C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014147 | |||||||
| chr5:53014168 | G | A | 6 | a0001c0011t0034g0084 a0002c0003t0017g0024 a0002c0003t0017g0025 others(3): Show |
6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-12580G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014168 | |||||||
| chr5:53014345 | C | T | 50 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(47): Show |
52 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.65-12403C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014345 | |||||||
| chr5:53014523 | G | A | 6 | a0001c0011t0034g0084 a0002c0003t0017g0024 a0002c0003t0017g0025 others(3): Show |
6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-12225G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014523 | |||||||
| chr5:53014580 | C | A | 1 | a0001c0002t0006g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.65-12168C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014580 | |||||||
| chr5:53014719 | G | T | 26 | a0001c0002t0042g0296 a0001c0004t0002g0329 a0001c0004t0008g0290 others(23): Show |
26 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.65-12029G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014719 | |||||||
| chr5:53014823 | A | C | 57 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(54): Show |
59 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.65-11925A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014823 | |||||||
| chr5:53015146 | T | C | 49 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(46): Show |
51 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.65-11602T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015146 | |||||||
| chr5:53015162 | G | A | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-11586G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015162 | |||||||
| chr5:53015333 | A | G | 341 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(338): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.65-11415A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015333 | |||||||
| chr5:53015471 | AT | A | 328 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(325): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.65-11266delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53015471 | ||||||
| chr5:53015471 | ATT | A | 9 | a0001c0001t0005g0261 a0001c0002t0004g0101 a0002c0007t0010g0162 others(6): Show |
9 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-11267_65-11266d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53015471 | ||||||
| chr5:53015493 | G | A | 33 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(30): Show |
35 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.65-11255G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015493 | |||||||
| chr5:53015786 | C | T | 11 | a0001c0001t0001g0227 a0001c0002t0003g0168 a0001c0002t0003g0178 others(8): Show |
11 | HG00609.hp1 NA18612.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-10962C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015786 | |||||||
| chr5:53015908 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-10840T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015908 | |||||||
| chr5:53015926 | CT | C | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(48): Show |
52 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.65-10821delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015926 | |||||||
| chr5:53016019 | C | T | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-10729C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016019 | |||||||
| chr5:53016086 | C | T | 1 | a0002c0003t0007g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.65-10662C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016086 | |||||||
| chr5:53016136 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.65-10612T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016136 | |||||||
| chr5:53016173 | A | G | 1 | a0001c0002t0003g0182 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.65-10575A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016173 | |||||||
| chr5:53016404 | T | C | 6 | a0001c0011t0034g0084 a0002c0003t0017g0024 a0002c0003t0017g0025 others(3): Show |
6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-10344T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016404 | |||||||
| chr5:53016521 | G | T | 64 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(61): Show |
68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.65-10227G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016521 | |||||||
| chr5:53016592 | A | G | 193 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(190): Show |
203 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.65-10156A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016592 | |||||||
| chr5:53016613 | T | C | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(46): Show |
50 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.65-10135T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016613 | |||||||
| chr5:53016667 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-10081T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016667 | |||||||
| chr5:53016673 | A | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-10075A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016673 | |||||||
| chr5:53016792 | T | C | 1 | a0002c0003t0026g0364 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-9956T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016792 | |||||||
| chr5:53016800 | C | T | 1 | a0001c0001t0036g0278 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.65-9948C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016800 | |||||||
| chr5:53016880 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.65-9868T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016880 | |||||||
| chr5:53016969 | T | C | 5 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 others(2): Show |
5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-9779T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016969 | |||||||
| chr5:53016985 | A | G | 3 | a0001c0002t0003g0186 a0001c0002t0003g0197 a0001c0002t0003g0198 |
3 | NA18989.hp1 NA19004.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.65-9763A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016985 | |||||||
| chr5:53017448 | T | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.65-9300T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017448 | |||||||
| chr5:53017681 | G | T | 2 | a0001c0001t0001g0086 a0001c0002t0004g0088 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.65-9067G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017681 | |||||||
| chr5:53017734 | G | A | 128 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0269 others(125): Show |
136 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.65-9014G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017734 | |||||||
| chr5:53017760 | T | C | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-8988T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017760 | |||||||
| chr5:53017991 | G | A | 1 | a0001c0002t0003g0032 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.65-8757G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017991 | |||||||
| chr5:53017998 | A | G | 38 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(35): Show |
40 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.65-8750A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017998 | |||||||
| chr5:53018217 | C | T | 45 | a0001c0001t0001g0301 a0001c0001t0001g0303 a0001c0001t0001g0304 others(42): Show |
47 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.65-8531C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018217 | |||||||
| chr5:53018222 | G | A | 2 | a0001c0001t0002g0362 a0001c0002t0047g0061 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-8526G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018222 | |||||||
| chr5:53018474 | T | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-8274T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018474 | |||||||
| chr5:53018494 | C | G | 1 | a0001c0001t0033g0339 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.65-8254C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018494 | |||||||
| chr5:53018552 | A | T | 64 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(61): Show |
68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.65-8196A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018552 | |||||||
| chr5:53018829 | C | T | 1 | a0001c0001t0005g0277 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.65-7919C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018829 | |||||||
| chr5:53018861 | C | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0313 |
2 | NA18946.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.65-7887C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018861 | |||||||
| chr5:53018962 | G | A | 2 | a0001c0001t0005g0287 a0001c0001t0005g0288 |
2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.65-7786G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018962 | |||||||
| chr5:53018972 | G | C | 1 | a0001c0001t0051g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.65-7776G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018972 | |||||||
| chr5:53018993 | G | A | 61 | a0001c0001t0001g0269 a0001c0001t0001g0281 a0001c0001t0001g0282 others(58): Show |
65 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.65-7755G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018993 | |||||||
| chr5:53019011 | C | T | 1 | a0001c0002t0006g0046 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.65-7737C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019011 | |||||||
| chr5:53019065 | A | AAAAT | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(58): Show |
63 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.65-7659_65-7656dup others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53019065 | ||||||
| chr5:53019065 | A | AAAATAAA others(1): Show |
3 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 |
3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.65-7663_65-7656dup others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53019065 | ||||||
| chr5:53019094 | G | A | 11 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0039 others(8): Show |
15 | HG01257.hp2 HG01496.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.65-7654G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019094 | |||||||
| chr5:53019147 | TA | T | 6 | a0001c0011t0034g0084 a0002c0003t0017g0024 a0002c0003t0017g0025 others(3): Show |
6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-7594delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53019147 | ||||||
| chr5:53019282 | T | C | 52 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(49): Show |
54 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.65-7466T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019282 | |||||||
| chr5:53019283 | A | G | 1 | a0002c0003t0017g0026 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.65-7465A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019283 | |||||||
| chr5:53019563 | T | C | 1 | a0001c0002t0004g0257 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.65-7185T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019563 | |||||||
| chr5:53019668 | G | C | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-7080G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019668 | |||||||
| chr5:53019673 | G | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.65-7075G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019673 | |||||||
| chr5:53019723 | C | G | 1 | a0002c0003t0007g0334 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.65-7025C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019723 | |||||||
| chr5:53019757 | C | T | 4 | a0001c0001t0005g0014 a0001c0001t0005g0133 a0004c0020t0003g0130 others(1): Show |
5 | HG02040.hp1 NA18940.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-6991C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019757 | |||||||
| chr5:53019762 | G | T | 1 | a0002c0003t0007g0021 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.65-6986G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019762 | |||||||
| chr5:53019852 | G | A | 2 | a0001c0002t0018g0102 a0001c0002t0018g0104 |
2 | HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.65-6896G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019852 | |||||||
| chr5:53019994 | A | G | 1 | a0014c0025t0003g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.65-6754A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019994 | |||||||
| chr5:53020189 | C | T | 1 | a0001c0002t0004g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.65-6559C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020189 | |||||||
| chr5:53020211 | A | C | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-6537A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020211 | |||||||
| chr5:53020342 | C | T | 128 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0269 others(125): Show |
136 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.65-6406C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020342 | |||||||
| chr5:53020486 | C | T | 3 | a0001c0001t0001g0181 a0001c0002t0003g0194 a0001c0002t0003g0195 |
3 | HG01106.hp2 HG02698.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.65-6262C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020486 | |||||||
| chr5:53020655 | C | T | 1 | a0001c0002t0003g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.65-6093C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020655 | |||||||
| chr5:53020689 | T | A | 45 | a0001c0001t0001g0324 a0001c0001t0002g0219 a0001c0001t0002g0220 others(42): Show |
47 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.65-6059T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020689 | |||||||
| chr5:53020848 | A | AT | 13 | a0001c0001t0001g0071 a0001c0001t0001g0098 a0001c0001t0002g0158 others(10): Show |
13 | HG01074.hp1 HG02015.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-5882dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53020848 | ||||||
| chr5:53020985 | G | A | 1 | a0001c0002t0004g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.65-5763G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020985 | |||||||
| chr5:53021137 | G | A | 1 | a0001c0001t0051g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.65-5611G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021137 | |||||||
| chr5:53021182 | A | G | 3 | a0001c0001t0014g0275 a0001c0001t0014g0276 a0001c0001t0014g0347 |
3 | NA18939.hp2 NA18951.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.65-5566A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021182 | |||||||
| chr5:53021227 | C | T | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.65-5521C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021227 | |||||||
| chr5:53021269 | T | C | 2 | a0002c0007t0010g0162 a0002c0007t0010g0163 |
2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-5479T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021269 | |||||||
| chr5:53021318 | A | G | 30 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(27): Show |
32 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-5430A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021318 | |||||||
| chr5:53021397 | T | C | 1 | a0001c0001t0015g0254 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.65-5351T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021397 | |||||||
| chr5:53021424 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.65-5324C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021424 | |||||||
| chr5:53021428 | C | G | 1 | a0001c0004t0002g0329 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.65-5320C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021428 | |||||||
| chr5:53021487 | C | T | 2 | a0001c0001t0002g0362 a0001c0002t0047g0061 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-5261C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021487 | |||||||
| chr5:53021775 | C | G | 1 | a0001c0001t0022g0045 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.65-4973C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021775 | |||||||
| chr5:53021883 | C | T | 1 | a0001c0002t0004g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.65-4865C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021883 | |||||||
| chr5:53022009 | T | C | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-4739T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022009 | |||||||
| chr5:53022024 | A | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-4724A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022024 | |||||||
| chr5:53022083 | A | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-4665A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022083 | |||||||
| chr5:53022086 | A | G | 1 | a0001c0002t0019g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.65-4662A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022086 | |||||||
| chr5:53022127 | A | G | 3 | a0001c0002t0003g0167 a0001c0002t0003g0182 a0001c0002t0003g0209 |
3 | HG00741.hp2 HG01433.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.65-4621A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022127 | |||||||
| chr5:53022208 | A | AT | 111 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(108): Show |
123 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.65-4529dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53022208 | ||||||
| chr5:53022218 | T | TG | 3 | a0001c0001t0002g0247 a0001c0001t0025g0367 a0001c0002t0048g0238 |
3 | HG00642.hp2 HG02559.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.65-4530_65-4529ins others(1): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022218 | |||||||
| chr5:53022219 | T | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(66): Show |
73 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.65-4529T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022219 | |||||||
| chr5:53022219 | T | TG | 144 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0076 others(141): Show |
150 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.65-4524dupG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53022219 | ||||||
| chr5:53022342 | G | C | 1 | a0001c0001t0002g0117 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.65-4406G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022342 | |||||||
| chr5:53022777 | GAC | G | 3 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 |
3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.65-3970_65-3969del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022777 | |||||||
| chr5:53022881 | T | C | 1 | a0001c0001t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.65-3867T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022881 | |||||||
| chr5:53022916 | A | G | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.65-3832A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022916 | |||||||
| chr5:53023076 | G | T | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-3672G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023076 | |||||||
| chr5:53023086 | C | T | 66 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(63): Show |
70 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-3662C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023086 | |||||||
| chr5:53023226 | T | G | 50 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(47): Show |
52 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.65-3522T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023226 | |||||||
| chr5:53023246 | C | T | 194 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
204 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.65-3502C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023246 | |||||||
| chr5:53023412 | C | A | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.65-3336C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023412 | |||||||
| chr5:53023464 | A | G | 1 | a0001c0001t0024g0285 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.65-3284A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023464 | |||||||
| chr5:53023532 | T | C | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-3216T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023532 | |||||||
| chr5:53023661 | T | A | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-3087T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023661 | |||||||
| chr5:53023769 | T | C | 6 | a0001c0002t0004g0101 a0002c0007t0010g0162 a0002c0007t0010g0163 others(3): Show |
6 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-2979T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023769 | |||||||
| chr5:53024020 | T | C | 6 | a0001c0011t0034g0084 a0002c0003t0017g0024 a0002c0003t0017g0025 others(3): Show |
6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-2728T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024020 | |||||||
| chr5:53024112 | G | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.65-2636G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024112 | |||||||
| chr5:53024199 | A | G | 67 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0301 others(64): Show |
71 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.65-2549A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024199 | |||||||
| chr5:53024325 | G | A | 2 | a0001c0001t0005g0308 a0001c0001t0005g0310 |
2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.65-2423G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024325 | |||||||
| chr5:53024403 | T | G | 4 | a0001c0001t0001g0326 a0001c0001t0001g0335 a0001c0001t0013g0325 others(1): Show |
4 | HG00408.hp2 NA18962.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2345T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024403 | |||||||
| chr5:53024490 | A | G | 3 | a0002c0003t0007g0210 a0002c0003t0007g0211 a0002c0003t0007g0212 |
3 | HG02055.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.65-2258A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024490 | |||||||
| chr5:53024493 | A | C | 2 | a0001c0001t0025g0366 a0001c0021t0050g0365 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.65-2255A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024493 | |||||||
| chr5:53024501 | T | A | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-2247T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024501 | |||||||
| chr5:53024689 | T | C | 1 | a0010c0017t0052g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-2059T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024689 | |||||||
| chr5:53024761 | A | C | 1 | a0001c0002t0004g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.65-1987A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024761 | |||||||
| chr5:53024900 | G | T | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-1848G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024900 | |||||||
| chr5:53024919 | T | C | 137 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0269 others(134): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.65-1829T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024919 | |||||||
| chr5:53025063 | T | C | 272 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(269): Show |
290 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.65-1685T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025063 | |||||||
| chr5:53025110 | G | A | 57 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(54): Show |
59 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.65-1638G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025110 | |||||||
| chr5:53025129 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0013g0139 |
2 | NA19000.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.65-1619C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025129 | |||||||
| chr5:53025197 | A | G | 3 | a0001c0002t0004g0101 a0002c0007t0010g0259 a0002c0007t0010g0260 |
3 | HG02280.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.65-1551A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025197 | |||||||
| chr5:53025209 | T | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(22): Show |
31 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.65-1539T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025209 | |||||||
| chr5:53025352 | A | C | 1 | a0001c0001t0038g0127 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.65-1396A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025352 | |||||||
| chr5:53025531 | C | T | 7 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 others(4): Show |
7 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-1217C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025531 | |||||||
| chr5:53025591 | A | G | 1 | a0001c0002t0006g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.65-1157A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025591 | |||||||
| chr5:53025602 | G | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(50): Show |
54 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.65-1146G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025602 | |||||||
| chr5:53025978 | A | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-770A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025978 | |||||||
| chr5:53026045 | T | C | 2 | a0001c0001t0002g0362 a0001c0002t0047g0061 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-703T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026045 | |||||||
| chr5:53026217 | C | A | 1 | a0003c0005t0003g0270 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65-531C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026217 | |||||||
| chr5:53026280 | G | A | 10 | a0001c0002t0003g0168 a0001c0002t0003g0178 a0001c0002t0003g0183 others(7): Show |
10 | HG00609.hp1 NA18612.hp1 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-468G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026280 | |||||||
| chr5:53026306 | C | A | 2 | a0001c0001t0005g0286 a0001c0001t0005g0311 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.65-442C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026306 | |||||||
| chr5:53026366 | C | T | 5 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 others(2): Show |
5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-382C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026366 | |||||||
| chr5:53026412 | A | T | 1 | a0001c0002t0004g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.65-336A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026412 | |||||||
| chr5:53026539 | G | A | 6 | a0001c0002t0004g0232 a0001c0002t0004g0239 a0001c0002t0004g0264 others(3): Show |
6 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-209G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026539 | |||||||
| chr5:53026577 | C | T | 4 | a0002c0003t0007g0323 a0002c0003t0007g0333 a0002c0003t0007g0341 others(1): Show |
4 | NA18989.hp2 NA19056.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-171C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026577 | |||||||
| chr5:53026691 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.65-57C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026691 | |||||||
| chr5:53026694 | C | T | 5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(2): Show |
5 | HG02080.hp2 HG02129.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-54C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026694 | |||||||
| chr5:53026891 | G | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0055 others(89): Show |
97 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.185+23G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53026891 | |||||||
| chr5:53026956 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.185+88G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53026956 | |||||||
| chr5:53027152 | T | TGATA | 53 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(50): Show |
55 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.185+287_185+290dup others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53027152 | ||||||
| chr5:53027182 | G | T | 5 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 others(2): Show |
5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+314G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027182 | |||||||
| chr5:53027276 | A | C | 1 | a0001c0002t0003g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.185+408A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027276 | |||||||
| chr5:53027414 | G | A | 2 | a0001c0002t0006g0111 a0001c0002t0006g0354 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.185+546G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027414 | |||||||
| chr5:53027623 | C | A | 118 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0269 others(115): Show |
123 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.185+755C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027623 | |||||||
| chr5:53027738 | A | G | 224 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(221): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.185+870A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027738 | |||||||
| chr5:53027790 | C | T | 4 | a0001c0011t0034g0084 a0002c0009t0016g0315 a0002c0009t0016g0316 others(1): Show |
4 | HG06807.hp1 NA18961.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+922C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027790 | |||||||
| chr5:53027890 | G | C | 8 | a0001c0002t0004g0101 a0002c0007t0010g0162 a0002c0007t0010g0163 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+1022G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027890 | |||||||
| chr5:53027927 | G | A | 304 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(301): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.185+1059G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027927 | |||||||
| chr5:53028099 | A | C | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+1231A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028099 | |||||||
| chr5:53028655 | C | T | 1 | a0001c0002t0003g0167 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.185+1787C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028655 | |||||||
| chr5:53028675 | C | T | 8 | a0001c0002t0004g0101 a0002c0007t0010g0162 a0002c0007t0010g0163 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+1807C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028675 | |||||||
| chr5:53028724 | C | T | 1 | a0001c0001t0005g0283 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.185+1856C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028724 | |||||||
| chr5:53028829 | C | T | 9 | a0001c0002t0003g0168 a0001c0002t0003g0178 a0001c0002t0003g0183 others(6): Show |
9 | HG00609.hp1 NA18612.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+1961C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028829 | |||||||
| chr5:53028851 | T | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.185+1983T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028851 | |||||||
| chr5:53028868 | C | T | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+2000C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028868 | |||||||
| chr5:53028886 | G | A | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.185+2018G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028886 | |||||||
| chr5:53029023 | G | C | 5 | a0001c0002t0018g0102 a0001c0002t0018g0104 a0001c0002t0018g0118 others(2): Show |
5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+2155G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029023 | |||||||
| chr5:53029141 | G | A | 8 | a0001c0002t0004g0101 a0002c0007t0010g0162 a0002c0007t0010g0163 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+2273G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029141 | |||||||
| chr5:53029211 | G | T | 2 | a0001c0002t0004g0232 a0001c0002t0004g0239 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.185+2343G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029211 | |||||||
| chr5:53029230 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | NA18940.hp2 NA18991.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.185+2362C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029230 | |||||||
| chr5:53029239 | T | A | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.185+2371T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029239 | |||||||
| chr5:53029484 | G | A | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+2616G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029484 | |||||||
| chr5:53029575 | T | C | 26 | a0001c0016t0005g0103 a0002c0003t0007g0022 a0002c0003t0007g0073 others(23): Show |
27 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.185+2707T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029575 | |||||||
| chr5:53029582 | A | G | 1 | a0001c0001t0002g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.185+2714A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029582 | |||||||
| chr5:53029945 | C | T | 112 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(109): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.185+3077C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029945 | |||||||
| chr5:53029955 | C | T | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185+3087C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029955 | |||||||
| chr5:53030218 | A | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+3350A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53030218 | |||||||
| chr5:53030468 | T | C | 1 | a0001c0002t0006g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.185+3600T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53030468 | |||||||
| chr5:53030613 | C | T | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+3745C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53030613 | |||||||
| chr5:53030630 | CAA | C | 8 | a0001c0002t0004g0101 a0002c0007t0010g0162 a0002c0007t0010g0163 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+3763_185+3764d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53030630 | |||||||
| chr5:53031305 | C | T | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185+4437C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031305 | |||||||
| chr5:53031379 | C | T | 1 | a0001c0008t0021g0016 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.185+4511C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031379 | |||||||
| chr5:53031400 | G | A | 104 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(101): Show |
109 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.185+4532G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031400 | |||||||
| chr5:53031521 | T | C | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+4653T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031521 | |||||||
| chr5:53031686 | C | G | 2 | a0001c0001t0005g0217 a0001c0001t0005g0218 |
2 | HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.185+4818C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031686 | |||||||
| chr5:53031866 | T | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | NA18991.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.185+4998T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031866 | |||||||
| chr5:53031937 | A | G | 8 | a0001c0002t0004g0101 a0002c0007t0010g0162 a0002c0007t0010g0163 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+5069A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031937 | |||||||
| chr5:53031977 | C | G | 104 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(101): Show |
109 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.185+5109C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031977 | |||||||
| chr5:53032173 | TA | T | 72 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(69): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.185+5313delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53032173 | ||||||
| chr5:53032363 | A | G | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.185+5495A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032363 | |||||||
| chr5:53032379 | T | C | 1 | a0001c0002t0004g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.185+5511T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032379 | |||||||
| chr5:53032402 | C | G | 4 | a0001c0001t0005g0216 a0001c0001t0005g0217 a0001c0001t0005g0218 others(1): Show |
4 | HG01993.hp2 HG02004.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+5534C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032402 | |||||||
| chr5:53032570 | C | T | 131 | a0001c0001t0002g0247 a0001c0002t0003g0003 a0001c0002t0003g0032 others(128): Show |
140 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.185+5702C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032570 | |||||||
| chr5:53032612 | T | G | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+5744T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032612 | |||||||
| chr5:53032824 | A | G | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.185+5956A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032824 | |||||||
| chr5:53032983 | C | T | 8 | a0001c0002t0004g0101 a0002c0007t0010g0162 a0002c0007t0010g0163 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+6115C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032983 | |||||||
| chr5:53032995 | C | T | 103 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(100): Show |
108 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.185+6127C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032995 | |||||||
| chr5:53033039 | G | A | 9 | a0001c0001t0001g0344 a0001c0002t0004g0101 a0002c0007t0010g0162 others(6): Show |
9 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+6171G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033039 | |||||||
| chr5:53033046 | T | C | 34 | a0001c0001t0005g0005 a0001c0001t0005g0020 a0001c0001t0005g0216 others(31): Show |
38 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.185+6178T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033046 | |||||||
| chr5:53033123 | G | A | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185+6255G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033123 | |||||||
| chr5:53033129 | C | T | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+6261C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033129 | |||||||
| chr5:53033130 | G | A | 78 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(75): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.185+6262G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033130 | |||||||
| chr5:53033132 | G | A | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.185+6264G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033132 | |||||||
| chr5:53033136 | G | A | 72 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(69): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.185+6268G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033136 | |||||||
| chr5:53033219 | A | G | 1 | a0003c0005t0003g0177 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.185+6351A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033219 | |||||||
| chr5:53033268 | CA | C | 159 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(156): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.185+6410delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53033268 | ||||||
| chr5:53033302 | A | G | 108 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(105): Show |
113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.185+6434A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033302 | |||||||
| chr5:53033418 | C | T | 3 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 |
3 | HG02818.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.185+6550C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033418 | |||||||
| chr5:53033511 | A | G | 243 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(240): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.185+6643A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033511 | |||||||
| chr5:53033607 | A | T | 39 | a0001c0001t0025g0367 a0001c0002t0047g0061 a0001c0008t0012g0159 others(36): Show |
41 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.185+6739A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033607 | |||||||
| chr5:53033611 | A | T | 218 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(215): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.185+6743A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033611 | |||||||
| chr5:53033751 | C | T | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+6883C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033751 | |||||||
| chr5:53033764 | AT | A | 130 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(127): Show |
140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.185+6913delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53033764 | ||||||
| chr5:53033764 | ATT | A | 110 | a0001c0001t0029g0137 a0001c0001t0039g0119 a0001c0002t0003g0003 others(107): Show |
115 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.185+6912_185+6913d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53033764 | ||||||
| chr5:53033786 | C | T | 10 | a0001c0002t0003g0168 a0001c0002t0003g0178 a0001c0002t0003g0183 others(7): Show |
10 | HG00609.hp1 HG00673.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+6918C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033786 | |||||||
| chr5:53033798 | C | A | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.185+6930C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033798 | |||||||
| chr5:53033832 | C | T | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185+6964C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033832 | |||||||
| chr5:53033850 | G | A | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+6982G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033850 | |||||||
| chr5:53034000 | A | G | 2 | a0001c0001t0005g0279 a0001c0001t0005g0280 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.185+7132A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034000 | |||||||
| chr5:53034021 | C | T | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.185+7153C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034021 | |||||||
| chr5:53034052 | G | T | 1 | a0001c0002t0003g0193 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.185+7184G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034052 | |||||||
| chr5:53034183 | A | T | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+7315A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034183 | |||||||
| chr5:53034193 | A | G | 137 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(134): Show |
147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.185+7325A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034193 | |||||||
| chr5:53034384 | G | A | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+7516G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034384 | |||||||
| chr5:53034407 | CA | C | 25 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(22): Show |
29 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.185+7553delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53034407 | ||||||
| chr5:53034407 | CAA | C | 111 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(108): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.185+7552_185+7553d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53034407 | ||||||
| chr5:53034501 | A | G | 26 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(23): Show |
30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.186-7611A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034501 | |||||||
| chr5:53034517 | A | AT | 26 | a0001c0016t0005g0103 a0002c0003t0007g0022 a0002c0003t0007g0073 others(23): Show |
27 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.186-7594dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53034517 | ||||||
| chr5:53034529 | C | T | 1 | a0001c0004t0008g0295 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.186-7583C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034529 | |||||||
| chr5:53034695 | A | T | 1 | a0015c0027t0006g0037 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-7417A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034695 | |||||||
| chr5:53034751 | A | G | 108 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(105): Show |
113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.186-7361A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034751 | |||||||
| chr5:53034813 | A | G | 26 | a0001c0016t0005g0103 a0002c0003t0007g0022 a0002c0003t0007g0073 others(23): Show |
27 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.186-7299A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034813 | |||||||
| chr5:53034859 | T | C | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.186-7253T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034859 | |||||||
| chr5:53034872 | T | A | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.186-7240T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034872 | |||||||
| chr5:53034915 | G | A | 243 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(240): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.186-7197G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034915 | |||||||
| chr5:53034962 | C | A | 5 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 others(2): Show |
5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-7150C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034962 | |||||||
| chr5:53035102 | G | C | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.186-7010G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035102 | |||||||
| chr5:53035195 | A | C | 108 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(105): Show |
113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.186-6917A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035195 | |||||||
| chr5:53035263 | G | C | 1 | a0001c0002t0003g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.186-6849G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035263 | |||||||
| chr5:53035304 | C | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186-6808C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035304 | |||||||
| chr5:53035314 | G | A | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.186-6798G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035314 | |||||||
| chr5:53035372 | G | A | 5 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-6740G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035372 | |||||||
| chr5:53035623 | A | G | 20 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(17): Show |
24 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.186-6489A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035623 | |||||||
| chr5:53035660 | C | T | 72 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(69): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.186-6452C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035660 | |||||||
| chr5:53035665 | A | G | 1 | a0001c0002t0004g0368 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.186-6447A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035665 | |||||||
| chr5:53035674 | G | A | 1 | a0001c0001t0002g0154 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.186-6438G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035674 | |||||||
| chr5:53036032 | G | A | 1 | a0004c0006t0003g0169 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.186-6080G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036032 | |||||||
| chr5:53036044 | T | TATTC | 28 | a0001c0001t0002g0136 a0001c0001t0002g0153 a0001c0002t0019g0237 others(25): Show |
29 | HG01074.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.186-6036_186-6033d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036044 | ||||||
| chr5:53036044 | T | TATTCATT others(1): Show |
100 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(97): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.186-6040_186-6033d others(10): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036044 | ||||||
| chr5:53036044 | T | TATTCATT others(5): Show |
8 | a0001c0001t0001g0306 a0001c0001t0002g0156 a0001c0001t0039g0119 others(5): Show |
8 | HG01099.hp2 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-6044_186-6033d others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036044 | ||||||
| chr5:53036044 | TATTC | T | 13 | a0001c0002t0006g0035 a0001c0002t0006g0036 a0001c0002t0006g0038 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-6036_186-6033d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036044 | ||||||
| chr5:53036259 | G | C | 245 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(242): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.186-5853G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036259 | |||||||
| chr5:53036271 | T | C | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.186-5841T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036271 | |||||||
| chr5:53036356 | C | T | 132 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(129): Show |
141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.186-5756C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036356 | |||||||
| chr5:53036605 | G | A | 268 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(265): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.186-5507G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036605 | |||||||
| chr5:53036678 | A | G | 1 | a0001c0001t0001g0322 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.186-5434A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036678 | |||||||
| chr5:53036756 | C | CT | 65 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(62): Show |
68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.186-5350dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036756 | ||||||
| chr5:53037303 | A | G | 1 | a0001c0002t0003g0167 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.186-4809A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037303 | |||||||
| chr5:53037383 | T | G | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.186-4729T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037383 | |||||||
| chr5:53037492 | G | A | 7 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(4): Show |
7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-4620G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037492 | |||||||
| chr5:53037590 | C | A | 132 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(129): Show |
141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.186-4522C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037590 | |||||||
| chr5:53037757 | T | G | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-4355T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037757 | |||||||
| chr5:53037914 | T | C | 221 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(218): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.186-4198T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037914 | |||||||
| chr5:53038090 | G | A | 2 | a0001c0002t0004g0228 a0001c0002t0004g0256 |
2 | HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.186-4022G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038090 | |||||||
| chr5:53038109 | A | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.186-4003A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038109 | |||||||
| chr5:53038207 | T | TAAA | 87 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0107 others(84): Show |
92 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.186-3892_186-3890d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53038207 | ||||||
| chr5:53038207 | T | TAAAA | 15 | a0001c0002t0003g0063 a0001c0002t0003g0070 a0001c0002t0003g0147 others(12): Show |
15 | HG00642.hp1 HG01175.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.186-3893_186-3890d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53038207 | ||||||
| chr5:53038207 | TA | T | 85 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(82): Show |
90 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.186-3890delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53038207 | ||||||
| chr5:53038207 | TAA | T | 30 | a0001c0001t0002g0106 a0001c0001t0002g0141 a0001c0001t0002g0263 others(27): Show |
32 | HG01192.hp1 HG01243.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.186-3891_186-3890d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53038207 | ||||||
| chr5:53038241 | G | A | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.186-3871G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038241 | |||||||
| chr5:53038307 | C | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186-3805C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038307 | |||||||
| chr5:53038488 | G | A | 108 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(105): Show |
115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.186-3624G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038488 | |||||||
| chr5:53038514 | A | G | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.186-3598A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038514 | |||||||
| chr5:53038662 | A | G | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.186-3450A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038662 | |||||||
| chr5:53038678 | C | G | 221 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(218): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.186-3434C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038678 | |||||||
| chr5:53038693 | C | T | 1 | a0001c0004t0008g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-3419C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038693 | |||||||
| chr5:53038697 | CGCACTTG others(7): Show |
C | 4 | a0002c0003t0007g0323 a0002c0003t0007g0333 a0002c0003t0007g0341 others(1): Show |
4 | NA18989.hp2 NA19056.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-3414_186-3401d others(16): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038697 | |||||||
| chr5:53038701 | C | A | 1 | a0001c0028t0004g0074 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.186-3411C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038701 | |||||||
| chr5:53038710 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.186-3402C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038710 | |||||||
| chr5:53038745 | A | G | 1 | a0001c0002t0041g0318 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.186-3367A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038745 | |||||||
| chr5:53038822 | G | C | 2 | a0001c0001t0005g0308 a0001c0001t0005g0310 |
2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.186-3290G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038822 | |||||||
| chr5:53038832 | A | T | 240 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(237): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.186-3280A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038832 | |||||||
| chr5:53038840 | C | A | 31 | a0001c0001t0005g0005 a0001c0001t0005g0020 a0001c0001t0005g0216 others(28): Show |
34 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.186-3272C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038840 | |||||||
| chr5:53038841 | A | G | 31 | a0001c0001t0005g0005 a0001c0001t0005g0020 a0001c0001t0005g0216 others(28): Show |
34 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.186-3271A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038841 | |||||||
| chr5:53038944 | A | G | 35 | a0001c0002t0004g0004 a0001c0002t0004g0088 a0001c0002t0004g0097 others(32): Show |
37 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-3168A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038944 | |||||||
| chr5:53038966 | G | A | 5 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-3146G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038966 | |||||||
| chr5:53039081 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-3031C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039081 | |||||||
| chr5:53039208 | T | G | 5 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-2904T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039208 | |||||||
| chr5:53039309 | GA | G | 106 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(103): Show |
111 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.186-2795delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039309 | ||||||
| chr5:53039342 | C | T | 1 | a0001c0004t0008g0295 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.186-2770C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039342 | |||||||
| chr5:53039401 | G | A | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.186-2711G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039401 | |||||||
| chr5:53039531 | G | A | 114 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(111): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.186-2581G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039531 | |||||||
| chr5:53039539 | G | T | 1 | a0001c0022t0002g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.186-2573G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039539 | |||||||
| chr5:53039572 | C | T | 78 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(75): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.186-2540C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039572 | |||||||
| chr5:53039611 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0033 |
3 | HG00673.hp2 HG02129.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.186-2501G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039611 | |||||||
| chr5:53039664 | C | T | 131 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(128): Show |
140 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.186-2448C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039664 | |||||||
| chr5:53039720 | A | G | 28 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.186-2392A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039720 | |||||||
| chr5:53039739 | C | CA | 84 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0065 others(81): Show |
90 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.186-2348dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039739 | ||||||
| chr5:53039739 | C | CAA | 12 | a0001c0001t0001g0305 a0001c0001t0001g0322 a0001c0001t0002g0121 others(9): Show |
12 | HG01261.hp2 HG01978.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.186-2349_186-2348d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039739 | ||||||
| chr5:53039739 | CA | C | 11 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0330 others(8): Show |
11 | HG01168.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.186-2348delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039739 | ||||||
| chr5:53039739 | CAAA | C | 22 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(19): Show |
26 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.186-2350_186-2348d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039739 | ||||||
| chr5:53039783 | A | C | 1 | a0001c0001t0005g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.186-2329A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039783 | |||||||
| chr5:53039952 | A | C | 10 | a0001c0002t0003g0063 a0001c0002t0003g0070 a0001c0002t0003g0147 others(7): Show |
11 | HG02015.hp1 NA18947.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.186-2160A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039952 | |||||||
| chr5:53040036 | G | A | 3 | a0001c0002t0004g0088 a0001c0002t0004g0231 a0001c0002t0004g0235 |
3 | HG02486.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.186-2076G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040036 | |||||||
| chr5:53040086 | C | A | 1 | a0001c0001t0005g0283 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.186-2026C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040086 | |||||||
| chr5:53040117 | T | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.186-1995T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040117 | |||||||
| chr5:53040237 | G | T | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.186-1875G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040237 | |||||||
| chr5:53040374 | A | C | 1 | a0002c0009t0016g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.186-1738A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040374 | |||||||
| chr5:53040462 | G | A | 1 | a0001c0004t0008g0349 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.186-1650G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040462 | |||||||
| chr5:53040641 | G | GA | 8 | a0001c0004t0008g0348 a0001c0004t0008g0351 a0001c0004t0008g0355 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-1465dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53040641 | ||||||
| chr5:53040703 | C | A | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.186-1409C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040703 | |||||||
| chr5:53040744 | C | T | 116 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(113): Show |
123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.186-1368C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040744 | |||||||
| chr5:53040751 | A | C | 221 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(218): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.186-1361A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040751 | |||||||
| chr5:53040812 | C | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186-1300C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040812 | |||||||
| chr5:53041010 | G | A | 1 | a0002c0007t0010g0260 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186-1102G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041010 | |||||||
| chr5:53041079 | T | G | 218 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(215): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.186-1033T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041079 | |||||||
| chr5:53041100 | T | G | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-1012T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041100 | |||||||
| chr5:53041115 | T | TA | 70 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(67): Show |
74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.186-996dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53041115 | ||||||
| chr5:53041152 | G | A | 218 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(215): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.186-960G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041152 | |||||||
| chr5:53041262 | T | C | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.186-850T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041262 | |||||||
| chr5:53041314 | C | T | 108 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(105): Show |
115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.186-798C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041314 | |||||||
| chr5:53041325 | T | C | 221 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(218): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.186-787T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041325 | |||||||
| chr5:53041426 | C | T | 221 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(218): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.186-686C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041426 | |||||||
| chr5:53041496 | G | T | 77 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(74): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.186-616G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041496 | |||||||
| chr5:53041573 | G | C | 114 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(111): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.186-539G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041573 | |||||||
| chr5:53041592 | C | T | 26 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(23): Show |
30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.186-520C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041592 | |||||||
| chr5:53041676 | C | A | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-436C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041676 | |||||||
| chr5:53041709 | C | T | 2 | a0001c0001t0025g0366 a0001c0021t0050g0365 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.186-403C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041709 | |||||||
| chr5:53041926 | A | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.186-186A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041926 | |||||||
| chr5:53041953 | T | C | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.186-159T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041953 | |||||||
| chr5:53042052 | G | T | 1 | a0008c0018t0037g0369 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-60G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53042052 | |||||||
| chr5:53042078 | C | T | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.186-34C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53042078 | |||||||
| chr5:53042253 | T | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.295+32T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042253 | |||||||
| chr5:53042310 | A | G | 4 | a0002c0003t0007g0323 a0002c0003t0007g0333 a0002c0003t0007g0341 others(1): Show |
4 | NA18989.hp2 NA19056.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+89A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042310 | |||||||
| chr5:53042411 | G | A | 72 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(69): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.295+190G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042411 | |||||||
| chr5:53042446 | T | C | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.295+225T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042446 | |||||||
| chr5:53042521 | T | C | 1 | a0001c0001t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.295+300T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042521 | |||||||
| chr5:53042834 | T | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.295+613T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042834 | |||||||
| chr5:53042837 | G | T | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.295+616G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042837 | |||||||
| chr5:53042847 | C | T | 20 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(17): Show |
22 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.295+626C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042847 | |||||||
| chr5:53042849 | T | TA | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.295+635dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53042849 | ||||||
| chr5:53042976 | A | C | 245 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(242): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.295+755A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042976 | |||||||
| chr5:53043026 | T | C | 2 | a0001c0001t0005g0279 a0001c0001t0005g0280 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.295+805T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043026 | |||||||
| chr5:53043196 | G | GTA | 6 | a0001c0001t0002g0117 a0001c0002t0003g0032 a0001c0002t0003g0107 others(3): Show |
6 | HG00741.hp1 HG01081.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+991_295+992dup others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53043196 | ||||||
| chr5:53043240 | GGAGT | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+1025_295+1028d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53043240 | ||||||
| chr5:53043277 | AT | A | 69 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(66): Show |
72 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.295+1060delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53043277 | ||||||
| chr5:53043284 | T | C | 78 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(75): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.295+1063T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043284 | |||||||
| chr5:53043380 | G | T | 1 | a0002c0007t0010g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.295+1159G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043380 | |||||||
| chr5:53043540 | G | T | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.295+1319G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043540 | |||||||
| chr5:53043660 | T | C | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.296-1341T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043660 | |||||||
| chr5:53043715 | G | A | 6 | a0001c0002t0009g0029 a0001c0002t0009g0173 a0001c0002t0009g0174 others(3): Show |
6 | HG00280.hp2 NA18995.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-1286G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043715 | |||||||
| chr5:53044013 | G | A | 8 | a0001c0001t0005g0020 a0001c0001t0005g0268 a0001c0001t0005g0277 others(5): Show |
9 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-988G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044013 | |||||||
| chr5:53044086 | G | A | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.296-915G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044086 | |||||||
| chr5:53044128 | A | G | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.296-873A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044128 | |||||||
| chr5:53044143 | T | C | 245 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(242): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.296-858T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044143 | |||||||
| chr5:53044199 | C | T | 1 | a0002c0003t0007g0267 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.296-802C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044199 | |||||||
| chr5:53044200 | G | A | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.296-801G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044200 | |||||||
| chr5:53044207 | A | G | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.296-794A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044207 | |||||||
| chr5:53044249 | T | C | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.296-752T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044249 | |||||||
| chr5:53044274 | C | CA | 62 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(59): Show |
68 | HG00408.hp2 HG00544.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.296-695dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAA | 43 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(40): Show |
44 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-696_296-695dup others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAA | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0005g0271 others(3): Show |
6 | HG01358.hp2 HG02071.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-697_296-695dup others(3): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAAAA | 5 | a0001c0001t0005g0020 a0001c0001t0005g0277 a0001c0001t0005g0279 others(2): Show |
6 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-699_296-695dup others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAAAAAA others(3): Show |
8 | a0002c0003t0007g0022 a0002c0003t0007g0267 a0002c0003t0007g0331 others(5): Show |
9 | HG01070.hp1 HG01192.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-704_296-695dup others(10): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAAAAAA others(4): Show |
6 | a0001c0008t0021g0016 a0002c0003t0007g0319 a0002c0003t0007g0320 others(3): Show |
7 | HG00323.hp2 HG01358.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-705_296-695dup others(11): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAAAAAA others(5): Show |
1 | a0001c0016t0005g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.296-706_296-695dup others(12): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAAAAAA others(6): Show |
2 | a0002c0003t0007g0021 a0002c0003t0007g0334 |
3 | HG01516.hp1 HG01517.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.296-707_296-695dup others(13): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAAAAAA others(7): Show |
1 | a0002c0003t0007g0328 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-708_296-695dup others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAAAAAA others(8): Show |
4 | a0001c0008t0012g0160 a0001c0008t0012g0161 a0002c0003t0007g0079 others(1): Show |
4 | HG00621.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-709_296-695dup others(15): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAAAAAA others(9): Show |
1 | a0001c0008t0012g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.296-710_296-695dup others(16): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | C | CAAAAAAA others(15): Show |
2 | a0002c0003t0007g0073 a0002c0003t0007g0080 |
2 | HG02132.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.296-716_296-695dup others(22): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | CAA | C | 11 | a0001c0002t0003g0107 a0001c0002t0003g0188 a0001c0002t0003g0189 others(8): Show |
11 | HG00544.hp2 HG01978.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.296-696_296-695del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | CAAA | C | 71 | a0001c0001t0001g0305 a0001c0001t0002g0131 a0001c0001t0002g0135 others(68): Show |
74 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.296-697_296-695del others(3): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | CAAAA | C | 96 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(93): Show |
102 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.296-698_296-695del others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | CAAAAA | C | 6 | a0001c0001t0002g0136 a0001c0001t0002g0140 a0001c0001t0002g0152 others(3): Show |
6 | HG00323.hp1 HG01168.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-699_296-695del others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0025g0366 a0001c0002t0004g0252 a0001c0021t0050g0365 |
3 | HG02615.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.296-705_296-695del others(11): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0049g0337 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.296-707_296-695del others(13): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | CAAAAAAA others(7): Show |
C | 21 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(18): Show |
25 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.296-708_296-695del others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | CAAAAAAA others(8): Show |
C | 1 | a0001c0002t0006g0041 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.296-709_296-695del others(15): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044274 | CAAAAAAA others(12): Show |
C | 1 | a0002c0003t0026g0364 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.296-713_296-695del others(19): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | ||||||
| chr5:53044305 | A | T | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.296-696A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044305 | |||||||
| chr5:53044311 | G | C | 1 | a0001c0001t0001g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.296-690G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044311 | |||||||
| chr5:53044443 | T | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0281 a0001c0001t0001g0282 |
3 | NA18963.hp1 NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.296-558T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044443 | |||||||
| chr5:53044470 | T | C | 1 | a0002c0003t0007g0328 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-531T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044470 | |||||||
| chr5:53044481 | C | T | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.296-520C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044481 | |||||||
| chr5:53044502 | G | A | 28 | a0001c0001t0005g0005 a0001c0001t0005g0020 a0001c0001t0005g0216 others(25): Show |
31 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.296-499G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044502 | |||||||
| chr5:53044504 | T | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.296-497T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044504 | |||||||
| chr5:53044536 | G | A | 2 | a0001c0001t0025g0366 a0001c0021t0050g0365 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.296-465G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044536 | |||||||
| chr5:53044678 | G | A | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.296-323G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044678 | |||||||
| chr5:53044704 | G | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.296-297G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044704 | |||||||
| chr5:53044745 | A | T | 1 | a0002c0003t0007g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.296-256A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044745 | |||||||
| chr5:53044777 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.296-224C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044777 | |||||||
| chr5:53044812 | A | G | 1 | a0001c0011t0002g0113 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.296-189A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044812 | |||||||
| chr5:53044844 | C | T | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.296-157C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044844 | |||||||
| chr5:53045149 | G | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.387+57G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045149 | |||||||
| chr5:53045234 | A | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.387+142A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045234 | |||||||
| chr5:53045280 | T | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.387+188T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045280 | |||||||
| chr5:53045391 | A | G | 1 | a0001c0002t0004g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.387+299A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045391 | |||||||
| chr5:53045529 | C | T | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.387+437C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045529 | |||||||
| chr5:53045564 | T | A | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.387+472T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045564 | |||||||
| chr5:53045572 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(17): Show |
22 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.387+480C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045572 | |||||||
| chr5:53045682 | A | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.387+590A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045682 | |||||||
| chr5:53045762 | G | C | 1 | a0001c0001t0005g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.387+670G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045762 | |||||||
| chr5:53045903 | TAGAG | T | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.387+814_387+817del others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53045903 | ||||||
| chr5:53045912 | T | A | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.387+820T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045912 | |||||||
| chr5:53045913 | G | T | 78 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(75): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.387+821G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045913 | |||||||
| chr5:53045916 | C | T | 20 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(17): Show |
22 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.387+824C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045916 | |||||||
| chr5:53045917 | G | A | 50 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(47): Show |
54 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.387+825G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045917 | |||||||
| chr5:53045926 | C | T | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+834C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045926 | |||||||
| chr5:53046006 | C | A | 1 | a0001c0002t0006g0050 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.387+914C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046006 | |||||||
| chr5:53046020 | A | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.387+928A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046020 | |||||||
| chr5:53046050 | G | C | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+958G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046050 | |||||||
| chr5:53046136 | A | G | 104 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(101): Show |
109 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.387+1044A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046136 | |||||||
| chr5:53046158 | G | A | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+1066G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046158 | |||||||
| chr5:53046194 | C | CA | 15 | a0001c0001t0001g0098 a0001c0001t0001g0134 a0001c0001t0001g0269 others(12): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.387+1123dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53046194 | ||||||
| chr5:53046194 | CA | C | 15 | a0001c0001t0001g0082 a0001c0001t0001g0301 a0001c0001t0002g0124 others(12): Show |
15 | HG01168.hp2 HG01243.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.387+1123delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53046194 | ||||||
| chr5:53046194 | CAA | C | 200 | a0001c0001t0001g0066 a0001c0001t0001g0303 a0001c0001t0001g0304 others(197): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.387+1122_387+1123d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53046194 | ||||||
| chr5:53046194 | CAAA | C | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+1121_387+1123d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53046194 | ||||||
| chr5:53046211 | A | G | 104 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(101): Show |
109 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.387+1119A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046211 | |||||||
| chr5:53046250 | AC | A | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+1159delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046250 | |||||||
| chr5:53046253 | C | T | 131 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(128): Show |
140 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.387+1161C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046253 | |||||||
| chr5:53046278 | G | A | 28 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.387+1186G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046278 | |||||||
| chr5:53046282 | T | C | 239 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(236): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.387+1190T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046282 | |||||||
| chr5:53046442 | G | C | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.387+1350G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046442 | |||||||
| chr5:53046489 | C | G | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.387+1397C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046489 | |||||||
| chr5:53046496 | G | A | 1 | a0002c0003t0007g0021 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.387+1404G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046496 | |||||||
| chr5:53046573 | C | T | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.387+1481C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046573 | |||||||
| chr5:53046579 | G | T | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.387+1487G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046579 | |||||||
| chr5:53046607 | C | T | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.387+1515C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046607 | |||||||
| chr5:53046668 | A | G | 300 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0001c0001t0001g0301 others(297): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.387+1576A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046668 | |||||||
| chr5:53046700 | G | A | 1 | a0002c0003t0007g0341 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.387+1608G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046700 | |||||||
| chr5:53046810 | T | A | 1 | a0006c0029t0001g0289 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.388-1553T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046810 | |||||||
| chr5:53046930 | A | T | 131 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(128): Show |
140 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.388-1433A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046930 | |||||||
| chr5:53046975 | AG | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.388-1387delG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046975 | |||||||
| chr5:53047060 | A | G | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.388-1303A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047060 | |||||||
| chr5:53047250 | A | G | 1 | a0001c0002t0049g0337 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.388-1113A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047250 | |||||||
| chr5:53047349 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.388-1014A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047349 | |||||||
| chr5:53047358 | T | G | 64 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(61): Show |
67 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.388-1005T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047358 | |||||||
| chr5:53047359 | G | A | 64 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(61): Show |
67 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.388-1004G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047359 | |||||||
| chr5:53047526 | C | G | 239 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(236): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.388-837C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047526 | |||||||
| chr5:53047621 | C | T | 24 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(21): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.388-742C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047621 | |||||||
| chr5:53047731 | A | G | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.388-632A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047731 | |||||||
| chr5:53047798 | A | G | 1 | a0001c0004t0008g0290 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.388-565A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047798 | |||||||
| chr5:53047963 | G | A | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.388-400G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047963 | |||||||
| chr5:53047972 | C | T | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.388-391C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047972 | |||||||
| chr5:53048000 | C | T | 1 | a0002c0003t0007g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.388-363C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048000 | |||||||
| chr5:53048071 | C | T | 72 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(69): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.388-292C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048071 | |||||||
| chr5:53048091 | G | C | 1 | a0001c0004t0008g0352 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.388-272G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048091 | |||||||
| chr5:53048120 | A | G | 1 | a0001c0002t0003g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.388-243A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048120 | |||||||
| chr5:53048121 | C | G | 1 | a0001c0001t0002g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.388-242C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048121 | |||||||
| chr5:53048150 | C | A | 4 | a0002c0003t0026g0363 a0002c0003t0026g0364 a0008c0018t0037g0369 others(1): Show |
4 | HG02451.hp2 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-213C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048150 | |||||||
| chr5:53048216 | G | A | 107 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(104): Show |
112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.388-147G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048216 | |||||||
| chr5:53048626 | C | T | 1 | a0001c0002t0003g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.503-17C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 5/29 | chr5 | 53048626 | |||||||
| chr5:53048780 | A | G | 268 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(265): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.630+10A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53048780 | |||||||
| chr5:53048950 | G | A | 31 | a0001c0002t0047g0061 a0001c0016t0005g0103 a0002c0003t0007g0021 others(28): Show |
33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+180G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53048950 | |||||||
| chr5:53048975 | C | A | 1 | a0001c0004t0008g0349 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.630+205C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53048975 | |||||||
| chr5:53049005 | G | A | 5 | a0001c0002t0003g0032 a0001c0002t0003g0107 a0001c0002t0003g0109 others(2): Show |
5 | HG01081.hp1 NA18963.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+235G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049005 | |||||||
| chr5:53049007 | C | T | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.630+237C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049007 | |||||||
| chr5:53049012 | C | CT | 8 | a0001c0001t0001g0096 a0001c0001t0005g0218 a0001c0002t0003g0168 others(5): Show |
8 | HG02293.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.630+258dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049012 | ||||||
| chr5:53049012 | CT | C | 7 | a0001c0001t0001g0092 a0001c0001t0002g0148 a0001c0001t0002g0152 others(4): Show |
7 | HG01081.hp2 HG02559.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.630+258delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049012 | ||||||
| chr5:53049012 | CTT | C | 34 | a0001c0002t0047g0061 a0001c0016t0005g0103 a0002c0003t0007g0021 others(31): Show |
36 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.630+257_630+258del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049012 | ||||||
| chr5:53049115 | G | T | 31 | a0001c0002t0047g0061 a0001c0016t0005g0103 a0002c0003t0007g0021 others(28): Show |
33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+345G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049115 | |||||||
| chr5:53049205 | T | G | 69 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(66): Show |
73 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.630+435T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049205 | |||||||
| chr5:53049234 | ACTC | A | 30 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(27): Show |
32 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.630+467_630+469del others(3): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049234 | ||||||
| chr5:53049243 | C | T | 30 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(27): Show |
32 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.630+473C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049243 | |||||||
| chr5:53049390 | G | A | 134 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(131): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.630+620G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049390 | |||||||
| chr5:53049417 | A | G | 31 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(28): Show |
33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+647A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049417 | |||||||
| chr5:53049434 | A | T | 1 | a0001c0001t0005g0283 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.630+664A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049434 | |||||||
| chr5:53049500 | C | T | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.630+730C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049500 | |||||||
| chr5:53049502 | G | C | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.630+732G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049502 | |||||||
| chr5:53049503 | C | A | 31 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(28): Show |
33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+733C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049503 | |||||||
| chr5:53049837 | C | T | 9 | a0003c0005t0003g0018 a0003c0005t0003g0019 a0003c0005t0003g0176 others(6): Show |
10 | HG02071.hp2 NA18964.hp1 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.630+1067C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049837 | |||||||
| chr5:53049852 | G | GTTGACA | 31 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(28): Show |
33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+1084_630+1089d others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049852 | ||||||
| chr5:53049858 | A | G | 2 | a0001c0002t0004g0115 a0001c0011t0034g0084 |
2 | HG03688.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.630+1088A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049858 | |||||||
| chr5:53049947 | T | C | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.630+1177T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049947 | |||||||
| chr5:53049974 | C | T | 2 | a0001c0002t0006g0111 a0001c0002t0006g0354 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.630+1204C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049974 | |||||||
| chr5:53050038 | C | T | 30 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(27): Show |
32 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.630+1268C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050038 | |||||||
| chr5:53050039 | G | A | 1 | a0001c0002t0004g0368 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.630+1269G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050039 | |||||||
| chr5:53050112 | T | C | 1 | a0001c0001t0023g0340 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.631-1299T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050112 | |||||||
| chr5:53050184 | T | C | 31 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(28): Show |
33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.631-1227T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050184 | |||||||
| chr5:53050208 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.631-1203G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050208 | |||||||
| chr5:53050219 | C | T | 5 | a0001c0002t0018g0102 a0001c0002t0018g0104 a0001c0002t0018g0118 others(2): Show |
5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-1192C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050219 | |||||||
| chr5:53050273 | C | T | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.631-1138C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050273 | |||||||
| chr5:53050283 | T | C | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.631-1128T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050283 | |||||||
| chr5:53050347 | G | C | 1 | a0001c0002t0043g0108 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.631-1064G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050347 | |||||||
| chr5:53050366 | G | A | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.631-1045G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050366 | |||||||
| chr5:53050562 | C | T | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.631-849C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050562 | |||||||
| chr5:53050697 | G | A | 5 | a0001c0001t0002g0012 a0001c0001t0002g0117 a0001c0001t0002g0135 others(2): Show |
6 | HG00741.hp1 HG01168.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-714G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050697 | |||||||
| chr5:53050724 | T | C | 1 | a0001c0002t0003g0183 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.631-687T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050724 | |||||||
| chr5:53050773 | T | C | 33 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.631-638T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050773 | |||||||
| chr5:53050847 | C | G | 23 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(20): Show |
25 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.631-564C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050847 | |||||||
| chr5:53050929 | C | T | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.631-482C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050929 | |||||||
| chr5:53051029 | C | T | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.631-382C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53051029 | |||||||
| chr5:53051057 | G | A | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.631-354G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53051057 | |||||||
| chr5:53051206 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.631-205G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53051206 | |||||||
| chr5:53051684 | AC | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.779+126delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53051684 | |||||||
| chr5:53051731 | G | A | 134 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(131): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.779+172G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53051731 | |||||||
| chr5:53051784 | C | T | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.779+225C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53051784 | |||||||
| chr5:53051995 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.779+436G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53051995 | |||||||
| chr5:53052050 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.779+491A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052050 | |||||||
| chr5:53052068 | AC | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.779+511delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr5 | 53052068 | ||||||
| chr5:53052242 | C | A | 1 | a0001c0002t0003g0109 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.779+683C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052242 | |||||||
| chr5:53052294 | T | G | 134 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(131): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.779+735T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052294 | |||||||
| chr5:53052426 | T | C | 134 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(131): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.779+867T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052426 | |||||||
| chr5:53052506 | C | T | 1 | a0001c0002t0004g0257 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.779+947C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052506 | |||||||
| chr5:53052524 | T | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.779+965T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052524 | |||||||
| chr5:53052537 | C | G | 33 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.779+978C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052537 | |||||||
| chr5:53052656 | T | C | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.779+1097T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052656 | |||||||
| chr5:53052801 | T | A | 1 | a0002c0003t0007g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.779+1242T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052801 | |||||||
| chr5:53052802 | C | A | 1 | a0002c0003t0007g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.779+1243C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052802 | |||||||
| chr5:53052821 | C | T | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.779+1262C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052821 | |||||||
| chr5:53052862 | G | A | 1 | a0001c0002t0004g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.779+1303G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052862 | |||||||
| chr5:53052868 | G | C | 28 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.779+1309G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052868 | |||||||
| chr5:53052918 | A | G | 2 | a0002c0003t0007g0319 a0002c0003t0007g0320 |
2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.779+1359A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052918 | |||||||
| chr5:53052991 | C | T | 28 | a0001c0001t0005g0005 a0001c0001t0005g0020 a0001c0001t0005g0216 others(25): Show |
31 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.779+1432C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052991 | |||||||
| chr5:53053023 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.779+1464C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053023 | |||||||
| chr5:53053153 | G | T | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.779+1594G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053153 | |||||||
| chr5:53053235 | G | A | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.779+1676G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053235 | |||||||
| chr5:53053242 | G | A | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.779+1683G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053242 | |||||||
| chr5:53053258 | G | C | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.779+1699G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053258 | |||||||
| chr5:53053559 | T | G | 2 | a0001c0001t0002g0219 a0001c0001t0002g0221 |
2 | HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.780-1979T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053559 | |||||||
| chr5:53053575 | T | C | 52 | a0001c0002t0003g0003 a0001c0002t0003g0063 a0001c0002t0003g0070 others(49): Show |
55 | HG00280.hp2 HG00609.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.780-1963T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053575 | |||||||
| chr5:53053831 | T | A | 301 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(298): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.780-1707T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053831 | |||||||
| chr5:53053836 | G | A | 2 | a0001c0004t0008g0291 a0001c0004t0008g0297 |
2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.780-1702G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053836 | |||||||
| chr5:53053992 | A | G | 6 | a0001c0001t0002g0154 a0001c0001t0002g0219 a0001c0001t0002g0220 others(3): Show |
6 | HG02080.hp2 HG02129.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.780-1546A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053992 | |||||||
| chr5:53054038 | G | A | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.780-1500G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054038 | |||||||
| chr5:53054163 | G | A | 28 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.780-1375G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054163 | |||||||
| chr5:53054186 | T | G | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.780-1352T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054186 | |||||||
| chr5:53054254 | C | T | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.780-1284C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054254 | |||||||
| chr5:53054266 | T | A | 1 | a0001c0016t0005g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.780-1272T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054266 | |||||||
| chr5:53054272 | G | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.780-1266G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054272 | |||||||
| chr5:53054301 | T | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.780-1237T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054301 | |||||||
| chr5:53054512 | T | A | 1 | a0008c0018t0037g0369 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.780-1026T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054512 | |||||||
| chr5:53054557 | T | G | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.780-981T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054557 | |||||||
| chr5:53054583 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.780-955G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054583 | |||||||
| chr5:53054608 | T | C | 28 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.780-930T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054608 | |||||||
| chr5:53054691 | G | A | 133 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(130): Show |
142 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.780-847G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054691 | |||||||
| chr5:53054781 | G | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.780-757G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054781 | |||||||
| chr5:53054799 | C | T | 1 | a0002c0003t0007g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.780-739C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054799 | |||||||
| chr5:53054889 | T | C | 4 | a0001c0002t0018g0102 a0001c0002t0018g0104 a0001c0002t0018g0118 others(1): Show |
4 | HG00642.hp1 HG01175.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.780-649T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054889 | |||||||
| chr5:53054912 | T | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0069 |
2 | NA18973.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.780-626T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054912 | |||||||
| chr5:53054985 | G | A | 1 | a0006c0029t0001g0289 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.780-553G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054985 | |||||||
| chr5:53055032 | G | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 |
5 | HG02080.hp1 HG02523.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.780-506G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055032 | |||||||
| chr5:53055313 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0362 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.780-225G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055313 | |||||||
| chr5:53055352 | A | G | 5 | a0001c0002t0018g0102 a0001c0002t0018g0104 a0001c0002t0018g0118 others(2): Show |
5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.780-186A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055352 | |||||||
| chr5:53055406 | C | T | 4 | a0001c0002t0004g0264 a0001c0002t0019g0229 a0001c0002t0019g0236 others(1): Show |
4 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.780-132C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055406 | |||||||
| chr5:53055412 | A | G | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.780-126A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055412 | |||||||
| chr5:53055527 | A | T | 1 | a0001c0001t0005g0271 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.780-11A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055527 | |||||||
| chr5:53055752 | T | C | 1 | a0001c0002t0006g0053 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.930+64T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/29 | chr5 | 53055752 | |||||||
| chr5:53055916 | G | A | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.931-68G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/29 | chr5 | 53055916 | |||||||
| chr5:53056159 | A | AT | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+11dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr5 | 53056159 | ||||||
| chr5:53056165 | T | A | 11 | a0001c0001t0002g0015 a0001c0001t0002g0143 a0001c0001t0002g0144 others(8): Show |
12 | HG00558.hp2 NA18957.hp1 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096+16T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056165 | |||||||
| chr5:53056497 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1096+348C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056497 | |||||||
| chr5:53056532 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1096+383G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056532 | |||||||
| chr5:53056546 | G | T | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1096+397G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056546 | |||||||
| chr5:53056548 | A | T | 136 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1096+399A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056548 | |||||||
| chr5:53056740 | T | C | 1 | a0004c0006t0003g0171 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1096+591T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056740 | |||||||
| chr5:53056857 | G | C | 28 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1096+708G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056857 | |||||||
| chr5:53056858 | T | C | 28 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1096+709T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056858 | |||||||
| chr5:53057003 | A | G | 166 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(163): Show |
177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1096+854A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057003 | |||||||
| chr5:53057169 | A | G | 1 | a0002c0003t0007g0267 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1097-856A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057169 | |||||||
| chr5:53057195 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1097-830T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057195 | |||||||
| chr5:53057384 | G | A | 28 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1097-641G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057384 | |||||||
| chr5:53057449 | A | G | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1097-576A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057449 | |||||||
| chr5:53057668 | A | C | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1097-357A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057668 | |||||||
| chr5:53057783 | A | G | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1097-242A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057783 | |||||||
| chr5:53058000 | C | T | 1 | a0001c0002t0004g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1097-25C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53058000 | |||||||
| chr5:53058129 | T | C | 28 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+28T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058129 | |||||||
| chr5:53058196 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1173+95A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058196 | |||||||
| chr5:53058199 | G | T | 1 | a0001c0002t0003g0184 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1173+98G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058199 | |||||||
| chr5:53058225 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1173+124G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058225 | |||||||
| chr5:53058226 | G | T | 1 | a0001c0002t0003g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1173+125G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058226 | |||||||
| chr5:53058255 | A | T | 3 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 |
3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1173+154A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058255 | |||||||
| chr5:53058273 | A | T | 299 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(296): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1173+172A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058273 | |||||||
| chr5:53058354 | C | T | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1173+253C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058354 | |||||||
| chr5:53058473 | G | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1173+372G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058473 | |||||||
| chr5:53058484 | G | T | 268 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(265): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1173+383G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058484 | |||||||
| chr5:53058594 | G | C | 64 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(61): Show |
67 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1173+493G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058594 | |||||||
| chr5:53058638 | T | C | 1 | a0002c0003t0007g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1173+537T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058638 | |||||||
| chr5:53058644 | T | G | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1173+543T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058644 | |||||||
| chr5:53058693 | A | G | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1173+592A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058693 | |||||||
| chr5:53058780 | A | G | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1173+679A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058780 | |||||||
| chr5:53058782 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1173+681C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058782 | |||||||
| chr5:53058982 | C | G | 1 | a0001c0001t0002g0106 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1173+881C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058982 | |||||||
| chr5:53059098 | A | G | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1174-776A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059098 | |||||||
| chr5:53059103 | C | T | 1 | a0001c0001t0036g0278 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1174-771C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059103 | |||||||
| chr5:53059258 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1174-616T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059258 | |||||||
| chr5:53059272 | C | T | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1174-602C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059272 | |||||||
| chr5:53059362 | G | C | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1174-512G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059362 | |||||||
| chr5:53059395 | G | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1174-479G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059395 | |||||||
| chr5:53059405 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1174-469C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059405 | |||||||
| chr5:53059419 | G | A | 1 | a0001c0001t0013g0139 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1174-455G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059419 | |||||||
| chr5:53059627 | G | A | 2 | a0001c0002t0003g0063 a0001c0002t0003g0070 |
2 | NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1174-247G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059627 | |||||||
| chr5:53059686 | G | A | 8 | a0001c0001t0005g0020 a0001c0001t0005g0268 a0001c0001t0005g0277 others(5): Show |
9 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-188G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059686 | |||||||
| chr5:53059736 | A | G | 37 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(34): Show |
39 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1174-138A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059736 | |||||||
| chr5:53060020 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG01433.hp1 | splice_region_variant&intron_variant | LOW | c.1312+8A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060020 | |||||||
| chr5:53060024 | T | C | 133 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(130): Show |
142 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1312+12T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060024 | |||||||
| chr5:53060176 | C | T | 67 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(64): Show |
71 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1312+164C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060176 | |||||||
| chr5:53060184 | C | T | 6 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(3): Show |
6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312+172C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060184 | |||||||
| chr5:53060376 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1312+364T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060376 | |||||||
| chr5:53060432 | C | G | 1 | a0001c0002t0003g0195 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1312+420C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060432 | |||||||
| chr5:53060440 | T | C | 3 | a0002c0003t0007g0078 a0002c0003t0007g0079 a0002c0003t0007g0080 |
3 | HG00544.hp2 HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1312+428T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060440 | |||||||
| chr5:53060494 | G | A | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-407G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060494 | |||||||
| chr5:53060602 | C | T | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1313-299C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060602 | |||||||
| chr5:53060694 | C | T | 1 | a0002c0003t0007g0334 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1313-207C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060694 | |||||||
| chr5:53060862 | T | C | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1313-39T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060862 | |||||||
| chr5:53060871 | T | G | 37 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(34): Show |
39 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1313-30T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060871 | |||||||
| chr5:53061135 | G | A | 1 | a0005c0010t0002g0120 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1458+89G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061135 | |||||||
| chr5:53061223 | C | T | 1 | a0001c0001t0005g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1458+177C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061223 | |||||||
| chr5:53061336 | A | G | 1 | a0001c0008t0021g0016 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1458+290A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061336 | |||||||
| chr5:53061502 | G | A | 2 | a0001c0001t0005g0287 a0001c0001t0005g0288 |
2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1458+456G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061502 | |||||||
| chr5:53061645 | C | T | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1458+599C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061645 | |||||||
| chr5:53061812 | G | T | 1 | a0001c0008t0021g0016 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1458+766G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061812 | |||||||
| chr5:53061879 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1458+833C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061879 | |||||||
| chr5:53062010 | G | C | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1459-776G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062010 | |||||||
| chr5:53062056 | C | T | 1 | a0010c0017t0052g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1459-730C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062056 | |||||||
| chr5:53062084 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0093 |
2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1459-702T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062084 | |||||||
| chr5:53062432 | A | G | 31 | a0001c0016t0005g0103 a0002c0003t0007g0021 a0002c0003t0007g0022 others(28): Show |
33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1459-354A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062432 | |||||||
| chr5:53062556 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1459-230C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062556 | |||||||
| chr5:53062650 | G | A | 1 | a0001c0002t0004g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1459-136G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062650 | |||||||
| chr5:53062652 | C | G | 1 | a0001c0002t0011g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1459-134C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062652 | |||||||
| chr5:53062747 | T | A | 1 | a0001c0001t0002g0145 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1459-39T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062747 | |||||||
| chr5:53062931 | TA | T | 6 | a0001c0002t0003g0192 a0002c0003t0017g0024 a0002c0003t0017g0025 others(3): Show |
6 | HG01243.hp2 HG01261.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602+15delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr5 | 53062931 | ||||||
| chr5:53063049 | A | G | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602+120A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063049 | |||||||
| chr5:53063057 | A | T | 19 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(16): Show |
21 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602+128A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063057 | |||||||
| chr5:53063205 | T | C | 6 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(3): Show |
6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602+276T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063205 | |||||||
| chr5:53063207 | G | A | 27 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(24): Show |
29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1602+278G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063207 | |||||||
| chr5:53063273 | G | T | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1602+344G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063273 | |||||||
| chr5:53063304 | C | G | 1 | a0001c0002t0009g0208 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1602+375C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063304 | |||||||
| chr5:53063477 | A | G | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1602+548A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063477 | |||||||
| chr5:53063531 | AT | A | 22 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(19): Show |
24 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1602+603delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063531 | |||||||
| chr5:53063687 | A | G | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1602+758A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063687 | |||||||
| chr5:53063859 | T | A | 7 | a0001c0002t0004g0004 a0001c0002t0004g0241 a0001c0002t0004g0242 others(4): Show |
9 | NA18942.hp2 NA18956.hp2 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602+930T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063859 | |||||||
| chr5:53063984 | A | G | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1603-928A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063984 | |||||||
| chr5:53064046 | T | C | 6 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(3): Show |
6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-866T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064046 | |||||||
| chr5:53064047 | G | C | 1 | a0002c0003t0007g0267 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1603-865G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064047 | |||||||
| chr5:53064104 | A | G | 172 | a0001c0001t0001g0269 a0001c0002t0003g0003 a0001c0002t0003g0032 others(169): Show |
183 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.1603-808A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064104 | |||||||
| chr5:53064261 | T | A | 1 | a0009c0026t0003g0206 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1603-651T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064261 | |||||||
| chr5:53064269 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1603-643A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064269 | |||||||
| chr5:53064329 | G | T | 1 | a0001c0001t0002g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1603-583G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064329 | |||||||
| chr5:53064349 | G | C | 1 | a0001c0001t0014g0347 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1603-563G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064349 | |||||||
| chr5:53064528 | T | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1603-384T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064528 | |||||||
| chr5:53064828 | A | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0075 others(2): Show |
5 | HG03704.hp1 NA18973.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-84A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064828 | |||||||
| chr5:53064830 | C | T | 1 | a0001c0002t0004g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1603-82C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064830 | |||||||
| chr5:53064876 | T | C | 1 | a0001c0001t0005g0271 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1603-36T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064876 | |||||||
| chr5:53065185 | T | G | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1806+70T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065185 | |||||||
| chr5:53065233 | C | T | 2 | a0008c0018t0037g0369 a0010c0017t0052g0262 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1806+118C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065233 | |||||||
| chr5:53065250 | G | T | 5 | a0001c0002t0003g0180 a0001c0002t0003g0199 a0001c0002t0003g0200 others(2): Show |
5 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1806+135G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065250 | |||||||
| chr5:53065346 | T | C | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1806+231T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065346 | |||||||
| chr5:53065389 | A | G | 301 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(298): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1806+274A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065389 | |||||||
| chr5:53065470 | G | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1806+355G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065470 | |||||||
| chr5:53065488 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1807-353T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065488 | |||||||
| chr5:53065573 | C | A | 1 | a0001c0001t0005g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1807-268C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065573 | |||||||
| chr5:53065708 | C | A | 1 | a0001c0004t0008g0349 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1807-133C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065708 | |||||||
| chr5:53066521 | C | T | 1 | a0011c0015t0002g0370 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1943+544C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066521 | |||||||
| chr5:53066572 | A | C | 1 | a0001c0002t0004g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1944-546A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066572 | |||||||
| chr5:53066575 | CATTT | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1944-542_1944-539d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066575 | |||||||
| chr5:53066859 | C | T | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1944-259C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066859 | |||||||
| chr5:53066935 | A | T | 65 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(62): Show |
69 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1944-183A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066935 | |||||||
| chr5:53066936 | A | T | 1 | a0001c0001t0002g0145 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1944-182A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066936 | |||||||
| chr5:53067077 | G | A | 1 | a0001c0002t0044g0222 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1944-41G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53067077 | |||||||
| chr5:53067352 | T | C | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2083+95T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067352 | |||||||
| chr5:53067449 | A | G | 3 | a0001c0001t0001g0326 a0001c0001t0001g0335 a0001c0001t0013g0325 |
3 | HG00408.hp2 NA18962.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2083+192A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067449 | |||||||
| chr5:53067614 | T | A | 1 | a0001c0002t0003g0070 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2083+357T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067614 | |||||||
| chr5:53067627 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2083+370A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067627 | |||||||
| chr5:53067647 | A | G | 33 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2083+390A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067647 | |||||||
| chr5:53067669 | C | T | 267 | a0001c0001t0001g0066 a0001c0001t0001g0301 a0001c0001t0001g0303 others(264): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2083+412C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067669 | |||||||
| chr5:53067670 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0181 |
2 | HG01106.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2083+413G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067670 | |||||||
| chr5:53067742 | T | C | 1 | a0001c0002t0004g0233 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2083+485T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067742 | |||||||
| chr5:53067796 | A | T | 60 | a0001c0002t0003g0003 a0001c0002t0003g0063 a0001c0002t0003g0070 others(57): Show |
63 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2083+539A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067796 | |||||||
| chr5:53067929 | A | G | 65 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(62): Show |
68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.2083+672A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067929 | |||||||
| chr5:53068256 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2083+999T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068256 | |||||||
| chr5:53068473 | G | A | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2083+1216G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068473 | |||||||
| chr5:53068624 | C | T | 1 | a0001c0001t0002g0028 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2083+1367C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068624 | |||||||
| chr5:53068845 | G | A | 1 | a0001c0004t0008g0359 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2084-1264G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068845 | |||||||
| chr5:53068925 | A | T | 2 | a0003c0005t0003g0019 a0003c0005t0003g0314 |
3 | NA18964.hp1 NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2084-1184A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068925 | |||||||
| chr5:53069270 | G | A | 1 | a0001c0002t0003g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2084-839G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069270 | |||||||
| chr5:53069364 | A | T | 3 | a0001c0002t0006g0040 a0001c0002t0006g0041 a0001c0002t0006g0046 |
3 | NA18959.hp2 NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2084-745A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069364 | |||||||
| chr5:53069541 | A | G | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2084-568A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069541 | |||||||
| chr5:53069555 | A | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2084-554A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069555 | |||||||
| chr5:53069663 | G | T | 2 | a0001c0002t0004g0228 a0001c0002t0004g0256 |
2 | HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2084-446G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069663 | |||||||
| chr5:53069736 | G | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2084-373G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069736 | |||||||
| chr5:53069775 | A | T | 1 | a0001c0001t0002g0362 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2084-334A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069775 | |||||||
| chr5:53069810 | AT | A | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2084-296delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr5 | 53069810 | ||||||
| chr5:53069843 | C | T | 1 | a0001c0002t0009g0174 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2084-266C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069843 | |||||||
| chr5:53069974 | A | G | 1 | a0001c0001t0005g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2084-135A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069974 | |||||||
| chr5:53070093 | A | ATT | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
splice_region_variant&intron_variant | LOW | c.2084-9_2084-8dupTT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr5 | 53070093 | ||||||
| chr5:53070102 | A | G | 1 | a0001c0002t0018g0104 | 1 | HG03710.hp1 | splice_region_variant&intron_variant | LOW | c.2084-7A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53070102 | |||||||
| chr5:53070308 | G | A | 259 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(256): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.2235+48G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070308 | |||||||
| chr5:53070332 | G | A | 65 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(62): Show |
68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.2235+72G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070332 | |||||||
| chr5:53070343 | A | C | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2235+83A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070343 | |||||||
| chr5:53070454 | G | A | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2235+194G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070454 | |||||||
| chr5:53070506 | T | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2235+246T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070506 | |||||||
| chr5:53070551 | A | G | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2235+291A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070551 | |||||||
| chr5:53070565 | G | C | 19 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(16): Show |
21 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.2235+305G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070565 | |||||||
| chr5:53070674 | T | C | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2235+414T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070674 | |||||||
| chr5:53070804 | G | A | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2235+544G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070804 | |||||||
| chr5:53070887 | T | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2235+627T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070887 | |||||||
| chr5:53070890 | C | CT | 22 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(19): Show |
24 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.2235+636dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr5 | 53070890 | ||||||
| chr5:53070928 | A | G | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2235+668A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070928 | |||||||
| chr5:53070948 | C | T | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2235+688C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070948 | |||||||
| chr5:53070949 | G | A | 40 | a0001c0002t0004g0004 a0001c0002t0004g0088 a0001c0002t0004g0097 others(37): Show |
42 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2235+689G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070949 | |||||||
| chr5:53071050 | A | C | 172 | a0001c0001t0024g0213 a0001c0002t0003g0003 a0001c0002t0003g0032 others(169): Show |
183 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.2235+790A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071050 | |||||||
| chr5:53071066 | T | C | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2235+806T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071066 | |||||||
| chr5:53071075 | A | G | 31 | a0001c0001t0005g0005 a0001c0001t0005g0020 a0001c0001t0005g0216 others(28): Show |
34 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.2235+815A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071075 | |||||||
| chr5:53071139 | C | T | 3 | a0001c0001t0002g0156 a0001c0001t0002g0266 a0001c0002t0003g0032 |
3 | HG01081.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2236-799C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071139 | |||||||
| chr5:53071259 | G | GA | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2236-673dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr5 | 53071259 | ||||||
| chr5:53071316 | C | T | 5 | a0001c0002t0018g0102 a0001c0002t0018g0104 a0001c0002t0018g0118 others(2): Show |
5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2236-622C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071316 | |||||||
| chr5:53071348 | C | T | 27 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(24): Show |
29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2236-590C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071348 | |||||||
| chr5:53071495 | C | A | 1 | a0001c0002t0003g0205 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2236-443C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071495 | |||||||
| chr5:53071719 | T | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2236-219T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071719 | |||||||
| chr5:53071836 | A | T | 292 | a0001c0001t0001g0086 a0001c0001t0002g0012 a0001c0001t0002g0013 others(289): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.2236-102A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071836 | |||||||
| chr5:53071876 | T | C | 171 | a0001c0001t0024g0213 a0001c0002t0003g0003 a0001c0002t0003g0032 others(168): Show |
182 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.2236-62T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071876 | |||||||
| chr5:53071885 | T | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2236-53T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071885 | |||||||
| chr5:53072126 | G | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0001g0089 others(11): Show |
14 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2346+78G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072126 | |||||||
| chr5:53072138 | C | T | 1 | a0001c0001t0005g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2346+90C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072138 | |||||||
| chr5:53072394 | G | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2347-219G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072394 | |||||||
| chr5:53072416 | TC | T | 40 | a0001c0002t0004g0004 a0001c0002t0004g0088 a0001c0002t0004g0097 others(37): Show |
42 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2347-192delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr5 | 53072416 | ||||||
| chr5:53072536 | A | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2347-77A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072536 | |||||||
| chr5:53072544 | A | G | 2 | a0002c0009t0016g0315 a0002c0009t0016g0316 |
2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2347-69A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072544 | |||||||
| chr5:53072562 | T | C | 1 | a0002c0003t0017g0024 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2347-51T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072562 | |||||||
| chr5:53072716 | T | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2429+21T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072716 | |||||||
| chr5:53072735 | A | T | 19 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(16): Show |
21 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.2429+40A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072735 | |||||||
| chr5:53072764 | C | T | 35 | a0001c0001t0001g0065 a0001c0001t0001g0313 a0002c0003t0007g0021 others(32): Show |
37 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.2429+69C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072764 | |||||||
| chr5:53072765 | G | C | 1 | a0001c0021t0050g0365 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2429+70G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072765 | |||||||
| chr5:53072896 | G | C | 1 | a0001c0004t0008g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2429+201G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072896 | |||||||
| chr5:53073025 | A | C | 1 | a0001c0002t0004g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2430-93A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53073025 | |||||||
| chr5:53073087 | G | A | 1 | a0001c0008t0021g0016 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2430-31G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53073087 | |||||||
| chr5:53073092 | T | A | 134 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(131): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.2430-26T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53073092 | |||||||
| chr5:53073111 | T | C | 1 | a0002c0003t0007g0333 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.2430-7T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53073111 | |||||||
| chr5:53073363 | A | G | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2571+104A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073363 | |||||||
| chr5:53073505 | A | G | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2571+246A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073505 | |||||||
| chr5:53073547 | C | G | 2 | a0001c0001t0005g0286 a0001c0001t0005g0311 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2571+288C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073547 | |||||||
| chr5:53073665 | C | T | 22 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(19): Show |
24 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.2571+406C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073665 | |||||||
| chr5:53073790 | T | C | 3 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 |
3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2571+531T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073790 | |||||||
| chr5:53073830 | T | G | 1 | a0001c0001t0005g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2572-555T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073830 | |||||||
| chr5:53073834 | G | A | 60 | a0001c0002t0003g0003 a0001c0002t0003g0063 a0001c0002t0003g0070 others(57): Show |
63 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2572-551G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073834 | |||||||
| chr5:53073913 | C | T | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2572-472C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073913 | |||||||
| chr5:53073944 | T | TA | 19 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0001g0134 others(16): Show |
19 | HG01106.hp1 HG01106.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2572-419dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr5 | 53073944 | ||||||
| chr5:53073944 | TA | T | 6 | a0001c0001t0001g0060 a0001c0001t0015g0157 a0001c0002t0003g0063 others(3): Show |
6 | HG00280.hp2 HG01257.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2572-419delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr5 | 53073944 | ||||||
| chr5:53073944 | TAAAA | T | 27 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(24): Show |
29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2572-422_2572-419d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr5 | 53073944 | ||||||
| chr5:53073944 | TAAAAA | T | 6 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(3): Show |
6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2572-423_2572-419d others(7): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr5 | 53073944 | ||||||
| chr5:53073960 | A | C | 22 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(19): Show |
26 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2572-425A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073960 | |||||||
| chr5:53074005 | T | C | 2 | a0001c0001t0005g0286 a0001c0001t0005g0311 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2572-380T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074005 | |||||||
| chr5:53074037 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2572-348A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074037 | |||||||
| chr5:53074098 | C | T | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0149 |
3 | NA18970.hp1 NA18985.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2572-287C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074098 | |||||||
| chr5:53074158 | T | C | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2572-227T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074158 | |||||||
| chr5:53074188 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2572-197C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074188 | |||||||
| chr5:53074252 | G | A | 4 | a0002c0003t0007g0323 a0002c0003t0007g0333 a0002c0003t0007g0341 others(1): Show |
4 | NA18989.hp2 NA19056.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.2572-133G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074252 | |||||||
| chr5:53074331 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2572-54A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074331 | |||||||
| chr5:53074344 | G | A | 172 | a0001c0001t0025g0367 a0001c0002t0003g0003 a0001c0002t0003g0032 others(169): Show |
183 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.2572-41G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074344 | |||||||
| chr5:53074557 | A | G | 3 | a0002c0003t0007g0210 a0002c0003t0007g0211 a0002c0003t0007g0212 |
3 | HG02055.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2664+80A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074557 | |||||||
| chr5:53074602 | G | C | 33 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2664+125G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074602 | |||||||
| chr5:53074663 | T | C | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2664+186T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074663 | |||||||
| chr5:53074844 | C | T | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2665-217C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074844 | |||||||
| chr5:53074886 | G | A | 1 | a0001c0002t0006g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2665-175G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074886 | |||||||
| chr5:53074902 | G | T | 33 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2665-159G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074902 | |||||||
| chr5:53074909 | A | G | 1 | a0003c0005t0003g0176 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2665-152A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074909 | |||||||
| chr5:53074941 | G | C | 14 | a0001c0002t0003g0003 a0001c0002t0003g0167 a0001c0002t0003g0182 others(11): Show |
15 | HG00741.hp2 HG01433.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.2665-120G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074941 | |||||||
| chr5:53075005 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2665-56C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53075005 | |||||||
| chr5:53075540 | C | T | 171 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(168): Show |
182 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.2825+236C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53075540 | |||||||
| chr5:53075770 | A | G | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2825+466A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53075770 | |||||||
| chr5:53075837 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2825+533C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53075837 | |||||||
| chr5:53075878 | G | GT | 27 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(24): Show |
29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2825+580dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr5 | 53075878 | ||||||
| chr5:53075978 | T | C | 23 | a0001c0004t0002g0329 a0001c0004t0008g0290 a0001c0004t0008g0291 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2825+674T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53075978 | |||||||
| chr5:53076044 | C | T | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2825+740C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076044 | |||||||
| chr5:53076189 | C | A | 1 | a0001c0001t0001g0224 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2825+885C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076189 | |||||||
| chr5:53076217 | G | A | 1 | a0001c0002t0006g0001 | 3 | HG01257.hp2 HG01496.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2825+913G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076217 | |||||||
| chr5:53076232 | C | T | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2825+928C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076232 | |||||||
| chr5:53076321 | C | G | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2825+1017C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076321 | |||||||
| chr5:53076358 | A | G | 1 | a0001c0001t0002g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2825+1054A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076358 | |||||||
| chr5:53076586 | C | T | 2 | a0001c0001t0014g0275 a0001c0001t0014g0276 |
2 | NA18939.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2825+1282C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076586 | |||||||
| chr5:53076620 | C | T | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2825+1316C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076620 | |||||||
| chr5:53076920 | T | A | 1 | a0001c0002t0003g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2825+1616T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076920 | |||||||
| chr5:53077057 | CAT | C | 33 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2826-1714_2826-171 others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077057 | |||||||
| chr5:53077296 | G | A | 14 | a0001c0002t0003g0003 a0001c0002t0003g0167 a0001c0002t0003g0182 others(11): Show |
15 | HG00741.hp2 HG01433.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.2826-1476G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077296 | |||||||
| chr5:53077382 | T | TA | 5 | a0001c0002t0018g0102 a0001c0002t0018g0104 a0001c0002t0018g0118 others(2): Show |
5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2826-1382dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr5 | 53077382 | ||||||
| chr5:53077408 | G | A | 135 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(132): Show |
144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.2826-1364G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077408 | |||||||
| chr5:53077411 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2826-1361A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077411 | |||||||
| chr5:53077446 | A | G | 3 | a0001c0002t0003g0063 a0001c0002t0003g0070 a0001c0002t0003g0147 |
3 | NA18948.hp1 NA19056.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2826-1326A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077446 | |||||||
| chr5:53077453 | T | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2826-1319T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077453 | |||||||
| chr5:53077572 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2826-1200C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077572 | |||||||
| chr5:53077599 | T | C | 135 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(132): Show |
144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.2826-1173T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077599 | |||||||
| chr5:53077622 | C | G | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2826-1150C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077622 | |||||||
| chr5:53077782 | G | A | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2826-990G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077782 | |||||||
| chr5:53077866 | C | T | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.2826-906C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077866 | |||||||
| chr5:53077872 | A | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2826-900A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077872 | |||||||
| chr5:53077980 | C | T | 58 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(55): Show |
62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.2826-792C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077980 | |||||||
| chr5:53078258 | T | C | 92 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(89): Show |
97 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2826-514T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078258 | |||||||
| chr5:53078366 | A | T | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | NA18980.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2826-406A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078366 | |||||||
| chr5:53078397 | A | C | 67 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(64): Show |
72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.2826-375A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078397 | |||||||
| chr5:53078622 | T | G | 1 | a0001c0021t0050g0365 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2826-150T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078622 | |||||||
| chr5:53078690 | AAGATACT others(5): Show |
A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-80_2826-69del others(12): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr5 | 53078690 | ||||||
| chr5:53078697 | TTAAA | T | 5 | a0001c0002t0018g0102 a0001c0002t0018g0104 a0001c0002t0018g0118 others(2): Show |
5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2826-70_2826-67del others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr5 | 53078697 | ||||||
| chr5:53078706 | A | G | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-66A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078706 | |||||||
| chr5:53078708 | A | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-64A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078708 | |||||||
| chr5:53078711 | T | A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-61T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078711 | |||||||
| chr5:53078715 | A | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-57A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078715 | |||||||
| chr5:53078718 | C | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-54C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078718 | |||||||
| chr5:53078720 | T | A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-52T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078720 | |||||||
| chr5:53078721 | C | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-51C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078721 | |||||||
| chr5:53078722 | A | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-50A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078722 | |||||||
| chr5:53078725 | A | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-47A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078725 | |||||||
| chr5:53078737 | C | A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-35C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078737 | |||||||
| chr5:53078743 | T | C | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-29T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078743 | |||||||
| chr5:53078746 | T | A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-26T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078746 | |||||||
| chr5:53078750 | C | G | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-22C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078750 | |||||||
| chr5:53078751 | T | C | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-21T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078751 | |||||||
| chr5:53078763 | A | G | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-9A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078763 | |||||||
| chr5:53078769 | C | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | splice_region_variant&intron_variant | LOW | c.2826-3C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078769 | |||||||
| chr5:53078770 | A | G | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.2826-2A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078770 | |||||||
| chr5:53078771 | G | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.2826-1G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078771 | |||||||
| chr5:53079009 | T | A | 1 | a0001c0002t0003g0190 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2928+135T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079009 | |||||||
| chr5:53079120 | A | T | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | NA18980.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2928+246A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079120 | |||||||
| chr5:53079152 | T | C | 1 | a0001c0001t0001g0313 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2928+278T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079152 | |||||||
| chr5:53079224 | G | C | 1 | a0001c0002t0003g0168 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2928+350G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079224 | |||||||
| chr5:53079290 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2928+416G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079290 | |||||||
| chr5:53079529 | G | A | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2928+655G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079529 | |||||||
| chr5:53079552 | A | G | 27 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(24): Show |
29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2928+678A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079552 | |||||||
| chr5:53079645 | TA | T | 7 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(4): Show |
7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2928+779delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr5 | 53079645 | ||||||
| chr5:53079706 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0362 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2929-805G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079706 | |||||||
| chr5:53079706 | G | C | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.2929-805G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079706 | |||||||
| chr5:53079753 | C | T | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2929-758C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079753 | |||||||
| chr5:53079754 | G | A | 3 | a0001c0001t0002g0131 a0001c0001t0038g0127 a0001c0022t0002g0250 |
3 | HG02602.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2929-757G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079754 | |||||||
| chr5:53079755 | C | T | 1 | a0001c0001t0025g0367 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2929-756C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079755 | |||||||
| chr5:53079923 | A | G | 1 | a0001c0001t0001g0335 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2929-588A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079923 | |||||||
| chr5:53080097 | C | T | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2929-414C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080097 | |||||||
| chr5:53080289 | G | A | 33 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2929-222G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080289 | |||||||
| chr5:53080335 | G | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2929-176G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080335 | |||||||
| chr5:53080417 | C | T | 1 | a0002c0003t0007g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2929-94C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080417 | |||||||
| chr5:53080438 | C | T | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2929-73C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080438 | |||||||
| chr5:53080439 | G | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2929-72G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080439 | |||||||
| chr5:53080442 | G | T | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2929-69G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080442 | |||||||
| chr5:53080694 | G | A | 4 | a0001c0008t0012g0159 a0001c0008t0012g0160 a0001c0008t0012g0161 others(1): Show |
5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3039+73G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080694 | |||||||
| chr5:53080888 | T | C | 1 | a0006c0029t0001g0289 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3039+267T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080888 | |||||||
| chr5:53080931 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3039+310T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080931 | |||||||
| chr5:53080989 | C | T | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3039+368C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080989 | |||||||
| chr5:53080990 | G | A | 33 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.3039+369G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080990 | |||||||
| chr5:53081086 | G | T | 291 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(288): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.3039+465G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081086 | |||||||
| chr5:53081133 | C | A | 1 | a0001c0001t0002g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3040-459C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081133 | |||||||
| chr5:53081285 | T | C | 3 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 |
3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3040-307T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081285 | |||||||
| chr5:53081347 | A | G | 2 | a0002c0003t0007g0319 a0002c0003t0007g0320 |
2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3040-245A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081347 | |||||||
| chr5:53081351 | T | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3040-241T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081351 | |||||||
| chr5:53081447 | A | T | 3 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 |
3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3040-145A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081447 | |||||||
| chr5:53081524 | A | G | 1 | a0001c0002t0003g0205 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3040-68A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081524 | |||||||
| chr5:53081783 | T | C | 7 | a0004c0006t0003g0017 a0004c0006t0003g0166 a0004c0006t0003g0169 others(4): Show |
8 | NA18947.hp1 NA18970.hp2 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.3144+87T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53081783 | |||||||
| chr5:53081784 | C | A | 1 | a0001c0001t0001g0303 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3144+88C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53081784 | |||||||
| chr5:53081818 | A | G | 1 | a0001c0021t0050g0365 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3144+122A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53081818 | |||||||
| chr5:53081886 | G | A | 1 | a0001c0002t0041g0318 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3144+190G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53081886 | |||||||
| chr5:53082104 | C | T | 1 | a0001c0001t0025g0366 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3144+408C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082104 | |||||||
| chr5:53082407 | T | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3144+711T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082407 | |||||||
| chr5:53082465 | G | A | 135 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(132): Show |
144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3144+769G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082465 | |||||||
| chr5:53082558 | G | C | 1 | a0001c0001t0001g0069 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3145-782G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082558 | |||||||
| chr5:53082606 | C | T | 38 | a0001c0002t0004g0004 a0001c0002t0004g0088 a0001c0002t0004g0097 others(35): Show |
40 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.3145-734C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082606 | |||||||
| chr5:53082679 | T | G | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3145-661T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082679 | |||||||
| chr5:53082692 | A | G | 6 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(3): Show |
6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3145-648A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082692 | |||||||
| chr5:53082779 | T | C | 5 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3145-561T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082779 | |||||||
| chr5:53082843 | C | T | 5 | a0001c0002t0018g0102 a0001c0002t0018g0104 a0001c0002t0018g0118 others(2): Show |
5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.3145-497C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082843 | |||||||
| chr5:53082922 | A | G | 1 | a0001c0002t0004g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3145-418A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082922 | |||||||
| chr5:53082961 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3145-379T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082961 | |||||||
| chr5:53083020 | GT | G | 134 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(131): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.3145-313delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr5 | 53083020 | ||||||
| chr5:53083089 | T | G | 5 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3145-251T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083089 | |||||||
| chr5:53083126 | G | A | 56 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(53): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3145-214G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083126 | |||||||
| chr5:53083130 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3145-210T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083130 | |||||||
| chr5:53083189 | G | A | 167 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(164): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.3145-151G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083189 | |||||||
| chr5:53083196 | T | C | 5 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3145-144T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083196 | |||||||
| chr5:53083293 | C | T | 1 | a0002c0009t0016g0215 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3145-47C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083293 | |||||||
| chr5:53083670 | A | G | 1 | a0001c0002t0003g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3258+217A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53083670 | |||||||
| chr5:53084292 | A | AT | 94 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(91): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.3258+849dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr5 | 53084292 | ||||||
| chr5:53084354 | AT | A | 6 | a0002c0007t0010g0162 a0002c0007t0010g0163 a0002c0007t0010g0164 others(3): Show |
6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3258+910delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr5 | 53084354 | ||||||
| chr5:53084677 | GT | G | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3258+1226delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr5 | 53084677 | ||||||
| chr5:53084765 | T | C | 3 | a0001c0002t0003g0199 a0001c0002t0003g0200 a0001c0002t0003g0201 |
3 | HG01515.hp1 HG01517.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3258+1312T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53084765 | |||||||
| chr5:53084791 | CACTG | C | 19 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(16): Show |
21 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.3258+1343_3258+134 others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr5 | 53084791 | ||||||
| chr5:53085093 | A | T | 38 | a0001c0002t0004g0004 a0001c0002t0004g0088 a0001c0002t0004g0097 others(35): Show |
40 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.3258+1640A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085093 | |||||||
| chr5:53085271 | T | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-1681T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085271 | |||||||
| chr5:53085290 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3259-1662G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085290 | |||||||
| chr5:53085291 | G | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-1661G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085291 | |||||||
| chr5:53085291 | G | T | 1 | a0001c0001t0002g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3259-1661G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085291 | |||||||
| chr5:53085294 | C | A | 1 | a0001c0001t0002g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3259-1658C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085294 | |||||||
| chr5:53085332 | A | C | 30 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(27): Show |
32 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.3259-1620A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085332 | |||||||
| chr5:53085334 | C | G | 22 | a0001c0004t0008g0290 a0001c0004t0008g0291 a0001c0004t0008g0292 others(19): Show |
22 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.3259-1618C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085334 | |||||||
| chr5:53085386 | T | C | 5 | a0001c0002t0018g0102 a0001c0002t0018g0104 a0001c0002t0018g0118 others(2): Show |
5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.3259-1566T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085386 | |||||||
| chr5:53085575 | T | C | 1 | a0001c0001t0051g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3259-1377T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085575 | |||||||
| chr5:53085822 | C | T | 1 | a0002c0003t0007g0267 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3259-1130C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085822 | |||||||
| chr5:53085922 | T | C | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3259-1030T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085922 | |||||||
| chr5:53086022 | C | T | 1 | a0001c0001t0038g0127 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3259-930C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086022 | |||||||
| chr5:53086030 | G | A | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3259-922G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086030 | |||||||
| chr5:53086051 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3259-901C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086051 | |||||||
| chr5:53086072 | T | C | 3 | a0002c0009t0016g0215 a0002c0009t0016g0315 a0002c0009t0016g0316 |
3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3259-880T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086072 | |||||||
| chr5:53086103 | T | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-849T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086103 | |||||||
| chr5:53086171 | C | T | 2 | a0001c0001t0025g0366 a0001c0001t0025g0367 |
2 | HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3259-781C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086171 | |||||||
| chr5:53086375 | G | T | 2 | a0002c0003t0007g0021 a0002c0003t0007g0267 |
3 | HG01070.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3259-577G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086375 | |||||||
| chr5:53086388 | C | G | 134 | a0001c0002t0003g0003 a0001c0002t0003g0032 a0001c0002t0003g0063 others(131): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.3259-564C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086388 | |||||||
| chr5:53086455 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3259-497T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086455 | |||||||
| chr5:53086481 | C | T | 22 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(19): Show |
26 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3259-471C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086481 | |||||||
| chr5:53086519 | T | C | 135 | a0001c0001t0024g0213 a0001c0002t0003g0003 a0001c0002t0003g0032 others(132): Show |
144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3259-433T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086519 | |||||||
| chr5:53086587 | A | G | 1 | a0001c0001t0029g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3259-365A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086587 | |||||||
| chr5:53086612 | G | A | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-340G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086612 | |||||||
| chr5:53086776 | C | T | 1 | a0001c0001t0001g0344 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3259-176C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086776 | |||||||
| chr5:53086825 | T | C | 33 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.3259-127T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086825 | |||||||
| chr5:53086873 | T | C | 2 | a0001c0001t0002g0307 a0001c0001t0002g0309 |
2 | HG00280.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.3259-79T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086873 | |||||||
| chr5:53086918 | A | T | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-34A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086918 | |||||||
| chr5:53087074 | A | G | 22 | a0001c0004t0008g0290 a0001c0004t0008g0291 a0001c0004t0008g0292 others(19): Show |
22 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.3348+33A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087074 | |||||||
| chr5:53087095 | C | T | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3348+54C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087095 | |||||||
| chr5:53087235 | C | T | 3 | a0002c0003t0007g0022 a0002c0003t0007g0331 a0002c0003t0007g0342 |
4 | HG01192.hp1 HG01884.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3348+194C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087235 | |||||||
| chr5:53087278 | C | G | 1 | a0001c0001t0001g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3348+237C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087278 | |||||||
| chr5:53087321 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3348+280A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087321 | |||||||
| chr5:53087414 | G | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3348+373G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087414 | |||||||
| chr5:53087414 | G | T | 1 | a0016c0019t0030g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3348+373G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087414 | |||||||
| chr5:53087463 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3348+422T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087463 | |||||||
| chr5:53087598 | G | A | 1 | a0001c0001t0029g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3348+557G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087598 | |||||||
| chr5:53087624 | T | TA | 46 | a0001c0001t0001g0269 a0001c0002t0003g0186 a0001c0002t0004g0004 others(43): Show |
48 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.3348+599dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53087624 | ||||||
| chr5:53087624 | T | TAA | 85 | a0001c0002t0003g0003 a0001c0002t0003g0063 a0001c0002t0003g0070 others(82): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.3348+598_3348+599d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53087624 | ||||||
| chr5:53087624 | T | TAAA | 7 | a0001c0001t0024g0213 a0001c0002t0003g0032 a0001c0002t0003g0107 others(4): Show |
7 | HG01081.hp1 HG01993.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.3348+597_3348+599d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53087624 | ||||||
| chr5:53087624 | TA | T | 9 | a0001c0001t0001g0058 a0001c0004t0008g0294 a0001c0011t0034g0084 others(6): Show |
9 | HG01070.hp2 HG01243.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.3348+599delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53087624 | ||||||
| chr5:53087721 | C | T | 1 | a0001c0001t0005g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3348+680C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087721 | |||||||
| chr5:53087808 | C | T | 23 | a0001c0002t0006g0001 a0001c0002t0006g0002 a0001c0002t0006g0035 others(20): Show |
27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.3348+767C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087808 | |||||||
| chr5:53087888 | C | G | 171 | a0001c0001t0024g0213 a0001c0002t0003g0003 a0001c0002t0003g0032 others(168): Show |
182 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.3348+847C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087888 | |||||||
| chr5:53088002 | T | C | 171 | a0001c0001t0024g0213 a0001c0002t0003g0003 a0001c0002t0003g0032 others(168): Show |
182 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.3348+961T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088002 | |||||||
| chr5:53088005 | G | A | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3348+964G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088005 | |||||||
| chr5:53088157 | G | A | 72 | a0001c0001t0024g0213 a0001c0002t0003g0003 a0001c0002t0003g0032 others(69): Show |
75 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.3348+1116G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088157 | |||||||
| chr5:53088175 | A | T | 5 | a0002c0003t0017g0024 a0002c0003t0017g0025 a0002c0003t0017g0026 others(2): Show |
5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.3348+1134A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088175 | |||||||
| chr5:53088391 | A | G | 1 | a0001c0001t0029g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3348+1350A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088391 | |||||||
| chr5:53088412 | A | G | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3348+1371A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088412 | |||||||
| chr5:53088462 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3348+1421A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088462 | |||||||
| chr5:53088484 | G | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3348+1443G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088484 | |||||||
| chr5:53088511 | A | C | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3349-1435A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088511 | |||||||
| chr5:53088602 | C | T | 1 | a0001c0004t0008g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3349-1344C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088602 | |||||||
| chr5:53088613 | G | A | 1 | a0001c0002t0004g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3349-1333G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088613 | |||||||
| chr5:53088685 | C | CA | 130 | a0001c0001t0001g0281 a0001c0001t0001g0301 a0001c0001t0024g0213 others(127): Show |
140 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.3349-1242dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53088685 | ||||||
| chr5:53088685 | C | CAA | 31 | a0001c0002t0003g0188 a0001c0002t0009g0175 a0002c0003t0007g0021 others(28): Show |
33 | HG00323.hp2 HG00621.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.3349-1243_3349-124 others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53088685 | ||||||
| chr5:53088685 | CA | C | 55 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(52): Show |
58 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.3349-1242delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53088685 | ||||||
| chr5:53088712 | G | A | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3349-1234G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088712 | |||||||
| chr5:53088833 | G | C | 259 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(256): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.3349-1113G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088833 | |||||||
| chr5:53088849 | C | T | 1 | a0001c0016t0005g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3349-1097C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088849 | |||||||
| chr5:53089056 | C | A | 6 | a0001c0002t0009g0029 a0001c0002t0009g0173 a0001c0002t0009g0174 others(3): Show |
6 | HG00280.hp2 NA18995.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.3349-890C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089056 | |||||||
| chr5:53089182 | C | A | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3349-764C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089182 | |||||||
| chr5:53089230 | C | T | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3349-716C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089230 | |||||||
| chr5:53089482 | C | T | 4 | a0001c0002t0004g0114 a0001c0002t0004g0142 a0001c0002t0048g0238 others(1): Show |
4 | HG02074.hp1 HG02293.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.3349-464C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089482 | |||||||
| chr5:53089574 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3349-372G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089574 | |||||||
| chr5:53089683 | T | C | 1 | a0001c0004t0008g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3349-263T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089683 | |||||||
| chr5:53089715 | T | C | 1 | a0001c0004t0008g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3349-231T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089715 | |||||||
| chr5:53090123 | A | G | 4 | a0001c0002t0004g0097 a0001c0002t0004g0240 a0001c0002t0004g0251 others(1): Show |
4 | HG02809.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3465+61A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090123 | |||||||
| chr5:53090225 | C | T | 1 | a0001c0008t0021g0016 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3465+163C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090225 | |||||||
| chr5:53090401 | C | T | 36 | a0002c0003t0007g0021 a0002c0003t0007g0022 a0002c0003t0007g0073 others(33): Show |
38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3466-118C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090401 | |||||||
| chr5:53090441 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3466-78G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090441 | |||||||
| chr5:53090485 | G | A | 4 | a0001c0002t0003g0180 a0001c0002t0003g0199 a0001c0002t0003g0200 others(1): Show |
4 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.3466-34G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090485 |