Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55258 |
| ensemblid | ENSG00000144115.18 |
| hgncid | 25602 |
| symbol | THNSL2 |
| name | threonine synthase like 2 |
| refseq_nuc | NM_018271.5 |
| refseq_prot | NP_060741.3 |
| ensembl_nuc | ENST00000674334.2 |
| ensembl_prot | ENSP00000501453.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 88170346 |
| end | 88186627 |
| strand | + |
| ver | v1.2 |
| region | chr2:88170346-88186627 |
| region5000 | chr2:88165346-88191627 |
| regionname0 | THNSL2_chr2_88170346_88186627 |
| regionname5000 | THNSL2_chr2_88165346_88191627 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 484 | 31 | 2 | 12 | 8 | 6 | 2 | 5 | THNSL2_chr2_88165346_88191627 | THNSL2 | MWYVS others(479): Show |
chr2 | 88165346 | 88191627 |
| a0002 | 1/0 | 484 | 15 | 1 | 7 | 2 | 2 | 2 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | MWYVS others(479): Show |
chr2 | 88165346 | 88191627 |
| a0003 | 0/0 | 484 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | MWYVS others(479): Show |
chr2 | 88165346 | 88191627 |
| a0004 | 0/0 | 484 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | MWYVS others(479): Show |
chr2 | 88165346 | 88191627 |
| a0005 | 0/0 | 484 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | MWYVS others(479): Show |
chr2 | 88165346 | 88191627 |
| a0006 | 0/0 | 484 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | MWYVS others(479): Show |
chr2 | 88165346 | 88191627 |
| a0007 | 0/0 | 250 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | MWYVS others(245): Show |
chr2 | 88165346 | 88191627 |
| a0008 | 0/0 | 484 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | MWYVS others(479): Show |
chr2 | 88165346 | 88191627 |
| a0009 | 0/0 | 258 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | MWYVS others(253): Show |
chr2 | 88165346 | 88191627 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1452 | 22 | 2 | 6 | 5 | 6 | 2 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1447): Show |
chr2 | 88165346 | 88191627 | ||
| a0001c0003 | 0/0 | 1452 | 6 | 0 | 4 | 2 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1447): Show |
chr2 | 88165346 | 88191627 | ||
| a0001c0004 | 0/0 | 1452 | 3 | 0 | 2 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1447): Show |
chr2 | 88165346 | 88191627 | ||
| a0002c0002 | 1/0 | 1452 | 15 | 1 | 7 | 2 | 2 | 2 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1447): Show |
chr2 | 88165346 | 88191627 | ||
| a0003c0005 | 0/0 | 1452 | 2 | 0 | 0 | 0 | 1 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1447): Show |
chr2 | 88165346 | 88191627 | ||
| a0004c0011 | 0/0 | 1452 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1447): Show |
chr2 | 88165346 | 88191627 | ||
| a0005c0008 | 0/0 | 1452 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1447): Show |
chr2 | 88165346 | 88191627 | ||
| a0006c0010 | 0/0 | 1452 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1447): Show |
chr2 | 88165346 | 88191627 | ||
| a0007c0009 | 0/0 | 1379 | 1 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1374): Show |
chr2 | 88165346 | 88191627 | ||
| a0008c0006 | 0/0 | 1452 | 1 | 0 | 0 | 0 | 0 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1447): Show |
chr2 | 88165346 | 88191627 | ||
| a0009c0007 | 0/0 | 1403 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ATGTG others(1398): Show |
chr2 | 88165346 | 88191627 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 2069 | 9 | 0 | 3 | 0 | 4 | 2 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2064): Show |
chr2 | 88165346 | 88191627 |
| a0001c0001t0004 | 0/0 | 2083 | 4 | 1 | 1 | 2 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2078): Show |
chr2 | 88165346 | 88191627 |
| a0001c0001t0005 | 0/0 | 2090 | 4 | 0 | 1 | 3 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2085): Show |
chr2 | 88165346 | 88191627 |
| a0001c0001t0009 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2071): Show |
chr2 | 88165346 | 88191627 |
| a0001c0001t0010 | 0/0 | 2111 | 1 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2106): Show |
chr2 | 88165346 | 88191627 |
| a0001c0001t0011 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2071): Show |
chr2 | 88165346 | 88191627 |
| a0001c0001t0012 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2085): Show |
chr2 | 88165346 | 88191627 |
| a0001c0001t0013 | 0/1 | 2104 | 1 | 0 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2099): Show |
chr2 | 88165346 | 88191627 |
| a0001c0003t0003 | 0/0 | 2068 | 5 | 0 | 4 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2063): Show |
chr2 | 88165346 | 88191627 |
| a0001c0003t0008 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2070): Show |
chr2 | 88165346 | 88191627 |
| a0001c0004t0003 | 0/0 | 2068 | 3 | 0 | 2 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2063): Show |
chr2 | 88165346 | 88191627 |
| a0002c0002t0001 | 1/0 | 2082 | 15 | 1 | 7 | 2 | 2 | 2 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2077): Show |
chr2 | 88165346 | 88191627 |
| a0003c0005t0006 | 0/0 | 2103 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2098): Show |
chr2 | 88165346 | 88191627 |
| a0003c0005t0007 | 0/0 | 2117 | 1 | 0 | 0 | 0 | 0 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2112): Show |
chr2 | 88165346 | 88191627 |
| a0004c0011t0001 | 0/0 | 2082 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2077): Show |
chr2 | 88165346 | 88191627 |
| a0005c0008t0006 | 0/0 | 2103 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2098): Show |
chr2 | 88165346 | 88191627 |
| a0006c0010t0003 | 0/0 | 2068 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2063): Show |
chr2 | 88165346 | 88191627 |
| a0007c0009t0002 | 0/0 | 1996 | 1 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(1991): Show |
chr2 | 88165346 | 88191627 |
| a0008c0006t0003 | 0/0 | 2068 | 1 | 0 | 0 | 0 | 0 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2063): Show |
chr2 | 88165346 | 88191627 |
| a0009c0007t0002 | 0/0 | 2020 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | ACCGT others(2015): Show |
chr2 | 88165346 | 88191627 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0011g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0001t0013g0030 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0003t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0003t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0003t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0003t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0003t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0003t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0004t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0001c0004t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0003c0005t0006g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0003c0005t0007g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0004c0011t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0005c0008t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0006c0010t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0007c0009t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0008c0006t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| a0009c0007t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0045 | EUR | GBR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG00099 | hp2 | a0001 | c0001 | t0012 | g0031 | EUR | GBR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG00140 | hp1 | a0003 | c0005 | t0006 | g0014 | EUR | GBR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0053 | EUR | GBR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | FIN | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG00323 | hp2 | a0001 | c0001 | t0009 | g0037 | EUR | FIN | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0050 | AMR | PUR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01074 | hp2 | a0004 | c0011 | t0001 | g0023 | AMR | PUR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0005 | AMR | PUR | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01258 | hp2 | a0001 | c0001 | t0011 | g0033 | AMR | CLM | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0051 | AMR | CLM | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01934 | hp1 | a0005 | c0008 | t0006 | g0015 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01943 | hp1 | a0001 | c0004 | t0003 | g0001 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01975 | hp2 | a0001 | c0003 | t0003 | g0007 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01981 | hp1 | a0006 | c0010 | t0003 | g0004 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | KHV | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0008 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02273 | hp2 | a0001 | c0004 | t0003 | g0001 | AMR | PEL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02523 | hp1 | a0001 | c0004 | t0003 | g0006 | EAS | KHV | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | KHV | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | GWD | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG03209 | hp1 | a0007 | c0009 | t0002 | g0040 | AFR | MSL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG03492 | hp1 | a0008 | c0006 | t0003 | g0046 | SAS | PJL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG03669 | hp1 | a0003 | c0005 | t0007 | g0013 | SAS | PJL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA18971 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA19081 | hp1 | a0001 | c0003 | t0008 | g0032 | EAS | JPT | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | TSI | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA20752 | hp2 | a0009 | c0007 | t0002 | g0047 | EUR | TSI | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | TSI | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0026 | EUR | TSI | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0030 | REF | REF | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0025 | REF | REF | THNSL2_chr2_88165346_88191627 | THNSL2 | chr2 | 88165346 | 88191627 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:88173272 | G | A | 7 | a0001 a0003 a0005 others(4): Show |
37 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(34): Show |
missense_variant | MODERATE | c.122G>A | p.Gly41Glu | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 2/9 | 245/2082 | 122/1455 | 41/484 | chr2 | 88173272 | |||
| chr2:88174647 | G | A | 2 | a0008 a0009 |
2 | HG03492.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.232G>A | p.Asp78Asn | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 3/9 | 355/2082 | 232/1455 | 78/484 | chr2 | 88174647 | |||
| chr2:88174818 | G | A | 1 | a0004 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.403G>A | p.Val135Ile | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 3/9 | 526/2082 | 403/1455 | 135/484 | chr2 | 88174818 | |||
| chr2:88178822 | C | A | 2 | a0003 a0005 |
3 | HG00140.hp1 HG01934.hp1 HG03669.hp1 |
missense_variant | MODERATE | c.611C>A | p.Thr204Asn | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/9 | 734/2082 | 611/1455 | 204/484 | chr2 | 88178822 | |||
| chr2:88178881 | AACTGGTC others(66): Show |
A | 1 | a0007 | 1 | HG03209.hp1 | frameshift_variant | HIGH | c.673_745delTGGTCCCG others(65): Show |
p.Trp225fs | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/9 | 796/2082 | 673/1455 | 225/484 | INFO_REALIGN_3_PRIME | chr2 | 88178881 | ||
| chr2:88178882 | A | C | 1 | a0002 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.671A>C | p.Asn224Thr | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/9 | 794/2082 | 671/1455 | 224/484 | chr2 | 88178882 | |||
| chr2:88178890 | C | G | 1 | a0002 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.679C>G | p.Arg227Gly | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/9 | 802/2082 | 679/1455 | 227/484 | chr2 | 88178890 | |||
| chr2:88178939 | C | T | 1 | a0001 | 3 | HG01433.hp1 HG01943.hp1 HG02273.hp2 |
missense_variant | MODERATE | c.728C>T | p.Thr243Met | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/9 | 851/2082 | 728/1455 | 243/484 | chr2 | 88178939 | |||
| chr2:88178964 | ACCCCTGG others(43): Show |
A | 1 | a0009 | 1 | NA20752.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.754_802+1delCCCCTG others(44): Show |
p.Pro252fs | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/9 | 877/2082 | 754/1455 | 252/484 | chr2 | 88178964 | |||
| chr2:88182740 | G | C | 1 | a0005 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.844G>C | p.Val282Leu | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 967/2082 | 844/1455 | 282/484 | chr2 | 88182740 | |||
| chr2:88182741 | T | A | 1 | a0005 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.845T>A | p.Val282Asp | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 968/2082 | 845/1455 | 282/484 | chr2 | 88182741 | |||
| chr2:88182744 | T | A | 1 | a0005 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.848T>A | p.Val283Glu | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 971/2082 | 848/1455 | 283/484 | chr2 | 88182744 | |||
| chr2:88182746 | G | A | 1 | a0005 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.850G>A | p.Ala284Thr | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 973/2082 | 850/1455 | 284/484 | chr2 | 88182746 | |||
| chr2:88182750 | T | A | 1 | a0005 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.854T>A | p.Val285Glu | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 977/2082 | 854/1455 | 285/484 | chr2 | 88182750 | |||
| chr2:88182752 | A | G | 1 | a0005 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.856A>G | p.Asn286Asp | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 979/2082 | 856/1455 | 286/484 | chr2 | 88182752 | |||
| chr2:88182755 | C | G | 1 | a0005 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.859C>G | p.Arg287Gly | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 982/2082 | 859/1455 | 287/484 | chr2 | 88182755 | |||
| chr2:88182756 | G | T | 1 | a0005 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.860G>T | p.Arg287Leu | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 983/2082 | 860/1455 | 287/484 | chr2 | 88182756 | |||
| chr2:88186106 | C | G | 1 | a0006 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1438C>G | p.Leu480Val | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 9/9 | 1561/2082 | 1438/1455 | 480/484 | chr2 | 88186106 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:88175259 | G | T | 1 | a0001c0004 | 3 | HG01943.hp1 HG02273.hp2 HG02523.hp1 |
synonymous_variant | LOW | c.429G>T | p.Gly143Gly | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/9 | 552/2082 | 429/1455 | 143/484 | chr2 | 88175259 | |||
| chr2:88182739 | G | A | 4 | a0001c0003 a0001c0004 a0006c0010 others(1): Show |
11 | HG01081.hp2 HG01433.hp1 HG01943.hp1 others(8): Show |
synonymous_variant | LOW | c.843G>A | p.Leu281Leu | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 966/2082 | 843/1455 | 281/484 | chr2 | 88182739 | |||
| chr2:88182745 | G | C | 1 | a0005c0008 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.849G>C | p.Val283Val | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 972/2082 | 849/1455 | 283/484 | chr2 | 88182745 | |||
| chr2:88182751 | G | C | 1 | a0005c0008 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.855G>C | p.Val285Val | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 978/2082 | 855/1455 | 285/484 | chr2 | 88182751 | |||
| chr2:88182754 | C | T | 1 | a0005c0008 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.858C>T | p.Asn286Asn | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 981/2082 | 858/1455 | 286/484 | chr2 | 88182754 | |||
| chr2:88182757 | C | T | 1 | a0005c0008 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.861C>T | p.Arg287Arg | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/9 | 984/2082 | 861/1455 | 287/484 | chr2 | 88182757 | |||
| chr2:88183055 | C | A | 1 | a0005c0008 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.1059C>A | p.Pro353Pro | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/9 | 1182/2082 | 1059/1455 | 353/484 | chr2 | 88183055 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:88170372 | G | T | 2 | a0001c0001t0011 a0001c0001t0012 |
2 | HG00099.hp2 HG01258.hp2 |
5_prime_UTR_variant | MODIFIER | c.-97G>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/9 | 2779 | chr2 | 88170372 | ||||||
| chr2:88170414 | T | TCGCGCAC others(14): Show |
2 | a0003c0005t0006 a0005c0008t0006 |
2 | HG00140.hp1 HG01934.hp1 |
5_prime_UTR_variant | MODIFIER | c.-50_-49insACCGGGCC others(13): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/9 | 2731 | INFO_REALIGN_3_PRIME | chr2 | 88170414 | |||||
| chr2:88170414 | T | TCGCGCAC others(28): Show |
1 | a0003c0005t0007 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-50_-49insACCGGGCC others(27): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/9 | 2731 | INFO_REALIGN_3_PRIME | chr2 | 88170414 | |||||
| chr2:88170414 | T | TCGCGCCC | 2 | a0001c0001t0005 a0001c0001t0012 |
5 | HG00099.hp2 HG00639.hp1 NA18971.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-23_-17dupGCCCCGC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/9 | 2698 | INFO_REALIGN_3_PRIME | chr2 | 88170414 | |||||
| chr2:88170414 | T | TCGCGCCC others(21): Show |
1 | a0001c0001t0010 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44_-17dupGCCCCGCG others(20): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/9 | 2698 | INFO_REALIGN_3_PRIME | chr2 | 88170414 | |||||
| chr2:88170414 | TCGCGCCC | T | 3 | a0001c0001t0009 a0001c0001t0011 a0001c0003t0008 |
3 | HG00323.hp2 HG01258.hp2 NA19081.hp1 |
5_prime_UTR_variant | MODIFIER | c.-23_-17delGCCCCGC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/9 | 2699 | INFO_REALIGN_3_PRIME | chr2 | 88170414 | |||||
| chr2:88170414 | TCGCGCCC others(7): Show |
T | 7 | a0001c0001t0002 a0001c0003t0003 a0001c0004t0003 others(4): Show |
21 | HG00099.hp1 HG00323.hp1 HG01070.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-30_-17delGCCCCGCG others(6): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/9 | 2699 | INFO_REALIGN_3_PRIME | chr2 | 88170414 | |||||
| chr2:88186182 | T | C | 1 | a0001c0003t0008 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 9/9 | 59 | chr2 | 88186182 | ||||||
| chr2:88186449 | A | AC | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(6): Show |
23 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*330dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 9/9 | 331 | INFO_REALIGN_3_PRIME | chr2 | 88186449 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:88170708 | G | GT | 3 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0053 |
3 | HG00140.hp2 HG01070.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-13+253dupT | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 88170708 | ||||||
| chr2:88170819 | C | G | 1 | a0002c0002t0001g0050 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-13+363C>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/8 | chr2 | 88170819 | |||||||
| chr2:88170851 | TG | T | 12 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13+399delG | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 88170851 | ||||||
| chr2:88171074 | G | A | 8 | a0001c0003t0003g0002 a0001c0003t0003g0003 a0001c0003t0003g0005 others(5): Show |
9 | HG01081.hp2 HG01433.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+618G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/8 | chr2 | 88171074 | |||||||
| chr2:88172277 | G | A | 12 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(9): Show |
13 | HG01074.hp1 HG01081.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-862G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/8 | chr2 | 88172277 | |||||||
| chr2:88172375 | G | T | 8 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(5): Show |
8 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-764G>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/8 | chr2 | 88172375 | |||||||
| chr2:88172622 | G | A | 8 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(5): Show |
8 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-517G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/8 | chr2 | 88172622 | |||||||
| chr2:88172730 | G | C | 15 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.-12-409G>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/8 | chr2 | 88172730 | |||||||
| chr2:88172761 | C | T | 37 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(34): Show |
38 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12-378C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 1/8 | chr2 | 88172761 | |||||||
| chr2:88173406 | A | G | 8 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(5): Show |
8 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.223+33A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 2/8 | chr2 | 88173406 | |||||||
| chr2:88173625 | T | TA | 8 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(5): Show |
8 | HG00099.hp2 HG00639.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+265dupA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 88173625 | ||||||
| chr2:88174056 | G | A | 8 | a0001c0003t0003g0002 a0001c0003t0003g0003 a0001c0003t0003g0005 others(5): Show |
9 | HG01081.hp2 HG01433.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-583G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 2/8 | chr2 | 88174056 | |||||||
| chr2:88174203 | A | G | 8 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(5): Show |
8 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.224-436A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 2/8 | chr2 | 88174203 | |||||||
| chr2:88174313 | G | A | 8 | a0001c0003t0003g0002 a0001c0003t0003g0003 a0001c0003t0003g0005 others(5): Show |
9 | HG01081.hp2 HG01433.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-326G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 2/8 | chr2 | 88174313 | |||||||
| chr2:88174378 | T | TA | 16 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.224-255dupA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 88174378 | ||||||
| chr2:88174851 | A | G | 36 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(33): Show |
37 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(34): Show |
intron_variant | MODIFIER | c.418+18A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 3/8 | chr2 | 88174851 | |||||||
| chr2:88175234 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.419-15T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 3/8 | chr2 | 88175234 | |||||||
| chr2:88175528 | G | A | 8 | a0001c0003t0003g0002 a0001c0003t0003g0003 a0001c0003t0003g0005 others(5): Show |
9 | HG01081.hp2 HG01433.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.571+127G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88175528 | |||||||
| chr2:88175683 | C | A | 8 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(5): Show |
8 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.571+282C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88175683 | |||||||
| chr2:88175863 | C | A | 1 | a0001c0003t0003g0002 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.571+462C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88175863 | |||||||
| chr2:88175892 | G | GT | 15 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.571+494dupT | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 88175892 | ||||||
| chr2:88175895 | T | G | 1 | a0002c0002t0001g0016 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.571+494T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88175895 | |||||||
| chr2:88176769 | A | G | 8 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(5): Show |
8 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.571+1368A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88176769 | |||||||
| chr2:88176924 | A | T | 1 | a0002c0002t0001g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571+1523A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88176924 | |||||||
| chr2:88177097 | A | G | 8 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(5): Show |
8 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.572-1686A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88177097 | |||||||
| chr2:88177234 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0048 a0001c0001t0002g0049 |
3 | HG01070.hp1 HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.572-1549A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88177234 | |||||||
| chr2:88177485 | G | C | 1 | a0002c0002t0001g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.572-1298G>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88177485 | |||||||
| chr2:88177501 | GAAGTAGC others(9): Show |
G | 1 | a0002c0002t0001g0017 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.572-1279_572-1264d others(18): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 88177501 | ||||||
| chr2:88177804 | A | T | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.572-979A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88177804 | |||||||
| chr2:88178012 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.572-771G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88178012 | |||||||
| chr2:88178058 | CCAATGGA others(6): Show |
C | 1 | a0002c0002t0001g0050 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.572-723_572-711del others(13): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 88178058 | ||||||
| chr2:88178403 | A | G | 1 | a0001c0001t0004g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.572-380A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88178403 | |||||||
| chr2:88178704 | G | C | 1 | a0001c0003t0003g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.572-79G>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 4/8 | chr2 | 88178704 | |||||||
| chr2:88179145 | C | T | 9 | a0001c0003t0003g0002 a0001c0003t0003g0003 a0001c0003t0003g0005 others(6): Show |
10 | HG01081.hp2 HG01433.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.802+132C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88179145 | |||||||
| chr2:88179308 | G | GC | 2 | a0001c0001t0002g0039 a0001c0003t0003g0003 |
2 | HG01433.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.802+297dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88179308 | ||||||
| chr2:88179427 | C | CACACCAC others(14): Show |
1 | a0001c0001t0004g0009 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.802+416_802+436dup others(21): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88179427 | ||||||
| chr2:88179667 | C | CATTTTCT others(27): Show |
1 | a0003c0005t0007g0013 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.802+655_802+688dup others(34): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88179667 | ||||||
| chr2:88179963 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.802+950C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88179963 | |||||||
| chr2:88180044 | A | G | 37 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(34): Show |
38 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+1031A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180044 | |||||||
| chr2:88180051 | TG | T | 2 | a0005c0008t0006g0015 a0006c0010t0003g0004 |
2 | HG01934.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.802+1041delG | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88180051 | ||||||
| chr2:88180136 | G | GC | 3 | a0001c0001t0004g0011 a0001c0001t0005g0036 a0001c0003t0003g0003 |
3 | HG00639.hp1 HG01433.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.802+1125dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88180136 | ||||||
| chr2:88180282 | T | C | 1 | a0001c0003t0003g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.802+1269T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180282 | |||||||
| chr2:88180407 | A | T | 1 | a0001c0001t0002g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.802+1394A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180407 | |||||||
| chr2:88180431 | G | T | 1 | a0009c0007t0002g0047 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.802+1418G>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180431 | |||||||
| chr2:88180482 | G | GA | 2 | a0001c0001t0005g0036 a0001c0001t0010g0029 |
2 | HG00639.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.802+1471dupA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88180482 | ||||||
| chr2:88180571 | C | CA | 9 | a0001c0001t0012g0031 a0002c0002t0001g0017 a0002c0002t0001g0018 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+1568dupA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88180571 | ||||||
| chr2:88180581 | AT | A | 21 | a0001c0001t0002g0039 a0001c0001t0002g0041 a0001c0001t0002g0043 others(18): Show |
22 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.802+1569delT | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180581 | |||||||
| chr2:88180582 | T | A | 14 | a0001c0001t0002g0038 a0001c0001t0004g0009 a0001c0001t0004g0011 others(11): Show |
14 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.802+1569T>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180582 | |||||||
| chr2:88180671 | GA | G | 2 | a0001c0001t0002g0045 a0001c0001t0010g0029 |
2 | HG00099.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.802+1661delA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88180671 | ||||||
| chr2:88180685 | T | TA | 2 | a0001c0001t0002g0039 a0001c0001t0010g0029 |
2 | HG02615.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.802+1676dupA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88180685 | ||||||
| chr2:88180734 | G | A | 2 | a0001c0001t0002g0048 a0001c0001t0005g0036 |
2 | HG00639.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.802+1721G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180734 | |||||||
| chr2:88180799 | T | C | 1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.802+1786T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180799 | |||||||
| chr2:88180800 | C | G | 3 | a0003c0005t0006g0014 a0003c0005t0007g0013 a0005c0008t0006g0015 |
3 | HG00140.hp1 HG01934.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.802+1787C>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180800 | |||||||
| chr2:88180815 | G | T | 3 | a0003c0005t0006g0014 a0003c0005t0007g0013 a0005c0008t0006g0015 |
3 | HG00140.hp1 HG01934.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.802+1802G>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180815 | |||||||
| chr2:88180823 | AG | A | 3 | a0001c0001t0002g0039 a0001c0001t0002g0045 a0005c0008t0006g0015 |
3 | HG00099.hp1 HG01934.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.802+1813delG | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88180823 | ||||||
| chr2:88180866 | A | T | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1833A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180866 | |||||||
| chr2:88180866 | AG | A | 2 | a0001c0001t0004g0011 a0002c0002t0001g0022 |
2 | HG02523.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.803-1830delG | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88180866 | ||||||
| chr2:88180870 | A | G | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1829A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180870 | |||||||
| chr2:88180872 | G | A | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1827G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180872 | |||||||
| chr2:88180882 | C | A | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1817C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180882 | |||||||
| chr2:88180900 | T | G | 1 | a0002c0002t0001g0017 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.803-1799T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180900 | |||||||
| chr2:88180911 | T | G | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1788T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180911 | |||||||
| chr2:88180930 | T | G | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1769T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180930 | |||||||
| chr2:88180958 | A | T | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1741A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180958 | |||||||
| chr2:88180960 | T | G | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1739T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180960 | |||||||
| chr2:88180963 | T | G | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1736T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180963 | |||||||
| chr2:88180965 | T | G | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1734T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180965 | |||||||
| chr2:88180971 | T | G | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1728T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180971 | |||||||
| chr2:88180996 | T | G | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1703T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88180996 | |||||||
| chr2:88180998 | A | AG | 2 | a0001c0001t0005g0036 a0002c0002t0001g0021 |
2 | HG00639.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.803-1700dupG | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88180998 | ||||||
| chr2:88181007 | T | G | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1692T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181007 | |||||||
| chr2:88181013 | A | G | 1 | a0002c0002t0001g0017 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.803-1686A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181013 | |||||||
| chr2:88181014 | C | A | 1 | a0002c0002t0001g0017 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.803-1685C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181014 | |||||||
| chr2:88181014 | CT | C | 2 | a0002c0002t0001g0021 a0002c0002t0001g0050 |
2 | HG00639.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.803-1682delT | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181014 | ||||||
| chr2:88181016 | T | G | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1683T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181016 | |||||||
| chr2:88181027 | CA | C | 2 | a0002c0002t0001g0017 a0005c0008t0006g0015 |
2 | HG01934.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.803-1671delA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181027 | |||||||
| chr2:88181035 | T | A | 1 | a0001c0001t0004g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-1664T>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181035 | |||||||
| chr2:88181035 | T | G | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1664T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181035 | |||||||
| chr2:88181040 | C | A | 1 | a0004c0011t0001g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.803-1659C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181040 | |||||||
| chr2:88181041 | A | C | 1 | a0004c0011t0001g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.803-1658A>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181041 | |||||||
| chr2:88181042 | T | TA | 2 | a0001c0003t0003g0003 a0007c0009t0002g0040 |
2 | HG01433.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.803-1653dupA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181042 | ||||||
| chr2:88181044 | A | T | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1655A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181044 | |||||||
| chr2:88181049 | G | C | 1 | a0002c0002t0001g0017 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.803-1650G>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181049 | |||||||
| chr2:88181054 | A | G | 1 | a0001c0001t0012g0031 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.803-1645A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181054 | |||||||
| chr2:88181055 | G | A | 1 | a0001c0001t0012g0031 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.803-1644G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181055 | |||||||
| chr2:88181055 | G | T | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1644G>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181055 | |||||||
| chr2:88181059 | T | G | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1640T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181059 | |||||||
| chr2:88181062 | T | A | 1 | a0001c0001t0002g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.803-1637T>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181062 | |||||||
| chr2:88181062 | T | G | 2 | a0001c0001t0005g0036 a0005c0008t0006g0015 |
2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.803-1637T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181062 | |||||||
| chr2:88181064 | A | T | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1635A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181064 | |||||||
| chr2:88181065 | T | A | 2 | a0001c0001t0005g0036 a0005c0008t0006g0015 |
2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.803-1634T>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181065 | |||||||
| chr2:88181067 | C | G | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1632C>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181067 | |||||||
| chr2:88181068 | A | ACGTGGCT others(511): Show |
1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1630_803-1629i others(520): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181068 | ||||||
| chr2:88181069 | C | A | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1630C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181069 | |||||||
| chr2:88181070 | T | C | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1629T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181070 | |||||||
| chr2:88181071 | C | CTAGCATA others(372): Show |
1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1628_803-1627i others(381): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181071 | |||||||
| chr2:88181072 | C | T | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1627C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181072 | |||||||
| chr2:88181073 | T | C | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1626T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181073 | |||||||
| chr2:88181074 | A | T | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1625A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181074 | |||||||
| chr2:88181075 | G | C | 2 | a0001c0001t0005g0036 a0005c0008t0006g0015 |
2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.803-1624G>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181075 | |||||||
| chr2:88181078 | A | C | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1621A>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181078 | |||||||
| chr2:88181078 | A | T | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1621A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181078 | |||||||
| chr2:88181079 | T | C | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1620T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181079 | |||||||
| chr2:88181080 | T | C | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1619T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181080 | |||||||
| chr2:88181080 | T | G | 1 | a0001c0001t0002g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.803-1619T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181080 | |||||||
| chr2:88181080 | TC | T | 4 | a0001c0001t0002g0041 a0001c0001t0002g0045 a0001c0001t0004g0027 others(1): Show |
4 | HG00099.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1616delC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181080 | ||||||
| chr2:88181081 | C | A | 1 | a0001c0001t0002g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.803-1618C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181081 | |||||||
| chr2:88181081 | C | T | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1618C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181081 | |||||||
| chr2:88181082 | C | T | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1617C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181082 | |||||||
| chr2:88181084 | A | T | 2 | a0001c0001t0005g0036 a0002c0002t0001g0021 |
2 | HG00639.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.803-1615A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181084 | |||||||
| chr2:88181085 | C | T | 21 | a0001c0001t0002g0038 a0001c0001t0002g0041 a0001c0001t0002g0042 others(18): Show |
21 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.803-1614C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181085 | |||||||
| chr2:88181086 | G | GAGAGCTA others(654): Show |
1 | a0001c0001t0002g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.803-1613_803-1612i others(663): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181086 | |||||||
| chr2:88181086 | G | T | 2 | a0001c0001t0005g0036 a0005c0008t0006g0015 |
2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.803-1613G>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181086 | |||||||
| chr2:88181090 | G | GCCTCTCT others(514): Show |
1 | a0002c0002t0001g0017 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.803-1608_803-1607i others(523): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181090 | ||||||
| chr2:88181090 | G | GCTCCTCC others(521): Show |
1 | a0002c0002t0001g0050 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.803-1606_803-1605i others(530): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181090 | ||||||
| chr2:88181090 | G | GCTCTCCT others(99): Show |
1 | a0002c0002t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803-1597_803-1596i others(108): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181090 | ||||||
| chr2:88181090 | G | T | 3 | a0001c0001t0002g0039 a0001c0001t0005g0036 a0005c0008t0006g0015 |
3 | HG00639.hp1 HG01934.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.803-1609G>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181090 | |||||||
| chr2:88181094 | T | C | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1605T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181094 | |||||||
| chr2:88181094 | T | TC | 3 | a0001c0003t0003g0003 a0002c0002t0001g0018 a0002c0002t0001g0021 |
3 | HG01433.hp1 HG02015.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.803-1603dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181094 | ||||||
| chr2:88181095 | C | T | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1604C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181095 | |||||||
| chr2:88181097 | T | TCTCTCCC others(212): Show |
1 | a0001c0001t0011g0033 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.803-1596_803-1595i others(221): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181097 | ||||||
| chr2:88181102 | C | CCTCTCTC others(116): Show |
1 | a0001c0004t0003g0006 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(125): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181102 | ||||||
| chr2:88181102 | C | CTCCTTCT others(485): Show |
1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1597_803-1596i others(494): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181102 | |||||||
| chr2:88181102 | C | CTCTCTCT others(242): Show |
1 | a0001c0001t0002g0048 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.803-1597_803-1596i others(251): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181102 | |||||||
| chr2:88181102 | C | CTCTCTCT others(529): Show |
1 | a0002c0002t0001g0018 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.803-1597_803-1596i others(538): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181102 | |||||||
| chr2:88181109 | C | CTCCTCTC others(583): Show |
1 | a0004c0011t0001g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(592): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181109 | ||||||
| chr2:88181111 | C | CTCCTCTC others(502): Show |
1 | a0003c0005t0007g0013 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.803-1588_803-1587i others(511): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181111 | |||||||
| chr2:88181111 | C | CTCCTCTC others(503): Show |
1 | a0003c0005t0006g0014 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.803-1588_803-1587i others(512): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181111 | |||||||
| chr2:88181111 | CCT | C | 4 | a0001c0001t0002g0038 a0001c0001t0004g0009 a0001c0001t0004g0011 others(1): Show |
4 | HG01070.hp1 HG02015.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1578_803-1577d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181111 | ||||||
| chr2:88181112 | C | T | 4 | a0001c0001t0002g0039 a0002c0002t0001g0017 a0002c0002t0001g0050 others(1): Show |
4 | HG00639.hp2 HG01934.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-1587C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181112 | |||||||
| chr2:88181113 | T | C | 4 | a0001c0001t0002g0039 a0002c0002t0001g0017 a0002c0002t0001g0050 others(1): Show |
4 | HG00639.hp2 HG01934.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-1586T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181113 | |||||||
| chr2:88181113 | T | TC | 2 | a0003c0005t0006g0014 a0003c0005t0007g0013 |
2 | HG00140.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.803-1585dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCCCTCTC others(707): Show |
1 | a0001c0001t0002g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.803-1585_803-1584i others(716): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(423): Show |
1 | a0001c0001t0004g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(432): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(676): Show |
1 | a0001c0001t0010g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(685): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(490): Show |
1 | a0001c0001t0005g0035 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(499): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(658): Show |
1 | a0001c0001t0009g0037 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(667): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(678): Show |
2 | a0001c0001t0002g0042 a0001c0001t0002g0049 |
2 | HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.803-1579_803-1578i others(687): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(689): Show |
1 | a0001c0001t0005g0034 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(698): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(314): Show |
1 | a0001c0001t0002g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(323): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(622): Show |
1 | a0001c0001t0002g0045 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(631): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(314): Show |
1 | a0001c0001t0002g0043 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(323): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(152): Show |
1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(161): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(343): Show |
1 | a0006c0010t0003g0004 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(352): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(344): Show |
1 | a0001c0004t0003g0001 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(353): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(343): Show |
1 | a0001c0004t0003g0001 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(352): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(511): Show |
1 | a0002c0002t0001g0052 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(520): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(511): Show |
2 | a0002c0002t0001g0026 a0002c0002t0001g0028 |
2 | HG03209.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.803-1579_803-1578i others(520): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(511): Show |
1 | a0002c0002t0001g0024 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(520): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(522): Show |
1 | a0002c0002t0001g0019 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(531): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(511): Show |
1 | a0002c0002t0001g0016 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(520): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(515): Show |
2 | a0002c0002t0001g0051 a0002c0002t0001g0053 |
2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.803-1579_803-1578i others(524): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(526): Show |
1 | a0002c0002t0001g0022 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(535): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(346): Show |
1 | a0001c0003t0003g0002 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.803-1579_803-1578i others(355): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTCTCTC others(347): Show |
1 | a0001c0003t0003g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.803-1577_803-1576i others(356): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181113 | T | TCTTCTCT others(355): Show |
1 | a0001c0003t0003g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.803-1584_803-1583i others(364): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181113 | ||||||
| chr2:88181115 | T | TCTCTCCT others(233): Show |
1 | a0001c0001t0004g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(242): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181115 | ||||||
| chr2:88181115 | T | TCTCTCCT others(654): Show |
1 | a0001c0001t0012g0031 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(663): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181115 | ||||||
| chr2:88181115 | T | TCTCTCCT others(123): Show |
1 | a0001c0003t0003g0005 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(132): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181115 | ||||||
| chr2:88181115 | T | TCTCTCCT others(125): Show |
1 | a0001c0003t0003g0007 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.803-1579_803-1578i others(134): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181115 | ||||||
| chr2:88181121 | T | C | 1 | a0008c0006t0003g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.803-1578T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181121 | |||||||
| chr2:88181122 | C | CCT | 2 | a0001c0001t0002g0048 a0002c0002t0001g0020 |
2 | HG01081.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.803-1569_803-1568d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181122 | ||||||
| chr2:88181122 | C | CCTCTCTC others(505): Show |
1 | a0007c0009t0002g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-1565_803-1564i others(514): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181122 | ||||||
| chr2:88181122 | C | T | 1 | a0008c0006t0003g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.803-1577C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181122 | |||||||
| chr2:88181123 | C | T | 1 | a0001c0001t0004g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-1576C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181123 | |||||||
| chr2:88181131 | C | CTCCTCCT others(3): Show |
1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1568_803-1567i others(12): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181131 | |||||||
| chr2:88181131 | C | T | 1 | a0001c0001t0011g0033 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.803-1568C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181131 | |||||||
| chr2:88181131 | CCT | C | 3 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0005g0010 |
3 | HG02015.hp2 HG02523.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.803-1558_803-1557d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181131 | ||||||
| chr2:88181133 | T | TCTCTCCT others(34): Show |
1 | a0008c0006t0003g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.803-1561_803-1560i others(43): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181133 | ||||||
| chr2:88181142 | C | CCTCTCTC others(351): Show |
1 | a0009c0007t0002g0047 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.803-1550_803-1549i others(360): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181142 | ||||||
| chr2:88181142 | C | T | 1 | a0007c0009t0002g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-1557C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181142 | |||||||
| chr2:88181146 | T | A | 1 | a0001c0001t0011g0033 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.803-1553T>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181146 | |||||||
| chr2:88181151 | C | T | 3 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0004g0012 |
3 | HG00323.hp1 HG01074.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.803-1548C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181151 | |||||||
| chr2:88181152 | T | C | 4 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0004g0012 others(1): Show |
4 | HG00323.hp1 HG01074.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1547T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181152 | |||||||
| chr2:88181153 | C | CCTCT | 2 | a0001c0001t0004g0027 a0001c0001t0005g0036 |
2 | HG00639.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.803-1542_803-1539d others(6): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181153 | ||||||
| chr2:88181153 | C | T | 4 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0004g0012 others(1): Show |
4 | HG00323.hp1 HG01074.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1546C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181153 | |||||||
| chr2:88181161 | C | T | 7 | a0001c0001t0005g0035 a0001c0001t0012g0031 a0001c0003t0003g0005 others(4): Show |
7 | HG00099.hp2 HG01081.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-1538C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181161 | |||||||
| chr2:88181162 | T | C | 5 | a0001c0001t0011g0033 a0001c0001t0012g0031 a0001c0003t0003g0005 others(2): Show |
5 | HG00099.hp2 HG01081.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-1537T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181162 | |||||||
| chr2:88181162 | T | TC | 2 | a0001c0001t0002g0048 a0002c0002t0001g0050 |
2 | HG00639.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.803-1536dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181162 | ||||||
| chr2:88181164 | T | TCTCTCTC others(798): Show |
1 | a0001c0001t0005g0010 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.803-1528_803-1527i others(807): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181164 | ||||||
| chr2:88181181 | T | C | 1 | a0001c0001t0012g0031 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.803-1518T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181181 | |||||||
| chr2:88181182 | C | T | 1 | a0001c0001t0012g0031 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.803-1517C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181182 | |||||||
| chr2:88181186 | T | C | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-1513T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181186 | |||||||
| chr2:88181189 | C | CCTCTCCT others(6): Show |
1 | a0001c0003t0003g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.803-1510_803-1509i others(15): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181189 | |||||||
| chr2:88181189 | CTCCCT | C | 2 | a0001c0001t0002g0038 a0001c0001t0004g0011 |
2 | HG01070.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.803-1509_803-1505d others(7): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181189 | |||||||
| chr2:88181190 | T | C | 1 | a0001c0003t0003g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.803-1509T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181190 | |||||||
| chr2:88181190 | TC | T | 17 | a0001c0001t0002g0039 a0001c0001t0002g0041 a0001c0001t0002g0045 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-1506delC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181190 | ||||||
| chr2:88181191 | C | CCTCTCTC others(1): Show |
6 | a0001c0001t0010g0029 a0002c0002t0001g0016 a0002c0002t0001g0017 others(3): Show |
6 | HG00639.hp2 HG01074.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-1507_803-1506i others(10): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181191 | ||||||
| chr2:88181191 | C | CCTCTCTC others(21): Show |
2 | a0001c0001t0002g0042 a0001c0001t0002g0049 |
2 | HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.803-1507_803-1506i others(30): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181191 | ||||||
| chr2:88181191 | C | CT | 13 | a0001c0001t0002g0043 a0001c0001t0004g0012 a0001c0001t0005g0035 others(10): Show |
13 | HG00323.hp1 HG01074.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.803-1508_803-1507i others(3): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181191 | |||||||
| chr2:88181191 | C | CTCCTCTC others(3): Show |
1 | a0001c0004t0003g0001 | 2 | HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.803-1508_803-1507i others(12): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181191 | |||||||
| chr2:88181191 | C | CTCTCCTC others(443): Show |
1 | a0001c0001t0004g0009 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.803-1508_803-1507i others(452): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181191 | |||||||
| chr2:88181191 | C | CTCTCTCC others(105): Show |
1 | a0001c0001t0004g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-1508_803-1507i others(114): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181191 | |||||||
| chr2:88181192 | C | CT | 3 | a0001c0001t0005g0010 a0001c0001t0005g0036 a0001c0001t0012g0031 |
3 | HG00099.hp2 HG00639.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.803-1507_803-1506i others(3): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181192 | |||||||
| chr2:88181192 | C | T | 1 | a0002c0002t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803-1507C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181192 | |||||||
| chr2:88181200 | T | C | 2 | a0001c0001t0005g0010 a0002c0002t0001g0020 |
2 | HG01981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.803-1499T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181200 | |||||||
| chr2:88181201 | C | T | 5 | a0001c0001t0005g0010 a0001c0001t0005g0035 a0001c0003t0008g0032 others(2): Show |
5 | HG01981.hp2 HG03209.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-1498C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181201 | |||||||
| chr2:88181202 | C | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0049 |
2 | HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.803-1497C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181202 | |||||||
| chr2:88181203 | T | C | 2 | a0001c0001t0002g0042 a0001c0001t0002g0049 |
2 | HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.803-1496T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181203 | |||||||
| chr2:88181203 | T | TCTCTCTC others(2): Show |
6 | a0002c0002t0001g0016 a0002c0002t0001g0017 a0002c0002t0001g0018 others(3): Show |
6 | HG00639.hp2 HG01074.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-1489_803-1488i others(11): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181203 | ||||||
| chr2:88181212 | T | TCTCTCTC others(391): Show |
1 | a0001c0001t0002g0043 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.803-1471_803-1470i others(400): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181212 | ||||||
| chr2:88181217 | C | T | 4 | a0001c0003t0003g0002 a0001c0003t0003g0008 a0001c0004t0003g0001 others(1): Show |
5 | HG01943.hp1 HG01981.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-1482C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181217 | |||||||
| chr2:88181221 | C | CCTCT | 3 | a0001c0001t0002g0044 a0001c0001t0004g0009 a0007c0009t0002g0040 |
3 | HG01934.hp2 HG02015.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.803-1474_803-1471d others(6): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181221 | ||||||
| chr2:88181221 | C | CCTCTCTC others(191): Show |
1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.803-1471_803-1470i others(200): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181221 | ||||||
| chr2:88181221 | C | CCTCTCTC others(226): Show |
1 | a0001c0003t0003g0007 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.803-1471_803-1470i others(235): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181221 | ||||||
| chr2:88181228 | C | CCTCTCT | 9 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0049 others(6): Show |
9 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.803-1465_803-1460d others(8): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181228 | ||||||
| chr2:88181228 | C | CCTCTCTC others(17): Show |
5 | a0002c0002t0001g0019 a0002c0002t0001g0022 a0002c0002t0001g0024 others(2): Show |
5 | HG00140.hp2 HG01943.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-1453_803-1452i others(26): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181228 | ||||||
| chr2:88181228 | C | CCTCTCTC others(720): Show |
1 | a0001c0001t0002g0038 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.803-1451_803-1450i others(729): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181228 | ||||||
| chr2:88181228 | C | CT | 6 | a0001c0001t0004g0012 a0001c0001t0005g0036 a0001c0001t0012g0031 others(3): Show |
6 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-1471_803-1470i others(3): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181228 | C | CTCTCCTC others(10): Show |
1 | a0002c0002t0001g0051 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.803-1471_803-1470i others(19): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181228 | C | CTCTCCTC others(29): Show |
1 | a0001c0001t0002g0045 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.803-1471_803-1470i others(38): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181228 | C | CTCTCCTC others(26): Show |
1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.803-1471_803-1470i others(35): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181228 | C | CTCTCCTC others(28): Show |
2 | a0003c0005t0006g0014 a0003c0005t0007g0013 |
2 | HG00140.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.803-1471_803-1470i others(37): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181228 | C | CTCTCCTC others(30): Show |
1 | a0001c0001t0002g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.803-1471_803-1470i others(39): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181228 | C | CTCTCCTC others(103): Show |
1 | a0001c0001t0009g0037 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.803-1471_803-1470i others(112): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181228 | C | CTCTCCTC others(114): Show |
1 | a0001c0001t0005g0034 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.803-1471_803-1470i others(123): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181228 | C | CTCTCCTC others(29): Show |
1 | a0001c0001t0002g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.803-1471_803-1470i others(38): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181228 | C | CTCTCCTC others(321): Show |
1 | a0001c0001t0005g0035 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.803-1471_803-1470i others(330): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181228 | |||||||
| chr2:88181229 | C | T | 4 | a0001c0001t0004g0027 a0001c0001t0011g0033 a0002c0002t0001g0020 others(1): Show |
4 | HG01258.hp2 HG01981.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1470C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181229 | |||||||
| chr2:88181230 | T | C | 1 | a0001c0001t0011g0033 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.803-1469T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181230 | |||||||
| chr2:88181230 | T | TC | 5 | a0001c0001t0004g0012 a0001c0001t0005g0036 a0001c0003t0003g0005 others(2): Show |
5 | HG00639.hp1 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-1468dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181230 | ||||||
| chr2:88181232 | T | TC | 3 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0009g0037 |
3 | HG00323.hp2 NA18971.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.803-1466dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181232 | ||||||
| chr2:88181238 | T | TCCTCTCT others(21): Show |
1 | a0002c0002t0001g0052 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.803-1451_803-1450i others(30): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181238 | ||||||
| chr2:88181239 | C | CCTCTCTC others(6): Show |
1 | a0001c0001t0010g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.803-1453_803-1452i others(15): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181239 | ||||||
| chr2:88181239 | C | T | 2 | a0001c0003t0003g0005 a0001c0004t0003g0006 |
2 | HG01081.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.803-1460C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181239 | |||||||
| chr2:88181249 | C | CTCTCTCT | 2 | a0001c0001t0005g0010 a0001c0003t0003g0007 |
2 | HG01975.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.803-1450_803-1449i others(9): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181249 | |||||||
| chr2:88181249 | C | T | 13 | a0001c0001t0002g0044 a0001c0001t0002g0048 a0001c0001t0004g0009 others(10): Show |
14 | HG01081.hp1 HG01934.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.803-1450C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181249 | |||||||
| chr2:88181250 | C | T | 10 | a0001c0001t0004g0012 a0001c0001t0005g0034 a0001c0001t0005g0035 others(7): Show |
10 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.803-1449C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181250 | |||||||
| chr2:88181259 | CCT | C | 3 | a0001c0001t0011g0033 a0001c0003t0003g0002 a0002c0002t0001g0024 |
3 | HG01258.hp2 HG01943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.803-1430_803-1429d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181259 | ||||||
| chr2:88181260 | C | T | 2 | a0001c0001t0004g0027 a0002c0002t0001g0020 |
2 | HG01981.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.803-1439C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181260 | |||||||
| chr2:88181261 | T | C | 2 | a0001c0001t0004g0027 a0002c0002t0001g0020 |
2 | HG01981.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.803-1438T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181261 | |||||||
| chr2:88181261 | T | TCTCTCTC | 3 | a0001c0003t0003g0008 a0001c0004t0003g0001 a0006c0010t0003g0004 |
4 | HG01943.hp1 HG01981.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-1437_803-1431d others(9): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181261 | ||||||
| chr2:88181264 | C | T | 3 | a0003c0005t0006g0014 a0003c0005t0007g0013 a0005c0008t0006g0015 |
3 | HG00140.hp1 HG01934.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.803-1435C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181264 | |||||||
| chr2:88181269 | T | C | 3 | a0001c0001t0002g0044 a0001c0001t0004g0009 a0007c0009t0002g0040 |
3 | HG01934.hp2 HG02015.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.803-1430T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181269 | |||||||
| chr2:88181270 | C | CCT | 2 | a0001c0001t0004g0012 a0002c0002t0001g0021 |
2 | HG01074.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.803-1421_803-1420d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181270 | ||||||
| chr2:88181270 | C | CCTCTCTC others(4): Show |
3 | a0003c0005t0006g0014 a0003c0005t0007g0013 a0005c0008t0006g0015 |
3 | HG00140.hp1 HG01934.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.803-1388_803-1378d others(13): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181270 | ||||||
| chr2:88181270 | C | T | 3 | a0001c0001t0002g0044 a0001c0001t0004g0009 a0007c0009t0002g0040 |
3 | HG01934.hp2 HG02015.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.803-1429C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181270 | |||||||
| chr2:88181278 | TC | T | 2 | a0001c0001t0005g0010 a0001c0003t0003g0007 |
2 | HG01975.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.803-1419delC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181278 | ||||||
| chr2:88181279 | C | CTCCTCTC others(1): Show |
3 | a0001c0003t0003g0008 a0001c0004t0003g0001 a0006c0010t0003g0004 |
3 | HG01981.hp1 HG02273.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.803-1420_803-1419i others(10): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181279 | |||||||
| chr2:88181279 | C | CTCCTCTC others(3): Show |
1 | a0001c0004t0003g0001 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.803-1420_803-1419i others(12): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181279 | |||||||
| chr2:88181279 | CCT | C | 3 | a0001c0001t0002g0048 a0002c0002t0001g0022 a0009c0007t0002g0047 |
3 | HG01081.hp1 NA19081.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.803-1410_803-1409d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181279 | ||||||
| chr2:88181280 | C | T | 3 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0009g0037 |
3 | HG00323.hp2 NA18971.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.803-1419C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181280 | |||||||
| chr2:88181281 | T | C | 3 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0009g0037 |
3 | HG00323.hp2 NA18971.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.803-1418T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181281 | |||||||
| chr2:88181281 | T | TCTCTCTC others(76): Show |
1 | a0001c0001t0002g0045 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.803-1409_803-1408i others(85): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181281 | ||||||
| chr2:88181282 | CT | C | 2 | a0001c0001t0005g0010 a0001c0003t0003g0007 |
2 | HG01975.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.803-1416delT | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181282 | |||||||
| chr2:88181283 | T | TC | 3 | a0001c0003t0003g0008 a0001c0004t0003g0001 a0006c0010t0003g0004 |
3 | HG01981.hp1 HG02273.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.803-1415dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181283 | ||||||
| chr2:88181283 | T | TCTCTCCT others(318): Show |
1 | a0008c0006t0003g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.803-1411_803-1410i others(327): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181283 | ||||||
| chr2:88181292 | T | C | 5 | a0001c0001t0002g0045 a0001c0001t0004g0009 a0001c0001t0005g0034 others(2): Show |
5 | HG00099.hp1 HG00323.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-1407T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181292 | |||||||
| chr2:88181303 | T | C | 4 | a0001c0001t0002g0045 a0001c0001t0005g0034 a0001c0001t0005g0035 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1396T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181303 | |||||||
| chr2:88181303 | T | TCTCTC | 6 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(3): Show |
6 | HG00323.hp1 HG01070.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-1395_803-1391d others(7): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181303 | ||||||
| chr2:88181303 | T | TCTCTCCT others(78): Show |
1 | a0001c0001t0012g0031 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.803-1391_803-1390i others(87): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181303 | ||||||
| chr2:88181303 | T | TCTCTCCT others(79): Show |
1 | a0001c0001t0010g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.803-1391_803-1390i others(88): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181303 | ||||||
| chr2:88181308 | C | CTCTCCTC others(5): Show |
1 | a0002c0002t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803-1380_803-1379i others(14): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181308 | ||||||
| chr2:88181312 | C | CCT | 8 | a0001c0001t0002g0048 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
9 | HG01074.hp1 HG01081.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.803-1379_803-1378d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181312 | ||||||
| chr2:88181312 | C | CCTCTCTC others(238): Show |
2 | a0001c0003t0003g0005 a0001c0004t0003g0006 |
2 | HG01081.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.803-1380_803-1379i others(247): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181312 | ||||||
| chr2:88181312 | C | CCTCTCTC others(6): Show |
1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.803-1378_803-1377i others(15): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181312 | ||||||
| chr2:88181313 | C | T | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1386C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181313 | |||||||
| chr2:88181314 | T | TCTCTCTC others(2): Show |
2 | a0001c0001t0002g0041 a0001c0003t0003g0003 |
2 | HG01433.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.803-1378_803-1377i others(11): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181314 | ||||||
| chr2:88181314 | T | TCTCTCTC others(264): Show |
1 | a0001c0001t0002g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.803-1378_803-1377i others(273): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181314 | ||||||
| chr2:88181318 | T | TCCTCTCT others(128): Show |
1 | a0007c0009t0002g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-1380_803-1379i others(137): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181318 | ||||||
| chr2:88181321 | C | T | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1378C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181321 | |||||||
| chr2:88181322 | C | T | 6 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0042 others(3): Show |
6 | HG00323.hp1 HG01070.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-1377C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181322 | |||||||
| chr2:88181323 | T | C | 6 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0042 others(3): Show |
6 | HG00323.hp1 HG01070.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-1376T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181323 | |||||||
| chr2:88181329 | T | TC | 2 | a0001c0001t0002g0041 a0009c0007t0002g0047 |
2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.803-1369dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181329 | ||||||
| chr2:88181331 | T | C | 8 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0042 others(5): Show |
8 | HG00323.hp1 HG01070.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.803-1368T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181331 | |||||||
| chr2:88181332 | C | CCTCTCTC others(4): Show |
6 | a0001c0003t0003g0005 a0001c0003t0003g0007 a0001c0003t0003g0008 others(3): Show |
7 | HG01081.hp2 HG01943.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-1350_803-1340d others(13): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181332 | ||||||
| chr2:88181332 | C | CCTCTCTC others(13): Show |
4 | a0001c0001t0002g0045 a0001c0001t0005g0034 a0001c0001t0005g0035 others(1): Show |
4 | HG00099.hp1 HG00099.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1351_803-1350i others(22): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181332 | ||||||
| chr2:88181332 | C | CCTCTCTC others(552): Show |
1 | a0001c0001t0002g0048 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.803-1360_803-1359i others(561): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181332 | ||||||
| chr2:88181332 | C | CCTCTCTC others(496): Show |
1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-1360_803-1359i others(505): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181332 | ||||||
| chr2:88181332 | C | CT | 3 | a0001c0001t0002g0041 a0001c0001t0004g0009 a0009c0007t0002g0047 |
3 | HG02015.hp2 NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.803-1367_803-1366i others(3): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181332 | |||||||
| chr2:88181332 | C | CTCTCTCC others(562): Show |
1 | a0001c0001t0011g0033 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.803-1367_803-1366i others(571): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181332 | |||||||
| chr2:88181332 | C | CTCTCTCT others(102): Show |
1 | a0001c0001t0004g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-1367_803-1366i others(111): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181332 | |||||||
| chr2:88181332 | C | T | 7 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0042 others(4): Show |
7 | HG00323.hp1 HG01070.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-1367C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181332 | |||||||
| chr2:88181334 | T | TCTCTCTC others(16): Show |
1 | a0001c0003t0003g0002 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.803-1360_803-1359i others(25): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181334 | ||||||
| chr2:88181341 | T | TCTCTCTC others(11): Show |
1 | a0001c0001t0010g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.803-1351_803-1350i others(20): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181341 | ||||||
| chr2:88181350 | C | CCT | 3 | a0001c0001t0002g0048 a0001c0001t0004g0009 a0002c0002t0001g0050 |
3 | HG00639.hp2 HG01081.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.803-1341_803-1340d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181350 | ||||||
| chr2:88181350 | C | CT | 2 | a0001c0001t0004g0027 a0001c0001t0010g0029 |
2 | HG02615.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.803-1349_803-1348i others(3): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181350 | |||||||
| chr2:88181350 | C | T | 1 | a0002c0002t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803-1349C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181350 | |||||||
| chr2:88181356 | T | TCTCCTCT others(3): Show |
1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.803-1339_803-1338i others(12): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181356 | ||||||
| chr2:88181359 | C | CTCCTCCT others(4): Show |
1 | a0001c0003t0003g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.803-1340_803-1339i others(13): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181359 | |||||||
| chr2:88181359 | C | CTCCTCTC others(3): Show |
2 | a0001c0001t0009g0037 a0006c0010t0003g0004 |
2 | HG00323.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.803-1340_803-1339i others(12): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181359 | |||||||
| chr2:88181360 | C | CTCTCTCT others(503): Show |
1 | a0001c0001t0004g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.803-1339_803-1338i others(512): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181360 | |||||||
| chr2:88181360 | C | T | 7 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0042 others(4): Show |
7 | HG00323.hp1 HG01070.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-1339C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181360 | |||||||
| chr2:88181361 | C | T | 4 | a0001c0001t0004g0009 a0001c0001t0004g0027 a0001c0001t0005g0010 others(1): Show |
4 | HG01981.hp2 HG02015.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1338C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181361 | |||||||
| chr2:88181368 | C | G | 1 | a0001c0001t0005g0010 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.803-1331C>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181368 | |||||||
| chr2:88181369 | T | TCC | 4 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0002g0043 others(1): Show |
4 | HG00323.hp1 HG01070.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-1329_803-1328d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181369 | ||||||
| chr2:88181370 | C | T | 1 | a0001c0001t0004g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.803-1329C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181370 | |||||||
| chr2:88181370 | CCTCT | C | 2 | a0003c0005t0006g0014 a0003c0005t0007g0013 |
2 | HG00140.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.803-1321_803-1318d others(6): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181370 | ||||||
| chr2:88181371 | C | T | 2 | a0002c0002t0001g0021 a0009c0007t0002g0047 |
2 | HG02015.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.803-1328C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181371 | |||||||
| chr2:88181372 | T | C | 11 | a0001c0001t0002g0039 a0001c0001t0002g0045 a0001c0001t0002g0048 others(8): Show |
11 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-1327T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181372 | |||||||
| chr2:88181380 | T | C | 5 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0002g0043 others(2): Show |
5 | HG00323.hp1 HG01070.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-1319T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181380 | |||||||
| chr2:88181380 | T | TCCTCTCT others(111): Show |
1 | a0001c0001t0002g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.803-1280_803-1279i others(120): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181380 | ||||||
| chr2:88181381 | C | T | 2 | a0001c0001t0004g0011 a0001c0001t0004g0012 |
2 | HG01074.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.803-1318C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181381 | |||||||
| chr2:88181390 | C | T | 1 | a0002c0002t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803-1309C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181390 | |||||||
| chr2:88181412 | CCT | C | 2 | a0002c0002t0001g0018 a0009c0007t0002g0047 |
2 | HG03492.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.803-1277_803-1276d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181412 | ||||||
| chr2:88181414 | T | TCTCTCTC others(230): Show |
1 | a0002c0002t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803-1278_803-1277i others(239): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181414 | ||||||
| chr2:88181422 | T | C | 1 | a0001c0001t0005g0010 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.803-1277T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181422 | |||||||
| chr2:88181423 | C | CCT | 3 | a0001c0001t0002g0039 a0001c0001t0004g0009 a0001c0001t0009g0037 |
3 | HG00323.hp2 HG02015.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.803-1268_803-1267d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181423 | ||||||
| chr2:88181428 | C | CTCTCTCC others(109): Show |
1 | a0007c0009t0002g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-1267_803-1266i others(118): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181428 | ||||||
| chr2:88181434 | T | C | 1 | a0001c0001t0005g0010 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.803-1265T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181434 | |||||||
| chr2:88181443 | C | CCTCTCTC others(494): Show |
1 | a0009c0007t0002g0047 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.803-1249_803-1248i others(503): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181443 | ||||||
| chr2:88181443 | C | T | 1 | a0001c0001t0004g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.803-1256C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181443 | |||||||
| chr2:88181451 | C | T | 1 | a0001c0001t0004g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.803-1248C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181451 | |||||||
| chr2:88181452 | T | C | 1 | a0001c0001t0004g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.803-1247T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181452 | |||||||
| chr2:88181460 | T | C | 1 | a0002c0002t0001g0018 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.803-1239T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181460 | |||||||
| chr2:88181461 | C | T | 1 | a0002c0002t0001g0018 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.803-1238C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181461 | |||||||
| chr2:88181471 | C | CTCTCTCT others(330): Show |
1 | a0001c0001t0004g0009 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.803-1228_803-1227i others(339): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181471 | |||||||
| chr2:88181471 | C | T | 4 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0027 others(1): Show |
4 | HG01074.hp1 HG02523.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1228C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181471 | |||||||
| chr2:88181472 | C | T | 1 | a0002c0002t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803-1227C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181472 | |||||||
| chr2:88181480 | TC | T | 3 | a0001c0001t0012g0031 a0002c0002t0001g0024 a0007c0009t0002g0040 |
3 | HG00099.hp2 HG01943.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.803-1215delC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181480 | ||||||
| chr2:88181481 | C | A | 1 | a0001c0001t0002g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.803-1218C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181481 | |||||||
| chr2:88181482 | C | T | 6 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(3): Show |
6 | HG01074.hp1 HG02015.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-1217C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181482 | |||||||
| chr2:88181483 | C | T | 1 | a0002c0002t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803-1216C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181483 | |||||||
| chr2:88181485 | TCTCTCTC others(4): Show |
T | 3 | a0003c0005t0006g0014 a0003c0005t0007g0013 a0005c0008t0006g0015 |
3 | HG00140.hp1 HG01934.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.803-1182_803-1172d others(13): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181485 | ||||||
| chr2:88181489 | T | TC | 4 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0027 others(1): Show |
4 | HG01074.hp1 HG01981.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1209dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181489 | ||||||
| chr2:88181493 | T | C | 2 | a0001c0001t0004g0009 a0009c0007t0002g0047 |
2 | HG02015.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.803-1206T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181493 | |||||||
| chr2:88181495 | T | C | 3 | a0001c0001t0004g0009 a0007c0009t0002g0040 a0009c0007t0002g0047 |
3 | HG02015.hp2 HG03209.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.803-1204T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181495 | |||||||
| chr2:88181495 | T | TC | 2 | a0001c0003t0003g0002 a0001c0003t0003g0003 |
2 | HG01433.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.803-1202dupC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181495 | ||||||
| chr2:88181496 | C | CTCCTCTC others(139): Show |
1 | a0002c0002t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803-1203_803-1202i others(148): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181496 | |||||||
| chr2:88181496 | C | CTCTCCTC others(314): Show |
1 | a0001c0001t0004g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-1203_803-1202i others(323): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181496 | |||||||
| chr2:88181496 | C | CTCTCCTC others(315): Show |
1 | a0001c0001t0004g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.803-1203_803-1202i others(324): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181496 | |||||||
| chr2:88181496 | C | CTCTCCTC others(370): Show |
1 | a0001c0001t0004g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.803-1203_803-1202i others(379): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181496 | |||||||
| chr2:88181496 | C | T | 2 | a0001c0001t0004g0009 a0009c0007t0002g0047 |
2 | HG02015.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.803-1203C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181496 | |||||||
| chr2:88181517 | T | C | 1 | a0002c0002t0001g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.803-1182T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181517 | |||||||
| chr2:88181528 | C | CCCTCTCT others(17): Show |
1 | a0001c0001t0005g0010 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.803-1161_803-1160i others(26): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181528 | ||||||
| chr2:88181528 | C | T | 7 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
7 | HG01074.hp1 HG01981.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-1171C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181528 | |||||||
| chr2:88181550 | C | CCCTCTCT others(5): Show |
1 | a0007c0009t0002g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-1138_803-1137i others(14): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181550 | ||||||
| chr2:88181555 | T | C | 1 | a0001c0003t0003g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.803-1144T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181555 | |||||||
| chr2:88181573 | C | CTG | 2 | a0001c0001t0004g0027 a0001c0001t0005g0036 |
2 | HG00639.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.803-1106_803-1105d others(4): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181573 | ||||||
| chr2:88181586 | T | C | 3 | a0003c0005t0006g0014 a0003c0005t0007g0013 a0005c0008t0006g0015 |
3 | HG00140.hp1 HG01934.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.803-1113T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181586 | |||||||
| chr2:88181628 | C | A | 3 | a0003c0005t0006g0014 a0003c0005t0007g0013 a0005c0008t0006g0015 |
3 | HG00140.hp1 HG01934.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.803-1071C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181628 | |||||||
| chr2:88181732 | TA | T | 3 | a0001c0001t0004g0009 a0001c0001t0004g0027 a0002c0002t0001g0052 |
3 | HG01070.hp2 HG02015.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.803-962delA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181732 | ||||||
| chr2:88181733 | A | C | 1 | a0007c0009t0002g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-966A>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181733 | |||||||
| chr2:88181737 | A | G | 1 | a0001c0003t0003g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.803-962A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181737 | |||||||
| chr2:88181738 | G | A | 1 | a0001c0003t0003g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.803-961G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181738 | |||||||
| chr2:88181801 | T | A | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-898T>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181801 | |||||||
| chr2:88181862 | T | C | 6 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(3): Show |
6 | HG01074.hp1 HG02015.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-837T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181862 | |||||||
| chr2:88181887 | CT | C | 2 | a0001c0003t0008g0032 a0007c0009t0002g0040 |
2 | HG03209.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.803-808delT | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181887 | ||||||
| chr2:88181916 | TGATGTTT others(4): Show |
T | 1 | a0002c0002t0001g0022 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.803-781_803-771del others(11): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88181916 | ||||||
| chr2:88181937 | A | C | 1 | a0007c0009t0002g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-762A>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181937 | |||||||
| chr2:88181972 | T | A | 1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.803-727T>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88181972 | |||||||
| chr2:88182256 | C | A | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-443C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88182256 | |||||||
| chr2:88182369 | A | ACATCTTT others(22): Show |
1 | a0002c0002t0001g0050 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.803-329_803-301dup others(29): Show |
THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 88182369 | ||||||
| chr2:88182422 | T | A | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-277T>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88182422 | |||||||
| chr2:88182617 | A | T | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.803-82A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88182617 | |||||||
| chr2:88182685 | T | C | 1 | a0001c0001t0005g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803-14T>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 5/8 | chr2 | 88182685 | |||||||
| chr2:88182850 | A | AG | 2 | a0001c0003t0003g0003 a0001c0004t0003g0006 |
2 | HG01433.hp1 HG02523.hp1 |
splice_region_variant&intron_variant | LOW | c.951+5dupG | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 88182850 | ||||||
| chr2:88183183 | G | C | 1 | a0005c0008t0006g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1077+110G>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88183183 | |||||||
| chr2:88183186 | A | T | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1077+113A>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88183186 | |||||||
| chr2:88183280 | TC | T | 2 | a0001c0001t0005g0036 a0001c0003t0008g0032 |
2 | HG00639.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1077+210delC | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 88183280 | ||||||
| chr2:88183396 | G | A | 6 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(3): Show |
6 | HG01074.hp1 HG02015.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+323G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88183396 | |||||||
| chr2:88183423 | C | A | 1 | a0001c0001t0002g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1077+350C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88183423 | |||||||
| chr2:88183453 | AT | A | 2 | a0002c0002t0001g0021 a0002c0002t0001g0050 |
2 | HG00639.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1077+382delT | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 88183453 | ||||||
| chr2:88183654 | C | T | 1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1077+581C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88183654 | |||||||
| chr2:88183715 | T | G | 3 | a0003c0005t0006g0014 a0003c0005t0007g0013 a0005c0008t0006g0015 |
3 | HG00140.hp1 HG01934.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1077+642T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88183715 | |||||||
| chr2:88183730 | T | G | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1077+657T>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88183730 | |||||||
| chr2:88183733 | G | A | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1077+660G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88183733 | |||||||
| chr2:88183735 | A | G | 1 | a0002c0002t0001g0021 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1077+662A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88183735 | |||||||
| chr2:88183785 | T | TA | 21 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(18): Show |
21 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.1077+725dupA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 88183785 | ||||||
| chr2:88183785 | TA | T | 5 | a0001c0003t0008g0032 a0002c0002t0001g0019 a0002c0002t0001g0021 others(2): Show |
5 | HG00639.hp2 HG02015.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077+725delA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 88183785 | ||||||
| chr2:88184056 | AT | A | 2 | a0001c0003t0008g0032 a0001c0004t0003g0006 |
2 | HG02523.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1077+987delT | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 88184056 | ||||||
| chr2:88184073 | T | A | 1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1077+1000T>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88184073 | |||||||
| chr2:88184095 | A | C | 1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1077+1022A>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88184095 | |||||||
| chr2:88184152 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1077+1079C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88184152 | |||||||
| chr2:88184500 | C | T | 1 | a0002c0002t0001g0022 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1078-828C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88184500 | |||||||
| chr2:88184590 | C | T | 6 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(3): Show |
6 | HG01074.hp1 HG02015.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-738C>T | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88184590 | |||||||
| chr2:88184602 | TA | T | 7 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
7 | HG01074.hp1 HG02015.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-711delA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 88184602 | ||||||
| chr2:88184611 | A | C | 9 | a0001c0003t0003g0002 a0001c0003t0003g0003 a0001c0003t0003g0005 others(6): Show |
10 | HG01081.hp2 HG01433.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1078-717A>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88184611 | |||||||
| chr2:88184781 | G | GA | 22 | a0001c0001t0002g0038 a0001c0001t0002g0041 a0001c0001t0002g0042 others(19): Show |
22 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1078-539dupA | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 88184781 | ||||||
| chr2:88185289 | C | A | 5 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(2): Show |
5 | HG01074.hp1 HG02015.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-39C>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 7/8 | chr2 | 88185289 | |||||||
| chr2:88185635 | A | G | 1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1229+156A>G | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 8/8 | chr2 | 88185635 | |||||||
| chr2:88185647 | G | A | 1 | a0001c0003t0008g0032 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1229+168G>A | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 8/8 | chr2 | 88185647 | |||||||
| chr2:88185873 | G | C | 36 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(33): Show |
37 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(34): Show |
intron_variant | MODIFIER | c.1230-25G>C | THNSL2 | ENSG00000144115.18 | transcript | ENST00000674334.2 | protein_coding | 8/8 | chr2 | 88185873 |