Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55020 |
| ensemblid | ENSG00000075234.17 |
| hgncid | 26082 |
| symbol | TTC38 |
| name | tetratricopeptide repeat domain 38 |
| refseq_nuc | NM_017931.4 |
| refseq_prot | NP_060401.3 |
| ensembl_nuc | ENST00000381031.8 |
| ensembl_prot | ENSP00000370419.3 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 46268008 |
| end | 46294008 |
| strand | + |
| ver | v1.2 |
| region | chr22:46268008-46294008 |
| region5000 | chr22:46263008-46299008 |
| regionname0 | TTC38_chr22_46268008_46294008 |
| regionname5000 | TTC38_chr22_46263008_46299008 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 469 | 211 | 81 | 50 | 40 | 10 | 29 | 18 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| a0002 | 0/0 | 469 | 8 | 1 | 3 | 0 | 2 | 2 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| a0003 | 0/0 | 469 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| a0004 | 0/0 | 469 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| a0005 | 0/0 | 324 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(319): Show |
chr22 | 46263008 | 46299008 |
| a0006 | 0/0 | 469 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| a0007 | 0/0 | 469 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| a0008 | 0/0 | 469 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| a0009 | 0/0 | 469 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAL others(464): Show |
chr22 | 46263008 | 46299008 |
| a0010 | 0/0 | 469 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| a0011 | 0/0 | 469 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| a0012 | 0/1 | 469 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | MAAAS others(464): Show |
chr22 | 46263008 | 46299008 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1407 | 145 | 28 | 43 | 39 | 10 | 24 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0002 | 0/0 | 1407 | 43 | 33 | 6 | 0 | 0 | 4 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0003 | 0/0 | 1407 | 11 | 10 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0005 | 0/0 | 1407 | 5 | 5 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0008 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0009 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0015 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0016 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0018 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0019 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0001c0020 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0002c0004 | 0/0 | 1407 | 8 | 1 | 3 | 0 | 2 | 2 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0003c0006 | 0/0 | 1407 | 3 | 3 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0004c0007 | 0/0 | 1407 | 2 | 2 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0005c0017 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0006c0011 | 0/0 | 1407 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0007c0012 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0008c0013 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0009c0022 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0010c0014 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0011c0021 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 | ||
| a0012c0010 | 0/1 | 1407 | 1 | 0 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | ATGGC others(1402): Show |
chr22 | 46263008 | 46299008 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2566 | 133 | 25 | 37 | 38 | 9 | 23 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0001t0002 | 0/0 | 2566 | 3 | 3 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0001t0003 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0001t0004 | 0/0 | 2566 | 5 | 0 | 4 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0001t0009 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0001t0010 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0001t0011 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0002t0001 | 0/0 | 2566 | 19 | 14 | 3 | 0 | 0 | 2 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0002t0002 | 0/0 | 2566 | 22 | 17 | 3 | 0 | 0 | 2 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0002t0006 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0003t0001 | 0/0 | 2566 | 11 | 10 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0005t0002 | 0/0 | 2566 | 5 | 5 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0008t0002 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0009t0002 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0015t0001 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0016t0007 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0018t0001 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0019t0001 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0001c0020t0001 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0002c0004t0003 | 0/0 | 2566 | 8 | 1 | 3 | 0 | 2 | 2 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0003c0006t0005 | 0/0 | 2566 | 3 | 3 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0004c0007t0005 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0005c0017t0001 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0006c0011t0001 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0007c0012t0001 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0008c0013t0001 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0009c0022t0001 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0010c0014t0001 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0011c0021t0008 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| a0012c0010t0012 | 0/1 | 2566 | 1 | 0 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | AGAGC others(2561): Show |
chr22 | 46263008 | 46299008 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 1 | 6 | 5 | 0 | 5 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0021 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0009g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0001t0011g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0002t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0003t0001g0002 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0005t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0005t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0005t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0005t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0008t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0009t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0015t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0016t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0018t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0019t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0001c0020t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0002c0004t0003g0011 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0002c0004t0003g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0002c0004t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0002c0004t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0002c0004t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0003c0006t0005g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0004c0007t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0005c0017t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0006c0011t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0007c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0008c0013t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0009c0022t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0010c0014t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0011c0021t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| a0012c0010t0012g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0047 | EUR | FIN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0129 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00673 | hp2 | a0005 | c0017 | t0001 | g0007 | EAS | CHS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00738 | hp1 | a0001 | c0001 | t0010 | g0157 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01070 | hp2 | a0002 | c0004 | t0003 | g0158 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01081 | hp1 | a0006 | c0011 | t0001 | g0111 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01106 | hp2 | a0002 | c0004 | t0003 | g0156 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01358 | hp1 | a0002 | c0004 | t0003 | g0031 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0127 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01975 | hp1 | a0001 | c0001 | t0011 | g0007 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02074 | hp2 | a0007 | c0012 | t0001 | g0001 | EAS | KHV | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02257 | hp1 | a0003 | c0006 | t0005 | g0012 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0117 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0139 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0145 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0149 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02572 | hp2 | a0003 | c0006 | t0005 | g0012 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0146 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02683 | hp1 | a0002 | c0004 | t0003 | g0011 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0140 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02723 | hp1 | a0003 | c0006 | t0005 | g0012 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0148 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02809 | hp1 | a0001 | c0005 | t0002 | g0130 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02818 | hp2 | a0001 | c0005 | t0002 | g0134 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02895 | hp1 | a0001 | c0005 | t0002 | g0128 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02965 | hp1 | a0001 | c0019 | t0001 | g0159 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0147 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03098 | hp1 | a0001 | c0020 | t0001 | g0008 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03098 | hp2 | a0001 | c0002 | t0006 | g0009 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03130 | hp2 | a0001 | c0009 | t0002 | g0160 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03195 | hp1 | a0001 | c0008 | t0002 | g0161 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03209 | hp1 | a0008 | c0013 | t0001 | g0022 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03209 | hp2 | a0009 | c0022 | t0001 | g0118 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03453 | hp1 | a0001 | c0002 | t0006 | g0009 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03540 | hp1 | a0001 | c0016 | t0007 | g0032 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | STU | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03710 | hp1 | a0001 | c0015 | t0001 | g0005 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03927 | hp1 | a0010 | c0014 | t0001 | g0005 | SAS | BEB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0166 | SAS | STU | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | YRI | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | YRI | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | YRI | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18959 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | LWK | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | LWK | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19043 | hp2 | a0001 | c0005 | t0002 | g0133 | AFR | LWK | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19090 | hp1 | a0001 | c0018 | t0001 | g0070 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA20752 | hp1 | a0002 | c0004 | t0003 | g0031 | EUR | TSI | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | TSI | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA20805 | hp2 | a0002 | c0004 | t0003 | g0011 | EUR | TSI | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA20905 | hp1 | a0002 | c0004 | t0003 | g0011 | SAS | GIH | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02486 | hp1 | a0001 | c0005 | t0002 | g0131 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG02559 | hp2 | a0004 | c0007 | t0005 | g0015 | AFR | ACB | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0141 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0144 | AFR | USA | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| HG06807 | hp2 | a0002 | c0004 | t0003 | g0155 | AFR | USA | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA20300 | hp1 | a0004 | c0007 | t0005 | g0015 | AFR | USA | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| NA21309 | hp2 | a0011 | c0021 | t0008 | g0033 | AFR | LWK | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| homoSapiens | chm13v2 | a0012 | c0010 | t0012 | g0090 | REF | REF | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0021 | REF | REF | TTC38_chr22_46263008_46299008 | TTC38 | chr22 | 46263008 | 46299008 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46268053 | C | T | 1 | a0009 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.14C>T | p.Ser5Leu | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 1/14 | 46/2566 | 14/1410 | 5/469 | chr22 | 46268053 | |||
| chr22:46275297 | C | T | 1 | a0011 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.415C>T | p.Pro139Ser | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/14 | 447/2566 | 415/1410 | 139/469 | chr22 | 46275297 | |||
| chr22:46278657 | A | G | 1 | a0003 | 3 | HG02257.hp1 HG02572.hp2 HG02723.hp1 |
missense_variant | MODERATE | c.611A>G | p.Lys204Arg | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/14 | 643/2566 | 611/1410 | 204/469 | chr22 | 46278657 | |||
| chr22:46285244 | G | A | 1 | a0006 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.799G>A | p.Glu267Lys | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/14 | 831/2566 | 799/1410 | 267/469 | chr22 | 46285244 | |||
| chr22:46287079 | C | T | 1 | a0002 | 8 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(5): Show |
missense_variant | MODERATE | c.841C>T | p.Pro281Ser | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/14 | 873/2566 | 841/1410 | 281/469 | chr22 | 46287079 | |||
| chr22:46287098 | A | G | 2 | a0003 a0004 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
missense_variant | MODERATE | c.860A>G | p.Asp287Gly | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/14 | 892/2566 | 860/1410 | 287/469 | chr22 | 46287098 | |||
| chr22:46287112 | G | A | 1 | a0007 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.874G>A | p.Val292Met | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/14 | 906/2566 | 874/1410 | 292/469 | chr22 | 46287112 | |||
| chr22:46288479 | C | T | 1 | a0005 | 1 | HG00673.hp2 | stop_gained | HIGH | c.973C>T | p.Arg325* | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/14 | 1005/2566 | 973/1410 | 325/469 | chr22 | 46288479 | |||
| chr22:46288480 | G | A | 1 | a0008 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.974G>A | p.Arg325Gln | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/14 | 1006/2566 | 974/1410 | 325/469 | chr22 | 46288480 | |||
| chr22:46288542 | C | G | 1 | a0011 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1036C>G | p.Pro346Ala | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/14 | 1068/2566 | 1036/1410 | 346/469 | chr22 | 46288542 | |||
| chr22:46289865 | A | G | 1 | a0010 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1282A>G | p.Asn428Asp | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/14 | 1314/2566 | 1282/1410 | 428/469 | chr22 | 46289865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46268534 | C | G | 5 | a0001c0002 a0001c0005 a0001c0020 others(2): Show |
51 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(48): Show |
synonymous_variant | LOW | c.54C>G | p.Leu18Leu | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/14 | 86/2566 | 54/1410 | 18/469 | chr22 | 46268534 | |||
| chr22:46275257 | G | A | 1 | a0001c0003 | 11 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(8): Show |
synonymous_variant | LOW | c.375G>A | p.Pro125Pro | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/14 | 407/2566 | 375/1410 | 125/469 | chr22 | 46275257 | |||
| chr22:46275299 | G | A | 2 | a0001c0008 a0001c0009 |
2 | HG03130.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.417G>A | p.Pro139Pro | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/14 | 449/2566 | 417/1410 | 139/469 | chr22 | 46275299 | |||
| chr22:46275344 | C | T | 1 | a0001c0019 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.462C>T | p.Tyr154Tyr | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/14 | 494/2566 | 462/1410 | 154/469 | chr22 | 46275344 | |||
| chr22:46285255 | C | T | 1 | a0001c0018 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.810C>T | p.Ala270Ala | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/14 | 842/2566 | 810/1410 | 270/469 | chr22 | 46285255 | |||
| chr22:46285276 | C | G | 2 | a0001c0005 a0001c0009 |
6 | HG02486.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
synonymous_variant | LOW | c.831C>G | p.Thr277Thr | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/14 | 863/2566 | 831/1410 | 277/469 | chr22 | 46285276 | |||
| chr22:46288574 | G | C | 1 | a0001c0020 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1068G>C | p.Leu356Leu | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/14 | 1100/2566 | 1068/1410 | 356/469 | chr22 | 46288574 | |||
| chr22:46289483 | C | T | 3 | a0001c0016 a0002c0004 a0011c0021 |
10 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(7): Show |
synonymous_variant | LOW | c.1164C>T | p.Asp388Asp | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 12/14 | 1196/2566 | 1164/1410 | 388/469 | chr22 | 46289483 | |||
| chr22:46289831 | C | T | 1 | a0001c0015 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.1248C>T | p.Asp416Asp | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/14 | 1280/2566 | 1248/1410 | 416/469 | chr22 | 46289831 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46292988 | G | C | 2 | a0001c0016t0007 a0011c0021t0008 |
2 | HG03540.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*104G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 14/14 | 104 | chr22 | 46292988 | ||||||
| chr22:46293046 | T | G | 1 | a0001c0001t0009 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 14/14 | 162 | chr22 | 46293046 | ||||||
| chr22:46293168 | T | C | 1 | a0001c0001t0004 | 5 | HG00323.hp2 HG00735.hp1 HG01175.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*284T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 14/14 | 284 | chr22 | 46293168 | ||||||
| chr22:46293257 | C | A | 1 | a0001c0001t0010 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 14/14 | 373 | chr22 | 46293257 | ||||||
| chr22:46293332 | C | T | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0006 others(3): Show |
34 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*448C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 14/14 | 448 | chr22 | 46293332 | ||||||
| chr22:46293450 | G | A | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0005t0002 others(3): Show |
33 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*566G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 14/14 | 566 | chr22 | 46293450 | ||||||
| chr22:46293539 | C | A | 1 | a0001c0001t0011 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 14/14 | 655 | chr22 | 46293539 | ||||||
| chr22:46293571 | G | A | 3 | a0001c0001t0003 a0001c0016t0007 a0002c0004t0003 |
10 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*687G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 14/14 | 687 | chr22 | 46293571 | ||||||
| chr22:46293612 | C | T | 2 | a0003c0006t0005 a0004c0007t0005 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*728C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 14/14 | 728 | chr22 | 46293612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46268170 | G | C | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.33+98G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 1/13 | chr22 | 46268170 | |||||||
| chr22:46268226 | C | A | 1 | a0011c0021t0008g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.33+154C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 1/13 | chr22 | 46268226 | |||||||
| chr22:46268667 | TTTTTG | T | 62 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0165 others(59): Show |
79 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.111+106_111+110del others(5): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 46268667 | ||||||
| chr22:46268667 | TTTTTGTT others(8): Show |
T | 1 | a0001c0002t0002g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.111+96_111+110delG others(14): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 46268667 | ||||||
| chr22:46268741 | G | A | 42 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(39): Show |
48 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.111+150G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46268741 | |||||||
| chr22:46268765 | AGCTTTGC others(4): Show |
A | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.111+175_111+185del others(11): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46268765 | |||||||
| chr22:46268777 | C | A | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.111+186C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46268777 | |||||||
| chr22:46268844 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
122 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.111+253T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46268844 | |||||||
| chr22:46268851 | A | AT | 13 | a0001c0002t0002g0010 a0001c0002t0002g0030 a0001c0002t0002g0034 others(10): Show |
16 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.111+268dupT | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 46268851 | ||||||
| chr22:46268881 | G | A | 1 | a0001c0002t0002g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.111+290G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46268881 | |||||||
| chr22:46268958 | A | G | 45 | a0001c0001t0002g0164 a0001c0002t0001g0008 a0001c0002t0001g0009 others(42): Show |
53 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.111+367A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46268958 | |||||||
| chr22:46269019 | T | A | 13 | a0001c0002t0002g0010 a0001c0002t0002g0030 a0001c0002t0002g0034 others(10): Show |
16 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.111+428T>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269019 | |||||||
| chr22:46269088 | G | GC | 28 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(25): Show |
38 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+507dupC | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 46269088 | ||||||
| chr22:46269088 | GC | G | 9 | a0001c0001t0010g0157 a0001c0002t0001g0154 a0001c0016t0007g0032 others(6): Show |
12 | HG00738.hp1 HG01070.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+507delC | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 46269088 | ||||||
| chr22:46269088 | GCC | G | 45 | a0001c0001t0002g0164 a0001c0002t0001g0008 a0001c0002t0001g0009 others(42): Show |
53 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.111+506_111+507del others(2): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 46269088 | ||||||
| chr22:46269092 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.111+501C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269092 | |||||||
| chr22:46269095 | C | CA | 5 | a0001c0003t0001g0002 a0001c0003t0001g0150 a0001c0003t0001g0151 others(2): Show |
11 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+504_111+505ins others(1): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269095 | |||||||
| chr22:46269096 | C | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0059 |
5 | HG00423.hp1 HG00673.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+505C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269096 | |||||||
| chr22:46269096 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.111+505C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269096 | |||||||
| chr22:46269098 | C | A | 6 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+507C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269098 | |||||||
| chr22:46269098 | C | G | 1 | a0001c0002t0002g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.111+507C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269098 | |||||||
| chr22:46269109 | A | G | 61 | a0001c0001t0002g0164 a0001c0001t0010g0157 a0001c0002t0001g0008 others(58): Show |
78 | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.111+518A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269109 | |||||||
| chr22:46269208 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.111+617C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269208 | |||||||
| chr22:46269219 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.111+628T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269219 | |||||||
| chr22:46269251 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.111+660G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269251 | |||||||
| chr22:46269312 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG01175.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.111+721G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269312 | |||||||
| chr22:46269435 | AC | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
16 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.111+845delC | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269435 | |||||||
| chr22:46269504 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.111+913C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269504 | |||||||
| chr22:46269622 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.111+1031G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269622 | |||||||
| chr22:46269773 | C | T | 39 | a0001c0001t0002g0164 a0001c0002t0001g0008 a0001c0002t0001g0009 others(36): Show |
45 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(42): Show |
intron_variant | MODIFIER | c.111+1182C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269773 | |||||||
| chr22:46269945 | A | G | 5 | a0001c0003t0001g0002 a0001c0003t0001g0150 a0001c0003t0001g0151 others(2): Show |
11 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+1354A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46269945 | |||||||
| chr22:46270254 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.111+1663C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46270254 | |||||||
| chr22:46270264 | T | C | 39 | a0001c0001t0002g0164 a0001c0002t0001g0008 a0001c0002t0001g0009 others(36): Show |
47 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(44): Show |
intron_variant | MODIFIER | c.111+1673T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46270264 | |||||||
| chr22:46270559 | G | A | 1 | a0001c0019t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.112-1776G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46270559 | |||||||
| chr22:46270678 | T | C | 53 | a0001c0001t0002g0164 a0001c0001t0010g0157 a0001c0002t0001g0008 others(50): Show |
64 | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.112-1657T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46270678 | |||||||
| chr22:46270765 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.112-1570T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46270765 | |||||||
| chr22:46270775 | A | G | 2 | a0001c0002t0002g0148 a0001c0002t0002g0149 |
2 | HG02572.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.112-1560A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46270775 | |||||||
| chr22:46270840 | GA | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0041 a0001c0001t0002g0042 others(1): Show |
6 | HG02559.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-1483delA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 46270840 | ||||||
| chr22:46270900 | G | A | 1 | a0001c0002t0001g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.112-1435G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46270900 | |||||||
| chr22:46270907 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
6 | HG00280.hp2 HG02015.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-1428C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46270907 | |||||||
| chr22:46271015 | T | TA | 38 | a0001c0001t0002g0164 a0001c0002t0001g0008 a0001c0002t0001g0009 others(35): Show |
44 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(41): Show |
intron_variant | MODIFIER | c.112-1310dupA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 46271015 | ||||||
| chr22:46271140 | T | C | 38 | a0001c0001t0002g0164 a0001c0002t0001g0008 a0001c0002t0001g0009 others(35): Show |
44 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(41): Show |
intron_variant | MODIFIER | c.112-1195T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46271140 | |||||||
| chr22:46271435 | G | A | 3 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 |
3 | HG02818.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.112-900G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46271435 | |||||||
| chr22:46271484 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.112-851C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46271484 | |||||||
| chr22:46271680 | T | TTTGTATT others(5): Show |
7 | a0001c0002t0002g0010 a0001c0002t0002g0030 a0001c0002t0002g0143 others(4): Show |
10 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.112-653_112-642dup others(12): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr22 | 46271680 | ||||||
| chr22:46271756 | C | T | 38 | a0001c0001t0002g0164 a0001c0002t0001g0008 a0001c0002t0001g0009 others(35): Show |
44 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(41): Show |
intron_variant | MODIFIER | c.112-579C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46271756 | |||||||
| chr22:46271819 | C | G | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.112-516C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46271819 | |||||||
| chr22:46272035 | A | T | 1 | a0001c0002t0002g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.112-300A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46272035 | |||||||
| chr22:46272100 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.112-235C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46272100 | |||||||
| chr22:46272182 | G | T | 40 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0002t0001g0008 others(37): Show |
48 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(45): Show |
intron_variant | MODIFIER | c.112-153G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46272182 | |||||||
| chr22:46272205 | G | C | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.112-130G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46272205 | |||||||
| chr22:46272243 | G | A | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.112-92G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46272243 | |||||||
| chr22:46272249 | C | T | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.112-86C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 2/13 | chr22 | 46272249 | |||||||
| chr22:46272455 | A | G | 41 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0002t0001g0008 others(38): Show |
49 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(46): Show |
intron_variant | MODIFIER | c.193+39A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46272455 | |||||||
| chr22:46272618 | T | A | 59 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0001t0010g0157 others(56): Show |
76 | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.193+202T>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46272618 | |||||||
| chr22:46272724 | T | C | 3 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 |
3 | HG02818.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.193+308T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46272724 | |||||||
| chr22:46272737 | A | G | 1 | a0001c0002t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.193+321A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46272737 | |||||||
| chr22:46272749 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.193+333G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46272749 | |||||||
| chr22:46272795 | C | T | 40 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0002t0001g0008 others(37): Show |
48 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(45): Show |
intron_variant | MODIFIER | c.193+379C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46272795 | |||||||
| chr22:46272829 | C | T | 40 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0002t0001g0008 others(37): Show |
48 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(45): Show |
intron_variant | MODIFIER | c.193+413C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46272829 | |||||||
| chr22:46272844 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.193+428G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46272844 | |||||||
| chr22:46273254 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.194-644A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46273254 | |||||||
| chr22:46273367 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.194-531C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46273367 | |||||||
| chr22:46273427 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.194-471G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46273427 | |||||||
| chr22:46273451 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.194-447C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46273451 | |||||||
| chr22:46273582 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.194-316T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 3/13 | chr22 | 46273582 | |||||||
| chr22:46274153 | G | A | 1 | a0011c0021t0008g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.365+84G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274153 | |||||||
| chr22:46274279 | C | G | 3 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 |
3 | HG02818.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.365+210C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274279 | |||||||
| chr22:46274441 | A | AC | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0009c0022t0001g0118 |
3 | HG02145.hp1 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.365+375dupC | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr22 | 46274441 | ||||||
| chr22:46274497 | T | C | 54 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0001t0010g0157 others(51): Show |
65 | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.365+428T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274497 | |||||||
| chr22:46274516 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.365+447C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274516 | |||||||
| chr22:46274581 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.365+512T>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274581 | |||||||
| chr22:46274596 | G | A | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0009c0022t0001g0118 |
3 | HG02145.hp1 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.365+527G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274596 | |||||||
| chr22:46274735 | GT | G | 42 | a0001c0001t0001g0069 a0001c0001t0002g0042 a0001c0001t0002g0164 others(39): Show |
48 | HG00639.hp2 HG01070.hp1 HG01433.hp1 others(45): Show |
intron_variant | MODIFIER | c.366-498delT | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr22 | 46274735 | ||||||
| chr22:46274774 | T | G | 3 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0001g0123 |
3 | HG01167.hp2 HG01169.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.366-474T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274774 | |||||||
| chr22:46274823 | G | C | 54 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0001t0010g0157 others(51): Show |
65 | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.366-425G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274823 | |||||||
| chr22:46274865 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.366-383G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274865 | |||||||
| chr22:46274894 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.366-354C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274894 | |||||||
| chr22:46274925 | T | C | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0009c0022t0001g0118 |
3 | HG02145.hp1 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.366-323T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274925 | |||||||
| chr22:46274948 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.366-300G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46274948 | |||||||
| chr22:46275057 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.366-191G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46275057 | |||||||
| chr22:46275059 | G | T | 1 | a0001c0002t0002g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.366-189G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 4/13 | chr22 | 46275059 | |||||||
| chr22:46275485 | A | G | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539+64A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46275485 | |||||||
| chr22:46275532 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0040 |
2 | HG00140.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.539+111C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46275532 | |||||||
| chr22:46275610 | C | T | 6 | a0001c0001t0010g0157 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG00738.hp1 HG01070.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.539+189C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46275610 | |||||||
| chr22:46275755 | A | G | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539+334A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46275755 | |||||||
| chr22:46275874 | G | A | 1 | a0001c0018t0001g0070 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.539+453G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46275874 | |||||||
| chr22:46275908 | G | A | 5 | a0001c0003t0001g0002 a0001c0003t0001g0150 a0001c0003t0001g0151 others(2): Show |
11 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.539+487G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46275908 | |||||||
| chr22:46276154 | A | C | 1 | a0001c0001t0001g0019 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.539+733A>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276154 | |||||||
| chr22:46276348 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.539+927C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276348 | |||||||
| chr22:46276350 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539+929C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276350 | |||||||
| chr22:46276358 | G | C | 2 | a0001c0002t0001g0008 a0001c0020t0001g0008 |
3 | HG02723.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.539+937G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276358 | |||||||
| chr22:46276403 | G | A | 4 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0154 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+982G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276403 | |||||||
| chr22:46276457 | C | T | 1 | a0001c0002t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.539+1036C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276457 | |||||||
| chr22:46276653 | C | G | 5 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0154 others(2): Show |
5 | HG02145.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+1232C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276653 | |||||||
| chr22:46276695 | A | T | 5 | a0001c0003t0001g0002 a0001c0003t0001g0150 a0001c0003t0001g0151 others(2): Show |
11 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.539+1274A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276695 | |||||||
| chr22:46276736 | A | T | 11 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0119 others(8): Show |
13 | HG01433.hp2 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.539+1315A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276736 | |||||||
| chr22:46276746 | A | T | 6 | a0001c0001t0010g0157 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG00738.hp1 HG01070.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.539+1325A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276746 | |||||||
| chr22:46276751 | C | CATATATT others(6): Show |
40 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0002t0001g0008 others(37): Show |
48 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(45): Show |
intron_variant | MODIFIER | c.539+1341_539+1353d others(15): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276751 | ||||||
| chr22:46276759 | AAAAATAT others(16): Show |
A | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.539+1354_539+1376d others(25): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276759 | ||||||
| chr22:46276800 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.539+1379T>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276800 | |||||||
| chr22:46276820 | A | T | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539+1399A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276820 | |||||||
| chr22:46276821 | T | A | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539+1400T>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276821 | |||||||
| chr22:46276822 | T | A | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539+1401T>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276822 | |||||||
| chr22:46276824 | A | AAT | 21 | a0001c0001t0001g0105 a0001c0001t0002g0042 a0001c0001t0010g0157 others(18): Show |
27 | HG00738.hp1 HG01070.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.539+1419_539+1420d others(4): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276824 | ||||||
| chr22:46276824 | A | AATAT | 14 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0124 others(11): Show |
16 | HG02451.hp2 HG02559.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.539+1417_539+1420d others(6): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276824 | ||||||
| chr22:46276824 | A | AATATAT | 6 | a0001c0001t0002g0164 a0001c0002t0002g0117 a0001c0002t0002g0132 others(3): Show |
6 | HG02258.hp1 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+1415_539+1420d others(8): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276824 | ||||||
| chr22:46276824 | A | AATATATA others(3): Show |
2 | a0001c0002t0001g0119 a0009c0022t0001g0118 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.539+1411_539+1420d others(12): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276824 | ||||||
| chr22:46276824 | A | AATATATA others(5): Show |
1 | a0001c0002t0001g0120 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.539+1409_539+1420d others(14): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276824 | ||||||
| chr22:46276824 | A | AATATATA others(15): Show |
1 | a0001c0002t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.539+1420_539+1421i others(24): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276824 | ||||||
| chr22:46276824 | A | AATATATA others(12): Show |
1 | a0003c0006t0005g0012 | 3 | HG02257.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.539+1415_539+1416i others(21): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276824 | ||||||
| chr22:46276824 | A | AATATATA others(31): Show |
1 | a0001c0019t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.539+1413_539+1414i others(40): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276824 | ||||||
| chr22:46276824 | A | T | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539+1403A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276824 | |||||||
| chr22:46276824 | AAT | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0044 others(8): Show |
21 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.539+1419_539+1420d others(4): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46276824 | ||||||
| chr22:46276858 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.539+1437A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46276858 | |||||||
| chr22:46277030 | AATACATA others(3): Show |
A | 2 | a0001c0002t0002g0143 a0001c0002t0002g0144 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.540-1548_540-1539d others(12): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277030 | ||||||
| chr22:46277033 | A | G | 8 | a0001c0001t0010g0157 a0001c0008t0002g0161 a0001c0016t0007g0032 others(5): Show |
11 | HG00738.hp1 HG01070.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.540-1553A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277033 | |||||||
| chr22:46277034 | CAT | C | 4 | a0001c0002t0001g0124 a0001c0002t0002g0117 a0001c0002t0002g0139 others(1): Show |
4 | HG02258.hp1 HG02258.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-1544_540-1543d others(4): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277034 | ||||||
| chr22:46277034 | CATAT | C | 12 | a0001c0001t0002g0164 a0001c0002t0001g0135 a0001c0002t0001g0136 others(9): Show |
13 | HG00639.hp2 HG02486.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.540-1546_540-1543d others(6): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277034 | ||||||
| chr22:46277034 | CATATAT | C | 5 | a0001c0002t0002g0010 a0001c0002t0002g0034 a0001c0002t0002g0142 others(2): Show |
6 | HG02451.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.540-1548_540-1543d others(8): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277034 | ||||||
| chr22:46277036 | TATATATA others(1): Show |
T | 4 | a0001c0001t0002g0042 a0001c0002t0002g0010 a0001c0002t0002g0147 others(1): Show |
4 | HG01496.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-1546_540-1539d others(10): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277036 | ||||||
| chr22:46277038 | T | C | 1 | a0001c0002t0002g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.540-1548T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277038 | |||||||
| chr22:46277038 | TATATAC | T | 14 | a0001c0001t0010g0157 a0001c0002t0001g0029 a0001c0002t0001g0125 others(11): Show |
18 | HG00738.hp1 HG01070.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.540-1544_540-1539d others(8): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277038 | ||||||
| chr22:46277038 | TATATACA others(3): Show |
T | 5 | a0001c0002t0001g0009 a0001c0002t0001g0119 a0001c0002t0001g0120 others(2): Show |
6 | HG02145.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-1546_540-1537d others(12): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277038 | ||||||
| chr22:46277038 | TATATACA others(5): Show |
T | 2 | a0001c0002t0001g0154 a0001c0019t0001g0159 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.540-1546_540-1535d others(14): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277038 | ||||||
| chr22:46277038 | TATATACA others(7): Show |
T | 2 | a0001c0002t0001g0008 a0001c0020t0001g0008 |
3 | HG02723.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.540-1546_540-1533d others(16): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277038 | ||||||
| chr22:46277040 | T | C | 4 | a0001c0002t0002g0127 a0001c0002t0002g0148 a0001c0005t0002g0130 others(1): Show |
4 | HG01433.hp1 HG02738.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-1546T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277040 | |||||||
| chr22:46277040 | TATACATA others(13): Show |
T | 1 | a0003c0006t0005g0012 | 3 | HG02257.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.540-1544_540-1525d others(22): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277040 | ||||||
| chr22:46277042 | T | C | 11 | a0001c0002t0001g0124 a0001c0002t0002g0030 a0001c0002t0002g0117 others(8): Show |
12 | HG01433.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.540-1544T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277042 | |||||||
| chr22:46277042 | TACATACA others(1): Show |
T | 4 | a0001c0003t0001g0002 a0001c0003t0001g0150 a0001c0003t0001g0151 others(1): Show |
10 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.540-1540_540-1533d others(10): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277042 | ||||||
| chr22:46277042 | TACATACA others(3): Show |
T | 1 | a0001c0003t0001g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.540-1540_540-1531d others(12): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277042 | ||||||
| chr22:46277046 | T | C | 34 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0002t0001g0029 others(31): Show |
38 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.540-1540T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277046 | |||||||
| chr22:46277046 | T | TAC | 3 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0108 |
4 | HG02109.hp1 HG03017.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-1502_540-1501d others(4): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277046 | ||||||
| chr22:46277046 | TAC | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(77): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.540-1502_540-1501d others(4): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277046 | ||||||
| chr22:46277046 | TACAC | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0091 others(3): Show |
9 | HG01081.hp1 HG01884.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-1504_540-1501d others(6): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277046 | ||||||
| chr22:46277046 | TACACAC | T | 9 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0071 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.540-1506_540-1501d others(8): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277046 | ||||||
| chr22:46277046 | TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0098 a0001c0001t0009g0024 |
3 | HG00621.hp1 HG02015.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.540-1508_540-1501d others(10): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277046 | ||||||
| chr22:46277065 | A | T | 6 | a0001c0001t0010g0157 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG00738.hp1 HG01070.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-1521A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277065 | |||||||
| chr22:46277084 | C | T | 1 | a0003c0006t0005g0012 | 3 | HG02257.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.540-1502C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277084 | |||||||
| chr22:46277086 | T | C | 8 | a0001c0002t0002g0132 a0001c0005t0002g0128 a0001c0005t0002g0130 others(5): Show |
8 | HG02486.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.540-1500T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277086 | |||||||
| chr22:46277255 | A | G | 1 | a0003c0006t0005g0012 | 3 | HG02257.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.540-1331A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277255 | |||||||
| chr22:46277334 | A | G | 5 | a0001c0003t0001g0002 a0001c0003t0001g0150 a0001c0003t0001g0151 others(2): Show |
11 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.540-1252A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277334 | |||||||
| chr22:46277503 | A | G | 41 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0002t0001g0008 others(38): Show |
49 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(46): Show |
intron_variant | MODIFIER | c.540-1083A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277503 | |||||||
| chr22:46277605 | CA | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.540-957delA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277605 | ||||||
| chr22:46277605 | CAA | C | 33 | a0001c0001t0001g0055 a0001c0001t0001g0092 a0001c0001t0002g0164 others(30): Show |
40 | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.540-958_540-957del others(2): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277605 | ||||||
| chr22:46277605 | CAAA | C | 8 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0135 others(5): Show |
10 | HG01433.hp2 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.540-959_540-957del others(3): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277605 | ||||||
| chr22:46277605 | CAAAAAAA others(6): Show |
C | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0009c0022t0001g0118 |
3 | HG02145.hp1 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.540-969_540-957del others(13): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr22 | 46277605 | ||||||
| chr22:46277622 | A | T | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.540-964A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277622 | |||||||
| chr22:46277628 | A | G | 14 | a0001c0001t0002g0042 a0001c0002t0002g0010 a0001c0002t0002g0030 others(11): Show |
17 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.540-958A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277628 | |||||||
| chr22:46277659 | G | A | 41 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0002t0001g0008 others(38): Show |
49 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(46): Show |
intron_variant | MODIFIER | c.540-927G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277659 | |||||||
| chr22:46277794 | T | C | 4 | a0001c0001t0002g0164 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG02818.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-792T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277794 | |||||||
| chr22:46277851 | G | C | 1 | a0001c0008t0002g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.540-735G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277851 | |||||||
| chr22:46277874 | G | A | 41 | a0001c0001t0002g0042 a0001c0001t0002g0164 a0001c0002t0001g0008 others(38): Show |
49 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(46): Show |
intron_variant | MODIFIER | c.540-712G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277874 | |||||||
| chr22:46277878 | T | C | 1 | a0001c0002t0002g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.540-708T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277878 | |||||||
| chr22:46277958 | T | G | 5 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0154 others(2): Show |
5 | HG02145.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-628T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46277958 | |||||||
| chr22:46278315 | A | G | 42 | a0001c0001t0001g0022 a0001c0001t0002g0042 a0001c0001t0002g0164 others(39): Show |
50 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(47): Show |
intron_variant | MODIFIER | c.540-271A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 5/13 | chr22 | 46278315 | |||||||
| chr22:46278706 | C | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0091 a0001c0001t0001g0095 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.615+45C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46278706 | |||||||
| chr22:46278742 | G | A | 55 | a0001c0001t0001g0063 a0001c0001t0001g0075 a0001c0001t0001g0099 others(52): Show |
66 | HG00609.hp1 HG00639.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.615+81G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46278742 | |||||||
| chr22:46278934 | C | T | 1 | a0011c0021t0008g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.615+273C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46278934 | |||||||
| chr22:46279006 | G | A | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.615+345G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279006 | |||||||
| chr22:46279155 | T | C | 1 | a0011c0021t0008g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.615+494T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279155 | |||||||
| chr22:46279339 | G | A | 1 | a0001c0002t0002g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.615+678G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279339 | |||||||
| chr22:46279392 | C | T | 1 | a0001c0002t0002g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.615+731C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279392 | |||||||
| chr22:46279533 | G | T | 6 | a0001c0005t0002g0128 a0001c0005t0002g0130 a0001c0005t0002g0131 others(3): Show |
6 | HG02486.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+872G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279533 | |||||||
| chr22:46279584 | T | C | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.615+923T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279584 | |||||||
| chr22:46279628 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0107 a0001c0001t0011g0007 others(1): Show |
4 | HG00438.hp1 HG00673.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+967T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279628 | |||||||
| chr22:46279822 | C | G | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.615+1161C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279822 | |||||||
| chr22:46279823 | C | T | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.615+1162C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279823 | |||||||
| chr22:46279830 | G | A | 3 | a0001c0002t0002g0127 a0001c0002t0002g0129 a0001c0002t0002g0166 |
3 | HG00639.hp2 HG01433.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.615+1169G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279830 | |||||||
| chr22:46279979 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0093 |
3 | HG02132.hp2 NA18747.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.615+1318G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46279979 | |||||||
| chr22:46280046 | G | A | 1 | a0011c0021t0008g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.615+1385G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280046 | |||||||
| chr22:46280113 | C | G | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+1452C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280113 | |||||||
| chr22:46280271 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.616-1328C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280271 | |||||||
| chr22:46280306 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.616-1293C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280306 | |||||||
| chr22:46280307 | G | A | 4 | a0001c0001t0004g0038 a0001c0001t0004g0047 a0001c0001t0004g0048 others(1): Show |
4 | HG00323.hp2 HG00735.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-1292G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280307 | |||||||
| chr22:46280360 | T | C | 2 | a0001c0001t0002g0056 a0001c0002t0002g0142 |
2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.616-1239T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280360 | |||||||
| chr22:46280377 | G | C | 2 | a0001c0002t0002g0132 a0001c0002t0002g0140 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.616-1222G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280377 | |||||||
| chr22:46280520 | C | T | 1 | a0001c0002t0002g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.616-1079C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280520 | |||||||
| chr22:46280523 | G | A | 1 | a0001c0002t0002g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.616-1076G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280523 | |||||||
| chr22:46280553 | A | G | 1 | a0001c0001t0004g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.616-1046A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280553 | |||||||
| chr22:46280780 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.616-819C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280780 | |||||||
| chr22:46280962 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.616-637G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46280962 | |||||||
| chr22:46281106 | C | T | 22 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(19): Show |
25 | HG00639.hp2 HG01433.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.616-493C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46281106 | |||||||
| chr22:46281401 | G | A | 5 | a0002c0004t0003g0011 a0002c0004t0003g0031 a0002c0004t0003g0155 others(2): Show |
8 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.616-198G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46281401 | |||||||
| chr22:46281474 | C | T | 6 | a0001c0005t0002g0128 a0001c0005t0002g0130 a0001c0005t0002g0131 others(3): Show |
6 | HG02486.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-125C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46281474 | |||||||
| chr22:46281517 | C | T | 8 | a0001c0002t0001g0009 a0001c0002t0001g0119 a0001c0002t0001g0120 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.616-82C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46281517 | |||||||
| chr22:46281532 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.616-67C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46281532 | |||||||
| chr22:46281533 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.616-66G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46281533 | |||||||
| chr22:46281586 | G | A | 3 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 |
3 | HG02818.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.616-13G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 6/13 | chr22 | 46281586 | |||||||
| chr22:46281806 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.735+88G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46281806 | |||||||
| chr22:46281823 | G | A | 14 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0002t0002g0010 others(11): Show |
17 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.735+105G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46281823 | |||||||
| chr22:46281851 | C | T | 3 | a0001c0002t0002g0132 a0001c0002t0002g0140 a0001c0008t0002g0161 |
3 | HG02717.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.735+133C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46281851 | |||||||
| chr22:46281966 | T | C | 8 | a0001c0002t0001g0009 a0001c0002t0001g0119 a0001c0002t0001g0120 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+248T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46281966 | |||||||
| chr22:46281969 | AG | A | 3 | a0001c0002t0002g0132 a0001c0002t0002g0140 a0001c0008t0002g0161 |
3 | HG02717.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.735+254delG | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 46281969 | ||||||
| chr22:46282007 | A | G | 29 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(26): Show |
35 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.735+289A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46282007 | |||||||
| chr22:46282100 | G | A | 26 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(23): Show |
29 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.735+382G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46282100 | |||||||
| chr22:46282491 | A | T | 1 | a0002c0004t0003g0156 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.735+773A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46282491 | |||||||
| chr22:46282718 | A | C | 62 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(59): Show |
79 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.735+1000A>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46282718 | |||||||
| chr22:46282769 | A | G | 27 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(24): Show |
30 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.735+1051A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46282769 | |||||||
| chr22:46283097 | T | TA | 7 | a0001c0002t0001g0008 a0001c0002t0001g0135 a0001c0002t0001g0136 others(4): Show |
8 | HG01433.hp2 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.736-869dupA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 46283097 | ||||||
| chr22:46283104 | AT | A | 8 | a0001c0002t0001g0009 a0001c0002t0001g0119 a0001c0002t0001g0120 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.736-857delT | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 46283104 | ||||||
| chr22:46283105 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.736-868T>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283105 | |||||||
| chr22:46283462 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.736-511A>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283462 | |||||||
| chr22:46283526 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.736-447A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283526 | |||||||
| chr22:46283579 | C | T | 6 | a0001c0002t0001g0008 a0001c0002t0001g0135 a0001c0002t0001g0136 others(3): Show |
7 | HG01433.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-394C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283579 | |||||||
| chr22:46283722 | C | T | 5 | a0002c0004t0003g0011 a0002c0004t0003g0031 a0002c0004t0003g0155 others(2): Show |
8 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.736-251C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283722 | |||||||
| chr22:46283760 | G | T | 26 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(23): Show |
29 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.736-213G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283760 | |||||||
| chr22:46283851 | C | CA | 13 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0091 others(10): Show |
13 | HG01081.hp1 HG01106.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.736-95dupA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 46283851 | ||||||
| chr22:46283851 | C | CAA | 6 | a0001c0002t0001g0009 a0001c0002t0001g0120 a0001c0002t0001g0121 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.736-96_736-95dupAA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 46283851 | ||||||
| chr22:46283851 | CA | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(38): Show |
51 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.736-95delA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 46283851 | ||||||
| chr22:46283851 | CAA | C | 23 | a0001c0001t0001g0054 a0001c0001t0002g0042 a0001c0001t0002g0056 others(20): Show |
30 | HG01070.hp2 HG01433.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.736-96_736-95delAA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 46283851 | ||||||
| chr22:46283941 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.736-32T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283941 | |||||||
| chr22:46283951 | C | CT | 2 | a0001c0002t0002g0149 a0011c0021t0008g0033 |
2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.736-21dupT | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr22 | 46283951 | ||||||
| chr22:46283953 | C | CG | 11 | a0001c0002t0001g0009 a0001c0002t0001g0119 a0001c0002t0001g0120 others(8): Show |
12 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.736-20_736-19insG | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283953 | |||||||
| chr22:46283953 | C | G | 2 | a0001c0002t0002g0149 a0011c0021t0008g0033 |
2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.736-20C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283953 | |||||||
| chr22:46283953 | C | T | 24 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(21): Show |
27 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.736-20C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283953 | |||||||
| chr22:46283954 | T | G | 44 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(41): Show |
54 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.736-19T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 7/13 | chr22 | 46283954 | |||||||
| chr22:46284075 | G | A | 1 | a0001c0002t0002g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.795+43G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284075 | |||||||
| chr22:46284086 | G | C | 6 | a0001c0005t0002g0128 a0001c0005t0002g0130 a0001c0005t0002g0131 others(3): Show |
6 | HG02486.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.795+54G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284086 | |||||||
| chr22:46284123 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.795+91G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284123 | |||||||
| chr22:46284124 | T | G | 27 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(24): Show |
30 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.795+92T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284124 | |||||||
| chr22:46284170 | T | C | 57 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(54): Show |
68 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(65): Show |
intron_variant | MODIFIER | c.795+138T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284170 | |||||||
| chr22:46284538 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.795+506A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284538 | |||||||
| chr22:46284729 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.796-512A>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284729 | |||||||
| chr22:46284737 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.796-504G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284737 | |||||||
| chr22:46284737 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0085 |
2 | HG01167.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.796-504G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284737 | |||||||
| chr22:46284799 | G | A | 5 | a0002c0004t0003g0011 a0002c0004t0003g0031 a0002c0004t0003g0155 others(2): Show |
8 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.796-442G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284799 | |||||||
| chr22:46284868 | CA | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.796-351delA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr22 | 46284868 | ||||||
| chr22:46284868 | CAA | C | 5 | a0001c0001t0001g0087 a0001c0001t0001g0097 a0001c0001t0001g0101 others(2): Show |
5 | HG00323.hp1 HG01081.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.796-352_796-351del others(2): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr22 | 46284868 | ||||||
| chr22:46284872 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.796-369A>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284872 | |||||||
| chr22:46284907 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.796-334A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46284907 | |||||||
| chr22:46285009 | C | T | 3 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 |
3 | HG02818.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.796-232C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 8/13 | chr22 | 46285009 | |||||||
| chr22:46285606 | AT | A | 33 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(30): Show |
37 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.834+341delT | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 46285606 | ||||||
| chr22:46285737 | G | T | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.834+458G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46285737 | |||||||
| chr22:46285748 | C | A | 6 | a0001c0001t0002g0164 a0001c0002t0002g0127 a0001c0002t0002g0129 others(3): Show |
6 | HG00639.hp2 HG01433.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.834+469C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46285748 | |||||||
| chr22:46285876 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0112 |
2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.834+597G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46285876 | |||||||
| chr22:46286014 | C | CAAAA | 8 | a0001c0002t0001g0009 a0001c0002t0001g0119 a0001c0002t0001g0120 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.834+749_834+752dup others(4): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 46286014 | ||||||
| chr22:46286014 | C | CAAAAA | 3 | a0001c0005t0002g0133 a0003c0006t0005g0012 a0004c0007t0005g0015 |
6 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.834+748_834+752dup others(5): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 46286014 | ||||||
| chr22:46286014 | C | CAAAAAA | 9 | a0001c0001t0004g0047 a0001c0001t0004g0048 a0001c0002t0002g0034 others(6): Show |
9 | HG00323.hp2 HG01257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.834+747_834+752dup others(6): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 46286014 | ||||||
| chr22:46286014 | C | CAAAAAAA | 61 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0016 others(58): Show |
81 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.834+746_834+752dup others(7): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 46286014 | ||||||
| chr22:46286014 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0004g0038 a0001c0001t0004g0049 a0001c0002t0001g0135 others(3): Show |
7 | HG00735.hp1 HG01175.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+745_834+752dup others(8): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 46286014 | ||||||
| chr22:46286014 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0001g0138 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.834+743_834+752dup others(10): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 46286014 | ||||||
| chr22:46286262 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0057 |
3 | HG02280.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835-811G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46286262 | |||||||
| chr22:46286311 | C | A | 8 | a0001c0002t0001g0009 a0001c0002t0001g0119 a0001c0002t0001g0120 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.835-762C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46286311 | |||||||
| chr22:46286389 | G | A | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.835-684G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46286389 | |||||||
| chr22:46286413 | C | G | 17 | a0001c0002t0001g0008 a0001c0002t0001g0135 a0001c0002t0001g0136 others(14): Show |
21 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.835-660C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46286413 | |||||||
| chr22:46286490 | A | G | 3 | a0001c0001t0001g0083 a0003c0006t0005g0012 a0004c0007t0005g0015 |
6 | HG00609.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-583A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46286490 | |||||||
| chr22:46286617 | C | T | 1 | a0001c0002t0002g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.835-456C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46286617 | |||||||
| chr22:46286661 | C | CA | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-396dupA | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 46286661 | ||||||
| chr22:46286872 | ACCTGGTG others(6): Show |
A | 1 | a0001c0001t0001g0104 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.835-199_835-187del others(13): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr22 | 46286872 | ||||||
| chr22:46287040 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.835-33C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46287040 | |||||||
| chr22:46287058 | C | T | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.835-15C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 9/13 | chr22 | 46287058 | |||||||
| chr22:46287218 | T | G | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+64T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46287218 | |||||||
| chr22:46287241 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0058 |
3 | HG02109.hp1 HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.916+87C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46287241 | |||||||
| chr22:46287302 | C | A | 1 | a0002c0004t0003g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.916+148C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46287302 | |||||||
| chr22:46287327 | C | G | 1 | a0001c0019t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.916+173C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46287327 | |||||||
| chr22:46287388 | G | A | 6 | a0001c0005t0002g0128 a0001c0005t0002g0130 a0001c0005t0002g0131 others(3): Show |
6 | HG02486.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.916+234G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46287388 | |||||||
| chr22:46287608 | G | A | 1 | a0001c0002t0002g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.916+454G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46287608 | |||||||
| chr22:46287725 | A | C | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+571A>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46287725 | |||||||
| chr22:46287822 | G | C | 1 | a0011c0021t0008g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.917-601G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46287822 | |||||||
| chr22:46287933 | C | T | 1 | a0001c0005t0002g0128 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.917-490C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46287933 | |||||||
| chr22:46288036 | G | A | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-387G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46288036 | |||||||
| chr22:46288373 | A | G | 1 | a0011c0021t0008g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.917-50A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 10/13 | chr22 | 46288373 | |||||||
| chr22:46288631 | C | T | 5 | a0002c0004t0003g0011 a0002c0004t0003g0031 a0002c0004t0003g0155 others(2): Show |
8 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1082+43C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288631 | |||||||
| chr22:46288661 | T | C | 57 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(54): Show |
68 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(65): Show |
intron_variant | MODIFIER | c.1082+73T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288661 | |||||||
| chr22:46288674 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1082+86G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288674 | |||||||
| chr22:46288754 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1082+166C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288754 | |||||||
| chr22:46288759 | G | T | 1 | a0001c0002t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1082+171G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288759 | |||||||
| chr22:46288781 | A | G | 57 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(54): Show |
68 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(65): Show |
intron_variant | MODIFIER | c.1082+193A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288781 | |||||||
| chr22:46288809 | C | G | 7 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(4): Show |
10 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1082+221C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288809 | |||||||
| chr22:46288911 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1082+323C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288911 | |||||||
| chr22:46288943 | C | T | 1 | a0011c0021t0008g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1082+355C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288943 | |||||||
| chr22:46288974 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1082+386C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288974 | |||||||
| chr22:46288992 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1082+404G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288992 | |||||||
| chr22:46288993 | A | G | 7 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(4): Show |
10 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1082+405A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46288993 | |||||||
| chr22:46289009 | G | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0081 |
2 | HG02300.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1083-393G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289009 | |||||||
| chr22:46289056 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0052 |
3 | HG01109.hp1 HG01943.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1083-346C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289056 | |||||||
| chr22:46289120 | G | A | 27 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(24): Show |
31 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.1083-282G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289120 | |||||||
| chr22:46289176 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1083-226A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289176 | |||||||
| chr22:46289207 | G | A | 1 | a0001c0001t0010g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1083-195G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289207 | |||||||
| chr22:46289234 | A | G | 7 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(4): Show |
10 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1083-168A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289234 | |||||||
| chr22:46289352 | G | A | 27 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(24): Show |
31 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.1083-50G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289352 | |||||||
| chr22:46289377 | T | C | 7 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(4): Show |
10 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1083-25T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289377 | |||||||
| chr22:46289387 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1083-15G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289387 | |||||||
| chr22:46289397 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03710.hp2 | splice_region_variant&intron_variant | LOW | c.1083-5C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 11/13 | chr22 | 46289397 | |||||||
| chr22:46289617 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(16): Show |
25 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1242+56G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 12/13 | chr22 | 46289617 | |||||||
| chr22:46289653 | G | A | 1 | a0002c0004t0003g0158 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1242+92G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 12/13 | chr22 | 46289653 | |||||||
| chr22:46289666 | G | A | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1242+105G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 12/13 | chr22 | 46289666 | |||||||
| chr22:46289706 | C | T | 5 | a0001c0003t0001g0002 a0001c0003t0001g0150 a0001c0003t0001g0151 others(2): Show |
11 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1243-120C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 12/13 | chr22 | 46289706 | |||||||
| chr22:46289707 | G | A | 1 | a0001c0002t0002g0129 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1243-119G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 12/13 | chr22 | 46289707 | |||||||
| chr22:46289726 | C | T | 1 | a0001c0002t0002g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1243-100C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 12/13 | chr22 | 46289726 | |||||||
| chr22:46289727 | A | G | 16 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0002t0001g0009 others(13): Show |
20 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1243-99A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 12/13 | chr22 | 46289727 | |||||||
| chr22:46289765 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1243-61C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 12/13 | chr22 | 46289765 | |||||||
| chr22:46290066 | G | A | 62 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(59): Show |
79 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.1316+167G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290066 | |||||||
| chr22:46290164 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1316+265C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290164 | |||||||
| chr22:46290198 | G | C | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1316+299G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290198 | |||||||
| chr22:46290218 | T | G | 7 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(4): Show |
10 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1316+319T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290218 | |||||||
| chr22:46290222 | T | A | 7 | a0001c0002t0001g0008 a0001c0002t0001g0135 a0001c0002t0001g0136 others(4): Show |
8 | HG01433.hp2 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1316+323T>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290222 | |||||||
| chr22:46290319 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1316+420A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290319 | |||||||
| chr22:46290356 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0081 |
2 | HG02300.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1316+457A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290356 | |||||||
| chr22:46290431 | C | G | 19 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(16): Show |
25 | HG01070.hp2 HG01106.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1316+532C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290431 | |||||||
| chr22:46290466 | G | GTAGGAGG others(81): Show |
24 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(21): Show |
28 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.1316+578_1316+579i others(90): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290466 | ||||||
| chr22:46290466 | G | GTAGGAGG others(81): Show |
1 | a0011c0021t0008g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1316+578_1316+579i others(90): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290466 | ||||||
| chr22:46290466 | G | GTAGGAGG others(52): Show |
1 | a0004c0007t0005g0015 | 2 | HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1316+578_1316+579i others(61): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290466 | ||||||
| chr22:46290466 | GTAGGAGG others(78): Show |
G | 7 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316+579_1316+663d others(87): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290466 | ||||||
| chr22:46290478 | C | T | 39 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(36): Show |
48 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.1316+579C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290478 | |||||||
| chr22:46290480 | T | G | 15 | a0001c0002t0002g0142 a0001c0005t0002g0128 a0001c0005t0002g0130 others(12): Show |
20 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1316+581T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290480 | |||||||
| chr22:46290486 | G | C | 14 | a0001c0002t0002g0142 a0001c0005t0002g0128 a0001c0005t0002g0130 others(11): Show |
19 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.1316+587G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290486 | |||||||
| chr22:46290498 | T | TAGG | 12 | a0001c0005t0002g0128 a0001c0005t0002g0130 a0001c0005t0002g0131 others(9): Show |
15 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1316+600_1316+602d others(5): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290498 | ||||||
| chr22:46290498 | T | TAGGAGGG others(77): Show |
1 | a0001c0002t0002g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1316+602_1316+603i others(86): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290498 | ||||||
| chr22:46290506 | C | T | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+607C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290506 | |||||||
| chr22:46290507 | A | G | 38 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(35): Show |
45 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1316+608A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290507 | |||||||
| chr22:46290508 | T | G | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+609T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290508 | |||||||
| chr22:46290521 | AGT | A | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+627_1316+628d others(4): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290521 | ||||||
| chr22:46290524 | G | GT | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316+626dupT | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290524 | ||||||
| chr22:46290526 | G | A | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316+627G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290526 | |||||||
| chr22:46290527 | T | G | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316+628T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290527 | |||||||
| chr22:46290528 | T | G | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316+629T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290528 | |||||||
| chr22:46290533 | C | T | 8 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(5): Show |
14 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1316+634C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290533 | |||||||
| chr22:46290534 | A | G | 8 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(5): Show |
14 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1316+635A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290534 | |||||||
| chr22:46290537 | G | A | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+638G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290537 | |||||||
| chr22:46290547 | G | GGTGA | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316+651_1316+652i others(6): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290547 | ||||||
| chr22:46290550 | G | GAGT | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+651_1316+652i others(5): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290550 | |||||||
| chr22:46290551 | T | G | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+652T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290551 | |||||||
| chr22:46290553 | A | G | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+654A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290553 | |||||||
| chr22:46290554 | G | T | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+655G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290554 | |||||||
| chr22:46290555 | G | T | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+656G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290555 | |||||||
| chr22:46290560 | T | C | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+661T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290560 | |||||||
| chr22:46290561 | G | A | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+662G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290561 | |||||||
| chr22:46290563 | T | C | 8 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(5): Show |
14 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1316+664T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290563 | |||||||
| chr22:46290563 | TGTGGCTG others(24): Show |
T | 1 | a0001c0002t0001g0138 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1316+705_1316+735d others(33): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290563 | ||||||
| chr22:46290565 | T | G | 7 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316+666T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290565 | |||||||
| chr22:46290571 | G | C | 7 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316+672G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290571 | |||||||
| chr22:46290574 | GGTGA | G | 6 | a0001c0016t0007g0032 a0002c0004t0003g0011 a0002c0004t0003g0031 others(3): Show |
9 | HG01070.hp2 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+679_1316+682d others(6): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290574 | ||||||
| chr22:46290583 | TAGG | T | 32 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(29): Show |
36 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.1316+688_1316+690d others(5): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290583 | ||||||
| chr22:46290586 | G | GAGGGTGG others(52): Show |
2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316+725_1316+726i others(61): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290586 | ||||||
| chr22:46290594 | C | T | 7 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316+695C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290594 | |||||||
| chr22:46290596 | T | G | 7 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316+697T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290596 | |||||||
| chr22:46290614 | TAGGAGGG others(84): Show |
T | 7 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316+719_1316+809d others(93): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46290614 | ||||||
| chr22:46290862 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1316+963G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290862 | |||||||
| chr22:46290895 | C | G | 62 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(59): Show |
79 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.1316+996C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290895 | |||||||
| chr22:46290931 | T | C | 1 | a0001c0002t0002g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1316+1032T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290931 | |||||||
| chr22:46290932 | C | T | 3 | a0001c0002t0002g0132 a0001c0002t0002g0140 a0001c0008t0002g0161 |
3 | HG02717.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1316+1033C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46290932 | |||||||
| chr22:46291044 | A | C | 1 | a0001c0016t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1316+1145A>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291044 | |||||||
| chr22:46291079 | T | C | 6 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316+1180T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291079 | |||||||
| chr22:46291245 | G | A | 4 | a0001c0005t0002g0130 a0001c0005t0002g0131 a0001c0005t0002g0133 others(1): Show |
4 | HG02486.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316+1346G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291245 | |||||||
| chr22:46291288 | G | C | 16 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0002t0001g0009 others(13): Show |
20 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1316+1389G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291288 | |||||||
| chr22:46291315 | A | G | 62 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(59): Show |
79 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.1316+1416A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291315 | |||||||
| chr22:46291323 | G | A | 31 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(28): Show |
35 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.1316+1424G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291323 | |||||||
| chr22:46291356 | G | A | 7 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1317-1435G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291356 | |||||||
| chr22:46291371 | G | A | 31 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(28): Show |
35 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.1317-1420G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291371 | |||||||
| chr22:46291553 | C | A | 2 | a0003c0006t0005g0012 a0004c0007t0005g0015 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1317-1238C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291553 | |||||||
| chr22:46291563 | T | G | 54 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(51): Show |
65 | HG00639.hp2 HG01070.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1317-1228T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291563 | |||||||
| chr22:46291784 | G | C | 4 | a0002c0004t0003g0011 a0002c0004t0003g0155 a0002c0004t0003g0156 others(1): Show |
6 | HG01070.hp2 HG01106.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317-1007G>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291784 | |||||||
| chr22:46291861 | C | A | 29 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(26): Show |
32 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.1317-930C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291861 | |||||||
| chr22:46291951 | A | G | 1 | a0001c0002t0002g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1317-840A>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291951 | |||||||
| chr22:46291962 | TTAAAAAA | T | 31 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(28): Show |
35 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.1317-823_1317-817d others(9): Show |
TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr22 | 46291962 | ||||||
| chr22:46291994 | T | G | 6 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317-797T>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46291994 | |||||||
| chr22:46292311 | C | A | 31 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(28): Show |
35 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.1317-480C>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46292311 | |||||||
| chr22:46292423 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1317-368C>G | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46292423 | |||||||
| chr22:46292424 | T | C | 31 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0164 others(28): Show |
35 | HG00639.hp2 HG01433.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.1317-367T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46292424 | |||||||
| chr22:46292516 | G | A | 6 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317-275G>A | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46292516 | |||||||
| chr22:46292525 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1317-266T>C | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46292525 | |||||||
| chr22:46292667 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1317-124C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46292667 | |||||||
| chr22:46292699 | C | T | 16 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0002t0001g0009 others(13): Show |
20 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1317-92C>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46292699 | |||||||
| chr22:46292736 | G | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
6 | HG00280.hp2 HG02015.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317-55G>T | TTC38 | ENSG00000075234.17 | transcript | ENST00000381031.8 | protein_coding | 13/13 | chr22 | 46292736 |