Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55633 |
| ensemblid | ENSG00000065491.8 |
| hgncid | 21602 |
| symbol | TBC1D22B |
| name | TBC1 domain family member 22B |
| refseq_nuc | NM_017772.4 |
| refseq_prot | NP_060242.2 |
| ensembl_nuc | ENST00000373491.3 |
| ensembl_prot | ENSP00000362590.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 37257772 |
| end | 37332970 |
| strand | + |
| ver | v1.2 |
| region | chr6:37257772-37332970 |
| region5000 | chr6:37252772-37337970 |
| regionname0 | TBC1D22B_chr6_37257772_37332970 |
| regionname5000 | TBC1D22B_chr6_37252772_37337970 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 505 | 220 | 82 | 54 | 46 | 10 | 26 | 32 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | MAAEN others(500): Show |
chr6 | 37252772 | 37337970 |
| a0002 | 0/0 | 505 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | MAAEN others(500): Show |
chr6 | 37252772 | 37337970 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1515 | 113 | 42 | 25 | 26 | 5 | 14 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ATGGC others(1510): Show |
chr6 | 37252772 | 37337970 | ||
| a0001c0002 | 0/0 | 1515 | 67 | 22 | 23 | 9 | 4 | 9 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ATGGC others(1510): Show |
chr6 | 37252772 | 37337970 | ||
| a0001c0003 | 1/0 | 1515 | 22 | 1 | 6 | 11 | 1 | 2 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ATGGC others(1510): Show |
chr6 | 37252772 | 37337970 | ||
| a0001c0004 | 0/0 | 1515 | 17 | 17 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ATGGC others(1510): Show |
chr6 | 37252772 | 37337970 | ||
| a0001c0006 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ATGGC others(1510): Show |
chr6 | 37252772 | 37337970 | ||
| a0002c0005 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ATGGC others(1510): Show |
chr6 | 37252772 | 37337970 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3462 | 78 | 21 | 21 | 20 | 4 | 11 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0002 | 0/0 | 3462 | 3 | 1 | 0 | 2 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0003 | 0/0 | 3462 | 16 | 11 | 1 | 3 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0006 | 0/0 | 3462 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0007 | 0/0 | 3462 | 4 | 0 | 2 | 0 | 1 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0008 | 0/0 | 3462 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0009 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0010 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0011 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0012 | 0/0 | 3462 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0014 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0001t0018 | 0/0 | 3462 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0001 | 0/0 | 3462 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0002 | 0/0 | 3462 | 35 | 5 | 17 | 5 | 3 | 5 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0003 | 0/0 | 3462 | 8 | 8 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0004 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0005 | 0/0 | 3462 | 8 | 1 | 3 | 1 | 0 | 3 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0006 | 0/0 | 3462 | 6 | 4 | 2 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0007 | 0/0 | 3462 | 3 | 0 | 1 | 0 | 1 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0013 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0016 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0002t0017 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0003t0004 | 1/0 | 3462 | 21 | 0 | 6 | 11 | 1 | 2 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0003t0015 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0004t0002 | 0/0 | 3462 | 11 | 11 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0004t0003 | 0/0 | 3462 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0004t0004 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0001c0006t0005 | 0/0 | 3462 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| a0002c0005t0004 | 0/0 | 3462 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | ACATC others(3457): Show |
chr6 | 37252772 | 37337970 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0005 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0007g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0014g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0001t0018g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0007g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0007g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0013g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0016g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0002t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0007 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0003t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0004t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0001c0006t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0002c0005t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| a0002c0005t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0179 | EUR | GBR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0065 | EUR | GBR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0089 | EUR | FIN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00609 | hp1 | a0001 | c0003 | t0004 | g0025 | EAS | CHS | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0077 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00642 | hp2 | a0002 | c0005 | t0004 | g0021 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00733 | hp1 | a0001 | c0003 | t0004 | g0028 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0066 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0180 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG00741 | hp2 | a0001 | c0003 | t0004 | g0013 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0105 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01069 | hp2 | a0001 | c0003 | t0004 | g0012 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01071 | hp1 | a0001 | c0003 | t0004 | g0011 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01074 | hp1 | a0001 | c0002 | t0005 | g0097 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01081 | hp1 | a0001 | c0002 | t0005 | g0092 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01099 | hp2 | a0001 | c0001 | t0018 | g0117 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0104 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0103 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0198 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01192 | hp1 | a0001 | c0003 | t0004 | g0026 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0075 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01243 | hp1 | a0001 | c0002 | t0006 | g0034 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0076 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01346 | hp1 | a0001 | c0003 | t0004 | g0023 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01358 | hp2 | a0001 | c0002 | t0005 | g0095 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01361 | hp1 | a0001 | c0002 | t0006 | g0032 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01433 | hp2 | a0001 | c0002 | t0007 | g0102 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01517 | hp1 | a0001 | c0003 | t0004 | g0024 | EUR | IBS | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | IBS | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01884 | hp2 | a0001 | c0004 | t0003 | g0049 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02015 | hp1 | a0001 | c0003 | t0004 | g0018 | EAS | KHV | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0074 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02055 | hp2 | a0001 | c0004 | t0003 | g0050 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | KHV | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02145 | hp2 | a0001 | c0004 | t0002 | g0061 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | CDX | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02257 | hp2 | a0001 | c0004 | t0002 | g0058 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0039 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02273 | hp2 | a0002 | c0005 | t0004 | g0030 | AMR | PEL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0167 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0127 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02451 | hp2 | a0001 | c0004 | t0003 | g0046 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | KHV | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02572 | hp1 | a0001 | c0004 | t0004 | g0051 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02572 | hp2 | a0001 | c0002 | t0013 | g0044 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02615 | hp1 | a0001 | c0002 | t0006 | g0031 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0129 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02630 | hp1 | a0001 | c0002 | t0016 | g0062 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02683 | hp1 | a0001 | c0002 | t0005 | g0098 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02723 | hp2 | a0001 | c0002 | t0006 | g0033 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02738 | hp1 | a0001 | c0002 | t0005 | g0093 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02886 | hp2 | a0001 | c0004 | t0002 | g0056 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0212 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02895 | hp2 | a0001 | c0004 | t0002 | g0045 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02896 | hp2 | a0001 | c0002 | t0006 | g0036 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02897 | hp1 | a0001 | c0002 | t0006 | g0037 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02897 | hp2 | a0001 | c0004 | t0002 | g0060 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02922 | hp1 | a0001 | c0004 | t0002 | g0054 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02965 | hp2 | a0001 | c0004 | t0002 | g0059 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0068 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03017 | hp1 | a0001 | c0001 | t0012 | g0216 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03017 | hp2 | a0001 | c0003 | t0004 | g0010 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0107 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0071 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03139 | hp1 | a0001 | c0004 | t0002 | g0053 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03139 | hp2 | a0001 | c0004 | t0002 | g0057 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03225 | hp1 | a0001 | c0002 | t0017 | g0063 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03453 | hp2 | a0001 | c0002 | t0005 | g0006 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0214 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03490 | hp1 | a0001 | c0002 | t0005 | g0094 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0170 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03704 | hp1 | a0001 | c0003 | t0004 | g0020 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0073 | SAS | BEB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | BEB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | BEB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0138 | SAS | BEB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG04204 | hp2 | a0001 | c0006 | t0005 | g0029 | SAS | STU | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0083 | SAS | STU | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | YRI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18964 | hp2 | a0001 | c0003 | t0004 | g0035 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18981 | hp2 | a0001 | c0003 | t0004 | g0014 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18992 | hp2 | a0001 | c0003 | t0004 | g0019 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19011 | hp1 | a0001 | c0002 | t0005 | g0096 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19011 | hp2 | a0001 | c0003 | t0004 | g0022 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0038 | AFR | LWK | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | LWK | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | LWK | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19065 | hp1 | a0001 | c0003 | t0004 | g0017 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19077 | hp1 | a0001 | c0003 | t0004 | g0008 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19088 | hp2 | a0001 | c0003 | t0004 | g0015 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19091 | hp1 | a0001 | c0003 | t0004 | g0027 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19240 | hp1 | a0001 | c0004 | t0003 | g0048 | AFR | YRI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA19240 | hp2 | a0001 | c0004 | t0003 | g0047 | AFR | YRI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20129 | hp1 | a0001 | c0003 | t0015 | g0009 | AFR | ASW | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0171 | AFR | ASW | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0079 | EUR | TSI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20805 | hp1 | a0001 | c0002 | t0007 | g0101 | EUR | TSI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20905 | hp1 | a0001 | c0002 | t0007 | g0100 | SAS | GIH | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | GIH | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0099 | AMR | CLM | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02109 | hp2 | a0001 | c0004 | t0002 | g0055 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0052 | AFR | ACB | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0042 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0108 | AFR | USA | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | USA | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18955 | hp1 | a0001 | c0003 | t0004 | g0016 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA18955 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | USA | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0109 | AFR | USA | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0201 | REF | REF | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0004 | g0007 | REF | REF | TBC1D22B_chr6_37252772_37337970 | TBC1D22B | chr6 | 37252772 | 37337970 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:37282292 | C | G | 1 | a0002 | 2 | HG00642.hp2 HG02273.hp2 |
missense_variant | MODERATE | c.529C>G | p.Pro177Ala | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 4/13 | 675/3462 | 529/1518 | 177/505 | chr6 | 37282292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:37279409 | C | T | 1 | a0001c0004 | 17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
synonymous_variant | LOW | c.219C>T | p.Gly73Gly | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/13 | 365/3462 | 219/1518 | 73/505 | chr6 | 37279409 | |||
| chr6:37282336 | A | G | 3 | a0001c0001 a0001c0002 a0001c0004 |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
synonymous_variant | LOW | c.573A>G | p.Gln191Gln | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 4/13 | 719/3462 | 573/1518 | 191/505 | chr6 | 37282336 | |||
| chr6:37284434 | C | T | 1 | a0001c0001 | 112 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(109): Show |
synonymous_variant | LOW | c.771C>T | p.Asn257Asn | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/13 | 917/3462 | 771/1518 | 257/505 | chr6 | 37284434 | |||
| chr6:37331052 | C | T | 1 | a0001c0006 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.1398C>T | p.Leu466Leu | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1544/3462 | 1398/1518 | 466/505 | chr6 | 37331052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:37331246 | C | T | 1 | a0001c0001t0018 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 74 | chr6 | 37331246 | ||||||
| chr6:37331337 | C | G | 8 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(5): Show |
43 | HG01243.hp1 HG01255.hp1 HG01361.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*165C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 165 | chr6 | 37331337 | ||||||
| chr6:37331418 | A | G | 1 | a0001c0003t0015 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 246 | chr6 | 37331418 | ||||||
| chr6:37331420 | A | G | 1 | a0001c0001t0014 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 248 | chr6 | 37331420 | ||||||
| chr6:37331440 | A | G | 1 | a0001c0002t0013 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*268A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 268 | chr6 | 37331440 | ||||||
| chr6:37331627 | G | C | 8 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(5): Show |
43 | HG01243.hp1 HG01255.hp1 HG01361.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*455G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 455 | chr6 | 37331627 | ||||||
| chr6:37331660 | G | A | 6 | a0001c0001t0003 a0001c0001t0008 a0001c0002t0003 others(3): Show |
35 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*488G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 488 | chr6 | 37331660 | ||||||
| chr6:37331872 | G | A | 2 | a0001c0001t0007 a0001c0002t0007 |
7 | HG00099.hp1 HG00735.hp1 HG01175.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*700G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 700 | chr6 | 37331872 | ||||||
| chr6:37332032 | T | C | 1 | a0001c0001t0009 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*860T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 860 | chr6 | 37332032 | ||||||
| chr6:37332180 | C | T | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0013 others(1): Show |
50 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1008C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1008 | chr6 | 37332180 | ||||||
| chr6:37332274 | C | G | 1 | a0001c0001t0012 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1102C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1102 | chr6 | 37332274 | ||||||
| chr6:37332373 | C | T | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(13): Show |
134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*1201C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1201 | chr6 | 37332373 | ||||||
| chr6:37332378 | C | T | 1 | a0001c0001t0011 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1206 | chr6 | 37332378 | ||||||
| chr6:37332385 | G | A | 1 | a0001c0002t0016 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1213G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1213 | chr6 | 37332385 | ||||||
| chr6:37332413 | G | A | 2 | a0001c0002t0005 a0001c0006t0005 |
9 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1241G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1241 | chr6 | 37332413 | ||||||
| chr6:37332508 | C | T | 6 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(3): Show |
41 | HG01243.hp1 HG01255.hp1 HG01361.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1336C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1336 | chr6 | 37332508 | ||||||
| chr6:37332619 | G | T | 1 | a0001c0001t0008 | 4 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1447G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1447 | chr6 | 37332619 | ||||||
| chr6:37332627 | G | A | 1 | a0001c0001t0010 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1455G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 13/13 | 1455 | chr6 | 37332627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:37258225 | C | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.56+252C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258225 | |||||||
| chr6:37258261 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+288A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258261 | |||||||
| chr6:37258288 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+315A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258288 | |||||||
| chr6:37258342 | C | T | 1 | a0001c0002t0002g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.56+369C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258342 | |||||||
| chr6:37258345 | C | T | 1 | a0001c0001t0012g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.56+372C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258345 | |||||||
| chr6:37258549 | T | C | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.56+576T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258549 | |||||||
| chr6:37258659 | T | C | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.56+686T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258659 | |||||||
| chr6:37258684 | C | T | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+711C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258684 | |||||||
| chr6:37258744 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.56+771A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258744 | |||||||
| chr6:37258920 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.56+947G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37258920 | |||||||
| chr6:37258957 | C | CT | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
184 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.56+995dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37258957 | ||||||
| chr6:37259015 | A | AT | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
115 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.56+1058dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37259015 | ||||||
| chr6:37259050 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG01255.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+1077G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37259050 | |||||||
| chr6:37259137 | C | T | 1 | a0001c0002t0003g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.56+1164C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37259137 | |||||||
| chr6:37259320 | T | G | 10 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0125 others(7): Show |
11 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.56+1347T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37259320 | |||||||
| chr6:37259460 | T | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+1487T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37259460 | |||||||
| chr6:37259558 | C | CT | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG01255.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+1592dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37259558 | ||||||
| chr6:37259714 | T | C | 1 | a0001c0001t0003g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.56+1741T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37259714 | |||||||
| chr6:37259740 | G | A | 1 | a0001c0002t0016g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.56+1767G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37259740 | |||||||
| chr6:37260110 | A | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.56+2137A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37260110 | |||||||
| chr6:37260200 | G | T | 11 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.56+2227G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37260200 | |||||||
| chr6:37260231 | G | A | 1 | a0001c0002t0017g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.56+2258G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37260231 | |||||||
| chr6:37260513 | T | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.56+2540T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37260513 | |||||||
| chr6:37260522 | C | T | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.56+2549C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37260522 | |||||||
| chr6:37260605 | A | G | 10 | a0001c0002t0002g0001 a0001c0002t0002g0065 a0001c0002t0002g0099 others(7): Show |
11 | HG00099.hp2 HG01069.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.56+2632A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37260605 | |||||||
| chr6:37260610 | G | A | 1 | a0001c0001t0006g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.56+2637G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37260610 | |||||||
| chr6:37260640 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.56+2667C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37260640 | |||||||
| chr6:37260849 | C | T | 1 | a0001c0001t0011g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.56+2876C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37260849 | |||||||
| chr6:37261165 | T | C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
161 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.56+3192T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37261165 | |||||||
| chr6:37261204 | G | A | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG00733.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.56+3231G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37261204 | |||||||
| chr6:37261387 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+3414G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37261387 | |||||||
| chr6:37261389 | G | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.56+3416G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37261389 | |||||||
| chr6:37261415 | G | C | 47 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(44): Show |
48 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.56+3442G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37261415 | |||||||
| chr6:37261432 | C | CA | 28 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0136 others(25): Show |
28 | HG01123.hp2 HG01255.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.56+3480dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261432 | ||||||
| chr6:37261432 | CA | C | 34 | a0001c0001t0001g0213 a0001c0002t0003g0038 a0001c0002t0004g0039 others(31): Show |
34 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.56+3480delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261432 | ||||||
| chr6:37261509 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.56+3536A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37261509 | |||||||
| chr6:37261637 | G | A | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0126 |
3 | HG02630.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.56+3664G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37261637 | |||||||
| chr6:37261669 | G | A | 16 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.56+3696G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37261669 | |||||||
| chr6:37261944 | A | AGT | 2 | a0001c0003t0004g0028 a0001c0003t0015g0009 |
2 | HG00733.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.56+4022_56+4023dup others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | A | AGTGT | 2 | a0001c0006t0005g0029 a0002c0005t0004g0030 |
2 | HG02273.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.56+4020_56+4023dup others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGT | A | 9 | a0001c0002t0005g0006 a0001c0002t0006g0036 a0001c0002t0006g0037 others(6): Show |
9 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.56+4022_56+4023del others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGT | A | 6 | a0001c0002t0002g0043 a0001c0002t0006g0032 a0001c0002t0006g0033 others(3): Show |
6 | HG00741.hp2 HG01243.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.56+4020_56+4023del others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGTGT | A | 9 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(6): Show |
9 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.56+4018_56+4023del others(6): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGTGTG others(1): Show |
A | 5 | a0001c0001t0009g0212 a0001c0002t0002g0066 a0001c0002t0002g0067 others(2): Show |
5 | HG00733.hp2 HG01243.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+4016_56+4023del others(8): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGTGTG others(3): Show |
A | 31 | a0001c0001t0001g0111 a0001c0001t0001g0137 a0001c0001t0001g0202 others(28): Show |
32 | HG00099.hp2 HG01069.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.56+4014_56+4023del others(10): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGTGTG others(5): Show |
A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0116 others(50): Show |
54 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.56+4012_56+4023del others(12): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGTGTG others(7): Show |
A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0114 others(50): Show |
54 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.56+4010_56+4023del others(14): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGTGTG others(9): Show |
A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0142 a0001c0001t0003g0131 |
3 | HG02647.hp2 HG02683.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.56+4008_56+4023del others(16): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGTGTG others(11): Show |
A | 13 | a0001c0001t0001g0141 a0001c0001t0003g0113 a0001c0001t0003g0123 others(10): Show |
14 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.56+4006_56+4023del others(18): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGTGTG others(13): Show |
A | 5 | a0001c0002t0003g0038 a0001c0004t0002g0061 a0001c0004t0003g0048 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+4004_56+4023del others(20): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261944 | AGTGTGTG others(15): Show |
A | 13 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(10): Show |
13 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.56+4002_56+4023del others(22): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37261944 | ||||||
| chr6:37261963 | G | T | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.56+3990G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37261963 | |||||||
| chr6:37262016 | G | GA | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.56+4053dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37262016 | ||||||
| chr6:37262030 | CCT | C | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+4058_56+4059del others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37262030 | |||||||
| chr6:37262031 | CT | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.56+4075delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37262031 | ||||||
| chr6:37262404 | A | T | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56+4431A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37262404 | |||||||
| chr6:37262442 | A | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.56+4469A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37262442 | |||||||
| chr6:37262517 | G | A | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.56+4544G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37262517 | |||||||
| chr6:37262555 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.56+4582G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37262555 | |||||||
| chr6:37262619 | G | C | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56+4646G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37262619 | |||||||
| chr6:37262837 | C | T | 4 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(1): Show |
4 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.56+4864C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37262837 | |||||||
| chr6:37262907 | C | G | 1 | a0001c0001t0003g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.56+4934C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37262907 | |||||||
| chr6:37262916 | T | C | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.56+4943T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37262916 | |||||||
| chr6:37263296 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.56+5323A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263296 | |||||||
| chr6:37263385 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+5412G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263385 | |||||||
| chr6:37263438 | T | C | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56+5465T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263438 | |||||||
| chr6:37263439 | G | A | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56+5466G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263439 | |||||||
| chr6:37263515 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.56+5542T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263515 | |||||||
| chr6:37263550 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+5577A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263550 | |||||||
| chr6:37263605 | C | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+5632C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263605 | |||||||
| chr6:37263636 | T | A | 1 | a0001c0002t0016g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.56+5663T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263636 | |||||||
| chr6:37263731 | G | A | 1 | a0001c0006t0005g0029 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.56+5758G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263731 | |||||||
| chr6:37263880 | G | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.57-5714G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37263880 | |||||||
| chr6:37264042 | AT | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.57-5540delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37264042 | ||||||
| chr6:37264338 | G | A | 1 | a0001c0002t0006g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.57-5256G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37264338 | |||||||
| chr6:37264381 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
98 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.57-5213C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37264381 | |||||||
| chr6:37264463 | C | T | 2 | a0001c0002t0003g0038 a0001c0002t0004g0039 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.57-5131C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37264463 | |||||||
| chr6:37264510 | T | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-5084T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37264510 | |||||||
| chr6:37264531 | GA | G | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.57-5061delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37264531 | ||||||
| chr6:37264690 | A | G | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.57-4904A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37264690 | |||||||
| chr6:37264827 | C | A | 7 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(4): Show |
7 | HG00741.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-4767C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37264827 | |||||||
| chr6:37265216 | C | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-4378C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37265216 | |||||||
| chr6:37265344 | T | C | 1 | a0001c0002t0005g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.57-4250T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37265344 | |||||||
| chr6:37265532 | G | GT | 8 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG01884.hp1 HG03486.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-4049dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37265532 | ||||||
| chr6:37265532 | GT | G | 22 | a0001c0001t0001g0202 a0001c0002t0003g0107 a0001c0002t0003g0108 others(19): Show |
22 | HG01257.hp2 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.57-4049delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37265532 | ||||||
| chr6:37265741 | G | A | 1 | a0001c0003t0004g0017 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.57-3853G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37265741 | |||||||
| chr6:37266188 | T | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-3406T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266188 | |||||||
| chr6:37266281 | C | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-3313C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266281 | |||||||
| chr6:37266332 | A | G | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57-3262A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266332 | |||||||
| chr6:37266369 | G | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-3225G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266369 | |||||||
| chr6:37266466 | CT | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.57-3115delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37266466 | ||||||
| chr6:37266484 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.57-3110C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266484 | |||||||
| chr6:37266497 | T | C | 1 | a0001c0002t0007g0100 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.57-3097T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266497 | |||||||
| chr6:37266733 | G | A | 1 | a0001c0004t0003g0048 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57-2861G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266733 | |||||||
| chr6:37266737 | A | G | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.57-2857A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266737 | |||||||
| chr6:37266740 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-2854G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266740 | |||||||
| chr6:37266790 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-2804A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266790 | |||||||
| chr6:37266927 | C | T | 1 | a0001c0002t0002g0090 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.57-2667C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37266927 | |||||||
| chr6:37266930 | C | CT | 6 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(3): Show |
6 | HG00741.hp1 HG00741.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-2640dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37266930 | ||||||
| chr6:37266930 | CT | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
112 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.57-2640delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37266930 | ||||||
| chr6:37266930 | CTT | C | 54 | a0001c0001t0001g0144 a0001c0001t0001g0176 a0001c0001t0012g0216 others(51): Show |
55 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.57-2641_57-2640del others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37266930 | ||||||
| chr6:37267156 | A | G | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57-2438A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267156 | |||||||
| chr6:37267194 | C | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-2400C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267194 | |||||||
| chr6:37267235 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-2359T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267235 | |||||||
| chr6:37267307 | CAT | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.57-2271_57-2270del others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267307 | ||||||
| chr6:37267311 | T | TATATATA others(6): Show |
17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-2272_57-2271ins others(13): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267311 | ||||||
| chr6:37267333 | C | CAT | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2255_57-2254dup others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267333 | ||||||
| chr6:37267333 | C | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
190 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.57-2261C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267333 | |||||||
| chr6:37267337 | TATAATAT others(12): Show |
T | 3 | a0001c0002t0006g0032 a0001c0002t0006g0033 a0001c0002t0006g0034 |
3 | HG01243.hp1 HG01361.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.57-2253_57-2235del others(19): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267337 | ||||||
| chr6:37267342 | TATATATA others(14): Show |
T | 10 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(7): Show |
10 | HG00741.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.57-2221_57-2201del others(21): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267342 | ||||||
| chr6:37267362 | T | A | 3 | a0001c0002t0006g0032 a0001c0002t0006g0033 a0001c0002t0006g0034 |
3 | HG01243.hp1 HG01361.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.57-2232T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267362 | |||||||
| chr6:37267363 | A | AAT | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2223_57-2222dup others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267363 | ||||||
| chr6:37267363 | A | ATAAT | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-2231_57-2230ins others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267363 | |||||||
| chr6:37267363 | A | T | 3 | a0001c0002t0006g0032 a0001c0002t0006g0033 a0001c0002t0006g0034 |
3 | HG01243.hp1 HG01361.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.57-2231A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267363 | |||||||
| chr6:37267373 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
160 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.57-2221C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267373 | |||||||
| chr6:37267377 | C | T | 1 | a0001c0002t0002g0075 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.57-2217C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267377 | |||||||
| chr6:37267384 | AAT | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
178 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.57-2200_57-2199del others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267384 | ||||||
| chr6:37267392 | TATAC | T | 4 | a0001c0002t0002g0076 a0001c0002t0006g0031 a0001c0002t0006g0036 others(1): Show |
4 | HG01257.hp1 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.57-2200_57-2197del others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267392 | ||||||
| chr6:37267400 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-2194C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267400 | |||||||
| chr6:37267402 | T | C | 1 | a0001c0002t0002g0076 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.57-2192T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267402 | |||||||
| chr6:37267406 | T | A | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2188T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267406 | |||||||
| chr6:37267407 | A | T | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2187A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267407 | |||||||
| chr6:37267412 | A | G | 7 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(4): Show |
7 | HG00741.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-2182A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267412 | |||||||
| chr6:37267415 | T | C | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2179T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267415 | |||||||
| chr6:37267417 | T | C | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2177T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267417 | |||||||
| chr6:37267421 | C | T | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2173C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267421 | |||||||
| chr6:37267421 | CATATA | C | 16 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.57-2167_57-2163del others(5): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267421 | ||||||
| chr6:37267436 | C | T | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2158C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267436 | |||||||
| chr6:37267448 | A | T | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2146A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267448 | |||||||
| chr6:37267449 | T | A | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2145T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267449 | |||||||
| chr6:37267461 | CA | C | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2132delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267461 | |||||||
| chr6:37267470 | A | AATAT | 2 | a0001c0002t0006g0036 a0001c0002t0006g0037 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2118_57-2115dup others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267470 | ||||||
| chr6:37267482 | CTATATAT others(15): Show |
C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.57-2094_57-2073del others(22): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267482 | ||||||
| chr6:37267482 | CTATATAT others(17): Show |
C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-2105_57-2082del others(24): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267482 | ||||||
| chr6:37267490 | A | AATAT | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.57-2098_57-2095dup others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267490 | ||||||
| chr6:37267490 | A | AATATATA others(21): Show |
3 | a0001c0002t0006g0032 a0001c0002t0006g0033 a0001c0002t0006g0034 |
3 | HG01243.hp1 HG01361.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.57-2095_57-2094ins others(28): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267490 | ||||||
| chr6:37267490 | A | ATAAT | 3 | a0001c0002t0006g0031 a0001c0002t0006g0036 a0001c0002t0006g0037 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-2104_57-2103ins others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267490 | |||||||
| chr6:37267490 | AATATATA others(17): Show |
A | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.57-2067_57-2044del others(24): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267490 | ||||||
| chr6:37267500 | C | T | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57-2094C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267500 | |||||||
| chr6:37267502 | C | CACATATA others(11): Show |
1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57-2092_57-2091ins others(18): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267502 | |||||||
| chr6:37267513 | A | T | 1 | a0001c0003t0015g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.57-2081A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267513 | |||||||
| chr6:37267527 | T | TATATATA others(16): Show |
1 | a0001c0003t0015g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.57-2057_57-2035dup others(23): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 37267527 | ||||||
| chr6:37267569 | A | G | 1 | a0001c0001t0009g0212 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.57-2025A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267569 | |||||||
| chr6:37267579 | A | T | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.57-2015A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267579 | |||||||
| chr6:37267777 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.57-1817C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267777 | |||||||
| chr6:37267977 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-1617A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37267977 | |||||||
| chr6:37268010 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.57-1584A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37268010 | |||||||
| chr6:37268266 | C | A | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.57-1328C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37268266 | |||||||
| chr6:37268341 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-1253G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37268341 | |||||||
| chr6:37268371 | G | A | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.57-1223G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37268371 | |||||||
| chr6:37268475 | T | A | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57-1119T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37268475 | |||||||
| chr6:37268890 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.57-704G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37268890 | |||||||
| chr6:37269046 | T | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | HG01070.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.57-548T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37269046 | |||||||
| chr6:37269140 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0006g0171 a0001c0001t0014g0167 |
3 | HG02280.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.57-454C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37269140 | |||||||
| chr6:37269405 | A | G | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.57-189A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37269405 | |||||||
| chr6:37269543 | T | C | 1 | a0001c0001t0008g0127 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.57-51T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 1/12 | chr6 | 37269543 | |||||||
| chr6:37269768 | T | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0116 others(14): Show |
18 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.113+118T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37269768 | |||||||
| chr6:37269774 | A | G | 47 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(44): Show |
48 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.113+124A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37269774 | |||||||
| chr6:37269834 | A | G | 1 | a0001c0001t0003g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.113+184A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37269834 | |||||||
| chr6:37269882 | T | C | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.113+232T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37269882 | |||||||
| chr6:37270054 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.113+404T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270054 | |||||||
| chr6:37270055 | A | G | 1 | a0001c0004t0003g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.113+405A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270055 | |||||||
| chr6:37270142 | A | G | 1 | a0001c0003t0004g0026 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.113+492A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270142 | |||||||
| chr6:37270293 | A | T | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.113+643A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270293 | |||||||
| chr6:37270325 | G | T | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.113+675G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270325 | |||||||
| chr6:37270438 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.113+788G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270438 | |||||||
| chr6:37270447 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0133 a0001c0001t0001g0146 others(2): Show |
6 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+797T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270447 | |||||||
| chr6:37270535 | A | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+885A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270535 | |||||||
| chr6:37270683 | A | G | 30 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(27): Show |
30 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.113+1033A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270683 | |||||||
| chr6:37270703 | G | A | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+1053G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37270703 | |||||||
| chr6:37271021 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.113+1371T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271021 | |||||||
| chr6:37271346 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+1696C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271346 | |||||||
| chr6:37271494 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.113+1844A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271494 | |||||||
| chr6:37271525 | G | A | 47 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(44): Show |
48 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.113+1875G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271525 | |||||||
| chr6:37271623 | G | T | 1 | a0001c0002t0005g0097 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.113+1973G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271623 | |||||||
| chr6:37271641 | C | T | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.113+1991C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271641 | |||||||
| chr6:37271801 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.113+2151T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271801 | |||||||
| chr6:37271849 | CT | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.113+2219delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37271849 | ||||||
| chr6:37271869 | T | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0154 others(1): Show |
4 | HG02886.hp1 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+2219T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271869 | |||||||
| chr6:37271885 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.113+2235A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271885 | |||||||
| chr6:37271935 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113+2285C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37271935 | |||||||
| chr6:37272089 | A | T | 3 | a0001c0001t0001g0166 a0001c0001t0003g0115 a0001c0001t0003g0165 |
3 | NA18964.hp1 NA18984.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.113+2439A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37272089 | |||||||
| chr6:37272147 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.113+2497C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37272147 | |||||||
| chr6:37272364 | C | CT | 10 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0003g0135 others(7): Show |
10 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.113+2730dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37272364 | ||||||
| chr6:37272364 | CT | C | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+2730delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37272364 | ||||||
| chr6:37272380 | T | C | 3 | a0001c0002t0007g0100 a0001c0002t0007g0101 a0001c0002t0007g0102 |
3 | HG01433.hp2 NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.113+2730T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37272380 | |||||||
| chr6:37272482 | T | A | 1 | a0001c0003t0004g0019 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.113+2832T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37272482 | |||||||
| chr6:37272517 | G | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.113+2867G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37272517 | |||||||
| chr6:37272539 | C | T | 9 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.113+2889C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37272539 | |||||||
| chr6:37272723 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.113+3073C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37272723 | |||||||
| chr6:37273028 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.113+3378G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273028 | |||||||
| chr6:37273120 | G | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.113+3470G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273120 | |||||||
| chr6:37273176 | C | T | 1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.113+3526C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273176 | |||||||
| chr6:37273182 | G | C | 1 | a0001c0003t0004g0019 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.113+3532G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273182 | |||||||
| chr6:37273183 | C | A | 1 | a0001c0003t0004g0019 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.113+3533C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273183 | |||||||
| chr6:37273183 | CA | C | 19 | a0001c0001t0001g0155 a0001c0001t0001g0169 a0001c0001t0001g0184 others(16): Show |
19 | HG00642.hp1 HG01106.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.113+3555delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37273183 | ||||||
| chr6:37273183 | CAA | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
142 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.113+3554_113+3555d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37273183 | ||||||
| chr6:37273183 | CAAA | C | 8 | a0001c0002t0002g0089 a0001c0002t0003g0107 a0001c0002t0003g0108 others(5): Show |
8 | HG00323.hp2 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.113+3553_113+3555d others(5): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37273183 | ||||||
| chr6:37273183 | CAAAA | C | 12 | a0001c0004t0002g0045 a0001c0004t0002g0053 a0001c0004t0002g0054 others(9): Show |
12 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+3552_113+3555d others(6): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37273183 | ||||||
| chr6:37273191 | A | C | 1 | a0001c0003t0004g0019 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.113+3541A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273191 | |||||||
| chr6:37273200 | A | G | 2 | a0001c0002t0003g0038 a0001c0002t0004g0039 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.113+3550A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273200 | |||||||
| chr6:37273205 | A | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG01517.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.113+3555A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273205 | |||||||
| chr6:37273241 | G | A | 1 | a0001c0003t0004g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.113+3591G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273241 | |||||||
| chr6:37273470 | C | T | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.113+3820C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273470 | |||||||
| chr6:37273677 | G | A | 1 | a0001c0002t0002g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.113+4027G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273677 | |||||||
| chr6:37273785 | A | G | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.113+4135A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273785 | |||||||
| chr6:37273867 | A | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.113+4217A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37273867 | |||||||
| chr6:37274008 | A | G | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.113+4358A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37274008 | |||||||
| chr6:37274049 | A | G | 3 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | NA18961.hp1 NA18999.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.113+4399A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37274049 | |||||||
| chr6:37274113 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0116 others(14): Show |
18 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.113+4463C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37274113 | |||||||
| chr6:37274426 | G | T | 1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.113+4776G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37274426 | |||||||
| chr6:37274496 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.114-4808C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37274496 | |||||||
| chr6:37274596 | T | C | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.114-4708T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37274596 | |||||||
| chr6:37274967 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-4337G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37274967 | |||||||
| chr6:37274975 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-4329C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37274975 | |||||||
| chr6:37274977 | G | A | 42 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(39): Show |
43 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.114-4327G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37274977 | |||||||
| chr6:37275049 | T | TTAA | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.114-4239_114-4237d others(5): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37275049 | ||||||
| chr6:37275092 | A | G | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
169 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.114-4212A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275092 | |||||||
| chr6:37275165 | G | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.114-4139G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275165 | |||||||
| chr6:37275337 | A | AT | 12 | a0001c0002t0002g0086 a0001c0004t0002g0045 a0001c0004t0002g0052 others(9): Show |
12 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.114-3956dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37275337 | ||||||
| chr6:37275402 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.114-3902A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275402 | |||||||
| chr6:37275498 | T | C | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.114-3806T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275498 | |||||||
| chr6:37275563 | C | T | 2 | a0001c0004t0003g0046 a0001c0004t0003g0047 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.114-3741C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275563 | |||||||
| chr6:37275692 | T | A | 1 | a0001c0002t0002g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.114-3612T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275692 | |||||||
| chr6:37275705 | CTGGTGAG others(19): Show |
C | 1 | a0001c0001t0003g0210 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114-3597_114-3572d others(28): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37275705 | ||||||
| chr6:37275708 | G | A | 5 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0154 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-3596G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275708 | |||||||
| chr6:37275732 | T | A | 1 | a0001c0001t0003g0210 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114-3572T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275732 | |||||||
| chr6:37275776 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-3528A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275776 | |||||||
| chr6:37275815 | A | G | 2 | a0001c0002t0003g0038 a0001c0002t0004g0039 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.114-3489A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275815 | |||||||
| chr6:37275909 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.114-3395T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37275909 | |||||||
| chr6:37275966 | C | CTTTTTT | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-3328_114-3323d others(8): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37275966 | ||||||
| chr6:37275966 | CT | C | 12 | a0001c0002t0003g0038 a0001c0002t0003g0170 a0001c0002t0004g0039 others(9): Show |
12 | HG01243.hp1 HG01361.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-3323delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37275966 | ||||||
| chr6:37276004 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-3300A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276004 | |||||||
| chr6:37276113 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.114-3191C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276113 | |||||||
| chr6:37276292 | C | T | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-3012C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276292 | |||||||
| chr6:37276360 | G | A | 2 | a0001c0002t0003g0038 a0001c0002t0004g0039 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.114-2944G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276360 | |||||||
| chr6:37276487 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-2817G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276487 | |||||||
| chr6:37276528 | A | G | 16 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.114-2776A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276528 | |||||||
| chr6:37276705 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.114-2599C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276705 | |||||||
| chr6:37276795 | G | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.114-2509G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276795 | |||||||
| chr6:37276903 | AAT | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-2387_114-2386d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37276903 | ||||||
| chr6:37276905 | T | A | 4 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(1): Show |
4 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-2399T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276905 | |||||||
| chr6:37276922 | C | T | 3 | a0001c0002t0003g0068 a0001c0002t0003g0070 a0001c0002t0003g0071 |
3 | HG02970.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.114-2382C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276922 | |||||||
| chr6:37276923 | G | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.114-2381G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276923 | |||||||
| chr6:37276947 | C | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-2357C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276947 | |||||||
| chr6:37276948 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.114-2356G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37276948 | |||||||
| chr6:37277180 | AT | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-2122delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37277180 | ||||||
| chr6:37277214 | A | G | 1 | a0001c0002t0002g0085 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.114-2090A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37277214 | |||||||
| chr6:37277234 | C | T | 4 | a0001c0001t0001g0163 a0001c0001t0001g0183 a0001c0001t0002g0194 others(1): Show |
4 | HG00438.hp2 HG00609.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2070C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37277234 | |||||||
| chr6:37277280 | A | G | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.114-2024A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37277280 | |||||||
| chr6:37277463 | C | CT | 18 | a0001c0001t0001g0215 a0001c0004t0002g0045 a0001c0004t0002g0052 others(15): Show |
18 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.114-1824dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37277463 | ||||||
| chr6:37277658 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.114-1646G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37277658 | |||||||
| chr6:37277686 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-1618T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37277686 | |||||||
| chr6:37277780 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-1524T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37277780 | |||||||
| chr6:37277965 | C | CA | 18 | a0001c0002t0004g0039 a0001c0004t0002g0045 a0001c0004t0002g0052 others(15): Show |
18 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.114-1327dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37277965 | ||||||
| chr6:37278269 | A | G | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.114-1035A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37278269 | |||||||
| chr6:37278552 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.114-752G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37278552 | |||||||
| chr6:37278927 | T | C | 1 | a0001c0003t0004g0025 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.114-377T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37278927 | |||||||
| chr6:37278928 | C | CA | 35 | a0001c0002t0003g0038 a0001c0002t0003g0170 a0001c0002t0004g0039 others(32): Show |
35 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.114-364dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 37278928 | ||||||
| chr6:37279133 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114-171G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 2/12 | chr6 | 37279133 | |||||||
| chr6:37279724 | A | G | 24 | a0001c0003t0004g0008 a0001c0003t0004g0010 a0001c0003t0004g0011 others(21): Show |
24 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.421+113A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37279724 | |||||||
| chr6:37279853 | C | T | 3 | a0001c0002t0003g0068 a0001c0002t0003g0070 a0001c0002t0003g0071 |
3 | HG02970.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.421+242C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37279853 | |||||||
| chr6:37279934 | C | T | 1 | a0001c0001t0006g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+323C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37279934 | |||||||
| chr6:37279953 | G | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.421+342G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37279953 | |||||||
| chr6:37280197 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0211 |
2 | HG04228.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.421+586A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280197 | |||||||
| chr6:37280227 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.421+616T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280227 | |||||||
| chr6:37280334 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.421+723G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280334 | |||||||
| chr6:37280379 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.421+768T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280379 | |||||||
| chr6:37280647 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.421+1036G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280647 | |||||||
| chr6:37280675 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+1064C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280675 | |||||||
| chr6:37280676 | C | T | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.421+1065C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280676 | |||||||
| chr6:37280703 | G | C | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.421+1092G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280703 | |||||||
| chr6:37280811 | C | T | 1 | a0001c0001t0006g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421+1200C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280811 | |||||||
| chr6:37280812 | G | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421+1201G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280812 | |||||||
| chr6:37280904 | A | C | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.422-1281A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280904 | |||||||
| chr6:37280957 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.422-1228C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280957 | |||||||
| chr6:37280962 | C | T | 55 | a0001c0002t0003g0038 a0001c0002t0003g0107 a0001c0002t0003g0108 others(52): Show |
55 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.422-1223C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37280962 | |||||||
| chr6:37281202 | A | G | 2 | a0001c0004t0003g0046 a0001c0004t0003g0047 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.422-983A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281202 | |||||||
| chr6:37281257 | T | C | 7 | a0001c0002t0003g0170 a0001c0002t0006g0031 a0001c0002t0006g0032 others(4): Show |
7 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.422-928T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281257 | |||||||
| chr6:37281496 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.422-689C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281496 | |||||||
| chr6:37281575 | C | T | 6 | a0001c0002t0006g0031 a0001c0002t0006g0032 a0001c0002t0006g0033 others(3): Show |
6 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-610C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281575 | |||||||
| chr6:37281599 | G | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-586G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281599 | |||||||
| chr6:37281632 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.422-553T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281632 | |||||||
| chr6:37281719 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.422-466T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281719 | |||||||
| chr6:37281839 | G | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.422-346G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281839 | |||||||
| chr6:37281942 | G | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-243G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281942 | |||||||
| chr6:37281980 | A | T | 1 | a0001c0002t0016g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.422-205A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37281980 | |||||||
| chr6:37282104 | T | C | 1 | a0001c0003t0004g0020 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.422-81T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37282104 | |||||||
| chr6:37282137 | C | A | 24 | a0001c0003t0004g0008 a0001c0003t0004g0010 a0001c0003t0004g0011 others(21): Show |
24 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.422-48C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 3/12 | chr6 | 37282137 | |||||||
| chr6:37282707 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.602-175G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 4/12 | chr6 | 37282707 | |||||||
| chr6:37282755 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.602-127G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 4/12 | chr6 | 37282755 | |||||||
| chr6:37283034 | C | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.672+82C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283034 | |||||||
| chr6:37283284 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.672+332G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283284 | |||||||
| chr6:37283323 | A | C | 1 | a0001c0001t0001g0149 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.672+371A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283323 | |||||||
| chr6:37283351 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.672+399T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283351 | |||||||
| chr6:37283358 | G | C | 3 | a0001c0003t0004g0014 a0001c0003t0004g0017 a0001c0003t0004g0019 |
3 | NA18981.hp2 NA18992.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.672+406G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283358 | |||||||
| chr6:37283379 | G | C | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.672+427G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283379 | |||||||
| chr6:37283395 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.672+443G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283395 | |||||||
| chr6:37283672 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.673-664A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283672 | |||||||
| chr6:37283777 | C | T | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.673-559C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283777 | |||||||
| chr6:37283801 | G | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.673-535G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283801 | |||||||
| chr6:37283844 | G | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0195 |
2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.673-492G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283844 | |||||||
| chr6:37283903 | A | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.673-433A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283903 | |||||||
| chr6:37283967 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.673-369A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283967 | |||||||
| chr6:37283992 | C | T | 1 | a0001c0002t0003g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.673-344C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 5/12 | chr6 | 37283992 | |||||||
| chr6:37284531 | C | T | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.801+67C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37284531 | |||||||
| chr6:37284545 | G | C | 8 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(5): Show |
8 | HG02109.hp2 HG02559.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+81G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37284545 | |||||||
| chr6:37284563 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18612.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.801+99C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37284563 | |||||||
| chr6:37284709 | A | G | 4 | a0001c0002t0002g0066 a0001c0002t0002g0067 a0001c0002t0003g0107 others(1): Show |
4 | HG00733.hp2 HG01243.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.801+245A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37284709 | |||||||
| chr6:37284953 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.801+489G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37284953 | |||||||
| chr6:37285026 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.801+562A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285026 | |||||||
| chr6:37285031 | G | T | 8 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(5): Show |
8 | HG02109.hp2 HG02559.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+567G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285031 | |||||||
| chr6:37285057 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.801+593G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285057 | |||||||
| chr6:37285063 | A | G | 1 | a0001c0001t0001g0005 | 2 | HG02723.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.801+599A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285063 | |||||||
| chr6:37285160 | T | TCTG | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.801+712_801+714dup others(3): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285160 | ||||||
| chr6:37285181 | A | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
112 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.801+717A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285181 | |||||||
| chr6:37285315 | C | CT | 5 | a0001c0001t0001g0213 a0001c0002t0005g0006 a0001c0002t0006g0034 others(2): Show |
5 | HG01243.hp1 HG01517.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.801+878dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTT | 7 | a0001c0001t0001g0143 a0001c0001t0003g0165 a0001c0001t0006g0132 others(4): Show |
7 | HG01081.hp1 HG01099.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+877_801+878dup others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTTT | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.801+876_801+878dup others(3): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTTTT | 36 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0001g0149 others(33): Show |
36 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.801+875_801+878dup others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTTTTTTT others(11): Show |
1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.801+861_801+878dup others(18): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTTTTTTT others(17): Show |
2 | a0001c0004t0003g0046 a0001c0004t0003g0047 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.801+855_801+878dup others(24): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTTTTTTT others(18): Show |
2 | a0001c0004t0002g0058 a0001c0004t0002g0059 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.801+854_801+878dup others(25): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTTTTTTT others(19): Show |
3 | a0001c0004t0002g0053 a0001c0004t0002g0057 a0001c0004t0002g0061 |
3 | HG02145.hp2 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.801+853_801+878dup others(26): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTTTTTTT others(20): Show |
3 | a0001c0004t0002g0052 a0001c0004t0002g0054 a0001c0004t0002g0060 |
3 | HG02559.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.801+852_801+878dup others(27): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTTTTTTT others(21): Show |
2 | a0001c0004t0002g0045 a0001c0004t0002g0055 |
2 | HG02109.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.801+878_801+879ins others(28): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285315 | C | CTTTTTTT others(23): Show |
1 | a0001c0004t0002g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.801+878_801+879ins others(30): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37285315 | ||||||
| chr6:37285485 | C | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.801+1021C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285485 | |||||||
| chr6:37285498 | C | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.801+1034C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285498 | |||||||
| chr6:37285557 | A | G | 1 | a0001c0002t0017g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.801+1093A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285557 | |||||||
| chr6:37285583 | G | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.801+1119G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285583 | |||||||
| chr6:37285609 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.801+1145C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285609 | |||||||
| chr6:37285789 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802-1218T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285789 | |||||||
| chr6:37285794 | G | A | 2 | a0001c0004t0002g0045 a0001c0004t0002g0060 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.802-1213G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285794 | |||||||
| chr6:37285920 | C | T | 1 | a0001c0002t0003g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.802-1087C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285920 | |||||||
| chr6:37285970 | T | C | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.802-1037T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285970 | |||||||
| chr6:37285973 | C | T | 2 | a0001c0002t0003g0038 a0001c0002t0004g0039 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.802-1034C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37285973 | |||||||
| chr6:37286001 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.802-1006T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286001 | |||||||
| chr6:37286025 | T | A | 9 | a0001c0002t0003g0170 a0001c0002t0006g0031 a0001c0002t0006g0032 others(6): Show |
9 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.802-982T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286025 | |||||||
| chr6:37286196 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.802-811A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286196 | |||||||
| chr6:37286204 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.802-803T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286204 | |||||||
| chr6:37286214 | G | A | 3 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | NA18961.hp1 NA18999.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.802-793G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286214 | |||||||
| chr6:37286235 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.802-772A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286235 | |||||||
| chr6:37286273 | T | C | 1 | a0001c0002t0016g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.802-734T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286273 | |||||||
| chr6:37286321 | C | CT | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.802-674dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37286321 | ||||||
| chr6:37286335 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.802-672A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286335 | |||||||
| chr6:37286355 | G | T | 1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.802-652G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286355 | |||||||
| chr6:37286378 | C | T | 1 | a0001c0002t0005g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.802-629C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286378 | |||||||
| chr6:37286408 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.802-599C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286408 | |||||||
| chr6:37286464 | C | T | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.802-543C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286464 | |||||||
| chr6:37286633 | T | TA | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.802-365dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37286633 | ||||||
| chr6:37286755 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.802-252T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286755 | |||||||
| chr6:37286858 | C | T | 3 | a0001c0003t0004g0023 a0001c0003t0004g0028 a0001c0003t0015g0009 |
3 | HG00733.hp1 HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.802-149C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286858 | |||||||
| chr6:37286909 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.802-98A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | chr6 | 37286909 | |||||||
| chr6:37286944 | C | CAAAA | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.802-59_802-56dupAA others(2): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37286944 | ||||||
| chr6:37286958 | C | CAAAACA | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.802-45_802-44insCA others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 37286958 | ||||||
| chr6:37287110 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+38C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287110 | |||||||
| chr6:37287171 | A | T | 3 | a0001c0002t0005g0094 a0001c0002t0005g0095 a0001c0002t0005g0098 |
3 | HG01358.hp2 HG02683.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.867+99A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287171 | |||||||
| chr6:37287209 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | HG01070.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.867+137A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287209 | |||||||
| chr6:37287214 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.867+142T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287214 | |||||||
| chr6:37287549 | C | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+477C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287549 | |||||||
| chr6:37287557 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+485T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287557 | |||||||
| chr6:37287595 | C | T | 52 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(49): Show |
53 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.867+523C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287595 | |||||||
| chr6:37287652 | A | G | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.867+580A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287652 | |||||||
| chr6:37287724 | G | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.867+652G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287724 | |||||||
| chr6:37287900 | G | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+828G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37287900 | |||||||
| chr6:37288026 | A | G | 1 | a0001c0002t0002g0041 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.867+954A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288026 | |||||||
| chr6:37288048 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+976C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288048 | |||||||
| chr6:37288080 | A | C | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+1008A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288080 | |||||||
| chr6:37288183 | C | A | 1 | a0001c0001t0006g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.867+1111C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288183 | |||||||
| chr6:37288184 | C | A | 1 | a0001c0001t0006g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.867+1112C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288184 | |||||||
| chr6:37288371 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+1299T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288371 | |||||||
| chr6:37288440 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+1368A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288440 | |||||||
| chr6:37288504 | G | A | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.867+1432G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288504 | |||||||
| chr6:37288589 | G | T | 2 | a0001c0001t0003g0140 a0001c0001t0006g0132 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.867+1517G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288589 | |||||||
| chr6:37288717 | G | C | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.867+1645G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288717 | |||||||
| chr6:37288741 | C | CA | 6 | a0001c0001t0001g0162 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): Show |
6 | HG01175.hp1 HG01175.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.867+1686dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 37288741 | ||||||
| chr6:37288869 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.867+1797C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288869 | |||||||
| chr6:37288883 | A | G | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.867+1811A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288883 | |||||||
| chr6:37288981 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.867+1909C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37288981 | |||||||
| chr6:37289073 | T | G | 7 | a0001c0001t0001g0166 a0001c0001t0001g0172 a0001c0001t0003g0115 others(4): Show |
7 | HG02280.hp2 HG03831.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.867+2001T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289073 | |||||||
| chr6:37289153 | C | G | 1 | a0001c0002t0002g0084 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.867+2081C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289153 | |||||||
| chr6:37289354 | T | A | 11 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.868-1889T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289354 | |||||||
| chr6:37289382 | C | T | 1 | a0001c0002t0003g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.868-1861C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289382 | |||||||
| chr6:37289450 | C | G | 3 | a0001c0003t0004g0015 a0001c0003t0004g0016 a0001c0003t0004g0027 |
3 | NA18955.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.868-1793C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289450 | |||||||
| chr6:37289452 | A | G | 1 | a0001c0002t0002g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.868-1791A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289452 | |||||||
| chr6:37289471 | T | G | 4 | a0001c0001t0001g0163 a0001c0001t0001g0183 a0001c0001t0002g0194 others(1): Show |
4 | HG00438.hp2 HG00609.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-1772T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289471 | |||||||
| chr6:37289561 | C | G | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.868-1682C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289561 | |||||||
| chr6:37289583 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.868-1660C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289583 | |||||||
| chr6:37289866 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.868-1377G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289866 | |||||||
| chr6:37289912 | T | A | 7 | a0001c0002t0003g0170 a0001c0002t0006g0031 a0001c0002t0006g0032 others(4): Show |
7 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.868-1331T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37289912 | |||||||
| chr6:37290011 | C | T | 52 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(49): Show |
53 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.868-1232C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37290011 | |||||||
| chr6:37290037 | G | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.868-1206G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37290037 | |||||||
| chr6:37290413 | G | T | 6 | a0001c0002t0002g0076 a0001c0002t0002g0082 a0001c0002t0002g0084 others(3): Show |
6 | HG00735.hp2 HG01257.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.868-830G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37290413 | |||||||
| chr6:37290825 | G | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.868-418G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37290825 | |||||||
| chr6:37290828 | C | CA | 20 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0002t0003g0038 others(17): Show |
20 | HG01070.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.868-402dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 37290828 | ||||||
| chr6:37290828 | CA | C | 8 | a0001c0001t0001g0191 a0001c0002t0005g0092 a0001c0002t0005g0093 others(5): Show |
8 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.868-402delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 37290828 | ||||||
| chr6:37290889 | G | C | 1 | a0001c0002t0003g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.868-354G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37290889 | |||||||
| chr6:37291195 | T | C | 1 | a0001c0002t0002g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.868-48T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 7/12 | chr6 | 37291195 | |||||||
| chr6:37291393 | G | A | 3 | a0001c0002t0003g0068 a0001c0002t0003g0070 a0001c0002t0003g0071 |
3 | HG02970.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.982+36G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37291393 | |||||||
| chr6:37291395 | T | C | 1 | a0001c0003t0004g0035 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.982+38T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37291395 | |||||||
| chr6:37291519 | C | T | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.982+162C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37291519 | |||||||
| chr6:37291703 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+346A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37291703 | |||||||
| chr6:37291827 | C | T | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982+470C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37291827 | |||||||
| chr6:37291917 | G | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+560G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37291917 | |||||||
| chr6:37291929 | G | A | 1 | a0001c0002t0002g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.982+572G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37291929 | |||||||
| chr6:37292020 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+663C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37292020 | |||||||
| chr6:37292248 | G | GT | 47 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(44): Show |
48 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.982+896dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37292248 | ||||||
| chr6:37292372 | G | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982+1015G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37292372 | |||||||
| chr6:37292413 | C | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.982+1056C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37292413 | |||||||
| chr6:37292925 | T | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.982+1568T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37292925 | |||||||
| chr6:37293062 | C | CATT | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.982+1727_982+1729d others(5): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37293062 | ||||||
| chr6:37293077 | TA | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+1721delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293077 | |||||||
| chr6:37293078 | A | T | 1 | a0001c0002t0006g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.982+1721A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293078 | |||||||
| chr6:37293081 | A | T | 16 | a0001c0001t0001g0122 a0001c0001t0001g0156 a0001c0001t0001g0168 others(13): Show |
16 | HG01243.hp1 HG01361.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.982+1724A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293081 | |||||||
| chr6:37293084 | A | T | 71 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0134 others(68): Show |
72 | HG00438.hp2 HG00609.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.982+1727A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293084 | |||||||
| chr6:37293087 | T | A | 1 | a0001c0002t0005g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.982+1730T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293087 | |||||||
| chr6:37293164 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+1807G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293164 | |||||||
| chr6:37293171 | G | A | 6 | a0001c0002t0006g0031 a0001c0002t0006g0032 a0001c0002t0006g0033 others(3): Show |
6 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+1814G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293171 | |||||||
| chr6:37293220 | G | A | 47 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(44): Show |
48 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.982+1863G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293220 | |||||||
| chr6:37293239 | G | A | 2 | a0001c0002t0002g0040 a0001c0002t0013g0044 |
2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.982+1882G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293239 | |||||||
| chr6:37293313 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0154 |
3 | HG03225.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.982+1956G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293313 | |||||||
| chr6:37293319 | C | T | 2 | a0001c0004t0002g0052 a0001c0004t0002g0054 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.982+1962C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293319 | |||||||
| chr6:37293603 | A | G | 3 | a0001c0001t0008g0002 a0001c0001t0008g0127 a0001c0001t0008g0129 |
4 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+2246A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293603 | |||||||
| chr6:37293620 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.982+2263G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293620 | |||||||
| chr6:37293621 | G | C | 1 | a0001c0001t0006g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.982+2264G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293621 | |||||||
| chr6:37293988 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+2631G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37293988 | |||||||
| chr6:37294025 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+2668A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37294025 | |||||||
| chr6:37294123 | G | A | 3 | a0001c0004t0003g0048 a0001c0004t0003g0049 a0001c0004t0003g0050 |
3 | HG01884.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.982+2766G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37294123 | |||||||
| chr6:37294202 | T | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0189 |
2 | HG01261.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.982+2845T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37294202 | |||||||
| chr6:37294271 | A | C | 3 | a0001c0004t0003g0048 a0001c0004t0003g0049 a0001c0004t0003g0050 |
3 | HG01884.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.982+2914A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37294271 | |||||||
| chr6:37294280 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.982+2923C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37294280 | |||||||
| chr6:37294288 | T | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.982+2931T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37294288 | |||||||
| chr6:37294796 | T | C | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982+3439T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37294796 | |||||||
| chr6:37294862 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.982+3505G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37294862 | |||||||
| chr6:37295128 | G | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982+3771G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37295128 | |||||||
| chr6:37295253 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.982+3896C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37295253 | |||||||
| chr6:37295298 | T | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+3941T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37295298 | |||||||
| chr6:37295394 | C | A | 1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.982+4037C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37295394 | |||||||
| chr6:37295564 | G | A | 193 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.982+4207G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37295564 | |||||||
| chr6:37295712 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.982+4355C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37295712 | |||||||
| chr6:37295743 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+4386C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37295743 | |||||||
| chr6:37295869 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+4512A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37295869 | |||||||
| chr6:37296065 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.982+4708G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296065 | |||||||
| chr6:37296233 | G | A | 52 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(49): Show |
53 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.982+4876G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296233 | |||||||
| chr6:37296289 | GTAT | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+4937_982+4939d others(5): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37296289 | ||||||
| chr6:37296302 | GTTGA | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+4956_982+4959d others(6): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37296302 | ||||||
| chr6:37296440 | G | C | 1 | a0001c0001t0003g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.982+5083G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296440 | |||||||
| chr6:37296485 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.982+5128A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296485 | |||||||
| chr6:37296542 | T | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+5185T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296542 | |||||||
| chr6:37296560 | G | A | 1 | a0001c0001t0003g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.982+5203G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296560 | |||||||
| chr6:37296634 | C | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0195 |
2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.982+5277C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296634 | |||||||
| chr6:37296635 | C | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0195 |
2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.982+5278C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296635 | |||||||
| chr6:37296658 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+5301C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296658 | |||||||
| chr6:37296772 | A | G | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.982+5415A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296772 | |||||||
| chr6:37296813 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+5456T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296813 | |||||||
| chr6:37296836 | G | GT | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+5489dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37296836 | ||||||
| chr6:37296836 | GT | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.982+5489delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37296836 | ||||||
| chr6:37296838 | T | G | 3 | a0001c0001t0008g0002 a0001c0001t0008g0127 a0001c0001t0008g0129 |
4 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+5481T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296838 | |||||||
| chr6:37296866 | G | A | 2 | a0001c0004t0003g0046 a0001c0004t0003g0047 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.982+5509G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296866 | |||||||
| chr6:37296876 | G | A | 1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.982+5519G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296876 | |||||||
| chr6:37296951 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+5594C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37296951 | |||||||
| chr6:37297067 | T | A | 2 | a0001c0004t0003g0046 a0001c0004t0003g0047 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.982+5710T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297067 | |||||||
| chr6:37297112 | C | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+5755C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297112 | |||||||
| chr6:37297178 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.982+5821A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297178 | |||||||
| chr6:37297215 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.982+5858G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297215 | |||||||
| chr6:37297304 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+5947C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297304 | |||||||
| chr6:37297502 | G | C | 1 | a0001c0002t0016g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.982+6145G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297502 | |||||||
| chr6:37297608 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.982+6251A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297608 | |||||||
| chr6:37297674 | A | T | 11 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(8): Show |
11 | HG02080.hp2 HG02165.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.982+6317A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297674 | |||||||
| chr6:37297712 | A | T | 1 | a0001c0001t0011g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.982+6355A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297712 | |||||||
| chr6:37297834 | A | G | 16 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.982+6477A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297834 | |||||||
| chr6:37297983 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.982+6626G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37297983 | |||||||
| chr6:37298159 | G | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.982+6802G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298159 | |||||||
| chr6:37298367 | T | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.982+7010T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298367 | |||||||
| chr6:37298482 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+7125C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298482 | |||||||
| chr6:37298539 | G | GTT | 6 | a0001c0002t0006g0031 a0001c0002t0006g0032 a0001c0002t0006g0033 others(3): Show |
6 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+7205_982+7206d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37298539 | ||||||
| chr6:37298539 | G | GTTTTGTT others(4): Show |
2 | a0001c0004t0002g0057 a0001c0004t0002g0061 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.982+7186_982+7187i others(13): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37298539 | ||||||
| chr6:37298539 | G | GTTTTTTT others(5): Show |
5 | a0001c0004t0002g0045 a0001c0004t0002g0053 a0001c0004t0002g0054 others(2): Show |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.982+7195_982+7206d others(14): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37298539 | ||||||
| chr6:37298539 | G | GTTTTTTT others(6): Show |
4 | a0001c0004t0002g0052 a0001c0004t0002g0055 a0001c0004t0002g0059 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+7194_982+7206d others(15): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37298539 | ||||||
| chr6:37298539 | G | GTTTTTTT others(7): Show |
4 | a0001c0004t0002g0056 a0001c0004t0003g0046 a0001c0004t0003g0049 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+7193_982+7206d others(16): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37298539 | ||||||
| chr6:37298539 | G | GTTTTTTT others(8): Show |
1 | a0001c0004t0003g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.982+7192_982+7206d others(17): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37298539 | ||||||
| chr6:37298539 | G | GTTTTTTT others(16): Show |
1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.982+7184_982+7206d others(25): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37298539 | ||||||
| chr6:37298539 | GT | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
109 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.982+7206delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37298539 | ||||||
| chr6:37298539 | GTT | G | 43 | a0001c0001t0001g0141 a0001c0001t0001g0161 a0001c0001t0003g0210 others(40): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.982+7205_982+7206d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37298539 | ||||||
| chr6:37298548 | T | G | 1 | a0001c0004t0002g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.982+7191T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298548 | |||||||
| chr6:37298569 | G | A | 7 | a0001c0002t0003g0170 a0001c0002t0006g0031 a0001c0002t0006g0032 others(4): Show |
7 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.982+7212G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298569 | |||||||
| chr6:37298572 | G | A | 2 | a0001c0004t0003g0048 a0001c0004t0003g0050 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.982+7215G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298572 | |||||||
| chr6:37298616 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.982+7259G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298616 | |||||||
| chr6:37298639 | G | A | 1 | a0001c0001t0011g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.982+7282G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298639 | |||||||
| chr6:37298670 | C | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982+7313C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298670 | |||||||
| chr6:37298695 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.982+7338G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298695 | |||||||
| chr6:37298735 | C | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.982+7378C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298735 | |||||||
| chr6:37298773 | C | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982+7416C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298773 | |||||||
| chr6:37298783 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.982+7426G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298783 | |||||||
| chr6:37298796 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+7439C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298796 | |||||||
| chr6:37298806 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+7449G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298806 | |||||||
| chr6:37298840 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+7483T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298840 | |||||||
| chr6:37298902 | A | G | 6 | a0001c0002t0006g0031 a0001c0002t0006g0032 a0001c0002t0006g0033 others(3): Show |
6 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+7545A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37298902 | |||||||
| chr6:37299032 | C | T | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.982+7675C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37299032 | |||||||
| chr6:37299124 | G | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+7767G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37299124 | |||||||
| chr6:37299179 | A | G | 16 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.982+7822A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37299179 | |||||||
| chr6:37299180 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.982+7823T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37299180 | |||||||
| chr6:37299377 | T | G | 4 | a0001c0001t0003g0118 a0001c0002t0003g0038 a0001c0004t0003g0048 others(1): Show |
4 | HG01255.hp1 HG02055.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+8020T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37299377 | |||||||
| chr6:37299519 | T | C | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982+8162T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37299519 | |||||||
| chr6:37299598 | A | C | 2 | a0001c0004t0002g0057 a0001c0004t0002g0061 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.982+8241A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37299598 | |||||||
| chr6:37299924 | G | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.982+8567G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37299924 | |||||||
| chr6:37300006 | C | CA | 6 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0003g0118 others(3): Show |
6 | HG01255.hp1 HG01261.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+8668dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37300006 | ||||||
| chr6:37300006 | C | CAA | 15 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(12): Show |
15 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.982+8667_982+8668d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37300006 | ||||||
| chr6:37300006 | CA | C | 6 | a0001c0001t0001g0116 a0001c0002t0002g0040 a0001c0002t0002g0041 others(3): Show |
6 | HG00741.hp1 HG01168.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.982+8668delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37300006 | ||||||
| chr6:37300036 | A | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.982+8679A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300036 | |||||||
| chr6:37300046 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.982+8689G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300046 | |||||||
| chr6:37300205 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982+8848C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300205 | |||||||
| chr6:37300337 | G | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0209 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.982+8980G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300337 | |||||||
| chr6:37300363 | A | T | 1 | a0001c0001t0001g0204 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.982+9006A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300363 | |||||||
| chr6:37300503 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.982+9146A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300503 | |||||||
| chr6:37300553 | G | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18612.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.982+9196G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300553 | |||||||
| chr6:37300601 | C | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.982+9244C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300601 | |||||||
| chr6:37300612 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+9255T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300612 | |||||||
| chr6:37300630 | G | A | 7 | a0001c0002t0005g0092 a0001c0002t0005g0093 a0001c0002t0005g0094 others(4): Show |
7 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+9273G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300630 | |||||||
| chr6:37300645 | A | G | 1 | a0001c0001t0009g0212 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.982+9288A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300645 | |||||||
| chr6:37300692 | A | T | 2 | a0001c0004t0003g0046 a0001c0004t0003g0047 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.982+9335A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300692 | |||||||
| chr6:37300855 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+9498G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300855 | |||||||
| chr6:37300873 | G | A | 7 | a0001c0002t0005g0092 a0001c0002t0005g0093 a0001c0002t0005g0094 others(4): Show |
7 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+9516G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300873 | |||||||
| chr6:37300888 | A | G | 1 | a0001c0001t0006g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.982+9531A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300888 | |||||||
| chr6:37300982 | CT | C | 6 | a0001c0001t0003g0118 a0001c0002t0003g0038 a0001c0002t0003g0107 others(3): Show |
6 | HG01255.hp1 HG02630.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+9626delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37300982 | |||||||
| chr6:37301039 | C | T | 1 | a0001c0002t0003g0107 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.982+9682C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301039 | |||||||
| chr6:37301176 | C | A | 1 | a0001c0004t0003g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.982+9819C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301176 | |||||||
| chr6:37301258 | G | A | 11 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.982+9901G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301258 | |||||||
| chr6:37301265 | A | G | 1 | a0001c0001t0003g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.982+9908A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301265 | |||||||
| chr6:37301276 | T | G | 1 | a0001c0001t0003g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.982+9919T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301276 | |||||||
| chr6:37301410 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.982+10053C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301410 | |||||||
| chr6:37301412 | T | C | 1 | a0001c0002t0002g0080 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.982+10055T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301412 | |||||||
| chr6:37301788 | G | A | 19 | a0001c0002t0003g0107 a0001c0002t0003g0108 a0001c0004t0002g0045 others(16): Show |
19 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.982+10431G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301788 | |||||||
| chr6:37301844 | A | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0147 a0001c0001t0001g0150 |
3 | HG01074.hp2 HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.982+10487A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301844 | |||||||
| chr6:37301903 | C | T | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.982+10546C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301903 | |||||||
| chr6:37301927 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.982+10570C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301927 | |||||||
| chr6:37301965 | T | C | 16 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.982+10608T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37301965 | |||||||
| chr6:37302326 | A | T | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.983-10592A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37302326 | |||||||
| chr6:37302593 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-10325G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37302593 | |||||||
| chr6:37302747 | A | G | 1 | a0001c0003t0004g0022 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.983-10171A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37302747 | |||||||
| chr6:37302929 | G | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-9989G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37302929 | |||||||
| chr6:37302980 | A | G | 16 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.983-9938A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37302980 | |||||||
| chr6:37303114 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-9804T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37303114 | |||||||
| chr6:37303128 | G | T | 1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.983-9790G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37303128 | |||||||
| chr6:37303255 | G | C | 4 | a0001c0001t0003g0118 a0001c0002t0003g0038 a0001c0004t0003g0048 others(1): Show |
4 | HG01255.hp1 HG02055.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-9663G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37303255 | |||||||
| chr6:37303446 | T | G | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.983-9472T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37303446 | |||||||
| chr6:37303522 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-9396G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37303522 | |||||||
| chr6:37303770 | G | A | 4 | a0001c0002t0003g0107 a0001c0002t0003g0108 a0001c0002t0016g0062 others(1): Show |
4 | HG02630.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-9148G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37303770 | |||||||
| chr6:37303830 | G | A | 3 | a0001c0004t0003g0048 a0001c0004t0003g0049 a0001c0004t0003g0050 |
3 | HG01884.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.983-9088G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37303830 | |||||||
| chr6:37303945 | G | A | 1 | a0001c0002t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.983-8973G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37303945 | |||||||
| chr6:37304129 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-8789T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304129 | |||||||
| chr6:37304161 | T | C | 4 | a0001c0002t0003g0107 a0001c0002t0003g0108 a0001c0002t0016g0062 others(1): Show |
4 | HG02630.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-8757T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304161 | |||||||
| chr6:37304235 | C | G | 1 | a0001c0002t0017g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.983-8683C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304235 | |||||||
| chr6:37304387 | C | T | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.983-8531C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304387 | |||||||
| chr6:37304454 | C | T | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.983-8464C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304454 | |||||||
| chr6:37304509 | G | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-8409G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304509 | |||||||
| chr6:37304592 | G | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.983-8326G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304592 | |||||||
| chr6:37304804 | T | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-8114T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304804 | |||||||
| chr6:37304846 | A | G | 1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.983-8072A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304846 | |||||||
| chr6:37304988 | T | C | 2 | a0001c0001t0003g0140 a0001c0001t0006g0132 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.983-7930T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37304988 | |||||||
| chr6:37305048 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-7870A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305048 | |||||||
| chr6:37305084 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.983-7834G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305084 | |||||||
| chr6:37305259 | C | T | 3 | a0001c0002t0007g0100 a0001c0002t0007g0101 a0001c0002t0007g0102 |
3 | HG01433.hp2 NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.983-7659C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305259 | |||||||
| chr6:37305346 | C | T | 3 | a0001c0004t0003g0048 a0001c0004t0003g0049 a0001c0004t0003g0050 |
3 | HG01884.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.983-7572C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305346 | |||||||
| chr6:37305379 | T | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.983-7539T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305379 | |||||||
| chr6:37305397 | C | T | 1 | a0001c0004t0002g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.983-7521C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305397 | |||||||
| chr6:37305523 | C | CT | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.983-7383dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37305523 | ||||||
| chr6:37305523 | C | CTT | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0141 others(11): Show |
14 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.983-7384_983-7383d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37305523 | ||||||
| chr6:37305523 | CT | C | 19 | a0001c0001t0003g0118 a0001c0002t0003g0038 a0001c0004t0002g0045 others(16): Show |
19 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.983-7383delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37305523 | ||||||
| chr6:37305541 | G | A | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.983-7377G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305541 | |||||||
| chr6:37305542 | G | A | 3 | a0001c0002t0003g0068 a0001c0002t0003g0070 a0001c0002t0003g0071 |
3 | HG02970.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.983-7376G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305542 | |||||||
| chr6:37305579 | G | A | 1 | a0001c0001t0003g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.983-7339G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305579 | |||||||
| chr6:37305686 | A | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-7232A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305686 | |||||||
| chr6:37305755 | C | T | 7 | a0001c0002t0003g0170 a0001c0002t0006g0031 a0001c0002t0006g0032 others(4): Show |
7 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.983-7163C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305755 | |||||||
| chr6:37305771 | C | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.983-7147C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305771 | |||||||
| chr6:37305802 | C | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.983-7116C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305802 | |||||||
| chr6:37305815 | C | T | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.983-7103C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305815 | |||||||
| chr6:37305816 | G | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.983-7102G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305816 | |||||||
| chr6:37305816 | G | C | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.983-7102G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37305816 | |||||||
| chr6:37306034 | G | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-6884G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306034 | |||||||
| chr6:37306126 | G | A | 1 | a0001c0001t0007g0179 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.983-6792G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306126 | |||||||
| chr6:37306179 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-6739T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306179 | |||||||
| chr6:37306335 | G | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.983-6583G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306335 | |||||||
| chr6:37306386 | G | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-6532G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306386 | |||||||
| chr6:37306416 | C | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.983-6502C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306416 | |||||||
| chr6:37306478 | A | G | 3 | a0001c0002t0003g0068 a0001c0002t0003g0070 a0001c0002t0003g0071 |
3 | HG02970.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.983-6440A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306478 | |||||||
| chr6:37306681 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.983-6237G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306681 | |||||||
| chr6:37306808 | G | A | 7 | a0001c0002t0003g0170 a0001c0002t0006g0031 a0001c0002t0006g0032 others(4): Show |
7 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.983-6110G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306808 | |||||||
| chr6:37306873 | A | G | 1 | a0001c0002t0003g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.983-6045A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306873 | |||||||
| chr6:37306909 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-6009C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306909 | |||||||
| chr6:37306929 | T | G | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.983-5989T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37306929 | |||||||
| chr6:37307105 | C | A | 1 | a0001c0001t0003g0210 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.983-5813C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307105 | |||||||
| chr6:37307153 | C | T | 1 | a0001c0001t0018g0117 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.983-5765C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307153 | |||||||
| chr6:37307219 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-5699A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307219 | |||||||
| chr6:37307273 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-5645G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307273 | |||||||
| chr6:37307357 | CTT | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-5549_983-5548d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37307357 | ||||||
| chr6:37307375 | C | T | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.983-5543C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307375 | |||||||
| chr6:37307388 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-5530C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307388 | |||||||
| chr6:37307434 | C | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.983-5484C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307434 | |||||||
| chr6:37307546 | G | A | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.983-5372G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307546 | |||||||
| chr6:37307638 | G | T | 52 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(49): Show |
53 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.983-5280G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307638 | |||||||
| chr6:37307721 | C | T | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.983-5197C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307721 | |||||||
| chr6:37307723 | A | G | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-5195A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307723 | |||||||
| chr6:37307878 | A | G | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.983-5040A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37307878 | |||||||
| chr6:37308085 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.983-4833G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37308085 | |||||||
| chr6:37308359 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.983-4559A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37308359 | |||||||
| chr6:37308367 | T | C | 3 | a0001c0004t0003g0048 a0001c0004t0003g0049 a0001c0004t0003g0050 |
3 | HG01884.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.983-4551T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37308367 | |||||||
| chr6:37308563 | T | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.983-4355T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37308563 | |||||||
| chr6:37308669 | T | C | 1 | a0001c0002t0002g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.983-4249T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37308669 | |||||||
| chr6:37308880 | TG | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-4035delG | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37308880 | ||||||
| chr6:37308944 | TA | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.983-3957delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37308944 | ||||||
| chr6:37308944 | TAA | T | 7 | a0001c0001t0001g0175 a0001c0001t0008g0127 a0001c0002t0002g0089 others(4): Show |
7 | HG00323.hp2 HG02451.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.983-3958_983-3957d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37308944 | ||||||
| chr6:37308981 | AT | A | 52 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(49): Show |
53 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.983-3936delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37308981 | |||||||
| chr6:37309047 | G | T | 1 | a0001c0003t0004g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.983-3871G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37309047 | |||||||
| chr6:37309142 | C | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.983-3776C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37309142 | |||||||
| chr6:37309187 | T | C | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.983-3731T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37309187 | |||||||
| chr6:37309191 | CAA | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0154 |
3 | HG03225.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.983-3725_983-3724d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37309191 | ||||||
| chr6:37309370 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.983-3548A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37309370 | |||||||
| chr6:37309529 | C | T | 1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.983-3389C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37309529 | |||||||
| chr6:37309847 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.983-3071G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37309847 | |||||||
| chr6:37309897 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-3021C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37309897 | |||||||
| chr6:37310266 | TAA | T | 3 | a0001c0004t0003g0048 a0001c0004t0003g0049 a0001c0004t0003g0050 |
3 | HG01884.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.983-2651_983-2650d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37310266 | |||||||
| chr6:37310387 | G | A | 6 | a0001c0002t0006g0031 a0001c0002t0006g0032 a0001c0002t0006g0033 others(3): Show |
6 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-2531G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37310387 | |||||||
| chr6:37310463 | G | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-2455G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37310463 | |||||||
| chr6:37310623 | G | A | 2 | a0001c0001t0003g0140 a0001c0001t0006g0132 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.983-2295G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37310623 | |||||||
| chr6:37310868 | A | G | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.983-2050A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37310868 | |||||||
| chr6:37310915 | G | A | 3 | a0001c0004t0003g0048 a0001c0004t0003g0049 a0001c0004t0003g0050 |
3 | HG01884.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.983-2003G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37310915 | |||||||
| chr6:37310975 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-1943T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37310975 | |||||||
| chr6:37311157 | T | C | 52 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0001g0088 others(49): Show |
53 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.983-1761T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37311157 | |||||||
| chr6:37311183 | AT | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.983-1722delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 37311183 | ||||||
| chr6:37311254 | G | T | 4 | a0001c0002t0003g0107 a0001c0002t0003g0108 a0001c0002t0016g0062 others(1): Show |
4 | HG02630.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-1664G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37311254 | |||||||
| chr6:37311315 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.983-1603G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37311315 | |||||||
| chr6:37311534 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-1384G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37311534 | |||||||
| chr6:37311619 | G | A | 4 | a0001c0002t0003g0107 a0001c0002t0003g0108 a0001c0002t0016g0062 others(1): Show |
4 | HG02630.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-1299G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37311619 | |||||||
| chr6:37311627 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-1291C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37311627 | |||||||
| chr6:37311717 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-1201T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37311717 | |||||||
| chr6:37311787 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.983-1131G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37311787 | |||||||
| chr6:37312032 | C | T | 1 | a0001c0001t0006g0171 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.983-886C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37312032 | |||||||
| chr6:37312851 | C | T | 1 | a0001c0002t0003g0107 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.983-67C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 8/12 | chr6 | 37312851 | |||||||
| chr6:37313068 | A | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1089+44A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 9/12 | chr6 | 37313068 | |||||||
| chr6:37313211 | C | CG | 6 | a0001c0001t0003g0118 a0001c0002t0003g0038 a0001c0002t0003g0107 others(3): Show |
6 | HG01255.hp1 HG02630.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1089+190dupG | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 37313211 | ||||||
| chr6:37313489 | CA | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1090-313delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 37313489 | ||||||
| chr6:37313550 | A | G | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1090-266A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 9/12 | chr6 | 37313550 | |||||||
| chr6:37313559 | T | G | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1090-257T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 9/12 | chr6 | 37313559 | |||||||
| chr6:37313640 | T | C | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1090-176T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 9/12 | chr6 | 37313640 | |||||||
| chr6:37314029 | C | T | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1165+138C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314029 | |||||||
| chr6:37314043 | A | C | 2 | a0001c0004t0003g0046 a0001c0004t0003g0047 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1165+152A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314043 | |||||||
| chr6:37314058 | T | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1165+167T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314058 | |||||||
| chr6:37314147 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1165+256T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314147 | |||||||
| chr6:37314158 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1165+267C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314158 | |||||||
| chr6:37314167 | C | T | 2 | a0001c0002t0002g0069 a0001c0002t0002g0073 |
2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1165+276C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314167 | |||||||
| chr6:37314222 | T | C | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1165+331T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314222 | |||||||
| chr6:37314240 | T | C | 1 | a0001c0003t0004g0024 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1165+349T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314240 | |||||||
| chr6:37314249 | C | T | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1165+358C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314249 | |||||||
| chr6:37314344 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1165+453C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314344 | |||||||
| chr6:37314423 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1165+532C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314423 | |||||||
| chr6:37314482 | G | A | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1165+591G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314482 | |||||||
| chr6:37314765 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1165+874T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314765 | |||||||
| chr6:37314826 | T | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG01517.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1165+935T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314826 | |||||||
| chr6:37314880 | G | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1165+989G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314880 | |||||||
| chr6:37314933 | AC | A | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1165+1043delC | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37314933 | |||||||
| chr6:37315100 | A | G | 5 | a0001c0001t0001g0122 a0001c0001t0001g0156 a0001c0001t0001g0168 others(2): Show |
5 | HG02622.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165+1209A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37315100 | |||||||
| chr6:37315171 | A | G | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165+1280A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37315171 | |||||||
| chr6:37315574 | C | T | 1 | a0001c0001t0003g0210 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1166-1129C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37315574 | |||||||
| chr6:37315733 | G | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1166-970G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37315733 | |||||||
| chr6:37315782 | C | G | 6 | a0001c0001t0001g0112 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG00323.hp1 HG02165.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.1166-921C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37315782 | |||||||
| chr6:37315786 | G | T | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1166-917G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37315786 | |||||||
| chr6:37315904 | G | T | 7 | a0001c0002t0003g0170 a0001c0002t0006g0031 a0001c0002t0006g0032 others(4): Show |
7 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1166-799G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37315904 | |||||||
| chr6:37315992 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1166-711G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37315992 | |||||||
| chr6:37316462 | C | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1166-241C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37316462 | |||||||
| chr6:37316501 | C | G | 16 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1166-202C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37316501 | |||||||
| chr6:37316572 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1166-131C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37316572 | |||||||
| chr6:37316674 | T | C | 1 | a0001c0002t0006g0032 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1166-29T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 10/12 | chr6 | 37316674 | |||||||
| chr6:37316961 | T | C | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1293+131T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 11/12 | chr6 | 37316961 | |||||||
| chr6:37317236 | G | A | 1 | a0001c0001t0007g0198 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1389+30G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37317236 | |||||||
| chr6:37317557 | C | G | 7 | a0001c0002t0003g0170 a0001c0002t0006g0031 a0001c0002t0006g0032 others(4): Show |
7 | HG01243.hp1 HG01361.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+351C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37317557 | |||||||
| chr6:37317569 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1389+363G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37317569 | |||||||
| chr6:37317589 | A | G | 1 | a0001c0002t0002g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1389+383A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37317589 | |||||||
| chr6:37317724 | C | T | 1 | a0001c0002t0016g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1389+518C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37317724 | |||||||
| chr6:37318535 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1389+1329G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37318535 | |||||||
| chr6:37318685 | G | T | 1 | a0001c0002t0006g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1389+1479G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37318685 | |||||||
| chr6:37318686 | C | T | 1 | a0001c0002t0006g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1389+1480C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37318686 | |||||||
| chr6:37318856 | G | A | 1 | a0001c0001t0006g0171 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1389+1650G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37318856 | |||||||
| chr6:37318906 | G | C | 3 | a0001c0001t0003g0118 a0001c0002t0003g0038 a0001c0002t0004g0039 |
3 | HG01255.hp1 HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1389+1700G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37318906 | |||||||
| chr6:37318965 | G | T | 1 | a0001c0003t0004g0020 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1389+1759G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37318965 | |||||||
| chr6:37318995 | T | C | 5 | a0001c0004t0002g0052 a0001c0004t0002g0053 a0001c0004t0002g0054 others(2): Show |
5 | HG02109.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1389+1789T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37318995 | |||||||
| chr6:37319037 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1389+1831G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37319037 | |||||||
| chr6:37319585 | A | G | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1389+2379A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37319585 | |||||||
| chr6:37319693 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1389+2487G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37319693 | |||||||
| chr6:37319696 | C | T | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1389+2490C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37319696 | |||||||
| chr6:37319904 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1389+2698G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37319904 | |||||||
| chr6:37320030 | A | C | 1 | a0001c0002t0002g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1389+2824A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320030 | |||||||
| chr6:37320152 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1389+2946A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320152 | |||||||
| chr6:37320153 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1389+2947G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320153 | |||||||
| chr6:37320160 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1389+2954A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320160 | |||||||
| chr6:37320253 | T | C | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+3047T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320253 | |||||||
| chr6:37320259 | C | T | 4 | a0001c0001t0003g0118 a0001c0002t0003g0038 a0001c0002t0016g0062 others(1): Show |
4 | HG01255.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+3053C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320259 | |||||||
| chr6:37320260 | A | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1389+3054A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320260 | |||||||
| chr6:37320373 | C | T | 1 | a0001c0004t0002g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1389+3167C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320373 | |||||||
| chr6:37320506 | G | A | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1389+3300G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320506 | |||||||
| chr6:37320575 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1389+3369G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320575 | |||||||
| chr6:37320678 | C | T | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1389+3472C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320678 | |||||||
| chr6:37320708 | G | T | 3 | a0001c0001t0008g0002 a0001c0001t0008g0127 a0001c0001t0008g0129 |
4 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+3502G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320708 | |||||||
| chr6:37320856 | C | T | 3 | a0001c0001t0008g0002 a0001c0001t0008g0127 a0001c0001t0008g0129 |
4 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+3650C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320856 | |||||||
| chr6:37320862 | C | T | 1 | a0001c0001t0003g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1389+3656C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37320862 | |||||||
| chr6:37321004 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1389+3798T>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37321004 | |||||||
| chr6:37321200 | A | AT | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1389+4006dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37321200 | ||||||
| chr6:37321375 | G | A | 1 | a0001c0002t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1389+4169G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37321375 | |||||||
| chr6:37321404 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1389+4198C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37321404 | |||||||
| chr6:37321596 | T | C | 19 | a0001c0002t0004g0039 a0001c0002t0005g0006 a0001c0004t0002g0045 others(16): Show |
19 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1389+4390T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37321596 | |||||||
| chr6:37321858 | A | G | 7 | a0001c0002t0005g0092 a0001c0002t0005g0093 a0001c0002t0005g0094 others(4): Show |
7 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1389+4652A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37321858 | |||||||
| chr6:37321895 | G | A | 1 | a0001c0004t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1389+4689G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37321895 | |||||||
| chr6:37322005 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1389+4799T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37322005 | |||||||
| chr6:37322030 | A | G | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1389+4824A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37322030 | |||||||
| chr6:37322070 | A | G | 1 | a0001c0003t0004g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1389+4864A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37322070 | |||||||
| chr6:37322155 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1389+4949G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37322155 | |||||||
| chr6:37322204 | G | T | 1 | a0001c0002t0005g0098 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1389+4998G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37322204 | |||||||
| chr6:37322306 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1389+5100G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37322306 | |||||||
| chr6:37322772 | G | A | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1389+5566G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37322772 | |||||||
| chr6:37322815 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1389+5609C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37322815 | |||||||
| chr6:37323009 | G | T | 7 | a0001c0002t0005g0092 a0001c0002t0005g0093 a0001c0002t0005g0094 others(4): Show |
7 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1389+5803G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323009 | |||||||
| chr6:37323065 | A | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0116 others(11): Show |
15 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1389+5859A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323065 | |||||||
| chr6:37323082 | AAGC | A | 4 | a0001c0002t0004g0039 a0001c0002t0005g0006 a0001c0002t0016g0062 others(1): Show |
4 | HG02258.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+5898_1389+590 others(7): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37323082 | ||||||
| chr6:37323279 | G | A | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02165.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1389+6073G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323279 | |||||||
| chr6:37323496 | T | C | 1 | a0001c0002t0002g0084 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1389+6290T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323496 | |||||||
| chr6:37323632 | A | G | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1389+6426A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323632 | |||||||
| chr6:37323713 | A | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1389+6507A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323713 | |||||||
| chr6:37323740 | G | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1389+6534G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323740 | |||||||
| chr6:37323819 | G | A | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1389+6613G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323819 | |||||||
| chr6:37323914 | C | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1389+6708C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323914 | |||||||
| chr6:37323925 | T | G | 3 | a0001c0001t0008g0002 a0001c0001t0008g0127 a0001c0001t0008g0129 |
4 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+6719T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37323925 | |||||||
| chr6:37324031 | A | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1389+6825A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37324031 | |||||||
| chr6:37324189 | A | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0164 a0001c0001t0001g0188 |
3 | HG00639.hp1 HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1390-6855A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37324189 | |||||||
| chr6:37324268 | T | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG01106.hp2 HG01517.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-6776T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37324268 | |||||||
| chr6:37324275 | GTAAAATT others(7): Show |
G | 1 | a0001c0003t0004g0012 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1390-6767_1390-675 others(18): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37324275 | ||||||
| chr6:37324563 | T | C | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1390-6481T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37324563 | |||||||
| chr6:37324592 | A | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1390-6452A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37324592 | |||||||
| chr6:37324667 | G | C | 3 | a0001c0001t0008g0002 a0001c0001t0008g0127 a0001c0001t0008g0129 |
4 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-6377G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37324667 | |||||||
| chr6:37325010 | G | A | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1390-6034G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325010 | |||||||
| chr6:37325121 | G | C | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1390-5923G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325121 | |||||||
| chr6:37325518 | C | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0195 |
2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1390-5526C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325518 | |||||||
| chr6:37325518 | C | T | 3 | a0001c0001t0008g0002 a0001c0001t0008g0127 a0001c0001t0008g0129 |
4 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-5526C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325518 | |||||||
| chr6:37325533 | G | A | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1390-5511G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325533 | |||||||
| chr6:37325540 | CT | C | 8 | a0001c0002t0003g0170 a0001c0002t0006g0032 a0001c0002t0006g0033 others(5): Show |
8 | HG01243.hp1 HG01361.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1390-5477delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37325540 | ||||||
| chr6:37325540 | CTTTTT | C | 46 | a0001c0002t0001g0064 a0001c0002t0001g0087 a0001c0002t0002g0001 others(43): Show |
47 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1390-5481_1390-547 others(9): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37325540 | ||||||
| chr6:37325540 | CTTTTTT | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1390-5482_1390-547 others(10): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37325540 | ||||||
| chr6:37325540 | CTTTTTTT | C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0150 a0001c0001t0009g0212 others(2): Show |
5 | HG01074.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-5483_1390-547 others(11): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37325540 | ||||||
| chr6:37325540 | CTTTTTTT others(1): Show |
C | 20 | a0001c0001t0003g0118 a0001c0002t0003g0038 a0001c0002t0004g0039 others(17): Show |
20 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1390-5484_1390-547 others(12): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37325540 | ||||||
| chr6:37325578 | C | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1390-5466C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325578 | |||||||
| chr6:37325588 | C | T | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1390-5456C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325588 | |||||||
| chr6:37325589 | G | A | 1 | a0001c0003t0004g0014 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1390-5455G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325589 | |||||||
| chr6:37325676 | T | C | 10 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0125 others(7): Show |
11 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1390-5368T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325676 | |||||||
| chr6:37325698 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1390-5346C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325698 | |||||||
| chr6:37325769 | C | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1390-5275C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325769 | |||||||
| chr6:37325798 | A | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1390-5246A>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325798 | |||||||
| chr6:37325863 | C | T | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1390-5181C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325863 | |||||||
| chr6:37325879 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1390-5165G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325879 | |||||||
| chr6:37325956 | C | T | 17 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1390-5088C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325956 | |||||||
| chr6:37325957 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1390-5087G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325957 | |||||||
| chr6:37325988 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
110 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1390-5056G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37325988 | |||||||
| chr6:37326002 | G | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1390-5042G>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326002 | |||||||
| chr6:37326110 | G | A | 2 | a0001c0004t0002g0057 a0001c0004t0002g0061 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1390-4934G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326110 | |||||||
| chr6:37326249 | G | A | 1 | a0001c0002t0006g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1390-4795G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326249 | |||||||
| chr6:37326376 | C | CA | 11 | a0001c0001t0001g0186 a0001c0002t0003g0108 a0001c0002t0003g0170 others(8): Show |
11 | HG01243.hp1 HG01361.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1390-4650dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37326376 | ||||||
| chr6:37326376 | C | CAA | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
102 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1390-4651_1390-465 others(6): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37326376 | ||||||
| chr6:37326376 | C | CAAA | 9 | a0001c0001t0001g0112 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG00323.hp1 HG00642.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1390-4652_1390-465 others(7): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37326376 | ||||||
| chr6:37326376 | CA | C | 7 | a0001c0002t0002g0076 a0001c0003t0004g0012 a0001c0004t0003g0046 others(4): Show |
7 | HG01069.hp2 HG01257.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1390-4650delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37326376 | ||||||
| chr6:37326376 | CAA | C | 11 | a0001c0004t0002g0045 a0001c0004t0002g0052 a0001c0004t0002g0053 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1390-4651_1390-465 others(6): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37326376 | ||||||
| chr6:37326392 | A | AG | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-4652_1390-465 others(5): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326392 | |||||||
| chr6:37326554 | C | T | 1 | a0001c0001t0007g0179 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1390-4490C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326554 | |||||||
| chr6:37326608 | A | G | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1390-4436A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326608 | |||||||
| chr6:37326737 | A | G | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
190 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1390-4307A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326737 | |||||||
| chr6:37326743 | A | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
189 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1390-4301A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326743 | |||||||
| chr6:37326783 | G | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0111 others(73): Show |
77 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1390-4261G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326783 | |||||||
| chr6:37326787 | C | CA | 46 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(43): Show |
47 | HG00438.hp2 HG00609.hp2 HG01261.hp2 others(44): Show |
intron_variant | MODIFIER | c.1390-4248dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37326787 | ||||||
| chr6:37326803 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | HG01070.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1390-4241A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37326803 | |||||||
| chr6:37327083 | G | A | 1 | a0001c0001t0003g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1390-3961G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327083 | |||||||
| chr6:37327099 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1390-3945G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327099 | |||||||
| chr6:37327177 | TAAAAAAT others(316): Show |
T | 65 | a0001c0001t0002g0194 a0001c0001t0002g0195 a0001c0001t0003g0113 others(62): Show |
67 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1390-3847_1390-352 others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37327177 | ||||||
| chr6:37327254 | G | A | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1390-3790G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327254 | |||||||
| chr6:37327306 | G | A | 1 | a0001c0002t0005g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1390-3738G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327306 | |||||||
| chr6:37327334 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0183 |
2 | HG00609.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1390-3710C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327334 | |||||||
| chr6:37327338 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1390-3706C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327338 | |||||||
| chr6:37327346 | T | C | 16 | a0001c0001t0001g0116 a0001c0001t0001g0146 a0001c0001t0001g0151 others(13): Show |
16 | HG00738.hp1 HG01123.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1390-3698T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327346 | |||||||
| chr6:37327371 | G | A | 4 | a0001c0001t0001g0187 a0001c0001t0001g0191 a0001c0001t0001g0213 others(1): Show |
4 | HG01081.hp2 HG02523.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-3673G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327371 | |||||||
| chr6:37327394 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
107 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1390-3650C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327394 | |||||||
| chr6:37327396 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1390-3648T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327396 | |||||||
| chr6:37327465 | C | G | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
129 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1390-3579C>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327465 | |||||||
| chr6:37327474 | A | T | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
129 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1390-3570A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327474 | |||||||
| chr6:37327477 | C | CA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
84 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.1390-3538dupA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37327477 | ||||||
| chr6:37327477 | C | CAA | 32 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0136 others(29): Show |
32 | HG00438.hp1 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1390-3539_1390-353 others(6): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37327477 | ||||||
| chr6:37327477 | CA | C | 8 | a0001c0001t0006g0171 a0001c0002t0003g0170 a0001c0002t0006g0031 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-3538delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37327477 | ||||||
| chr6:37327641 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1390-3403G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327641 | |||||||
| chr6:37327738 | G | A | 18 | a0001c0001t0003g0113 a0001c0001t0003g0115 a0001c0001t0003g0123 others(15): Show |
19 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1390-3306G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327738 | |||||||
| chr6:37327854 | A | G | 87 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0154 others(84): Show |
89 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1390-3190A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37327854 | |||||||
| chr6:37328040 | G | A | 92 | a0001c0001t0002g0153 a0001c0001t0002g0194 a0001c0001t0002g0195 others(89): Show |
94 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1390-3004G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328040 | |||||||
| chr6:37328042 | G | A | 90 | a0001c0001t0002g0153 a0001c0001t0002g0194 a0001c0001t0002g0195 others(87): Show |
92 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1390-3002G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328042 | |||||||
| chr6:37328085 | G | A | 2 | a0001c0002t0003g0107 a0001c0002t0003g0108 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1390-2959G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328085 | |||||||
| chr6:37328086 | G | T | 1 | a0001c0002t0004g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1390-2958G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328086 | |||||||
| chr6:37328095 | C | T | 1 | a0001c0002t0002g0099 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1390-2949C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328095 | |||||||
| chr6:37328097 | TGAGGTCA others(1): Show |
T | 87 | a0001c0001t0002g0153 a0001c0001t0002g0194 a0001c0001t0002g0195 others(84): Show |
89 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1390-2943_1390-293 others(12): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37328097 | ||||||
| chr6:37328220 | G | A | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG00741.hp1 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-2824G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328220 | |||||||
| chr6:37328264 | C | T | 49 | a0001c0001t0002g0153 a0001c0001t0002g0194 a0001c0001t0002g0195 others(46): Show |
50 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1390-2780C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328264 | |||||||
| chr6:37328315 | AATAG | A | 6 | a0001c0002t0003g0068 a0001c0002t0003g0070 a0001c0002t0003g0071 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1390-2717_1390-271 others(8): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37328315 | ||||||
| chr6:37328328 | A | G | 89 | a0001c0001t0002g0153 a0001c0001t0002g0194 a0001c0001t0002g0195 others(86): Show |
91 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1390-2716A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328328 | |||||||
| chr6:37328335 | T | C | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1390-2709T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328335 | |||||||
| chr6:37328720 | T | G | 89 | a0001c0001t0002g0153 a0001c0001t0002g0194 a0001c0001t0002g0195 others(86): Show |
91 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1390-2324T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328720 | |||||||
| chr6:37328762 | C | T | 89 | a0001c0001t0002g0153 a0001c0001t0002g0194 a0001c0001t0002g0195 others(86): Show |
91 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1390-2282C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328762 | |||||||
| chr6:37328788 | G | A | 1 | a0001c0002t0002g0090 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1390-2256G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328788 | |||||||
| chr6:37328947 | A | G | 89 | a0001c0001t0002g0153 a0001c0001t0002g0194 a0001c0001t0002g0195 others(86): Show |
91 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1390-2097A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37328947 | |||||||
| chr6:37329042 | TA | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
106 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1390-1992delA | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37329042 | ||||||
| chr6:37329204 | T | C | 1 | a0001c0002t0003g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1390-1840T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37329204 | |||||||
| chr6:37329221 | T | C | 25 | a0001c0001t0003g0113 a0001c0001t0003g0115 a0001c0001t0003g0123 others(22): Show |
26 | HG01243.hp1 HG01361.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1390-1823T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37329221 | |||||||
| chr6:37329253 | G | T | 89 | a0001c0001t0002g0153 a0001c0001t0002g0194 a0001c0001t0002g0195 others(86): Show |
91 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1390-1791G>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37329253 | |||||||
| chr6:37329415 | G | A | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1390-1629G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37329415 | |||||||
| chr6:37329456 | C | A | 2 | a0001c0001t0003g0118 a0001c0002t0003g0038 |
2 | HG01255.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1390-1588C>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37329456 | |||||||
| chr6:37329493 | T | C | 1 | a0001c0001t0003g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1390-1551T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37329493 | |||||||
| chr6:37329620 | C | T | 1 | a0001c0002t0003g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1390-1424C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37329620 | |||||||
| chr6:37329716 | A | G | 10 | a0001c0002t0004g0039 a0001c0002t0005g0006 a0001c0002t0005g0092 others(7): Show |
10 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1390-1328A>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37329716 | |||||||
| chr6:37329936 | A | T | 1 | a0001c0002t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1390-1108A>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37329936 | |||||||
| chr6:37330222 | C | CT | 16 | a0001c0001t0002g0194 a0001c0001t0002g0195 a0001c0002t0002g0001 others(13): Show |
17 | HG00323.hp2 HG00438.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.1390-787dupT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330222 | C | CTT | 7 | a0001c0002t0002g0041 a0001c0002t0002g0067 a0001c0002t0005g0092 others(4): Show |
7 | HG00642.hp2 HG00741.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-788_1390-787d others(4): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330222 | CT | C | 20 | a0001c0002t0002g0077 a0001c0002t0002g0078 a0001c0002t0002g0110 others(17): Show |
20 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1390-787delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330222 | CTTTTTT | C | 8 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0126 others(5): Show |
8 | HG02622.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1390-792_1390-787d others(8): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330222 | CTTTTTTT | C | 18 | a0001c0001t0003g0113 a0001c0001t0003g0115 a0001c0001t0003g0123 others(15): Show |
19 | HG01243.hp1 HG01361.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1390-793_1390-787d others(9): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330222 | CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0003g0118 a0001c0002t0003g0038 a0001c0002t0003g0070 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1390-796_1390-787d others(12): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330222 | CTTTTTTT others(4): Show |
C | 6 | a0001c0002t0002g0076 a0001c0002t0002g0082 a0001c0002t0002g0084 others(3): Show |
6 | HG00735.hp2 HG01257.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1390-797_1390-787d others(13): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330222 | CTTTTTTT others(9): Show |
C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1390-802_1390-787d others(18): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330222 | CTTTTTTT others(11): Show |
C | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02165.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1390-804_1390-787d others(20): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330222 | CTTTTTTT others(16): Show |
C | 1 | a0001c0003t0004g0025 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1390-809_1390-787d others(25): Show |
TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330222 | ||||||
| chr6:37330302 | G | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1390-742G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37330302 | |||||||
| chr6:37330395 | T | G | 2 | a0001c0002t0002g0069 a0001c0002t0002g0073 |
2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1390-649T>G | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37330395 | |||||||
| chr6:37330462 | C | T | 8 | a0001c0002t0005g0092 a0001c0002t0005g0093 a0001c0002t0005g0094 others(5): Show |
8 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1390-582C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37330462 | |||||||
| chr6:37330515 | C | T | 11 | a0001c0002t0004g0039 a0001c0002t0005g0006 a0001c0002t0005g0092 others(8): Show |
11 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1390-529C>T | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37330515 | |||||||
| chr6:37330688 | T | C | 2 | a0001c0002t0016g0062 a0001c0002t0017g0063 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1390-356T>C | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37330688 | |||||||
| chr6:37330800 | GT | G | 44 | a0001c0001t0003g0113 a0001c0001t0003g0115 a0001c0001t0003g0118 others(41): Show |
45 | HG01243.hp1 HG01255.hp1 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.1390-238delT | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 37330800 | ||||||
| chr6:37330899 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1390-145G>A | TBC1D22B | ENSG00000065491.8 | transcript | ENST00000373491.3 | protein_coding | 12/12 | chr6 | 37330899 |