Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55761 |
| ensemblid | ENSG00000052841.16 |
| hgncid | 25596 |
| symbol | TTC17 |
| name | tetratricopeptide repeat domain 17 |
| refseq_nuc | NM_018259.6 |
| refseq_prot | NP_060729.2 |
| ensembl_nuc | ENST00000039989.9 |
| ensembl_prot | ENSP00000039989.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 43358920 |
| end | 43494931 |
| strand | + |
| ver | v1.2 |
| region | chr11:43358920-43494931 |
| region5000 | chr11:43353920-43499931 |
| regionname0 | TTC17_chr11_43358920_43494931 |
| regionname5000 | TTC17_chr11_43353920_43499931 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1141 | 271 | 54 | 64 | 101 | 14 | 36 | 77 | TTC17_chr11_43353920_43499931 | TTC17 | MAAAV others(1136): Show |
chr11 | 43353920 | 43499931 |
| a0002 | 0/0 | 1141 | 21 | 19 | 2 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | MAAAV others(1136): Show |
chr11 | 43353920 | 43499931 |
| a0003 | 0/0 | 1141 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | MAAAV others(1136): Show |
chr11 | 43353920 | 43499931 |
| a0004 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | MAAAV others(1136): Show |
chr11 | 43353920 | 43499931 |
| a0005 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | MAAAV others(1136): Show |
chr11 | 43353920 | 43499931 |
| a0006 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | MAAAV others(1136): Show |
chr11 | 43353920 | 43499931 |
| a0007 | 0/0 | 1141 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | MAAAV others(1136): Show |
chr11 | 43353920 | 43499931 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3423 | 246 | 53 | 50 | 94 | 14 | 34 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 | ||
| a0001c0002 | 0/1 | 3423 | 23 | 0 | 13 | 7 | 0 | 2 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 | ||
| a0001c0006 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 | ||
| a0001c0008 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 | ||
| a0002c0003 | 0/0 | 3423 | 21 | 19 | 2 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 | ||
| a0003c0004 | 0/0 | 3423 | 2 | 2 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 | ||
| a0004c0009 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 | ||
| a0005c0010 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 | ||
| a0006c0005 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 | ||
| a0007c0007 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | ATGGC others(3418): Show |
chr11 | 43353920 | 43499931 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4488 | 225 | 53 | 46 | 84 | 11 | 30 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0001c0001t0003 | 0/0 | 4488 | 13 | 0 | 2 | 7 | 3 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0001c0001t0004 | 0/0 | 4488 | 3 | 0 | 2 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0001c0001t0005 | 0/0 | 4488 | 3 | 0 | 0 | 3 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0001c0001t0007 | 0/0 | 4488 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0001c0001t0008 | 0/0 | 4488 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0001c0002t0001 | 0/1 | 4488 | 23 | 0 | 13 | 7 | 0 | 2 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0001c0006t0001 | 0/0 | 4488 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0001c0008t0006 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0002c0003t0001 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0002c0003t0002 | 0/0 | 4488 | 20 | 18 | 2 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0003c0004t0001 | 0/0 | 4488 | 2 | 2 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0004c0009t0001 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0005c0010t0001 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0006c0005t0001 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| a0007c0007t0001 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | GCTTC others(4483): Show |
chr11 | 43353920 | 43499931 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0006t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0008t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0003c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0003c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0004c0009t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0005c0010t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0006c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0007c0007t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0093 | EUR | GBR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00738 | hp1 | a0001 | c0006 | t0001 | g0200 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0218 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01496 | hp2 | a0002 | c0003 | t0002 | g0213 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0031 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0220 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01891 | hp2 | a0003 | c0004 | t0001 | g0246 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02622 | hp1 | a0002 | c0003 | t0002 | g0225 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02717 | hp1 | a0002 | c0003 | t0002 | g0215 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02809 | hp1 | a0002 | c0003 | t0002 | g0214 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02818 | hp1 | a0002 | c0003 | t0002 | g0224 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02897 | hp2 | a0002 | c0003 | t0002 | g0051 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02922 | hp1 | a0002 | c0003 | t0002 | g0222 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02965 | hp1 | a0002 | c0003 | t0002 | g0210 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02970 | hp2 | a0002 | c0003 | t0002 | g0211 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0208 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0219 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03195 | hp1 | a0001 | c0008 | t0006 | g0064 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03195 | hp2 | a0002 | c0003 | t0002 | g0212 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03516 | hp1 | a0002 | c0003 | t0002 | g0209 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0226 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0149 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04199 | hp2 | a0001 | c0001 | t0008 | g0088 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0247 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18943 | hp2 | a0004 | c0009 | t0001 | g0186 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18979 | hp2 | a0005 | c0010 | t0001 | g0119 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19084 | hp1 | a0006 | c0005 | t0001 | g0274 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19240 | hp2 | a0002 | c0003 | t0002 | g0217 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | TSI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | GIH | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | GIH | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02109 | hp2 | a0002 | c0003 | t0002 | g0216 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02559 | hp2 | a0002 | c0003 | t0002 | g0221 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03471 | hp2 | a0002 | c0003 | t0002 | g0003 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | USA | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0223 | AFR | USA | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA21309 | hp2 | a0007 | c0007 | t0001 | g0046 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0249 | REF | REF | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0084 | REF | REF | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43359060 | G | A | 1 | a0006 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.106G>A | p.Ala36Thr | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/24 | 141/4488 | 106/3426 | 36/1141 | chr11 | 43359060 | |||
| chr11:43391478 | A | C | 1 | a0002 | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
missense_variant | MODERATE | c.433A>C | p.Ile145Leu | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/24 | 468/4488 | 433/3426 | 145/1141 | chr11 | 43391478 | |||
| chr11:43405577 | G | A | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1543G>A | p.Val515Ile | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 12/24 | 1578/4488 | 1543/3426 | 515/1141 | chr11 | 43405577 | |||
| chr11:43443511 | G | T | 1 | a0003 | 2 | HG01891.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.2438G>T | p.Gly813Val | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 17/24 | 2473/4488 | 2438/3426 | 813/1141 | chr11 | 43443511 | |||
| chr11:43448010 | C | T | 1 | a0005 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.2674C>T | p.Arg892Cys | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/24 | 2709/4488 | 2674/3426 | 892/1141 | chr11 | 43448010 | |||
| chr11:43490341 | G | T | 1 | a0004 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.3133G>T | p.Ala1045Ser | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/24 | 3168/4488 | 3133/3426 | 1045/1141 | chr11 | 43490341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43359083 | C | A | 1 | a0001c0006 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.129C>A | p.Val43Val | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/24 | 164/4488 | 129/3426 | 43/1141 | chr11 | 43359083 | |||
| chr11:43444109 | T | C | 1 | a0001c0008 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2565T>C | p.Thr855Thr | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/24 | 2600/4488 | 2565/3426 | 855/1141 | chr11 | 43444109 | |||
| chr11:43451196 | C | T | 3 | a0001c0002 a0001c0006 a0004c0009 |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
synonymous_variant | LOW | c.2961C>T | p.Leu987Leu | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/24 | 2996/4488 | 2961/3426 | 987/1141 | chr11 | 43451196 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43493945 | A | T | 1 | a0001c0001t0005 | 3 | HG00609.hp2 HG02040.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*41A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 41 | chr11 | 43493945 | ||||||
| chr11:43494313 | A | G | 1 | a0001c0001t0008 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 409 | chr11 | 43494313 | ||||||
| chr11:43494358 | G | A | 1 | a0001c0008t0006 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 454 | chr11 | 43494358 | ||||||
| chr11:43494375 | T | G | 2 | a0001c0001t0003 a0001c0001t0008 |
14 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*471T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 471 | chr11 | 43494375 | ||||||
| chr11:43494489 | A | G | 1 | a0002c0003t0002 | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*585A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 585 | chr11 | 43494489 | ||||||
| chr11:43494547 | A | C | 1 | a0001c0001t0004 | 3 | HG00639.hp2 HG01106.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*643A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 643 | chr11 | 43494547 | ||||||
| chr11:43494765 | T | C | 1 | a0001c0001t0007 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*861T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 861 | chr11 | 43494765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43359272 | C | A | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.159+159C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359272 | |||||||
| chr11:43359440 | G | A | 1 | a0002c0003t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.159+327G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359440 | |||||||
| chr11:43359446 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.159+333C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359446 | |||||||
| chr11:43359484 | C | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.159+371C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359484 | |||||||
| chr11:43359748 | C | G | 1 | a0001c0002t0001g0294 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.159+635C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359748 | |||||||
| chr11:43359750 | G | A | 1 | a0001c0002t0001g0294 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.159+637G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359750 | |||||||
| chr11:43359775 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.159+662G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359775 | |||||||
| chr11:43359867 | C | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG01346.hp1 HG01496.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+754C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359867 | |||||||
| chr11:43360108 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.159+995G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360108 | |||||||
| chr11:43360122 | GTGTAATG others(2): Show |
G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+1011_159+1019d others(11): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43360122 | ||||||
| chr11:43360165 | A | T | 1 | a0001c0001t0001g0293 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.159+1052A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360165 | |||||||
| chr11:43360185 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.159+1072C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360185 | |||||||
| chr11:43360203 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.159+1090A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360203 | |||||||
| chr11:43360377 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.159+1264A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360377 | |||||||
| chr11:43360418 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.159+1305T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360418 | |||||||
| chr11:43360663 | A | G | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+1550A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360663 | |||||||
| chr11:43360709 | A | AT | 6 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
6 | HG01884.hp2 HG02080.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+1612dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43360709 | ||||||
| chr11:43360709 | AT | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(34): Show |
37 | HG01069.hp1 HG01069.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.159+1612delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43360709 | ||||||
| chr11:43360742 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.159+1629T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360742 | |||||||
| chr11:43360777 | G | T | 23 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(20): Show |
23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.159+1664G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360777 | |||||||
| chr11:43360793 | A | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(4): Show |
7 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+1680A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360793 | |||||||
| chr11:43360809 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.159+1696C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360809 | |||||||
| chr11:43360838 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.159+1725T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360838 | |||||||
| chr11:43360877 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.159+1764G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360877 | |||||||
| chr11:43360895 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.159+1782C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360895 | |||||||
| chr11:43361178 | C | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(59): Show |
62 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.159+2065C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361178 | |||||||
| chr11:43361332 | C | T | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.159+2219C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361332 | |||||||
| chr11:43361397 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.159+2284G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361397 | |||||||
| chr11:43361481 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.159+2368A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361481 | |||||||
| chr11:43361733 | A | T | 5 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(2): Show |
5 | NA18940.hp1 NA18967.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+2620A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361733 | |||||||
| chr11:43361777 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.159+2664G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361777 | |||||||
| chr11:43361848 | T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.159+2735T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361848 | |||||||
| chr11:43361868 | C | A | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.159+2755C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361868 | |||||||
| chr11:43361978 | C | CT | 23 | a0001c0001t0001g0030 a0001c0001t0001g0290 a0001c0002t0001g0294 others(20): Show |
23 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.159+2884dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43361978 | ||||||
| chr11:43361978 | CT | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0068 others(7): Show |
10 | HG02145.hp2 HG02486.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.159+2884delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43361978 | ||||||
| chr11:43362061 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.159+2948A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362061 | |||||||
| chr11:43362149 | T | G | 1 | a0001c0001t0001g0248 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.159+3036T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362149 | |||||||
| chr11:43362149 | T | TTG | 17 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0145 others(14): Show |
17 | HG00099.hp2 HG01255.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.159+3080_159+3081d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | T | TTGTG | 16 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0065 others(13): Show |
16 | HG00609.hp1 HG00741.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.159+3078_159+3081d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | T | TTGTGTG | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG02486.hp1 NA18979.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+3076_159+3081d others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.159+3072_159+3081d others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | TTG | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(33): Show |
36 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.159+3080_159+3081d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | TTGTG | T | 88 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(85): Show |
88 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.159+3078_159+3081d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | TTGTGTG | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
34 | HG00438.hp2 HG00639.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.159+3076_159+3081d others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | TTGTGTGT others(1): Show |
T | 6 | a0001c0001t0001g0075 a0001c0001t0001g0112 a0001c0001t0001g0133 others(3): Show |
6 | HG00408.hp2 HG00438.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+3074_159+3081d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0115 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.159+3072_159+3081d others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.159+3070_159+3081d others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | TTGTGTGT others(7): Show |
T | 16 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0190 others(13): Show |
16 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.159+3068_159+3081d others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | TTGTGTGT others(9): Show |
T | 8 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0192 others(5): Show |
8 | HG00735.hp1 HG01070.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+3066_159+3081d others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362149 | TTGTGTGT others(11): Show |
T | 1 | a0002c0003t0002g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.159+3064_159+3081d others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | ||||||
| chr11:43362177 | G | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0184 |
2 | HG00438.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.159+3064G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362177 | |||||||
| chr11:43362179 | G | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0184 |
2 | HG00438.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.159+3066G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362179 | |||||||
| chr11:43362261 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.159+3148C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362261 | |||||||
| chr11:43362355 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+3242A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362355 | |||||||
| chr11:43362454 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159+3341G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362454 | |||||||
| chr11:43362898 | A | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
156 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.159+3785A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362898 | |||||||
| chr11:43363000 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.159+3887A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363000 | |||||||
| chr11:43363036 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.159+3923G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363036 | |||||||
| chr11:43363383 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.159+4270A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363383 | |||||||
| chr11:43363404 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.159+4291G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363404 | |||||||
| chr11:43363544 | A | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.159+4431A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363544 | |||||||
| chr11:43363621 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+4508C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363621 | |||||||
| chr11:43363800 | T | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG03688.hp2 HG03834.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.159+4687T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363800 | |||||||
| chr11:43363979 | A | T | 8 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(5): Show |
8 | HG01070.hp2 HG01081.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+4866A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363979 | |||||||
| chr11:43364047 | C | CT | 53 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0036 others(50): Show |
53 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.159+4960dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43364047 | ||||||
| chr11:43364047 | CT | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0052 others(29): Show |
32 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.159+4960delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43364047 | ||||||
| chr11:43364225 | T | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+5112T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364225 | |||||||
| chr11:43364295 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.159+5182G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364295 | |||||||
| chr11:43364407 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+5294T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364407 | |||||||
| chr11:43364512 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.159+5399G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364512 | |||||||
| chr11:43364951 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.159+5838A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364951 | |||||||
| chr11:43365146 | G | T | 1 | a0001c0002t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.159+6033G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365146 | |||||||
| chr11:43365250 | A | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.159+6137A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365250 | |||||||
| chr11:43365303 | A | G | 1 | a0001c0006t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.159+6190A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365303 | |||||||
| chr11:43365305 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.159+6192G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365305 | |||||||
| chr11:43365332 | G | A | 1 | a0001c0001t0003g0086 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.159+6219G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365332 | |||||||
| chr11:43365399 | G | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.159+6286G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365399 | |||||||
| chr11:43365445 | T | G | 1 | a0004c0009t0001g0186 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.159+6332T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365445 | |||||||
| chr11:43365466 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.159+6353G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365466 | |||||||
| chr11:43365494 | C | G | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+6381C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365494 | |||||||
| chr11:43365555 | G | A | 19 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(16): Show |
19 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.159+6442G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365555 | |||||||
| chr11:43365933 | T | C | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+6820T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365933 | |||||||
| chr11:43366063 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.159+6950C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366063 | |||||||
| chr11:43366105 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.159+6992C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366105 | |||||||
| chr11:43366126 | C | T | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.159+7013C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366126 | |||||||
| chr11:43366127 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+7014G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366127 | |||||||
| chr11:43366308 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.159+7195C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366308 | |||||||
| chr11:43366433 | G | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): Show |
36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.159+7320G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366433 | |||||||
| chr11:43366483 | G | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(4): Show |
7 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+7370G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366483 | |||||||
| chr11:43366505 | C | CA | 35 | a0001c0001t0001g0087 a0001c0001t0001g0251 a0001c0001t0001g0252 others(32): Show |
35 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.159+7408dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43366505 | ||||||
| chr11:43366505 | CA | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(61): Show |
64 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.159+7408delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43366505 | ||||||
| chr11:43366611 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.159+7498C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366611 | |||||||
| chr11:43366702 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+7589T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366702 | |||||||
| chr11:43366801 | C | T | 24 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(21): Show |
24 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.159+7688C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366801 | |||||||
| chr11:43366813 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.159+7700A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366813 | |||||||
| chr11:43366904 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG01074.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.159+7791C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366904 | |||||||
| chr11:43366933 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.159+7820C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366933 | |||||||
| chr11:43367260 | G | A | 4 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(1): Show |
4 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+8147G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367260 | |||||||
| chr11:43367344 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.159+8231A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367344 | |||||||
| chr11:43367367 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): Show |
36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.159+8254G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367367 | |||||||
| chr11:43367520 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159+8407C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367520 | |||||||
| chr11:43367527 | G | C | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.159+8414G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367527 | |||||||
| chr11:43367617 | C | G | 23 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0262 others(20): Show |
23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.159+8504C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367617 | |||||||
| chr11:43367623 | T | C | 1 | a0001c0001t0008g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.159+8510T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367623 | |||||||
| chr11:43367714 | C | CTG | 35 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(32): Show |
35 | HG00558.hp2 HG00741.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.159+8633_159+8634d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43367714 | ||||||
| chr11:43367714 | CTG | C | 182 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.159+8633_159+8634d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43367714 | ||||||
| chr11:43367714 | CTGTG | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0002c0003t0001g0226 |
3 | HG02145.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.159+8631_159+8634d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43367714 | ||||||
| chr11:43367781 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.159+8668C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367781 | |||||||
| chr11:43367822 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159+8709C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367822 | |||||||
| chr11:43368054 | C | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.159+8941C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368054 | |||||||
| chr11:43368087 | G | A | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.159+8974G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368087 | |||||||
| chr11:43368321 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.159+9208A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368321 | |||||||
| chr11:43368582 | C | A | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.159+9469C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368582 | |||||||
| chr11:43368607 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.159+9494G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368607 | |||||||
| chr11:43368766 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.159+9653A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368766 | |||||||
| chr11:43368975 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159+9862C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368975 | |||||||
| chr11:43369096 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+9983A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369096 | |||||||
| chr11:43369252 | C | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-9981C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369252 | |||||||
| chr11:43369294 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-9939C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369294 | |||||||
| chr11:43369475 | A | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-9758A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369475 | |||||||
| chr11:43369556 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.160-9677T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369556 | |||||||
| chr11:43369732 | T | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0255 |
2 | HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.160-9501T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369732 | |||||||
| chr11:43369742 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.160-9491G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369742 | |||||||
| chr11:43369862 | C | T | 1 | a0001c0001t0008g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.160-9371C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369862 | |||||||
| chr11:43370098 | C | T | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-9135C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370098 | |||||||
| chr11:43370111 | A | G | 1 | a0001c0002t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.160-9122A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370111 | |||||||
| chr11:43370142 | C | A | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160-9091C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370142 | |||||||
| chr11:43370160 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160-9073T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370160 | |||||||
| chr11:43370179 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.160-9054A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370179 | |||||||
| chr11:43370329 | A | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.160-8904A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370329 | |||||||
| chr11:43370396 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.160-8837A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370396 | |||||||
| chr11:43370719 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0134 a0001c0001t0001g0163 |
3 | NA18953.hp1 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.160-8514G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370719 | |||||||
| chr11:43370736 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.160-8497A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370736 | |||||||
| chr11:43370776 | T | A | 11 | a0002c0003t0002g0051 a0002c0003t0002g0208 a0002c0003t0002g0209 others(8): Show |
11 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.160-8457T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370776 | |||||||
| chr11:43370782 | AAG | A | 10 | a0002c0003t0002g0051 a0002c0003t0002g0208 a0002c0003t0002g0210 others(7): Show |
10 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.160-8446_160-8445d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43370782 | ||||||
| chr11:43370795 | G | GGTTT | 79 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0001t0001g0251 others(76): Show |
79 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.160-8409_160-8406d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43370795 | ||||||
| chr11:43370795 | G | GGTTTGTT others(1): Show |
5 | a0001c0001t0001g0280 a0001c0001t0001g0283 a0001c0001t0003g0031 others(2): Show |
5 | HG01070.hp2 HG01081.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-8413_160-8406d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43370795 | ||||||
| chr11:43370795 | GGTTTGTT others(1): Show |
G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-8413_160-8406d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43370795 | ||||||
| chr11:43371023 | T | TG | 26 | a0001c0001t0001g0033 a0001c0001t0001g0074 a0001c0001t0001g0075 others(23): Show |
26 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.160-8199dupG | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43371023 | ||||||
| chr11:43371023 | TG | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
82 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.160-8199delG | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43371023 | ||||||
| chr11:43371023 | TGG | T | 60 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0028 others(57): Show |
60 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.160-8200_160-8199d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43371023 | ||||||
| chr11:43371025 | G | C | 1 | a0002c0003t0002g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.160-8208G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371025 | |||||||
| chr11:43371025 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.160-8208G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371025 | |||||||
| chr11:43371143 | A | G | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-8090A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371143 | |||||||
| chr11:43371346 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.160-7887A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371346 | |||||||
| chr11:43371402 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-7831T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371402 | |||||||
| chr11:43371404 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.160-7829C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371404 | |||||||
| chr11:43371440 | T | C | 1 | a0002c0003t0002g0051 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.160-7793T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371440 | |||||||
| chr11:43371534 | A | G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
23 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.160-7699A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371534 | |||||||
| chr11:43371560 | G | A | 2 | a0001c0001t0003g0104 a0001c0001t0005g0103 |
2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.160-7673G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371560 | |||||||
| chr11:43372051 | G | A | 19 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(16): Show |
19 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.160-7182G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372051 | |||||||
| chr11:43372149 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(255): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.160-7084A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372149 | |||||||
| chr11:43372202 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.160-7031A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372202 | |||||||
| chr11:43372231 | G | GTA | 34 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(31): Show |
34 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.160-6999_160-6998d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372231 | ||||||
| chr11:43372305 | C | T | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.160-6928C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372305 | |||||||
| chr11:43372306 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(59): Show |
62 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.160-6927A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372306 | |||||||
| chr11:43372372 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.160-6861C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372372 | |||||||
| chr11:43372428 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.160-6805G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372428 | |||||||
| chr11:43372482 | T | TTTTA | 58 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(55): Show |
58 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.160-6719_160-6716d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | ||||||
| chr11:43372482 | T | TTTTATTT others(1): Show |
6 | a0002c0003t0001g0226 a0002c0003t0002g0217 a0002c0003t0002g0218 others(3): Show |
6 | HG01243.hp2 HG01891.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-6723_160-6716d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | ||||||
| chr11:43372482 | T | TTTTATTT others(5): Show |
14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.160-6727_160-6716d others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | ||||||
| chr11:43372482 | T | TTTTATTT others(9): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.160-6731_160-6716d others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | ||||||
| chr11:43372482 | T | TTTTATTT others(13): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG01261.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.160-6735_160-6716d others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | ||||||
| chr11:43372571 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.160-6662A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372571 | |||||||
| chr11:43372971 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-6262A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372971 | |||||||
| chr11:43373082 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-6151T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373082 | |||||||
| chr11:43373324 | C | CT | 11 | a0001c0001t0001g0024 a0001c0001t0001g0101 a0001c0001t0001g0169 others(8): Show |
11 | HG01168.hp2 HG01361.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-5892dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43373324 | ||||||
| chr11:43373351 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.160-5882T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373351 | |||||||
| chr11:43373361 | T | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0134 a0001c0001t0001g0163 |
3 | NA18953.hp1 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.160-5872T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373361 | |||||||
| chr11:43373384 | C | T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0164 others(1): Show |
4 | NA18962.hp1 NA18970.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-5849C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373384 | |||||||
| chr11:43373427 | C | T | 44 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(41): Show |
44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.160-5806C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373427 | |||||||
| chr11:43373504 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(12): Show |
15 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.160-5729T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373504 | |||||||
| chr11:43373566 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.160-5667A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373566 | |||||||
| chr11:43373972 | A | G | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-5261A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373972 | |||||||
| chr11:43373979 | G | C | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.160-5254G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373979 | |||||||
| chr11:43374018 | T | C | 10 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(7): Show |
10 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-5215T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374018 | |||||||
| chr11:43374390 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160-4843A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374390 | |||||||
| chr11:43374636 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.160-4597C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374636 | |||||||
| chr11:43374663 | A | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.160-4570A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374663 | |||||||
| chr11:43374749 | C | CA | 20 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(17): Show |
20 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-4468dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43374749 | ||||||
| chr11:43374749 | CA | C | 44 | a0001c0001t0001g0042 a0001c0001t0001g0251 a0001c0001t0001g0252 others(41): Show |
44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.160-4468delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43374749 | ||||||
| chr11:43374752 | A | G | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(2): Show |
5 | NA18943.hp1 NA18953.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-4481A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374752 | |||||||
| chr11:43375284 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.160-3949G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375284 | |||||||
| chr11:43375330 | G | C | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.160-3903G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375330 | |||||||
| chr11:43375340 | T | C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
23 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.160-3893T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375340 | |||||||
| chr11:43375641 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.160-3592C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375641 | |||||||
| chr11:43375682 | AG | A | 33 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0081 others(30): Show |
33 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.160-3550delG | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375682 | |||||||
| chr11:43375684 | A | C | 33 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0081 others(30): Show |
33 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.160-3549A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375684 | |||||||
| chr11:43375687 | A | G | 33 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0081 others(30): Show |
33 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.160-3546A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375687 | |||||||
| chr11:43375827 | A | C | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.160-3406A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375827 | |||||||
| chr11:43376115 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.160-3118C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43376115 | |||||||
| chr11:43376591 | C | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.160-2642C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43376591 | |||||||
| chr11:43376613 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0229 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.160-2620G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43376613 | |||||||
| chr11:43377020 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): Show |
36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.160-2213C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377020 | |||||||
| chr11:43377065 | G | A | 25 | a0001c0001t0001g0052 a0001c0002t0001g0050 a0001c0002t0001g0187 others(22): Show |
25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.160-2168G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377065 | |||||||
| chr11:43377110 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.160-2123G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377110 | |||||||
| chr11:43377111 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160-2122G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377111 | |||||||
| chr11:43377208 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-2025G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377208 | |||||||
| chr11:43377276 | G | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.160-1957G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377276 | |||||||
| chr11:43377301 | A | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-1932A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377301 | |||||||
| chr11:43377545 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.160-1688G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377545 | |||||||
| chr11:43377627 | TCTG | T | 4 | a0001c0001t0001g0105 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG01928.hp1 HG01952.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-1603_160-1601d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43377627 | ||||||
| chr11:43377652 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.160-1581C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377652 | |||||||
| chr11:43377751 | A | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.160-1482A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377751 | |||||||
| chr11:43377810 | C | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.160-1423C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377810 | |||||||
| chr11:43377851 | A | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(4): Show |
7 | HG01255.hp1 HG01515.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-1382A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377851 | |||||||
| chr11:43377934 | C | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.160-1299C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377934 | |||||||
| chr11:43377990 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(59): Show |
62 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.160-1243A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377990 | |||||||
| chr11:43378108 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): Show |
36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.160-1125G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378108 | |||||||
| chr11:43378154 | C | T | 1 | a0001c0002t0001g0199 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.160-1079C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378154 | |||||||
| chr11:43378205 | G | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(12): Show |
15 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.160-1028G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378205 | |||||||
| chr11:43378243 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.160-990G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378243 | |||||||
| chr11:43378387 | T | C | 1 | a0002c0003t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160-846T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378387 | |||||||
| chr11:43378575 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.160-658T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378575 | |||||||
| chr11:43378734 | C | T | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-499C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378734 | |||||||
| chr11:43378913 | A | G | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.160-320A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378913 | |||||||
| chr11:43379202 | C | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-31C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43379202 | |||||||
| chr11:43379458 | A | ATG | 22 | a0001c0001t0001g0116 a0001c0001t0001g0179 a0001c0001t0001g0180 others(19): Show |
22 | HG01243.hp1 HG01243.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.249+158_249+159dup others(2): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43379458 | ||||||
| chr11:43379480 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.249+158G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379480 | |||||||
| chr11:43379482 | T | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): Show |
36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.249+160T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379482 | |||||||
| chr11:43379776 | T | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(45): Show |
49 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.249+454T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379776 | |||||||
| chr11:43379792 | C | A | 1 | a0002c0003t0002g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.249+470C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379792 | |||||||
| chr11:43379818 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.249+496A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379818 | |||||||
| chr11:43380083 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.249+761T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380083 | |||||||
| chr11:43380235 | G | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+913G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380235 | |||||||
| chr11:43380302 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.249+980C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380302 | |||||||
| chr11:43380444 | C | T | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+1122C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380444 | |||||||
| chr11:43380500 | C | A | 1 | a0001c0001t0007g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.249+1178C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380500 | |||||||
| chr11:43380530 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+1208C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380530 | |||||||
| chr11:43380545 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.249+1223G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380545 | |||||||
| chr11:43380546 | T | C | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.249+1224T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380546 | |||||||
| chr11:43380637 | G | A | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.249+1315G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380637 | |||||||
| chr11:43380678 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.249+1356T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380678 | |||||||
| chr11:43380941 | G | A | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+1619G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380941 | |||||||
| chr11:43380974 | A | T | 23 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(20): Show |
23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.249+1652A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380974 | |||||||
| chr11:43381239 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.249+1917T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381239 | |||||||
| chr11:43381308 | C | G | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | HG02922.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.249+1986C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381308 | |||||||
| chr11:43381311 | TA | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0048 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1992delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43381311 | ||||||
| chr11:43381368 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.249+2046T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381368 | |||||||
| chr11:43381616 | A | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0229 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.249+2294A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381616 | |||||||
| chr11:43381966 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.249+2644T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381966 | |||||||
| chr11:43382152 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): Show |
36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.249+2830A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382152 | |||||||
| chr11:43382199 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.249+2877T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382199 | |||||||
| chr11:43382224 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.249+2902G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382224 | |||||||
| chr11:43382241 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.249+2919C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382241 | |||||||
| chr11:43382369 | C | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0133 others(1): Show |
4 | HG00408.hp2 HG00438.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+3047C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382369 | |||||||
| chr11:43382475 | G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.249+3153G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382475 | |||||||
| chr11:43382590 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+3268A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382590 | |||||||
| chr11:43382625 | A | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0229 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.249+3303A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382625 | |||||||
| chr11:43382646 | T | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.249+3324T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382646 | |||||||
| chr11:43382721 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.249+3399T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382721 | |||||||
| chr11:43382791 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.249+3469C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382791 | |||||||
| chr11:43382849 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.249+3527C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382849 | |||||||
| chr11:43382889 | ATTTTCTT others(8): Show |
A | 5 | a0002c0003t0002g0210 a0002c0003t0002g0211 a0002c0003t0002g0212 others(2): Show |
5 | HG01496.hp2 HG02109.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+3581_249+3595d others(17): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43382889 | ||||||
| chr11:43383004 | A | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.249+3682A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383004 | |||||||
| chr11:43383232 | G | A | 23 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0262 others(20): Show |
23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.249+3910G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383232 | |||||||
| chr11:43383554 | G | A | 1 | a0001c0001t0003g0077 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.249+4232G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383554 | |||||||
| chr11:43383608 | G | A | 60 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(57): Show |
60 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.249+4286G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383608 | |||||||
| chr11:43383619 | C | T | 6 | a0001c0001t0003g0077 a0001c0001t0003g0086 a0001c0001t0003g0094 others(3): Show |
6 | HG02080.hp2 NA18944.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+4297C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383619 | |||||||
| chr11:43383658 | C | T | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+4336C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383658 | |||||||
| chr11:43383796 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.249+4474C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383796 | |||||||
| chr11:43383832 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+4510G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383832 | |||||||
| chr11:43383880 | A | G | 25 | a0001c0001t0001g0052 a0001c0002t0001g0050 a0001c0002t0001g0187 others(22): Show |
25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.249+4558A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383880 | |||||||
| chr11:43383946 | T | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.249+4624T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383946 | |||||||
| chr11:43384037 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+4715G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384037 | |||||||
| chr11:43384144 | CA | C | 254 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.249+4835delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43384144 | ||||||
| chr11:43384144 | CAA | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(13): Show |
16 | HG00741.hp2 HG01069.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.249+4834_249+4835d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43384144 | ||||||
| chr11:43384175 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.249+4853A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384175 | |||||||
| chr11:43384387 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.249+5065G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384387 | |||||||
| chr11:43384446 | G | A | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+5124G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384446 | |||||||
| chr11:43384618 | C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.250-5034C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384618 | |||||||
| chr11:43384903 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250-4749A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384903 | |||||||
| chr11:43384928 | C | G | 9 | a0001c0001t0001g0251 a0001c0001t0001g0279 a0001c0001t0001g0280 others(6): Show |
9 | HG01070.hp2 HG01081.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-4724C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384928 | |||||||
| chr11:43385174 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.250-4478C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385174 | |||||||
| chr11:43385256 | T | A | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.250-4396T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385256 | |||||||
| chr11:43385421 | AAG | A | 7 | a0001c0001t0003g0077 a0001c0001t0003g0086 a0001c0001t0003g0094 others(4): Show |
7 | HG02040.hp2 HG02080.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-4225_250-4224d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43385421 | ||||||
| chr11:43385456 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.250-4196G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385456 | |||||||
| chr11:43385508 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): Show |
36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.250-4144A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385508 | |||||||
| chr11:43385536 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18747.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.250-4116C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385536 | |||||||
| chr11:43385541 | A | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.250-4111A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385541 | |||||||
| chr11:43385787 | A | C | 7 | a0001c0001t0003g0077 a0001c0001t0003g0086 a0001c0001t0003g0094 others(4): Show |
7 | HG02040.hp2 HG02080.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-3865A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385787 | |||||||
| chr11:43386104 | A | G | 2 | a0003c0004t0001g0246 a0003c0004t0001g0247 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.250-3548A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386104 | |||||||
| chr11:43386323 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.250-3329C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386323 | |||||||
| chr11:43386357 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.250-3295G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386357 | |||||||
| chr11:43386694 | G | A | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-2958G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386694 | |||||||
| chr11:43386768 | C | CGTAT | 3 | a0001c0001t0001g0165 a0001c0001t0003g0091 a0001c0002t0001g0194 |
3 | HG02129.hp2 HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.250-2875_250-2872d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43386768 | ||||||
| chr11:43386777 | G | GTATT | 22 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(19): Show |
22 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.250-2858_250-2855d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43386777 | ||||||
| chr11:43386781 | T | G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
23 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.250-2871T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386781 | |||||||
| chr11:43386869 | C | T | 60 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(57): Show |
60 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.250-2783C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386869 | |||||||
| chr11:43387025 | C | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.250-2627C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387025 | |||||||
| chr11:43387232 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.250-2420A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387232 | |||||||
| chr11:43387269 | G | C | 1 | a0001c0001t0001g0009 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.250-2383G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387269 | |||||||
| chr11:43387507 | TTAA | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.250-2138_250-2136d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43387507 | ||||||
| chr11:43387692 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.250-1960G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387692 | |||||||
| chr11:43387800 | A | G | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-1852A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387800 | |||||||
| chr11:43388008 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250-1644T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388008 | |||||||
| chr11:43388120 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250-1532A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388120 | |||||||
| chr11:43388166 | T | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.250-1486T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388166 | |||||||
| chr11:43388167 | TAAAG | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-1482_250-1479d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43388167 | ||||||
| chr11:43388183 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.250-1469A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388183 | |||||||
| chr11:43388258 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0245 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.250-1394G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388258 | |||||||
| chr11:43388397 | TAGG | T | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.250-1252_250-1250d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43388397 | ||||||
| chr11:43388612 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.250-1040A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388612 | |||||||
| chr11:43388782 | T | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.250-870T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388782 | |||||||
| chr11:43388974 | C | CA | 45 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0068 others(42): Show |
45 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.250-662dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43388974 | ||||||
| chr11:43388990 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.250-662A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388990 | |||||||
| chr11:43389017 | T | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-635T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43389017 | |||||||
| chr11:43389138 | C | CA | 31 | a0001c0001t0001g0052 a0001c0001t0001g0150 a0001c0001t0001g0151 others(28): Show |
31 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.250-501dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43389138 | ||||||
| chr11:43389393 | C | T | 2 | a0001c0001t0001g0207 a0001c0002t0001g0201 |
2 | HG03834.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.250-259C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43389393 | |||||||
| chr11:43389396 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.250-256G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43389396 | |||||||
| chr11:43389543 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.250-109C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43389543 | |||||||
| chr11:43389978 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.419+157A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43389978 | |||||||
| chr11:43389990 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.419+169A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43389990 | |||||||
| chr11:43390033 | G | A | 31 | a0001c0001t0001g0036 a0001c0001t0001g0071 a0001c0001t0001g0080 others(28): Show |
31 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.419+212G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390033 | |||||||
| chr11:43390117 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.419+296G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390117 | |||||||
| chr11:43390127 | C | T | 42 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(39): Show |
42 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.419+306C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390127 | |||||||
| chr11:43390156 | T | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0184 |
3 | HG00438.hp2 NA18957.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.419+335T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390156 | |||||||
| chr11:43390212 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.419+391A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390212 | |||||||
| chr11:43390336 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.419+515C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390336 | |||||||
| chr11:43390343 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): Show |
36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.419+522G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390343 | |||||||
| chr11:43390561 | AGCCAAGA others(3): Show |
A | 32 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(29): Show |
32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+741_419+750del others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390561 | |||||||
| chr11:43390571 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.419+750G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390571 | |||||||
| chr11:43390574 | C | G | 32 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(29): Show |
32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+753C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390574 | |||||||
| chr11:43390575 | CACTG | C | 32 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(29): Show |
32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+755_419+758del others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390575 | |||||||
| chr11:43390582 | C | G | 32 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(29): Show |
32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+761C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390582 | |||||||
| chr11:43390583 | T | C | 32 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(29): Show |
32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+762T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390583 | |||||||
| chr11:43390610 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.419+789C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390610 | |||||||
| chr11:43390650 | AAAAAATA others(6): Show |
A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02976.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.420-803_420-791del others(13): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | 43390650 | ||||||
| chr11:43390901 | C | G | 1 | a0001c0002t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.420-564C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390901 | |||||||
| chr11:43390935 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0245 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.420-530A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390935 | |||||||
| chr11:43391126 | C | CA | 44 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(41): Show |
44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.420-338dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | 43391126 | ||||||
| chr11:43391393 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.420-72T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43391393 | |||||||
| chr11:43391596 | A | AT | 33 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(30): Show |
33 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.531+33dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | 43391596 | ||||||
| chr11:43391596 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.531+20A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/23 | chr11 | 43391596 | |||||||
| chr11:43391608 | TTGCG | T | 239 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.531+34_531+37delGC others(2): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | 43391608 | ||||||
| chr11:43391609 | TGCG | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0026 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.531+34_531+36delGC others(1): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/23 | chr11 | 43391609 | |||||||
| chr11:43392187 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.663+235C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43392187 | |||||||
| chr11:43392379 | C | CT | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.663+430dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | 43392379 | ||||||
| chr11:43392582 | A | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.663+630A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43392582 | |||||||
| chr11:43392950 | C | G | 1 | a0001c0001t0001g0278 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.663+998C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43392950 | |||||||
| chr11:43393378 | C | T | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.663+1426C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393378 | |||||||
| chr11:43393384 | A | C | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.663+1432A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393384 | |||||||
| chr11:43393394 | A | G | 2 | a0001c0002t0001g0195 a0001c0002t0001g0196 |
2 | HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.663+1442A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393394 | |||||||
| chr11:43393437 | TC | T | 24 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(21): Show |
24 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.663+1487delC | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | 43393437 | ||||||
| chr11:43393528 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.663+1576C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393528 | |||||||
| chr11:43393620 | G | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.663+1668G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393620 | |||||||
| chr11:43393661 | C | T | 2 | a0003c0004t0001g0246 a0003c0004t0001g0247 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.663+1709C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393661 | |||||||
| chr11:43394020 | A | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.663+2068A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43394020 | |||||||
| chr11:43394330 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.663+2378G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43394330 | |||||||
| chr11:43394788 | G | C | 1 | a0001c0002t0001g0197 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.664-1921G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43394788 | |||||||
| chr11:43395099 | C | CT | 6 | a0001c0001t0001g0049 a0001c0001t0001g0128 a0001c0001t0001g0182 others(3): Show |
6 | HG01175.hp2 HG02083.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-1591dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | 43395099 | ||||||
| chr11:43395136 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.664-1573T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395136 | |||||||
| chr11:43395139 | C | T | 7 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01928.hp2 NA18943.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.664-1570C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395139 | |||||||
| chr11:43395201 | C | T | 3 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0006t0001g0200 |
3 | HG00738.hp1 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.664-1508C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395201 | |||||||
| chr11:43395231 | G | C | 5 | a0001c0001t0001g0089 a0001c0001t0001g0101 a0001c0001t0001g0139 others(2): Show |
5 | HG01978.hp2 NA18949.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-1478G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395231 | |||||||
| chr11:43395247 | C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.664-1462C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395247 | |||||||
| chr11:43395422 | C | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0101 a0001c0001t0001g0139 others(2): Show |
5 | HG01978.hp2 NA18949.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-1287C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395422 | |||||||
| chr11:43396069 | A | G | 1 | a0001c0001t0008g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.664-640A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396069 | |||||||
| chr11:43396114 | T | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-595T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396114 | |||||||
| chr11:43396118 | T | C | 1 | a0002c0003t0002g0220 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.664-591T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396118 | |||||||
| chr11:43396172 | C | A | 1 | a0001c0001t0001g0034 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.664-537C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396172 | |||||||
| chr11:43396232 | T | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.664-477T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396232 | |||||||
| chr11:43396353 | A | G | 23 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0262 others(20): Show |
23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.664-356A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396353 | |||||||
| chr11:43396634 | A | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.664-75A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396634 | |||||||
| chr11:43396646 | T | C | 1 | a0001c0001t0003g0093 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.664-63T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396646 | |||||||
| chr11:43396957 | C | CA | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
27 | HG00639.hp1 HG00639.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.773+155dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr11 | 43396957 | ||||||
| chr11:43397123 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0173 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.774-224C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 6/23 | chr11 | 43397123 | |||||||
| chr11:43397181 | T | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.774-166T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 6/23 | chr11 | 43397181 | |||||||
| chr11:43397321 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0155 |
2 | NA18985.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.774-26C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 6/23 | chr11 | 43397321 | |||||||
| chr11:43397536 | T | C | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.918+45T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | chr11 | 43397536 | |||||||
| chr11:43397537 | C | CT | 149 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
150 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.918+62dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397537 | ||||||
| chr11:43397568 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.918+77G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | chr11 | 43397568 | |||||||
| chr11:43397684 | A | G | 25 | a0001c0001t0001g0052 a0001c0002t0001g0050 a0001c0002t0001g0187 others(22): Show |
25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.918+193A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | chr11 | 43397684 | |||||||
| chr11:43397789 | C | CTGGTCAC others(12): Show |
3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0229 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919-175_919-157dup others(19): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397789 | ||||||
| chr11:43397873 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.919-101A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | chr11 | 43397873 | |||||||
| chr11:43397901 | C | CGT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0098 others(9): Show |
12 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.919-24_919-23dupGT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | C | CGTGT | 3 | a0001c0001t0001g0078 a0001c0001t0001g0090 a0001c0001t0001g0115 |
3 | HG01256.hp2 HG01258.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.919-26_919-23dupGT others(2): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0003g0104 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.919-34_919-23dupGT others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGT | C | 28 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0033 others(25): Show |
28 | HG01081.hp1 HG01099.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.919-24_919-23delGT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGT | C | 44 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0044 others(41): Show |
44 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.919-26_919-23delGT others(2): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGT | C | 55 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(52): Show |
55 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.919-28_919-23delGT others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(1): Show |
C | 18 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0061 others(15): Show |
18 | HG00099.hp1 HG00738.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.919-30_919-23delGT others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(3): Show |
C | 22 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0067 others(19): Show |
22 | HG00408.hp1 HG00639.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.919-32_919-23delGT others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(5): Show |
C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0029 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.919-34_919-23delGT others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0002c0003t0002g0215 |
3 | HG01884.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.919-36_919-23delGT others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(9): Show |
C | 20 | a0001c0001t0001g0042 a0002c0003t0002g0003 a0002c0003t0002g0051 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.919-38_919-23delGT others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0001g0110 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.919-40_919-23delGT others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(13): Show |
C | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.919-42_919-23delGT others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(15): Show |
C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
19 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.919-44_919-23delGT others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(19): Show |
C | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.919-48_919-23delGT others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(21): Show |
C | 15 | a0001c0001t0001g0278 a0001c0001t0003g0031 a0001c0001t0003g0032 others(12): Show |
15 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.919-50_919-23delGT others(26): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43397901 | CGTGTGTG others(25): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.919-54_919-23delGT others(30): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | ||||||
| chr11:43398227 | C | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1058+114C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398227 | |||||||
| chr11:43398305 | T | C | 5 | a0001c0001t0001g0089 a0001c0001t0001g0101 a0001c0001t0001g0139 others(2): Show |
5 | HG01978.hp2 NA18949.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+192T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398305 | |||||||
| chr11:43398360 | A | G | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1058+247A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398360 | |||||||
| chr11:43398603 | G | A | 1 | a0002c0003t0002g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1058+490G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398603 | |||||||
| chr11:43398847 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1058+734A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398847 | |||||||
| chr11:43398889 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1058+776A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398889 | |||||||
| chr11:43398935 | T | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1058+822T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398935 | |||||||
| chr11:43398971 | ATCTT | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG01074.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1058+860_1058+863d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr11 | 43398971 | ||||||
| chr11:43399056 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1059-832C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43399056 | |||||||
| chr11:43399057 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1059-831A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43399057 | |||||||
| chr11:43399158 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0134 a0001c0001t0001g0163 |
3 | NA18953.hp1 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1059-730G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43399158 | |||||||
| chr11:43399835 | A | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0163 |
2 | NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1059-53A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43399835 | |||||||
| chr11:43400090 | T | G | 1 | a0007c0007t0001g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1219+42T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400090 | |||||||
| chr11:43400172 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1219+124C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400172 | |||||||
| chr11:43400173 | G | A | 23 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0262 others(20): Show |
23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.1219+125G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400173 | |||||||
| chr11:43400277 | T | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1219+229T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400277 | |||||||
| chr11:43400457 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0277 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1219+409C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400457 | |||||||
| chr11:43400535 | A | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1219+487A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400535 | |||||||
| chr11:43400673 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1219+625T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400673 | |||||||
| chr11:43401011 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1220-435T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43401011 | |||||||
| chr11:43401085 | A | G | 23 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(20): Show |
23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1220-361A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43401085 | |||||||
| chr11:43401318 | C | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1220-128C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43401318 | |||||||
| chr11:43401398 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1220-48C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43401398 | |||||||
| chr11:43401607 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1332+49G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43401607 | |||||||
| chr11:43401884 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1332+326G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43401884 | |||||||
| chr11:43401963 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0245 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1332+405G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43401963 | |||||||
| chr11:43401980 | A | AAAAT | 16 | a0001c0001t0001g0044 a0001c0001t0001g0102 a0001c0001t0001g0123 others(13): Show |
16 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.1332+470_1332+473d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | ||||||
| chr11:43401980 | AAAAT | A | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1332+470_1332+473d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | ||||||
| chr11:43401980 | AAAATAAA others(1): Show |
A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(39): Show |
42 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1332+466_1332+473d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | ||||||
| chr11:43401980 | AAAATAAA others(5): Show |
A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0107 a0001c0001t0001g0108 others(5): Show |
8 | HG02055.hp2 HG02622.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332+462_1332+473d others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | ||||||
| chr11:43401980 | AAAATAAA others(9): Show |
A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(36): Show |
39 | HG00438.hp1 HG01069.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.1332+458_1332+473d others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | ||||||
| chr11:43401980 | AAAATAAA others(13): Show |
A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1332+454_1332+473d others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | ||||||
| chr11:43401980 | AAAATAAA others(21): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1332+446_1332+473d others(30): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | ||||||
| chr11:43402032 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1332+474G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402032 | |||||||
| chr11:43402062 | T | C | 1 | a0002c0003t0002g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1332+504T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402062 | |||||||
| chr11:43402112 | A | G | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1332+554A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402112 | |||||||
| chr11:43402190 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0228 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1332+632G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402190 | |||||||
| chr11:43402228 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1332+670G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402228 | |||||||
| chr11:43402256 | A | T | 1 | a0001c0001t0001g0176 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1332+698A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402256 | |||||||
| chr11:43402404 | C | T | 5 | a0001c0001t0001g0252 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | NA18942.hp1 NA18948.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332+846C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402404 | |||||||
| chr11:43402434 | G | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.1332+876G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402434 | |||||||
| chr11:43402616 | A | G | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1332+1058A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402616 | |||||||
| chr11:43402709 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1332+1151A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402709 | |||||||
| chr11:43402762 | G | T | 25 | a0001c0001t0001g0052 a0001c0002t0001g0050 a0001c0002t0001g0187 others(22): Show |
25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1332+1204G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402762 | |||||||
| chr11:43402828 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0277 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1333-1170G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402828 | |||||||
| chr11:43402862 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1333-1136G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402862 | |||||||
| chr11:43402920 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1333-1078C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402920 | |||||||
| chr11:43403014 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0133 others(1): Show |
4 | HG00408.hp2 HG00438.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333-984G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403014 | |||||||
| chr11:43403078 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1333-920A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403078 | |||||||
| chr11:43403079 | TAAAG | T | 42 | a0001c0001t0001g0143 a0001c0001t0001g0251 a0001c0001t0001g0252 others(39): Show |
42 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1333-916_1333-913d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43403079 | ||||||
| chr11:43403117 | C | CT | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0164 |
3 | NA18962.hp1 NA18970.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1333-878dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43403117 | ||||||
| chr11:43403221 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1333-777C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403221 | |||||||
| chr11:43403261 | A | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1333-737A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403261 | |||||||
| chr11:43403275 | C | T | 14 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0035 others(11): Show |
14 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1333-723C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403275 | |||||||
| chr11:43403399 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1333-599A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403399 | |||||||
| chr11:43403493 | C | T | 1 | a0005c0010t0001g0119 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1333-505C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403493 | |||||||
| chr11:43403622 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333-376C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403622 | |||||||
| chr11:43403632 | A | G | 1 | a0002c0003t0002g0223 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1333-366A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403632 | |||||||
| chr11:43403694 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1333-304A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403694 | |||||||
| chr11:43403743 | G | GGGACAGG others(33): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1333-216_1333-215i others(42): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43403743 | ||||||
| chr11:43403756 | G | A | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1333-242G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403756 | |||||||
| chr11:43403862 | A | G | 9 | a0001c0001t0001g0137 a0001c0001t0001g0144 a0001c0001t0001g0152 others(6): Show |
9 | HG00558.hp2 HG01256.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.1333-136A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403862 | |||||||
| chr11:43403959 | C | T | 1 | a0002c0003t0002g0051 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1333-39C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403959 | |||||||
| chr11:43403977 | AC | A | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1333-20delC | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403977 | |||||||
| chr11:43403988 | C | A | 1 | a0001c0002t0001g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1333-10C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403988 | |||||||
| chr11:43404305 | A | G | 25 | a0001c0001t0001g0052 a0001c0002t0001g0050 a0001c0002t0001g0187 others(22): Show |
25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1479+161A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404305 | |||||||
| chr11:43404419 | C | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1479+275C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404419 | |||||||
| chr11:43404641 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1479+497C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404641 | |||||||
| chr11:43404787 | ATTTAAGT | A | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1479+646_1479+652d others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr11 | 43404787 | ||||||
| chr11:43404887 | A | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1480-627A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404887 | |||||||
| chr11:43404942 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1480-572G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404942 | |||||||
| chr11:43405094 | CT | C | 25 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0295 others(22): Show |
25 | HG01243.hp2 HG01256.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1480-403delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr11 | 43405094 | ||||||
| chr11:43405164 | A | G | 13 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0069 others(10): Show |
13 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.1480-350A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43405164 | |||||||
| chr11:43405323 | C | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
14 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1480-191C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43405323 | |||||||
| chr11:43405396 | T | C | 60 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(57): Show |
60 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1480-118T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43405396 | |||||||
| chr11:43405452 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1480-62T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43405452 | |||||||
| chr11:43405707 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1595+78G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 12/23 | chr11 | 43405707 | |||||||
| chr11:43405718 | G | A | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | HG01099.hp2 HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1596-68G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 12/23 | chr11 | 43405718 | |||||||
| chr11:43406115 | G | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761+164G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406115 | |||||||
| chr11:43406156 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0166 |
2 | NA18945.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1761+205C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406156 | |||||||
| chr11:43406369 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1761+418G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406369 | |||||||
| chr11:43406449 | T | C | 93 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(90): Show |
93 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1761+498T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406449 | |||||||
| chr11:43406566 | CTTT | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1762-563_1762-561d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr11 | 43406566 | ||||||
| chr11:43406639 | C | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG00639.hp1 HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1762-499C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406639 | |||||||
| chr11:43406823 | G | T | 1 | a0002c0003t0002g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1762-315G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406823 | |||||||
| chr11:43406969 | C | G | 2 | a0001c0001t0001g0162 a0001c0008t0006g0064 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1762-169C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406969 | |||||||
| chr11:43406971 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1762-167A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406971 | |||||||
| chr11:43407051 | TAAGAA | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1762-82_1762-78del others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr11 | 43407051 | ||||||
| chr11:43407299 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1840-54T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 14/23 | chr11 | 43407299 | |||||||
| chr11:43407790 | GT | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | HG01168.hp2 HG01261.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2064+226delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43407790 | ||||||
| chr11:43408276 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2064+699A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408276 | |||||||
| chr11:43408523 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2064+946A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408523 | |||||||
| chr11:43408545 | C | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064+968C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408545 | |||||||
| chr11:43408720 | C | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0145 a0001c0001t0001g0175 others(2): Show |
5 | HG02129.hp1 NA18945.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.2064+1143C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408720 | |||||||
| chr11:43408909 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG01255.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2064+1332A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408909 | |||||||
| chr11:43408930 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0138 |
2 | HG02083.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.2064+1353A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408930 | |||||||
| chr11:43409002 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2064+1425A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409002 | |||||||
| chr11:43409032 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2064+1455C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409032 | |||||||
| chr11:43409241 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2064+1664A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409241 | |||||||
| chr11:43409312 | C | T | 6 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0125 others(3): Show |
6 | HG00642.hp2 HG01081.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.2064+1735C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409312 | |||||||
| chr11:43409761 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+2184G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409761 | |||||||
| chr11:43410007 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0134 a0001c0001t0001g0163 |
3 | NA18953.hp1 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2064+2430A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410007 | |||||||
| chr11:43410130 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064+2553G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410130 | |||||||
| chr11:43410462 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2064+2885G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410462 | |||||||
| chr11:43410496 | A | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(106): Show |
109 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.2064+2919A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410496 | |||||||
| chr11:43410543 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2064+2966G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410543 | |||||||
| chr11:43410569 | G | A | 23 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(20): Show |
23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.2064+2992G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410569 | |||||||
| chr11:43410730 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2064+3153A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410730 | |||||||
| chr11:43410740 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.2064+3163C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410740 | |||||||
| chr11:43410756 | T | C | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2064+3179T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410756 | |||||||
| chr11:43410875 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.2064+3298G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410875 | |||||||
| chr11:43411000 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2064+3423G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411000 | |||||||
| chr11:43411072 | A | G | 1 | a0001c0002t0001g0197 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2064+3495A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411072 | |||||||
| chr11:43411102 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(106): Show |
109 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.2065-3488T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411102 | |||||||
| chr11:43411296 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2065-3294A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411296 | |||||||
| chr11:43411479 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0245 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2065-3111C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411479 | |||||||
| chr11:43411559 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2065-3031G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411559 | |||||||
| chr11:43411666 | A | T | 1 | a0002c0003t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2065-2924A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411666 | |||||||
| chr11:43411722 | CTT | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2065-2866_2065-286 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43411722 | ||||||
| chr11:43411798 | T | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(62): Show |
65 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.2065-2792T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411798 | |||||||
| chr11:43411957 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2065-2633A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411957 | |||||||
| chr11:43412069 | A | T | 1 | a0001c0002t0001g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2065-2521A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412069 | |||||||
| chr11:43412263 | C | T | 4 | a0001c0001t0001g0105 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG01928.hp1 HG01952.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-2327C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412263 | |||||||
| chr11:43412343 | C | T | 16 | a0001c0001t0001g0059 a0001c0001t0001g0230 a0001c0001t0001g0231 others(13): Show |
16 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.2065-2247C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412343 | |||||||
| chr11:43412426 | C | T | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2065-2164C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412426 | |||||||
| chr11:43412561 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2065-2029A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412561 | |||||||
| chr11:43412700 | T | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2065-1890T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412700 | |||||||
| chr11:43412893 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2065-1697A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412893 | |||||||
| chr11:43412926 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2065-1664T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412926 | |||||||
| chr11:43412981 | G | GAC | 30 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
30 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.2065-1563_2065-156 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | G | GACAC | 10 | a0001c0001t0001g0058 a0001c0001t0001g0083 a0001c0001t0001g0154 others(7): Show |
10 | HG00558.hp2 HG01255.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2065-1565_2065-156 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | G | GACACAC | 6 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0116 others(3): Show |
6 | HG01256.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2065-1567_2065-156 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | G | GACACACA others(1): Show |
5 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0172 others(2): Show |
5 | HG01891.hp2 HG02886.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2065-1569_2065-156 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | G | GACACACA others(3): Show |
1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2065-1571_2065-156 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | GAC | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00642.hp1 HG01069.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.2065-1563_2065-156 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | GACAC | G | 28 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(25): Show |
28 | HG00738.hp2 HG01243.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.2065-1565_2065-156 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | GACACAC | G | 41 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0044 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.2065-1567_2065-156 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | GACACACA others(1): Show |
G | 54 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(51): Show |
54 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2065-1569_2065-156 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | GACACACA others(3): Show |
G | 38 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0251 others(35): Show |
38 | HG00609.hp1 HG00741.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2065-1571_2065-156 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | GACACACA others(5): Show |
G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0026 others(2): Show |
5 | HG02300.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2065-1573_2065-156 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | GACACACA others(7): Show |
G | 1 | a0001c0001t0003g0104 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2065-1575_2065-156 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412981 | GACACACA others(11): Show |
G | 1 | a0001c0001t0001g0132 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2065-1579_2065-156 others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | ||||||
| chr11:43412985 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2065-1605C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412985 | |||||||
| chr11:43413017 | CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2065-1571_2065-156 others(15): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43413017 | ||||||
| chr11:43413027 | C | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
21 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.2065-1563C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413027 | |||||||
| chr11:43413028 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2065-1562_2065-156 others(15): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413028 | |||||||
| chr11:43413419 | C | A | 1 | a0001c0001t0005g0117 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2065-1171C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413419 | |||||||
| chr11:43413545 | TAGAC | T | 14 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0069 others(11): Show |
14 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.2065-1041_2065-103 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43413545 | ||||||
| chr11:43413706 | G | GA | 8 | a0001c0001t0001g0138 a0001c0001t0001g0230 a0001c0001t0001g0262 others(5): Show |
8 | HG02109.hp2 HG02486.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.2065-872dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43413706 | ||||||
| chr11:43413848 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2065-742A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413848 | |||||||
| chr11:43413950 | G | A | 9 | a0002c0003t0002g0208 a0002c0003t0002g0210 a0002c0003t0002g0211 others(6): Show |
9 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2065-640G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413950 | |||||||
| chr11:43414396 | A | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2065-194A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43414396 | |||||||
| chr11:43414452 | G | C | 1 | a0001c0001t0001g0293 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2065-138G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43414452 | |||||||
| chr11:43414521 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2065-69T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43414521 | |||||||
| chr11:43414528 | G | A | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2065-62G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43414528 | |||||||
| chr11:43414888 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0182 |
2 | HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2251+112C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43414888 | |||||||
| chr11:43415104 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2251+328T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415104 | |||||||
| chr11:43415439 | G | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.2251+663G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415439 | |||||||
| chr11:43415456 | G | C | 1 | a0001c0001t0003g0086 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2251+680G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415456 | |||||||
| chr11:43415919 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(41): Show |
44 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.2251+1143G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415919 | |||||||
| chr11:43415980 | T | C | 1 | a0002c0003t0002g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2251+1204T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415980 | |||||||
| chr11:43416292 | A | G | 1 | a0001c0002t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2251+1516A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416292 | |||||||
| chr11:43416299 | C | T | 93 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(90): Show |
93 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.2251+1523C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416299 | |||||||
| chr11:43416307 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2251+1531T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416307 | |||||||
| chr11:43416466 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(41): Show |
44 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.2251+1690T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416466 | |||||||
| chr11:43416551 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+1775G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416551 | |||||||
| chr11:43416651 | G | C | 1 | a0001c0001t0001g0276 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2251+1875G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416651 | |||||||
| chr11:43416660 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2251+1884T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416660 | |||||||
| chr11:43416690 | T | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18979.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2251+1914T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416690 | |||||||
| chr11:43416819 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+2043C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416819 | |||||||
| chr11:43416906 | C | G | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2251+2130C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416906 | |||||||
| chr11:43417358 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2251+2582G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417358 | |||||||
| chr11:43417493 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2251+2717A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417493 | |||||||
| chr11:43417562 | A | G | 1 | a0001c0001t0003g0096 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2251+2786A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417562 | |||||||
| chr11:43417664 | C | A | 1 | a0001c0002t0001g0250 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2251+2888C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417664 | |||||||
| chr11:43417781 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2251+3005G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417781 | |||||||
| chr11:43417792 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(253): Show |
257 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.2251+3016G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417792 | |||||||
| chr11:43417813 | C | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(199): Show |
202 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.2251+3037C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417813 | |||||||
| chr11:43418275 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0286 |
2 | HG01346.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2251+3499C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418275 | |||||||
| chr11:43418284 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2251+3508A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418284 | |||||||
| chr11:43418370 | T | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+3594T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418370 | |||||||
| chr11:43418443 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2251+3667G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418443 | |||||||
| chr11:43418458 | C | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0245 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2251+3682C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418458 | |||||||
| chr11:43418561 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2251+3785G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418561 | |||||||
| chr11:43418649 | AAAAACAG others(14): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2251+3878_2251+389 others(25): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43418649 | ||||||
| chr11:43419050 | C | T | 1 | a0001c0002t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2251+4274C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419050 | |||||||
| chr11:43419133 | T | G | 1 | a0002c0003t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2251+4357T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419133 | |||||||
| chr11:43419381 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2251+4605A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419381 | |||||||
| chr11:43419405 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2251+4629A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419405 | |||||||
| chr11:43419740 | G | A | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+4964G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419740 | |||||||
| chr11:43419848 | A | C | 1 | a0002c0003t0002g0208 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2251+5072A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419848 | |||||||
| chr11:43419945 | T | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0055 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2251+5169T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419945 | |||||||
| chr11:43420007 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2251+5231G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420007 | |||||||
| chr11:43420087 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0286 |
2 | HG01346.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2251+5311A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420087 | |||||||
| chr11:43420404 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0283 |
2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2251+5628G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420404 | |||||||
| chr11:43420671 | G | C | 1 | a0001c0001t0003g0096 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2251+5895G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420671 | |||||||
| chr11:43420774 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2251+5998T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420774 | |||||||
| chr11:43420853 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2251+6077A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420853 | |||||||
| chr11:43420854 | G | C | 1 | a0001c0001t0001g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2251+6078G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420854 | |||||||
| chr11:43420998 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0228 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2251+6222A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420998 | |||||||
| chr11:43421051 | C | T | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+6275C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421051 | |||||||
| chr11:43421158 | T | A | 23 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0262 others(20): Show |
23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.2251+6382T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421158 | |||||||
| chr11:43421167 | T | G | 30 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(27): Show |
30 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.2251+6391T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421167 | |||||||
| chr11:43421206 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2251+6430G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421206 | |||||||
| chr11:43421235 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2251+6459A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421235 | |||||||
| chr11:43421609 | A | C | 1 | a0001c0002t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2251+6833A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421609 | |||||||
| chr11:43421870 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+7094G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421870 | |||||||
| chr11:43421938 | A | T | 1 | a0001c0001t0001g0252 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2251+7162A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421938 | |||||||
| chr11:43422072 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2251+7296T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422072 | |||||||
| chr11:43422124 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2251+7348G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422124 | |||||||
| chr11:43422127 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2251+7351A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422127 | |||||||
| chr11:43422290 | G | C | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2251+7514G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422290 | |||||||
| chr11:43422299 | A | C | 3 | a0002c0003t0002g0220 a0002c0003t0002g0222 a0002c0003t0002g0223 |
3 | HG01891.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2251+7523A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422299 | |||||||
| chr11:43422328 | G | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2251+7552G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422328 | |||||||
| chr11:43422438 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2251+7662G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422438 | |||||||
| chr11:43422461 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2251+7685C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422461 | |||||||
| chr11:43422957 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2251+8181A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422957 | |||||||
| chr11:43423279 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2251+8503G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43423279 | |||||||
| chr11:43423360 | CAT | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2251+8585_2251+858 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43423360 | |||||||
| chr11:43423930 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2251+9154A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43423930 | |||||||
| chr11:43424006 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2251+9230A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424006 | |||||||
| chr11:43424087 | C | CT | 11 | a0001c0001t0001g0047 a0001c0001t0001g0100 a0002c0003t0002g0208 others(8): Show |
11 | HG00642.hp2 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2251+9326dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43424087 | ||||||
| chr11:43424122 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+9346C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424122 | |||||||
| chr11:43424123 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2251+9347G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424123 | |||||||
| chr11:43424260 | T | C | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+9484T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424260 | |||||||
| chr11:43424283 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2251+9507G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424283 | |||||||
| chr11:43424290 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.2251+9514C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424290 | |||||||
| chr11:43424442 | GA | G | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+9669delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43424442 | ||||||
| chr11:43424535 | C | T | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2251+9759C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424535 | |||||||
| chr11:43424695 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0115 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2251+9919G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424695 | |||||||
| chr11:43424799 | T | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+10023T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424799 | |||||||
| chr11:43424867 | A | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2251+10091A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424867 | |||||||
| chr11:43424935 | A | G | 23 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0262 others(20): Show |
23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.2251+10159A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424935 | |||||||
| chr11:43425019 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2251+10243G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425019 | |||||||
| chr11:43425153 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2251+10377C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425153 | |||||||
| chr11:43425286 | T | G | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+10510T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425286 | |||||||
| chr11:43425333 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2251+10557T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425333 | |||||||
| chr11:43425383 | G | A | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2251+10607G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425383 | |||||||
| chr11:43425476 | C | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+10700C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425476 | |||||||
| chr11:43425600 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2251+10824C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425600 | |||||||
| chr11:43425882 | G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2251+11106G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425882 | |||||||
| chr11:43425899 | A | T | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2251+11123A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425899 | |||||||
| chr11:43426066 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2251+11290G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426066 | |||||||
| chr11:43426202 | T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2251+11426T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426202 | |||||||
| chr11:43426386 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2251+11610C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426386 | |||||||
| chr11:43426481 | C | T | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+11705C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426481 | |||||||
| chr11:43426510 | G | A | 25 | a0001c0001t0001g0052 a0001c0002t0001g0050 a0001c0002t0001g0187 others(22): Show |
25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.2251+11734G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426510 | |||||||
| chr11:43426583 | A | T | 1 | a0001c0001t0005g0117 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2251+11807A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426583 | |||||||
| chr11:43426624 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2251+11848A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426624 | |||||||
| chr11:43426632 | C | T | 1 | a0002c0003t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2251+11856C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426632 | |||||||
| chr11:43426917 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2251+12141A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426917 | |||||||
| chr11:43426931 | G | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+12155G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426931 | |||||||
| chr11:43427250 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2251+12474A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427250 | |||||||
| chr11:43427293 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2251+12517C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427293 | |||||||
| chr11:43427396 | C | T | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2251+12620C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427396 | |||||||
| chr11:43427398 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2251+12622G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427398 | |||||||
| chr11:43427520 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2251+12744G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427520 | |||||||
| chr11:43427539 | A | G | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | HG02922.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2251+12763A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427539 | |||||||
| chr11:43427555 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2251+12779C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427555 | |||||||
| chr11:43427735 | T | C | 34 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(31): Show |
34 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.2251+12959T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427735 | |||||||
| chr11:43427823 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2251+13047C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427823 | |||||||
| chr11:43427913 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2251+13137C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427913 | |||||||
| chr11:43428305 | TA | T | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2251+13539delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43428305 | ||||||
| chr11:43428524 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2251+13748G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428524 | |||||||
| chr11:43428540 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2251+13764G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428540 | |||||||
| chr11:43428811 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2251+14035A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428811 | |||||||
| chr11:43428839 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2251+14063C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428839 | |||||||
| chr11:43428993 | A | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+14217A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428993 | |||||||
| chr11:43429038 | A | G | 13 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(10): Show |
13 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.2251+14262A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429038 | |||||||
| chr11:43429057 | C | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2252-14268C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429057 | |||||||
| chr11:43429314 | G | T | 18 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0255 others(15): Show |
18 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-14011G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429314 | |||||||
| chr11:43429331 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2252-13994T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429331 | |||||||
| chr11:43429377 | C | T | 42 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(39): Show |
42 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.2252-13948C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429377 | |||||||
| chr11:43429599 | A | G | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0164 others(1): Show |
4 | NA18962.hp1 NA18970.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2252-13726A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429599 | |||||||
| chr11:43429698 | GAAAT | G | 30 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(27): Show |
30 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.2252-13626_2252-13 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429698 | |||||||
| chr11:43429740 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2252-13585A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429740 | |||||||
| chr11:43429746 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2252-13579G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429746 | |||||||
| chr11:43429907 | C | T | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.2252-13418C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429907 | |||||||
| chr11:43429960 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2252-13365A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429960 | |||||||
| chr11:43430569 | C | T | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2252-12756C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430569 | |||||||
| chr11:43430607 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2252-12718G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430607 | |||||||
| chr11:43430704 | T | TACACACA others(11): Show |
1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2252-12617_2252-12 others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430704 | ||||||
| chr11:43430709 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2252-12616G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430709 | |||||||
| chr11:43430709 | G | GCA | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(55): Show |
58 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2252-12577_2252-12 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | G | GCACA | 40 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(37): Show |
40 | HG00609.hp1 HG00639.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2252-12579_2252-12 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | G | GCACACA | 23 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0045 others(20): Show |
23 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.2252-12581_2252-12 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | G | GCACACAC others(1): Show |
17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(14): Show |
17 | HG00597.hp2 HG01070.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.2252-12583_2252-12 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | G | GCACACAC others(3): Show |
14 | a0001c0001t0001g0021 a0001c0001t0001g0048 a0001c0001t0001g0049 others(11): Show |
14 | HG00408.hp1 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2252-12585_2252-12 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | G | GCACACAC others(5): Show |
11 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0057 others(8): Show |
12 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.2252-12587_2252-12 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | G | GCACACAC others(7): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.2252-12589_2252-12 others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | G | GCGCA | 3 | a0002c0003t0002g0214 a0002c0003t0002g0215 a0002c0003t0002g0225 |
3 | HG02622.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2252-12615_2252-12 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | G | GCGCACAC others(3): Show |
2 | a0001c0001t0001g0027 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2252-12615_2252-12 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | GCA | G | 39 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0081 others(36): Show |
39 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2252-12577_2252-12 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | GCACA | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0052 a0001c0001t0001g0058 others(4): Show |
7 | HG01243.hp1 HG02280.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2252-12579_2252-12 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | GCACACA | G | 12 | a0001c0001t0001g0132 a0001c0002t0001g0050 a0001c0002t0001g0187 others(9): Show |
12 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.2252-12581_2252-12 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | GCACACAC others(1): Show |
G | 15 | a0001c0001t0001g0172 a0001c0001t0004g0004 a0001c0002t0001g0190 others(12): Show |
15 | HG00558.hp2 HG00738.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2252-12583_2252-12 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | GCACACAC others(3): Show |
G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2252-12585_2252-12 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430709 | GCACACAC others(5): Show |
G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2252-12587_2252-12 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | ||||||
| chr11:43430711 | A | G | 2 | a0001c0001t0001g0028 a0001c0008t0006g0064 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2252-12614A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430711 | |||||||
| chr11:43430749 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2252-12576_2252-12 others(17): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430749 | |||||||
| chr11:43430836 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2252-12489T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430836 | |||||||
| chr11:43431291 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2252-12034A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43431291 | |||||||
| chr11:43431427 | A | G | 3 | a0002c0003t0002g0214 a0002c0003t0002g0215 a0002c0003t0002g0225 |
3 | HG02622.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2252-11898A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43431427 | |||||||
| chr11:43431616 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2252-11709A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43431616 | |||||||
| chr11:43431803 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18979.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2252-11522C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43431803 | |||||||
| chr11:43432057 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2252-11268C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432057 | |||||||
| chr11:43432235 | A | AG | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2252-11089dupG | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432235 | ||||||
| chr11:43432454 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2252-10871G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432454 | |||||||
| chr11:43432678 | G | A | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2252-10647G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432678 | |||||||
| chr11:43432784 | C | CT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
14 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.2252-10534dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432784 | ||||||
| chr11:43432845 | T | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2252-10480T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432845 | |||||||
| chr11:43432919 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2252-10406A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432919 | |||||||
| chr11:43432989 | G | GTGTTT | 29 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(26): Show |
29 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2252-10311_2252-10 others(11): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432989 | ||||||
| chr11:43432989 | G | GTGTTTTG others(3): Show |
14 | a0002c0003t0002g0051 a0002c0003t0002g0208 a0002c0003t0002g0209 others(11): Show |
14 | HG01496.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2252-10316_2252-10 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432989 | ||||||
| chr11:43432989 | G | GTGTTTTG others(8): Show |
5 | a0002c0003t0002g0003 a0002c0003t0002g0215 a0002c0003t0002g0220 others(2): Show |
5 | HG01891.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2252-10321_2252-10 others(21): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432989 | ||||||
| chr11:43432989 | G | GTGTTTTG others(13): Show |
1 | a0002c0003t0002g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2252-10326_2252-10 others(26): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432989 | ||||||
| chr11:43433075 | G | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2252-10250G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433075 | |||||||
| chr11:43433225 | T | C | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2252-10100T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433225 | |||||||
| chr11:43433251 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
163 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.2252-10074A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433251 | |||||||
| chr11:43433290 | C | T | 39 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(36): Show |
39 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2252-10035C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433290 | |||||||
| chr11:43433474 | C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-9851C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433474 | |||||||
| chr11:43433501 | T | C | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2252-9824T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433501 | |||||||
| chr11:43433634 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2252-9691A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433634 | |||||||
| chr11:43433674 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2252-9651A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433674 | |||||||
| chr11:43433692 | G | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2252-9633G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433692 | |||||||
| chr11:43433824 | A | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2252-9501A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433824 | |||||||
| chr11:43434018 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2252-9307T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434018 | |||||||
| chr11:43434036 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2252-9289C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434036 | |||||||
| chr11:43434122 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | HG02922.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2252-9203C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434122 | |||||||
| chr11:43434128 | T | G | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2252-9197T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434128 | |||||||
| chr11:43434168 | G | GAC | 3 | a0001c0001t0001g0019 a0001c0001t0001g0116 a0001c0001t0001g0181 |
3 | HG02818.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2252-9094_2252-909 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | G | GACACACA others(3): Show |
1 | a0001c0001t0001g0060 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2252-9102_2252-909 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GAC | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0043 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.2252-9094_2252-909 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACAC | G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(12): Show |
16 | HG00558.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.2252-9096_2252-909 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACAC | G | 20 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0065 others(17): Show |
20 | HG00099.hp1 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2252-9098_2252-909 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(1): Show |
G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(8): Show |
11 | HG01433.hp2 HG01515.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.2252-9100_2252-909 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(3): Show |
G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0087 a0001c0001t0001g0090 others(6): Show |
9 | HG01243.hp2 HG01516.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2252-9102_2252-909 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(5): Show |
G | 18 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0042 others(15): Show |
18 | HG00438.hp2 HG00639.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-9104_2252-909 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(7): Show |
G | 53 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0053 others(50): Show |
53 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2252-9106_2252-909 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(9): Show |
G | 28 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0037 others(25): Show |
28 | HG00609.hp2 HG01069.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.2252-9108_2252-909 others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(11): Show |
G | 13 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0047 others(10): Show |
13 | HG00099.hp2 HG00408.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.2252-9110_2252-909 others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(13): Show |
G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0038 others(12): Show |
15 | HG00323.hp1 HG00609.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.2252-9112_2252-909 others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(15): Show |
G | 39 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(36): Show |
39 | HG00741.hp1 HG01099.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.2252-9114_2252-909 others(26): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(17): Show |
G | 22 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0278 others(19): Show |
22 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.2252-9116_2252-909 others(28): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(19): Show |
G | 5 | a0001c0001t0001g0183 a0001c0002t0001g0195 a0001c0002t0001g0196 others(2): Show |
5 | HG01257.hp1 HG01361.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2252-9118_2252-909 others(30): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(23): Show |
G | 10 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0002c0003t0002g0208 others(7): Show |
10 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2252-9122_2252-909 others(34): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(25): Show |
G | 2 | a0001c0001t0001g0256 a0002c0003t0002g0215 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2252-9124_2252-909 others(36): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434168 | GACACACA others(27): Show |
G | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2252-9126_2252-909 others(38): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | ||||||
| chr11:43434169 | ACACACAC others(6): Show |
A | 1 | a0001c0001t0001g0171 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2252-9155_2252-914 others(17): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434169 | |||||||
| chr11:43434169 | ACACACAC others(16): Show |
A | 1 | a0001c0001t0001g0281 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2252-9155_2252-913 others(27): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434169 | |||||||
| chr11:43434407 | C | G | 10 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(7): Show |
10 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.2252-8918C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434407 | |||||||
| chr11:43434480 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2252-8845A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434480 | |||||||
| chr11:43434541 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2252-8784C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434541 | |||||||
| chr11:43434676 | T | C | 1 | a0001c0006t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2252-8649T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434676 | |||||||
| chr11:43435009 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2252-8316A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435009 | |||||||
| chr11:43435031 | CAT | C | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2252-8293_2252-829 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435031 | |||||||
| chr11:43435070 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2252-8255G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435070 | |||||||
| chr11:43435077 | T | TGATA | 70 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(67): Show |
70 | HG00323.hp1 HG00408.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.2252-8196_2252-819 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | ||||||
| chr11:43435077 | T | TGATAGAT others(1): Show |
30 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0030 others(27): Show |
31 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.2252-8200_2252-819 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | ||||||
| chr11:43435077 | T | TGATAGAT others(5): Show |
11 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0027 others(8): Show |
11 | HG00609.hp1 HG01943.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.2252-8204_2252-819 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | ||||||
| chr11:43435077 | TGATA | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(40): Show |
43 | HG00558.hp2 HG00735.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.2252-8196_2252-819 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | ||||||
| chr11:43435077 | TGATAGAT others(1): Show |
T | 36 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0043 others(33): Show |
36 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.2252-8200_2252-819 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | ||||||
| chr11:43435077 | TGATAGAT others(5): Show |
T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0112 a0001c0001t0001g0185 others(1): Show |
4 | HG00438.hp1 NA18944.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.2252-8204_2252-819 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | ||||||
| chr11:43435077 | TGATAGAT others(9): Show |
T | 2 | a0001c0001t0003g0077 a0001c0001t0003g0135 |
2 | NA18964.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.2252-8208_2252-819 others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | ||||||
| chr11:43435089 | A | T | 1 | a0001c0001t0001g0171 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2252-8236A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435089 | |||||||
| chr11:43435100 | T | TAGATAGA others(5): Show |
1 | a0001c0001t0001g0230 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2252-8214_2252-821 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435100 | ||||||
| chr11:43435210 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2252-8115A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435210 | |||||||
| chr11:43435772 | A | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(36): Show |
39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.2252-7553A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435772 | |||||||
| chr11:43435779 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2252-7546A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435779 | |||||||
| chr11:43435790 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2252-7535A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435790 | |||||||
| chr11:43435915 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18747.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2252-7410T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435915 | |||||||
| chr11:43435995 | C | T | 1 | a0001c0002t0001g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2252-7330C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435995 | |||||||
| chr11:43436438 | A | G | 1 | a0002c0003t0002g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2252-6887A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436438 | |||||||
| chr11:43436583 | T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-6742T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436583 | |||||||
| chr11:43436594 | A | G | 18 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0255 others(15): Show |
18 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-6731A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436594 | |||||||
| chr11:43436721 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2252-6604A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436721 | |||||||
| chr11:43436723 | T | G | 16 | a0001c0001t0001g0059 a0001c0001t0001g0230 a0001c0001t0001g0231 others(13): Show |
16 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.2252-6602T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436723 | |||||||
| chr11:43437006 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2252-6319A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437006 | |||||||
| chr11:43437035 | C | T | 1 | a0002c0003t0002g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2252-6290C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437035 | |||||||
| chr11:43437395 | T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-5930T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437395 | |||||||
| chr11:43437560 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2252-5765C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437560 | |||||||
| chr11:43437578 | C | T | 44 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(41): Show |
44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.2252-5747C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437578 | |||||||
| chr11:43437612 | A | G | 18 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0255 others(15): Show |
18 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-5713A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437612 | |||||||
| chr11:43437772 | C | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-5553C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437772 | |||||||
| chr11:43437870 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.2252-5455A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437870 | |||||||
| chr11:43437898 | A | G | 14 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0035 others(11): Show |
14 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2252-5427A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437898 | |||||||
| chr11:43437975 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2252-5350A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437975 | |||||||
| chr11:43438160 | A | G | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2252-5165A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438160 | |||||||
| chr11:43438440 | C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-4885C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438440 | |||||||
| chr11:43438881 | A | T | 1 | a0001c0001t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2252-4444A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438881 | |||||||
| chr11:43438901 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2252-4424A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438901 | |||||||
| chr11:43438910 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2252-4415A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438910 | |||||||
| chr11:43438931 | C | T | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2252-4394C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438931 | |||||||
| chr11:43439059 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2252-4266G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439059 | |||||||
| chr11:43439199 | A | C | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2252-4126A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439199 | |||||||
| chr11:43439262 | G | A | 1 | a0001c0001t0003g0093 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2252-4063G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439262 | |||||||
| chr11:43439469 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2252-3856G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439469 | |||||||
| chr11:43439471 | T | G | 3 | a0001c0001t0003g0104 a0001c0001t0005g0103 a0001c0001t0005g0126 |
3 | HG00609.hp2 HG02040.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2252-3854T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439471 | |||||||
| chr11:43439488 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2252-3837G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439488 | |||||||
| chr11:43439613 | T | C | 34 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(31): Show |
34 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.2252-3712T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439613 | |||||||
| chr11:43439631 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2252-3694G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439631 | |||||||
| chr11:43439916 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | HG02922.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2252-3409G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439916 | |||||||
| chr11:43439953 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2252-3372C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439953 | |||||||
| chr11:43440503 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2252-2822C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43440503 | |||||||
| chr11:43440592 | T | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2252-2733T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43440592 | |||||||
| chr11:43440671 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2252-2654G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43440671 | |||||||
| chr11:43440868 | T | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-2457T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43440868 | |||||||
| chr11:43440961 | TA | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.2252-2352delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43440961 | ||||||
| chr11:43441114 | C | CAAAAAAA others(329): Show |
1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2252-2193_2252-219 others(340): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | ||||||
| chr11:43441114 | C | CAAAAAAA others(310): Show |
20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2252-2193_2252-219 others(321): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | ||||||
| chr11:43441114 | C | CAAAAAAA others(312): Show |
6 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0047 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2252-2193_2252-219 others(323): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | ||||||
| chr11:43441114 | C | CAAAAAAA others(329): Show |
1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2252-2193_2252-219 others(340): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | ||||||
| chr11:43441114 | C | CAAAAAAA others(330): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0053 |
2 | HG02055.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.2252-2193_2252-219 others(341): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | ||||||
| chr11:43441114 | C | CAAAAAAA others(331): Show |
8 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
8 | HG01069.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.2252-2193_2252-219 others(342): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | ||||||
| chr11:43441114 | C | CAAAAAAA others(332): Show |
1 | a0001c0001t0001g0228 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2252-2193_2252-219 others(343): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | ||||||
| chr11:43441130 | G | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2252-2195G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441130 | |||||||
| chr11:43441227 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0245 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2252-2098C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441227 | |||||||
| chr11:43441267 | C | T | 44 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(41): Show |
44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.2252-2058C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441267 | |||||||
| chr11:43441403 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(62): Show |
65 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.2252-1922C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441403 | |||||||
| chr11:43441432 | A | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02976.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2252-1893A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441432 | |||||||
| chr11:43441499 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2252-1826G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441499 | |||||||
| chr11:43441606 | T | C | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG01074.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2252-1719T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441606 | |||||||
| chr11:43441864 | A | G | 23 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(20): Show |
23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.2252-1461A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441864 | |||||||
| chr11:43441983 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-1342G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441983 | |||||||
| chr11:43442051 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2252-1274C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43442051 | |||||||
| chr11:43442206 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2252-1119A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43442206 | |||||||
| chr11:43442474 | T | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2252-851T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43442474 | |||||||
| chr11:43442743 | G | C | 44 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(41): Show |
44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.2252-582G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43442743 | |||||||
| chr11:43443094 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2252-231C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43443094 | |||||||
| chr11:43443228 | G | A | 3 | a0002c0003t0002g0217 a0002c0003t0002g0219 a0002c0003t0002g0221 |
3 | HG02559.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2252-97G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43443228 | |||||||
| chr11:43443289 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2252-36G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43443289 | |||||||
| chr11:43443752 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0182 |
2 | HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2511+168T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 17/23 | chr11 | 43443752 | |||||||
| chr11:43444015 | T | A | 2 | a0001c0001t0003g0104 a0001c0001t0005g0103 |
2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2512-41T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 17/23 | chr11 | 43444015 | |||||||
| chr11:43444017 | A | C | 2 | a0001c0001t0003g0104 a0001c0001t0005g0103 |
2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2512-39A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 17/23 | chr11 | 43444017 | |||||||
| chr11:43444452 | G | C | 1 | a0002c0003t0002g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2665+243G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43444452 | |||||||
| chr11:43444722 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2665+513T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43444722 | |||||||
| chr11:43444722 | T | TAC | 111 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(108): Show |
112 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.2665+549_2665+550d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | ||||||
| chr11:43444722 | T | TACAC | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2665+547_2665+550d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | ||||||
| chr11:43444722 | T | TACACAC | 19 | a0001c0001t0001g0012 a0001c0001t0001g0162 a0001c0001t0001g0251 others(16): Show |
19 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2665+545_2665+550d others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | ||||||
| chr11:43444722 | T | TACACACA others(1): Show |
6 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0256 others(3): Show |
6 | HG01361.hp1 HG02293.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2665+543_2665+550d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | ||||||
| chr11:43444722 | TAC | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(16): Show |
19 | HG00741.hp2 HG01243.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2665+549_2665+550d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | ||||||
| chr11:43444722 | TACACAC | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0228 |
3 | HG01069.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2665+545_2665+550d others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | ||||||
| chr11:43444900 | C | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(255): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2665+691C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43444900 | |||||||
| chr11:43444951 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2665+742A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43444951 | |||||||
| chr11:43445562 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2665+1353C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43445562 | |||||||
| chr11:43445897 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | NA18949.hp2 NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2665+1688A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43445897 | |||||||
| chr11:43445935 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2665+1726A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43445935 | |||||||
| chr11:43446131 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2666-1871C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446131 | |||||||
| chr11:43446194 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2666-1808T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446194 | |||||||
| chr11:43446250 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2666-1752T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446250 | |||||||
| chr11:43446345 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2666-1657C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446345 | |||||||
| chr11:43446620 | C | T | 1 | a0002c0003t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2666-1382C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446620 | |||||||
| chr11:43446708 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2666-1294C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446708 | |||||||
| chr11:43446814 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2666-1188A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446814 | |||||||
| chr11:43446950 | G | C | 9 | a0002c0003t0002g0208 a0002c0003t0002g0210 a0002c0003t0002g0211 others(6): Show |
9 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2666-1052G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446950 | |||||||
| chr11:43447038 | G | A | 1 | a0001c0001t0005g0126 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2666-964G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447038 | |||||||
| chr11:43447253 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2666-749T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447253 | |||||||
| chr11:43447293 | G | A | 2 | a0001c0001t0004g0001 a0001c0001t0004g0004 |
3 | HG00639.hp2 HG01106.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2666-709G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447293 | |||||||
| chr11:43447598 | C | T | 47 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(44): Show |
47 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.2666-404C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447598 | |||||||
| chr11:43447822 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2666-180A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447822 | |||||||
| chr11:43448147 | C | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2786+25C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448147 | |||||||
| chr11:43448208 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2786+86G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448208 | |||||||
| chr11:43448333 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2786+211G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448333 | |||||||
| chr11:43448388 | C | A | 1 | a0002c0003t0002g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2786+266C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448388 | |||||||
| chr11:43448425 | G | C | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2786+303G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448425 | |||||||
| chr11:43448705 | C | A | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2786+583C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448705 | |||||||
| chr11:43448714 | A | G | 2 | a0001c0001t0001g0236 a0002c0003t0001g0226 |
2 | HG02132.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2786+592A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448714 | |||||||
| chr11:43449058 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2786+936C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43449058 | |||||||
| chr11:43449098 | T | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02976.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2786+976T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43449098 | |||||||
| chr11:43449884 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG00323.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.2787-198G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43449884 | |||||||
| chr11:43450291 | G | A | 2 | a0001c0001t0003g0104 a0001c0001t0005g0103 |
2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2946+50G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450291 | |||||||
| chr11:43450298 | G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2946+57G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450298 | |||||||
| chr11:43450325 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2946+84G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450325 | |||||||
| chr11:43450400 | T | C | 2 | a0002c0003t0002g0222 a0002c0003t0002g0223 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2946+159T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450400 | |||||||
| chr11:43450681 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0021 |
2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2946+440G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450681 | |||||||
| chr11:43450787 | G | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(36): Show |
39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.2947-395G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450787 | |||||||
| chr11:43451027 | G | A | 3 | a0002c0003t0002g0217 a0002c0003t0002g0219 a0002c0003t0002g0221 |
3 | HG02559.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2947-155G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43451027 | |||||||
| chr11:43451143 | G | A | 3 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0006t0001g0200 |
3 | HG00738.hp1 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2947-39G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43451143 | |||||||
| chr11:43451345 | G | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(255): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.3030+80G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451345 | |||||||
| chr11:43451507 | C | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3030+242C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451507 | |||||||
| chr11:43451557 | T | C | 4 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(1): Show |
4 | HG00323.hp1 HG01099.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.3030+292T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451557 | |||||||
| chr11:43451650 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3030+385T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451650 | |||||||
| chr11:43451773 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3030+508G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451773 | |||||||
| chr11:43451781 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3030+516T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451781 | |||||||
| chr11:43451804 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3030+539G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451804 | |||||||
| chr11:43451932 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0229 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3030+667G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451932 | |||||||
| chr11:43451932 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3030+667G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451932 | |||||||
| chr11:43452217 | C | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3030+952C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452217 | |||||||
| chr11:43452222 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3030+957G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452222 | |||||||
| chr11:43452356 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3030+1091C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452356 | |||||||
| chr11:43452455 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0166 |
2 | NA18945.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.3030+1190C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452455 | |||||||
| chr11:43452573 | C | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3030+1308C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452573 | |||||||
| chr11:43452768 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3030+1503C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452768 | |||||||
| chr11:43452871 | T | C | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.3030+1606T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452871 | |||||||
| chr11:43453113 | C | T | 1 | a0002c0003t0002g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3030+1848C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453113 | |||||||
| chr11:43453180 | A | AAAAT | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.3030+1916_3030+191 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43453180 | ||||||
| chr11:43453469 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(36): Show |
39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3030+2204T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453469 | |||||||
| chr11:43453695 | T | G | 1 | a0007c0007t0001g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3030+2430T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453695 | |||||||
| chr11:43453910 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3030+2645T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453910 | |||||||
| chr11:43453949 | C | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0157 |
3 | NA18979.hp1 NA19083.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3030+2684C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453949 | |||||||
| chr11:43454041 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3030+2776G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454041 | |||||||
| chr11:43454092 | G | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3030+2827G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454092 | |||||||
| chr11:43454268 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.3030+3003A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454268 | |||||||
| chr11:43454378 | C | G | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3030+3113C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454378 | |||||||
| chr11:43454448 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3030+3183T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454448 | |||||||
| chr11:43454531 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3030+3266A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454531 | |||||||
| chr11:43454862 | A | G | 1 | a0003c0004t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3030+3597A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454862 | |||||||
| chr11:43455037 | C | T | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0008t0006g0064 |
3 | HG02145.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3030+3772C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455037 | |||||||
| chr11:43455172 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3030+3907G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455172 | |||||||
| chr11:43455232 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0277 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3030+3967C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455232 | |||||||
| chr11:43455272 | G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3030+4007G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455272 | |||||||
| chr11:43455428 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3030+4163G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455428 | |||||||
| chr11:43456039 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3030+4774A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456039 | |||||||
| chr11:43456179 | A | AAC | 40 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0023 others(37): Show |
40 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3030+4947_3030+494 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | ||||||
| chr11:43456179 | A | AACAC | 29 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0047 others(26): Show |
29 | HG00735.hp2 HG01069.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3030+4945_3030+494 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | ||||||
| chr11:43456179 | A | AACACAC | 4 | a0001c0001t0001g0002 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG00323.hp2 HG01346.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.3030+4943_3030+494 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | ||||||
| chr11:43456179 | AAC | A | 18 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0069 others(15): Show |
18 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.3030+4947_3030+494 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | ||||||
| chr11:43456179 | AACAC | A | 29 | a0001c0001t0001g0033 a0001c0001t0001g0065 a0001c0001t0001g0066 others(26): Show |
29 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.3030+4945_3030+494 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | ||||||
| chr11:43456179 | AACACACA others(1): Show |
A | 24 | a0001c0001t0001g0052 a0001c0002t0001g0050 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00735.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.3030+4941_3030+494 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | ||||||
| chr11:43456179 | AACACACA others(3): Show |
A | 1 | a0001c0001t0001g0166 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3030+4939_3030+494 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | ||||||
| chr11:43456179 | AACACACA others(5): Show |
A | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3030+4937_3030+494 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | ||||||
| chr11:43456195 | C | T | 34 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(31): Show |
34 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.3030+4930C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456195 | |||||||
| chr11:43456574 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3030+5309A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456574 | |||||||
| chr11:43456729 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3030+5464G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456729 | |||||||
| chr11:43456906 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3030+5641G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456906 | |||||||
| chr11:43456951 | G | A | 1 | a0002c0003t0002g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3030+5686G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456951 | |||||||
| chr11:43457272 | A | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3030+6007A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457272 | |||||||
| chr11:43457322 | C | A | 1 | a0001c0001t0001g0009 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3030+6057C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457322 | |||||||
| chr11:43457609 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3030+6344A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457609 | |||||||
| chr11:43457671 | G | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
155 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.3030+6406G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457671 | |||||||
| chr11:43457881 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3030+6616G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457881 | |||||||
| chr11:43457897 | T | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3030+6632T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457897 | |||||||
| chr11:43458156 | T | C | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3030+6891T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458156 | |||||||
| chr11:43458157 | T | A | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3030+6892T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458157 | |||||||
| chr11:43458174 | G | A | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3030+6909G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458174 | |||||||
| chr11:43458206 | A | C | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.3030+6941A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458206 | |||||||
| chr11:43458246 | G | T | 16 | a0001c0001t0001g0059 a0001c0001t0001g0230 a0001c0001t0001g0231 others(13): Show |
16 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.3030+6981G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458246 | |||||||
| chr11:43458296 | G | A | 1 | a0001c0002t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3030+7031G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458296 | |||||||
| chr11:43458354 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3030+7089C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458354 | |||||||
| chr11:43458624 | G | A | 18 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0255 others(15): Show |
18 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.3030+7359G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458624 | |||||||
| chr11:43458808 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0008t0006g0064 |
3 | HG02145.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3030+7543G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458808 | |||||||
| chr11:43458926 | T | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0168 |
2 | HG02132.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3030+7661T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458926 | |||||||
| chr11:43458948 | TAATAGTT others(13): Show |
T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+7704_3030+772 others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43458948 | ||||||
| chr11:43458963 | G | A | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3030+7698G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458963 | |||||||
| chr11:43459031 | A | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(36): Show |
39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3030+7766A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459031 | |||||||
| chr11:43459057 | C | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | NA18949.hp2 NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.3030+7792C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459057 | |||||||
| chr11:43459339 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3030+8074C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459339 | |||||||
| chr11:43459374 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3030+8109T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459374 | |||||||
| chr11:43459663 | T | C | 1 | a0007c0007t0001g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3030+8398T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459663 | |||||||
| chr11:43459692 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3030+8427T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459692 | |||||||
| chr11:43459760 | T | C | 1 | a0001c0001t0004g0001 | 2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.3030+8495T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459760 | |||||||
| chr11:43460090 | C | T | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3030+8825C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460090 | |||||||
| chr11:43460105 | A | AT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(21): Show |
24 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.3030+8853dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43460105 | ||||||
| chr11:43460356 | A | G | 1 | a0001c0002t0001g0189 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3030+9091A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460356 | |||||||
| chr11:43460399 | T | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.3030+9134T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460399 | |||||||
| chr11:43460472 | C | T | 23 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0262 others(20): Show |
23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.3030+9207C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460472 | |||||||
| chr11:43460494 | C | G | 3 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0035 |
3 | HG01433.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3030+9229C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460494 | |||||||
| chr11:43460668 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3030+9403G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460668 | |||||||
| chr11:43461011 | A | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3030+9746A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461011 | |||||||
| chr11:43461111 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3030+9846G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461111 | |||||||
| chr11:43461133 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3030+9868C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461133 | |||||||
| chr11:43461212 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
14 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.3030+9947G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461212 | |||||||
| chr11:43461213 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.3030+9948C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461213 | |||||||
| chr11:43461241 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0048 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3030+9976G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461241 | |||||||
| chr11:43461311 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3030+10046G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461311 | |||||||
| chr11:43461390 | C | CA | 57 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0024 others(54): Show |
57 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.3030+10151dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | ||||||
| chr11:43461390 | C | CAA | 47 | a0001c0001t0001g0022 a0001c0001t0001g0052 a0001c0001t0001g0061 others(44): Show |
47 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.3030+10150_3030+10 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | ||||||
| chr11:43461390 | C | CAAA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0272 a0001c0001t0001g0276 others(3): Show |
6 | HG01433.hp1 HG02055.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.3030+10149_3030+10 others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | ||||||
| chr11:43461390 | CAAAAAAA others(2): Show |
C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3030+10143_3030+10 others(15): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | ||||||
| chr11:43461390 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3030+10136_3030+10 others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | ||||||
| chr11:43461672 | T | C | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+10407T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461672 | |||||||
| chr11:43461943 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3030+10678C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461943 | |||||||
| chr11:43462089 | T | TA | 65 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0026 others(62): Show |
65 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.3030+10840dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462089 | ||||||
| chr11:43462089 | T | TAA | 7 | a0001c0001t0001g0230 a0001c0001t0001g0233 a0001c0002t0001g0187 others(4): Show |
7 | HG00642.hp1 HG01175.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.3030+10839_3030+10 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462089 | ||||||
| chr11:43462223 | C | G | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.3030+10958C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43462223 | |||||||
| chr11:43462567 | A | G | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.3030+11302A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43462567 | |||||||
| chr11:43462645 | T | A | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+11380T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43462645 | |||||||
| chr11:43462695 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3030+11430G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43462695 | |||||||
| chr11:43462921 | C | CT | 24 | a0001c0001t0001g0007 a0001c0001t0001g0059 a0001c0001t0001g0060 others(21): Show |
24 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.3030+11668dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT | 40 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(37): Show |
40 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.3030+11662_3030+11 others(13): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(4): Show |
14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG00558.hp2 HG01069.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.3030+11658_3030+11 others(17): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3030+11657_3030+11 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0207 a0001c0002t0001g0203 |
2 | HG01943.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(20): Show |
5 | a0002c0003t0002g0051 a0002c0003t0002g0210 a0002c0003t0002g0212 others(2): Show |
5 | HG01496.hp2 HG02559.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(33): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(21): Show |
5 | a0002c0003t0002g0003 a0002c0003t0002g0208 a0002c0003t0002g0211 others(2): Show |
5 | HG02818.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(34): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(22): Show |
9 | a0002c0003t0002g0209 a0002c0003t0002g0214 a0002c0003t0002g0215 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(35): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(23): Show |
3 | a0001c0002t0001g0195 a0002c0003t0001g0226 a0002c0003t0002g0218 |
3 | HG01243.hp2 HG01257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(36): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(24): Show |
6 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0001c0002t0001g0199 others(3): Show |
6 | HG00738.hp1 HG01361.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(37): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(25): Show |
10 | a0001c0001t0001g0030 a0001c0002t0001g0187 a0001c0002t0001g0192 others(7): Show |
10 | HG00642.hp1 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(38): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(26): Show |
6 | a0001c0001t0001g0052 a0001c0002t0001g0050 a0001c0002t0001g0188 others(3): Show |
6 | HG01069.hp2 HG01074.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(39): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(27): Show |
1 | a0001c0002t0001g0189 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3030+11668_3030+11 others(40): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(28): Show |
2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(41): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462921 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3030+11668_3030+11 others(42): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | ||||||
| chr11:43462990 | ACTGCAAC | A | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3030+11728_3030+11 others(13): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462990 | ||||||
| chr11:43463104 | C | T | 23 | a0001c0001t0001g0239 a0001c0001t0001g0241 a0002c0003t0001g0226 others(20): Show |
23 | HG01243.hp2 HG01496.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.3030+11839C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463104 | |||||||
| chr11:43463204 | G | A | 19 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(16): Show |
19 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.3030+11939G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463204 | |||||||
| chr11:43463508 | AT | A | 12 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.3030+12253delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43463508 | ||||||
| chr11:43463821 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3030+12556A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463821 | |||||||
| chr11:43463945 | A | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG02083.hp1 NA18949.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.3030+12680A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463945 | |||||||
| chr11:43463983 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3030+12718T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463983 | |||||||
| chr11:43464114 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3030+12849A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464114 | |||||||
| chr11:43464164 | C | T | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3030+12899C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464164 | |||||||
| chr11:43464279 | C | CA | 12 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(9): Show |
12 | HG01261.hp2 HG02055.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.3030+13030dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43464279 | ||||||
| chr11:43464316 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0004g0001 others(1): Show |
5 | HG00639.hp2 HG01106.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.3030+13051A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464316 | |||||||
| chr11:43464432 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0177 |
2 | HG02129.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.3030+13167T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464432 | |||||||
| chr11:43464493 | A | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(42): Show |
45 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.3030+13228A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464493 | |||||||
| chr11:43464517 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3030+13252C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464517 | |||||||
| chr11:43464518 | G | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3030+13253G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464518 | |||||||
| chr11:43464561 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3030+13296T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464561 | |||||||
| chr11:43464569 | A | G | 8 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(5): Show |
8 | HG01070.hp2 HG01081.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.3030+13304A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464569 | |||||||
| chr11:43464599 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3030+13334A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464599 | |||||||
| chr11:43464743 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3030+13478T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464743 | |||||||
| chr11:43465076 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3030+13811C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465076 | |||||||
| chr11:43465134 | C | T | 62 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(59): Show |
62 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.3030+13869C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465134 | |||||||
| chr11:43465224 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3030+13959T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465224 | |||||||
| chr11:43465262 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3030+13997G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465262 | |||||||
| chr11:43465415 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18945.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3030+14150A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465415 | |||||||
| chr11:43465578 | C | T | 1 | a0005c0010t0001g0119 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3030+14313C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465578 | |||||||
| chr11:43465867 | C | CA | 39 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(36): Show |
39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3030+14604dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43465867 | ||||||
| chr11:43465942 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3030+14677A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465942 | |||||||
| chr11:43466067 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3030+14802C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466067 | |||||||
| chr11:43466115 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3030+14850A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466115 | |||||||
| chr11:43466223 | G | A | 1 | a0001c0002t0001g0198 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3030+14958G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466223 | |||||||
| chr11:43466301 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3030+15036T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466301 | |||||||
| chr11:43466366 | C | A | 1 | a0002c0003t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3030+15101C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466366 | |||||||
| chr11:43466486 | C | T | 10 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(7): Show |
10 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.3030+15221C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466486 | |||||||
| chr11:43466937 | C | T | 16 | a0001c0001t0001g0059 a0001c0001t0001g0230 a0001c0001t0001g0231 others(13): Show |
16 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.3030+15672C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466937 | |||||||
| chr11:43466938 | G | A | 1 | a0001c0002t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3030+15673G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466938 | |||||||
| chr11:43466953 | C | T | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0008t0006g0064 |
3 | HG02145.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3030+15688C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466953 | |||||||
| chr11:43467026 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3030+15761G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467026 | |||||||
| chr11:43467075 | CAAA | C | 15 | a0001c0001t0001g0155 a0001c0001t0003g0031 a0001c0001t0003g0032 others(12): Show |
15 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.3030+15817_3030+15 others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43467075 | ||||||
| chr11:43467138 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3030+15873G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467138 | |||||||
| chr11:43467403 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3030+16138A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467403 | |||||||
| chr11:43467564 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3030+16299A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467564 | |||||||
| chr11:43467568 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3030+16303G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467568 | |||||||
| chr11:43467656 | G | A | 62 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(59): Show |
62 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.3030+16391G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467656 | |||||||
| chr11:43467786 | G | T | 5 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(2): Show |
5 | NA18940.hp1 NA18967.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3030+16521G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467786 | |||||||
| chr11:43467856 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3030+16591G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467856 | |||||||
| chr11:43467874 | C | CA | 30 | a0001c0001t0001g0085 a0001c0001t0001g0159 a0001c0001t0001g0160 others(27): Show |
30 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.3030+16623dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43467874 | ||||||
| chr11:43467960 | CAG | C | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3030+16697_3030+16 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43467960 | ||||||
| chr11:43468041 | G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3030+16776G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468041 | |||||||
| chr11:43468181 | C | T | 1 | a0001c0002t0001g0197 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3030+16916C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468181 | |||||||
| chr11:43468488 | A | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0101 a0001c0001t0001g0139 others(2): Show |
5 | HG01978.hp2 NA18949.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.3030+17223A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468488 | |||||||
| chr11:43468494 | G | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0048 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3030+17229G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468494 | |||||||
| chr11:43468734 | A | G | 8 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(5): Show |
8 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.3030+17469A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468734 | |||||||
| chr11:43468880 | G | A | 1 | a0001c0002t0001g0195 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3030+17615G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468880 | |||||||
| chr11:43468908 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3030+17643A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468908 | |||||||
| chr11:43468974 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3030+17709G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468974 | |||||||
| chr11:43469074 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(106): Show |
109 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.3030+17809T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469074 | |||||||
| chr11:43469273 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3030+18008A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469273 | |||||||
| chr11:43469299 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3030+18034A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469299 | |||||||
| chr11:43469391 | A | G | 1 | a0002c0003t0002g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3030+18126A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469391 | |||||||
| chr11:43469757 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+18492G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469757 | |||||||
| chr11:43469853 | A | T | 1 | a0002c0003t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3030+18588A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469853 | |||||||
| chr11:43469872 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0112 others(1): Show |
4 | HG00408.hp2 HG00438.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.3030+18607T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469872 | |||||||
| chr11:43469940 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0245 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3030+18675C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469940 | |||||||
| chr11:43470120 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3030+18855A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470120 | |||||||
| chr11:43470175 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0140 |
3 | HG02922.hp2 HG02976.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.3030+18910C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470175 | |||||||
| chr11:43470264 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3030+18999A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470264 | |||||||
| chr11:43470290 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3030+19025T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470290 | |||||||
| chr11:43470584 | C | T | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+19319C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470584 | |||||||
| chr11:43470654 | C | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3030+19389C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470654 | |||||||
| chr11:43470963 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-19276C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470963 | |||||||
| chr11:43471096 | C | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3031-19143C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471096 | |||||||
| chr11:43471184 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3031-19055C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471184 | |||||||
| chr11:43471198 | A | C | 11 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(8): Show |
11 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.3031-19041A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471198 | |||||||
| chr11:43471236 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-19003A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471236 | |||||||
| chr11:43471276 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3031-18963T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471276 | |||||||
| chr11:43471513 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3031-18726C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471513 | |||||||
| chr11:43471525 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3031-18714G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471525 | |||||||
| chr11:43471590 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(36): Show |
39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3031-18649T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471590 | |||||||
| chr11:43471616 | G | A | 42 | a0001c0001t0001g0240 a0001c0001t0001g0251 a0001c0001t0001g0252 others(39): Show |
42 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.3031-18623G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471616 | |||||||
| chr11:43471731 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(106): Show |
109 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.3031-18508C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471731 | |||||||
| chr11:43472391 | G | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0156 others(2): Show |
5 | HG02148.hp2 NA18964.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-17848G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472391 | |||||||
| chr11:43472406 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3031-17833T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472406 | |||||||
| chr11:43472418 | T | C | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3031-17821T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472418 | |||||||
| chr11:43472674 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3031-17565A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472674 | |||||||
| chr11:43472728 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3031-17511A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472728 | |||||||
| chr11:43472841 | T | TA | 45 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0068 others(42): Show |
45 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.3031-17381dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43472841 | ||||||
| chr11:43472841 | TA | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(5): Show |
8 | HG01884.hp2 HG01928.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.3031-17381delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43472841 | ||||||
| chr11:43472876 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3031-17363G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472876 | |||||||
| chr11:43472903 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3031-17336G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472903 | |||||||
| chr11:43472951 | G | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG00609.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.3031-17288G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472951 | |||||||
| chr11:43473046 | G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3031-17193G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473046 | |||||||
| chr11:43473183 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3031-17056A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473183 | |||||||
| chr11:43473216 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3031-17023A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473216 | |||||||
| chr11:43473597 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3031-16642G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473597 | |||||||
| chr11:43473624 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3031-16615T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473624 | |||||||
| chr11:43473684 | G | A | 1 | a0002c0003t0002g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3031-16555G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473684 | |||||||
| chr11:43473825 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3031-16414G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473825 | |||||||
| chr11:43473882 | C | CA | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG01081.hp2 HG01261.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3031-16340dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43473882 | ||||||
| chr11:43473961 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3031-16278A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473961 | |||||||
| chr11:43473979 | C | T | 1 | a0001c0002t0001g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3031-16260C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473979 | |||||||
| chr11:43474320 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3031-15919T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474320 | |||||||
| chr11:43474401 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3031-15838T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474401 | |||||||
| chr11:43474406 | A | G | 24 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0060 others(21): Show |
24 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.3031-15833A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474406 | |||||||
| chr11:43474493 | C | T | 1 | a0001c0002t0001g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3031-15746C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474493 | |||||||
| chr11:43474580 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
155 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.3031-15659C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474580 | |||||||
| chr11:43474849 | TAAG | T | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3031-15387_3031-15 others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43474849 | ||||||
| chr11:43474963 | G | A | 41 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(38): Show |
41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3031-15276G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474963 | |||||||
| chr11:43474974 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02976.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3031-15265G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474974 | |||||||
| chr11:43475019 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3031-15220G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475019 | |||||||
| chr11:43475033 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3031-15206A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475033 | |||||||
| chr11:43475057 | G | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(77): Show |
80 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.3031-15182G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475057 | |||||||
| chr11:43475078 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0021 |
2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3031-15161G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475078 | |||||||
| chr11:43475160 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3031-15079C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475160 | |||||||
| chr11:43475247 | G | A | 34 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0081 others(31): Show |
34 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.3031-14992G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475247 | |||||||
| chr11:43475949 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.3031-14290C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475949 | |||||||
| chr11:43476024 | T | A | 5 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 others(2): Show |
5 | HG00558.hp2 HG01256.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.3031-14215T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476024 | |||||||
| chr11:43476026 | C | T | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-14213C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476026 | |||||||
| chr11:43476057 | A | G | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-14182A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476057 | |||||||
| chr11:43476319 | A | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.3031-13920A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476319 | |||||||
| chr11:43476356 | A | G | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-13883A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476356 | |||||||
| chr11:43476505 | G | A | 1 | a0002c0003t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3031-13734G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476505 | |||||||
| chr11:43476676 | G | A | 24 | a0001c0002t0001g0050 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.3031-13563G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476676 | |||||||
| chr11:43476746 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3031-13493C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476746 | |||||||
| chr11:43476916 | C | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3031-13323C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476916 | |||||||
| chr11:43477083 | T | C | 1 | a0001c0006t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3031-13156T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477083 | |||||||
| chr11:43477268 | C | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-12971C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477268 | |||||||
| chr11:43477411 | T | G | 1 | a0001c0001t0001g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3031-12828T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477411 | |||||||
| chr11:43477743 | A | G | 1 | a0007c0007t0001g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3031-12496A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477743 | |||||||
| chr11:43477870 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0047 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-12369G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477870 | |||||||
| chr11:43477902 | T | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.3031-12337T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477902 | |||||||
| chr11:43478005 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-12234A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478005 | |||||||
| chr11:43478276 | C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3031-11963C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478276 | |||||||
| chr11:43478378 | G | A | 34 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0081 others(31): Show |
34 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.3031-11861G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478378 | |||||||
| chr11:43478405 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG00558.hp1 NA18948.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.3031-11834T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478405 | |||||||
| chr11:43478455 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0021 |
2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3031-11784C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478455 | |||||||
| chr11:43478592 | A | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-11647A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478592 | |||||||
| chr11:43478715 | C | G | 1 | a0002c0003t0002g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3031-11524C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478715 | |||||||
| chr11:43478721 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3031-11518C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478721 | |||||||
| chr11:43478743 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3031-11496C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478743 | |||||||
| chr11:43478744 | G | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-11495G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478744 | |||||||
| chr11:43478800 | A | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(36): Show |
39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3031-11439A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478800 | |||||||
| chr11:43478918 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(77): Show |
80 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.3031-11321C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478918 | |||||||
| chr11:43478919 | G | A | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-11320G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478919 | |||||||
| chr11:43478962 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3031-11277C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478962 | |||||||
| chr11:43479092 | T | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3031-11147T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479092 | |||||||
| chr11:43479164 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(12): Show |
15 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.3031-11075C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479164 | |||||||
| chr11:43479196 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG01074.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.3031-11043C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479196 | |||||||
| chr11:43479239 | C | CAAA | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-10995_3031-10 others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43479239 | ||||||
| chr11:43479247 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-10992G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479247 | |||||||
| chr11:43479476 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3031-10763A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479476 | |||||||
| chr11:43479784 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3031-10455A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479784 | |||||||
| chr11:43479793 | T | C | 1 | a0002c0003t0002g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3031-10446T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479793 | |||||||
| chr11:43480055 | A | T | 21 | a0002c0003t0001g0226 a0002c0003t0002g0003 a0002c0003t0002g0051 others(18): Show |
21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3031-10184A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480055 | |||||||
| chr11:43480168 | C | A | 25 | a0001c0001t0001g0052 a0001c0002t0001g0050 a0001c0002t0001g0187 others(22): Show |
25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.3031-10071C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480168 | |||||||
| chr11:43480436 | A | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0174 |
3 | NA18964.hp2 NA18972.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3031-9803A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480436 | |||||||
| chr11:43480632 | G | A | 3 | a0002c0003t0002g0220 a0002c0003t0002g0222 a0002c0003t0002g0223 |
3 | HG01891.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3031-9607G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480632 | |||||||
| chr11:43480887 | C | CA | 23 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(20): Show |
23 | HG00099.hp1 HG00639.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.3031-9338dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43480887 | ||||||
| chr11:43480887 | CA | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
21 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.3031-9338delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43480887 | ||||||
| chr11:43480917 | G | A | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-9322G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480917 | |||||||
| chr11:43481057 | AGGT | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3031-9181_3031-917 others(7): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481057 | |||||||
| chr11:43481058 | GGTA | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.3031-9176_3031-917 others(7): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43481058 | ||||||
| chr11:43481146 | T | A | 1 | a0001c0001t0001g0252 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3031-9093T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481146 | |||||||
| chr11:43481151 | T | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-9088T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481151 | |||||||
| chr11:43481186 | C | T | 1 | a0002c0003t0002g0223 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3031-9053C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481186 | |||||||
| chr11:43481231 | AAAAG | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-9002_3031-899 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43481231 | ||||||
| chr11:43481269 | G | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0245 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3031-8970G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481269 | |||||||
| chr11:43481360 | T | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3031-8879T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481360 | |||||||
| chr11:43481445 | G | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-8794G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481445 | |||||||
| chr11:43481486 | G | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3031-8753G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481486 | |||||||
| chr11:43481727 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0173 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3031-8512T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481727 | |||||||
| chr11:43481779 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG01928.hp1 HG01952.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.3031-8460G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481779 | |||||||
| chr11:43481920 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3031-8319G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481920 | |||||||
| chr11:43482258 | GT | G | 45 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
46 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.3031-7969delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43482258 | ||||||
| chr11:43482490 | C | G | 34 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0081 others(31): Show |
34 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.3031-7749C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43482490 | |||||||
| chr11:43482529 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3031-7710T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43482529 | |||||||
| chr11:43482800 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.3031-7439G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43482800 | |||||||
| chr11:43482986 | T | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3031-7253T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43482986 | |||||||
| chr11:43483152 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-7087A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43483152 | |||||||
| chr11:43483174 | TTAAG | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-7062_3031-705 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43483174 | ||||||
| chr11:43483190 | T | TA | 80 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0030 others(77): Show |
80 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.3031-7043dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43483190 | ||||||
| chr11:43483383 | A | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-6856A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43483383 | |||||||
| chr11:43483667 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3031-6572A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43483667 | |||||||
| chr11:43484112 | A | G | 34 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0081 others(31): Show |
34 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.3031-6127A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484112 | |||||||
| chr11:43484157 | T | G | 31 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(28): Show |
32 | HG00099.hp2 HG00639.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3031-6082T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484157 | |||||||
| chr11:43484418 | T | A | 2 | a0001c0001t0005g0103 a0001c0001t0005g0117 |
2 | HG00609.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.3031-5821T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484418 | |||||||
| chr11:43484607 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3031-5632T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484607 | |||||||
| chr11:43484897 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
19 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.3031-5342G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484897 | |||||||
| chr11:43485074 | T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3031-5165T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485074 | |||||||
| chr11:43485245 | A | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3031-4994A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485245 | |||||||
| chr11:43485392 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3031-4847T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485392 | |||||||
| chr11:43485601 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3031-4638A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485601 | |||||||
| chr11:43485699 | T | C | 31 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0081 others(28): Show |
31 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.3031-4540T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485699 | |||||||
| chr11:43485828 | G | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3031-4411G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485828 | |||||||
| chr11:43485851 | T | A | 1 | a0001c0002t0001g0202 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3031-4388T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485851 | |||||||
| chr11:43485883 | G | GT | 10 | a0001c0001t0001g0066 a0001c0001t0001g0099 a0001c0001t0001g0112 others(7): Show |
10 | HG00438.hp1 HG00597.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.3031-4336dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43485883 | ||||||
| chr11:43485883 | GT | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(80): Show |
83 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.3031-4336delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43485883 | ||||||
| chr11:43485883 | GTT | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(17): Show |
21 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.3031-4337_3031-433 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43485883 | ||||||
| chr11:43486157 | T | TC | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
95 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.3031-4075dupC | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43486157 | ||||||
| chr11:43486426 | C | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3031-3813C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486426 | |||||||
| chr11:43486508 | T | C | 1 | a0001c0001t0007g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3031-3731T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486508 | |||||||
| chr11:43486606 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
22 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.3031-3633A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486606 | |||||||
| chr11:43486662 | G | A | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-3577G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486662 | |||||||
| chr11:43486700 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0245 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3031-3539A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486700 | |||||||
| chr11:43486717 | A | G | 1 | a0001c0002t0001g0193 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3031-3522A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486717 | |||||||
| chr11:43486768 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3031-3471A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486768 | |||||||
| chr11:43487131 | A | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.3031-3108A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487131 | |||||||
| chr11:43487206 | C | T | 1 | a0002c0003t0002g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3031-3033C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487206 | |||||||
| chr11:43487292 | C | A | 1 | a0001c0001t0001g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3031-2947C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487292 | |||||||
| chr11:43487334 | C | T | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-2905C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487334 | |||||||
| chr11:43487365 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | HG02886.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3031-2874C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487365 | |||||||
| chr11:43487369 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3031-2870C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487369 | |||||||
| chr11:43487619 | A | C | 26 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0002t0001g0050 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-2620A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487619 | |||||||
| chr11:43487808 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3031-2431C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487808 | |||||||
| chr11:43488031 | A | G | 1 | a0002c0003t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3031-2208A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43488031 | |||||||
| chr11:43488719 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3031-1520G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43488719 | |||||||
| chr11:43489375 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(1): Show |
4 | HG01255.hp1 HG01943.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.3031-864T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489375 | |||||||
| chr11:43489471 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3031-768C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489471 | |||||||
| chr11:43489536 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3031-703G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489536 | |||||||
| chr11:43489717 | G | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
25 | HG00408.hp1 HG00639.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.3031-522G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489717 | |||||||
| chr11:43489718 | A | G | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-521A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489718 | |||||||
| chr11:43489757 | A | AGGAGGGG | 13 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(10): Show |
13 | HG01069.hp1 HG01169.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3031-469_3031-463d others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43489757 | ||||||
| chr11:43489857 | A | G | 68 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(65): Show |
69 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.3031-382A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489857 | |||||||
| chr11:43489966 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3031-273G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489966 | |||||||
| chr11:43490070 | T | A | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-169T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43490070 | |||||||
| chr11:43490079 | G | C | 20 | a0002c0003t0002g0003 a0002c0003t0002g0051 a0002c0003t0002g0208 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-160G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43490079 | |||||||
| chr11:43490181 | G | C | 1 | a0002c0003t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3031-58G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43490181 | |||||||
| chr11:43490231 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.3031-8C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43490231 | |||||||
| chr11:43490574 | G | A | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3150+216G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43490574 | |||||||
| chr11:43490668 | A | C | 19 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(16): Show |
19 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.3150+310A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43490668 | |||||||
| chr11:43490854 | C | CA | 68 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(65): Show |
68 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.3150+524dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | ||||||
| chr11:43490854 | C | CAA | 29 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0028 others(26): Show |
29 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.3150+523_3150+524d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | ||||||
| chr11:43490854 | C | CAAA | 6 | a0001c0002t0001g0193 a0001c0002t0001g0196 a0001c0002t0001g0198 others(3): Show |
6 | HG00738.hp1 HG01175.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+522_3150+524d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | ||||||
| chr11:43490854 | CA | C | 28 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0038 others(25): Show |
28 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.3150+524delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | ||||||
| chr11:43490854 | CAA | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0239 others(3): Show |
6 | HG01243.hp2 HG01516.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+523_3150+524d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | ||||||
| chr11:43490854 | CAAA | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(27): Show |
31 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.3150+522_3150+524d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | ||||||
| chr11:43490854 | CAAAA | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+521_3150+524d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | ||||||
| chr11:43491048 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3150+690G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491048 | |||||||
| chr11:43491230 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
22 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.3151-790C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491230 | |||||||
| chr11:43491303 | A | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3151-717A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491303 | |||||||
| chr11:43491421 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3151-599G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491421 | |||||||
| chr11:43491800 | C | T | 23 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0262 others(20): Show |
23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.3151-220C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491800 | |||||||
| chr11:43491813 | C | T | 33 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(30): Show |
33 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.3151-207C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491813 | |||||||
| chr11:43491995 | C | T | 2 | a0003c0004t0001g0246 a0003c0004t0001g0247 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3151-25C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491995 | |||||||
| chr11:43491999 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18945.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3151-21C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491999 | |||||||
| chr11:43492385 | A | G | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3294+222A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492385 | |||||||
| chr11:43492508 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3294+345T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492508 | |||||||
| chr11:43492630 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3294+467T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492630 | |||||||
| chr11:43492731 | G | A | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3294+568G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492731 | |||||||
| chr11:43492980 | A | G | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
46 | HG00099.hp2 HG00323.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.3295-793A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492980 | |||||||
| chr11:43493160 | T | G | 11 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(8): Show |
11 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.3295-613T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493160 | |||||||
| chr11:43493201 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3295-572A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493201 | |||||||
| chr11:43493202 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3295-571C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493202 | |||||||
| chr11:43493381 | G | A | 47 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(44): Show |
48 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.3295-392G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493381 | |||||||
| chr11:43493754 | C | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
115 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.3295-19C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493754 |