Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7267 |
| ensemblid | ENSG00000182670.14 |
| hgncid | 12393 |
| symbol | TTC3 |
| name | tetratricopeptide repeat domain 3 |
| refseq_nuc | NM_001330683.2 |
| refseq_prot | NP_001317612.1 |
| ensembl_nuc | ENST00000418766.6 |
| ensembl_prot | ENSP00000403943.2 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 37073254 |
| end | 37203107 |
| strand | + |
| ver | v1.2 |
| region | chr21:37073254-37203107 |
| region5000 | chr21:37068254-37208107 |
| regionname0 | TTC3_chr21_37073254_37203107 |
| regionname5000 | TTC3_chr21_37068254_37208107 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 2025 | 176 | 51 | 37 | 78 | 3 | 7 | 61 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0002 | 1/1 | 2025 | 72 | 3 | 22 | 30 | 5 | 10 | 25 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0003 | 0/0 | 2025 | 57 | 17 | 6 | 34 | 0 | 0 | 26 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0004 | 0/0 | 2025 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0005 | 0/0 | 2025 | 6 | 0 | 2 | 0 | 2 | 2 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0006 | 0/0 | 2025 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0007 | 0/0 | 2025 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0008 | 0/0 | 2025 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0009 | 0/0 | 2025 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0010 | 0/0 | 2025 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0011 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0012 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0013 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| a0014 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | MDNFA others(2020): Show |
chr21 | 37068254 | 37208107 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 6075 | 99 | 20 | 12 | 59 | 1 | 7 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0001c0004 | 0/0 | 6075 | 39 | 14 | 15 | 10 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0001c0005 | 0/0 | 6075 | 33 | 14 | 9 | 9 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0001c0014 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0001c0021 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0001c0022 | 0/0 | 6075 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0001c0023 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0001c0024 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0002c0002 | 1/1 | 6075 | 72 | 3 | 22 | 30 | 5 | 10 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0003c0003 | 0/0 | 6075 | 54 | 16 | 6 | 32 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0003c0013 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0003c0016 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0003c0018 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0004c0006 | 0/0 | 6075 | 11 | 9 | 2 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0005c0007 | 0/0 | 6075 | 6 | 0 | 2 | 0 | 2 | 2 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0006c0011 | 0/0 | 6075 | 3 | 2 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0007c0008 | 0/0 | 6075 | 3 | 0 | 1 | 2 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0008c0009 | 0/0 | 6075 | 3 | 0 | 2 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0009c0010 | 0/0 | 6075 | 3 | 3 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0010c0012 | 0/0 | 6075 | 2 | 0 | 0 | 0 | 0 | 2 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0011c0020 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0012c0019 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0013c0017 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 | ||
| a0014c0015 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ATGGA others(6070): Show |
chr21 | 37068254 | 37208107 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 7842 | 90 | 12 | 12 | 58 | 1 | 7 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0001c0001t0007 | 0/0 | 7829 | 7 | 7 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7824): Show |
chr21 | 37068254 | 37208107 |
| a0001c0001t0013 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCAG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0001c0001t0016 | 0/0 | 7829 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7824): Show |
chr21 | 37068254 | 37208107 |
| a0001c0004t0003 | 0/0 | 7842 | 33 | 9 | 14 | 10 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0001c0004t0010 | 0/0 | 7839 | 5 | 5 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7834): Show |
chr21 | 37068254 | 37208107 |
| a0001c0004t0015 | 0/0 | 7842 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0001c0005t0002 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0001c0005t0004 | 0/0 | 7842 | 25 | 10 | 6 | 9 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0001c0005t0008 | 0/0 | 7845 | 6 | 2 | 3 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0001c0005t0022 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0001c0014t0006 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0001c0021t0002 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0001c0022t0002 | 0/0 | 7842 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0001c0023t0008 | 0/0 | 7845 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0001c0024t0002 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0002c0002t0001 | 0/1 | 7845 | 62 | 2 | 18 | 29 | 5 | 7 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0002c0002t0009 | 1/0 | 7842 | 5 | 0 | 3 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0002c0002t0014 | 0/0 | 7860 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7855): Show |
chr21 | 37068254 | 37208107 |
| a0002c0002t0018 | 0/0 | 7845 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0002c0002t0019 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0002c0002t0020 | 0/0 | 7845 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0002c0002t0021 | 0/0 | 7845 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0003c0003t0001 | 0/0 | 7845 | 44 | 12 | 6 | 26 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0003c0003t0009 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0003c0003t0011 | 0/0 | 7848 | 4 | 4 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7843): Show |
chr21 | 37068254 | 37208107 |
| a0003c0003t0012 | 0/0 | 7845 | 2 | 0 | 0 | 2 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0003c0003t0017 | 0/0 | 7845 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0003c0003t0023 | 0/0 | 7845 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0003c0003t0024 | 0/0 | 7848 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7843): Show |
chr21 | 37068254 | 37208107 |
| a0003c0013t0001 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0003c0016t0001 | 0/0 | 7845 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0003c0018t0001 | 0/0 | 7845 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0004c0006t0005 | 0/0 | 7839 | 11 | 9 | 2 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7834): Show |
chr21 | 37068254 | 37208107 |
| a0005c0007t0002 | 0/0 | 7842 | 6 | 0 | 2 | 0 | 2 | 2 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0006c0011t0001 | 0/0 | 7845 | 3 | 2 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0007c0008t0006 | 0/0 | 7845 | 3 | 0 | 1 | 2 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0008c0009t0006 | 0/0 | 7845 | 3 | 0 | 2 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0009c0010t0006 | 0/0 | 7845 | 3 | 3 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0010c0012t0002 | 0/0 | 7842 | 2 | 0 | 0 | 0 | 0 | 2 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0011c0020t0002 | 0/0 | 7842 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7837): Show |
chr21 | 37068254 | 37208107 |
| a0012c0019t0001 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0013c0017t0001 | 0/0 | 7845 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| a0014c0015t0001 | 0/0 | 7845 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | ACCCG others(7840): Show |
chr21 | 37068254 | 37208107 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0001t0016g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0010g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0010g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0010g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0004t0015g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0008g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0008g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0008g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0008g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0008g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0005t0022g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0014t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0021t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0022t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0023t0008g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0001c0024t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0009g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0009g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0009g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0009g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0014g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0018g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0019g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0020g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0002c0002t0021g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0011g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0011g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0011g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0012g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0012g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0017g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0023g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0003t0024g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0013t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0016t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0003c0018t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0004c0006t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0005c0007t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0005c0007t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0005c0007t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0005c0007t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0005c0007t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0005c0007t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0006c0011t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0006c0011t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0006c0011t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0007c0008t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0007c0008t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0007c0008t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0008c0009t0006g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0008c0009t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0008c0009t0006g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0009c0010t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0009c0010t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0009c0010t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0010c0012t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0010c0012t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0011c0020t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0012c0019t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0013c0017t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| a0014c0015t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0007 | t0002 | g0044 | EUR | GBR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00099 | hp2 | a0001 | c0005 | t0008 | g0324 | EUR | GBR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00544 | hp2 | a0001 | c0004 | t0003 | g0024 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0238 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0257 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00621 | hp1 | a0002 | c0002 | t0009 | g0116 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00621 | hp2 | a0003 | c0003 | t0017 | g0230 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00639 | hp2 | a0001 | c0004 | t0015 | g0294 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0260 | EAS | CHS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00733 | hp1 | a0001 | c0005 | t0004 | g0315 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00735 | hp2 | a0003 | c0003 | t0001 | g0187 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00738 | hp2 | a0005 | c0007 | t0002 | g0109 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG00741 | hp2 | a0001 | c0004 | t0003 | g0289 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01069 | hp1 | a0002 | c0002 | t0018 | g0174 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01069 | hp2 | a0001 | c0004 | t0003 | g0010 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01071 | hp2 | a0001 | c0004 | t0003 | g0012 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01099 | hp1 | a0006 | c0011 | t0001 | g0221 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01106 | hp1 | a0005 | c0007 | t0002 | g0115 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01106 | hp2 | a0004 | c0006 | t0005 | g0287 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01109 | hp1 | a0001 | c0005 | t0008 | g0322 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01109 | hp2 | a0004 | c0006 | t0005 | g0283 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0188 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01243 | hp1 | a0008 | c0009 | t0006 | g0263 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01243 | hp2 | a0001 | c0004 | t0003 | g0291 | AMR | PUR | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01255 | hp2 | a0001 | c0005 | t0004 | g0318 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01257 | hp1 | a0001 | c0004 | t0003 | g0295 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01257 | hp2 | a0001 | c0004 | t0003 | g0008 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01258 | hp1 | a0001 | c0004 | t0003 | g0296 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01261 | hp1 | a0001 | c0004 | t0003 | g0009 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01261 | hp2 | a0001 | c0005 | t0008 | g0243 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01346 | hp1 | a0001 | c0004 | t0003 | g0013 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0305 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01361 | hp2 | a0001 | c0005 | t0004 | g0325 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0149 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01433 | hp2 | a0011 | c0020 | t0002 | g0050 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0192 | EUR | IBS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01515 | hp2 | a0005 | c0007 | t0002 | g0051 | EUR | IBS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0103 | EUR | IBS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0177 | EUR | IBS | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0189 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01884 | hp2 | a0003 | c0003 | t0011 | g0250 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0216 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01928 | hp1 | a0001 | c0004 | t0003 | g0006 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01928 | hp2 | a0001 | c0023 | t0008 | g0259 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01934 | hp1 | a0001 | c0005 | t0004 | g0328 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0223 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01943 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0224 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01975 | hp1 | a0001 | c0005 | t0004 | g0319 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01978 | hp1 | a0008 | c0009 | t0006 | g0265 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01978 | hp2 | a0001 | c0004 | t0003 | g0021 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01981 | hp1 | a0001 | c0004 | t0003 | g0005 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01993 | hp2 | a0002 | c0002 | t0009 | g0030 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02004 | hp1 | a0002 | c0002 | t0009 | g0064 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02004 | hp2 | a0001 | c0005 | t0004 | g0320 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02055 | hp2 | a0003 | c0003 | t0011 | g0252 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02071 | hp2 | a0003 | c0018 | t0001 | g0231 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02080 | hp1 | a0001 | c0005 | t0004 | g0326 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02129 | hp1 | a0003 | c0016 | t0001 | g0241 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02145 | hp2 | a0001 | c0004 | t0003 | g0300 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02148 | hp1 | a0001 | c0005 | t0008 | g0262 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0136 | EAS | CDX | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CDX | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02257 | hp1 | a0001 | c0005 | t0008 | g0330 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0184 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02258 | hp1 | a0004 | c0006 | t0005 | g0280 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02258 | hp2 | a0001 | c0005 | t0004 | g0321 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02273 | hp1 | a0001 | c0004 | t0003 | g0016 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02273 | hp2 | a0002 | c0002 | t0009 | g0063 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02293 | hp1 | a0003 | c0003 | t0001 | g0143 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02300 | hp2 | a0003 | c0003 | t0001 | g0144 | AMR | PEL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02451 | hp1 | a0001 | c0004 | t0003 | g0290 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02451 | hp2 | a0002 | c0002 | t0019 | g0214 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02572 | hp1 | a0001 | c0004 | t0003 | g0299 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0198 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02615 | hp1 | a0006 | c0011 | t0001 | g0222 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02615 | hp2 | a0001 | c0024 | t0002 | g0135 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02622 | hp1 | a0001 | c0005 | t0004 | g0333 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02622 | hp2 | a0001 | c0014 | t0006 | g0307 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0303 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02630 | hp2 | a0001 | c0004 | t0010 | g0272 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02647 | hp1 | a0004 | c0006 | t0005 | g0285 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02647 | hp2 | a0001 | c0004 | t0003 | g0297 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0185 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02717 | hp2 | a0004 | c0006 | t0005 | g0279 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02723 | hp2 | a0001 | c0004 | t0003 | g0292 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02735 | hp1 | a0002 | c0002 | t0014 | g0153 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02809 | hp1 | a0001 | c0005 | t0004 | g0312 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02809 | hp2 | a0006 | c0011 | t0001 | g0306 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0266 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0276 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0275 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02886 | hp2 | a0004 | c0006 | t0005 | g0282 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02895 | hp2 | a0001 | c0004 | t0010 | g0268 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02896 | hp1 | a0001 | c0021 | t0002 | g0097 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02896 | hp2 | a0001 | c0005 | t0004 | g0310 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02897 | hp2 | a0001 | c0005 | t0004 | g0311 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02922 | hp2 | a0004 | c0006 | t0005 | g0277 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02965 | hp1 | a0001 | c0004 | t0010 | g0271 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0186 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02976 | hp1 | a0009 | c0010 | t0006 | g0213 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02976 | hp2 | a0001 | c0004 | t0003 | g0288 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03041 | hp1 | a0003 | c0003 | t0011 | g0251 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03098 | hp1 | a0009 | c0010 | t0006 | g0137 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0267 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03130 | hp2 | a0001 | c0005 | t0004 | g0313 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03139 | hp1 | a0001 | c0004 | t0003 | g0298 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0254 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03195 | hp1 | a0001 | c0005 | t0004 | g0332 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03195 | hp2 | a0001 | c0005 | t0022 | g0308 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0255 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03209 | hp2 | a0001 | c0004 | t0010 | g0270 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0203 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03486 | hp1 | a0004 | c0006 | t0005 | g0284 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03490 | hp1 | a0010 | c0012 | t0002 | g0068 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03516 | hp1 | a0009 | c0010 | t0006 | g0138 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03516 | hp2 | a0004 | c0006 | t0005 | g0286 | AFR | ESN | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03540 | hp2 | a0003 | c0003 | t0011 | g0253 | AFR | GWD | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03579 | hp1 | a0001 | c0005 | t0002 | g0033 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03579 | hp2 | a0001 | c0005 | t0004 | g0336 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | STU | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03688 | hp2 | a0002 | c0002 | t0021 | g0196 | SAS | STU | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03704 | hp1 | a0005 | c0007 | t0002 | g0078 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0194 | SAS | BEB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG04184 | hp1 | a0002 | c0002 | t0020 | g0155 | SAS | BEB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | BEB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG04199 | hp1 | a0008 | c0009 | t0006 | g0264 | SAS | STU | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG04199 | hp2 | a0005 | c0007 | t0002 | g0069 | SAS | STU | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | STU | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0204 | SAS | STU | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0197 | AFR | YRI | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | YRI | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | CHB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0225 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18947 | hp1 | a0001 | c0004 | t0003 | g0023 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18948 | hp1 | a0003 | c0003 | t0009 | g0057 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18954 | hp2 | a0001 | c0004 | t0003 | g0011 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18956 | hp2 | a0001 | c0004 | t0003 | g0017 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18960 | hp1 | a0003 | c0003 | t0001 | g0240 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0228 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18964 | hp2 | a0001 | c0005 | t0004 | g0316 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0239 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18967 | hp1 | a0001 | c0005 | t0004 | g0329 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0229 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18970 | hp2 | a0003 | c0003 | t0001 | g0237 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18971 | hp1 | a0003 | c0003 | t0001 | g0248 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18973 | hp2 | a0001 | c0005 | t0004 | g0327 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18979 | hp2 | a0001 | c0005 | t0004 | g0337 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18981 | hp2 | a0003 | c0003 | t0012 | g0234 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18983 | hp1 | a0007 | c0008 | t0006 | g0140 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0244 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18986 | hp2 | a0001 | c0004 | t0003 | g0007 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18988 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18991 | hp1 | a0003 | c0003 | t0001 | g0246 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18994 | hp1 | a0001 | c0004 | t0003 | g0015 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18995 | hp1 | a0013 | c0017 | t0001 | g0181 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18998 | hp2 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0232 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19004 | hp1 | a0001 | c0005 | t0004 | g0323 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19004 | hp2 | a0003 | c0003 | t0012 | g0235 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19005 | hp1 | a0001 | c0004 | t0003 | g0018 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0226 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19011 | hp2 | a0003 | c0003 | t0024 | g0233 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19030 | hp1 | a0001 | c0005 | t0004 | g0334 | AFR | LWK | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19030 | hp2 | a0003 | c0013 | t0001 | g0218 | AFR | LWK | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0301 | AFR | LWK | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0273 | AFR | LWK | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19054 | hp2 | a0001 | c0004 | t0003 | g0022 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19062 | hp1 | a0001 | c0001 | t0013 | g0134 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19062 | hp2 | a0014 | c0015 | t0001 | g0164 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19067 | hp2 | a0003 | c0003 | t0023 | g0256 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19068 | hp1 | a0001 | c0005 | t0004 | g0314 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0245 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19072 | hp1 | a0001 | c0004 | t0003 | g0020 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19075 | hp2 | a0001 | c0005 | t0004 | g0309 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19080 | hp2 | a0003 | c0003 | t0001 | g0258 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19085 | hp1 | a0001 | c0005 | t0004 | g0317 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0227 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0242 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19240 | hp1 | a0004 | c0006 | t0005 | g0278 | AFR | YRI | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0096 | AFR | YRI | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20129 | hp1 | a0001 | c0005 | t0004 | g0335 | AFR | ASW | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20129 | hp2 | a0001 | c0005 | t0008 | g0331 | AFR | ASW | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0210 | EUR | TSI | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20752 | hp2 | a0001 | c0022 | t0002 | g0067 | EUR | TSI | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0211 | EUR | TSI | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0173 | EUR | TSI | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0208 | SAS | GIH | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20905 | hp2 | a0010 | c0012 | t0002 | g0098 | SAS | GIH | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG01123 | hp2 | a0007 | c0008 | t0006 | g0141 | AMR | CLM | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02109 | hp2 | a0001 | c0004 | t0010 | g0269 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02486 | hp1 | a0004 | c0006 | t0005 | g0281 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0217 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0274 | AFR | MSL | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG06807 | hp1 | a0012 | c0019 | t0001 | g0302 | AFR | USA | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| HG06807 | hp2 | a0001 | c0004 | t0003 | g0293 | AFR | USA | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18955 | hp1 | a0007 | c0008 | t0006 | g0142 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | USA | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| NA20300 | hp2 | a0001 | c0004 | t0003 | g0014 | AFR | USA | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0025 | REF | REF | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0009 | g0090 | REF | REF | TTC3_chr21_37068254_37208107 | TTC3 | chr21 | 37068254 | 37208107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:37121973 | C | G | 1 | a0005 | 6 | HG00099.hp1 HG00738.hp2 HG01106.hp1 others(3): Show |
missense_variant | MODERATE | c.1057C>G | p.Leu353Val | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/46 | 1288/7842 | 1057/6078 | 353/2025 | chr21 | 37121973 | |||
| chr21:37153056 | T | C | 8 | a0001 a0004 a0005 others(5): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
missense_variant | MODERATE | c.2519T>C | p.Met840Thr | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/46 | 2750/7842 | 2519/6078 | 840/2025 | chr21 | 37153056 | |||
| chr21:37156685 | G | A | 1 | a0011 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.2771G>A | p.Arg924His | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/46 | 3002/7842 | 2771/6078 | 924/2025 | chr21 | 37156685 | |||
| chr21:37164083 | C | T | 1 | a0012 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.3203C>T | p.Ala1068Val | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 32/46 | 3434/7842 | 3203/6078 | 1068/2025 | chr21 | 37164083 | |||
| chr21:37165716 | T | C | 1 | a0007 | 3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
missense_variant | MODERATE | c.3502T>C | p.Cys1168Arg | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/46 | 3733/7842 | 3502/6078 | 1168/2025 | chr21 | 37165716 | |||
| chr21:37165881 | G | A | 1 | a0014 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.3667G>A | p.Val1223Met | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/46 | 3898/7842 | 3667/6078 | 1223/2025 | chr21 | 37165881 | |||
| chr21:37165989 | G | A | 1 | a0006 | 3 | HG01099.hp1 HG02615.hp1 HG02809.hp2 |
missense_variant | MODERATE | c.3775G>A | p.Asp1259Asn | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/46 | 4006/7842 | 3775/6078 | 1259/2025 | chr21 | 37165989 | |||
| chr21:37166017 | A | G | 1 | a0004 | 11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
missense_variant | MODERATE | c.3803A>G | p.Asp1268Gly | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/46 | 4034/7842 | 3803/6078 | 1268/2025 | chr21 | 37166017 | |||
| chr21:37185741 | A | G | 1 | a0009 | 3 | HG02976.hp1 HG03098.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.4793A>G | p.His1598Arg | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/46 | 5024/7842 | 4793/6078 | 1598/2025 | chr21 | 37185741 | |||
| chr21:37191338 | C | T | 2 | a0008 a0009 |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
missense_variant | MODERATE | c.5029C>T | p.Pro1677Ser | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 40/46 | 5260/7842 | 5029/6078 | 1677/2025 | chr21 | 37191338 | |||
| chr21:37191385 | G | C | 1 | a0010 | 2 | HG03490.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.5076G>C | p.Leu1692Phe | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 40/46 | 5307/7842 | 5076/6078 | 1692/2025 | chr21 | 37191385 | |||
| chr21:37195708 | G | C | 11 | a0001 a0003 a0004 others(8): Show |
264 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(261): Show |
missense_variant | MODERATE | c.5251G>C | p.Asp1751His | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/46 | 5482/7842 | 5251/6078 | 1751/2025 | chr21 | 37195708 | |||
| chr21:37195747 | A | T | 1 | a0013 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.5290A>T | p.Thr1764Ser | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/46 | 5521/7842 | 5290/6078 | 1764/2025 | chr21 | 37195747 | |||
| chr21:37195958 | C | T | 1 | a0007 | 3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
missense_variant | MODERATE | c.5501C>T | p.Ala1834Val | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/46 | 5732/7842 | 5501/6078 | 1834/2025 | chr21 | 37195958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:37087323 | C | T | 1 | a0001c0024 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.66C>T | p.His22His | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 2/46 | 297/7842 | 66/6078 | 22/2025 | chr21 | 37087323 | |||
| chr21:37126118 | T | C | 1 | a0003c0013 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1272T>C | p.Cys424Cys | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/46 | 1503/7842 | 1272/6078 | 424/2025 | chr21 | 37126118 | |||
| chr21:37140656 | A | G | 11 | a0001c0001 a0001c0004 a0001c0005 others(8): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
synonymous_variant | LOW | c.1755A>G | p.Val585Val | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/46 | 1986/7842 | 1755/6078 | 585/2025 | chr21 | 37140656 | |||
| chr21:37151926 | A | G | 2 | a0001c0004 a0004c0006 |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
synonymous_variant | LOW | c.2310A>G | p.Lys770Lys | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/46 | 2541/7842 | 2310/6078 | 770/2025 | chr21 | 37151926 | |||
| chr21:37153144 | A | G | 1 | a0001c0014 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.2607A>G | p.Ala869Ala | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/46 | 2838/7842 | 2607/6078 | 869/2025 | chr21 | 37153144 | |||
| chr21:37165898 | A | G | 1 | a0003c0018 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.3684A>G | p.Ser1228Ser | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/46 | 3915/7842 | 3684/6078 | 1228/2025 | chr21 | 37165898 | |||
| chr21:37165982 | A | G | 1 | a0001c0023 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.3768A>G | p.Pro1256Pro | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/46 | 3999/7842 | 3768/6078 | 1256/2025 | chr21 | 37165982 | |||
| chr21:37166321 | G | A | 1 | a0001c0021 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.4107G>A | p.Pro1369Pro | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/46 | 4338/7842 | 4107/6078 | 1369/2025 | chr21 | 37166321 | |||
| chr21:37191424 | G | A | 8 | a0001c0001 a0001c0021 a0001c0022 others(5): Show |
112 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(109): Show |
splice_region_variant&synonymous_variant | LOW | c.5115G>A | p.Lys1705Lys | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 40/46 | 5346/7842 | 5115/6078 | 1705/2025 | chr21 | 37191424 | |||
| chr21:37195914 | C | T | 1 | a0007c0008 | 3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
synonymous_variant | LOW | c.5457C>T | p.Ser1819Ser | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/46 | 5688/7842 | 5457/6078 | 1819/2025 | chr21 | 37195914 | |||
| chr21:37196007 | C | T | 11 | a0001c0001 a0001c0004 a0001c0005 others(8): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
synonymous_variant | LOW | c.5550C>T | p.His1850His | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/46 | 5781/7842 | 5550/6078 | 1850/2025 | chr21 | 37196007 | |||
| chr21:37197573 | T | C | 1 | a0001c0022 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.5583T>C | p.Thr1861Thr | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 43/46 | 5814/7842 | 5583/6078 | 1861/2025 | chr21 | 37197573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:37073257 | C | A | 1 | a0001c0001t0013 | 1 | NA19062.hp1 | 5_prime_UTR_variant | MODIFIER | c.-228C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/46 | 14001 | chr21 | 37073257 | ||||||
| chr21:37073296 | TGGC | T | 2 | a0001c0004t0010 a0004c0006t0005 |
16 | HG01106.hp2 HG01109.hp2 HG02109.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-170_-168delGGC | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/46 | 13941 | INFO_REALIGN_3_PRIME | chr21 | 37073296 | |||||
| chr21:37073315 | G | GGCT | 23 | a0001c0005t0008 a0001c0005t0022 a0001c0014t0006 others(20): Show |
140 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(137): Show |
5_prime_UTR_variant | MODIFIER | c.-155_-153dupTGC | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/46 | 13925 | INFO_REALIGN_3_PRIME | chr21 | 37073315 | |||||
| chr21:37073315 | G | GGCTGCT | 2 | a0003c0003t0011 a0003c0003t0024 |
5 | HG01884.hp2 HG02055.hp2 HG03041.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-158_-153dupTGCTGC | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/46 | 13925 | INFO_REALIGN_3_PRIME | chr21 | 37073315 | |||||
| chr21:37073315 | G | GGCTGCTG others(11): Show |
1 | a0002c0002t0014 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-156_-155insGGCTGC others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/46 | 13928 | INFO_REALIGN_3_PRIME | chr21 | 37073315 | |||||
| chr21:37073361 | C | T | 1 | a0003c0003t0023 | 1 | NA19067.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/46 | 13897 | chr21 | 37073361 | ||||||
| chr21:37073397 | C | T | 1 | a0001c0005t0022 | 1 | HG03195.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-88C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/46 | chr21 | 37073397 | |||||||
| chr21:37201715 | C | T | 2 | a0003c0003t0012 a0003c0003t0024 |
3 | NA18981.hp2 NA19004.hp2 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 141 | chr21 | 37201715 | ||||||
| chr21:37201717 | C | T | 23 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(20): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*143C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 143 | chr21 | 37201717 | ||||||
| chr21:37201791 | A | G | 3 | a0001c0005t0004 a0001c0005t0008 a0001c0023t0008 |
32 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*217A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 217 | chr21 | 37201791 | ||||||
| chr21:37201818 | G | C | 1 | a0003c0003t0017 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*244G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 244 | chr21 | 37201818 | ||||||
| chr21:37201912 | G | A | 3 | a0001c0004t0003 a0001c0004t0010 a0001c0004t0015 |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*338G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 338 | chr21 | 37201912 | ||||||
| chr21:37201912 | GCCCCACG others(6): Show |
G | 2 | a0001c0001t0007 a0001c0001t0016 |
8 | HG02109.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*356_*368delACGTTT others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 356 | INFO_REALIGN_3_PRIME | chr21 | 37201912 | |||||
| chr21:37202145 | A | G | 1 | a0002c0002t0021 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*571A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 571 | chr21 | 37202145 | ||||||
| chr21:37202203 | G | A | 1 | a0001c0001t0016 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*629G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 629 | chr21 | 37202203 | ||||||
| chr21:37202373 | C | G | 19 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(16): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*799C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 799 | chr21 | 37202373 | ||||||
| chr21:37202374 | T | C | 19 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(16): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*800T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 800 | chr21 | 37202374 | ||||||
| chr21:37202379 | T | C | 23 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(20): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*805T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 805 | chr21 | 37202379 | ||||||
| chr21:37202528 | A | G | 1 | a0002c0002t0020 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*954A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 954 | chr21 | 37202528 | ||||||
| chr21:37202555 | C | T | 1 | a0002c0002t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 981 | chr21 | 37202555 | ||||||
| chr21:37202583 | A | T | 1 | a0002c0002t0018 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1009A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 1009 | chr21 | 37202583 | ||||||
| chr21:37202945 | A | G | 1 | a0001c0004t0015 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 46/46 | 1371 | chr21 | 37202945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:37073536 | G | A | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+63G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073536 | |||||||
| chr21:37073579 | A | G | 225 | a0001c0001t0007g0266 a0001c0001t0007g0273 a0001c0001t0007g0274 others(222): Show |
227 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(224): Show |
intron_variant | MODIFIER | c.-12+106A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073579 | |||||||
| chr21:37073593 | G | GC | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+125dupC | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37073593 | ||||||
| chr21:37073668 | C | T | 31 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-12+195C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073668 | |||||||
| chr21:37073673 | C | T | 1 | a0006c0011t0001g0306 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12+200C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073673 | |||||||
| chr21:37073729 | C | G | 2 | a0002c0002t0001g0304 a0002c0002t0001g0305 |
2 | HG01255.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-12+256C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073729 | |||||||
| chr21:37073754 | T | C | 225 | a0001c0001t0007g0266 a0001c0001t0007g0273 a0001c0001t0007g0274 others(222): Show |
227 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(224): Show |
intron_variant | MODIFIER | c.-12+281T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073754 | |||||||
| chr21:37073813 | G | C | 1 | a0003c0003t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-12+340G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073813 | |||||||
| chr21:37073838 | T | A | 1 | a0001c0001t0002g0026 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-12+365T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073838 | |||||||
| chr21:37073892 | C | T | 1 | a0001c0005t0004g0337 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-12+419C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073892 | |||||||
| chr21:37073932 | G | A | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+459G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37073932 | |||||||
| chr21:37074017 | GTA | G | 3 | a0003c0003t0001g0301 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-12+546_-12+547del others(2): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37074017 | ||||||
| chr21:37074019 | A | G | 145 | a0001c0001t0002g0040 a0001c0001t0002g0047 a0001c0001t0002g0048 others(142): Show |
147 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.-12+546A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074019 | |||||||
| chr21:37074021 | C | G | 3 | a0003c0003t0001g0301 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-12+548C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074021 | |||||||
| chr21:37074055 | G | C | 1 | a0001c0001t0002g0027 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-12+582G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074055 | |||||||
| chr21:37074159 | CA | C | 34 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(31): Show |
34 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12+687delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074159 | |||||||
| chr21:37074163 | A | G | 34 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(31): Show |
34 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12+690A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074163 | |||||||
| chr21:37074166 | G | C | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+693G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074166 | |||||||
| chr21:37074281 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+808T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074281 | |||||||
| chr21:37074292 | G | A | 2 | a0009c0010t0006g0137 a0009c0010t0006g0138 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-12+819G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074292 | |||||||
| chr21:37074321 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+848A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074321 | |||||||
| chr21:37074521 | A | G | 1 | a0001c0024t0002g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-12+1048A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074521 | |||||||
| chr21:37074618 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+1145A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074618 | |||||||
| chr21:37074655 | A | AT | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+1188dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37074655 | ||||||
| chr21:37074740 | C | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+1267C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074740 | |||||||
| chr21:37074764 | A | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+1291A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074764 | |||||||
| chr21:37074781 | G | T | 1 | a0001c0001t0013g0134 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-12+1308G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074781 | |||||||
| chr21:37074801 | G | A | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-12+1328G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074801 | |||||||
| chr21:37074832 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+1359T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37074832 | |||||||
| chr21:37075084 | A | T | 223 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(220): Show |
225 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(222): Show |
intron_variant | MODIFIER | c.-12+1611A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075084 | |||||||
| chr21:37075123 | A | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+1650A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075123 | |||||||
| chr21:37075166 | C | CT | 168 | a0001c0001t0002g0133 a0001c0005t0004g0309 a0001c0005t0004g0310 others(165): Show |
170 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.-12+1706dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37075166 | ||||||
| chr21:37075181 | C | T | 1 | a0001c0004t0003g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-12+1708C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075181 | |||||||
| chr21:37075189 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+1716C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075189 | |||||||
| chr21:37075284 | T | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-12+1811T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075284 | |||||||
| chr21:37075306 | C | T | 41 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(38): Show |
41 | HG00099.hp2 HG00733.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.-12+1833C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075306 | |||||||
| chr21:37075333 | C | T | 2 | a0003c0003t0001g0303 a0012c0019t0001g0302 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-12+1860C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075333 | |||||||
| chr21:37075441 | C | T | 2 | a0004c0006t0005g0286 a0004c0006t0005g0287 |
2 | HG01106.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-12+1968C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075441 | |||||||
| chr21:37075554 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-12+2081A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075554 | |||||||
| chr21:37075639 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+2166A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075639 | |||||||
| chr21:37075725 | A | G | 136 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(133): Show |
138 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.-12+2252A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075725 | |||||||
| chr21:37075769 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+2296G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075769 | |||||||
| chr21:37075895 | A | G | 3 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 |
3 | HG01243.hp1 HG01978.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-12+2422A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37075895 | |||||||
| chr21:37076300 | A | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+2827A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37076300 | |||||||
| chr21:37076386 | T | G | 2 | a0003c0003t0001g0143 a0003c0003t0001g0144 |
2 | HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-12+2913T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37076386 | |||||||
| chr21:37076544 | G | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+3071G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37076544 | |||||||
| chr21:37076580 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+3107T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37076580 | |||||||
| chr21:37076694 | A | AT | 25 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(22): Show |
25 | HG00621.hp1 HG01106.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.-12+3247dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATT | 13 | a0001c0001t0002g0131 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00597.hp1 HG00639.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+3246_-12+3247d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATTT | 40 | a0001c0001t0002g0132 a0001c0004t0003g0004 a0001c0004t0003g0005 others(37): Show |
40 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.-12+3245_-12+3247d others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATTTT | 29 | a0001c0004t0003g0016 a0001c0004t0003g0017 a0001c0004t0003g0018 others(26): Show |
29 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-12+3244_-12+3247d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATTTTT | 45 | a0001c0005t0008g0243 a0002c0002t0001g0236 a0002c0002t0001g0247 others(42): Show |
47 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.-12+3243_-12+3247d others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATTTTTT | 8 | a0001c0005t0004g0314 a0001c0005t0008g0262 a0001c0023t0008g0259 others(5): Show |
8 | HG00597.hp2 HG00673.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+3242_-12+3247d others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATTTTTTT | 10 | a0001c0005t0004g0315 a0001c0005t0004g0316 a0001c0005t0004g0317 others(7): Show |
10 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+3241_-12+3247d others(9): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATTTTTTT others(1): Show |
8 | a0001c0005t0004g0325 a0001c0005t0004g0326 a0001c0005t0004g0327 others(5): Show |
8 | HG01361.hp2 HG01934.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+3240_-12+3247d others(10): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATTTTTTT others(3): Show |
2 | a0001c0005t0004g0332 a0001c0005t0004g0333 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-12+3238_-12+3247d others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATTTTTTT others(4): Show |
3 | a0001c0005t0004g0334 a0001c0005t0004g0335 a0001c0005t0004g0336 |
3 | HG03579.hp2 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-12+3237_-12+3247d others(13): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | A | ATTTTTTT others(10): Show |
1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-12+3231_-12+3247d others(19): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | AT | A | 11 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0031 others(8): Show |
11 | HG00673.hp1 HG01169.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+3247delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | ATTTTTT | A | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+3242_-12+3247d others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076694 | ATTTTTTT others(3): Show |
A | 41 | a0002c0002t0001g0145 a0002c0002t0001g0146 a0002c0002t0001g0147 others(38): Show |
41 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-12+3238_-12+3247d others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37076694 | ||||||
| chr21:37076948 | G | A | 41 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(38): Show |
41 | HG00099.hp2 HG00733.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.-12+3475G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37076948 | |||||||
| chr21:37077092 | T | C | 1 | a0001c0005t0004g0334 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12+3619T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077092 | |||||||
| chr21:37077100 | C | CT | 138 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(135): Show |
140 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.-12+3637dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37077100 | ||||||
| chr21:37077118 | C | A | 2 | a0003c0003t0001g0223 a0003c0003t0001g0224 |
2 | HG01943.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-12+3645C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077118 | |||||||
| chr21:37077210 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+3737G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077210 | |||||||
| chr21:37077225 | C | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-12+3752C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077225 | |||||||
| chr21:37077246 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-12+3773A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077246 | |||||||
| chr21:37077252 | A | T | 3 | a0001c0001t0002g0001 a0001c0001t0002g0113 a0001c0001t0002g0114 |
4 | HG02056.hp2 NA18747.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+3779A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077252 | |||||||
| chr21:37077266 | T | A | 1 | a0001c0001t0002g0113 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-12+3793T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077266 | |||||||
| chr21:37077329 | A | G | 1 | a0004c0006t0005g0287 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12+3856A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077329 | |||||||
| chr21:37077504 | T | G | 1 | a0001c0004t0003g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-12+4031T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077504 | |||||||
| chr21:37077643 | T | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+4170T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077643 | |||||||
| chr21:37077708 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+4235T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077708 | |||||||
| chr21:37077725 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+4252T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077725 | |||||||
| chr21:37077800 | C | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-12+4327C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077800 | |||||||
| chr21:37077803 | T | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-12+4330T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077803 | |||||||
| chr21:37077842 | G | C | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | NA18984.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-12+4369G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077842 | |||||||
| chr21:37077958 | G | A | 2 | a0003c0003t0001g0002 a0003c0003t0023g0256 |
3 | NA18988.hp1 NA19056.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-12+4485G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077958 | |||||||
| chr21:37077970 | A | T | 2 | a0004c0006t0005g0286 a0004c0006t0005g0287 |
2 | HG01106.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-12+4497A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37077970 | |||||||
| chr21:37078017 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+4544G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37078017 | |||||||
| chr21:37078042 | T | A | 1 | a0005c0007t0002g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-12+4569T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37078042 | |||||||
| chr21:37078257 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+4784C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37078257 | |||||||
| chr21:37078350 | G | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+4877G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37078350 | |||||||
| chr21:37078467 | G | A | 1 | a0005c0007t0002g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-12+4994G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37078467 | |||||||
| chr21:37078606 | C | CTTAT | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+5135_-12+5138d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37078606 | ||||||
| chr21:37078646 | T | C | 2 | a0001c0001t0007g0266 a0001c0001t0016g0267 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-12+5173T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37078646 | |||||||
| chr21:37078830 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+5357C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37078830 | |||||||
| chr21:37078929 | A | G | 1 | a0001c0001t0016g0267 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12+5456A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37078929 | |||||||
| chr21:37079034 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+5561T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079034 | |||||||
| chr21:37079064 | T | A | 1 | a0002c0002t0019g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-12+5591T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079064 | |||||||
| chr21:37079517 | G | GT | 11 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0107 others(8): Show |
11 | HG00673.hp1 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+6078dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37079517 | ||||||
| chr21:37079517 | GT | G | 62 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(59): Show |
62 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-12+6078delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37079517 | ||||||
| chr21:37079517 | GTT | G | 28 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(25): Show |
28 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-12+6077_-12+6078d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37079517 | ||||||
| chr21:37079517 | GTTT | G | 9 | a0001c0004t0003g0004 a0001c0004t0003g0289 a0001c0004t0003g0290 others(6): Show |
9 | HG00741.hp2 HG01243.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+6076_-12+6078d others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37079517 | ||||||
| chr21:37079517 | GTTTT | G | 13 | a0001c0004t0003g0288 a0001c0004t0003g0298 a0002c0002t0001g0139 others(10): Show |
13 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+6075_-12+6078d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37079517 | ||||||
| chr21:37079517 | GTTTTT | G | 139 | a0001c0005t0004g0333 a0001c0005t0008g0243 a0001c0005t0008g0262 others(136): Show |
141 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+6074_-12+6078d others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37079517 | ||||||
| chr21:37079517 | GTTTTTT | G | 14 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(11): Show |
14 | HG01109.hp1 HG01515.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+6073_-12+6078d others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37079517 | ||||||
| chr21:37079517 | GTTTTTTT | G | 15 | a0001c0005t0004g0309 a0001c0005t0004g0315 a0001c0005t0004g0316 others(12): Show |
15 | HG00733.hp1 HG01255.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+6072_-12+6078d others(9): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37079517 | ||||||
| chr21:37079517 | GTTTTTTT others(12): Show |
G | 1 | a0002c0002t0009g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-12+6060_-12+6078d others(21): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37079517 | ||||||
| chr21:37079531 | T | G | 1 | a0008c0009t0006g0265 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-12+6058T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079531 | |||||||
| chr21:37079532 | T | G | 2 | a0002c0002t0001g0183 a0008c0009t0006g0264 |
2 | HG04199.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-12+6059T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079532 | |||||||
| chr21:37079533 | T | G | 135 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(132): Show |
137 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.-12+6060T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079533 | |||||||
| chr21:37079534 | T | G | 1 | a0002c0002t0001g0192 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-12+6061T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079534 | |||||||
| chr21:37079536 | T | G | 1 | a0002c0002t0001g0183 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-12+6063T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079536 | |||||||
| chr21:37079537 | T | G | 134 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(131): Show |
136 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.-12+6064T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079537 | |||||||
| chr21:37079538 | T | G | 1 | a0002c0002t0001g0192 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-12+6065T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079538 | |||||||
| chr21:37079540 | T | G | 1 | a0002c0002t0001g0183 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-12+6067T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079540 | |||||||
| chr21:37079541 | T | G | 127 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(124): Show |
129 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.-12+6068T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079541 | |||||||
| chr21:37079542 | T | G | 1 | a0002c0002t0001g0192 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-12+6069T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079542 | |||||||
| chr21:37079545 | T | G | 47 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(44): Show |
49 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-12+6072T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079545 | |||||||
| chr21:37079566 | C | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-12+6093C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079566 | |||||||
| chr21:37079626 | A | G | 219 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(216): Show |
221 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(218): Show |
intron_variant | MODIFIER | c.-12+6153A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079626 | |||||||
| chr21:37079670 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+6197T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079670 | |||||||
| chr21:37079677 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+6204G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079677 | |||||||
| chr21:37079722 | C | T | 141 | a0001c0001t0007g0266 a0001c0001t0016g0267 a0001c0005t0008g0243 others(138): Show |
143 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.-12+6249C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079722 | |||||||
| chr21:37079727 | T | A | 24 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(21): Show |
24 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-12+6254T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079727 | |||||||
| chr21:37079827 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+6354C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079827 | |||||||
| chr21:37079900 | A | G | 11 | a0001c0001t0002g0027 a0001c0001t0002g0032 a0001c0001t0002g0035 others(8): Show |
11 | HG00639.hp1 HG00733.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+6427A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079900 | |||||||
| chr21:37079952 | A | T | 1 | a0002c0002t0021g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-12+6479A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079952 | |||||||
| chr21:37079994 | G | T | 5 | a0002c0002t0001g0180 a0002c0002t0001g0182 a0002c0002t0001g0183 others(2): Show |
5 | NA18947.hp2 NA18984.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+6521G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37079994 | |||||||
| chr21:37080049 | T | G | 1 | a0002c0002t0001g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-12+6576T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080049 | |||||||
| chr21:37080079 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+6606T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080079 | |||||||
| chr21:37080079 | T | G | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+6606T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080079 | |||||||
| chr21:37080092 | C | T | 2 | a0002c0002t0001g0177 a0002c0002t0001g0178 |
2 | HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-12+6619C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080092 | |||||||
| chr21:37080120 | C | T | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+6647C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080120 | |||||||
| chr21:37080186 | A | G | 6 | a0003c0003t0001g0254 a0003c0003t0001g0255 a0003c0003t0011g0250 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+6713A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080186 | |||||||
| chr21:37080334 | C | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+6861C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080334 | |||||||
| chr21:37080368 | A | AT | 13 | a0001c0001t0002g0114 a0001c0005t0004g0309 a0004c0006t0005g0277 others(10): Show |
13 | HG01106.hp2 HG01109.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-6866dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37080368 | ||||||
| chr21:37080368 | AT | A | 16 | a0001c0001t0002g0040 a0001c0001t0002g0047 a0001c0001t0002g0048 others(13): Show |
16 | HG00741.hp1 HG01433.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-6866delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37080368 | ||||||
| chr21:37080368 | ATT | A | 139 | a0001c0004t0010g0271 a0001c0004t0010g0272 a0001c0005t0008g0243 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-6867_-11-6866d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37080368 | ||||||
| chr21:37080383 | C | G | 1 | a0002c0002t0001g0192 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-11-6864C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080383 | |||||||
| chr21:37080753 | G | A | 5 | a0002c0002t0001g0150 a0002c0002t0001g0151 a0002c0002t0001g0152 others(2): Show |
5 | HG00738.hp1 HG01071.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-6494G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080753 | |||||||
| chr21:37080766 | T | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-6481T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080766 | |||||||
| chr21:37080883 | A | G | 136 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(133): Show |
138 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.-11-6364A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080883 | |||||||
| chr21:37080906 | G | A | 6 | a0001c0001t0002g0027 a0001c0001t0002g0032 a0001c0001t0002g0046 others(3): Show |
6 | HG00733.hp2 HG01516.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-6341G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080906 | |||||||
| chr21:37080927 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-6320T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37080927 | |||||||
| chr21:37080964 | T | TA | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-6279dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37080964 | ||||||
| chr21:37081012 | A | C | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-6235A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081012 | |||||||
| chr21:37081058 | A | ATAC | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-11-6186_-11-6184d others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081058 | ||||||
| chr21:37081089 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-11-6158G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081089 | |||||||
| chr21:37081109 | C | CT | 32 | a0001c0001t0002g0026 a0001c0001t0002g0034 a0001c0001t0002g0045 others(29): Show |
32 | HG00099.hp2 HG01106.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11-6111dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081109 | ||||||
| chr21:37081109 | C | CTT | 10 | a0001c0001t0002g0102 a0001c0001t0002g0128 a0001c0005t0004g0329 others(7): Show |
10 | HG01106.hp2 HG01175.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-6112_-11-6111d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081109 | ||||||
| chr21:37081109 | C | CTTT | 40 | a0001c0005t0004g0333 a0001c0005t0008g0243 a0001c0023t0008g0259 others(37): Show |
42 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.-11-6113_-11-6111d others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081109 | ||||||
| chr21:37081109 | C | CTTTT | 11 | a0001c0005t0008g0262 a0002c0002t0001g0247 a0003c0003t0001g0143 others(8): Show |
11 | HG00673.hp2 HG02148.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-6114_-11-6111d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081109 | ||||||
| chr21:37081109 | CT | C | 97 | a0001c0001t0002g0028 a0001c0001t0002g0032 a0001c0001t0002g0082 others(94): Show |
97 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.-11-6111delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081109 | ||||||
| chr21:37081109 | CTTTTTTT others(6): Show |
C | 2 | a0001c0005t0002g0033 a0001c0005t0022g0308 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-6123_-11-6111d others(15): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081109 | ||||||
| chr21:37081150 | G | A | 1 | a0003c0003t0001g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-11-6097G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081150 | |||||||
| chr21:37081159 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-6088T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081159 | |||||||
| chr21:37081173 | A | G | 1 | a0001c0001t0002g0100 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-11-6074A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081173 | |||||||
| chr21:37081179 | G | A | 3 | a0001c0005t0004g0309 a0001c0005t0004g0323 a0001c0005t0004g0329 |
3 | NA18967.hp1 NA19004.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-11-6068G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081179 | |||||||
| chr21:37081182 | A | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0082 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-11-6065A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081182 | |||||||
| chr21:37081210 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-6037T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081210 | |||||||
| chr21:37081368 | A | G | 3 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 |
3 | HG01261.hp2 HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-11-5879A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081368 | |||||||
| chr21:37081395 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-5852C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081395 | |||||||
| chr21:37081408 | A | G | 226 | a0001c0001t0007g0266 a0001c0001t0007g0273 a0001c0001t0007g0274 others(223): Show |
228 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(225): Show |
intron_variant | MODIFIER | c.-11-5839A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081408 | |||||||
| chr21:37081424 | C | T | 2 | a0001c0001t0002g0074 a0001c0001t0002g0127 |
2 | HG02132.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.-11-5823C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081424 | |||||||
| chr21:37081482 | G | C | 1 | a0008c0009t0006g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-11-5765G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081482 | |||||||
| chr21:37081865 | C | CT | 12 | a0002c0002t0001g0176 a0004c0006t0005g0277 a0004c0006t0005g0278 others(9): Show |
12 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-5365dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081865 | ||||||
| chr21:37081865 | C | CTT | 31 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-11-5366_-11-5365d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081865 | ||||||
| chr21:37081865 | CT | C | 40 | a0001c0001t0002g0029 a0001c0001t0002g0039 a0001c0001t0002g0048 others(37): Show |
40 | HG00544.hp2 HG00673.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-11-5365delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37081865 | ||||||
| chr21:37081866 | T | C | 1 | a0001c0001t0002g0077 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-11-5381T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081866 | |||||||
| chr21:37081904 | G | A | 2 | a0002c0002t0009g0116 a0003c0003t0001g0179 |
2 | HG00621.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-11-5343G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081904 | |||||||
| chr21:37081952 | C | T | 19 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(16): Show |
19 | HG00733.hp1 HG01255.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.-11-5295C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081952 | |||||||
| chr21:37081957 | C | T | 5 | a0001c0001t0002g0046 a0001c0001t0007g0273 a0001c0001t0007g0274 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-5290C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37081957 | |||||||
| chr21:37082021 | C | A | 3 | a0002c0002t0001g0180 a0002c0002t0001g0182 a0013c0017t0001g0181 |
3 | NA18947.hp2 NA18995.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-11-5226C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082021 | |||||||
| chr21:37082039 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-5208G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082039 | |||||||
| chr21:37082145 | A | G | 31 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-11-5102A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082145 | |||||||
| chr21:37082156 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-5091T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082156 | |||||||
| chr21:37082160 | C | T | 2 | a0001c0005t0022g0308 a0003c0003t0001g0226 |
2 | HG03195.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-11-5087C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082160 | |||||||
| chr21:37082259 | A | G | 1 | a0002c0002t0001g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-4988A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082259 | |||||||
| chr21:37082312 | A | AG | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-4930dupG | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37082312 | ||||||
| chr21:37082403 | T | C | 49 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(46): Show |
51 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-11-4844T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082403 | |||||||
| chr21:37082570 | T | C | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-4677T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082570 | |||||||
| chr21:37082651 | G | A | 1 | a0002c0002t0019g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11-4596G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082651 | |||||||
| chr21:37082715 | T | G | 84 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(81): Show |
84 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.-11-4532T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082715 | |||||||
| chr21:37082726 | A | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-11-4521A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082726 | |||||||
| chr21:37082733 | G | A | 1 | a0002c0002t0020g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-11-4514G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082733 | |||||||
| chr21:37082853 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-4394A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37082853 | |||||||
| chr21:37083024 | C | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-4223C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083024 | |||||||
| chr21:37083056 | A | G | 1 | a0002c0002t0019g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11-4191A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083056 | |||||||
| chr21:37083299 | A | G | 5 | a0002c0002t0001g0150 a0002c0002t0001g0151 a0002c0002t0001g0152 others(2): Show |
5 | HG00738.hp1 HG01071.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-3948A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083299 | |||||||
| chr21:37083310 | A | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-11-3937A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083310 | |||||||
| chr21:37083359 | G | T | 1 | a0002c0002t0001g0182 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-11-3888G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083359 | |||||||
| chr21:37083387 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-11-3860A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083387 | |||||||
| chr21:37083608 | C | T | 5 | a0001c0005t0004g0314 a0001c0005t0008g0322 a0001c0005t0008g0324 others(2): Show |
5 | HG00099.hp2 HG01109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-3639C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083608 | |||||||
| chr21:37083612 | G | T | 30 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(27): Show |
30 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-11-3635G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083612 | |||||||
| chr21:37083636 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-3611A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083636 | |||||||
| chr21:37083699 | T | G | 75 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(72): Show |
75 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11-3548T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083699 | |||||||
| chr21:37083818 | C | T | 2 | a0004c0006t0005g0280 a0004c0006t0005g0281 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-11-3429C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37083818 | |||||||
| chr21:37084096 | C | T | 48 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(45): Show |
48 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-11-3151C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37084096 | |||||||
| chr21:37084104 | G | T | 1 | a0001c0005t0008g0262 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-11-3143G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37084104 | |||||||
| chr21:37084327 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-11-2920G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37084327 | |||||||
| chr21:37084437 | T | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-2810T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37084437 | |||||||
| chr21:37084532 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-2715C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37084532 | |||||||
| chr21:37084769 | C | T | 129 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(126): Show |
131 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.-11-2478C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37084769 | |||||||
| chr21:37084891 | G | T | 1 | a0001c0001t0007g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-11-2356G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37084891 | |||||||
| chr21:37084948 | G | A | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11-2299G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37084948 | |||||||
| chr21:37084972 | G | A | 129 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(126): Show |
131 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.-11-2275G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37084972 | |||||||
| chr21:37084991 | T | TCAAA | 60 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(57): Show |
62 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-11-2238_-11-2235d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37084991 | ||||||
| chr21:37084991 | T | TCAAACAA others(1): Show |
74 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(71): Show |
74 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11-2242_-11-2235d others(10): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37084991 | ||||||
| chr21:37085054 | T | TAA | 10 | a0003c0003t0001g0003 a0003c0003t0001g0136 a0003c0003t0001g0227 others(7): Show |
11 | HG00408.hp2 HG00597.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-2192_-11-2191i others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37085054 | ||||||
| chr21:37085063 | A | G | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-2184A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085063 | |||||||
| chr21:37085093 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-2154C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085093 | |||||||
| chr21:37085116 | C | A | 1 | a0001c0001t0002g0133 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-11-2131C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085116 | |||||||
| chr21:37085126 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-11-2121G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085126 | |||||||
| chr21:37085136 | C | T | 1 | a0001c0004t0003g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-11-2111C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085136 | |||||||
| chr21:37085157 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-2090T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085157 | |||||||
| chr21:37085367 | A | T | 1 | a0003c0016t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-11-1880A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085367 | |||||||
| chr21:37085371 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-1876T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085371 | |||||||
| chr21:37085407 | C | A | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-1840C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085407 | |||||||
| chr21:37085408 | C | T | 70 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(67): Show |
70 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.-11-1839C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085408 | |||||||
| chr21:37085620 | C | T | 1 | a0002c0002t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-11-1627C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085620 | |||||||
| chr21:37085665 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11-1582T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085665 | |||||||
| chr21:37085748 | G | A | 6 | a0002c0002t0001g0193 a0002c0002t0001g0195 a0002c0002t0001g0199 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-1499G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085748 | |||||||
| chr21:37085817 | C | T | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.-11-1430C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085817 | |||||||
| chr21:37085859 | A | T | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-1388A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085859 | |||||||
| chr21:37085900 | T | A | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.-11-1347T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37085900 | |||||||
| chr21:37086445 | G | GA | 140 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(137): Show |
142 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.-11-794dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr21 | 37086445 | ||||||
| chr21:37086473 | C | G | 141 | a0001c0001t0002g0029 a0001c0001t0002g0081 a0001c0005t0008g0243 others(138): Show |
143 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.-11-774C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37086473 | |||||||
| chr21:37086554 | C | T | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11-693C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37086554 | |||||||
| chr21:37086760 | C | T | 2 | a0003c0003t0001g0254 a0003c0003t0001g0255 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-11-487C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37086760 | |||||||
| chr21:37086784 | G | C | 1 | a0001c0001t0002g0085 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-11-463G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37086784 | |||||||
| chr21:37086835 | A | G | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11-412A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37086835 | |||||||
| chr21:37086974 | A | C | 1 | a0002c0002t0009g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-11-273A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37086974 | |||||||
| chr21:37087141 | G | A | 2 | a0001c0005t0004g0310 a0001c0005t0004g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-11-106G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37087141 | |||||||
| chr21:37087169 | A | G | 2 | a0004c0006t0005g0282 a0004c0006t0005g0283 |
2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-11-78A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 1/45 | chr21 | 37087169 | |||||||
| chr21:37087425 | A | G | 84 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(81): Show |
84 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.144+24A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 2/45 | chr21 | 37087425 | |||||||
| chr21:37087469 | T | G | 1 | a0002c0002t0001g0199 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.144+68T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 2/45 | chr21 | 37087469 | |||||||
| chr21:37087651 | T | C | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.145-182T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 2/45 | chr21 | 37087651 | |||||||
| chr21:37087665 | G | C | 3 | a0006c0011t0001g0221 a0006c0011t0001g0222 a0006c0011t0001g0306 |
3 | HG01099.hp1 HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.145-168G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 2/45 | chr21 | 37087665 | |||||||
| chr21:37087702 | T | A | 1 | a0001c0004t0003g0300 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.145-131T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 2/45 | chr21 | 37087702 | |||||||
| chr21:37087807 | A | G | 2 | a0003c0003t0001g0303 a0012c0019t0001g0302 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.145-26A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 2/45 | chr21 | 37087807 | |||||||
| chr21:37087947 | G | A | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.187+72G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 3/45 | chr21 | 37087947 | |||||||
| chr21:37088038 | T | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.188-158T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 3/45 | chr21 | 37088038 | |||||||
| chr21:37088188 | T | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
splice_region_variant&intron_variant | LOW | c.188-8T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 3/45 | chr21 | 37088188 | |||||||
| chr21:37088454 | C | T | 5 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(2): Show |
5 | NA18959.hp1 NA18966.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.338+108C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 4/45 | chr21 | 37088454 | |||||||
| chr21:37088590 | G | T | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.339-209G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 4/45 | chr21 | 37088590 | |||||||
| chr21:37088591 | G | T | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.339-208G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 4/45 | chr21 | 37088591 | |||||||
| chr21:37088777 | A | T | 1 | a0001c0001t0002g0122 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.339-22A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 4/45 | chr21 | 37088777 | |||||||
| chr21:37088783 | T | A | 1 | a0001c0001t0002g0122 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.339-16T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 4/45 | chr21 | 37088783 | |||||||
| chr21:37088784 | A | T | 1 | a0001c0001t0002g0122 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.339-15A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 4/45 | chr21 | 37088784 | |||||||
| chr21:37089026 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.426+140G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | chr21 | 37089026 | |||||||
| chr21:37089154 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.426+268A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | chr21 | 37089154 | |||||||
| chr21:37089440 | T | C | 3 | a0002c0002t0001g0156 a0002c0002t0001g0157 a0002c0002t0001g0191 |
3 | NA18940.hp1 NA18975.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.426+554T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | chr21 | 37089440 | |||||||
| chr21:37089495 | A | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.426+609A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | chr21 | 37089495 | |||||||
| chr21:37089512 | T | TTAG | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.426+628_426+629ins others(3): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr21 | 37089512 | ||||||
| chr21:37089578 | A | G | 1 | a0003c0003t0001g0187 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.427-655A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | chr21 | 37089578 | |||||||
| chr21:37089595 | T | C | 19 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(16): Show |
19 | HG00733.hp1 HG01255.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.427-638T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | chr21 | 37089595 | |||||||
| chr21:37089728 | G | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.427-505G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | chr21 | 37089728 | |||||||
| chr21:37089739 | C | T | 1 | a0003c0003t0001g0258 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.427-494C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | chr21 | 37089739 | |||||||
| chr21:37089941 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.427-292C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | chr21 | 37089941 | |||||||
| chr21:37089984 | C | CA | 140 | a0001c0001t0002g0045 a0001c0004t0010g0268 a0001c0005t0008g0243 others(137): Show |
142 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.427-235dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr21 | 37089984 | ||||||
| chr21:37090314 | A | G | 136 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(133): Show |
138 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.480+28A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090314 | |||||||
| chr21:37090416 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.480+130A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090416 | |||||||
| chr21:37090457 | C | A | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.480+171C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090457 | |||||||
| chr21:37090467 | CT | C | 102 | a0001c0001t0002g0001 a0001c0001t0002g0113 a0001c0001t0002g0114 others(99): Show |
105 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.480+195delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | INFO_REALIGN_3_PRIME | chr21 | 37090467 | ||||||
| chr21:37090467 | CTT | C | 27 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(24): Show |
27 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.480+194_480+195del others(2): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | INFO_REALIGN_3_PRIME | chr21 | 37090467 | ||||||
| chr21:37090469 | T | C | 2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | HG00597.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.480+183T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090469 | |||||||
| chr21:37090470 | T | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+184T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090470 | |||||||
| chr21:37090481 | T | A | 23 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(20): Show |
23 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.480+195T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090481 | |||||||
| chr21:37090530 | T | C | 1 | a0003c0003t0011g0250 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+244T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090530 | |||||||
| chr21:37090609 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.480+323T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090609 | |||||||
| chr21:37090626 | C | A | 1 | a0003c0003t0001g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.480+340C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090626 | |||||||
| chr21:37090636 | A | G | 1 | a0003c0003t0001g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.480+350A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090636 | |||||||
| chr21:37090659 | T | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.480+373T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090659 | |||||||
| chr21:37090809 | A | C | 136 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(133): Show |
138 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.481-484A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37090809 | |||||||
| chr21:37091042 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.481-251A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37091042 | |||||||
| chr21:37091090 | A | G | 1 | a0001c0023t0008g0259 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.481-203A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37091090 | |||||||
| chr21:37091106 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.481-187A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37091106 | |||||||
| chr21:37091136 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.481-157T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37091136 | |||||||
| chr21:37091152 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.481-141T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 6/45 | chr21 | 37091152 | |||||||
| chr21:37091527 | A | G | 1 | a0002c0002t0001g0172 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.601+114A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37091527 | |||||||
| chr21:37091568 | A | ATTAT | 5 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0007c0008t0006g0140 others(2): Show |
5 | HG00733.hp2 HG01123.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+182_601+185dup others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | INFO_REALIGN_3_PRIME | chr21 | 37091568 | ||||||
| chr21:37091568 | A | ATTATTTA others(1): Show |
122 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(119): Show |
124 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.601+178_601+185dup others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | INFO_REALIGN_3_PRIME | chr21 | 37091568 | ||||||
| chr21:37091568 | A | ATTATTTA others(5): Show |
10 | a0001c0014t0006g0307 a0002c0002t0001g0211 a0002c0002t0001g0304 others(7): Show |
10 | HG01099.hp1 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.601+174_601+185dup others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | INFO_REALIGN_3_PRIME | chr21 | 37091568 | ||||||
| chr21:37091568 | A | ATTATTTA others(9): Show |
3 | a0003c0003t0001g0197 a0003c0003t0001g0228 a0006c0011t0001g0222 |
3 | HG02615.hp1 NA18522.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.601+170_601+185dup others(16): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | INFO_REALIGN_3_PRIME | chr21 | 37091568 | ||||||
| chr21:37091568 | ATTAT | A | 87 | a0001c0001t0007g0266 a0001c0001t0007g0273 a0001c0001t0007g0274 others(84): Show |
87 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.601+182_601+185del others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | INFO_REALIGN_3_PRIME | chr21 | 37091568 | ||||||
| chr21:37091667 | C | T | 136 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(133): Show |
138 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.601+254C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37091667 | |||||||
| chr21:37092039 | A | G | 49 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(46): Show |
51 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.601+626A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37092039 | |||||||
| chr21:37092087 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.601+674G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37092087 | |||||||
| chr21:37092180 | A | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.601+767A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37092180 | |||||||
| chr21:37092278 | A | G | 5 | a0002c0002t0001g0148 a0002c0002t0001g0247 a0003c0003t0001g0225 others(2): Show |
5 | NA18946.hp1 NA18960.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+865A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37092278 | |||||||
| chr21:37092516 | G | A | 1 | a0002c0002t0021g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.601+1103G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37092516 | |||||||
| chr21:37092757 | A | G | 1 | a0009c0010t0006g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.602-1248A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37092757 | |||||||
| chr21:37092897 | A | G | 1 | a0003c0003t0001g0224 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.602-1108A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37092897 | |||||||
| chr21:37093045 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.602-960C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093045 | |||||||
| chr21:37093098 | C | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.602-907C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093098 | |||||||
| chr21:37093227 | A | C | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.602-778A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093227 | |||||||
| chr21:37093320 | G | A | 136 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(133): Show |
138 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.602-685G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093320 | |||||||
| chr21:37093379 | C | CA | 83 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0001c0001t0002g0034 others(80): Show |
83 | HG00544.hp2 HG00639.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.602-603dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | INFO_REALIGN_3_PRIME | chr21 | 37093379 | ||||||
| chr21:37093379 | C | CAA | 19 | a0001c0001t0002g0053 a0001c0001t0002g0075 a0001c0004t0003g0005 others(16): Show |
19 | HG00099.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.602-604_602-603dup others(2): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | INFO_REALIGN_3_PRIME | chr21 | 37093379 | ||||||
| chr21:37093379 | CAAAAAAA others(3): Show |
C | 7 | a0001c0014t0006g0307 a0008c0009t0006g0263 a0008c0009t0006g0264 others(4): Show |
7 | HG01243.hp1 HG01978.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.602-612_602-603del others(10): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | INFO_REALIGN_3_PRIME | chr21 | 37093379 | ||||||
| chr21:37093402 | A | AAG | 9 | a0002c0002t0001g0156 a0002c0002t0001g0158 a0002c0002t0001g0175 others(6): Show |
9 | HG00621.hp2 HG01175.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.602-603_602-602ins others(2): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093402 | |||||||
| chr21:37093402 | A | AG | 117 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(114): Show |
119 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.602-601dupG | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | INFO_REALIGN_3_PRIME | chr21 | 37093402 | ||||||
| chr21:37093402 | A | G | 13 | a0001c0014t0006g0307 a0002c0002t0001g0170 a0002c0002t0001g0171 others(10): Show |
13 | HG01123.hp2 HG01243.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.602-603A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093402 | |||||||
| chr21:37093513 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.602-492A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093513 | |||||||
| chr21:37093556 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.602-449T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093556 | |||||||
| chr21:37093573 | G | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.602-432G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093573 | |||||||
| chr21:37093593 | A | G | 2 | a0001c0001t0002g0058 a0003c0003t0009g0057 |
2 | NA18948.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.602-412A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093593 | |||||||
| chr21:37093611 | G | T | 20 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0001c0001t0002g0034 others(17): Show |
20 | HG01081.hp2 HG01981.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.602-394G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093611 | |||||||
| chr21:37093764 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.602-241G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093764 | |||||||
| chr21:37093902 | C | T | 1 | a0001c0004t0003g0023 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.602-103C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093902 | |||||||
| chr21:37093903 | G | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.602-102G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093903 | |||||||
| chr21:37093923 | A | G | 1 | a0008c0009t0006g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.602-82A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093923 | |||||||
| chr21:37093961 | T | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.602-44T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 7/45 | chr21 | 37093961 | |||||||
| chr21:37094239 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.687+149C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094239 | |||||||
| chr21:37094257 | C | G | 47 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(44): Show |
47 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.687+167C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094257 | |||||||
| chr21:37094315 | A | G | 74 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(71): Show |
74 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.687+225A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094315 | |||||||
| chr21:37094369 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.687+279T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094369 | |||||||
| chr21:37094571 | A | G | 1 | a0001c0005t0004g0325 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.687+481A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094571 | |||||||
| chr21:37094637 | G | T | 136 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(133): Show |
138 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.687+547G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094637 | |||||||
| chr21:37094686 | A | AT | 31 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.687+602dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37094686 | ||||||
| chr21:37094710 | A | G | 1 | a0001c0001t0002g0126 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.687+620A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094710 | |||||||
| chr21:37094743 | A | G | 5 | a0001c0005t0004g0313 a0001c0005t0004g0321 a0001c0005t0004g0334 others(2): Show |
5 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.688-607A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094743 | |||||||
| chr21:37094792 | T | C | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | HG02074.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.688-558T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094792 | |||||||
| chr21:37094910 | G | A | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.688-440G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37094910 | |||||||
| chr21:37095137 | A | ATG | 32 | a0001c0001t0002g0043 a0001c0001t0002g0058 a0001c0001t0002g0099 others(29): Show |
32 | HG00099.hp1 HG00544.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.688-187_688-186dup others(2): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | ATGTGTG | 3 | a0002c0002t0001g0146 a0006c0011t0001g0221 a0006c0011t0001g0306 |
3 | HG01099.hp1 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.688-191_688-186dup others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | ATGTGTGT others(1): Show |
10 | a0003c0003t0001g0254 a0003c0003t0001g0255 a0003c0003t0001g0301 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.688-193_688-186dup others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | ATGTGTGT others(3): Show |
4 | a0002c0002t0001g0172 a0002c0002t0001g0203 a0008c0009t0006g0263 others(1): Show |
4 | HG01243.hp1 HG03239.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.688-195_688-186dup others(10): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | ATGTGTGT others(5): Show |
12 | a0002c0002t0001g0249 a0003c0003t0001g0184 a0003c0003t0001g0185 others(9): Show |
12 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.688-197_688-186dup others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | ATGTGTGT others(7): Show |
48 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(45): Show |
49 | HG00408.hp2 HG01069.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.688-199_688-186dup others(14): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | ATGTGTGT others(9): Show |
15 | a0002c0002t0001g0145 a0002c0002t0001g0147 a0003c0003t0001g0002 others(12): Show |
16 | HG00558.hp2 HG00597.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.688-201_688-186dup others(16): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | ATGTGTGT others(11): Show |
20 | a0002c0002t0001g0139 a0002c0002t0001g0149 a0002c0002t0001g0150 others(17): Show |
20 | HG00735.hp1 HG00738.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.688-203_688-186dup others(18): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | ATGTGTGT others(13): Show |
15 | a0002c0002t0001g0154 a0002c0002t0001g0159 a0002c0002t0001g0160 others(12): Show |
15 | HG00673.hp2 HG02055.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.688-205_688-186dup others(20): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | ATGTGTGT others(15): Show |
8 | a0002c0002t0001g0156 a0002c0002t0001g0157 a0002c0002t0001g0158 others(5): Show |
8 | NA18940.hp1 NA18947.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.688-207_688-186dup others(22): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095137 | A | G | 32 | a0001c0001t0007g0266 a0001c0001t0016g0267 a0001c0005t0004g0309 others(29): Show |
32 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.688-213A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37095137 | |||||||
| chr21:37095137 | ATG | A | 22 | a0001c0001t0002g0041 a0001c0001t0002g0045 a0001c0001t0002g0076 others(19): Show |
22 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.688-187_688-186del others(2): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr21 | 37095137 | ||||||
| chr21:37095256 | G | A | 31 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.688-94G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37095256 | |||||||
| chr21:37095316 | C | A | 138 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(135): Show |
140 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.688-34C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 8/45 | chr21 | 37095316 | |||||||
| chr21:37095557 | C | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.782+113C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 9/45 | chr21 | 37095557 | |||||||
| chr21:37095565 | A | G | 1 | a0003c0003t0001g0215 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.782+121A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 9/45 | chr21 | 37095565 | |||||||
| chr21:37095606 | G | C | 1 | a0001c0001t0002g0103 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.782+162G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 9/45 | chr21 | 37095606 | |||||||
| chr21:37096076 | G | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.783-505G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 9/45 | chr21 | 37096076 | |||||||
| chr21:37096149 | A | C | 1 | a0003c0003t0023g0256 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.783-432A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 9/45 | chr21 | 37096149 | |||||||
| chr21:37096150 | C | G | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.783-431C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 9/45 | chr21 | 37096150 | |||||||
| chr21:37096271 | G | A | 1 | a0003c0003t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.783-310G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 9/45 | chr21 | 37096271 | |||||||
| chr21:37096406 | A | C | 1 | a0001c0001t0002g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.783-175A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 9/45 | chr21 | 37096406 | |||||||
| chr21:37096658 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.845+15A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37096658 | |||||||
| chr21:37096706 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.845+63G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37096706 | |||||||
| chr21:37096717 | T | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.845+74T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37096717 | |||||||
| chr21:37096769 | G | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.845+126G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37096769 | |||||||
| chr21:37096911 | G | A | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.845+268G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37096911 | |||||||
| chr21:37096913 | A | G | 1 | a0001c0005t0004g0321 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.845+270A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37096913 | |||||||
| chr21:37096944 | G | A | 49 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(46): Show |
51 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.845+301G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37096944 | |||||||
| chr21:37097223 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.845+580A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097223 | |||||||
| chr21:37097314 | A | C | 1 | a0003c0003t0023g0256 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.845+671A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097314 | |||||||
| chr21:37097423 | T | G | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.845+780T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097423 | |||||||
| chr21:37097482 | A | G | 1 | a0002c0002t0001g0171 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.845+839A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097482 | |||||||
| chr21:37097493 | C | T | 3 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0169 |
3 | HG02056.hp1 HG02132.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.845+850C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097493 | |||||||
| chr21:37097496 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.845+853A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097496 | |||||||
| chr21:37097509 | A | T | 1 | a0002c0002t0014g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.845+866A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097509 | |||||||
| chr21:37097537 | A | G | 224 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(221): Show |
226 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(223): Show |
intron_variant | MODIFIER | c.845+894A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097537 | |||||||
| chr21:37097669 | T | A | 3 | a0003c0003t0001g0301 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.845+1026T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097669 | |||||||
| chr21:37097751 | A | G | 5 | a0001c0005t0004g0313 a0001c0005t0004g0321 a0001c0005t0004g0334 others(2): Show |
5 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.845+1108A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097751 | |||||||
| chr21:37097820 | G | A | 31 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.845+1177G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37097820 | |||||||
| chr21:37098125 | G | A | 1 | a0002c0002t0001g0171 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.845+1482G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37098125 | |||||||
| chr21:37098156 | T | C | 1 | a0002c0002t0001g0165 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.845+1513T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37098156 | |||||||
| chr21:37098204 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.845+1561T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37098204 | |||||||
| chr21:37098237 | A | C | 2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | HG00597.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.845+1594A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37098237 | |||||||
| chr21:37098663 | G | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845+2020G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37098663 | |||||||
| chr21:37098893 | A | G | 1 | a0007c0008t0006g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.845+2250A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37098893 | |||||||
| chr21:37099016 | G | A | 2 | a0001c0001t0007g0266 a0001c0001t0016g0267 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.845+2373G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37099016 | |||||||
| chr21:37099060 | A | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.845+2417A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37099060 | |||||||
| chr21:37099116 | G | A | 1 | a0003c0018t0001g0231 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.845+2473G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37099116 | |||||||
| chr21:37099215 | T | C | 1 | a0002c0002t0001g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.845+2572T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37099215 | |||||||
| chr21:37099325 | C | T | 10 | a0001c0001t0002g0027 a0001c0001t0002g0032 a0001c0001t0002g0035 others(7): Show |
10 | HG00639.hp1 HG00733.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.845+2682C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37099325 | |||||||
| chr21:37099326 | G | A | 1 | a0001c0005t0004g0325 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.845+2683G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37099326 | |||||||
| chr21:37099663 | G | T | 136 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(133): Show |
138 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.845+3020G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37099663 | |||||||
| chr21:37099890 | C | A | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.845+3247C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37099890 | |||||||
| chr21:37100001 | T | C | 1 | a0001c0001t0002g0120 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.845+3358T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100001 | |||||||
| chr21:37100114 | G | A | 1 | a0002c0002t0021g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.845+3471G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100114 | |||||||
| chr21:37100121 | A | T | 5 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(2): Show |
5 | HG01175.hp2 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.845+3478A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100121 | |||||||
| chr21:37100154 | G | A | 24 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(21): Show |
24 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.845+3511G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100154 | |||||||
| chr21:37100160 | G | A | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845+3517G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100160 | |||||||
| chr21:37100405 | A | G | 63 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(60): Show |
63 | HG00099.hp2 HG00544.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.845+3762A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100405 | |||||||
| chr21:37100476 | G | A | 4 | a0001c0001t0002g0047 a0001c0001t0002g0084 a0001c0001t0002g0119 others(1): Show |
4 | HG02071.hp1 HG02080.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.845+3833G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100476 | |||||||
| chr21:37100492 | A | G | 3 | a0002c0002t0001g0210 a0002c0002t0001g0212 a0002c0002t0001g0220 |
3 | HG01258.hp2 HG01952.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.845+3849A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100492 | |||||||
| chr21:37100516 | C | CAAACA | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.845+3873_845+3874i others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100516 | |||||||
| chr21:37100544 | T | G | 1 | a0001c0001t0002g0026 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.845+3901T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100544 | |||||||
| chr21:37100707 | C | T | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.845+4064C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100707 | |||||||
| chr21:37100771 | G | C | 2 | a0001c0001t0002g0085 a0001c0001t0002g0108 |
2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.845+4128G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100771 | |||||||
| chr21:37100780 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.845+4137G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100780 | |||||||
| chr21:37100873 | A | G | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.845+4230A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100873 | |||||||
| chr21:37100892 | G | A | 1 | a0001c0004t0003g0020 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.845+4249G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100892 | |||||||
| chr21:37100932 | G | T | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.845+4289G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100932 | |||||||
| chr21:37100959 | A | G | 1 | a0003c0003t0001g0187 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.845+4316A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100959 | |||||||
| chr21:37100984 | G | T | 1 | a0002c0002t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.845+4341G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100984 | |||||||
| chr21:37100985 | G | T | 1 | a0002c0002t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.845+4342G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100985 | |||||||
| chr21:37100990 | G | A | 1 | a0005c0007t0002g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.845+4347G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37100990 | |||||||
| chr21:37101248 | A | G | 3 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0122 |
3 | NA18971.hp2 NA19075.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.845+4605A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37101248 | |||||||
| chr21:37101351 | T | TTG | 16 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0060 others(13): Show |
16 | HG00544.hp1 HG00738.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.845+4742_845+4743d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37101351 | ||||||
| chr21:37101351 | T | TTGTG | 10 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0052 others(7): Show |
10 | HG01081.hp2 HG02109.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.845+4740_845+4743d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37101351 | ||||||
| chr21:37101351 | TTG | T | 29 | a0001c0001t0002g0056 a0001c0001t0002g0100 a0001c0004t0003g0004 others(26): Show |
29 | HG00099.hp2 HG00733.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.845+4742_845+4743d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37101351 | ||||||
| chr21:37101351 | TTGTG | T | 78 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(75): Show |
80 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.845+4740_845+4743d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37101351 | ||||||
| chr21:37101351 | TTGTGTG | T | 70 | a0001c0005t0004g0313 a0001c0005t0004g0321 a0001c0005t0004g0334 others(67): Show |
70 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.845+4738_845+4743d others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37101351 | ||||||
| chr21:37101367 | G | T | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.845+4724G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37101367 | |||||||
| chr21:37101443 | T | C | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.845+4800T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37101443 | |||||||
| chr21:37101497 | G | A | 2 | a0001c0005t0004g0309 a0001c0005t0004g0323 |
2 | NA19004.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.845+4854G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37101497 | |||||||
| chr21:37101570 | G | GT | 3 | a0009c0010t0006g0137 a0009c0010t0006g0138 a0009c0010t0006g0213 |
3 | HG02976.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.845+4927_845+4928i others(3): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37101570 | |||||||
| chr21:37101743 | G | C | 1 | a0003c0003t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.845+5100G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37101743 | |||||||
| chr21:37101779 | C | CT | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845+5146dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37101779 | ||||||
| chr21:37101918 | T | TTA | 69 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(66): Show |
71 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.845+5287_845+5288d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37101918 | ||||||
| chr21:37101918 | T | TTATA | 70 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(67): Show |
70 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.845+5285_845+5288d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37101918 | ||||||
| chr21:37102041 | TTTAC | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.845+5402_845+5405d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37102041 | ||||||
| chr21:37102603 | A | C | 1 | a0003c0003t0001g0215 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.846-5789A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37102603 | |||||||
| chr21:37102719 | A | G | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.846-5673A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37102719 | |||||||
| chr21:37102863 | G | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0046 |
2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.846-5529G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37102863 | |||||||
| chr21:37102864 | G | C | 70 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(67): Show |
70 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.846-5528G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37102864 | |||||||
| chr21:37103098 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.846-5294G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37103098 | |||||||
| chr21:37103127 | A | C | 3 | a0001c0005t0004g0334 a0001c0005t0004g0335 a0001c0005t0004g0336 |
3 | HG03579.hp2 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.846-5265A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37103127 | |||||||
| chr21:37103129 | A | G | 1 | a0005c0007t0002g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.846-5263A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37103129 | |||||||
| chr21:37103254 | A | C | 3 | a0003c0003t0001g0301 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.846-5138A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37103254 | |||||||
| chr21:37103285 | A | G | 3 | a0009c0010t0006g0137 a0009c0010t0006g0138 a0009c0010t0006g0213 |
3 | HG02976.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.846-5107A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37103285 | |||||||
| chr21:37103448 | T | A | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.846-4944T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37103448 | |||||||
| chr21:37103622 | C | A | 1 | a0001c0004t0003g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.846-4770C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37103622 | |||||||
| chr21:37103829 | G | C | 1 | a0003c0003t0001g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.846-4563G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37103829 | |||||||
| chr21:37103865 | TGTA | T | 48 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(45): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.846-4525_846-4523d others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37103865 | ||||||
| chr21:37104050 | C | T | 1 | a0008c0009t0006g0264 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.846-4342C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37104050 | |||||||
| chr21:37104356 | G | A | 1 | a0002c0002t0001g0249 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.846-4036G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37104356 | |||||||
| chr21:37104566 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.846-3826G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37104566 | |||||||
| chr21:37104569 | G | A | 19 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(16): Show |
19 | HG00733.hp1 HG01255.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.846-3823G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37104569 | |||||||
| chr21:37104588 | C | CA | 67 | a0001c0001t0002g0029 a0001c0001t0002g0041 a0001c0001t0002g0061 others(64): Show |
67 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.846-3783dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37104588 | ||||||
| chr21:37104588 | C | CAA | 6 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(3): Show |
6 | HG01934.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.846-3784_846-3783d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37104588 | ||||||
| chr21:37104588 | C | CAAAAAAA others(3): Show |
1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.846-3792_846-3783d others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37104588 | ||||||
| chr21:37104588 | C | CAAAAAAA others(11): Show |
3 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 |
3 | HG01243.hp1 HG01978.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.846-3800_846-3783d others(20): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37104588 | ||||||
| chr21:37104588 | C | CAAAAAAA others(12): Show |
3 | a0009c0010t0006g0137 a0009c0010t0006g0138 a0009c0010t0006g0213 |
3 | HG02976.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.846-3801_846-3783d others(21): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37104588 | ||||||
| chr21:37104588 | CA | C | 11 | a0001c0001t0002g0046 a0001c0001t0002g0055 a0001c0001t0002g0120 others(8): Show |
11 | HG01891.hp2 HG02083.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.846-3783delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37104588 | ||||||
| chr21:37104588 | CAA | C | 122 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(119): Show |
124 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.846-3784_846-3783d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37104588 | ||||||
| chr21:37104588 | CAAAAAAA others(3): Show |
C | 2 | a0004c0006t0005g0280 a0004c0006t0005g0281 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.846-3792_846-3783d others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37104588 | ||||||
| chr21:37104601 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.846-3791A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37104601 | |||||||
| chr21:37104853 | G | C | 1 | a0002c0002t0001g0158 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.846-3539G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37104853 | |||||||
| chr21:37104862 | T | C | 1 | a0001c0001t0002g0072 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.846-3530T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37104862 | |||||||
| chr21:37104912 | C | T | 1 | a0001c0004t0003g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.846-3480C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37104912 | |||||||
| chr21:37104994 | A | G | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.846-3398A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37104994 | |||||||
| chr21:37105010 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.846-3382C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37105010 | |||||||
| chr21:37105030 | G | A | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.846-3362G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37105030 | |||||||
| chr21:37105091 | G | T | 1 | a0001c0001t0002g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.846-3301G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37105091 | |||||||
| chr21:37105271 | G | A | 226 | a0001c0001t0007g0266 a0001c0001t0007g0273 a0001c0001t0007g0274 others(223): Show |
228 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(225): Show |
intron_variant | MODIFIER | c.846-3121G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37105271 | |||||||
| chr21:37105511 | C | A | 1 | a0001c0004t0003g0008 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.846-2881C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37105511 | |||||||
| chr21:37105617 | C | T | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.846-2775C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37105617 | |||||||
| chr21:37105657 | A | G | 1 | a0005c0007t0002g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.846-2735A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37105657 | |||||||
| chr21:37105680 | A | C | 1 | a0001c0001t0002g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.846-2712A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37105680 | |||||||
| chr21:37105814 | G | T | 3 | a0006c0011t0001g0221 a0006c0011t0001g0222 a0006c0011t0001g0306 |
3 | HG01099.hp1 HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.846-2578G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37105814 | |||||||
| chr21:37106102 | A | G | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.846-2290A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37106102 | |||||||
| chr21:37106129 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.846-2263G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37106129 | |||||||
| chr21:37106313 | A | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.846-2079A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37106313 | |||||||
| chr21:37106421 | C | A | 24 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(21): Show |
24 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.846-1971C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37106421 | |||||||
| chr21:37106498 | A | G | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.846-1894A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37106498 | |||||||
| chr21:37106853 | C | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.846-1539C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37106853 | |||||||
| chr21:37107076 | G | GT | 6 | a0001c0001t0002g0077 a0001c0001t0002g0124 a0001c0001t0002g0127 others(3): Show |
6 | HG01934.hp1 HG02145.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.846-1301dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37107076 | ||||||
| chr21:37107076 | GT | G | 137 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(134): Show |
139 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.846-1301delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37107076 | ||||||
| chr21:37107090 | T | G | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.846-1302T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107090 | |||||||
| chr21:37107096 | G | A | 5 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.846-1296G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107096 | |||||||
| chr21:37107153 | C | CT | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.846-1237dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr21 | 37107153 | ||||||
| chr21:37107229 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.846-1163T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107229 | |||||||
| chr21:37107578 | A | T | 48 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(45): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.846-814A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107578 | |||||||
| chr21:37107585 | A | G | 136 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(133): Show |
138 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.846-807A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107585 | |||||||
| chr21:37107672 | A | G | 1 | a0007c0008t0006g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.846-720A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107672 | |||||||
| chr21:37107874 | A | G | 1 | a0002c0002t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.846-518A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107874 | |||||||
| chr21:37107942 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.846-450G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107942 | |||||||
| chr21:37107955 | T | C | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.846-437T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107955 | |||||||
| chr21:37107969 | T | C | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.846-423T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37107969 | |||||||
| chr21:37108054 | C | T | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.846-338C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37108054 | |||||||
| chr21:37108063 | C | T | 42 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(39): Show |
42 | HG00099.hp2 HG00733.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.846-329C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37108063 | |||||||
| chr21:37108071 | C | T | 8 | a0001c0001t0002g0059 a0001c0001t0007g0096 a0001c0001t0007g0130 others(5): Show |
8 | HG02109.hp1 HG02615.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.846-321C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37108071 | |||||||
| chr21:37108294 | A | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0082 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.846-98A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 10/45 | chr21 | 37108294 | |||||||
| chr21:37108466 | T | C | 1 | a0003c0016t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.900+20T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108466 | |||||||
| chr21:37108494 | T | C | 2 | a0001c0004t0010g0268 a0001c0004t0010g0269 |
2 | HG02109.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.900+48T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108494 | |||||||
| chr21:37108551 | G | A | 3 | a0003c0003t0001g0301 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.900+105G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108551 | |||||||
| chr21:37108573 | G | T | 2 | a0002c0002t0001g0304 a0002c0002t0001g0305 |
2 | HG01255.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.900+127G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108573 | |||||||
| chr21:37108632 | G | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.900+186G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108632 | |||||||
| chr21:37108744 | C | G | 1 | a0001c0001t0002g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.900+298C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108744 | |||||||
| chr21:37108831 | C | T | 1 | a0002c0002t0009g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.900+385C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108831 | |||||||
| chr21:37108948 | C | T | 226 | a0001c0001t0007g0266 a0001c0001t0007g0273 a0001c0001t0007g0274 others(223): Show |
228 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(225): Show |
intron_variant | MODIFIER | c.900+502C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108948 | |||||||
| chr21:37108988 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0083 |
2 | HG00639.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.900+542C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108988 | |||||||
| chr21:37108992 | G | A | 129 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(126): Show |
131 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.900+546G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37108992 | |||||||
| chr21:37109062 | G | T | 1 | a0001c0001t0002g0113 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.900+616G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109062 | |||||||
| chr21:37109135 | C | T | 7 | a0001c0014t0006g0307 a0008c0009t0006g0263 a0008c0009t0006g0264 others(4): Show |
7 | HG01243.hp1 HG01978.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.900+689C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109135 | |||||||
| chr21:37109136 | G | T | 129 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(126): Show |
131 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.900+690G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109136 | |||||||
| chr21:37109205 | A | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.900+759A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109205 | |||||||
| chr21:37109232 | C | T | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.900+786C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109232 | |||||||
| chr21:37109263 | C | T | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.900+817C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109263 | |||||||
| chr21:37109520 | G | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.900+1074G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109520 | |||||||
| chr21:37109570 | G | A | 1 | a0001c0001t0007g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.900+1124G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109570 | |||||||
| chr21:37109716 | G | T | 6 | a0003c0003t0001g0254 a0003c0003t0001g0255 a0003c0003t0011g0250 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+1270G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109716 | |||||||
| chr21:37109774 | C | T | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+1328C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109774 | |||||||
| chr21:37109780 | C | T | 4 | a0001c0005t0004g0313 a0001c0005t0004g0334 a0001c0005t0004g0335 others(1): Show |
4 | HG03130.hp2 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+1334C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109780 | |||||||
| chr21:37109956 | C | A | 3 | a0003c0003t0001g0143 a0003c0003t0001g0144 a0003c0003t0001g0246 |
3 | HG02293.hp1 HG02300.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.900+1510C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37109956 | |||||||
| chr21:37110004 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.900+1558G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110004 | |||||||
| chr21:37110038 | AC | A | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.900+1594delC | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37110038 | ||||||
| chr21:37110087 | A | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.900+1641A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110087 | |||||||
| chr21:37110205 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.900+1759G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110205 | |||||||
| chr21:37110236 | G | A | 3 | a0003c0003t0012g0234 a0003c0003t0012g0235 a0003c0003t0024g0233 |
3 | NA18981.hp2 NA19004.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.900+1790G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110236 | |||||||
| chr21:37110400 | A | G | 2 | a0004c0006t0005g0282 a0004c0006t0005g0283 |
2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.900+1954A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110400 | |||||||
| chr21:37110414 | C | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.900+1968C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110414 | |||||||
| chr21:37110417 | A | G | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.900+1971A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110417 | |||||||
| chr21:37110460 | G | A | 4 | a0003c0003t0011g0250 a0003c0003t0011g0251 a0003c0003t0011g0252 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+2014G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110460 | |||||||
| chr21:37110529 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.900+2083C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110529 | |||||||
| chr21:37110540 | A | G | 1 | a0001c0004t0010g0270 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.900+2094A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110540 | |||||||
| chr21:37110580 | A | G | 3 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 |
3 | HG01243.hp1 HG01978.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.900+2134A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110580 | |||||||
| chr21:37110852 | ATC | A | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+2411_900+2412d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37110852 | ||||||
| chr21:37110896 | A | G | 1 | a0002c0002t0001g0211 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.900+2450A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110896 | |||||||
| chr21:37110945 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.900+2499C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37110945 | |||||||
| chr21:37111054 | G | A | 31 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.900+2608G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111054 | |||||||
| chr21:37111079 | G | A | 1 | a0002c0002t0001g0204 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.900+2633G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111079 | |||||||
| chr21:37111107 | T | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.900+2661T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111107 | |||||||
| chr21:37111151 | G | A | 4 | a0001c0001t0002g0053 a0001c0004t0003g0290 a0001c0004t0003g0293 others(1): Show |
4 | HG00639.hp2 HG02074.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+2705G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111151 | |||||||
| chr21:37111282 | C | T | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.900+2836C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111282 | |||||||
| chr21:37111283 | G | C | 2 | a0001c0004t0003g0298 a0001c0004t0003g0300 |
2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.900+2837G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111283 | |||||||
| chr21:37111330 | T | C | 5 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+2884T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111330 | |||||||
| chr21:37111351 | G | A | 1 | a0002c0002t0001g0204 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.900+2905G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111351 | |||||||
| chr21:37111538 | G | T | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+3092G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111538 | |||||||
| chr21:37111698 | C | T | 1 | a0001c0024t0002g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.900+3252C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111698 | |||||||
| chr21:37111725 | C | T | 39 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(36): Show |
41 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.900+3279C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111725 | |||||||
| chr21:37111731 | A | G | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+3285A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111731 | |||||||
| chr21:37111741 | T | C | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | NA18959.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.900+3295T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111741 | |||||||
| chr21:37111875 | G | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.900+3429G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111875 | |||||||
| chr21:37111959 | T | TA | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.900+3514dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37111959 | ||||||
| chr21:37111960 | A | AG | 120 | a0001c0001t0002g0027 a0001c0001t0002g0032 a0001c0001t0002g0035 others(117): Show |
120 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.900+3514_900+3515i others(3): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111960 | |||||||
| chr21:37111999 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.900+3553A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37111999 | |||||||
| chr21:37112000 | C | T | 15 | a0001c0001t0002g0036 a0001c0001t0002g0061 a0001c0001t0002g0080 others(12): Show |
15 | HG00408.hp1 HG01243.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.900+3554C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112000 | |||||||
| chr21:37112084 | C | A | 7 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.900+3638C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112084 | |||||||
| chr21:37112095 | A | G | 20 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0001c0001t0002g0034 others(17): Show |
20 | HG01081.hp2 HG01981.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.900+3649A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112095 | |||||||
| chr21:37112140 | G | C | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.900+3694G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112140 | |||||||
| chr21:37112260 | G | A | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+3814G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112260 | |||||||
| chr21:37112272 | G | C | 1 | a0001c0001t0002g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.900+3826G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112272 | |||||||
| chr21:37112376 | G | A | 224 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(221): Show |
226 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(223): Show |
intron_variant | MODIFIER | c.900+3930G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112376 | |||||||
| chr21:37112470 | A | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.900+4024A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112470 | |||||||
| chr21:37112540 | C | T | 1 | a0014c0015t0001g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.900+4094C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112540 | |||||||
| chr21:37112561 | T | C | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.900+4115T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112561 | |||||||
| chr21:37112596 | G | A | 1 | a0001c0004t0003g0016 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.900+4150G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112596 | |||||||
| chr21:37112694 | A | G | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.900+4248A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112694 | |||||||
| chr21:37112810 | G | A | 1 | a0001c0001t0002g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.900+4364G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112810 | |||||||
| chr21:37112865 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.900+4419T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112865 | |||||||
| chr21:37112878 | C | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.900+4432C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112878 | |||||||
| chr21:37112989 | C | G | 1 | a0002c0002t0001g0209 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.900+4543C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37112989 | |||||||
| chr21:37113080 | A | G | 3 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0122 |
3 | NA18971.hp2 NA19075.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.900+4634A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37113080 | |||||||
| chr21:37113233 | A | T | 1 | a0001c0004t0003g0300 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.900+4787A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37113233 | |||||||
| chr21:37113431 | C | T | 1 | a0001c0021t0002g0097 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.900+4985C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37113431 | |||||||
| chr21:37113499 | A | C | 1 | a0001c0005t0004g0309 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.900+5053A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37113499 | |||||||
| chr21:37114029 | A | T | 3 | a0001c0001t0002g0095 a0001c0001t0002g0111 a0001c0001t0002g0112 |
3 | HG02922.hp1 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.900+5583A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114029 | |||||||
| chr21:37114157 | G | C | 5 | a0003c0003t0001g0002 a0003c0003t0001g0238 a0003c0003t0001g0239 others(2): Show |
6 | HG00558.hp2 NA18966.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+5711G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114157 | |||||||
| chr21:37114289 | T | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.900+5843T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114289 | |||||||
| chr21:37114371 | G | A | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.900+5925G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114371 | |||||||
| chr21:37114412 | T | C | 1 | a0001c0004t0003g0013 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.900+5966T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114412 | |||||||
| chr21:37114487 | A | G | 1 | a0001c0005t0004g0333 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.900+6041A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114487 | |||||||
| chr21:37114591 | A | C | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.900+6145A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114591 | |||||||
| chr21:37114745 | T | C | 140 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(137): Show |
142 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.900+6299T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114745 | |||||||
| chr21:37114750 | G | C | 140 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(137): Show |
142 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.900+6304G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114750 | |||||||
| chr21:37114845 | A | G | 4 | a0002c0002t0019g0214 a0008c0009t0006g0263 a0008c0009t0006g0264 others(1): Show |
4 | HG01243.hp1 HG01978.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.900+6399A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114845 | |||||||
| chr21:37114974 | T | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.900+6528T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114974 | |||||||
| chr21:37114987 | G | A | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.900+6541G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37114987 | |||||||
| chr21:37115126 | C | A | 1 | a0002c0002t0001g0205 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.900+6680C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37115126 | |||||||
| chr21:37115174 | T | TATA | 118 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0028 others(115): Show |
119 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.901-6617_901-6615d others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37115174 | ||||||
| chr21:37115174 | T | TATAATA | 37 | a0001c0001t0002g0027 a0001c0001t0002g0032 a0001c0001t0002g0066 others(34): Show |
38 | HG00099.hp2 HG00558.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.901-6620_901-6615d others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37115174 | ||||||
| chr21:37115174 | T | TATAATAA others(2): Show |
108 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(105): Show |
108 | HG00544.hp2 HG00733.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.901-6623_901-6615d others(11): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37115174 | ||||||
| chr21:37115174 | T | TATAATAA others(5): Show |
37 | a0001c0004t0003g0008 a0001c0004t0003g0013 a0001c0005t0008g0243 others(34): Show |
38 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.901-6626_901-6615d others(14): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37115174 | ||||||
| chr21:37115174 | T | TATAATAA others(8): Show |
12 | a0001c0004t0003g0299 a0002c0002t0001g0148 a0002c0002t0001g0158 others(9): Show |
12 | HG00597.hp2 HG01943.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.901-6629_901-6615d others(17): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37115174 | ||||||
| chr21:37115174 | T | TATAATAA others(11): Show |
12 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(9): Show |
12 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.901-6632_901-6615d others(20): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37115174 | ||||||
| chr21:37115174 | T | TATAATAA others(14): Show |
3 | a0001c0004t0003g0292 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.901-6635_901-6615d others(23): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37115174 | ||||||
| chr21:37115200 | T | TAATAATA others(5): Show |
1 | a0003c0003t0001g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.901-6615_901-6614i others(14): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37115200 | ||||||
| chr21:37115203 | A | T | 1 | a0001c0004t0010g0268 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.901-6614A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37115203 | |||||||
| chr21:37115261 | G | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.901-6556G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37115261 | |||||||
| chr21:37115678 | C | A | 1 | a0001c0001t0002g0054 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.901-6139C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37115678 | |||||||
| chr21:37115692 | G | C | 1 | a0001c0004t0010g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.901-6125G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37115692 | |||||||
| chr21:37115790 | C | G | 1 | a0003c0003t0001g0237 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.901-6027C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37115790 | |||||||
| chr21:37115985 | G | A | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.901-5832G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37115985 | |||||||
| chr21:37116033 | G | C | 29 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(26): Show |
29 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.901-5784G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37116033 | |||||||
| chr21:37116059 | T | C | 1 | a0003c0003t0001g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.901-5758T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37116059 | |||||||
| chr21:37116296 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.901-5521C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37116296 | |||||||
| chr21:37116608 | A | G | 220 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(217): Show |
222 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.901-5209A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37116608 | |||||||
| chr21:37116622 | CA | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.901-5193delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37116622 | ||||||
| chr21:37116657 | A | T | 1 | a0001c0001t0002g0035 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.901-5160A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37116657 | |||||||
| chr21:37116895 | C | T | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.901-4922C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37116895 | |||||||
| chr21:37116945 | G | T | 224 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(221): Show |
226 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(223): Show |
intron_variant | MODIFIER | c.901-4872G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37116945 | |||||||
| chr21:37116994 | C | T | 2 | a0002c0002t0001g0209 a0002c0002t0001g0249 |
2 | NA18957.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.901-4823C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37116994 | |||||||
| chr21:37117052 | A | ACTTTC | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.901-4761_901-4760i others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37117052 | ||||||
| chr21:37117178 | G | T | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.901-4639G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117178 | |||||||
| chr21:37117289 | A | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0089 |
2 | HG02293.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.901-4528A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117289 | |||||||
| chr21:37117453 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.901-4364T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117453 | |||||||
| chr21:37117474 | A | G | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.901-4343A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117474 | |||||||
| chr21:37117486 | T | G | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.901-4331T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117486 | |||||||
| chr21:37117576 | C | T | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-4241C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117576 | |||||||
| chr21:37117657 | G | A | 3 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 |
3 | HG01243.hp1 HG01978.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.901-4160G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117657 | |||||||
| chr21:37117706 | T | C | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.901-4111T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117706 | |||||||
| chr21:37117729 | G | A | 1 | a0007c0008t0006g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.901-4088G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117729 | |||||||
| chr21:37117814 | C | T | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.901-4003C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117814 | |||||||
| chr21:37117815 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.901-4002G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117815 | |||||||
| chr21:37117835 | C | CA | 55 | a0001c0001t0002g0040 a0001c0001t0002g0048 a0001c0001t0002g0049 others(52): Show |
55 | HG00544.hp2 HG00741.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.901-3964dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37117835 | ||||||
| chr21:37117835 | CA | C | 18 | a0001c0001t0002g0046 a0001c0001t0002g0099 a0001c0001t0002g0120 others(15): Show |
18 | HG01123.hp2 HG01243.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.901-3964delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37117835 | ||||||
| chr21:37117850 | AAAAG | A | 11 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0291 others(8): Show |
11 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.901-3963_901-3960d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37117850 | ||||||
| chr21:37117859 | A | G | 12 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0291 others(9): Show |
12 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.901-3958A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117859 | |||||||
| chr21:37117988 | C | T | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.901-3829C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37117988 | |||||||
| chr21:37118004 | T | C | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.901-3813T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118004 | |||||||
| chr21:37118029 | C | T | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.901-3788C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118029 | |||||||
| chr21:37118121 | CT | C | 227 | a0001c0001t0002g0084 a0001c0001t0002g0087 a0001c0001t0007g0266 others(224): Show |
229 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(226): Show |
intron_variant | MODIFIER | c.901-3686delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37118121 | ||||||
| chr21:37118131 | T | A | 14 | a0001c0001t0002g0034 a0001c0004t0003g0288 a0001c0004t0003g0289 others(11): Show |
14 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.901-3686T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118131 | |||||||
| chr21:37118229 | T | A | 2 | a0001c0001t0007g0266 a0001c0001t0016g0267 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.901-3588T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118229 | |||||||
| chr21:37118272 | A | G | 1 | a0001c0005t0004g0314 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.901-3545A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118272 | |||||||
| chr21:37118434 | T | A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.901-3383T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118434 | |||||||
| chr21:37118511 | C | T | 2 | a0001c0001t0007g0275 a0001c0001t0007g0276 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.901-3306C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118511 | |||||||
| chr21:37118524 | C | T | 1 | a0002c0002t0019g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.901-3293C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118524 | |||||||
| chr21:37118551 | G | C | 70 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(67): Show |
70 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.901-3266G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118551 | |||||||
| chr21:37118601 | A | G | 2 | a0001c0001t0007g0266 a0001c0001t0016g0267 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.901-3216A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118601 | |||||||
| chr21:37118630 | T | C | 1 | a0002c0002t0001g0249 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.901-3187T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118630 | |||||||
| chr21:37118663 | G | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0133 |
2 | NA18991.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.901-3154G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118663 | |||||||
| chr21:37118795 | A | G | 140 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(137): Show |
142 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.901-3022A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37118795 | |||||||
| chr21:37119048 | G | C | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.901-2769G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119048 | |||||||
| chr21:37119079 | G | A | 1 | a0001c0004t0003g0293 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.901-2738G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119079 | |||||||
| chr21:37119259 | ATTT | A | 4 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0284 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-2554_901-2552d others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr21 | 37119259 | ||||||
| chr21:37119341 | T | C | 3 | a0009c0010t0006g0137 a0009c0010t0006g0138 a0009c0010t0006g0213 |
3 | HG02976.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.901-2476T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119341 | |||||||
| chr21:37119380 | T | C | 8 | a0001c0001t0002g0059 a0001c0001t0007g0096 a0001c0001t0007g0130 others(5): Show |
8 | HG02109.hp1 HG02615.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.901-2437T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119380 | |||||||
| chr21:37119404 | G | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.901-2413G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119404 | |||||||
| chr21:37119441 | C | T | 1 | a0003c0003t0001g0226 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.901-2376C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119441 | |||||||
| chr21:37119457 | T | C | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.901-2360T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119457 | |||||||
| chr21:37119578 | G | A | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.901-2239G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119578 | |||||||
| chr21:37119592 | A | T | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.901-2225A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119592 | |||||||
| chr21:37119673 | T | G | 140 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(137): Show |
142 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.901-2144T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119673 | |||||||
| chr21:37119811 | T | A | 1 | a0002c0002t0009g0063 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.901-2006T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119811 | |||||||
| chr21:37119847 | G | C | 140 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(137): Show |
142 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.901-1970G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37119847 | |||||||
| chr21:37120357 | T | G | 130 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(127): Show |
132 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.901-1460T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37120357 | |||||||
| chr21:37120472 | T | A | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-1345T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37120472 | |||||||
| chr21:37120780 | T | C | 1 | a0002c0002t0001g0165 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.901-1037T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37120780 | |||||||
| chr21:37121155 | A | G | 140 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(137): Show |
142 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.901-662A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37121155 | |||||||
| chr21:37121369 | A | G | 2 | a0002c0002t0001g0204 a0002c0002t0001g0219 |
2 | HG01081.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.901-448A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37121369 | |||||||
| chr21:37121397 | C | T | 31 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.901-420C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37121397 | |||||||
| chr21:37121440 | T | G | 5 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(2): Show |
5 | HG01106.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.901-377T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37121440 | |||||||
| chr21:37121542 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.901-275A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37121542 | |||||||
| chr21:37121767 | T | A | 1 | a0001c0001t0002g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.901-50T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 11/45 | chr21 | 37121767 | |||||||
| chr21:37121998 | T | A | 1 | a0001c0001t0002g0046 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1063+19T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37121998 | |||||||
| chr21:37122031 | T | C | 1 | a0002c0002t0001g0183 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1063+52T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122031 | |||||||
| chr21:37122119 | C | T | 2 | a0002c0002t0001g0304 a0002c0002t0001g0305 |
2 | HG01255.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1063+140C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122119 | |||||||
| chr21:37122195 | AT | A | 3 | a0009c0010t0006g0137 a0009c0010t0006g0138 a0009c0010t0006g0213 |
3 | HG02976.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1063+219delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122195 | ||||||
| chr21:37122273 | T | A | 1 | a0002c0002t0001g0206 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1063+294T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122273 | |||||||
| chr21:37122373 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1063+394G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122373 | |||||||
| chr21:37122417 | ATAATATA others(16): Show |
A | 139 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0014t0006g0307 others(136): Show |
141 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.1063+439_1063+461d others(25): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122417 | |||||||
| chr21:37122419 | A | AAT | 17 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0045 others(14): Show |
17 | HG00558.hp1 HG01109.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.1063+457_1063+458d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122419 | ||||||
| chr21:37122419 | A | AATATATA others(111): Show |
1 | a0001c0004t0003g0298 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1063+456_1063+457i others(120): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122419 | ||||||
| chr21:37122419 | A | T | 2 | a0004c0006t0005g0280 a0004c0006t0005g0281 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1063+440A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122419 | |||||||
| chr21:37122420 | A | T | 1 | a0011c0020t0002g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1063+441A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122420 | |||||||
| chr21:37122421 | T | A | 1 | a0011c0020t0002g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1063+442T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122421 | |||||||
| chr21:37122421 | T | TATATATA others(79): Show |
1 | a0001c0004t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1063+456_1063+457i others(88): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122421 | ||||||
| chr21:37122422 | A | ATATATAT others(146): Show |
1 | a0001c0004t0003g0006 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1063+454_1063+455i others(155): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122422 | ||||||
| chr21:37122422 | A | ATATATAT others(146): Show |
1 | a0001c0004t0003g0015 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1063+454_1063+455i others(155): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122422 | ||||||
| chr21:37122422 | A | ATATATAT others(172): Show |
1 | a0001c0004t0003g0013 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1063+454_1063+455i others(181): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122422 | ||||||
| chr21:37122422 | A | ATATATAT others(148): Show |
12 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0009 others(9): Show |
12 | HG01069.hp2 HG01071.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1063+454_1063+455i others(157): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122422 | ||||||
| chr21:37122422 | A | ATATATAT others(144): Show |
2 | a0001c0004t0003g0019 a0001c0004t0003g0022 |
2 | NA18998.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1063+454_1063+455i others(153): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122422 | ||||||
| chr21:37122422 | A | ATATATAT others(150): Show |
1 | a0001c0004t0003g0008 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1063+454_1063+455i others(159): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122422 | ||||||
| chr21:37122422 | A | ATATATAT others(120): Show |
1 | a0001c0004t0003g0024 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1063+454_1063+455i others(129): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122422 | ||||||
| chr21:37122422 | A | ATATATAT others(152): Show |
1 | a0001c0004t0003g0007 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1063+454_1063+455i others(161): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122422 | ||||||
| chr21:37122422 | A | ATATATAT others(170): Show |
1 | a0001c0004t0003g0023 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1063+452_1063+453i others(179): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122422 | ||||||
| chr21:37122423 | T | TATATATA others(103): Show |
1 | a0001c0004t0003g0300 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1063+456_1063+457i others(112): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122423 | ||||||
| chr21:37122423 | TATATATA others(9): Show |
T | 29 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(26): Show |
29 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1063+445_1063+460d others(18): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122423 | |||||||
| chr21:37122434 | A | ATTATATA others(46): Show |
1 | a0001c0004t0010g0270 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1063+456_1063+457i others(55): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122434 | ||||||
| chr21:37122434 | A | ATTATATA others(74): Show |
3 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0271 |
3 | HG02109.hp2 HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1063+456_1063+457i others(83): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122434 | ||||||
| chr21:37122435 | TATTA | T | 10 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(7): Show |
10 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1063+457_1063+460d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122435 | |||||||
| chr21:37122436 | A | T | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1063+457A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122436 | |||||||
| chr21:37122437 | T | A | 22 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(19): Show |
22 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1063+458T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122437 | |||||||
| chr21:37122437 | T | TA | 4 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(1): Show |
4 | HG02109.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+458_1063+459i others(3): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122437 | |||||||
| chr21:37122437 | T | TATATATA others(70): Show |
1 | a0001c0004t0010g0272 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1063+458_1063+459i others(79): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122437 | |||||||
| chr21:37122437 | TTA | T | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063+473_1063+474d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122437 | ||||||
| chr21:37122438 | T | A | 2 | a0004c0006t0005g0286 a0004c0006t0005g0287 |
2 | HG01106.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1063+459T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122438 | |||||||
| chr21:37122439 | A | T | 2 | a0004c0006t0005g0286 a0004c0006t0005g0287 |
2 | HG01106.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1063+460A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122439 | |||||||
| chr21:37122440 | T | TATATATA others(62): Show |
1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1063+470_1063+471i others(71): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122440 | ||||||
| chr21:37122440 | T | TATATATA others(6): Show |
1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1063+464_1063+476d others(15): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr21 | 37122440 | ||||||
| chr21:37122441 | A | T | 29 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(26): Show |
29 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1063+462A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122441 | |||||||
| chr21:37122443 | A | T | 29 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(26): Show |
29 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1063+464A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122443 | |||||||
| chr21:37122618 | G | A | 129 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(126): Show |
131 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.1064-365G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122618 | |||||||
| chr21:37122621 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0060 |
2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1064-362G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122621 | |||||||
| chr21:37122654 | G | A | 1 | a0001c0004t0003g0013 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1064-329G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122654 | |||||||
| chr21:37122827 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1064-156A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122827 | |||||||
| chr21:37122893 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1064-90T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 12/45 | chr21 | 37122893 | |||||||
| chr21:37123107 | C | T | 1 | a0001c0004t0003g0015 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1109+79C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123107 | |||||||
| chr21:37123360 | C | G | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1109+332C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123360 | |||||||
| chr21:37123362 | G | T | 1 | a0003c0003t0001g0179 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1109+334G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123362 | |||||||
| chr21:37123393 | G | A | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1109+365G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123393 | |||||||
| chr21:37123499 | A | G | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1109+471A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123499 | |||||||
| chr21:37123549 | A | G | 217 | a0001c0001t0002g0028 a0001c0001t0002g0052 a0001c0004t0003g0004 others(214): Show |
219 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(216): Show |
intron_variant | MODIFIER | c.1109+521A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123549 | |||||||
| chr21:37123549 | A | T | 5 | a0001c0005t0004g0313 a0001c0005t0004g0321 a0001c0005t0004g0334 others(2): Show |
5 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1109+521A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123549 | |||||||
| chr21:37123634 | A | G | 1 | a0001c0024t0002g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1109+606A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123634 | |||||||
| chr21:37123732 | A | G | 31 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1109+704A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123732 | |||||||
| chr21:37123929 | G | A | 6 | a0003c0003t0001g0254 a0003c0003t0001g0255 a0003c0003t0011g0250 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110-690G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123929 | |||||||
| chr21:37123979 | CCT | C | 4 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0284 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110-638_1110-637d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37123979 | ||||||
| chr21:37123995 | C | T | 1 | a0001c0005t0004g0334 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110-624C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37123995 | |||||||
| chr21:37124074 | TA | T | 5 | a0001c0005t0004g0314 a0001c0005t0008g0322 a0001c0005t0008g0324 others(2): Show |
5 | HG00099.hp2 HG01109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110-542delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124074 | ||||||
| chr21:37124087 | G | A | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1110-532G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124087 | |||||||
| chr21:37124112 | C | CTT | 13 | a0001c0001t0002g0001 a0001c0001t0002g0056 a0001c0001t0002g0065 others(10): Show |
14 | HG00621.hp2 HG01943.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110-485_1110-484d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTT | 48 | a0001c0001t0002g0038 a0001c0001t0002g0053 a0001c0001t0002g0071 others(45): Show |
48 | HG00621.hp1 HG00673.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.1110-487_1110-484d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTT | 41 | a0001c0001t0002g0047 a0001c0001t0002g0055 a0001c0001t0002g0084 others(38): Show |
41 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1110-488_1110-484d others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTT | 19 | a0001c0001t0002g0107 a0001c0001t0002g0119 a0001c0001t0002g0129 others(16): Show |
19 | HG00639.hp2 HG00741.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1110-489_1110-484d others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT | 20 | a0001c0001t0002g0123 a0001c0004t0003g0005 a0001c0004t0003g0006 others(17): Show |
20 | HG00544.hp2 HG00741.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1110-490_1110-484d others(9): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(1): Show |
7 | a0001c0004t0003g0012 a0001c0004t0003g0014 a0001c0004t0003g0015 others(4): Show |
7 | HG01071.hp2 NA18947.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110-491_1110-484d others(10): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(3): Show |
1 | a0001c0021t0002g0097 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1110-493_1110-484d others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1110-496_1110-484d others(15): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1110-500_1110-484d others(19): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0002g0035 a0001c0001t0002g0046 a0001c0001t0002g0103 |
3 | HG01169.hp2 HG01516.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1110-501_1110-484d others(20): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0027 a0001c0001t0002g0032 a0001c0001t0002g0082 |
3 | HG02895.hp1 HG02897.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1110-502_1110-484d others(21): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(13): Show |
1 | a0010c0012t0002g0098 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1110-503_1110-484d others(22): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1110-505_1110-484d others(24): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0002g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1110-506_1110-484d others(25): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1110-484_1110-483i others(26): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0007g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1110-484_1110-483i others(28): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(22): Show |
1 | a0001c0024t0002g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1110-484_1110-483i others(31): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(24): Show |
1 | a0010c0012t0002g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1110-484_1110-483i others(33): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(30): Show |
1 | a0001c0001t0007g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110-484_1110-483i others(39): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124112 | C | CTTTTTTT others(31): Show |
1 | a0001c0001t0007g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1110-484_1110-483i others(40): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | INFO_REALIGN_3_PRIME | chr21 | 37124112 | ||||||
| chr21:37124146 | C | G | 1 | a0001c0004t0003g0298 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1110-473C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124146 | |||||||
| chr21:37124206 | A | C | 2 | a0003c0003t0001g0225 a0003c0003t0001g0240 |
2 | NA18946.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1110-413A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124206 | |||||||
| chr21:37124206 | A | G | 1 | a0002c0002t0001g0157 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1110-413A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124206 | |||||||
| chr21:37124281 | A | G | 3 | a0001c0021t0002g0097 a0001c0022t0002g0067 a0001c0024t0002g0135 |
3 | HG02615.hp2 HG02896.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1110-338A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124281 | |||||||
| chr21:37124290 | A | C | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1110-329A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124290 | |||||||
| chr21:37124314 | A | C | 1 | a0003c0003t0001g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1110-305A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124314 | |||||||
| chr21:37124455 | T | C | 1 | a0003c0003t0001g0223 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1110-164T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124455 | |||||||
| chr21:37124533 | G | C | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110-86G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124533 | |||||||
| chr21:37124542 | C | T | 40 | a0001c0005t0008g0243 a0001c0005t0008g0262 a0001c0023t0008g0259 others(37): Show |
42 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1110-77C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124542 | |||||||
| chr21:37124583 | A | G | 196 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1110-36A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 13/45 | chr21 | 37124583 | |||||||
| chr21:37124749 | T | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
splice_region_variant&intron_variant | LOW | c.1233+7T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37124749 | |||||||
| chr21:37124765 | G | GT | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.1233+30dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | INFO_REALIGN_3_PRIME | chr21 | 37124765 | ||||||
| chr21:37124780 | A | G | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1233+38A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37124780 | |||||||
| chr21:37124837 | C | T | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1233+95C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37124837 | |||||||
| chr21:37124918 | G | A | 1 | a0002c0002t0020g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1233+176G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37124918 | |||||||
| chr21:37125003 | G | A | 196 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1233+261G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37125003 | |||||||
| chr21:37125004 | C | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(112): Show |
116 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1233+262C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37125004 | |||||||
| chr21:37125010 | T | G | 1 | a0008c0009t0006g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1233+268T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37125010 | |||||||
| chr21:37125028 | G | A | 1 | a0002c0002t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1233+286G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37125028 | |||||||
| chr21:37125155 | AT | A | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+414delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37125155 | |||||||
| chr21:37125190 | C | G | 196 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1233+448C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37125190 | |||||||
| chr21:37125839 | G | A | 1 | a0001c0005t0004g0313 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1234-241G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37125839 | |||||||
| chr21:37125948 | T | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1234-132T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37125948 | |||||||
| chr21:37126040 | TG | T | 18 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(15): Show |
18 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1234-39delG | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | chr21 | 37126040 | |||||||
| chr21:37126041 | G | GT | 31 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1234-25dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 14/45 | INFO_REALIGN_3_PRIME | chr21 | 37126041 | ||||||
| chr21:37126285 | G | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(100): Show |
104 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1297+142G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37126285 | |||||||
| chr21:37126582 | G | A | 1 | a0004c0006t0005g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1297+439G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37126582 | |||||||
| chr21:37126772 | C | T | 1 | a0003c0003t0001g0215 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1297+629C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37126772 | |||||||
| chr21:37126773 | C | T | 2 | a0002c0002t0001g0206 a0002c0002t0001g0208 |
2 | HG01358.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1297+630C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37126773 | |||||||
| chr21:37127083 | G | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1297+940G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37127083 | |||||||
| chr21:37127310 | C | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1297+1167C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37127310 | |||||||
| chr21:37127331 | A | G | 1 | a0001c0004t0003g0006 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1297+1188A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37127331 | |||||||
| chr21:37127484 | C | A | 48 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(45): Show |
48 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1297+1341C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37127484 | |||||||
| chr21:37127527 | T | G | 1 | a0001c0005t0004g0318 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1297+1384T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37127527 | |||||||
| chr21:37127772 | A | G | 1 | a0006c0011t0001g0221 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1298-1231A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37127772 | |||||||
| chr21:37127917 | C | G | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1298-1086C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37127917 | |||||||
| chr21:37127942 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1298-1061A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37127942 | |||||||
| chr21:37128389 | G | C | 193 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.1298-614G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37128389 | |||||||
| chr21:37128410 | C | G | 193 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.1298-593C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37128410 | |||||||
| chr21:37128431 | T | C | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298-572T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37128431 | |||||||
| chr21:37128577 | G | A | 1 | a0004c0006t0005g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1298-426G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37128577 | |||||||
| chr21:37128721 | A | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1298-282A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37128721 | |||||||
| chr21:37128734 | A | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1298-269A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37128734 | |||||||
| chr21:37128885 | C | T | 5 | a0002c0002t0001g0150 a0002c0002t0001g0151 a0002c0002t0001g0152 others(2): Show |
5 | HG00738.hp1 HG01071.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1298-118C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37128885 | |||||||
| chr21:37128915 | T | C | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.1298-88T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37128915 | |||||||
| chr21:37128979 | G | A | 27 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(24): Show |
27 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1298-24G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 15/45 | chr21 | 37128979 | |||||||
| chr21:37129318 | C | T | 5 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358+255C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37129318 | |||||||
| chr21:37129415 | C | T | 47 | a0002c0002t0001g0236 a0002c0002t0001g0247 a0003c0003t0001g0002 others(44): Show |
49 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1358+352C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37129415 | |||||||
| chr21:37129513 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1358+450A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37129513 | |||||||
| chr21:37129627 | C | T | 1 | a0001c0001t0002g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1358+564C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37129627 | |||||||
| chr21:37129712 | G | C | 197 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1358+649G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37129712 | |||||||
| chr21:37130093 | C | T | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1358+1030C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130093 | |||||||
| chr21:37130257 | T | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1358+1194T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130257 | |||||||
| chr21:37130366 | CAG | C | 11 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(8): Show |
11 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1358+1306_1358+130 others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | INFO_REALIGN_3_PRIME | chr21 | 37130366 | ||||||
| chr21:37130471 | T | C | 5 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358+1408T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130471 | |||||||
| chr21:37130504 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1358+1441G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130504 | |||||||
| chr21:37130568 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1358+1505C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130568 | |||||||
| chr21:37130584 | T | C | 3 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0169 |
3 | HG02056.hp1 HG02132.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1358+1521T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130584 | |||||||
| chr21:37130682 | C | T | 1 | a0001c0001t0002g0117 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1358+1619C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130682 | |||||||
| chr21:37130792 | T | C | 1 | a0001c0001t0002g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1358+1729T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130792 | |||||||
| chr21:37130800 | C | CTTTCT | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1358+1739_1358+174 others(9): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | INFO_REALIGN_3_PRIME | chr21 | 37130800 | ||||||
| chr21:37130826 | A | G | 204 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1358+1763A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130826 | |||||||
| chr21:37130852 | A | G | 1 | a0001c0004t0003g0018 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1358+1789A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37130852 | |||||||
| chr21:37131098 | A | G | 1 | a0002c0002t0001g0175 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1359-1584A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131098 | |||||||
| chr21:37131143 | C | T | 5 | a0001c0005t0004g0314 a0001c0005t0008g0322 a0001c0005t0008g0324 others(2): Show |
5 | HG00099.hp2 HG01109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359-1539C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131143 | |||||||
| chr21:37131255 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1359-1427G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131255 | |||||||
| chr21:37131288 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1359-1394A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131288 | |||||||
| chr21:37131294 | A | G | 32 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(29): Show |
32 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1359-1388A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131294 | |||||||
| chr21:37131359 | A | G | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1359-1323A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131359 | |||||||
| chr21:37131462 | T | G | 197 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1359-1220T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131462 | |||||||
| chr21:37131570 | T | G | 5 | a0001c0005t0004g0314 a0001c0005t0008g0322 a0001c0005t0008g0324 others(2): Show |
5 | HG00099.hp2 HG01109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359-1112T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131570 | |||||||
| chr21:37131577 | T | C | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1359-1105T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131577 | |||||||
| chr21:37131628 | AG | A | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1359-1051delG | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | INFO_REALIGN_3_PRIME | chr21 | 37131628 | ||||||
| chr21:37131674 | G | T | 22 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(19): Show |
22 | HG00733.hp1 HG01255.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1359-1008G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131674 | |||||||
| chr21:37131717 | C | T | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1359-965C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131717 | |||||||
| chr21:37131809 | A | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1359-873A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37131809 | |||||||
| chr21:37132024 | T | G | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1359-658T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132024 | |||||||
| chr21:37132028 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1359-654G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132028 | |||||||
| chr21:37132113 | C | G | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1359-569C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132113 | |||||||
| chr21:37132195 | A | G | 1 | a0001c0004t0003g0015 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1359-487A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132195 | |||||||
| chr21:37132200 | C | T | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1359-482C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132200 | |||||||
| chr21:37132330 | T | A | 1 | a0001c0004t0003g0300 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1359-352T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132330 | |||||||
| chr21:37132335 | CT | C | 126 | a0001c0001t0002g0027 a0001c0001t0002g0032 a0001c0001t0002g0035 others(123): Show |
126 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.1359-333delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | INFO_REALIGN_3_PRIME | chr21 | 37132335 | ||||||
| chr21:37132353 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1359-329T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132353 | |||||||
| chr21:37132532 | C | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1359-150C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132532 | |||||||
| chr21:37132564 | C | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1359-118C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132564 | |||||||
| chr21:37132628 | A | G | 45 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(42): Show |
45 | HG00099.hp2 HG00733.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1359-54A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 16/45 | chr21 | 37132628 | |||||||
| chr21:37132858 | G | GT | 5 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1443+100dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | INFO_REALIGN_3_PRIME | chr21 | 37132858 | ||||||
| chr21:37133025 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1443+259A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37133025 | |||||||
| chr21:37133080 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1443+314C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37133080 | |||||||
| chr21:37133271 | A | G | 1 | a0003c0003t0001g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1443+505A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37133271 | |||||||
| chr21:37133280 | A | T | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1443+514A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37133280 | |||||||
| chr21:37133281 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1443+515C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37133281 | |||||||
| chr21:37133282 | G | A | 1 | a0006c0011t0001g0306 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1443+516G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37133282 | |||||||
| chr21:37133396 | C | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1443+630C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37133396 | |||||||
| chr21:37133669 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1443+903G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37133669 | |||||||
| chr21:37134129 | G | A | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1444-1251G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134129 | |||||||
| chr21:37134142 | T | C | 1 | a0010c0012t0002g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1444-1238T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134142 | |||||||
| chr21:37134143 | T | C | 1 | a0003c0003t0001g0240 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1444-1237T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134143 | |||||||
| chr21:37134184 | T | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1444-1196T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134184 | |||||||
| chr21:37134271 | G | A | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1444-1109G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134271 | |||||||
| chr21:37134354 | A | G | 1 | a0009c0010t0006g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1444-1026A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134354 | |||||||
| chr21:37134387 | T | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1444-993T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134387 | |||||||
| chr21:37134396 | G | A | 1 | a0003c0018t0001g0231 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1444-984G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134396 | |||||||
| chr21:37134448 | CA | C | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1444-921delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | INFO_REALIGN_3_PRIME | chr21 | 37134448 | ||||||
| chr21:37134455 | A | C | 1 | a0001c0001t0002g0107 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1444-925A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134455 | |||||||
| chr21:37134467 | G | A | 4 | a0001c0005t0004g0313 a0001c0005t0004g0334 a0001c0005t0004g0335 others(1): Show |
4 | HG03130.hp2 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444-913G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134467 | |||||||
| chr21:37134625 | T | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1444-755T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134625 | |||||||
| chr21:37134629 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1444-751G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134629 | |||||||
| chr21:37134837 | A | G | 3 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 |
3 | HG01243.hp1 HG01978.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1444-543A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134837 | |||||||
| chr21:37134842 | T | C | 1 | a0002c0002t0001g0171 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1444-538T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134842 | |||||||
| chr21:37134871 | A | G | 1 | a0011c0020t0002g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1444-509A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37134871 | |||||||
| chr21:37135017 | A | G | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.1444-363A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37135017 | |||||||
| chr21:37135227 | G | T | 1 | a0002c0002t0009g0030 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1444-153G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37135227 | |||||||
| chr21:37135272 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1444-108T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 17/45 | chr21 | 37135272 | |||||||
| chr21:37136017 | G | A | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1578+503G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37136017 | |||||||
| chr21:37136097 | A | T | 1 | a0002c0002t0001g0205 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1578+583A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37136097 | |||||||
| chr21:37136201 | T | TAATGACC others(4): Show |
1 | a0002c0002t0001g0166 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1578+692_1578+702d others(13): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | INFO_REALIGN_3_PRIME | chr21 | 37136201 | ||||||
| chr21:37136319 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1578+805C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37136319 | |||||||
| chr21:37136462 | T | C | 1 | a0003c0003t0001g0188 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1578+948T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37136462 | |||||||
| chr21:37136573 | A | G | 1 | a0002c0002t0001g0160 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1578+1059A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37136573 | |||||||
| chr21:37136939 | A | G | 2 | a0001c0004t0003g0007 a0001c0004t0003g0011 |
2 | NA18954.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1578+1425A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37136939 | |||||||
| chr21:37137053 | A | G | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1578+1539A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137053 | |||||||
| chr21:37137268 | A | G | 1 | a0001c0005t0004g0321 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1579-1366A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137268 | |||||||
| chr21:37137405 | G | A | 32 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(29): Show |
32 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1579-1229G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137405 | |||||||
| chr21:37137407 | A | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1579-1227A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137407 | |||||||
| chr21:37137418 | C | T | 1 | a0003c0016t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1579-1216C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137418 | |||||||
| chr21:37137508 | G | A | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1579-1126G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137508 | |||||||
| chr21:37137722 | A | T | 3 | a0001c0004t0003g0290 a0001c0004t0003g0293 a0001c0004t0015g0294 |
3 | HG00639.hp2 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1579-912A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137722 | |||||||
| chr21:37137882 | A | C | 2 | a0001c0005t0002g0033 a0001c0005t0022g0308 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1579-752A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137882 | |||||||
| chr21:37137903 | G | C | 1 | a0005c0007t0002g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1579-731G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137903 | |||||||
| chr21:37137911 | C | A | 3 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 |
3 | HG01243.hp1 HG01978.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1579-723C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137911 | |||||||
| chr21:37137951 | C | CA | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1579-682dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | INFO_REALIGN_3_PRIME | chr21 | 37137951 | ||||||
| chr21:37137962 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1579-672T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137962 | |||||||
| chr21:37137970 | G | A | 1 | a0003c0016t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1579-664G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37137970 | |||||||
| chr21:37138038 | T | A | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1579-596T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37138038 | |||||||
| chr21:37138177 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0104 |
2 | HG00733.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1579-457C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37138177 | |||||||
| chr21:37138270 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0002g0123 |
2 | HG02071.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1579-364C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37138270 | |||||||
| chr21:37138316 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1579-318G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37138316 | |||||||
| chr21:37138344 | A | G | 1 | a0001c0021t0002g0097 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1579-290A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37138344 | |||||||
| chr21:37138498 | T | C | 1 | a0003c0003t0001g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1579-136T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37138498 | |||||||
| chr21:37138627 | T | A | 1 | a0002c0002t0001g0151 | 1 | HG00738.hp1 | splice_region_variant&intron_variant | LOW | c.1579-7T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37138627 | |||||||
| chr21:37138629 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG00738.hp1 | splice_region_variant&intron_variant | LOW | c.1579-5G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 18/45 | chr21 | 37138629 | |||||||
| chr21:37138956 | T | G | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1659+242T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37138956 | |||||||
| chr21:37139146 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1659+432C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139146 | |||||||
| chr21:37139187 | C | T | 1 | a0003c0003t0001g0187 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1659+473C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139187 | |||||||
| chr21:37139231 | C | T | 60 | a0001c0014t0006g0307 a0002c0002t0001g0236 a0003c0003t0001g0002 others(57): Show |
62 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1659+517C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139231 | |||||||
| chr21:37139308 | A | T | 1 | a0001c0001t0002g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1659+594A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139308 | |||||||
| chr21:37139323 | A | G | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1659+609A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139323 | |||||||
| chr21:37139533 | A | G | 1 | a0009c0010t0006g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1659+819A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139533 | |||||||
| chr21:37139555 | C | G | 37 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(34): Show |
37 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1659+841C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139555 | |||||||
| chr21:37139616 | A | T | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1659+902A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139616 | |||||||
| chr21:37139678 | T | C | 1 | a0002c0002t0001g0159 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1660-883T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139678 | |||||||
| chr21:37139809 | GA | G | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1660-742delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | INFO_REALIGN_3_PRIME | chr21 | 37139809 | ||||||
| chr21:37139875 | C | T | 2 | a0001c0004t0003g0298 a0001c0004t0003g0300 |
2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1660-686C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139875 | |||||||
| chr21:37139957 | T | C | 102 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(99): Show |
103 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1660-604T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37139957 | |||||||
| chr21:37140141 | A | T | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1660-420A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37140141 | |||||||
| chr21:37140187 | C | CA | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660-374_1660-373i others(3): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37140187 | |||||||
| chr21:37140191 | A | AGTGCT | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660-370_1660-369i others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37140191 | |||||||
| chr21:37140192 | T | A | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660-369T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37140192 | |||||||
| chr21:37140345 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1660-216C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37140345 | |||||||
| chr21:37140398 | A | G | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1660-163A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 19/45 | chr21 | 37140398 | |||||||
| chr21:37140763 | A | G | 1 | a0001c0004t0003g0300 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1772+90A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37140763 | |||||||
| chr21:37140844 | C | T | 4 | a0001c0004t0003g0017 a0001c0004t0003g0018 a0001c0004t0003g0020 others(1): Show |
4 | NA18956.hp2 NA19005.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1772+171C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37140844 | |||||||
| chr21:37141066 | A | T | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1772+393A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37141066 | |||||||
| chr21:37141078 | A | G | 1 | a0001c0005t0004g0327 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1772+405A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37141078 | |||||||
| chr21:37141215 | T | A | 1 | a0001c0001t0002g0100 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1772+542T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37141215 | |||||||
| chr21:37141215 | T | C | 1 | a0001c0004t0003g0005 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1772+542T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37141215 | |||||||
| chr21:37141412 | T | TC | 35 | a0001c0004t0003g0298 a0001c0004t0003g0300 a0001c0005t0002g0033 others(32): Show |
35 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1772+748dupC | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | INFO_REALIGN_3_PRIME | chr21 | 37141412 | ||||||
| chr21:37141412 | T | TCC | 140 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(137): Show |
141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1772+747_1772+748d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | INFO_REALIGN_3_PRIME | chr21 | 37141412 | ||||||
| chr21:37141418 | C | CCCCCCAG others(3): Show |
1 | a0004c0006t0005g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1772+748_1772+749i others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | INFO_REALIGN_3_PRIME | chr21 | 37141418 | ||||||
| chr21:37141745 | G | T | 1 | a0001c0001t0002g0091 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1772+1072G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37141745 | |||||||
| chr21:37141869 | C | T | 1 | a0002c0002t0001g0157 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1772+1196C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37141869 | |||||||
| chr21:37142174 | C | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1772+1501C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37142174 | |||||||
| chr21:37142195 | T | C | 1 | a0002c0002t0019g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1772+1522T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37142195 | |||||||
| chr21:37142350 | C | A | 1 | a0014c0015t0001g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1772+1677C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37142350 | |||||||
| chr21:37142458 | C | G | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1772+1785C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37142458 | |||||||
| chr21:37142588 | A | G | 1 | a0002c0002t0020g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1772+1915A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37142588 | |||||||
| chr21:37142672 | A | G | 1 | a0003c0003t0001g0215 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1773-1853A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37142672 | |||||||
| chr21:37142717 | A | C | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1773-1808A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37142717 | |||||||
| chr21:37143007 | A | G | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1773-1518A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143007 | |||||||
| chr21:37143117 | A | G | 1 | a0001c0005t0004g0327 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1773-1408A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143117 | |||||||
| chr21:37143157 | A | G | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1773-1368A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143157 | |||||||
| chr21:37143179 | G | A | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1773-1346G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143179 | |||||||
| chr21:37143345 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1773-1180C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143345 | |||||||
| chr21:37143353 | G | A | 35 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(32): Show |
35 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1773-1172G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143353 | |||||||
| chr21:37143484 | A | G | 1 | a0003c0016t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1773-1041A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143484 | |||||||
| chr21:37143509 | C | A | 17 | a0001c0005t0004g0309 a0001c0005t0004g0315 a0001c0005t0004g0316 others(14): Show |
17 | HG00733.hp1 HG01255.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1773-1016C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143509 | |||||||
| chr21:37143559 | G | T | 1 | a0002c0002t0001g0175 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1773-966G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143559 | |||||||
| chr21:37143570 | G | A | 1 | a0002c0002t0001g0175 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1773-955G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143570 | |||||||
| chr21:37143577 | A | C | 3 | a0003c0003t0001g0301 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1773-948A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143577 | |||||||
| chr21:37143586 | A | G | 3 | a0003c0003t0001g0301 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1773-939A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143586 | |||||||
| chr21:37143633 | A | G | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1773-892A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143633 | |||||||
| chr21:37143640 | T | C | 1 | a0001c0001t0002g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1773-885T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143640 | |||||||
| chr21:37143663 | A | G | 5 | a0001c0005t0004g0313 a0001c0005t0004g0321 a0001c0005t0004g0334 others(2): Show |
5 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1773-862A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143663 | |||||||
| chr21:37143741 | C | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1773-784C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143741 | |||||||
| chr21:37143742 | G | A | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1773-783G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143742 | |||||||
| chr21:37143852 | C | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1773-673C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143852 | |||||||
| chr21:37143853 | T | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1773-672T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143853 | |||||||
| chr21:37143856 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1773-669G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143856 | |||||||
| chr21:37143906 | A | T | 262 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(259): Show |
265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1773-619A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143906 | |||||||
| chr21:37143911 | C | A | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1773-614C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143911 | |||||||
| chr21:37143921 | G | T | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1773-604G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37143921 | |||||||
| chr21:37144023 | C | T | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1773-502C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37144023 | |||||||
| chr21:37144024 | G | A | 11 | a0002c0002t0001g0192 a0002c0002t0001g0204 a0002c0002t0001g0205 others(8): Show |
11 | HG00735.hp2 HG01081.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1773-501G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37144024 | |||||||
| chr21:37144156 | T | C | 5 | a0002c0002t0001g0150 a0002c0002t0001g0151 a0002c0002t0001g0152 others(2): Show |
5 | HG00738.hp1 HG01071.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1773-369T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37144156 | |||||||
| chr21:37144208 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1773-317G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37144208 | |||||||
| chr21:37144242 | TAA | T | 26 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(23): Show |
26 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1773-276_1773-275d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | INFO_REALIGN_3_PRIME | chr21 | 37144242 | ||||||
| chr21:37144249 | A | T | 167 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(164): Show |
168 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1773-276A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37144249 | |||||||
| chr21:37144264 | A | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1773-261A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37144264 | |||||||
| chr21:37144336 | A | G | 1 | a0001c0005t0008g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1773-189A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37144336 | |||||||
| chr21:37144359 | T | C | 1 | a0001c0001t0007g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1773-166T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 20/45 | chr21 | 37144359 | |||||||
| chr21:37144711 | A | G | 2 | a0005c0007t0002g0044 a0005c0007t0002g0115 |
2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1893+66A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37144711 | |||||||
| chr21:37144721 | G | A | 102 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(99): Show |
103 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1893+76G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37144721 | |||||||
| chr21:37144758 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1893+113C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37144758 | |||||||
| chr21:37144813 | G | A | 1 | a0002c0002t0001g0212 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1893+168G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37144813 | |||||||
| chr21:37144840 | A | G | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1893+195A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37144840 | |||||||
| chr21:37144964 | T | C | 252 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(249): Show |
255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1893+319T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37144964 | |||||||
| chr21:37145227 | T | G | 1 | a0010c0012t0002g0098 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1893+582T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37145227 | |||||||
| chr21:37145303 | A | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1893+658A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37145303 | |||||||
| chr21:37145579 | A | C | 2 | a0001c0001t0002g0088 a0001c0001t0002g0101 |
2 | NA18988.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1893+934A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37145579 | |||||||
| chr21:37145906 | A | C | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893+1261A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37145906 | |||||||
| chr21:37146120 | G | C | 1 | a0001c0004t0003g0020 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1894-1361G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37146120 | |||||||
| chr21:37146134 | A | G | 5 | a0002c0002t0001g0192 a0002c0002t0001g0204 a0002c0002t0001g0205 others(2): Show |
5 | HG01081.hp1 HG01515.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-1347A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37146134 | |||||||
| chr21:37146660 | T | C | 1 | a0001c0021t0002g0097 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1894-821T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37146660 | |||||||
| chr21:37146664 | A | G | 2 | a0001c0001t0002g0088 a0001c0001t0002g0101 |
2 | NA18988.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1894-817A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37146664 | |||||||
| chr21:37146681 | T | C | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1894-800T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37146681 | |||||||
| chr21:37146717 | G | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0052 |
2 | HG01081.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1894-764G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37146717 | |||||||
| chr21:37146758 | A | C | 29 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(26): Show |
29 | HG00639.hp2 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1894-723A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37146758 | |||||||
| chr21:37146768 | G | A | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894-713G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37146768 | |||||||
| chr21:37147200 | A | G | 1 | a0001c0005t0004g0314 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1894-281A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37147200 | |||||||
| chr21:37147227 | A | G | 313 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(310): Show |
316 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.1894-254A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37147227 | |||||||
| chr21:37147380 | A | C | 1 | a0001c0001t0002g0123 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1894-101A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 21/45 | chr21 | 37147380 | |||||||
| chr21:37147712 | C | T | 1 | a0013c0017t0001g0181 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2016+109C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | chr21 | 37147712 | |||||||
| chr21:37147731 | A | AT | 20 | a0001c0001t0002g0087 a0001c0001t0002g0114 a0002c0002t0001g0150 others(17): Show |
20 | HG00738.hp1 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2016+144dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | INFO_REALIGN_3_PRIME | chr21 | 37147731 | ||||||
| chr21:37147731 | A | ATT | 6 | a0001c0001t0007g0130 a0004c0006t0005g0286 a0004c0006t0005g0287 others(3): Show |
6 | HG01106.hp2 HG01123.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2016+143_2016+144d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | INFO_REALIGN_3_PRIME | chr21 | 37147731 | ||||||
| chr21:37147791 | C | T | 102 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(99): Show |
103 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2016+188C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | chr21 | 37147791 | |||||||
| chr21:37147873 | C | T | 7 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2016+270C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | chr21 | 37147873 | |||||||
| chr21:37147903 | A | G | 4 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(1): Show |
4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2016+300A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | chr21 | 37147903 | |||||||
| chr21:37147932 | T | C | 1 | a0003c0003t0001g0187 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2016+329T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | chr21 | 37147932 | |||||||
| chr21:37148125 | C | T | 4 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0284 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2017-421C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | chr21 | 37148125 | |||||||
| chr21:37148274 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2017-272A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | chr21 | 37148274 | |||||||
| chr21:37148420 | G | A | 254 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(251): Show |
257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.2017-126G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 22/45 | chr21 | 37148420 | |||||||
| chr21:37148658 | A | C | 1 | a0002c0002t0001g0202 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2118+11A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | chr21 | 37148658 | |||||||
| chr21:37148873 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2118+226C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | chr21 | 37148873 | |||||||
| chr21:37148948 | CA | C | 102 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(99): Show |
103 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2118+304delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | INFO_REALIGN_3_PRIME | chr21 | 37148948 | ||||||
| chr21:37149233 | G | A | 2 | a0001c0005t0002g0033 a0001c0005t0022g0308 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2118+586G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | chr21 | 37149233 | |||||||
| chr21:37149360 | A | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.2118+713A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | chr21 | 37149360 | |||||||
| chr21:37149378 | C | CA | 155 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.2119-699dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | INFO_REALIGN_3_PRIME | chr21 | 37149378 | ||||||
| chr21:37149542 | A | G | 197 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.2119-536A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | chr21 | 37149542 | |||||||
| chr21:37149644 | G | T | 3 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 |
3 | HG01243.hp1 HG01978.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2119-434G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | chr21 | 37149644 | |||||||
| chr21:37149649 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2119-429G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | chr21 | 37149649 | |||||||
| chr21:37149762 | G | A | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.2119-316G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | chr21 | 37149762 | |||||||
| chr21:37149866 | G | A | 2 | a0001c0001t0007g0275 a0001c0001t0007g0276 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2119-212G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | chr21 | 37149866 | |||||||
| chr21:37150053 | GT | G | 191 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.2119-11delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | INFO_REALIGN_3_PRIME | chr21 | 37150053 | ||||||
| chr21:37150053 | GTT | G | 7 | a0001c0001t0002g0046 a0001c0001t0002g0059 a0001c0021t0002g0097 others(4): Show |
7 | HG02615.hp2 HG02896.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.2119-12_2119-11del others(2): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 23/45 | INFO_REALIGN_3_PRIME | chr21 | 37150053 | ||||||
| chr21:37150186 | G | T | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2211+16G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 24/45 | chr21 | 37150186 | |||||||
| chr21:37150318 | G | T | 197 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.2211+148G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 24/45 | chr21 | 37150318 | |||||||
| chr21:37150390 | T | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2211+220T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 24/45 | chr21 | 37150390 | |||||||
| chr21:37150396 | A | G | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2211+226A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 24/45 | chr21 | 37150396 | |||||||
| chr21:37150410 | A | G | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2211+240A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 24/45 | chr21 | 37150410 | |||||||
| chr21:37150477 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2211+307A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 24/45 | chr21 | 37150477 | |||||||
| chr21:37150507 | A | G | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212-313A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 24/45 | chr21 | 37150507 | |||||||
| chr21:37150966 | C | A | 144 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.2276+82C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 25/45 | chr21 | 37150966 | |||||||
| chr21:37151046 | A | G | 1 | a0002c0002t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2276+162A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 25/45 | chr21 | 37151046 | |||||||
| chr21:37151109 | G | C | 2 | a0001c0005t0008g0324 a0001c0005t0008g0331 |
2 | HG00099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2276+225G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 25/45 | chr21 | 37151109 | |||||||
| chr21:37151139 | G | A | 13 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2276+255G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 25/45 | chr21 | 37151139 | |||||||
| chr21:37151412 | A | AT | 10 | a0003c0003t0001g0003 a0003c0003t0001g0136 a0003c0003t0001g0227 others(7): Show |
11 | HG00408.hp2 HG00597.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.2277-472dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 25/45 | INFO_REALIGN_3_PRIME | chr21 | 37151412 | ||||||
| chr21:37151607 | G | A | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2277-286G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 25/45 | chr21 | 37151607 | |||||||
| chr21:37151772 | G | A | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | HG02074.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2277-121G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 25/45 | chr21 | 37151772 | |||||||
| chr21:37151824 | A | C | 1 | a0002c0002t0014g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2277-69A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 25/45 | chr21 | 37151824 | |||||||
| chr21:37152158 | T | C | 2 | a0003c0003t0001g0136 a0003c0003t0001g0245 |
2 | HG02165.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2413+129T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152158 | |||||||
| chr21:37152204 | GAAC | G | 32 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0028 others(29): Show |
33 | HG00673.hp1 HG01081.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.2413+177_2413+179d others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr21 | 37152204 | ||||||
| chr21:37152357 | C | T | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2413+328C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152357 | |||||||
| chr21:37152358 | G | A | 2 | a0002c0002t0001g0177 a0002c0002t0001g0178 |
2 | HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2413+329G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152358 | |||||||
| chr21:37152379 | GT | G | 192 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.2413+362delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr21 | 37152379 | ||||||
| chr21:37152389 | T | G | 3 | a0003c0003t0001g0301 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2413+360T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152389 | |||||||
| chr21:37152455 | C | T | 2 | a0009c0010t0006g0137 a0009c0010t0006g0138 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2413+426C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152455 | |||||||
| chr21:37152587 | C | T | 47 | a0002c0002t0001g0236 a0002c0002t0001g0247 a0003c0003t0001g0002 others(44): Show |
49 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.2414-364C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152587 | |||||||
| chr21:37152588 | G | A | 32 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(29): Show |
32 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.2414-363G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152588 | |||||||
| chr21:37152719 | G | A | 204 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.2414-232G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152719 | |||||||
| chr21:37152814 | T | A | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2414-137T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152814 | |||||||
| chr21:37152866 | A | G | 1 | a0005c0007t0002g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2414-85A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152866 | |||||||
| chr21:37152898 | G | A | 313 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(310): Show |
316 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.2414-53G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 26/45 | chr21 | 37152898 | |||||||
| chr21:37153303 | A | G | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2740+26A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153303 | |||||||
| chr21:37153327 | T | C | 1 | a0001c0005t0004g0332 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2740+50T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153327 | |||||||
| chr21:37153352 | T | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.2740+75T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153352 | |||||||
| chr21:37153506 | C | G | 47 | a0002c0002t0001g0236 a0002c0002t0001g0247 a0003c0003t0001g0002 others(44): Show |
49 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.2740+229C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153506 | |||||||
| chr21:37153521 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2740+244A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153521 | |||||||
| chr21:37153680 | A | G | 1 | a0003c0003t0001g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2740+403A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153680 | |||||||
| chr21:37153846 | T | C | 1 | a0002c0002t0001g0191 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2740+569T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153846 | |||||||
| chr21:37153860 | C | CA | 7 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2740+584dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | INFO_REALIGN_3_PRIME | chr21 | 37153860 | ||||||
| chr21:37153912 | G | C | 9 | a0002c0002t0001g0193 a0002c0002t0001g0195 a0002c0002t0001g0199 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2740+635G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153912 | |||||||
| chr21:37153966 | TC | T | 4 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0284 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2740+690delC | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153966 | |||||||
| chr21:37153993 | G | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2740+716G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37153993 | |||||||
| chr21:37154181 | G | A | 2 | a0007c0008t0006g0140 a0007c0008t0006g0142 |
2 | NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2740+904G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154181 | |||||||
| chr21:37154255 | T | A | 1 | a0009c0010t0006g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2740+978T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154255 | |||||||
| chr21:37154303 | T | G | 1 | a0001c0001t0002g0027 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2740+1026T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154303 | |||||||
| chr21:37154318 | T | A | 3 | a0003c0003t0001g0223 a0003c0003t0001g0224 a0003c0003t0017g0230 |
3 | HG00621.hp2 HG01943.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.2740+1041T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154318 | |||||||
| chr21:37154364 | G | A | 4 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0284 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2740+1087G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154364 | |||||||
| chr21:37154366 | T | G | 1 | a0002c0002t0001g0202 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2740+1089T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154366 | |||||||
| chr21:37154530 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2740+1253C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154530 | |||||||
| chr21:37154581 | A | G | 1 | a0002c0002t0001g0158 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2740+1304A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154581 | |||||||
| chr21:37154690 | T | G | 4 | a0002c0002t0001g0247 a0003c0003t0001g0225 a0003c0003t0001g0240 others(1): Show |
4 | HG03704.hp1 NA18946.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2740+1413T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154690 | |||||||
| chr21:37154694 | G | T | 2 | a0001c0004t0003g0289 a0001c0004t0003g0291 |
2 | HG00741.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2740+1417G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154694 | |||||||
| chr21:37154740 | G | T | 2 | a0002c0002t0001g0148 a0002c0002t0001g0158 |
2 | NA18993.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2740+1463G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154740 | |||||||
| chr21:37154878 | G | T | 5 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2740+1601G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154878 | |||||||
| chr21:37154930 | C | T | 2 | a0001c0001t0002g0093 a0001c0001t0002g0094 |
2 | NA18955.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2740+1653C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154930 | |||||||
| chr21:37154962 | T | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2740+1685T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154962 | |||||||
| chr21:37154987 | G | A | 4 | a0002c0002t0001g0193 a0002c0002t0001g0195 a0002c0002t0001g0200 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2741-1668G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37154987 | |||||||
| chr21:37155195 | C | T | 1 | a0002c0002t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2741-1460C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155195 | |||||||
| chr21:37155198 | C | T | 1 | a0002c0002t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2741-1457C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155198 | |||||||
| chr21:37155212 | T | C | 4 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(1): Show |
4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2741-1443T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155212 | |||||||
| chr21:37155408 | G | C | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.2741-1247G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155408 | |||||||
| chr21:37155453 | A | G | 1 | a0003c0013t0001g0218 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2741-1202A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155453 | |||||||
| chr21:37155455 | C | T | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.2741-1200C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155455 | |||||||
| chr21:37155551 | C | G | 1 | a0001c0004t0003g0021 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2741-1104C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155551 | |||||||
| chr21:37155573 | A | C | 3 | a0001c0001t0002g0031 a0001c0001t0002g0038 a0001c0001t0002g0039 |
3 | NA18984.hp1 NA19087.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2741-1082A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155573 | |||||||
| chr21:37155934 | T | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2741-721T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155934 | |||||||
| chr21:37155969 | T | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.2741-686T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37155969 | |||||||
| chr21:37156041 | TG | T | 192 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.2741-613delG | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37156041 | |||||||
| chr21:37156042 | G | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0111 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2741-613G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37156042 | |||||||
| chr21:37156208 | T | TTTTG | 256 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(253): Show |
259 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.2741-444_2741-443i others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | INFO_REALIGN_3_PRIME | chr21 | 37156208 | ||||||
| chr21:37156306 | G | A | 4 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0284 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2741-349G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37156306 | |||||||
| chr21:37156312 | C | T | 10 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(7): Show |
10 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.2741-343C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37156312 | |||||||
| chr21:37156554 | A | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2741-101A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37156554 | |||||||
| chr21:37156565 | A | G | 203 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2741-90A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37156565 | |||||||
| chr21:37156588 | A | C | 4 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2741-67A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 27/45 | chr21 | 37156588 | |||||||
| chr21:37157022 | C | T | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2992+116C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37157022 | |||||||
| chr21:37157079 | A | G | 2 | a0001c0004t0003g0289 a0001c0004t0003g0291 |
2 | HG00741.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2992+173A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37157079 | |||||||
| chr21:37157139 | C | T | 2 | a0001c0005t0002g0033 a0001c0005t0022g0308 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2992+233C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37157139 | |||||||
| chr21:37157180 | G | A | 2 | a0001c0001t0002g0085 a0001c0001t0002g0108 |
2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2992+274G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37157180 | |||||||
| chr21:37157218 | A | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2992+312A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37157218 | |||||||
| chr21:37157410 | T | G | 5 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(2): Show |
5 | HG01106.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2992+504T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37157410 | |||||||
| chr21:37158042 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2992+1136A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37158042 | |||||||
| chr21:37158222 | G | A | 1 | a0001c0001t0002g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2992+1316G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37158222 | |||||||
| chr21:37158250 | G | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2992+1344G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37158250 | |||||||
| chr21:37158357 | C | T | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2993-1342C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37158357 | |||||||
| chr21:37158589 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2993-1110G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37158589 | |||||||
| chr21:37158826 | T | G | 2 | a0002c0002t0001g0145 a0002c0002t0001g0147 |
2 | NA18747.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2993-873T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37158826 | |||||||
| chr21:37158870 | C | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2993-829C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37158870 | |||||||
| chr21:37159106 | C | T | 1 | a0003c0016t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2993-593C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37159106 | |||||||
| chr21:37159202 | C | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2993-497C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37159202 | |||||||
| chr21:37159377 | G | A | 1 | a0001c0005t0004g0321 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2993-322G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37159377 | |||||||
| chr21:37159475 | A | G | 1 | a0002c0002t0019g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2993-224A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37159475 | |||||||
| chr21:37159569 | T | C | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.2993-130T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37159569 | |||||||
| chr21:37159679 | C | T | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2993-20C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37159679 | |||||||
| chr21:37159695 | A | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | NA18984.hp1 NA19087.hp1 |
splice_region_variant&intron_variant | LOW | c.2993-4A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 28/45 | chr21 | 37159695 | |||||||
| chr21:37159763 | C | A | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.3039+18C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 29/45 | chr21 | 37159763 | |||||||
| chr21:37160158 | GT | G | 10 | a0001c0014t0006g0307 a0007c0008t0006g0140 a0007c0008t0006g0141 others(7): Show |
10 | HG01123.hp2 HG01243.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.3039+415delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 29/45 | INFO_REALIGN_3_PRIME | chr21 | 37160158 | ||||||
| chr21:37160168 | T | C | 1 | a0001c0005t0004g0321 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3039+423T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 29/45 | chr21 | 37160168 | |||||||
| chr21:37160335 | G | A | 2 | a0001c0005t0004g0334 a0001c0005t0004g0335 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3040-467G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 29/45 | chr21 | 37160335 | |||||||
| chr21:37160356 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3040-446C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 29/45 | chr21 | 37160356 | |||||||
| chr21:37160551 | C | G | 1 | a0001c0005t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3040-251C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 29/45 | chr21 | 37160551 | |||||||
| chr21:37160695 | G | A | 5 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3040-107G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 29/45 | chr21 | 37160695 | |||||||
| chr21:37160762 | GTTAT | G | 3 | a0002c0002t0001g0145 a0002c0002t0001g0147 a0002c0002t0001g0176 |
3 | NA18747.hp2 NA18954.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.3040-37_3040-34del others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 29/45 | INFO_REALIGN_3_PRIME | chr21 | 37160762 | ||||||
| chr21:37160877 | A | G | 1 | a0009c0010t0006g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3096+19A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37160877 | |||||||
| chr21:37160998 | G | A | 5 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(2): Show |
5 | HG01106.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3096+140G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37160998 | |||||||
| chr21:37161039 | A | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.3096+181A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161039 | |||||||
| chr21:37161088 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.3096+230C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161088 | |||||||
| chr21:37161103 | T | TA | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.3096+257dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | INFO_REALIGN_3_PRIME | chr21 | 37161103 | ||||||
| chr21:37161165 | A | T | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3096+307A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161165 | |||||||
| chr21:37161283 | T | C | 1 | a0001c0005t0004g0319 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3096+425T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161283 | |||||||
| chr21:37161316 | C | A | 2 | a0001c0005t0008g0324 a0001c0005t0008g0331 |
2 | HG00099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3096+458C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161316 | |||||||
| chr21:37161421 | G | T | 1 | a0001c0022t0002g0067 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3096+563G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161421 | |||||||
| chr21:37161447 | T | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.3097-543T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161447 | |||||||
| chr21:37161507 | G | A | 6 | a0003c0003t0001g0254 a0003c0003t0001g0255 a0003c0003t0011g0250 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3097-483G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161507 | |||||||
| chr21:37161515 | G | T | 1 | a0003c0003t0009g0057 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3097-475G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161515 | |||||||
| chr21:37161654 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3097-336A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161654 | |||||||
| chr21:37161714 | T | G | 1 | a0001c0001t0002g0083 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3097-276T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161714 | |||||||
| chr21:37161961 | C | T | 4 | a0001c0005t0004g0313 a0001c0005t0004g0334 a0001c0005t0004g0335 others(1): Show |
4 | HG03130.hp2 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3097-29C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161961 | |||||||
| chr21:37161987 | C | A | 4 | a0003c0003t0011g0250 a0003c0003t0011g0251 a0003c0003t0011g0252 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG03041.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3097-3C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 30/45 | chr21 | 37161987 | |||||||
| chr21:37162092 | A | C | 1 | a0001c0001t0002g0091 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3170+29A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37162092 | |||||||
| chr21:37162143 | A | T | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.3170+80A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37162143 | |||||||
| chr21:37162231 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.3170+168T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37162231 | |||||||
| chr21:37162309 | A | G | 1 | a0002c0002t0021g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3170+246A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37162309 | |||||||
| chr21:37162673 | C | T | 1 | a0001c0022t0002g0067 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3170+610C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37162673 | |||||||
| chr21:37162723 | C | T | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3170+660C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37162723 | |||||||
| chr21:37162732 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.3170+669G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37162732 | |||||||
| chr21:37162800 | A | G | 3 | a0009c0010t0006g0137 a0009c0010t0006g0138 a0009c0010t0006g0213 |
3 | HG02976.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3170+737A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37162800 | |||||||
| chr21:37163044 | A | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.3170+981A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37163044 | |||||||
| chr21:37163214 | C | G | 1 | a0001c0001t0002g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3171-837C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37163214 | |||||||
| chr21:37163306 | A | C | 3 | a0003c0003t0001g0301 a0003c0003t0001g0303 a0012c0019t0001g0302 |
3 | HG02630.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3171-745A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37163306 | |||||||
| chr21:37163507 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3171-544C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37163507 | |||||||
| chr21:37163509 | C | A | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3171-542C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37163509 | |||||||
| chr21:37163524 | A | G | 3 | a0003c0003t0012g0234 a0003c0003t0012g0235 a0003c0003t0024g0233 |
3 | NA18981.hp2 NA19004.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.3171-527A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37163524 | |||||||
| chr21:37163546 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.3171-505T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37163546 | |||||||
| chr21:37163759 | T | C | 2 | a0002c0002t0001g0177 a0002c0002t0001g0178 |
2 | HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.3171-292T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37163759 | |||||||
| chr21:37163778 | T | A | 1 | a0001c0005t0004g0333 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3171-273T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37163778 | |||||||
| chr21:37164046 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
splice_region_variant&intron_variant | LOW | c.3171-5A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 31/45 | chr21 | 37164046 | |||||||
| chr21:37164265 | A | G | 2 | a0004c0006t0005g0280 a0004c0006t0005g0281 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3335+50A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 32/45 | chr21 | 37164265 | |||||||
| chr21:37164340 | AT | A | 84 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(81): Show |
84 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.3335+141delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 32/45 | INFO_REALIGN_3_PRIME | chr21 | 37164340 | ||||||
| chr21:37164527 | A | G | 1 | a0003c0003t0001g0248 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3335+312A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 32/45 | chr21 | 37164527 | |||||||
| chr21:37164714 | G | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.3335+499G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 32/45 | chr21 | 37164714 | |||||||
| chr21:37165078 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.3336-472G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 32/45 | chr21 | 37165078 | |||||||
| chr21:37165441 | A | C | 45 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(42): Show |
45 | HG00099.hp2 HG00733.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.3336-109A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 32/45 | chr21 | 37165441 | |||||||
| chr21:37165477 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.3336-73A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 32/45 | chr21 | 37165477 | |||||||
| chr21:37166764 | A | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4401+149A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/45 | chr21 | 37166764 | |||||||
| chr21:37166817 | A | G | 313 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(310): Show |
316 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.4401+202A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/45 | chr21 | 37166817 | |||||||
| chr21:37166910 | G | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4401+295G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/45 | chr21 | 37166910 | |||||||
| chr21:37167055 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4401+440C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/45 | chr21 | 37167055 | |||||||
| chr21:37167356 | G | A | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.4402-199G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/45 | chr21 | 37167356 | |||||||
| chr21:37167416 | G | A | 197 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.4402-139G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/45 | chr21 | 37167416 | |||||||
| chr21:37167463 | T | G | 1 | a0005c0007t0002g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4402-92T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/45 | chr21 | 37167463 | |||||||
| chr21:37167542 | G | A | 113 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(110): Show |
114 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.4402-13G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 33/45 | chr21 | 37167542 | |||||||
| chr21:37167787 | T | A | 197 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.4467+167T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37167787 | |||||||
| chr21:37168204 | A | G | 197 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.4467+584A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37168204 | |||||||
| chr21:37168366 | T | C | 2 | a0001c0014t0006g0307 a0003c0003t0001g0187 |
2 | HG00735.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.4467+746T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37168366 | |||||||
| chr21:37168576 | G | A | 1 | a0003c0003t0001g0246 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4467+956G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37168576 | |||||||
| chr21:37168604 | A | G | 1 | a0001c0001t0007g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4467+984A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37168604 | |||||||
| chr21:37169054 | G | A | 197 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.4467+1434G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169054 | |||||||
| chr21:37169345 | G | A | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4467+1725G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169345 | |||||||
| chr21:37169476 | G | A | 55 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(52): Show |
55 | HG00099.hp2 HG00544.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.4467+1856G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169476 | |||||||
| chr21:37169561 | G | A | 11 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(8): Show |
11 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.4467+1941G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169561 | |||||||
| chr21:37169736 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4467+2116T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169736 | |||||||
| chr21:37169746 | G | A | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.4467+2126G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169746 | |||||||
| chr21:37169804 | C | T | 5 | a0002c0002t0001g0210 a0002c0002t0001g0212 a0002c0002t0001g0220 others(2): Show |
5 | HG01258.hp2 HG01952.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.4467+2184C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169804 | |||||||
| chr21:37169847 | C | CA | 6 | a0001c0001t0002g0076 a0003c0003t0001g0261 a0004c0006t0005g0277 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4467+2240dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | INFO_REALIGN_3_PRIME | chr21 | 37169847 | ||||||
| chr21:37169856 | A | AC | 7 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.4467+2236_4467+223 others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169856 | |||||||
| chr21:37169874 | C | T | 5 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(2): Show |
5 | HG01106.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4467+2254C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169874 | |||||||
| chr21:37169875 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4467+2255G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169875 | |||||||
| chr21:37169916 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4467+2296A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169916 | |||||||
| chr21:37169921 | T | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4467+2301T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37169921 | |||||||
| chr21:37170031 | A | T | 3 | a0001c0001t0002g0095 a0001c0001t0002g0111 a0001c0001t0002g0112 |
3 | HG02922.hp1 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4467+2411A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170031 | |||||||
| chr21:37170062 | T | C | 1 | a0003c0003t0001g0229 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4467+2442T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170062 | |||||||
| chr21:37170255 | A | G | 4 | a0002c0002t0001g0145 a0002c0002t0001g0147 a0002c0002t0001g0172 others(1): Show |
4 | NA18747.hp2 NA18954.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.4468-2340A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170255 | |||||||
| chr21:37170406 | A | G | 1 | a0002c0002t0001g0165 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4468-2189A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170406 | |||||||
| chr21:37170447 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4468-2148G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170447 | |||||||
| chr21:37170459 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4468-2136G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170459 | |||||||
| chr21:37170463 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4468-2132C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170463 | |||||||
| chr21:37170472 | C | G | 1 | a0001c0021t0002g0097 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4468-2123C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170472 | |||||||
| chr21:37170494 | A | G | 1 | a0001c0001t0002g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4468-2101A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170494 | |||||||
| chr21:37170520 | G | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0028 others(68): Show |
72 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.4468-2075G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170520 | |||||||
| chr21:37170579 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4468-2016G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170579 | |||||||
| chr21:37170654 | A | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4468-1941A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170654 | |||||||
| chr21:37170712 | T | A | 1 | a0001c0001t0002g0035 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4468-1883T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170712 | |||||||
| chr21:37170791 | T | A | 4 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(1): Show |
4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4468-1804T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37170791 | |||||||
| chr21:37171000 | T | A | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.4468-1595T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171000 | |||||||
| chr21:37171210 | G | T | 1 | a0001c0001t0002g0085 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4468-1385G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171210 | |||||||
| chr21:37171239 | A | G | 47 | a0002c0002t0001g0247 a0003c0003t0001g0002 a0003c0003t0001g0003 others(44): Show |
49 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.4468-1356A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171239 | |||||||
| chr21:37171382 | C | T | 1 | a0003c0003t0011g0252 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4468-1213C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171382 | |||||||
| chr21:37171411 | T | C | 4 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0284 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4468-1184T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171411 | |||||||
| chr21:37171569 | T | C | 4 | a0002c0002t0001g0145 a0002c0002t0001g0147 a0002c0002t0001g0172 others(1): Show |
4 | NA18747.hp2 NA18954.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.4468-1026T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171569 | |||||||
| chr21:37171755 | A | T | 1 | a0004c0006t0005g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4468-840A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171755 | |||||||
| chr21:37171770 | A | G | 1 | a0001c0001t0002g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4468-825A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171770 | |||||||
| chr21:37171796 | T | G | 1 | a0001c0023t0008g0259 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4468-799T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171796 | |||||||
| chr21:37171944 | A | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4468-651A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 34/45 | chr21 | 37171944 | |||||||
| chr21:37172854 | A | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4617+110A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37172854 | |||||||
| chr21:37173154 | T | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4617+410T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37173154 | |||||||
| chr21:37173308 | G | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4617+564G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37173308 | |||||||
| chr21:37173328 | T | C | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4617+584T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37173328 | |||||||
| chr21:37173380 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4617+636A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37173380 | |||||||
| chr21:37173398 | T | A | 1 | a0002c0002t0001g0157 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4617+654T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37173398 | |||||||
| chr21:37173426 | G | A | 2 | a0010c0012t0002g0068 a0010c0012t0002g0098 |
2 | HG03490.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.4617+682G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37173426 | |||||||
| chr21:37173466 | G | C | 1 | a0002c0002t0001g0166 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.4617+722G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37173466 | |||||||
| chr21:37173920 | C | T | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.4617+1176C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37173920 | |||||||
| chr21:37174080 | T | C | 106 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(103): Show |
107 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.4617+1336T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174080 | |||||||
| chr21:37174113 | TAA | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.4617+1371_4617+137 others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37174113 | ||||||
| chr21:37174171 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4617+1427T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174171 | |||||||
| chr21:37174268 | T | A | 2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | HG00597.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.4617+1524T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174268 | |||||||
| chr21:37174272 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4617+1528G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174272 | |||||||
| chr21:37174333 | A | T | 1 | a0001c0001t0002g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4617+1589A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174333 | |||||||
| chr21:37174380 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4617+1636G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174380 | |||||||
| chr21:37174471 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4617+1727C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174471 | |||||||
| chr21:37174504 | TAGAA | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4617+1766_4617+176 others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37174504 | ||||||
| chr21:37174686 | G | A | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.4617+1942G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174686 | |||||||
| chr21:37174736 | A | C | 1 | a0001c0022t0002g0067 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4617+1992A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174736 | |||||||
| chr21:37174901 | A | G | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4617+2157A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174901 | |||||||
| chr21:37174913 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4617+2169G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174913 | |||||||
| chr21:37174984 | G | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4617+2240G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174984 | |||||||
| chr21:37174984 | G | C | 8 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0037 others(5): Show |
9 | HG00673.hp1 HG02056.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.4617+2240G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37174984 | |||||||
| chr21:37175037 | C | T | 1 | a0003c0003t0001g0242 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4617+2293C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175037 | |||||||
| chr21:37175082 | C | T | 113 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(110): Show |
114 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.4617+2338C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175082 | |||||||
| chr21:37175083 | G | A | 1 | a0002c0002t0001g0171 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4617+2339G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175083 | |||||||
| chr21:37175099 | C | CA | 220 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.4617+2370dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37175099 | ||||||
| chr21:37175099 | C | CAA | 15 | a0001c0005t0002g0033 a0001c0005t0022g0308 a0003c0003t0001g0254 others(12): Show |
15 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.4617+2369_4617+237 others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37175099 | ||||||
| chr21:37175188 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4617+2444C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175188 | |||||||
| chr21:37175207 | C | T | 1 | a0005c0007t0002g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4617+2463C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175207 | |||||||
| chr21:37175234 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4617+2490C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175234 | |||||||
| chr21:37175263 | C | CA | 18 | a0001c0001t0002g0028 a0001c0001t0002g0034 a0001c0001t0002g0080 others(15): Show |
18 | HG00741.hp1 HG01243.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.4617+2542dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37175263 | ||||||
| chr21:37175263 | CA | C | 44 | a0001c0001t0002g0029 a0001c0004t0003g0297 a0002c0002t0001g0149 others(41): Show |
46 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.4617+2542delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37175263 | ||||||
| chr21:37175263 | CAA | C | 47 | a0001c0004t0003g0004 a0001c0004t0003g0006 a0001c0004t0003g0007 others(44): Show |
47 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.4617+2541_4617+254 others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37175263 | ||||||
| chr21:37175263 | CAAA | C | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.4617+2540_4617+254 others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37175263 | ||||||
| chr21:37175315 | C | T | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4617+2571C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175315 | |||||||
| chr21:37175339 | G | A | 32 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(29): Show |
32 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.4617+2595G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175339 | |||||||
| chr21:37175469 | C | T | 1 | a0001c0001t0007g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4617+2725C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175469 | |||||||
| chr21:37175597 | C | CA | 19 | a0001c0001t0002g0114 a0001c0001t0002g0117 a0001c0001t0002g0133 others(16): Show |
19 | HG00735.hp2 HG01123.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.4617+2873dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37175597 | ||||||
| chr21:37175597 | CA | C | 8 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(5): Show |
8 | HG01433.hp2 HG02273.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4617+2873delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37175597 | ||||||
| chr21:37175752 | C | T | 110 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.4617+3008C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37175752 | |||||||
| chr21:37176023 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4617+3279G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37176023 | |||||||
| chr21:37176042 | AAGGCACC others(22): Show |
A | 1 | a0003c0003t0001g0237 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.4617+3321_4617+334 others(33): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37176042 | ||||||
| chr21:37176069 | G | A | 1 | a0001c0005t0004g0333 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4617+3325G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37176069 | |||||||
| chr21:37176110 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4617+3366A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37176110 | |||||||
| chr21:37176934 | A | G | 259 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(256): Show |
262 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.4617+4190A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37176934 | |||||||
| chr21:37177001 | C | A | 33 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(30): Show |
33 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.4617+4257C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37177001 | |||||||
| chr21:37177102 | G | A | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | HG01168.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.4617+4358G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37177102 | |||||||
| chr21:37177269 | C | T | 1 | a0001c0005t0004g0313 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4617+4525C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37177269 | |||||||
| chr21:37177299 | G | T | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4617+4555G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37177299 | |||||||
| chr21:37177317 | G | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4617+4573G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37177317 | |||||||
| chr21:37177447 | C | T | 5 | a0002c0002t0001g0192 a0002c0002t0001g0204 a0002c0002t0001g0205 others(2): Show |
5 | HG01081.hp1 HG01515.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.4617+4703C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37177447 | |||||||
| chr21:37177466 | G | A | 1 | a0009c0010t0006g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4617+4722G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37177466 | |||||||
| chr21:37177956 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4618-4818T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37177956 | |||||||
| chr21:37178370 | A | C | 12 | a0001c0001t0002g0036 a0001c0001t0002g0061 a0001c0001t0002g0080 others(9): Show |
12 | HG00408.hp1 HG02293.hp2 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.4618-4404A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37178370 | |||||||
| chr21:37178799 | A | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0082 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4618-3975A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37178799 | |||||||
| chr21:37178917 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4618-3857T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37178917 | |||||||
| chr21:37179134 | A | G | 1 | a0002c0002t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4618-3640A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179134 | |||||||
| chr21:37179162 | C | T | 2 | a0009c0010t0006g0137 a0009c0010t0006g0138 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4618-3612C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179162 | |||||||
| chr21:37179240 | T | A | 136 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.4618-3534T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179240 | |||||||
| chr21:37179287 | A | T | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4618-3487A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179287 | |||||||
| chr21:37179413 | T | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4618-3361T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179413 | |||||||
| chr21:37179485 | C | G | 1 | a0001c0024t0002g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4618-3289C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179485 | |||||||
| chr21:37179534 | G | A | 1 | a0002c0002t0020g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4618-3240G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179534 | |||||||
| chr21:37179546 | C | T | 4 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0284 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4618-3228C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179546 | |||||||
| chr21:37179674 | A | G | 210 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(207): Show |
211 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.4618-3100A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179674 | |||||||
| chr21:37179683 | G | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4618-3091G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179683 | |||||||
| chr21:37179768 | A | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4618-3006A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179768 | |||||||
| chr21:37179814 | A | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4618-2960A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179814 | |||||||
| chr21:37179928 | A | G | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.4618-2846A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179928 | |||||||
| chr21:37179943 | C | A | 2 | a0001c0004t0003g0292 a0001c0004t0003g0297 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4618-2831C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37179943 | |||||||
| chr21:37180068 | C | G | 1 | a0006c0011t0001g0306 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4618-2706C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180068 | |||||||
| chr21:37180315 | C | T | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.4618-2459C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180315 | |||||||
| chr21:37180348 | G | C | 1 | a0001c0005t0008g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4618-2426G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180348 | |||||||
| chr21:37180349 | C | T | 1 | a0001c0005t0008g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4618-2425C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180349 | |||||||
| chr21:37180397 | C | CT | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.4618-2368dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37180397 | ||||||
| chr21:37180425 | C | T | 1 | a0002c0002t0001g0161 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4618-2349C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180425 | |||||||
| chr21:37180501 | A | G | 1 | a0003c0018t0001g0231 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4618-2273A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180501 | |||||||
| chr21:37180503 | C | T | 1 | a0001c0004t0003g0300 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4618-2271C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180503 | |||||||
| chr21:37180526 | T | C | 4 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(1): Show |
4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4618-2248T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180526 | |||||||
| chr21:37180540 | C | T | 1 | a0001c0004t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4618-2234C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180540 | |||||||
| chr21:37180616 | G | C | 1 | a0001c0005t0022g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4618-2158G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180616 | |||||||
| chr21:37180624 | G | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4618-2150G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180624 | |||||||
| chr21:37180636 | G | A | 8 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(5): Show |
8 | HG02109.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4618-2138G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180636 | |||||||
| chr21:37180643 | G | A | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4618-2131G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180643 | |||||||
| chr21:37180760 | TA | T | 197 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.4618-2005delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37180760 | ||||||
| chr21:37180843 | TA | T | 8 | a0003c0003t0001g0261 a0004c0006t0005g0282 a0008c0009t0006g0263 others(5): Show |
8 | HG01243.hp1 HG01978.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4618-1918delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37180843 | ||||||
| chr21:37180905 | A | T | 39 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(36): Show |
39 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.4618-1869A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37180905 | |||||||
| chr21:37181391 | G | A | 5 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4618-1383G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37181391 | |||||||
| chr21:37181784 | C | T | 19 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.4618-990C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37181784 | |||||||
| chr21:37181786 | T | C | 2 | a0001c0005t0004g0315 a0001c0005t0004g0325 |
2 | HG00733.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.4618-988T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37181786 | |||||||
| chr21:37181880 | C | T | 1 | a0006c0011t0001g0221 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4618-894C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37181880 | |||||||
| chr21:37181942 | TAA | T | 22 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(19): Show |
22 | HG00733.hp1 HG01255.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.4618-829_4618-828d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | INFO_REALIGN_3_PRIME | chr21 | 37181942 | ||||||
| chr21:37182027 | G | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4618-747G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37182027 | |||||||
| chr21:37182541 | G | T | 84 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(81): Show |
84 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.4618-233G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37182541 | |||||||
| chr21:37182638 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4618-136C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 35/45 | chr21 | 37182638 | |||||||
| chr21:37183042 | GT | G | 10 | a0001c0005t0004g0309 a0001c0005t0004g0316 a0001c0005t0004g0317 others(7): Show |
10 | HG01261.hp2 HG01928.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.4757+133delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | INFO_REALIGN_3_PRIME | chr21 | 37183042 | ||||||
| chr21:37183126 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4757+213A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37183126 | |||||||
| chr21:37183212 | C | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4757+299C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37183212 | |||||||
| chr21:37183349 | G | A | 1 | a0002c0002t0001g0209 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4757+436G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37183349 | |||||||
| chr21:37183401 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0104 |
2 | HG00733.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.4757+488G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37183401 | |||||||
| chr21:37183624 | G | A | 1 | a0001c0001t0007g0266 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4757+711G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37183624 | |||||||
| chr21:37183977 | A | G | 1 | a0002c0002t0001g0172 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.4757+1064A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37183977 | |||||||
| chr21:37184065 | AAC | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4757+1155_4757+115 others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | INFO_REALIGN_3_PRIME | chr21 | 37184065 | ||||||
| chr21:37184133 | A | G | 1 | a0002c0002t0001g0180 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4757+1220A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37184133 | |||||||
| chr21:37184143 | C | G | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4757+1230C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37184143 | |||||||
| chr21:37184155 | T | C | 22 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0001c0001t0002g0034 others(19): Show |
22 | HG01081.hp2 HG01981.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.4757+1242T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37184155 | |||||||
| chr21:37184485 | G | C | 195 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.4758-1221G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37184485 | |||||||
| chr21:37184511 | A | G | 2 | a0001c0004t0003g0295 a0001c0004t0003g0296 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.4758-1195A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37184511 | |||||||
| chr21:37184629 | A | AT | 87 | a0001c0001t0007g0096 a0001c0001t0007g0266 a0001c0001t0007g0273 others(84): Show |
89 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.4758-1058dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | INFO_REALIGN_3_PRIME | chr21 | 37184629 | ||||||
| chr21:37184629 | A | ATT | 11 | a0001c0001t0007g0130 a0001c0004t0010g0268 a0001c0004t0010g0269 others(8): Show |
11 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.4758-1059_4758-105 others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | INFO_REALIGN_3_PRIME | chr21 | 37184629 | ||||||
| chr21:37184629 | A | ATTT | 18 | a0001c0001t0002g0041 a0001c0001t0002g0061 a0001c0001t0002g0086 others(15): Show |
18 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.4758-1060_4758-105 others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | INFO_REALIGN_3_PRIME | chr21 | 37184629 | ||||||
| chr21:37184629 | A | ATTTT | 114 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.4758-1061_4758-105 others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | INFO_REALIGN_3_PRIME | chr21 | 37184629 | ||||||
| chr21:37184629 | A | ATTTTT | 13 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0037 others(10): Show |
14 | HG00673.hp1 HG00741.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.4758-1062_4758-105 others(9): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | INFO_REALIGN_3_PRIME | chr21 | 37184629 | ||||||
| chr21:37184697 | G | C | 2 | a0001c0005t0008g0324 a0001c0005t0008g0331 |
2 | HG00099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4758-1009G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37184697 | |||||||
| chr21:37184836 | C | A | 51 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(48): Show |
51 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.4758-870C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37184836 | |||||||
| chr21:37184931 | G | A | 1 | a0003c0003t0001g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4758-775G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37184931 | |||||||
| chr21:37185106 | G | T | 195 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.4758-600G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37185106 | |||||||
| chr21:37185264 | T | C | 1 | a0002c0002t0001g0212 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4758-442T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37185264 | |||||||
| chr21:37185492 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.4758-214A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37185492 | |||||||
| chr21:37185623 | G | C | 3 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0169 |
3 | HG02056.hp1 HG02132.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.4758-83G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37185623 | |||||||
| chr21:37185666 | T | G | 41 | a0001c0001t0002g0111 a0001c0004t0003g0004 a0001c0004t0003g0005 others(38): Show |
41 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.4758-40T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 36/45 | chr21 | 37185666 | |||||||
| chr21:37186284 | T | TC | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4826+511dupC | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | INFO_REALIGN_3_PRIME | chr21 | 37186284 | ||||||
| chr21:37186304 | C | A | 1 | a0001c0001t0002g0120 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4826+530C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | chr21 | 37186304 | |||||||
| chr21:37186318 | G | C | 27 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(24): Show |
27 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.4826+544G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | chr21 | 37186318 | |||||||
| chr21:37186335 | G | A | 195 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.4826+561G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | chr21 | 37186335 | |||||||
| chr21:37186362 | C | G | 2 | a0001c0005t0002g0033 a0001c0005t0022g0308 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4826+588C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | chr21 | 37186362 | |||||||
| chr21:37186511 | T | G | 195 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.4827-538T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | chr21 | 37186511 | |||||||
| chr21:37186587 | C | T | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.4827-462C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | chr21 | 37186587 | |||||||
| chr21:37186605 | T | C | 10 | a0001c0014t0006g0307 a0007c0008t0006g0140 a0007c0008t0006g0141 others(7): Show |
10 | HG01123.hp2 HG01243.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.4827-444T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | chr21 | 37186605 | |||||||
| chr21:37187022 | GT | G | 17 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(14): Show |
17 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.4827-17delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | INFO_REALIGN_3_PRIME | chr21 | 37187022 | ||||||
| chr21:37187033 | C | T | 2 | a0010c0012t0002g0068 a0010c0012t0002g0098 |
2 | HG03490.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.4827-16C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 37/45 | chr21 | 37187033 | |||||||
| chr21:37187410 | T | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.4923+265T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 38/45 | chr21 | 37187410 | |||||||
| chr21:37187568 | T | TAG | 105 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(102): Show |
106 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.4923+424_4923+425d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 38/45 | INFO_REALIGN_3_PRIME | chr21 | 37187568 | ||||||
| chr21:37187761 | A | G | 2 | a0001c0005t0002g0033 a0001c0005t0022g0308 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4923+616A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 38/45 | chr21 | 37187761 | |||||||
| chr21:37187834 | A | G | 4 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(1): Show |
4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4924-661A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 38/45 | chr21 | 37187834 | |||||||
| chr21:37188033 | T | C | 195 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.4924-462T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 38/45 | chr21 | 37188033 | |||||||
| chr21:37188057 | T | A | 8 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(5): Show |
8 | HG02109.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4924-438T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 38/45 | chr21 | 37188057 | |||||||
| chr21:37188100 | G | A | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.4924-395G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 38/45 | chr21 | 37188100 | |||||||
| chr21:37188165 | G | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4924-330G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 38/45 | chr21 | 37188165 | |||||||
| chr21:37188764 | C | A | 1 | a0002c0002t0001g0236 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5024+169C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37188764 | |||||||
| chr21:37189084 | A | AT | 198 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.5024+492dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr21 | 37189084 | ||||||
| chr21:37189182 | G | C | 1 | a0002c0002t0001g0209 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5024+587G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189182 | |||||||
| chr21:37189333 | C | T | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.5024+738C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189333 | |||||||
| chr21:37189431 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5024+836A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189431 | |||||||
| chr21:37189479 | C | T | 1 | a0003c0003t0011g0253 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5024+884C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189479 | |||||||
| chr21:37189485 | C | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.5024+890C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189485 | |||||||
| chr21:37189549 | CTTGT | C | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.5024+965_5024+968d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr21 | 37189549 | ||||||
| chr21:37189575 | T | G | 1 | a0002c0002t0001g0169 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5024+980T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189575 | |||||||
| chr21:37189587 | G | A | 1 | a0001c0005t0008g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5024+992G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189587 | |||||||
| chr21:37189600 | T | A | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.5024+1005T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189600 | |||||||
| chr21:37189616 | C | T | 1 | a0003c0003t0001g0245 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.5024+1021C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189616 | |||||||
| chr21:37189617 | G | A | 34 | a0001c0005t0002g0033 a0001c0005t0004g0309 a0001c0005t0004g0310 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.5024+1022G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189617 | |||||||
| chr21:37189621 | C | T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0083 a0001c0001t0002g0105 others(1): Show |
4 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.5024+1026C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189621 | |||||||
| chr21:37189625 | G | A | 2 | a0001c0001t0002g0045 a0001c0001t0002g0076 |
2 | NA18975.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.5024+1030G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189625 | |||||||
| chr21:37189640 | C | T | 111 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(108): Show |
112 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.5024+1045C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189640 | |||||||
| chr21:37189738 | G | T | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.5024+1143G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189738 | |||||||
| chr21:37189899 | C | T | 1 | a0006c0011t0001g0306 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5024+1304C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189899 | |||||||
| chr21:37189945 | T | C | 1 | a0001c0004t0003g0021 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5024+1350T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189945 | |||||||
| chr21:37189983 | C | T | 4 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(1): Show |
4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5025-1351C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37189983 | |||||||
| chr21:37190130 | C | CT | 27 | a0001c0014t0006g0307 a0002c0002t0001g0139 a0002c0002t0001g0149 others(24): Show |
27 | HG00558.hp2 HG01081.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.5025-1175dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr21 | 37190130 | ||||||
| chr21:37190130 | C | CTT | 27 | a0002c0002t0001g0190 a0002c0002t0001g0194 a0002c0002t0001g0209 others(24): Show |
28 | HG00621.hp2 HG00673.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5025-1176_5025-117 others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr21 | 37190130 | ||||||
| chr21:37190130 | C | CTTT | 15 | a0003c0003t0001g0003 a0003c0003t0001g0136 a0003c0003t0001g0143 others(12): Show |
16 | HG00408.hp2 HG00597.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.5025-1177_5025-117 others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr21 | 37190130 | ||||||
| chr21:37190130 | C | CTTTT | 7 | a0003c0003t0001g0185 a0003c0003t0001g0186 a0003c0003t0001g0188 others(4): Show |
7 | HG01175.hp2 HG01884.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.5025-1178_5025-117 others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr21 | 37190130 | ||||||
| chr21:37190130 | CTTTT | C | 17 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0059 others(14): Show |
17 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.5025-1178_5025-117 others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr21 | 37190130 | ||||||
| chr21:37190130 | CTTTTT | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0028 others(100): Show |
104 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.5025-1179_5025-117 others(9): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr21 | 37190130 | ||||||
| chr21:37190130 | CTTTTTT | C | 70 | a0001c0001t0002g0026 a0001c0001t0002g0031 a0001c0001t0002g0032 others(67): Show |
70 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.5025-1180_5025-117 others(10): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr21 | 37190130 | ||||||
| chr21:37190134 | T | C | 1 | a0002c0002t0001g0183 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.5025-1200T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190134 | |||||||
| chr21:37190142 | T | C | 10 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(7): Show |
10 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.5025-1192T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190142 | |||||||
| chr21:37190143 | T | C | 1 | a0001c0004t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5025-1191T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190143 | |||||||
| chr21:37190146 | T | C | 10 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(7): Show |
10 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.5025-1188T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190146 | |||||||
| chr21:37190147 | T | C | 1 | a0001c0004t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5025-1187T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190147 | |||||||
| chr21:37190261 | G | T | 6 | a0001c0001t0002g0029 a0001c0001t0002g0043 a0001c0001t0002g0060 others(3): Show |
6 | HG00544.hp1 HG02165.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.5025-1073G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190261 | |||||||
| chr21:37190346 | T | G | 195 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.5025-988T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190346 | |||||||
| chr21:37190476 | T | C | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.5025-858T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190476 | |||||||
| chr21:37190541 | G | C | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.5025-793G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190541 | |||||||
| chr21:37190766 | A | G | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5025-568A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190766 | |||||||
| chr21:37190786 | C | T | 1 | a0003c0003t0011g0253 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5025-548C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37190786 | |||||||
| chr21:37191284 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5025-50G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 39/45 | chr21 | 37191284 | |||||||
| chr21:37191534 | A | T | 50 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
50 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.5115+110A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 40/45 | chr21 | 37191534 | |||||||
| chr21:37191618 | G | T | 1 | a0001c0001t0002g0061 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.5115+194G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 40/45 | chr21 | 37191618 | |||||||
| chr21:37191731 | A | G | 22 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0001c0001t0002g0034 others(19): Show |
22 | HG01081.hp2 HG01981.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.5115+307A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 40/45 | chr21 | 37191731 | |||||||
| chr21:37191900 | T | C | 21 | a0001c0004t0003g0004 a0001c0004t0003g0005 a0001c0004t0003g0006 others(18): Show |
21 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.5116-212T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 40/45 | chr21 | 37191900 | |||||||
| chr21:37191987 | G | A | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.5116-125G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 40/45 | chr21 | 37191987 | |||||||
| chr21:37192002 | T | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.5116-110T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 40/45 | chr21 | 37192002 | |||||||
| chr21:37192229 | CT | C | 9 | a0001c0001t0002g0039 a0001c0001t0002g0086 a0001c0001t0002g0112 others(6): Show |
9 | HG01069.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.5217+30delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192229 | ||||||
| chr21:37192339 | A | C | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.5217+126A>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192339 | |||||||
| chr21:37192385 | T | C | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.5217+172T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192385 | |||||||
| chr21:37192405 | C | T | 3 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 |
3 | HG01243.hp1 HG01978.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.5217+192C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192405 | |||||||
| chr21:37192491 | T | TGTGTGTG others(4): Show |
1 | a0004c0006t0005g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5217+278_5217+279i others(13): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192491 | |||||||
| chr21:37192491 | T | TGTGTGTG others(6): Show |
2 | a0001c0001t0002g0121 a0001c0004t0003g0019 |
2 | HG04228.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.5217+278_5217+279i others(15): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192491 | |||||||
| chr21:37192491 | T | TGTGTGTG others(8): Show |
2 | a0001c0001t0002g0055 a0001c0001t0002g0070 |
2 | HG02083.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.5217+278_5217+279i others(17): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192491 | |||||||
| chr21:37192491 | T | TGTGTGTG others(10): Show |
2 | a0001c0001t0002g0038 a0001c0001t0002g0047 |
2 | HG02083.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.5217+278_5217+279i others(19): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192491 | |||||||
| chr21:37192491 | T | TTG | 11 | a0001c0001t0002g0091 a0002c0002t0001g0201 a0002c0002t0021g0196 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.5217+310_5217+311d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTG | 4 | a0002c0002t0001g0165 a0007c0008t0006g0140 a0007c0008t0006g0141 others(1): Show |
4 | HG01123.hp2 NA18943.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.5217+308_5217+311d others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTGTG | 39 | a0002c0002t0001g0139 a0002c0002t0001g0145 a0002c0002t0001g0146 others(36): Show |
39 | HG00621.hp1 HG00735.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.5217+306_5217+311d others(8): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTGTGT others(1): Show |
11 | a0001c0004t0003g0006 a0001c0004t0003g0013 a0001c0004t0003g0288 others(8): Show |
11 | HG01069.hp1 HG01346.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.5217+304_5217+311d others(10): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTGTGT others(3): Show |
24 | a0001c0001t0002g0062 a0001c0001t0007g0096 a0001c0001t0007g0130 others(21): Show |
24 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.5217+302_5217+311d others(12): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTGTGT others(5): Show |
44 | a0001c0001t0002g0043 a0001c0001t0002g0056 a0001c0001t0002g0059 others(41): Show |
44 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.5217+300_5217+311d others(14): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTGTGT others(7): Show |
59 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0028 others(56): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.5217+298_5217+311d others(16): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTGTGT others(9): Show |
34 | a0001c0001t0002g0027 a0001c0001t0002g0029 a0001c0001t0002g0035 others(31): Show |
34 | HG00738.hp2 HG01081.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.5217+296_5217+311d others(18): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTGTGT others(11): Show |
18 | a0001c0001t0002g0040 a0001c0001t0002g0048 a0001c0001t0002g0083 others(15): Show |
18 | HG00639.hp1 HG00741.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.5217+294_5217+311d others(20): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTGTGT others(13): Show |
4 | a0001c0001t0002g0108 a0001c0004t0010g0268 a0001c0005t0004g0316 others(1): Show |
4 | HG01358.hp1 HG02895.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5217+292_5217+311d others(22): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | T | TTGTGTGT others(17): Show |
1 | a0001c0001t0002g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5217+288_5217+311d others(26): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192491 | TTG | T | 9 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(6): Show |
9 | HG00735.hp2 HG01175.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.5217+310_5217+311d others(4): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37192491 | ||||||
| chr21:37192542 | C | G | 1 | a0003c0003t0001g0229 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5217+329C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192542 | |||||||
| chr21:37192707 | G | A | 1 | a0003c0003t0001g0187 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.5217+494G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192707 | |||||||
| chr21:37192763 | T | C | 198 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.5217+550T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192763 | |||||||
| chr21:37192900 | A | G | 195 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.5217+687A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37192900 | |||||||
| chr21:37193216 | C | T | 10 | a0001c0001t0002g0027 a0001c0001t0002g0032 a0001c0001t0002g0035 others(7): Show |
10 | HG00639.hp1 HG00733.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.5217+1003C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193216 | |||||||
| chr21:37193329 | G | T | 1 | a0001c0005t0008g0243 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5217+1116G>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193329 | |||||||
| chr21:37193365 | G | GA | 231 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(228): Show |
234 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.5217+1164dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37193365 | ||||||
| chr21:37193365 | G | GAA | 72 | a0001c0001t0002g0085 a0001c0004t0003g0004 a0001c0004t0003g0005 others(69): Show |
72 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.5217+1163_5217+116 others(6): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37193365 | ||||||
| chr21:37193365 | G | GAAA | 8 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(5): Show |
8 | HG00733.hp1 HG01361.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.5217+1162_5217+116 others(7): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr21 | 37193365 | ||||||
| chr21:37193452 | G | C | 1 | a0001c0001t0007g0266 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5217+1239G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193452 | |||||||
| chr21:37193541 | C | T | 1 | a0014c0015t0001g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.5217+1328C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193541 | |||||||
| chr21:37193655 | G | C | 1 | a0003c0003t0001g0187 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.5217+1442G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193655 | |||||||
| chr21:37193689 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5217+1476G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193689 | |||||||
| chr21:37193851 | G | A | 12 | a0001c0004t0003g0288 a0001c0004t0003g0289 a0001c0004t0003g0290 others(9): Show |
12 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.5217+1638G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193851 | |||||||
| chr21:37193877 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5217+1664T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193877 | |||||||
| chr21:37193963 | G | A | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.5218-1712G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193963 | |||||||
| chr21:37193982 | G | A | 1 | a0001c0005t0004g0313 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5218-1693G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37193982 | |||||||
| chr21:37194031 | A | G | 3 | a0002c0002t0001g0209 a0002c0002t0001g0247 a0002c0002t0001g0249 |
3 | NA18957.hp2 NA19000.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.5218-1644A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37194031 | |||||||
| chr21:37194095 | G | A | 7 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.5218-1580G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37194095 | |||||||
| chr21:37194230 | C | T | 3 | a0002c0002t0001g0193 a0002c0002t0001g0195 a0002c0002t0001g0200 |
3 | HG01168.hp2 HG01169.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.5218-1445C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37194230 | |||||||
| chr21:37194265 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.5218-1410C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37194265 | |||||||
| chr21:37194326 | C | G | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.5218-1349C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37194326 | |||||||
| chr21:37194333 | A | G | 5 | a0003c0003t0001g0197 a0003c0003t0001g0198 a0003c0003t0001g0216 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.5218-1342A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37194333 | |||||||
| chr21:37194556 | G | A | 1 | a0003c0003t0001g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5218-1119G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37194556 | |||||||
| chr21:37194667 | A | T | 11 | a0004c0006t0005g0277 a0004c0006t0005g0278 a0004c0006t0005g0279 others(8): Show |
11 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.5218-1008A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37194667 | |||||||
| chr21:37195008 | G | A | 6 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0186 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.5218-667G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37195008 | |||||||
| chr21:37195319 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.5218-356G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37195319 | |||||||
| chr21:37195563 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.5218-112G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37195563 | |||||||
| chr21:37195582 | C | T | 1 | a0003c0003t0001g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5218-93C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37195582 | |||||||
| chr21:37195601 | C | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.5218-74C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37195601 | |||||||
| chr21:37195610 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.5218-65T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37195610 | |||||||
| chr21:37195614 | T | C | 1 | a0002c0002t0001g0209 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5218-61T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 41/45 | chr21 | 37195614 | |||||||
| chr21:37196174 | A | T | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.5579+138A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37196174 | |||||||
| chr21:37196237 | C | CT | 7 | a0002c0002t0001g0205 a0002c0002t0001g0247 a0003c0003t0001g0197 others(4): Show |
7 | HG01891.hp2 HG01993.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.5579+218dupT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | INFO_REALIGN_3_PRIME | chr21 | 37196237 | ||||||
| chr21:37196237 | C | CTTT | 46 | a0003c0003t0001g0002 a0003c0003t0001g0003 a0003c0003t0001g0136 others(43): Show |
48 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.5579+216_5579+218d others(5): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | INFO_REALIGN_3_PRIME | chr21 | 37196237 | ||||||
| chr21:37196237 | CT | C | 202 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(199): Show |
203 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.5579+218delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | INFO_REALIGN_3_PRIME | chr21 | 37196237 | ||||||
| chr21:37196543 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.5579+507A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37196543 | |||||||
| chr21:37196581 | G | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.5579+545G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37196581 | |||||||
| chr21:37196606 | C | T | 27 | a0001c0005t0004g0309 a0001c0005t0004g0310 a0001c0005t0004g0311 others(24): Show |
27 | HG00099.hp2 HG00733.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.5579+570C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37196606 | |||||||
| chr21:37196613 | A | T | 2 | a0002c0002t0001g0206 a0002c0002t0001g0208 |
2 | HG01358.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.5579+577A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37196613 | |||||||
| chr21:37196666 | T | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.5579+630T>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37196666 | |||||||
| chr21:37196746 | C | T | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.5579+710C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37196746 | |||||||
| chr21:37196765 | G | A | 8 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(5): Show |
8 | HG02109.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5579+729G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37196765 | |||||||
| chr21:37197204 | C | A | 1 | a0001c0001t0007g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5580-366C>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37197204 | |||||||
| chr21:37197322 | A | G | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.5580-248A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37197322 | |||||||
| chr21:37197342 | C | T | 7 | a0001c0014t0006g0307 a0008c0009t0006g0263 a0008c0009t0006g0264 others(4): Show |
7 | HG01243.hp1 HG01978.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.5580-228C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37197342 | |||||||
| chr21:37197387 | C | CA | 9 | a0001c0004t0003g0293 a0002c0002t0001g0157 a0003c0003t0024g0233 others(6): Show |
9 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.5580-168dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | INFO_REALIGN_3_PRIME | chr21 | 37197387 | ||||||
| chr21:37197387 | CA | C | 6 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0005t0002g0033 others(3): Show |
6 | HG01106.hp2 HG02109.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.5580-168delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | INFO_REALIGN_3_PRIME | chr21 | 37197387 | ||||||
| chr21:37197517 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5580-53T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 42/45 | chr21 | 37197517 | |||||||
| chr21:37197706 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.5706+10C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 43/45 | chr21 | 37197706 | |||||||
| chr21:37197754 | T | TA | 23 | a0001c0001t0002g0061 a0001c0001t0002g0105 a0001c0001t0002g0122 others(20): Show |
23 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.5706+72dupA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 43/45 | INFO_REALIGN_3_PRIME | chr21 | 37197754 | ||||||
| chr21:37197754 | T | TAA | 174 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0028 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.5706+71_5706+72dup others(2): Show |
TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 43/45 | INFO_REALIGN_3_PRIME | chr21 | 37197754 | ||||||
| chr21:37197754 | TA | T | 7 | a0003c0003t0001g0002 a0003c0003t0001g0143 a0003c0003t0001g0144 others(4): Show |
8 | HG02293.hp1 HG02300.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.5706+72delA | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 43/45 | INFO_REALIGN_3_PRIME | chr21 | 37197754 | ||||||
| chr21:37197859 | C | T | 1 | a0001c0004t0003g0016 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5707-23C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 43/45 | chr21 | 37197859 | |||||||
| chr21:37198100 | C | G | 1 | a0005c0007t0002g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5850+75C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37198100 | |||||||
| chr21:37198476 | C | G | 1 | a0003c0003t0001g0237 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5850+451C>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37198476 | |||||||
| chr21:37198708 | A | G | 4 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5850+683A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37198708 | |||||||
| chr21:37198756 | T | G | 3 | a0001c0001t0002g0001 a0001c0001t0002g0113 a0001c0001t0002g0114 |
4 | HG02056.hp2 NA18747.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.5850+731T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37198756 | |||||||
| chr21:37198850 | A | T | 1 | a0001c0014t0006g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5850+825A>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37198850 | |||||||
| chr21:37198850 | AT | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.5850+836delT | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | INFO_REALIGN_3_PRIME | chr21 | 37198850 | ||||||
| chr21:37199126 | T | C | 1 | a0001c0001t0002g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5850+1101T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37199126 | |||||||
| chr21:37199181 | G | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.5851-1051G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37199181 | |||||||
| chr21:37199208 | G | A | 1 | a0003c0003t0001g0224 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5851-1024G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37199208 | |||||||
| chr21:37199439 | G | A | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.5851-793G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37199439 | |||||||
| chr21:37199906 | T | C | 2 | a0002c0002t0001g0148 a0002c0002t0001g0158 |
2 | NA18993.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.5851-326T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37199906 | |||||||
| chr21:37199919 | C | T | 12 | a0002c0002t0001g0160 a0002c0002t0001g0161 a0002c0002t0001g0163 others(9): Show |
12 | HG02056.hp1 HG02074.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.5851-313C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37199919 | |||||||
| chr21:37199957 | G | A | 6 | a0008c0009t0006g0263 a0008c0009t0006g0264 a0008c0009t0006g0265 others(3): Show |
6 | HG01243.hp1 HG01978.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.5851-275G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37199957 | |||||||
| chr21:37200109 | T | C | 1 | a0001c0004t0003g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.5851-123T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37200109 | |||||||
| chr21:37200115 | T | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0120 |
2 | NA18957.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.5851-117T>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37200115 | |||||||
| chr21:37200134 | T | C | 5 | a0001c0004t0010g0268 a0001c0004t0010g0269 a0001c0004t0010g0270 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.5851-98T>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37200134 | |||||||
| chr21:37200171 | A | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0123 |
2 | HG02071.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.5851-61A>G | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37200171 | |||||||
| chr21:37200175 | G | C | 2 | a0001c0001t0002g0119 a0001c0001t0002g0123 |
2 | HG02071.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.5851-57G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37200175 | |||||||
| chr21:37200214 | G | A | 47 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(44): Show |
47 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.5851-18G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 44/45 | chr21 | 37200214 | |||||||
| chr21:37200518 | C | T | 47 | a0001c0001t0007g0096 a0001c0001t0007g0130 a0001c0001t0007g0266 others(44): Show |
47 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.5943+194C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37200518 | |||||||
| chr21:37200537 | G | C | 7 | a0004c0006t0005g0279 a0004c0006t0005g0280 a0004c0006t0005g0281 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.5943+213G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37200537 | |||||||
| chr21:37200760 | G | A | 2 | a0002c0002t0001g0304 a0002c0002t0001g0305 |
2 | HG01255.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.5943+436G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37200760 | |||||||
| chr21:37200798 | G | C | 1 | a0001c0001t0002g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5943+474G>C | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37200798 | |||||||
| chr21:37200893 | C | T | 1 | a0002c0002t0001g0182 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5944-547C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37200893 | |||||||
| chr21:37200945 | G | A | 5 | a0001c0005t0004g0314 a0001c0005t0008g0322 a0001c0005t0008g0324 others(2): Show |
5 | HG00099.hp2 HG01109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.5944-495G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37200945 | |||||||
| chr21:37200949 | C | T | 1 | a0005c0007t0002g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5944-491C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37200949 | |||||||
| chr21:37201073 | A | AG | 3 | a0007c0008t0006g0140 a0007c0008t0006g0141 a0007c0008t0006g0142 |
3 | HG01123.hp2 NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.5944-365dupG | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | INFO_REALIGN_3_PRIME | chr21 | 37201073 | ||||||
| chr21:37201128 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.5944-312G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37201128 | |||||||
| chr21:37201223 | C | T | 1 | a0002c0002t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5944-217C>T | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37201223 | |||||||
| chr21:37201290 | G | A | 1 | a0001c0004t0003g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5944-150G>A | TTC3 | ENSG00000182670.14 | transcript | ENST00000418766.6 | protein_coding | 45/45 | chr21 | 37201290 |