Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3685 |
| ensemblid | ENSG00000138448.13 |
| hgncid | 6150 |
| symbol | ITGAV |
| name | integrin subunit alpha V |
| refseq_nuc | NM_002210.5 |
| refseq_prot | NP_002201.2 |
| ensembl_nuc | ENST00000261023.8 |
| ensembl_prot | ENSP00000261023.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 186590056 |
| end | 186680901 |
| strand | + |
| ver | v1.2 |
| region | chr2:186590056-186680901 |
| region5000 | chr2:186585056-186685901 |
| regionname0 | ITGAV_chr2_186590056_186680901 |
| regionname5000 | ITGAV_chr2_186585056_186685901 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1048 | 275 | 74 | 60 | 88 | 14 | 38 | 56 | ITGAV_chr2_186585056_186685901 | ITGAV | MAFPP others(1043): Show |
chr2 | 186585056 | 186685901 |
| a0002 | 0/0 | 1048 | 23 | 7 | 6 | 10 | 0 | 0 | 9 | ITGAV_chr2_186585056_186685901 | ITGAV | MAFPP others(1043): Show |
chr2 | 186585056 | 186685901 |
| a0003 | 1/0 | 1048 | 7 | 6 | 0 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | MAFPP others(1043): Show |
chr2 | 186585056 | 186685901 |
| a0004 | 0/0 | 1048 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | MAFPP others(1043): Show |
chr2 | 186585056 | 186685901 |
| a0005 | 0/0 | 1048 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | MAFPP others(1043): Show |
chr2 | 186585056 | 186685901 |
| a0006 | 0/0 | 1048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | MAFPP others(1043): Show |
chr2 | 186585056 | 186685901 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3144 | 264 | 63 | 60 | 88 | 14 | 38 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 | ||
| a0001c0003 | 0/0 | 3144 | 7 | 7 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 | ||
| a0001c0005 | 0/0 | 3144 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 | ||
| a0001c0008 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 | ||
| a0002c0002 | 0/0 | 3144 | 22 | 7 | 5 | 10 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 | ||
| a0002c0006 | 0/0 | 3144 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 | ||
| a0003c0004 | 1/0 | 3144 | 7 | 6 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 | ||
| a0004c0007 | 0/0 | 3144 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 | ||
| a0005c0010 | 0/0 | 3144 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 | ||
| a0006c0009 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | ATGGC others(3139): Show |
chr2 | 186585056 | 186685901 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7039 | 119 | 26 | 24 | 45 | 6 | 17 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0002 | 0/0 | 7034 | 65 | 4 | 22 | 23 | 4 | 12 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7029): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0003 | 0/0 | 7037 | 50 | 11 | 13 | 14 | 4 | 8 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7032): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0005 | 0/0 | 7041 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7036): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0006 | 0/0 | 7040 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7035): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0008 | 0/0 | 7039 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0009 | 0/0 | 7034 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7029): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0010 | 0/0 | 7042 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7037): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0011 | 0/0 | 7039 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0012 | 0/0 | 7039 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0013 | 0/0 | 7037 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7032): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0014 | 0/0 | 7041 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7036): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0015 | 0/0 | 7041 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7036): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0016 | 0/0 | 7040 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7035): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0017 | 0/0 | 7041 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7036): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0018 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0019 | 0/0 | 7034 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7029): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0021 | 0/0 | 7034 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7029): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0023 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0001c0001t0024 | 0/0 | 7041 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7036): Show |
chr2 | 186585056 | 186685901 |
| a0001c0003t0001 | 0/0 | 7039 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0001c0003t0002 | 0/0 | 7034 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7029): Show |
chr2 | 186585056 | 186685901 |
| a0001c0005t0002 | 0/0 | 7034 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7029): Show |
chr2 | 186585056 | 186685901 |
| a0001c0008t0020 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7032): Show |
chr2 | 186585056 | 186685901 |
| a0002c0002t0001 | 0/0 | 7039 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0002c0002t0002 | 0/0 | 7034 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7029): Show |
chr2 | 186585056 | 186685901 |
| a0002c0002t0004 | 0/0 | 7039 | 15 | 2 | 3 | 10 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0002c0002t0007 | 0/0 | 7037 | 3 | 2 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7032): Show |
chr2 | 186585056 | 186685901 |
| a0002c0002t0022 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0002c0006t0001 | 0/0 | 7039 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0003c0004t0001 | 1/0 | 7039 | 7 | 6 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7034): Show |
chr2 | 186585056 | 186685901 |
| a0004c0007t0003 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7032): Show |
chr2 | 186585056 | 186685901 |
| a0005c0010t0003 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7032): Show |
chr2 | 186585056 | 186685901 |
| a0006c0009t0003 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | AGTCC others(7032): Show |
chr2 | 186585056 | 186685901 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0010g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0010g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0013g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0013g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0015g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0016g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0017g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0018g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0019g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0021g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0023g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0001t0024g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0003t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0003t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0005t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0005t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0001c0008t0020g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0007g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0002t0022g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0002c0006t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0003c0004t0001g0002 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0003c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0003c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0003c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0003c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0003c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0004c0007t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0005c0010t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| a0006c0009t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0241 | EUR | GBR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0253 | EUR | FIN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | FIN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0135 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01081 | hp1 | a0001 | c0001 | t0015 | g0280 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01099 | hp1 | a0002 | c0006 | t0001 | g0292 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01192 | hp2 | a0002 | c0002 | t0007 | g0140 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | IBS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01884 | hp1 | a0001 | c0001 | t0019 | g0032 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01952 | hp1 | a0002 | c0002 | t0004 | g0131 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01975 | hp1 | a0002 | c0002 | t0004 | g0130 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02015 | hp1 | a0004 | c0007 | t0003 | g0008 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02148 | hp1 | a0002 | c0002 | t0004 | g0227 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CDX | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CDX | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CDX | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02257 | hp2 | a0001 | c0005 | t0002 | g0066 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0289 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02615 | hp2 | a0001 | c0005 | t0002 | g0033 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02630 | hp2 | a0002 | c0002 | t0004 | g0260 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02647 | hp2 | a0002 | c0002 | t0004 | g0158 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02723 | hp1 | a0003 | c0004 | t0001 | g0086 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02886 | hp1 | a0001 | c0008 | t0020 | g0022 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0160 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02896 | hp2 | a0001 | c0001 | t0023 | g0071 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0142 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0077 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0118 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0002 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03098 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0287 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0097 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0286 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03209 | hp2 | a0001 | c0001 | t0012 | g0098 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03453 | hp1 | a0001 | c0001 | t0024 | g0107 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0082 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03486 | hp1 | a0001 | c0001 | t0017 | g0106 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03516 | hp1 | a0003 | c0004 | t0001 | g0081 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0110 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0290 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0246 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0272 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04204 | hp1 | a0001 | c0001 | t0021 | g0231 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18522 | hp2 | a0003 | c0004 | t0001 | g0083 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0288 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18948 | hp2 | a0002 | c0002 | t0004 | g0124 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18950 | hp1 | a0001 | c0001 | t0010 | g0164 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18950 | hp2 | a0002 | c0002 | t0004 | g0127 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18951 | hp1 | a0002 | c0002 | t0004 | g0138 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18964 | hp1 | a0002 | c0002 | t0004 | g0129 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18967 | hp1 | a0001 | c0001 | t0013 | g0056 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18972 | hp2 | a0002 | c0002 | t0004 | g0133 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18989 | hp1 | a0002 | c0002 | t0004 | g0125 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18992 | hp1 | a0001 | c0001 | t0010 | g0282 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18993 | hp1 | a0002 | c0002 | t0004 | g0132 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19009 | hp1 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19030 | hp1 | a0002 | c0002 | t0022 | g0090 | AFR | LWK | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | LWK | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19080 | hp2 | a0001 | c0001 | t0013 | g0055 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19083 | hp1 | a0005 | c0010 | t0003 | g0070 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19085 | hp1 | a0002 | c0002 | t0004 | g0134 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19088 | hp2 | a0001 | c0001 | t0009 | g0074 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA19240 | hp2 | a0001 | c0005 | t0002 | g0065 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | ASW | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | ASW | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | TSI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0247 | EUR | TSI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | GIH | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0034 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0136 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03471 | hp1 | a0001 | c0001 | t0018 | g0156 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG03471 | hp2 | a0002 | c0002 | t0007 | g0141 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG06807 | hp1 | a0002 | c0002 | t0007 | g0139 | AFR | USA | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | USA | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA18955 | hp2 | a0002 | c0002 | t0004 | g0126 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20300 | hp1 | a0006 | c0009 | t0003 | g0277 | AFR | USA | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | USA | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | LWK | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0146 | REF | REF | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| homoSapiens | grch38p0 | a0003 | c0004 | t0001 | g0002 | REF | REF | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:186638460 | G | A | 1 | a0004 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.898G>A | p.Glu300Lys | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/30 | 1181/7039 | 898/3147 | 300/1048 | chr2 | 186638460 | |||
| chr2:186646739 | A | G | 1 | a0002 | 23 | HG00423.hp2 HG01099.hp1 HG01192.hp2 others(20): Show |
missense_variant | MODERATE | c.1213A>G | p.Ile405Val | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/30 | 1496/7039 | 1213/3147 | 405/1048 | chr2 | 186646739 | |||
| chr2:186656364 | G | T | 1 | a0005 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.1682G>T | p.Gly561Val | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/30 | 1965/7039 | 1682/3147 | 561/1048 | chr2 | 186656364 | |||
| chr2:186667690 | G | A | 5 | a0001 a0002 a0004 others(2): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
missense_variant | MODERATE | c.2347G>A | p.Val783Ile | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/30 | 2630/7039 | 2347/3147 | 783/1048 | chr2 | 186667690 | |||
| chr2:186668906 | C | T | 1 | a0006 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.2578C>T | p.Pro860Ser | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/30 | 2861/7039 | 2578/3147 | 860/1048 | chr2 | 186668906 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:186625505 | G | A | 2 | a0001c0003 a0002c0006 |
8 | HG01099.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.441G>A | p.Glu147Glu | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/30 | 724/7039 | 441/3147 | 147/1048 | chr2 | 186625505 | |||
| chr2:186666727 | T | C | 1 | a0001c0008 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.2190T>C | p.Ser730Ser | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 22/30 | 2473/7039 | 2190/3147 | 730/1048 | chr2 | 186666727 | |||
| chr2:186675918 | C | T | 1 | a0001c0005 | 3 | HG02257.hp2 HG02615.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.2919C>T | p.Asn973Asn | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/30 | 3202/7039 | 2919/3147 | 973/1048 | chr2 | 186675918 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:186590107 | G | C | 1 | a0001c0001t0009 | 2 | NA19009.hp1 NA19088.hp2 |
5_prime_UTR_variant | MODIFIER | c.-232G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 232 | chr2 | 186590107 | ||||||
| chr2:186590127 | C | A | 1 | a0001c0001t0014 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-212C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 212 | chr2 | 186590127 | ||||||
| chr2:186590127 | C | G | 1 | a0001c0001t0024 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 212 | chr2 | 186590127 | ||||||
| chr2:186590132 | C | T | 1 | a0001c0001t0023 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-207C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 207 | chr2 | 186590132 | ||||||
| chr2:186590153 | G | T | 1 | a0002c0002t0022 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-186G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 186 | chr2 | 186590153 | ||||||
| chr2:186590288 | G | A | 2 | a0001c0001t0014 a0001c0001t0015 |
2 | HG01081.hp1 HG02895.hp2 |
5_prime_UTR_variant | MODIFIER | c.-51G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 51 | chr2 | 186590288 | ||||||
| chr2:186677555 | A | G | 1 | a0001c0001t0021 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 263 | chr2 | 186677555 | ||||||
| chr2:186677629 | C | T | 1 | a0001c0008t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 337 | chr2 | 186677629 | ||||||
| chr2:186677639 | T | TTTG | 7 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0014 others(4): Show |
14 | HG01081.hp1 HG01192.hp2 HG02622.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*377_*379dupGTT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 380 | INFO_REALIGN_3_PRIME | chr2 | 186677639 | |||||
| chr2:186677639 | T | TTTGTTG | 2 | a0001c0001t0006 a0001c0001t0016 |
4 | HG02976.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*374_*379dupGTTGTT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 380 | INFO_REALIGN_3_PRIME | chr2 | 186677639 | |||||
| chr2:186677912 | C | T | 1 | a0001c0001t0006 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*620C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 620 | chr2 | 186677912 | ||||||
| chr2:186678209 | TAGTA | T | 10 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(7): Show |
82 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*922_*925delAGTA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 922 | INFO_REALIGN_3_PRIME | chr2 | 186678209 | |||||
| chr2:186678341 | A | C | 1 | a0001c0008t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1049A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1049 | chr2 | 186678341 | ||||||
| chr2:186678396 | A | T | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0008t0020 others(3): Show |
56 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1104A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1104 | chr2 | 186678396 | ||||||
| chr2:186678500 | G | C | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0008t0020 others(3): Show |
56 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1208G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1208 | chr2 | 186678500 | ||||||
| chr2:186678575 | G | A | 1 | a0002c0002t0004 | 15 | HG00423.hp2 HG01952.hp1 HG01975.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1283G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1283 | chr2 | 186678575 | ||||||
| chr2:186678647 | C | T | 10 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(7): Show |
82 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1355C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1355 | chr2 | 186678647 | ||||||
| chr2:186679201 | C | G | 1 | a0001c0008t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1909C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1909 | chr2 | 186679201 | ||||||
| chr2:186679282 | T | C | 1 | a0001c0001t0011 | 2 | HG02970.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1990T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1990 | chr2 | 186679282 | ||||||
| chr2:186679495 | AT | A | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(12): Show |
91 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2212delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2212 | INFO_REALIGN_3_PRIME | chr2 | 186679495 | |||||
| chr2:186679495 | ATT | A | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0008t0020 others(3): Show |
56 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2211_*2212delTT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2211 | INFO_REALIGN_3_PRIME | chr2 | 186679495 | |||||
| chr2:186679525 | A | T | 1 | a0001c0001t0005 | 5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2233A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2233 | chr2 | 186679525 | ||||||
| chr2:186679873 | A | G | 5 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0015 others(2): Show |
9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2581A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2581 | chr2 | 186679873 | ||||||
| chr2:186680036 | T | C | 1 | a0001c0008t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2744T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2744 | chr2 | 186680036 | ||||||
| chr2:186680037 | A | G | 2 | a0001c0001t0008 a0001c0001t0023 |
4 | HG02486.hp2 HG02896.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2745A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2745 | chr2 | 186680037 | ||||||
| chr2:186680263 | T | C | 1 | a0001c0001t0011 | 2 | HG02970.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2971T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2971 | chr2 | 186680263 | ||||||
| chr2:186680478 | A | G | 1 | a0001c0001t0013 | 2 | NA18967.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3186A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3186 | chr2 | 186680478 | ||||||
| chr2:186680518 | A | T | 1 | a0001c0001t0012 | 2 | HG03139.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3226A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3226 | chr2 | 186680518 | ||||||
| chr2:186680589 | A | C | 5 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0015 others(2): Show |
9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3297A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3297 | chr2 | 186680589 | ||||||
| chr2:186680649 | C | T | 1 | a0001c0001t0018 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3357C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3357 | chr2 | 186680649 | ||||||
| chr2:186680719 | A | G | 1 | a0001c0001t0019 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3427A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3427 | chr2 | 186680719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:186590551 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(182): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.185+28C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590551 | |||||||
| chr2:186590578 | A | C | 1 | a0001c0001t0003g0014 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.185+55A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590578 | |||||||
| chr2:186590593 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.185+70A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590593 | |||||||
| chr2:186590685 | G | T | 1 | a0001c0001t0003g0293 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.185+162G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590685 | |||||||
| chr2:186590840 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.185+317C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590840 | |||||||
| chr2:186590886 | A | G | 1 | a0002c0006t0001g0292 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.185+363A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590886 | |||||||
| chr2:186590900 | T | C | 2 | a0001c0001t0003g0119 a0001c0001t0016g0118 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+377T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590900 | |||||||
| chr2:186590952 | C | T | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
4 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+429C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590952 | |||||||
| chr2:186590982 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.185+459C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590982 | |||||||
| chr2:186591020 | T | C | 1 | a0001c0001t0003g0120 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.185+497T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186591020 | |||||||
| chr2:186591184 | T | C | 25 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0137 others(22): Show |
25 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.185+661T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186591184 | |||||||
| chr2:186591394 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(157): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.185+871A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186591394 | |||||||
| chr2:186591751 | GATTAGAT others(1502): Show |
G | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+1230_185+2738d others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186591751 | ||||||
| chr2:186591947 | C | G | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.185+1424C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186591947 | |||||||
| chr2:186592045 | A | T | 1 | a0001c0001t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.185+1522A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592045 | |||||||
| chr2:186592046 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.185+1523G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592046 | |||||||
| chr2:186592152 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185+1629T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592152 | |||||||
| chr2:186592243 | A | C | 1 | a0001c0001t0002g0069 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.185+1720A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592243 | |||||||
| chr2:186592334 | G | A | 1 | a0001c0001t0003g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.185+1811G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592334 | |||||||
| chr2:186592536 | T | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | NA18949.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.185+2013T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592536 | |||||||
| chr2:186592574 | GT | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(171): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.185+2063delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186592574 | ||||||
| chr2:186592581 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.185+2058T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592581 | |||||||
| chr2:186592600 | A | G | 1 | a0001c0001t0002g0006 | 2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.185+2077A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592600 | |||||||
| chr2:186592656 | A | T | 1 | a0001c0001t0003g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.185+2133A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592656 | |||||||
| chr2:186592762 | G | T | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.185+2239G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592762 | |||||||
| chr2:186592861 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(193): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.185+2338A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592861 | |||||||
| chr2:186592890 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.185+2367C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592890 | |||||||
| chr2:186592916 | C | T | 2 | a0001c0001t0003g0119 a0001c0001t0016g0118 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+2393C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592916 | |||||||
| chr2:186593265 | T | G | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2742T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593265 | |||||||
| chr2:186593266 | A | T | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2743A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593266 | |||||||
| chr2:186593270 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2747T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593270 | |||||||
| chr2:186593273 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2750A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593273 | |||||||
| chr2:186593274 | A | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2751A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593274 | |||||||
| chr2:186593277 | A | T | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2754A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593277 | |||||||
| chr2:186593284 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2761T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593284 | |||||||
| chr2:186593285 | A | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2762A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593285 | |||||||
| chr2:186593286 | G | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2763G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593286 | |||||||
| chr2:186593290 | A | T | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2767A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593290 | |||||||
| chr2:186593292 | A | T | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2769A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593292 | |||||||
| chr2:186593293 | G | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2770G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593293 | |||||||
| chr2:186593295 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2772T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593295 | |||||||
| chr2:186593301 | G | T | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2778G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593301 | |||||||
| chr2:186593303 | G | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2780G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593303 | |||||||
| chr2:186593315 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2792A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593315 | |||||||
| chr2:186593320 | T | G | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2797T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593320 | |||||||
| chr2:186593324 | T | A | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2801T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593324 | |||||||
| chr2:186593326 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2803T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593326 | |||||||
| chr2:186593328 | A | C | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2805A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593328 | |||||||
| chr2:186593331 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2808G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593331 | |||||||
| chr2:186593332 | G | T | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2809G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593332 | |||||||
| chr2:186593337 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2814G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593337 | |||||||
| chr2:186593339 | C | G | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2816C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593339 | |||||||
| chr2:186593351 | C | A | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2828C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593351 | |||||||
| chr2:186593352 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2829A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593352 | |||||||
| chr2:186593355 | ATGTTAAG others(332): Show |
A | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2833_185+3171d others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593355 | |||||||
| chr2:186593459 | C | G | 1 | a0001c0001t0003g0276 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.185+2936C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593459 | |||||||
| chr2:186593461 | G | GT | 185 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(182): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.185+2947dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186593461 | ||||||
| chr2:186593530 | A | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.185+3007A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593530 | |||||||
| chr2:186593780 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.185+3257G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593780 | |||||||
| chr2:186593786 | G | GT | 186 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(183): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.185+3264dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186593786 | ||||||
| chr2:186593910 | A | C | 1 | a0001c0001t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.185+3387A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593910 | |||||||
| chr2:186593948 | A | T | 1 | a0001c0001t0002g0109 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.185+3425A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593948 | |||||||
| chr2:186594005 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.185+3482C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594005 | |||||||
| chr2:186594350 | T | A | 1 | a0001c0001t0003g0148 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.185+3827T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594350 | |||||||
| chr2:186594388 | C | A | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.185+3865C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594388 | |||||||
| chr2:186594477 | T | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.185+3954T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594477 | |||||||
| chr2:186594556 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.185+4033G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594556 | |||||||
| chr2:186594655 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.185+4132T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594655 | |||||||
| chr2:186594739 | A | G | 6 | a0001c0003t0001g0012 a0001c0003t0001g0288 a0001c0003t0001g0289 others(3): Show |
8 | HG01099.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+4216A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594739 | |||||||
| chr2:186594770 | C | G | 28 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0122 others(25): Show |
28 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+4247C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594770 | |||||||
| chr2:186594844 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185+4321G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594844 | |||||||
| chr2:186594849 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185+4326T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594849 | |||||||
| chr2:186594920 | C | T | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.185+4397C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594920 | |||||||
| chr2:186595374 | G | T | 1 | a0001c0001t0002g0116 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.185+4851G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186595374 | |||||||
| chr2:186595688 | TA | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(187): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.185+5176delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186595688 | ||||||
| chr2:186595796 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.185+5273A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186595796 | |||||||
| chr2:186596122 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.185+5599A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186596122 | |||||||
| chr2:186596372 | T | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0002g0006 others(2): Show |
6 | HG01975.hp2 HG02004.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-5649T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186596372 | |||||||
| chr2:186596452 | C | CT | 5 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
6 | HG00597.hp1 HG00642.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-5554dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186596452 | ||||||
| chr2:186596815 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.186-5206T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186596815 | |||||||
| chr2:186597002 | T | G | 1 | a0001c0001t0002g0020 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.186-5019T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597002 | |||||||
| chr2:186597151 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.186-4870A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597151 | |||||||
| chr2:186597404 | C | T | 1 | a0001c0001t0015g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.186-4617C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597404 | |||||||
| chr2:186597655 | C | A | 1 | a0002c0002t0004g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.186-4366C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597655 | |||||||
| chr2:186597854 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(203): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.186-4167A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597854 | |||||||
| chr2:186597875 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.186-4146A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597875 | |||||||
| chr2:186598292 | T | TAC | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-3728_186-3727i others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598292 | ||||||
| chr2:186598292 | T | TACACAC | 2 | a0001c0001t0001g0003 a0001c0001t0001g0089 |
3 | HG02257.hp1 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.186-3728_186-3727i others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598292 | ||||||
| chr2:186598294 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-3727T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186598294 | |||||||
| chr2:186598294 | T | TAC | 9 | a0001c0001t0001g0078 a0001c0001t0001g0105 a0001c0001t0001g0159 others(6): Show |
9 | HG00544.hp1 HG02622.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-3693_186-3692d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | T | TACAC | 9 | a0001c0001t0001g0100 a0001c0001t0002g0004 a0001c0001t0002g0019 others(6): Show |
10 | HG01069.hp1 HG01071.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-3695_186-3692d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | T | TACACAC | 44 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0049 others(41): Show |
46 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.186-3697_186-3692d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | T | TACACACA others(1): Show |
14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0015 others(11): Show |
14 | HG01256.hp2 HG01884.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.186-3699_186-3692d others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | T | TACACACA others(3): Show |
6 | a0001c0001t0002g0023 a0001c0001t0002g0112 a0001c0001t0002g0113 others(3): Show |
6 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-3701_186-3692d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | T | TACACACA others(5): Show |
2 | a0001c0001t0008g0110 a0001c0008t0020g0022 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.186-3703_186-3692d others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0021 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-3705_186-3692d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | TAC | T | 11 | a0001c0001t0001g0111 a0001c0001t0001g0122 a0001c0001t0001g0137 others(8): Show |
11 | HG01168.hp2 HG01192.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.186-3693_186-3692d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | TACAC | T | 18 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0002g0161 others(15): Show |
18 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.186-3695_186-3692d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | TACACAC | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(133): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.186-3697_186-3692d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.186-3701_186-3692d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598294 | TACACACA others(5): Show |
T | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.186-3703_186-3692d others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | ||||||
| chr2:186598436 | A | AT | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(187): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.186-3566dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598436 | ||||||
| chr2:186598436 | A | ATT | 8 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(5): Show |
8 | HG01099.hp2 HG01243.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-3567_186-3566d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598436 | ||||||
| chr2:186598436 | AT | A | 8 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0002g0024 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-3566delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598436 | ||||||
| chr2:186599020 | A | T | 1 | a0001c0001t0002g0019 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.186-3001A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599020 | |||||||
| chr2:186599197 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.186-2824T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599197 | |||||||
| chr2:186599349 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.186-2672C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599349 | |||||||
| chr2:186599385 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.186-2636G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599385 | |||||||
| chr2:186599694 | G | A | 3 | a0001c0001t0008g0026 a0001c0001t0008g0034 a0001c0001t0023g0071 |
3 | HG02486.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.186-2327G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599694 | |||||||
| chr2:186599761 | T | C | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | NA18949.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.186-2260T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599761 | |||||||
| chr2:186600142 | G | T | 1 | a0003c0004t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.186-1879G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186600142 | |||||||
| chr2:186600167 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.186-1854G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186600167 | |||||||
| chr2:186600894 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.186-1127G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186600894 | |||||||
| chr2:186600959 | C | CA | 12 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(9): Show |
12 | HG01168.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.186-1047dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186600959 | ||||||
| chr2:186600997 | G | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(286): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.186-1024G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186600997 | |||||||
| chr2:186601292 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.186-729C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601292 | |||||||
| chr2:186601301 | T | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(282): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.186-720T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601301 | |||||||
| chr2:186601309 | A | T | 1 | a0002c0002t0004g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.186-712A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601309 | |||||||
| chr2:186601452 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(284): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.186-569T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601452 | |||||||
| chr2:186601453 | G | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(201): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.186-568G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601453 | |||||||
| chr2:186601461 | TA | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(17): Show |
21 | HG01168.hp2 HG01891.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.186-548delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186601461 | ||||||
| chr2:186601894 | T | C | 1 | a0001c0001t0002g0027 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.186-127T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601894 | |||||||
| chr2:186602194 | A | AT | 9 | a0001c0001t0001g0111 a0001c0001t0001g0137 a0001c0001t0001g0144 others(6): Show |
9 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+53dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186602194 | ||||||
| chr2:186602257 | C | A | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+106C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186602257 | |||||||
| chr2:186602460 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316+309G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186602460 | |||||||
| chr2:186602728 | T | C | 1 | a0001c0001t0002g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.316+577T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186602728 | |||||||
| chr2:186602876 | TA | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(239): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.316+744delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186602876 | ||||||
| chr2:186603023 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(204): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.316+872A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603023 | |||||||
| chr2:186603278 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0002g0006 others(2): Show |
6 | HG01975.hp2 HG02004.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+1127T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603278 | |||||||
| chr2:186603353 | A | G | 2 | a0001c0001t0003g0119 a0001c0001t0016g0118 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.316+1202A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603353 | |||||||
| chr2:186603398 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(284): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.316+1247A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603398 | |||||||
| chr2:186603496 | G | A | 10 | a0001c0001t0002g0020 a0001c0001t0002g0036 a0001c0001t0002g0037 others(7): Show |
10 | HG00544.hp2 HG00558.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+1345G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603496 | |||||||
| chr2:186603513 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.316+1362T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603513 | |||||||
| chr2:186603603 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.316+1452A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603603 | |||||||
| chr2:186603668 | T | G | 1 | a0001c0001t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316+1517T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603668 | |||||||
| chr2:186603830 | A | T | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+1679A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603830 | |||||||
| chr2:186603886 | A | G | 1 | a0001c0003t0002g0013 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.316+1735A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603886 | |||||||
| chr2:186604171 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.316+2020A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186604171 | |||||||
| chr2:186604323 | G | A | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+2172G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186604323 | |||||||
| chr2:186604499 | A | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.316+2348A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186604499 | |||||||
| chr2:186604656 | G | A | 1 | a0001c0001t0005g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.316+2505G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186604656 | |||||||
| chr2:186604704 | TTTAA | T | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+2558_316+2561d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186604704 | ||||||
| chr2:186605092 | T | A | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+2941T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605092 | |||||||
| chr2:186605157 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.316+3006A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605157 | |||||||
| chr2:186605458 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(284): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.316+3307T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605458 | |||||||
| chr2:186605463 | T | G | 81 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(78): Show |
84 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.316+3312T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605463 | |||||||
| chr2:186605584 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(151): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.316+3433C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605584 | |||||||
| chr2:186605617 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0147 others(76): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.316+3466G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605617 | |||||||
| chr2:186605640 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.316+3489C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605640 | |||||||
| chr2:186605726 | G | T | 2 | a0001c0001t0003g0011 a0001c0001t0003g0265 |
3 | HG01168.hp1 HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.316+3575G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605726 | |||||||
| chr2:186605740 | GTA | G | 77 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(74): Show |
78 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.316+3607_316+3608d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605740 | ||||||
| chr2:186605740 | GTATA | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(17): Show |
21 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.316+3605_316+3608d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605740 | ||||||
| chr2:186605746 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.316+3595A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605746 | |||||||
| chr2:186605753 | T | TATTTATA others(10): Show |
8 | a0001c0001t0001g0178 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
8 | HG01496.hp1 HG01884.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+3604_316+3605i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605753 | ||||||
| chr2:186605755 | T | TTTATATG others(43): Show |
170 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(167): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.316+3604_316+3605i others(52): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605755 | |||||||
| chr2:186605755 | T | TTTATATG others(70): Show |
4 | a0001c0001t0001g0157 a0001c0001t0001g0184 a0001c0001t0003g0235 others(1): Show |
4 | HG01981.hp2 HG02486.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+3604_316+3605i others(79): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605755 | |||||||
| chr2:186605755 | T | TTTATATG others(97): Show |
1 | a0001c0001t0002g0234 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.316+3604_316+3605i others(106): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605755 | |||||||
| chr2:186605755 | T | TTTATATG others(124): Show |
1 | a0001c0001t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.316+3604_316+3605i others(133): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605755 | |||||||
| chr2:186605756 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(173): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.316+3605A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605756 | |||||||
| chr2:186605760 | T | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(173): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.316+3609T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605760 | |||||||
| chr2:186605760 | T | TCTTATG | 8 | a0001c0001t0001g0178 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
8 | HG01496.hp1 HG01884.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+3609_316+3610i others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605760 | |||||||
| chr2:186605797 | A | AATAC | 184 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(181): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.316+3649_316+3650i others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186605797 | A | AATATATT others(47): Show |
8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+3697_316+3750d others(56): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186605797 | A | AATATATT others(74): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0096 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+3670_316+3750d others(83): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186605797 | A | AATATATT others(101): Show |
7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(110): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186605797 | A | AATATATT others(128): Show |
8 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0002g0064 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(137): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186605797 | A | AATATATT others(155): Show |
5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0002g0075 others(2): Show |
5 | HG01243.hp1 HG02132.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(164): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186605797 | A | AATATATT others(182): Show |
66 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 others(63): Show |
67 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(191): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186605797 | A | AATATATT others(209): Show |
3 | a0001c0001t0002g0005 a0001c0001t0009g0076 a0001c0008t0020g0022 |
4 | HG01516.hp2 HG01517.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(218): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186605797 | A | AATATATT others(236): Show |
1 | a0001c0001t0002g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.316+3750_316+3751i others(245): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186605797 | A | AATATATT others(70): Show |
1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+3672_316+3673i others(79): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | ||||||
| chr2:186606281 | G | A | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+4130G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606281 | |||||||
| chr2:186606532 | C | T | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+4381C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606532 | |||||||
| chr2:186606557 | C | G | 6 | a0001c0003t0001g0012 a0001c0003t0001g0288 a0001c0003t0001g0289 others(3): Show |
8 | HG01099.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+4406C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606557 | |||||||
| chr2:186606563 | A | C | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+4412A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606563 | |||||||
| chr2:186606754 | G | C | 81 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(78): Show |
84 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.316+4603G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606754 | |||||||
| chr2:186606806 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.316+4655G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606806 | |||||||
| chr2:186606818 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.316+4667A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606818 | |||||||
| chr2:186606959 | G | A | 6 | a0001c0003t0001g0012 a0001c0003t0001g0288 a0001c0003t0001g0289 others(3): Show |
8 | HG01099.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+4808G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606959 | |||||||
| chr2:186607091 | T | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0002g0112 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+4940T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186607091 | |||||||
| chr2:186607331 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.316+5180C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186607331 | |||||||
| chr2:186607585 | A | T | 8 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0108 others(5): Show |
8 | HG02622.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+5434A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186607585 | |||||||
| chr2:186607596 | A | G | 4 | a0001c0001t0003g0235 a0001c0001t0003g0261 a0001c0001t0014g0160 others(1): Show |
4 | HG01081.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+5445A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186607596 | |||||||
| chr2:186608041 | A | G | 4 | a0001c0001t0008g0026 a0001c0001t0008g0034 a0001c0001t0008g0110 others(1): Show |
4 | HG02486.hp2 HG02896.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+5890A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608041 | |||||||
| chr2:186608257 | T | C | 28 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0122 others(25): Show |
28 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.316+6106T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608257 | |||||||
| chr2:186608412 | A | G | 2 | a0001c0001t0002g0279 a0001c0001t0021g0231 |
2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.316+6261A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608412 | |||||||
| chr2:186608580 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.316+6429G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608580 | |||||||
| chr2:186608616 | G | A | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+6465G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608616 | |||||||
| chr2:186608712 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.316+6561C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608712 | |||||||
| chr2:186608905 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.316+6754C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608905 | |||||||
| chr2:186608980 | A | C | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 |
3 | HG01243.hp1 HG01258.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.316+6829A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608980 | |||||||
| chr2:186609793 | C | CAT | 187 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(184): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.316+7653_316+7654d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186609793 | ||||||
| chr2:186609945 | T | G | 1 | a0001c0001t0002g0047 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.316+7794T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186609945 | |||||||
| chr2:186610085 | C | A | 1 | a0003c0004t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.316+7934C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610085 | |||||||
| chr2:186610132 | A | G | 1 | a0001c0001t0002g0025 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.316+7981A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610132 | |||||||
| chr2:186610377 | G | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(193): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.316+8226G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610377 | |||||||
| chr2:186610443 | A | C | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+8292A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610443 | |||||||
| chr2:186610466 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316+8315C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610466 | |||||||
| chr2:186610598 | T | A | 2 | a0001c0001t0003g0119 a0001c0001t0016g0118 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.316+8447T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610598 | |||||||
| chr2:186610630 | C | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(181): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.316+8479C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610630 | |||||||
| chr2:186610842 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.316+8691C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610842 | |||||||
| chr2:186610929 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.316+8778C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610929 | |||||||
| chr2:186611342 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0266 |
2 | HG00558.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.316+9191C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186611342 | |||||||
| chr2:186611434 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316+9283C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186611434 | |||||||
| chr2:186611664 | A | C | 1 | a0001c0001t0003g0174 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.316+9513A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186611664 | |||||||
| chr2:186611932 | A | C | 1 | a0001c0001t0012g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.316+9781A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186611932 | |||||||
| chr2:186612071 | A | G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+9920A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612071 | |||||||
| chr2:186612135 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(181): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.316+9984C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612135 | |||||||
| chr2:186612219 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.316+10068A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612219 | |||||||
| chr2:186612369 | A | AT | 102 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(99): Show |
105 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.317-9955dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186612369 | ||||||
| chr2:186612369 | AT | A | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0003g0181 others(3): Show |
6 | HG01123.hp2 HG01358.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-9955delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186612369 | ||||||
| chr2:186612754 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-9585A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612754 | |||||||
| chr2:186612801 | G | C | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.317-9538G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612801 | |||||||
| chr2:186612964 | A | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(203): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.317-9375A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612964 | |||||||
| chr2:186613013 | C | T | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.317-9326C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613013 | |||||||
| chr2:186613317 | G | T | 1 | a0001c0008t0020g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.317-9022G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613317 | |||||||
| chr2:186613474 | C | T | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-8865C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613474 | |||||||
| chr2:186613721 | C | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-8618C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613721 | |||||||
| chr2:186613773 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(183): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.317-8566A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613773 | |||||||
| chr2:186614188 | C | T | 1 | a0002c0002t0004g0134 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.317-8151C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614188 | |||||||
| chr2:186614248 | G | A | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-8091G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614248 | |||||||
| chr2:186614605 | T | G | 5 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(2): Show |
5 | HG02622.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-7734T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614605 | |||||||
| chr2:186614627 | T | C | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(2): Show |
5 | HG00673.hp2 HG02056.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-7712T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614627 | |||||||
| chr2:186614683 | C | T | 1 | a0002c0002t0004g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.317-7656C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614683 | |||||||
| chr2:186614738 | T | G | 1 | a0001c0001t0003g0268 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.317-7601T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614738 | |||||||
| chr2:186614780 | T | C | 1 | a0001c0001t0003g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.317-7559T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614780 | |||||||
| chr2:186614812 | A | G | 1 | a0001c0001t0010g0164 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.317-7527A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614812 | |||||||
| chr2:186614921 | A | G | 32 | a0001c0001t0001g0007 a0001c0001t0001g0163 a0001c0001t0001g0184 others(29): Show |
33 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.317-7418A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614921 | |||||||
| chr2:186615029 | C | A | 79 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(76): Show |
82 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.317-7310C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615029 | |||||||
| chr2:186615084 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.317-7255T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615084 | |||||||
| chr2:186615244 | T | G | 4 | a0001c0001t0003g0235 a0001c0001t0003g0261 a0001c0001t0014g0160 others(1): Show |
4 | HG01081.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-7095T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615244 | |||||||
| chr2:186615279 | T | C | 28 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0122 others(25): Show |
28 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.317-7060T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615279 | |||||||
| chr2:186615575 | T | A | 7 | a0001c0001t0001g0242 a0001c0001t0002g0165 a0001c0001t0002g0166 others(4): Show |
7 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-6764T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615575 | |||||||
| chr2:186615679 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.317-6660C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615679 | |||||||
| chr2:186615680 | G | GT | 16 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0208 others(13): Show |
16 | HG01496.hp1 HG01496.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.317-6649dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186615680 | ||||||
| chr2:186615825 | A | G | 5 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(2): Show |
5 | HG02622.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-6514A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615825 | |||||||
| chr2:186615936 | G | A | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(284): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.317-6403G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615936 | |||||||
| chr2:186615948 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.317-6391C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615948 | |||||||
| chr2:186616261 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.317-6078A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616261 | |||||||
| chr2:186616273 | AT | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(229): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.317-6043delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186616273 | ||||||
| chr2:186616291 | T | A | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.317-6048T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616291 | |||||||
| chr2:186616404 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(284): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.317-5935A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616404 | |||||||
| chr2:186616432 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-5907G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616432 | |||||||
| chr2:186616604 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0096 |
4 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-5735G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616604 | |||||||
| chr2:186616643 | C | T | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-5696C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616643 | |||||||
| chr2:186617037 | G | GT | 8 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0108 others(5): Show |
8 | HG02622.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.317-5291dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186617037 | ||||||
| chr2:186617037 | GT | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(173): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.317-5291delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186617037 | ||||||
| chr2:186617108 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0147 others(76): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.317-5231A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617108 | |||||||
| chr2:186617278 | T | C | 1 | a0003c0004t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.317-5061T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617278 | |||||||
| chr2:186617529 | C | A | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-4810C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617529 | |||||||
| chr2:186617571 | C | G | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-4768C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617571 | |||||||
| chr2:186617575 | C | CAA | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-4762_317-4761d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186617575 | ||||||
| chr2:186617755 | A | G | 2 | a0001c0001t0001g0285 a0001c0001t0003g0271 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.317-4584A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617755 | |||||||
| chr2:186618104 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.317-4235T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618104 | |||||||
| chr2:186618214 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.317-4125A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618214 | |||||||
| chr2:186618425 | A | G | 14 | a0001c0001t0003g0123 a0002c0002t0002g0128 a0002c0002t0004g0124 others(11): Show |
14 | HG00423.hp2 HG01943.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.317-3914A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618425 | |||||||
| chr2:186618505 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.317-3834A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618505 | |||||||
| chr2:186618615 | G | C | 4 | a0001c0001t0003g0235 a0001c0001t0003g0261 a0001c0001t0014g0160 others(1): Show |
4 | HG01081.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-3724G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618615 | |||||||
| chr2:186618687 | G | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0096 |
4 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-3652G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618687 | |||||||
| chr2:186618744 | GC | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(181): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.317-3594delC | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618744 | |||||||
| chr2:186618748 | C | T | 1 | a0001c0001t0009g0074 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.317-3591C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618748 | |||||||
| chr2:186618925 | T | A | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-3414T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618925 | |||||||
| chr2:186619043 | GTGTGTAT others(9): Show |
G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0096 |
4 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-3286_317-3271d others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186619043 | ||||||
| chr2:186619063 | G | GTA | 9 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0100 others(6): Show |
9 | HG02622.hp1 HG02723.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.317-3264_317-3263d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186619063 | ||||||
| chr2:186619073 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.317-3266A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619073 | |||||||
| chr2:186619111 | TTA | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0147 others(83): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.317-3212_317-3211d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186619111 | ||||||
| chr2:186619291 | A | G | 27 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0122 others(24): Show |
27 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.317-3048A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619291 | |||||||
| chr2:186619313 | A | T | 7 | a0001c0001t0001g0242 a0001c0001t0002g0165 a0001c0001t0002g0166 others(4): Show |
7 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-3026A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619313 | |||||||
| chr2:186619375 | T | G | 1 | a0001c0001t0003g0276 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.317-2964T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619375 | |||||||
| chr2:186619566 | CA | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(193): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.317-2766delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186619566 | ||||||
| chr2:186619575 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.317-2764G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619575 | |||||||
| chr2:186619653 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-2686A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619653 | |||||||
| chr2:186619713 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(201): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.317-2626A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619713 | |||||||
| chr2:186619897 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.317-2442C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619897 | |||||||
| chr2:186620075 | C | A | 1 | a0001c0001t0002g0048 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.317-2264C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620075 | |||||||
| chr2:186620093 | C | T | 2 | a0001c0001t0003g0235 a0001c0001t0003g0261 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.317-2246C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620093 | |||||||
| chr2:186620127 | G | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(181): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.317-2212G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620127 | |||||||
| chr2:186620200 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0003g0011 a0001c0001t0003g0265 |
5 | HG01168.hp1 HG01169.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-2139C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620200 | |||||||
| chr2:186620547 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.317-1792G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620547 | |||||||
| chr2:186620670 | G | C | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.317-1669G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620670 | |||||||
| chr2:186620673 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.317-1666G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620673 | |||||||
| chr2:186620974 | G | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-1365G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620974 | |||||||
| chr2:186621138 | G | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-1201G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621138 | |||||||
| chr2:186621270 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.317-1069A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621270 | |||||||
| chr2:186621404 | CATT | C | 4 | a0001c0001t0008g0026 a0001c0001t0008g0034 a0001c0001t0008g0110 others(1): Show |
4 | HG02486.hp2 HG02896.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-929_317-927del others(3): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186621404 | ||||||
| chr2:186621430 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.317-909A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621430 | |||||||
| chr2:186621490 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.317-849A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621490 | |||||||
| chr2:186621500 | T | A | 2 | a0001c0001t0006g0286 a0001c0001t0006g0287 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.317-839T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621500 | |||||||
| chr2:186621712 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.317-627A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621712 | |||||||
| chr2:186621915 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0117 |
2 | HG01175.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.317-424G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621915 | |||||||
| chr2:186621918 | T | A | 2 | a0001c0001t0006g0286 a0001c0001t0006g0287 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.317-421T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621918 | |||||||
| chr2:186621928 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.317-411C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621928 | |||||||
| chr2:186621988 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.317-351G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621988 | |||||||
| chr2:186621996 | G | T | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-343G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621996 | |||||||
| chr2:186622180 | A | C | 10 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(7): Show |
10 | HG00323.hp1 HG00673.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-159A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186622180 | |||||||
| chr2:186622181 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02056.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.317-158G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186622181 | |||||||
| chr2:186622294 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.317-45G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186622294 | |||||||
| chr2:186622433 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(201): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
splice_region_variant&intron_variant | LOW | c.408+3G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186622433 | |||||||
| chr2:186622542 | G | T | 81 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(78): Show |
84 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.408+112G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186622542 | |||||||
| chr2:186622643 | T | A | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+213T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186622643 | |||||||
| chr2:186622730 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.408+300A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186622730 | |||||||
| chr2:186623019 | C | T | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+589C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623019 | |||||||
| chr2:186623049 | G | C | 2 | a0001c0001t0003g0235 a0001c0001t0003g0261 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.408+619G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623049 | |||||||
| chr2:186623301 | AT | A | 5 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0044 others(2): Show |
7 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+876delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 186623301 | ||||||
| chr2:186623581 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.408+1151C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623581 | |||||||
| chr2:186623592 | A | G | 1 | a0001c0001t0003g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.408+1162A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623592 | |||||||
| chr2:186623602 | T | G | 1 | a0001c0001t0002g0116 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.408+1172T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623602 | |||||||
| chr2:186623772 | A | G | 1 | a0001c0001t0003g0182 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.408+1342A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623772 | |||||||
| chr2:186624267 | G | A | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.409-1206G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624267 | |||||||
| chr2:186624285 | C | T | 1 | a0002c0002t0004g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.409-1188C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624285 | |||||||
| chr2:186624405 | GA | G | 4 | a0001c0001t0003g0235 a0001c0001t0003g0261 a0001c0001t0014g0160 others(1): Show |
4 | HG01081.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-1066delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 186624405 | ||||||
| chr2:186624621 | A | G | 2 | a0001c0001t0003g0235 a0001c0001t0003g0261 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.409-852A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624621 | |||||||
| chr2:186624701 | C | T | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.409-772C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624701 | |||||||
| chr2:186624902 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.409-571A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624902 | |||||||
| chr2:186624920 | C | A | 39 | a0001c0001t0001g0050 a0001c0001t0002g0004 a0001c0001t0002g0005 others(36): Show |
41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.409-553C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624920 | |||||||
| chr2:186624952 | G | GA | 281 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(278): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.409-511dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 186624952 | ||||||
| chr2:186625365 | C | G | 1 | a0001c0001t0015g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.409-108C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186625365 | |||||||
| chr2:186625644 | T | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(183): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.523+57T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625644 | |||||||
| chr2:186625651 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0003g0259 a0001c0001t0005g0183 |
2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.523+65_523+74dupTG others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625651 | ||||||
| chr2:186625651 | A | ATGTGTGT others(5): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0096 |
4 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+74_523+75insTG others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625651 | ||||||
| chr2:186625662 | G | GGTGT | 3 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0108 |
3 | HG02630.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.523+89_523+92dupTG others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625662 | ||||||
| chr2:186625662 | G | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(195): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.523+75G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625662 | |||||||
| chr2:186625669 | G | GTGTGTA | 3 | a0001c0001t0012g0097 a0001c0001t0012g0098 a0002c0002t0022g0090 |
3 | HG03139.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.523+87_523+88insAT others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625669 | ||||||
| chr2:186625669 | G | GTGTGTGT others(1): Show |
5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+89_523+90insAT others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625669 | ||||||
| chr2:186625676 | T | A | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.523+89T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625676 | |||||||
| chr2:186625678 | T | A | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.523+91T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625678 | |||||||
| chr2:186625678 | T | TGTGA | 5 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(2): Show |
5 | HG02622.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | ||||||
| chr2:186625678 | T | TGTGTGA | 3 | a0001c0001t0003g0235 a0001c0001t0006g0149 a0001c0003t0002g0013 |
4 | HG02486.hp1 HG03098.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | ||||||
| chr2:186625678 | T | TGTGTGTG others(1): Show |
78 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0121 others(75): Show |
82 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | ||||||
| chr2:186625678 | T | TGTGTGTG others(3): Show |
73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0147 others(70): Show |
77 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | ||||||
| chr2:186625678 | T | TGTGTGTG others(5): Show |
20 | a0001c0001t0001g0176 a0001c0001t0001g0180 a0001c0001t0001g0198 others(17): Show |
20 | HG00597.hp2 HG00642.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | ||||||
| chr2:186625678 | T | TGTGTGTG others(7): Show |
8 | a0001c0001t0001g0162 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG00558.hp2 HG02155.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | ||||||
| chr2:186625678 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.523+92_523+93insTG others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | ||||||
| chr2:186625678 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.523+92_523+93insTG others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | ||||||
| chr2:186625678 | TGAGA | T | 68 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 others(65): Show |
71 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.523+100_523+103del others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | ||||||
| chr2:186625712 | T | G | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.523+125T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625712 | |||||||
| chr2:186625813 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.523+226C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625813 | |||||||
| chr2:186625814 | G | A | 1 | a0002c0002t0004g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.523+227G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625814 | |||||||
| chr2:186625820 | A | G | 5 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(2): Show |
5 | HG00323.hp1 NA18612.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+233A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625820 | |||||||
| chr2:186626046 | T | A | 1 | a0002c0002t0022g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.523+459T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626046 | |||||||
| chr2:186626317 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.523+730C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626317 | |||||||
| chr2:186626413 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(201): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.523+826G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626413 | |||||||
| chr2:186626442 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.523+855C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626442 | |||||||
| chr2:186626595 | T | G | 1 | a0001c0001t0002g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.523+1008T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626595 | |||||||
| chr2:186626876 | T | C | 1 | a0001c0001t0012g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.523+1289T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626876 | |||||||
| chr2:186627093 | A | G | 5 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(2): Show |
5 | HG02622.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+1506A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627093 | |||||||
| chr2:186627159 | T | C | 2 | a0002c0002t0001g0142 a0002c0002t0001g0143 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.523+1572T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627159 | |||||||
| chr2:186627173 | A | T | 1 | a0001c0001t0002g0151 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.523+1586A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627173 | |||||||
| chr2:186627199 | C | T | 5 | a0001c0001t0001g0162 a0001c0001t0001g0204 a0001c0001t0001g0207 others(2): Show |
5 | HG02165.hp1 NA18949.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+1612C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627199 | |||||||
| chr2:186627324 | G | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(284): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.523+1737G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627324 | |||||||
| chr2:186627425 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.523+1838C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627425 | |||||||
| chr2:186627733 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(201): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.523+2146G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627733 | |||||||
| chr2:186627738 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.523+2151G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627738 | |||||||
| chr2:186627872 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.523+2285G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627872 | |||||||
| chr2:186627923 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.523+2336A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627923 | |||||||
| chr2:186627966 | A | C | 5 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0061 others(2): Show |
5 | HG00673.hp1 HG02135.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+2379A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627966 | |||||||
| chr2:186628015 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(153): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.523+2428G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628015 | |||||||
| chr2:186628048 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.523+2461T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628048 | |||||||
| chr2:186628096 | G | C | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG00323.hp1 NA18612.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+2509G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628096 | |||||||
| chr2:186628200 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
2 | HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.524-2597C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628200 | |||||||
| chr2:186628237 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(192): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.524-2560A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628237 | |||||||
| chr2:186628704 | G | A | 7 | a0001c0001t0001g0242 a0001c0001t0002g0165 a0001c0001t0002g0166 others(4): Show |
7 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.524-2093G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628704 | |||||||
| chr2:186628843 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-1954T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628843 | |||||||
| chr2:186629051 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.524-1746A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629051 | |||||||
| chr2:186629114 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(181): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.524-1683A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629114 | |||||||
| chr2:186629125 | A | G | 1 | a0001c0001t0003g0171 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.524-1672A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629125 | |||||||
| chr2:186629208 | A | G | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.524-1589A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629208 | |||||||
| chr2:186629385 | A | C | 1 | a0001c0001t0002g0027 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.524-1412A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629385 | |||||||
| chr2:186629601 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-1196A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629601 | |||||||
| chr2:186629620 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-1177T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629620 | |||||||
| chr2:186629674 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.524-1123G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629674 | |||||||
| chr2:186629690 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.524-1107G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629690 | |||||||
| chr2:186629700 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(190): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.524-1097G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629700 | |||||||
| chr2:186629829 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.524-968C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629829 | |||||||
| chr2:186629851 | T | A | 1 | a0001c0001t0001g0273 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.524-946T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629851 | |||||||
| chr2:186629919 | A | G | 1 | a0002c0002t0004g0132 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.524-878A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629919 | |||||||
| chr2:186630485 | G | A | 1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.524-312G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186630485 | |||||||
| chr2:186630547 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.524-250A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186630547 | |||||||
| chr2:186630553 | G | A | 1 | a0002c0002t0004g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.524-244G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186630553 | |||||||
| chr2:186630773 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.524-24A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186630773 | |||||||
| chr2:186630901 | AT | A | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+45delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr2 | 186630901 | ||||||
| chr2:186631422 | A | G | 8 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0108 others(5): Show |
8 | HG02622.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.585+564A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186631422 | |||||||
| chr2:186631633 | C | T | 1 | a0001c0001t0002g0064 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.585+775C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186631633 | |||||||
| chr2:186631649 | T | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0002g0112 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+791T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186631649 | |||||||
| chr2:186631691 | T | G | 1 | a0001c0001t0002g0069 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.585+833T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186631691 | |||||||
| chr2:186632113 | C | A | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.586-1216C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632113 | |||||||
| chr2:186632192 | G | A | 12 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(9): Show |
12 | HG01168.hp2 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.586-1137G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632192 | |||||||
| chr2:186632203 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.586-1126T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632203 | |||||||
| chr2:186632355 | G | T | 1 | a0001c0001t0002g0234 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.586-974G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632355 | |||||||
| chr2:186632390 | G | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0263 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-939G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632390 | |||||||
| chr2:186632418 | G | GC | 16 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0093 others(13): Show |
16 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.586-911_586-910ins others(1): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632418 | |||||||
| chr2:186632419 | T | G | 16 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0093 others(13): Show |
16 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.586-910T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632419 | |||||||
| chr2:186632419 | T | TG | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(83): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.586-910_586-909ins others(1): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632419 | |||||||
| chr2:186632427 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.586-902C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632427 | |||||||
| chr2:186632649 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.586-680A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632649 | |||||||
| chr2:186632981 | C | CTAGA | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.586-329_586-326dup others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr2 | 186632981 | ||||||
| chr2:186632981 | CTAGA | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.586-329_586-326del others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr2 | 186632981 | ||||||
| chr2:186633004 | C | G | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.586-325C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633004 | |||||||
| chr2:186633014 | T | C | 1 | a0001c0001t0002g0020 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.586-315T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633014 | |||||||
| chr2:186633091 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.586-238C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633091 | |||||||
| chr2:186633141 | C | CA | 12 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0220 others(9): Show |
12 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.586-174dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr2 | 186633141 | ||||||
| chr2:186633226 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.586-103C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633226 | |||||||
| chr2:186633260 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.586-69C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633260 | |||||||
| chr2:186633261 | A | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(14): Show |
18 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.586-68A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633261 | |||||||
| chr2:186633380 | T | C | 58 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0015 others(55): Show |
60 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
splice_region_variant&intron_variant | LOW | c.631+6T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633380 | |||||||
| chr2:186633527 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(54): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+153T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633527 | |||||||
| chr2:186633631 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.631+257A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633631 | |||||||
| chr2:186633765 | A | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(122): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.631+391A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633765 | |||||||
| chr2:186633835 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(124): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.631+461A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633835 | |||||||
| chr2:186633921 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.631+547G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633921 | |||||||
| chr2:186633972 | G | A | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+598G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633972 | |||||||
| chr2:186634257 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.631+883A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186634257 | |||||||
| chr2:186634282 | CAT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.631+909_631+910del others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186634282 | |||||||
| chr2:186634460 | G | GA | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(235): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.631+1090dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr2 | 186634460 | ||||||
| chr2:186634985 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0089 others(1): Show |
5 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-1097G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186634985 | |||||||
| chr2:186635302 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(13): Show |
17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.632-780A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635302 | |||||||
| chr2:186635311 | T | G | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.632-771T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635311 | |||||||
| chr2:186635418 | C | T | 3 | a0001c0005t0002g0033 a0001c0005t0002g0065 a0001c0005t0002g0066 |
3 | HG02257.hp2 HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.632-664C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635418 | |||||||
| chr2:186635495 | C | T | 1 | a0001c0001t0013g0056 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.632-587C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635495 | |||||||
| chr2:186635515 | T | C | 2 | a0001c0001t0011g0059 a0001c0001t0011g0077 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.632-567T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635515 | |||||||
| chr2:186635540 | C | G | 1 | a0001c0001t0002g0062 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.632-542C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635540 | |||||||
| chr2:186635633 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.632-449T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635633 | |||||||
| chr2:186635955 | A | G | 65 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(62): Show |
68 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.632-127A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635955 | |||||||
| chr2:186636395 | A | T | 2 | a0001c0001t0006g0286 a0001c0001t0006g0287 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.757+188A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636395 | |||||||
| chr2:186636428 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.757+221T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636428 | |||||||
| chr2:186636702 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.758-363C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636702 | |||||||
| chr2:186636720 | A | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.758-345A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636720 | |||||||
| chr2:186636919 | A | G | 1 | a0001c0003t0001g0289 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.758-146A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636919 | |||||||
| chr2:186636921 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(13): Show |
17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.758-144A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636921 | |||||||
| chr2:186636955 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(202): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.758-110G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636955 | |||||||
| chr2:186637015 | G | A | 14 | a0002c0002t0002g0128 a0002c0002t0004g0124 a0002c0002t0004g0125 others(11): Show |
14 | HG00423.hp2 HG01943.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.758-50G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186637015 | |||||||
| chr2:186637024 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.758-41G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186637024 | |||||||
| chr2:186637167 | CAT | C | 26 | a0001c0001t0001g0256 a0001c0003t0001g0012 a0001c0003t0001g0288 others(23): Show |
27 | HG00423.hp2 HG01099.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+59_802+60delAT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637167 | |||||||
| chr2:186637270 | C | T | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.802+161C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637270 | |||||||
| chr2:186637339 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.802+230G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637339 | |||||||
| chr2:186637481 | C | CA | 6 | a0001c0001t0002g0057 a0001c0001t0002g0099 a0001c0001t0002g0113 others(3): Show |
6 | HG00558.hp1 HG01243.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+390dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 186637481 | ||||||
| chr2:186637481 | CA | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(198): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.802+390delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 186637481 | ||||||
| chr2:186637501 | G | A | 2 | a0001c0001t0012g0097 a0001c0001t0012g0098 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.802+392G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637501 | |||||||
| chr2:186637532 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.802+423A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637532 | |||||||
| chr2:186637650 | T | G | 1 | a0001c0001t0010g0164 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.802+541T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637650 | |||||||
| chr2:186637828 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0211 |
2 | HG02135.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.803-449C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637828 | |||||||
| chr2:186637944 | A | G | 2 | a0001c0001t0002g0023 a0001c0001t0002g0084 |
2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.803-333A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637944 | |||||||
| chr2:186637947 | A | G | 1 | a0001c0001t0003g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.803-330A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637947 | |||||||
| chr2:186638119 | T | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(13): Show |
17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-158T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186638119 | |||||||
| chr2:186638476 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.903+11A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638476 | |||||||
| chr2:186638499 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(140): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.903+34T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638499 | |||||||
| chr2:186638631 | C | CGT | 23 | a0001c0001t0001g0080 a0001c0001t0001g0093 a0001c0001t0001g0094 others(20): Show |
24 | HG00423.hp2 HG00558.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.903+205_903+206dup others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | C | CGTGT | 31 | a0001c0001t0001g0137 a0001c0001t0001g0238 a0001c0001t0002g0017 others(28): Show |
31 | HG00544.hp2 HG00673.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.903+203_903+206dup others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | C | CGTGTGT | 25 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0122 others(22): Show |
27 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.903+201_903+206dup others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0018 a0001c0001t0001g0121 a0001c0001t0002g0006 others(5): Show |
9 | HG01934.hp1 HG02004.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+199_903+206dup others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0002g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.903+197_903+206dup others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | C | CGTGTGTG others(5): Show |
1 | a0001c0005t0002g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.903+195_903+206dup others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | CGT | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.903+205_903+206del others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | CGTGT | C | 11 | a0001c0001t0001g0050 a0001c0001t0001g0152 a0001c0001t0001g0154 others(8): Show |
11 | HG00639.hp1 HG01081.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.903+203_903+206del others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | CGTGTGT | C | 37 | a0001c0001t0001g0191 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.903+201_903+206del others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0003g0181 a0001c0001t0003g0236 a0001c0001t0003g0247 others(1): Show |
4 | HG01123.hp2 HG02055.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+199_903+206del others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638631 | CGTGTGTG others(3): Show |
C | 6 | a0001c0001t0002g0068 a0001c0001t0005g0101 a0001c0001t0005g0102 others(3): Show |
6 | HG01192.hp1 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+197_903+206del others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | ||||||
| chr2:186638668 | GTGTA | G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0155 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.903+204_903+207del others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638668 | |||||||
| chr2:186638670 | GTA | G | 2 | a0001c0001t0002g0112 a0001c0003t0002g0013 |
3 | HG02145.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.903+206_903+207del others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638670 | |||||||
| chr2:186638672 | A | G | 23 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(20): Show |
24 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.903+207A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638672 | |||||||
| chr2:186638897 | C | CT | 26 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0100 others(23): Show |
27 | HG00597.hp1 HG01192.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.903+448dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638897 | ||||||
| chr2:186638897 | CT | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
19 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.903+448delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638897 | ||||||
| chr2:186638965 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0211 |
2 | HG02135.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.903+500T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638965 | |||||||
| chr2:186639044 | A | G | 1 | a0001c0001t0010g0282 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.903+579A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639044 | |||||||
| chr2:186639070 | T | G | 1 | a0001c0001t0002g0038 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.903+605T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639070 | |||||||
| chr2:186639144 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.903+679A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639144 | |||||||
| chr2:186639204 | A | G | 1 | a0001c0001t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.903+739A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639204 | |||||||
| chr2:186639478 | G | T | 5 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(2): Show |
5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.903+1013G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639478 | |||||||
| chr2:186639482 | C | T | 1 | a0002c0002t0022g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.903+1017C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639482 | |||||||
| chr2:186639625 | C | T | 2 | a0001c0001t0011g0059 a0001c0001t0011g0077 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.903+1160C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639625 | |||||||
| chr2:186639721 | T | C | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0155 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-1194T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639721 | |||||||
| chr2:186639809 | G | A | 1 | a0001c0001t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.904-1106G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639809 | |||||||
| chr2:186640074 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.904-841G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640074 | |||||||
| chr2:186640414 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.904-501C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640414 | |||||||
| chr2:186640419 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0284 |
2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.904-496G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640419 | |||||||
| chr2:186640440 | G | A | 52 | a0001c0001t0001g0285 a0001c0001t0003g0008 a0001c0001t0003g0009 others(49): Show |
55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.904-475G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640440 | |||||||
| chr2:186640619 | A | G | 7 | a0002c0002t0002g0128 a0002c0002t0004g0129 a0002c0002t0004g0130 others(4): Show |
7 | HG00423.hp2 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-296A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640619 | |||||||
| chr2:186640670 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.904-245A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640670 | |||||||
| chr2:186640759 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(135): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.904-156A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640759 | |||||||
| chr2:186640780 | AAAGAC | A | 3 | a0001c0001t0013g0055 a0001c0001t0013g0056 a0005c0010t0003g0070 |
3 | NA18967.hp1 NA19080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.904-128_904-124del others(5): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186640780 | ||||||
| chr2:186640975 | T | A | 5 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(2): Show |
5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.956+8T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 11/29 | chr2 | 186640975 | |||||||
| chr2:186640976 | A | G | 2 | a0002c0002t0004g0126 a0002c0002t0004g0133 |
2 | NA18955.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.956+9A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 11/29 | chr2 | 186640976 | |||||||
| chr2:186641170 | C | T | 10 | a0001c0001t0002g0112 a0001c0001t0002g0161 a0001c0001t0002g0173 others(7): Show |
11 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.956+203C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 11/29 | chr2 | 186641170 | |||||||
| chr2:186641631 | G | A | 1 | a0001c0001t0019g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1159+43G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186641631 | |||||||
| chr2:186641675 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1159+87C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186641675 | |||||||
| chr2:186641834 | T | A | 1 | a0001c0001t0003g0248 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1159+246T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186641834 | |||||||
| chr2:186641947 | T | TA | 10 | a0001c0001t0002g0112 a0001c0001t0002g0161 a0001c0001t0002g0173 others(7): Show |
11 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+368dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186641947 | ||||||
| chr2:186642022 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1159+434A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642022 | |||||||
| chr2:186642059 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1159+471A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642059 | |||||||
| chr2:186642061 | A | G | 1 | a0001c0001t0023g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1159+473A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642061 | |||||||
| chr2:186642110 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1159+522T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642110 | |||||||
| chr2:186642120 | C | T | 1 | a0003c0004t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1159+532C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642120 | |||||||
| chr2:186642124 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1159+536T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642124 | |||||||
| chr2:186642150 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1159+562C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642150 | |||||||
| chr2:186642271 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1159+683G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642271 | |||||||
| chr2:186642381 | CTTG | C | 64 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(61): Show |
67 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1159+798_1159+800d others(5): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186642381 | ||||||
| chr2:186642535 | CT | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(184): Show |
196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1159+964delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186642535 | ||||||
| chr2:186642551 | T | C | 1 | a0001c0001t0003g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1159+963T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642551 | |||||||
| chr2:186642688 | C | T | 1 | a0001c0001t0005g0104 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1159+1100C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642688 | |||||||
| chr2:186642701 | A | AT | 68 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1159+1121dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186642701 | ||||||
| chr2:186642732 | G | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0195 |
2 | HG00408.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1159+1144G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642732 | |||||||
| chr2:186642950 | T | C | 5 | a0001c0001t0001g0177 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | NA18942.hp1 NA18960.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159+1362T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642950 | |||||||
| chr2:186643245 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(210): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1159+1657C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186643245 | |||||||
| chr2:186643471 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(210): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1159+1883C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186643471 | |||||||
| chr2:186643706 | T | G | 4 | a0001c0001t0014g0160 a0001c0001t0015g0280 a0001c0001t0017g0106 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1159+2118T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186643706 | |||||||
| chr2:186643770 | A | G | 2 | a0002c0002t0004g0158 a0002c0002t0004g0260 |
2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1159+2182A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186643770 | |||||||
| chr2:186644119 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1159+2531T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644119 | |||||||
| chr2:186644170 | CT | C | 4 | a0001c0001t0014g0160 a0001c0001t0015g0280 a0001c0001t0017g0106 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160-2515delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644170 | |||||||
| chr2:186644270 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(122): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1160-2416A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644270 | |||||||
| chr2:186644314 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1160-2372G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644314 | |||||||
| chr2:186644335 | G | T | 1 | a0001c0001t0003g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1160-2351G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644335 | |||||||
| chr2:186644393 | T | G | 1 | a0002c0002t0004g0130 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1160-2293T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644393 | |||||||
| chr2:186644395 | G | A | 1 | a0001c0001t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1160-2291G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644395 | |||||||
| chr2:186644560 | G | A | 8 | a0001c0001t0003g0119 a0001c0001t0003g0150 a0001c0001t0003g0171 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160-2126G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644560 | |||||||
| chr2:186644820 | T | TA | 66 | a0001c0001t0001g0049 a0001c0001t0001g0078 a0001c0001t0001g0079 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1160-1854dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186644820 | ||||||
| chr2:186644879 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
10 | HG01169.hp1 HG01255.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-1807G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644879 | |||||||
| chr2:186644937 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(217): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1160-1749T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644937 | |||||||
| chr2:186644976 | G | A | 50 | a0001c0001t0001g0285 a0001c0001t0003g0008 a0001c0001t0003g0009 others(47): Show |
53 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1160-1710G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644976 | |||||||
| chr2:186645178 | A | G | 1 | a0001c0001t0002g0291 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1160-1508A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645178 | |||||||
| chr2:186645322 | T | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(13): Show |
17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1160-1364T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645322 | |||||||
| chr2:186645336 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1160-1350T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645336 | |||||||
| chr2:186645519 | A | G | 1 | a0001c0001t0002g0048 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1160-1167A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645519 | |||||||
| chr2:186645524 | A | C | 1 | a0001c0001t0015g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1160-1162A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645524 | |||||||
| chr2:186645626 | C | G | 1 | a0001c0001t0002g0054 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1160-1060C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645626 | |||||||
| chr2:186645734 | G | A | 1 | a0001c0001t0003g0120 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1160-952G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645734 | |||||||
| chr2:186645865 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0284 |
2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1160-821G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645865 | |||||||
| chr2:186645943 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1160-743G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645943 | |||||||
| chr2:186646026 | G | A | 5 | a0001c0001t0001g0256 a0001c0003t0001g0012 a0001c0003t0001g0288 others(2): Show |
6 | HG02451.hp2 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-660G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646026 | |||||||
| chr2:186646139 | G | T | 1 | a0002c0002t0004g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1160-547G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646139 | |||||||
| chr2:186646150 | A | G | 2 | a0001c0001t0006g0286 a0001c0001t0006g0287 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1160-536A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646150 | |||||||
| chr2:186646199 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1160-487C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646199 | |||||||
| chr2:186646203 | T | C | 1 | a0002c0006t0001g0292 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1160-483T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646203 | |||||||
| chr2:186646345 | G | A | 52 | a0001c0001t0001g0285 a0001c0001t0003g0008 a0001c0001t0003g0009 others(49): Show |
55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1160-341G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646345 | |||||||
| chr2:186646461 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1160-225G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646461 | |||||||
| chr2:186647080 | G | A | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1351+203G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186647080 | |||||||
| chr2:186647238 | A | AT | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(172): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1351+376dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186647238 | ||||||
| chr2:186647628 | A | T | 4 | a0001c0001t0014g0160 a0001c0001t0015g0280 a0001c0001t0017g0106 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+751A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186647628 | |||||||
| chr2:186647672 | C | A | 4 | a0001c0001t0014g0160 a0001c0001t0015g0280 a0001c0001t0017g0106 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+795C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186647672 | |||||||
| chr2:186648003 | G | A | 4 | a0001c0001t0014g0160 a0001c0001t0015g0280 a0001c0001t0017g0106 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+1126G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648003 | |||||||
| chr2:186648248 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1351+1371G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648248 | |||||||
| chr2:186648375 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1352-1465A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648375 | |||||||
| chr2:186648554 | G | A | 65 | a0001c0001t0001g0018 a0001c0001t0002g0004 a0001c0001t0002g0005 others(62): Show |
68 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1352-1286G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648554 | |||||||
| chr2:186648614 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(218): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1352-1226A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648614 | |||||||
| chr2:186648666 | T | C | 1 | a0001c0001t0003g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1352-1174T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648666 | |||||||
| chr2:186648746 | A | G | 2 | a0001c0001t0002g0045 a0001c0001t0002g0112 |
2 | HG00323.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1352-1094A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648746 | |||||||
| chr2:186648787 | C | G | 2 | a0001c0001t0002g0173 a0001c0003t0002g0013 |
3 | HG02615.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1352-1053C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648787 | |||||||
| chr2:186648788 | C | T | 1 | a0002c0002t0004g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1352-1052C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648788 | |||||||
| chr2:186648933 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1352-907T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648933 | |||||||
| chr2:186648936 | A | G | 1 | a0001c0001t0003g0259 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1352-904A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648936 | |||||||
| chr2:186648943 | TACATTTG others(53): Show |
T | 1 | a0001c0001t0003g0250 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1352-875_1352-816d others(62): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186648943 | ||||||
| chr2:186648956 | A | G | 2 | a0001c0001t0003g0235 a0001c0001t0003g0261 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1352-884A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648956 | |||||||
| chr2:186648981 | TACATTTG others(15): Show |
T | 129 | a0001c0001t0001g0018 a0001c0001t0001g0100 a0001c0001t0001g0108 others(126): Show |
135 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1352-811_1352-790d others(24): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186648981 | ||||||
| chr2:186648981 | TACATTTG others(37): Show |
T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(122): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1352-833_1352-790d others(46): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186648981 | ||||||
| chr2:186648994 | ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0105 a0001c0001t0002g0084 |
2 | HG00738.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1352-837_1352-818d others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186648994 | ||||||
| chr2:186649003 | C | T | 15 | a0001c0001t0001g0222 a0001c0001t0002g0112 a0001c0001t0002g0161 others(12): Show |
16 | HG01884.hp1 HG01928.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1352-837C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649003 | |||||||
| chr2:186649010 | GTGTGTA | G | 13 | a0001c0001t0001g0222 a0001c0001t0002g0112 a0001c0001t0002g0161 others(10): Show |
14 | HG01884.hp1 HG01928.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1352-828_1352-823d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186649010 | ||||||
| chr2:186649016 | ATATATAT others(13): Show |
A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(13): Show |
17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1352-815_1352-796d others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186649016 | ||||||
| chr2:186649025 | C | T | 13 | a0001c0001t0001g0222 a0001c0001t0002g0112 a0001c0001t0002g0161 others(10): Show |
14 | HG01884.hp1 HG01928.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1352-815C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649025 | |||||||
| chr2:186649082 | TC | T | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1352-757delC | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649082 | |||||||
| chr2:186649083 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(212): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1352-757C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649083 | |||||||
| chr2:186649100 | A | C | 1 | a0001c0001t0002g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1352-740A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649100 | |||||||
| chr2:186649131 | A | G | 65 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(62): Show |
68 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1352-709A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649131 | |||||||
| chr2:186649393 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1352-447G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649393 | |||||||
| chr2:186649394 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1352-446A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649394 | |||||||
| chr2:186649455 | T | C | 65 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(62): Show |
68 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1352-385T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649455 | |||||||
| chr2:186649703 | A | G | 14 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0155 others(11): Show |
15 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1352-137A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649703 | |||||||
| chr2:186649814 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1352-26A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649814 | |||||||
| chr2:186650094 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1397+209G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650094 | |||||||
| chr2:186650227 | T | A | 1 | a0001c0001t0001g0219 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1397+342T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650227 | |||||||
| chr2:186650270 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1397+385G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650270 | |||||||
| chr2:186650361 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0214 |
2 | HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1397+476G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650361 | |||||||
| chr2:186650748 | C | T | 2 | a0001c0001t0011g0059 a0001c0001t0011g0077 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1397+863C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650748 | |||||||
| chr2:186650942 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0089 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1398-1040A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650942 | |||||||
| chr2:186651017 | A | G | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1398-965A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651017 | |||||||
| chr2:186651050 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1398-932A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651050 | |||||||
| chr2:186651262 | T | A | 4 | a0001c0001t0014g0160 a0001c0001t0015g0280 a0001c0001t0017g0106 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-720T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651262 | |||||||
| chr2:186651319 | A | G | 4 | a0001c0001t0014g0160 a0001c0001t0015g0280 a0001c0001t0017g0106 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-663A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651319 | |||||||
| chr2:186651644 | C | A | 1 | a0002c0002t0004g0130 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1398-338C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651644 | |||||||
| chr2:186651649 | C | A | 3 | a0001c0001t0003g0014 a0001c0001t0003g0240 a0001c0001t0003g0251 |
4 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-333C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651649 | |||||||
| chr2:186651650 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1398-332G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651650 | |||||||
| chr2:186651719 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1398-263A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651719 | |||||||
| chr2:186651855 | A | T | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1398-127A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651855 | |||||||
| chr2:186652131 | G | T | 1 | a0001c0001t0003g0293 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1505+42G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652131 | |||||||
| chr2:186652181 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1505+92T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652181 | |||||||
| chr2:186652478 | C | CCATT | 28 | a0001c0001t0001g0256 a0001c0003t0001g0012 a0001c0003t0001g0288 others(25): Show |
29 | HG00423.hp2 HG01099.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.1505+390_1505+393d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652478 | ||||||
| chr2:186652928 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1505+839T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652928 | |||||||
| chr2:186652931 | A | AT | 29 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0108 others(26): Show |
29 | HG01099.hp1 HG01123.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1505+867dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652931 | ||||||
| chr2:186652931 | A | ATTT | 9 | a0002c0002t0004g0124 a0002c0002t0004g0126 a0002c0002t0004g0129 others(6): Show |
9 | HG00423.hp2 HG01952.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1505+865_1505+867d others(5): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652931 | ||||||
| chr2:186652931 | AT | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1505+867delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652931 | ||||||
| chr2:186652931 | ATT | A | 42 | a0001c0001t0001g0092 a0001c0001t0001g0224 a0001c0001t0001g0285 others(39): Show |
45 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1505+866_1505+867d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652931 | ||||||
| chr2:186652961 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1505+872C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652961 | |||||||
| chr2:186652994 | A | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(198): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1505+905A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652994 | |||||||
| chr2:186653071 | G | T | 4 | a0001c0001t0014g0160 a0001c0001t0015g0280 a0001c0001t0017g0106 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1505+982G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653071 | |||||||
| chr2:186653090 | C | T | 4 | a0001c0001t0014g0160 a0001c0001t0015g0280 a0001c0001t0017g0106 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1505+1001C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653090 | |||||||
| chr2:186653121 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1505+1032A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653121 | |||||||
| chr2:186653196 | C | T | 2 | a0001c0001t0003g0235 a0001c0001t0003g0261 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1505+1107C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653196 | |||||||
| chr2:186653301 | T | C | 7 | a0001c0001t0002g0161 a0001c0001t0002g0173 a0001c0001t0008g0026 others(4): Show |
8 | HG02486.hp2 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1505+1212T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653301 | |||||||
| chr2:186653371 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1506-1279A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653371 | |||||||
| chr2:186653420 | C | T | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1506-1230C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653420 | |||||||
| chr2:186653432 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1506-1218A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653432 | |||||||
| chr2:186653533 | A | G | 52 | a0001c0001t0001g0285 a0001c0001t0003g0008 a0001c0001t0003g0009 others(49): Show |
55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506-1117A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653533 | |||||||
| chr2:186653562 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1506-1088A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653562 | |||||||
| chr2:186653947 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1506-703A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653947 | |||||||
| chr2:186653988 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1506-662T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653988 | |||||||
| chr2:186654098 | C | A | 5 | a0001c0001t0001g0177 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | NA18942.hp1 NA18960.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506-552C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654098 | |||||||
| chr2:186654222 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1506-428A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654222 | |||||||
| chr2:186654281 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1506-369C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654281 | |||||||
| chr2:186654332 | C | CA | 8 | a0001c0001t0001g0159 a0001c0001t0001g0208 a0001c0001t0001g0242 others(5): Show |
8 | HG00544.hp1 HG01361.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506-301dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186654332 | ||||||
| chr2:186654332 | CA | C | 7 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0001g0274 others(4): Show |
7 | HG01081.hp1 HG01255.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1506-301delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186654332 | ||||||
| chr2:186654545 | G | T | 1 | a0001c0001t0002g0017 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1506-105G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654545 | |||||||
| chr2:186654611 | G | T | 43 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0017 others(40): Show |
45 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1506-39G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654611 | |||||||
| chr2:186654908 | T | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | NA18942.hp1 NA18960.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1564+200T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186654908 | |||||||
| chr2:186654935 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1564+227C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186654935 | |||||||
| chr2:186655006 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1564+298A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655006 | |||||||
| chr2:186655381 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1564+673G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655381 | |||||||
| chr2:186655565 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1565-682T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655565 | |||||||
| chr2:186655602 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1565-645C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655602 | |||||||
| chr2:186655603 | G | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0121 others(5): Show |
9 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565-644G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655603 | |||||||
| chr2:186655639 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1565-608A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655639 | |||||||
| chr2:186656054 | T | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG00323.hp1 NA18612.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1565-193T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186656054 | |||||||
| chr2:186656446 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1719+45T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656446 | |||||||
| chr2:186656533 | C | A | 65 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(62): Show |
68 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1719+132C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656533 | |||||||
| chr2:186656572 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0105 |
2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1719+171C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656572 | |||||||
| chr2:186656694 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1719+293A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656694 | |||||||
| chr2:186656711 | A | G | 3 | a0002c0002t0007g0139 a0002c0002t0007g0140 a0002c0002t0007g0141 |
3 | HG01192.hp2 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1719+310A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656711 | |||||||
| chr2:186656736 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1719+335C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656736 | |||||||
| chr2:186656806 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1719+405A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656806 | |||||||
| chr2:186656816 | T | G | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1719+415T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656816 | |||||||
| chr2:186656868 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1719+467C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656868 | |||||||
| chr2:186656987 | A | AACAC | 5 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(2): Show |
5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1719+620_1719+623d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | ||||||
| chr2:186656987 | AAC | A | 65 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(62): Show |
68 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1719+622_1719+623d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | ||||||
| chr2:186656987 | AACAC | A | 98 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0091 others(95): Show |
102 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1719+620_1719+623d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | ||||||
| chr2:186656987 | AACACAC | A | 20 | a0001c0001t0019g0032 a0001c0003t0001g0012 a0001c0003t0001g0290 others(17): Show |
21 | HG00423.hp2 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1719+618_1719+623d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | ||||||
| chr2:186656987 | AACACACA others(3): Show |
A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1719+614_1719+623d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | ||||||
| chr2:186656987 | AACACACA others(7): Show |
A | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1719+610_1719+623d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | ||||||
| chr2:186657011 | CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1719+612_1719+625d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186657011 | ||||||
| chr2:186657015 | CACACACA others(3): Show |
C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(71): Show |
78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1719+616_1719+625d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186657015 | ||||||
| chr2:186657017 | CACACACA others(1): Show |
C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0200 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1719+618_1719+625d others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186657017 | ||||||
| chr2:186657217 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0031 |
2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1719+816T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657217 | |||||||
| chr2:186657567 | A | G | 1 | a0001c0001t0016g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1719+1166A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657567 | |||||||
| chr2:186657594 | T | C | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1719+1193T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657594 | |||||||
| chr2:186657679 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(191): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1719+1278G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657679 | |||||||
| chr2:186657885 | G | C | 63 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(60): Show |
66 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1720-1153G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657885 | |||||||
| chr2:186657953 | GA | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1720-1075delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186657953 | ||||||
| chr2:186657954 | A | G | 65 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(62): Show |
68 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1720-1084A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657954 | |||||||
| chr2:186658023 | G | T | 58 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0015 others(55): Show |
60 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1720-1015G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658023 | |||||||
| chr2:186658061 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(119): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1720-977A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658061 | |||||||
| chr2:186658064 | G | A | 2 | a0002c0002t0004g0129 a0002c0002t0004g0132 |
2 | NA18964.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1720-974G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658064 | |||||||
| chr2:186658146 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1720-892C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658146 | |||||||
| chr2:186658239 | G | A | 1 | a0001c0001t0019g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1720-799G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658239 | |||||||
| chr2:186658768 | GTGTT | G | 24 | a0001c0001t0001g0256 a0001c0003t0001g0012 a0001c0003t0001g0288 others(21): Show |
25 | HG00423.hp2 HG01099.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1720-267_1720-264d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186658768 | ||||||
| chr2:186658807 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1720-231C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658807 | |||||||
| chr2:186658968 | G | A | 2 | a0001c0001t0011g0059 a0001c0001t0011g0077 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1720-70G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658968 | |||||||
| chr2:186659307 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1857+132G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186659307 | |||||||
| chr2:186659795 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1857+620T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186659795 | |||||||
| chr2:186660091 | T | C | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1857+916T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660091 | |||||||
| chr2:186660228 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1857+1053C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660228 | |||||||
| chr2:186660299 | G | A | 7 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0005g0101 others(4): Show |
7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1857+1124G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660299 | |||||||
| chr2:186660466 | C | T | 52 | a0001c0001t0001g0285 a0001c0001t0003g0008 a0001c0001t0003g0009 others(49): Show |
55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1857+1291C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660466 | |||||||
| chr2:186660545 | G | A | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0022g0090 others(1): Show |
4 | HG01099.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1857+1370G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660545 | |||||||
| chr2:186660971 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0002g0048 |
2 | HG02630.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1857+1796G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660971 | |||||||
| chr2:186661235 | A | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(13): Show |
17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1857+2060A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661235 | |||||||
| chr2:186661268 | A | C | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1857+2093A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661268 | |||||||
| chr2:186661363 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(119): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1857+2188T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661363 | |||||||
| chr2:186661453 | A | T | 63 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(60): Show |
66 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1857+2278A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661453 | |||||||
| chr2:186661539 | G | T | 1 | a0001c0001t0003g0251 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1858-2229G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661539 | |||||||
| chr2:186661586 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1858-2182T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661586 | |||||||
| chr2:186661598 | GT | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(212): Show |
225 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1858-2153delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr2 | 186661598 | ||||||
| chr2:186661603 | T | TG | 9 | a0001c0001t0001g0285 a0001c0001t0003g0119 a0001c0001t0003g0150 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1858-2165_1858-216 others(5): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661603 | |||||||
| chr2:186661604 | T | G | 59 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(56): Show |
62 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1858-2164T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661604 | |||||||
| chr2:186661605 | T | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(120): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1858-2163T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661605 | |||||||
| chr2:186661611 | T | G | 1 | a0003c0004t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1858-2157T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661611 | |||||||
| chr2:186661707 | C | T | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1858-2061C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661707 | |||||||
| chr2:186661757 | C | T | 1 | a0001c0001t0017g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1858-2011C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661757 | |||||||
| chr2:186661758 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
10 | HG01169.hp1 HG01255.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1858-2010G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661758 | |||||||
| chr2:186661830 | C | T | 1 | a0001c0001t0003g0247 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1858-1938C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661830 | |||||||
| chr2:186661884 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0228 |
3 | HG02083.hp1 HG02155.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1858-1884C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661884 | |||||||
| chr2:186661887 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(216): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1858-1881A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661887 | |||||||
| chr2:186661945 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(118): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1858-1823G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661945 | |||||||
| chr2:186661963 | G | A | 2 | a0001c0001t0017g0106 a0001c0001t0024g0107 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1858-1805G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661963 | |||||||
| chr2:186662017 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1858-1751T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662017 | |||||||
| chr2:186662060 | T | C | 1 | a0002c0002t0004g0126 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1858-1708T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662060 | |||||||
| chr2:186662205 | T | C | 1 | a0001c0001t0003g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1858-1563T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662205 | |||||||
| chr2:186662237 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0011g0059 a0001c0001t0011g0077 |
3 | HG02970.hp1 HG03209.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1858-1531G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662237 | |||||||
| chr2:186662305 | G | A | 1 | a0002c0002t0004g0260 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1858-1463G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662305 | |||||||
| chr2:186663243 | A | G | 1 | a0002c0002t0004g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1858-525A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186663243 | |||||||
| chr2:186663424 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1858-344A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186663424 | |||||||
| chr2:186663692 | A | G | 1 | a0001c0001t0006g0287 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1858-76A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186663692 | |||||||
| chr2:186663908 | A | G | 77 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(74): Show |
81 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1925+73A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 19/29 | chr2 | 186663908 | |||||||
| chr2:186663968 | A | G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0078 others(9): Show |
12 | HG00140.hp1 HG00738.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1925+133A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 19/29 | chr2 | 186663968 | |||||||
| chr2:186664883 | C | G | 1 | a0001c0001t0003g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2073+242C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | chr2 | 186664883 | |||||||
| chr2:186664885 | A | G | 1 | a0001c0008t0020g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2074-241A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | chr2 | 186664885 | |||||||
| chr2:186664925 | T | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(285): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.2074-201T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | chr2 | 186664925 | |||||||
| chr2:186665096 | A | AT | 6 | a0001c0001t0001g0210 a0001c0001t0001g0214 a0001c0001t0002g0024 others(3): Show |
6 | HG01361.hp1 HG02132.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.2074-13dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr2 | 186665096 | ||||||
| chr2:186665096 | AT | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(192): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2074-13delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr2 | 186665096 | ||||||
| chr2:186665096 | ATT | A | 17 | a0001c0001t0003g0014 a0001c0001t0003g0240 a0001c0001t0003g0251 others(14): Show |
18 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2074-14_2074-13del others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr2 | 186665096 | ||||||
| chr2:186665389 | C | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(11): Show |
15 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.2166+171C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665389 | |||||||
| chr2:186665399 | T | G | 5 | a0001c0001t0001g0162 a0001c0001t0001g0204 a0001c0001t0001g0207 others(2): Show |
5 | HG02165.hp1 NA18949.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.2166+181T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665399 | |||||||
| chr2:186665505 | G | T | 2 | a0001c0001t0008g0026 a0001c0001t0008g0034 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2166+287G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665505 | |||||||
| chr2:186665654 | G | A | 3 | a0001c0001t0008g0026 a0001c0001t0008g0034 a0001c0001t0023g0071 |
3 | HG02486.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2166+436G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665654 | |||||||
| chr2:186665691 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2166+473A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665691 | |||||||
| chr2:186665694 | G | A | 1 | a0001c0001t0002g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2166+476G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665694 | |||||||
| chr2:186665793 | T | C | 77 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(74): Show |
81 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2166+575T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665793 | |||||||
| chr2:186665972 | T | C | 1 | a0001c0001t0018g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2167-732T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665972 | |||||||
| chr2:186666308 | T | C | 1 | a0001c0001t0003g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2167-396T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666308 | |||||||
| chr2:186666364 | T | C | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2167-340T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666364 | |||||||
| chr2:186666445 | T | G | 1 | a0001c0001t0002g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2167-259T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666445 | |||||||
| chr2:186666468 | T | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0084 |
2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2167-236T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666468 | |||||||
| chr2:186666575 | C | T | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2167-129C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666575 | |||||||
| chr2:186666639 | A | G | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2167-65A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666639 | |||||||
| chr2:186667283 | G | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.2327+53G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 23/29 | chr2 | 186667283 | |||||||
| chr2:186667507 | G | A | 51 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0011 others(48): Show |
54 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2328-164G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 23/29 | chr2 | 186667507 | |||||||
| chr2:186667646 | T | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(11): Show |
15 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.2328-25T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 23/29 | chr2 | 186667646 | |||||||
| chr2:186668041 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2433+265T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668041 | |||||||
| chr2:186668090 | G | A | 1 | a0001c0008t0020g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2433+314G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668090 | |||||||
| chr2:186668185 | C | CAT | 3 | a0001c0001t0005g0101 a0003c0004t0001g0082 a0003c0004t0001g0086 |
3 | HG02723.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2433+440_2433+441d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | C | CATATAT | 5 | a0001c0001t0001g0137 a0002c0002t0004g0126 a0002c0002t0004g0130 others(2): Show |
5 | HG01168.hp2 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+436_2433+441d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | C | CATATATA others(1): Show |
3 | a0001c0001t0008g0110 a0002c0002t0004g0133 a0002c0002t0004g0135 |
3 | HG00423.hp2 HG03540.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.2433+434_2433+441d others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | C | CATATATA others(3): Show |
3 | a0002c0002t0004g0125 a0002c0002t0004g0127 a0002c0002t0004g0134 |
3 | NA18950.hp2 NA18989.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2433+432_2433+441d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | C | CATATATA others(5): Show |
1 | a0002c0002t0004g0124 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2433+430_2433+441d others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | C | CATATATA others(7): Show |
1 | a0002c0002t0004g0260 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2433+428_2433+441d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | C | CATATATA others(15): Show |
1 | a0001c0001t0003g0241 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2433+420_2433+441d others(24): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | C | CATATATG others(3): Show |
1 | a0001c0001t0002g0029 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2433+415_2433+416i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | CATATAT | C | 4 | a0001c0001t0001g0176 a0001c0001t0001g0215 a0001c0001t0003g0148 others(1): Show |
4 | HG01081.hp2 HG01993.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+436_2433+441d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | CATATATA others(1): Show |
C | 26 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0119 others(23): Show |
28 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2433+434_2433+441d others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | CATATATA others(3): Show |
C | 3 | a0001c0001t0003g0248 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2433+432_2433+441d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2433+430_2433+441d others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668185 | CATATATA others(7): Show |
C | 1 | a0001c0001t0001g0229 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2433+428_2433+441d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | ||||||
| chr2:186668186 | A | ATATATGT others(3): Show |
1 | a0001c0001t0019g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2433+415_2433+416i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668186 | ||||||
| chr2:186668189 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0197 |
2 | HG01256.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2433+413T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668189 | |||||||
| chr2:186668190 | A | ATGTATAT others(7): Show |
1 | a0001c0001t0002g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2433+415_2433+416i others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668190 | ||||||
| chr2:186668192 | A | G | 74 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(71): Show |
78 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.2433+416A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668192 | |||||||
| chr2:186668205 | TATATATA | T | 6 | a0001c0001t0001g0267 a0001c0001t0003g0011 a0001c0001t0003g0039 others(3): Show |
7 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2433+430_2433+436d others(9): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668205 | |||||||
| chr2:186668205 | TATATATA others(2): Show |
T | 7 | a0001c0001t0003g0008 a0001c0001t0003g0123 a0001c0001t0003g0174 others(4): Show |
7 | HG01069.hp2 HG03710.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.2433+430_2433+438d others(11): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668205 | |||||||
| chr2:186668207 | TATATATA others(2): Show |
T | 3 | a0001c0001t0003g0243 a0001c0001t0003g0247 a0004c0007t0003g0008 |
3 | HG02015.hp1 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2433+432_2433+440d others(11): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668207 | |||||||
| chr2:186668210 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2433+434A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668210 | |||||||
| chr2:186668210 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2433+436_2433+445d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668210 | ||||||
| chr2:186668212 | A | T | 15 | a0001c0001t0001g0018 a0001c0001t0001g0152 a0001c0001t0001g0176 others(12): Show |
16 | HG00280.hp1 HG00558.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.2433+436A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668212 | |||||||
| chr2:186668214 | A | T | 47 | a0001c0001t0001g0018 a0001c0001t0001g0152 a0001c0001t0001g0159 others(44): Show |
50 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.2433+438A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668214 | |||||||
| chr2:186668216 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0222 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0206 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(30): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(26): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(18): Show |
4 | a0001c0001t0001g0007 a0001c0001t0001g0185 a0001c0001t0001g0194 others(1): Show |
4 | HG00423.hp1 HG01169.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(27): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0162 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(28): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0270 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(29): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0175 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(25): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0274 |
2 | HG01934.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(26): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(18): Show |
2 | a0001c0001t0001g0204 a0001c0001t0001g0208 |
2 | NA18949.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(27): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(21): Show |
3 | a0001c0001t0001g0197 a0001c0001t0001g0224 a0001c0001t0001g0273 |
3 | HG01952.hp2 NA18960.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(30): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0199 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0213 a0001c0001t0001g0218 |
2 | HG01255.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(24): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(16): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0184 a0001c0001t0001g0186 others(1): Show |
4 | HG00280.hp2 HG01358.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(25): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0269 |
2 | HG02015.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(26): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0192 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(27): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0030 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(28): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0228 |
2 | HG02083.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0203 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0190 a0001c0001t0001g0195 |
2 | HG00408.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(24): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0223 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(25): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0147 a0001c0001t0001g0217 |
2 | NA18747.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(26): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(28): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0105 a0001c0001t0001g0163 |
2 | HG02135.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(10): Show |
1 | a0002c0002t0002g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0196 a0001c0001t0002g0045 |
3 | HG00323.hp2 HG01258.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0016 a0001c0001t0002g0052 |
2 | HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(13): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0078 a0001c0001t0001g0191 others(2): Show |
5 | HG02155.hp1 HG02451.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0157 a0001c0001t0001g0180 a0001c0001t0001g0193 others(1): Show |
4 | HG01981.hp1 NA18979.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0284 a0001c0001t0002g0004 |
2 | HG00642.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(11): Show |
5 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0044 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0189 a0001c0001t0001g0275 a0001c0001t0002g0069 |
3 | HG01123.hp1 NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(13): Show |
5 | a0001c0001t0001g0079 a0001c0001t0001g0100 a0001c0001t0001g0177 others(2): Show |
5 | HG01993.hp1 HG02622.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0080 a0001c0001t0001g0214 |
2 | HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0121 a0001c0001t0002g0279 a0001c0001t0010g0164 |
3 | HG03017.hp1 HG03704.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0226 a0001c0001t0001g0283 |
2 | HG00597.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(12): Show |
5 | a0001c0001t0001g0091 a0001c0001t0002g0057 a0001c0001t0002g0058 others(2): Show |
5 | HG01928.hp2 HG02738.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0092 a0001c0001t0001g0153 |
2 | HG02300.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0179 a0001c0001t0001g0232 |
2 | HG02056.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(4): Show |
2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG01256.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(13): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0285 a0001c0001t0002g0114 a0001c0001t0002g0234 |
3 | HG01258.hp2 HG03490.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0010 a0001c0001t0002g0048 |
3 | HG03490.hp2 HG03492.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0085 a0001c0001t0001g0096 a0001c0001t0001g0201 |
3 | HG00738.hp2 HG02572.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(17): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0200 a0001c0001t0002g0062 |
2 | HG02683.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(10): Show |
1 | a0001c0001t0024g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0005 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0155 a0001c0001t0001g0230 |
2 | HG02965.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0225 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0219 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(3): Show |
1 | a0001c0003t0002g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0093 a0001c0001t0001g0145 a0001c0001t0002g0025 others(6): Show |
9 | HG02132.hp1 HG02258.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(13): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(5): Show |
7 | a0001c0001t0002g0084 a0001c0001t0002g0099 a0001c0001t0002g0115 others(4): Show |
7 | HG00558.hp1 HG00738.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(6): Show |
3 | a0001c0001t0002g0020 a0001c0001t0002g0037 a0001c0001t0002g0166 |
3 | HG02602.hp1 NA18949.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(17): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0089 |
2 | HG02258.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0221 a0001c0001t0018g0156 |
2 | HG00323.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATTT others(3): Show |
3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0002c0002t0022g0090 |
3 | HG01891.hp1 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATTT others(4): Show |
4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0036 others(1): Show |
4 | HG03927.hp2 NA18954.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(13): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATTT others(5): Show |
13 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0017 others(10): Show |
14 | HG00544.hp2 HG01496.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATTT others(6): Show |
5 | a0001c0001t0002g0028 a0001c0001t0002g0040 a0001c0001t0002g0117 others(2): Show |
5 | HG01106.hp1 HG01175.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATTT others(7): Show |
4 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0068 others(1): Show |
4 | HG00673.hp1 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATTT others(8): Show |
1 | a0001c0001t0001g0003 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(17): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATTT others(9): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0154 |
2 | HG01496.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATATTT others(11): Show |
1 | a0001c0001t0001g0220 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATTTTT others(3): Show |
1 | a0001c0001t0015g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATTTTT others(4): Show |
3 | a0001c0001t0002g0046 a0001c0001t0009g0076 a0001c0005t0002g0065 |
3 | NA19009.hp1 NA19060.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(13): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATTTTT others(5): Show |
4 | a0001c0001t0002g0061 a0001c0001t0002g0165 a0001c0005t0002g0033 others(1): Show |
4 | HG01358.hp1 HG02135.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATTTTT others(6): Show |
3 | a0001c0001t0002g0041 a0002c0002t0007g0139 a0002c0002t0007g0141 |
3 | HG02056.hp2 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | ATATTTTT others(7): Show |
1 | a0001c0001t0002g0167 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | ||||||
| chr2:186668216 | A | T | 62 | a0001c0001t0001g0018 a0001c0001t0001g0152 a0001c0001t0001g0159 others(59): Show |
65 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2433+440A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668216 | |||||||
| chr2:186668218 | T | A | 11 | a0001c0001t0008g0110 a0002c0002t0004g0124 a0002c0002t0004g0125 others(8): Show |
11 | HG01952.hp1 HG02148.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2433+442T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668218 | |||||||
| chr2:186668219 | T | A | 3 | a0001c0001t0008g0026 a0001c0001t0008g0034 a0001c0001t0023g0071 |
3 | HG02486.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2433+443T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668219 | |||||||
| chr2:186668220 | T | A | 7 | a0001c0001t0008g0110 a0002c0002t0004g0124 a0002c0002t0004g0125 others(4): Show |
7 | HG03540.hp1 NA18948.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.2433+444T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668220 | |||||||
| chr2:186668222 | T | A | 1 | a0001c0001t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2433+446T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668222 | |||||||
| chr2:186668224 | T | A | 1 | a0001c0001t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2433+448T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668224 | |||||||
| chr2:186668225 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2433+449T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668225 | |||||||
| chr2:186668226 | T | A | 1 | a0001c0001t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2433+450T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668226 | |||||||
| chr2:186668289 | G | C | 51 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0011 others(48): Show |
54 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2434-473G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668289 | |||||||
| chr2:186668361 | G | T | 1 | a0001c0001t0001g0206 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2434-401G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668361 | |||||||
| chr2:186668641 | C | T | 77 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(74): Show |
81 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2434-121C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668641 | |||||||
| chr2:186669014 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(102): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2592+94T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669014 | |||||||
| chr2:186669032 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2592+112T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669032 | |||||||
| chr2:186669131 | A | G | 1 | a0001c0001t0019g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2592+211A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669131 | |||||||
| chr2:186669388 | A | T | 9 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(6): Show |
9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2593-313A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669388 | |||||||
| chr2:186669456 | T | G | 78 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0049 others(75): Show |
82 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2593-245T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669456 | |||||||
| chr2:186669498 | A | T | 1 | a0001c0001t0002g0112 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2593-203A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669498 | |||||||
| chr2:186669859 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2706+45T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186669859 | |||||||
| chr2:186669984 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2706+170A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186669984 | |||||||
| chr2:186670051 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0228 |
3 | HG02083.hp1 HG02155.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2706+237C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670051 | |||||||
| chr2:186670292 | T | TTTTG | 77 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(74): Show |
81 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2706+498_2706+501d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 186670292 | ||||||
| chr2:186670335 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2706+521T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670335 | |||||||
| chr2:186670352 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2706+538G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670352 | |||||||
| chr2:186670544 | G | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(11): Show |
15 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.2706+730G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670544 | |||||||
| chr2:186670607 | A | G | 1 | a0001c0008t0020g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2706+793A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670607 | |||||||
| chr2:186670616 | A | T | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2706+802A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670616 | |||||||
| chr2:186671088 | A | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0155 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2706+1274A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671088 | |||||||
| chr2:186671144 | G | C | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2706+1330G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671144 | |||||||
| chr2:186671423 | T | A | 1 | a0001c0001t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2706+1609T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671423 | |||||||
| chr2:186671428 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(86): Show |
93 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.2706+1614C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671428 | |||||||
| chr2:186671472 | C | T | 2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | NA18940.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2706+1658C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671472 | |||||||
| chr2:186671582 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2706+1768C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671582 | |||||||
| chr2:186671640 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2706+1826A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671640 | |||||||
| chr2:186671921 | A | G | 2 | a0001c0001t0011g0059 a0001c0001t0011g0077 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2706+2107A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671921 | |||||||
| chr2:186671938 | A | G | 1 | a0001c0001t0002g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2706+2124A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671938 | |||||||
| chr2:186671945 | C | CT | 102 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(99): Show |
107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.2706+2147dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 186671945 | ||||||
| chr2:186671945 | C | CTT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(157): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2706+2146_2706+214 others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 186671945 | ||||||
| chr2:186671962 | C | G | 1 | a0001c0001t0002g0064 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2706+2148C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671962 | |||||||
| chr2:186672045 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2706+2231G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672045 | |||||||
| chr2:186672201 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2706+2387C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672201 | |||||||
| chr2:186672695 | C | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0137 a0001c0001t0001g0144 |
3 | HG01168.hp2 HG01255.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2706+2881C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672695 | |||||||
| chr2:186672806 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2707-2798A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672806 | |||||||
| chr2:186672977 | T | A | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2707-2627T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672977 | |||||||
| chr2:186673009 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2707-2595T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673009 | |||||||
| chr2:186673120 | T | C | 75 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(72): Show |
79 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2707-2484T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673120 | |||||||
| chr2:186673243 | T | C | 2 | a0001c0001t0017g0106 a0001c0001t0024g0107 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2707-2361T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673243 | |||||||
| chr2:186673546 | GTTTA | G | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2707-2051_2707-204 others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 186673546 | ||||||
| chr2:186673619 | T | A | 9 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(6): Show |
9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2707-1985T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673619 | |||||||
| chr2:186673619 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(255): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.2707-1985T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673619 | |||||||
| chr2:186673756 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2707-1848C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673756 | |||||||
| chr2:186673935 | T | A | 1 | a0001c0001t0003g0172 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2707-1669T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673935 | |||||||
| chr2:186673937 | C | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0085 |
2 | HG00738.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2707-1667C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673937 | |||||||
| chr2:186674058 | C | T | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2707-1546C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674058 | |||||||
| chr2:186674253 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2707-1351G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674253 | |||||||
| chr2:186674360 | G | C | 2 | a0001c0001t0006g0286 a0001c0001t0006g0287 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2707-1244G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674360 | |||||||
| chr2:186674453 | A | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2707-1151A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674453 | |||||||
| chr2:186674488 | C | G | 1 | a0001c0001t0002g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2707-1116C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674488 | |||||||
| chr2:186674502 | A | T | 1 | a0001c0001t0003g0253 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2707-1102A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674502 | |||||||
| chr2:186674590 | C | A | 1 | a0001c0008t0020g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2707-1014C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674590 | |||||||
| chr2:186674628 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(264): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.2707-976T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674628 | |||||||
| chr2:186674735 | C | T | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0022g0090 others(1): Show |
4 | HG01099.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2707-869C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674735 | |||||||
| chr2:186674754 | C | G | 5 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(2): Show |
5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2707-850C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674754 | |||||||
| chr2:186674850 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2707-754C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674850 | |||||||
| chr2:186674951 | A | G | 1 | a0002c0002t0007g0140 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2707-653A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674951 | |||||||
| chr2:186674994 | G | A | 52 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0011 others(49): Show |
55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2707-610G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674994 | |||||||
| chr2:186675133 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2707-471C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186675133 | |||||||
| chr2:186675353 | C | T | 1 | a0002c0002t0022g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2707-251C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186675353 | |||||||
| chr2:186675429 | C | T | 1 | a0001c0001t0003g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2707-175C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186675429 | |||||||
| chr2:186675742 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2820+25G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 27/29 | chr2 | 186675742 | |||||||
| chr2:186675757 | G | A | 1 | a0001c0001t0015g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2820+40G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 27/29 | chr2 | 186675757 | |||||||
| chr2:186676005 | G | A | 139 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(136): Show |
146 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.2928+78G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676005 | |||||||
| chr2:186676198 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2928+271G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676198 | |||||||
| chr2:186676240 | G | T | 51 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0011 others(48): Show |
54 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2928+313G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676240 | |||||||
| chr2:186676271 | G | A | 9 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(6): Show |
9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2928+344G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676271 | |||||||
| chr2:186676385 | T | C | 5 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0103 others(2): Show |
5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2929-428T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676385 | |||||||
| chr2:186676403 | A | G | 3 | a0001c0001t0006g0149 a0001c0001t0006g0286 a0001c0001t0006g0287 |
3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2929-410A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676403 | |||||||
| chr2:186676408 | C | T | 2 | a0001c0001t0003g0235 a0001c0001t0003g0261 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2929-405C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676408 | |||||||
| chr2:186676480 | T | G | 1 | a0001c0001t0002g0084 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2929-333T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676480 | |||||||
| chr2:186676529 | G | A | 1 | a0001c0001t0003g0252 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2929-284G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676529 | |||||||
| chr2:186676589 | A | G | 1 | a0001c0001t0002g0020 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2929-224A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676589 | |||||||
| chr2:186676591 | G | A | 139 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(136): Show |
146 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.2929-222G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676591 | |||||||
| chr2:186676650 | G | A | 75 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(72): Show |
79 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2929-163G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676650 | |||||||
| chr2:186676953 | AAAG | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG02056.hp1 NA18951.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.3051+22_3051+24del others(3): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr2 | 186676953 | ||||||
| chr2:186677083 | T | C | 51 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0011 others(48): Show |
54 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.3052-114T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 29/29 | chr2 | 186677083 |