Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26010 |
| ensemblid | ENSG00000196141.14 |
| hgncid | 24574 |
| symbol | SPATS2L |
| name | spermatogenesis associated serine rich 2 like |
| refseq_nuc | NM_001100423.2 |
| refseq_prot | NP_001093893.1 |
| ensembl_nuc | ENST00000409140.8 |
| ensembl_prot | ENSP00000386730.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 200306693 |
| end | 200482264 |
| strand | + |
| ver | v1.2 |
| region | chr2:200306693-200482264 |
| region5000 | chr2:200301693-200487264 |
| regionname0 | SPATS2L_chr2_200306693_200482264 |
| regionname5000 | SPATS2L_chr2_200301693_200487264 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 558 | 282 | 60 | 47 | 129 | 6 | 38 | 97 | SPATS2L_chr2_200301693_200487264 | SPATS2L | MAELN others(553): Show |
chr2 | 200301693 | 200487264 |
| a0002 | 0/0 | 558 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | MAELN others(553): Show |
chr2 | 200301693 | 200487264 |
| a0003 | 0/0 | 558 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | MAELN others(553): Show |
chr2 | 200301693 | 200487264 |
| a0004 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | MAELN others(553): Show |
chr2 | 200301693 | 200487264 |
| a0005 | 0/0 | 558 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | MAELN others(553): Show |
chr2 | 200301693 | 200487264 |
| a0006 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | MAELN others(553): Show |
chr2 | 200301693 | 200487264 |
| a0007 | 0/0 | 558 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | MAELN others(553): Show |
chr2 | 200301693 | 200487264 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1674 | 231 | 39 | 44 | 105 | 6 | 36 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0001c0002 | 0/1 | 1674 | 28 | 20 | 0 | 6 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0001c0003 | 0/0 | 1674 | 18 | 0 | 3 | 15 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0001c0005 | 0/0 | 1674 | 3 | 0 | 0 | 3 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0001c0010 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0001c0013 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0002c0004 | 0/0 | 1674 | 11 | 11 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0003c0006 | 0/0 | 1674 | 2 | 1 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0003c0008 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0004c0009 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0005c0011 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0006c0007 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 | ||
| a0007c0012 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | ATGGC others(1669): Show |
chr2 | 200301693 | 200487264 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6210 | 21 | 0 | 6 | 11 | 0 | 4 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0002 | 0/0 | 6210 | 31 | 0 | 3 | 21 | 0 | 7 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0003 | 0/0 | 6212 | 15 | 2 | 3 | 8 | 0 | 2 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0004 | 0/0 | 6212 | 14 | 1 | 1 | 11 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0005 | 0/0 | 6210 | 12 | 0 | 1 | 11 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0006 | 0/0 | 6167 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6162): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0007 | 0/0 | 6211 | 11 | 0 | 5 | 4 | 0 | 2 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0008 | 0/0 | 6212 | 11 | 3 | 2 | 4 | 0 | 2 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0009 | 0/0 | 6206 | 9 | 1 | 6 | 2 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6201): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0010 | 1/0 | 6212 | 8 | 7 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0011 | 0/0 | 6210 | 7 | 0 | 0 | 4 | 0 | 3 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0012 | 0/0 | 6213 | 3 | 3 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6208): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0013 | 0/0 | 6212 | 3 | 3 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0014 | 0/0 | 6212 | 6 | 2 | 4 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0015 | 0/0 | 6210 | 4 | 0 | 2 | 0 | 1 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0017 | 0/0 | 6211 | 4 | 4 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0018 | 0/0 | 6212 | 5 | 1 | 0 | 3 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0020 | 0/0 | 6212 | 4 | 0 | 1 | 2 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0021 | 0/0 | 6212 | 4 | 4 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0022 | 0/0 | 6210 | 3 | 0 | 0 | 3 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0023 | 0/0 | 6210 | 3 | 0 | 2 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0025 | 0/0 | 6209 | 2 | 0 | 1 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6204): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0026 | 0/0 | 6210 | 2 | 0 | 0 | 2 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0027 | 0/0 | 6211 | 2 | 0 | 0 | 2 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0028 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0031 | 0/0 | 6212 | 2 | 0 | 1 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0032 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0033 | 0/0 | 6212 | 2 | 0 | 0 | 2 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0034 | 0/0 | 6213 | 2 | 2 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6208): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0035 | 0/0 | 6212 | 2 | 0 | 0 | 0 | 0 | 2 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0036 | 0/0 | 6212 | 2 | 0 | 1 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0037 | 0/0 | 6212 | 2 | 0 | 1 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0039 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0040 | 0/0 | 6210 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0041 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6204): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0042 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0043 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0044 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0046 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0048 | 0/0 | 6211 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0049 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6204): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0050 | 0/0 | 6210 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0051 | 0/0 | 6165 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6160): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0052 | 0/0 | 6206 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6201): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0053 | 0/0 | 6206 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6201): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0054 | 0/0 | 6210 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0055 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6204): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0056 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0057 | 0/0 | 6210 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0059 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0060 | 0/0 | 6212 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0064 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0066 | 0/0 | 6211 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0067 | 0/0 | 6211 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0071 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0072 | 0/0 | 6212 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0073 | 0/0 | 6212 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0074 | 0/0 | 6211 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0075 | 0/0 | 6211 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0076 | 0/0 | 6212 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0077 | 0/0 | 6211 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0078 | 0/0 | 6213 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6208): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0079 | 0/0 | 6212 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0001t0080 | 0/0 | 6212 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0002t0006 | 0/1 | 6167 | 11 | 4 | 0 | 6 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6162): Show |
chr2 | 200301693 | 200487264 |
| a0001c0002t0013 | 0/0 | 6212 | 5 | 5 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0002t0016 | 0/0 | 6165 | 5 | 5 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6160): Show |
chr2 | 200301693 | 200487264 |
| a0001c0002t0030 | 0/0 | 6213 | 2 | 2 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6208): Show |
chr2 | 200301693 | 200487264 |
| a0001c0002t0045 | 0/0 | 6165 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6160): Show |
chr2 | 200301693 | 200487264 |
| a0001c0002t0062 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0002t0069 | 0/0 | 6211 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0001c0002t0070 | 0/0 | 6167 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6162): Show |
chr2 | 200301693 | 200487264 |
| a0001c0002t0081 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0003t0001 | 0/0 | 6210 | 10 | 0 | 3 | 7 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0003t0003 | 0/0 | 6212 | 2 | 0 | 0 | 2 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0003t0024 | 0/0 | 6210 | 3 | 0 | 0 | 3 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0003t0028 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0003t0038 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0003t0061 | 0/0 | 6212 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0005t0011 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0001c0005t0029 | 0/0 | 6206 | 2 | 0 | 0 | 2 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6201): Show |
chr2 | 200301693 | 200487264 |
| a0001c0010t0065 | 0/0 | 6212 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0001c0013t0010 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0002c0004t0012 | 0/0 | 6213 | 5 | 5 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6208): Show |
chr2 | 200301693 | 200487264 |
| a0002c0004t0019 | 0/0 | 6211 | 4 | 4 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0002c0004t0063 | 0/0 | 6213 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6208): Show |
chr2 | 200301693 | 200487264 |
| a0002c0004t0068 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0003c0006t0017 | 0/0 | 6211 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6206): Show |
chr2 | 200301693 | 200487264 |
| a0003c0006t0032 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0003c0008t0058 | 0/0 | 6213 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6208): Show |
chr2 | 200301693 | 200487264 |
| a0004c0009t0003 | 0/0 | 6212 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6207): Show |
chr2 | 200301693 | 200487264 |
| a0005c0011t0001 | 0/0 | 6210 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0006c0007t0047 | 0/0 | 6210 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| a0007c0012t0015 | 0/0 | 6210 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | AGTTG others(6205): Show |
chr2 | 200301693 | 200487264 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0007g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0009g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0009g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0009g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0009g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0009g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0010g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0011g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0011g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0011g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0011g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0012g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0012g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0012g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0013g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0014g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0014g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0014g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0014g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0014g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0015g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0015g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0015g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0015g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0017g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0017g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0017g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0018g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0018g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0018g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0018g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0018g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0020g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0020g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0020g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0020g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0021g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0021g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0021g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0021g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0022g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0022g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0022g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0023g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0023g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0023g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0025g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0025g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0026g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0026g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0027g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0027g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0028g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0031g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0031g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0032g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0033g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0033g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0034g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0034g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0035g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0035g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0036g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0036g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0037g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0037g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0039g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0040g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0041g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0042g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0043g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0044g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0046g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0048g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0049g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0050g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0051g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0052g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0053g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0054g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0055g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0056g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0057g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0059g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0060g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0064g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0066g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0067g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0071g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0072g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0073g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0074g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0075g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0076g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0077g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0078g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0079g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0001t0080g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0013g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0013g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0013g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0016g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0016g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0016g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0016g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0030g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0030g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0045g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0062g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0069g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0070g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0002t0081g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0024g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0024g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0024g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0028g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0038g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0003t0061g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0005t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0005t0029g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0005t0029g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0010t0065g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0001c0013t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0019g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0019g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0019g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0019g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0063g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0002c0004t0068g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0003c0006t0017g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0003c0006t0032g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0003c0008t0058g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0004c0009t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0005c0011t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0006c0007t0047g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| a0007c0012t0015g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0036 | g0076 | EUR | GBR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00099 | hp2 | a0001 | c0001 | t0057 | g0298 | EUR | GBR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00408 | hp2 | a0001 | c0005 | t0011 | g0001 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00423 | hp1 | a0001 | c0003 | t0038 | g0168 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00438 | hp1 | a0001 | c0001 | t0080 | g0016 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0185 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0255 | EAS | CHS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00639 | hp2 | a0001 | c0001 | t0015 | g0188 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00733 | hp2 | a0001 | c0001 | t0008 | g0080 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0172 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00735 | hp2 | a0001 | c0001 | t0023 | g0208 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00738 | hp1 | a0001 | c0001 | t0053 | g0167 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00741 | hp1 | a0001 | c0001 | t0015 | g0297 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0152 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01070 | hp1 | a0001 | c0001 | t0014 | g0110 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0269 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0088 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01074 | hp2 | a0001 | c0001 | t0014 | g0050 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01099 | hp1 | a0001 | c0001 | t0014 | g0128 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01106 | hp1 | a0001 | c0001 | t0020 | g0106 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01106 | hp2 | a0001 | c0001 | t0023 | g0207 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01175 | hp2 | a0001 | c0001 | t0036 | g0034 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0161 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0217 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01243 | hp1 | a0003 | c0006 | t0017 | g0130 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01243 | hp2 | a0001 | c0001 | t0037 | g0060 | AMR | PUR | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01257 | hp1 | a0001 | c0001 | t0052 | g0164 | AMR | CLM | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01257 | hp2 | a0001 | c0001 | t0048 | g0221 | AMR | CLM | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0171 | AMR | CLM | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01361 | hp2 | a0001 | c0001 | t0014 | g0105 | AMR | CLM | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01496 | hp1 | a0001 | c0001 | t0025 | g0247 | AMR | CLM | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01496 | hp2 | a0001 | c0001 | t0077 | g0073 | AMR | CLM | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01517 | hp1 | a0001 | c0001 | t0076 | g0091 | EUR | IBS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0046 | EUR | IBS | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01884 | hp1 | a0001 | c0001 | t0059 | g0026 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01884 | hp2 | a0001 | c0002 | t0062 | g0107 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0153 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01891 | hp2 | a0001 | c0002 | t0081 | g0137 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0184 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01975 | hp1 | a0001 | c0001 | t0031 | g0052 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01975 | hp2 | a0001 | c0001 | t0009 | g0162 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0250 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01978 | hp2 | a0001 | c0001 | t0009 | g0155 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02004 | hp1 | a0001 | c0001 | t0009 | g0165 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0256 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02015 | hp1 | a0001 | c0001 | t0026 | g0236 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02015 | hp2 | a0001 | c0001 | t0018 | g0079 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0198 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02055 | hp2 | a0001 | c0001 | t0017 | g0087 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02056 | hp1 | a0001 | c0001 | t0020 | g0051 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02056 | hp2 | a0001 | c0001 | t0042 | g0189 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0229 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02129 | hp1 | a0001 | c0001 | t0020 | g0118 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02129 | hp2 | a0001 | c0001 | t0007 | g0218 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02135 | hp2 | a0001 | c0003 | t0024 | g0242 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02145 | hp1 | a0001 | c0013 | t0010 | g0005 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02145 | hp2 | a0003 | c0008 | t0058 | g0099 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02148 | hp1 | a0001 | c0001 | t0009 | g0166 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0289 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02155 | hp1 | a0001 | c0003 | t0024 | g0169 | EAS | CDX | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02155 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | CDX | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02165 | hp1 | a0001 | c0003 | t0024 | g0270 | EAS | CDX | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02165 | hp2 | a0001 | c0001 | t0056 | g0294 | EAS | CDX | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02258 | hp1 | a0001 | c0002 | t0030 | g0141 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02258 | hp2 | a0001 | c0002 | t0016 | g0279 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02280 | hp1 | a0001 | c0001 | t0034 | g0144 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02280 | hp2 | a0001 | c0002 | t0016 | g0280 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02293 | hp2 | a0001 | c0001 | t0009 | g0163 | AMR | PEL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02523 | hp1 | a0001 | c0001 | t0055 | g0293 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0191 | EAS | KHV | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02572 | hp1 | a0001 | c0002 | t0006 | g0019 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02572 | hp2 | a0001 | c0001 | t0021 | g0032 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02602 | hp1 | a0001 | c0001 | t0011 | g0248 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02602 | hp2 | a0001 | c0001 | t0008 | g0063 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02615 | hp1 | a0001 | c0001 | t0041 | g0283 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02615 | hp2 | a0001 | c0002 | t0070 | g0147 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0078 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0071 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02647 | hp2 | a0002 | c0004 | t0012 | g0132 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02717 | hp1 | a0001 | c0001 | t0064 | g0070 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02717 | hp2 | a0001 | c0002 | t0013 | g0104 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02723 | hp1 | a0001 | c0002 | t0006 | g0094 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02723 | hp2 | a0002 | c0004 | t0019 | g0285 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02735 | hp1 | a0001 | c0001 | t0049 | g0245 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02735 | hp2 | a0001 | c0010 | t0065 | g0004 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02738 | hp1 | a0001 | c0001 | t0020 | g0109 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02738 | hp2 | a0001 | c0001 | t0050 | g0203 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02809 | hp2 | a0001 | c0002 | t0006 | g0133 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02818 | hp1 | a0002 | c0004 | t0012 | g0020 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02818 | hp2 | a0001 | c0002 | t0016 | g0282 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02886 | hp1 | a0002 | c0004 | t0068 | g0002 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02886 | hp2 | a0002 | c0004 | t0019 | g0286 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02895 | hp1 | a0001 | c0002 | t0006 | g0093 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02895 | hp2 | a0002 | c0004 | t0063 | g0102 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02896 | hp1 | a0001 | c0001 | t0017 | g0143 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02896 | hp2 | a0003 | c0006 | t0032 | g0012 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02922 | hp1 | a0001 | c0001 | t0021 | g0075 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02922 | hp2 | a0002 | c0004 | t0019 | g0131 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02976 | hp1 | a0001 | c0001 | t0021 | g0014 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0096 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0136 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0007 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03139 | hp1 | a0004 | c0009 | t0003 | g0084 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0095 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0140 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03225 | hp1 | a0001 | c0002 | t0045 | g0291 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03225 | hp2 | a0001 | c0001 | t0014 | g0134 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03239 | hp2 | a0001 | c0001 | t0035 | g0059 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03453 | hp1 | a0001 | c0001 | t0071 | g0139 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03453 | hp2 | a0002 | c0004 | t0012 | g0098 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03486 | hp1 | a0001 | c0002 | t0013 | g0011 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03486 | hp2 | a0002 | c0004 | t0012 | g0101 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0272 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03490 | hp2 | a0001 | c0001 | t0074 | g0062 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03491 | hp1 | a0001 | c0001 | t0015 | g0212 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03491 | hp2 | a0001 | c0001 | t0054 | g0296 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03516 | hp1 | a0001 | c0002 | t0016 | g0284 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03516 | hp2 | a0001 | c0001 | t0018 | g0072 | AFR | ESN | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03540 | hp1 | a0002 | c0004 | t0019 | g0135 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03579 | hp1 | a0001 | c0001 | t0021 | g0074 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03579 | hp2 | a0001 | c0002 | t0016 | g0281 | AFR | MSL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03654 | hp2 | a0001 | c0001 | t0011 | g0295 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03669 | hp1 | a0001 | c0001 | t0035 | g0061 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | STU | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03688 | hp2 | a0001 | c0001 | t0011 | g0299 | SAS | STU | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03704 | hp1 | a0001 | c0001 | t0018 | g0055 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03831 | hp1 | a0001 | c0002 | t0069 | g0053 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0027 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03834 | hp2 | a0005 | c0011 | t0001 | g0222 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0033 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03942 | hp1 | a0001 | c0001 | t0031 | g0021 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | BEB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG04199 | hp1 | a0001 | c0001 | t0079 | g0081 | SAS | STU | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0240 | SAS | STU | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG04204 | hp1 | a0001 | c0001 | t0072 | g0057 | SAS | STU | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG04204 | hp2 | a0001 | c0001 | t0040 | g0197 | SAS | STU | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | STU | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG04228 | hp2 | a0001 | c0001 | t0073 | g0090 | SAS | STU | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18522 | hp1 | a0001 | c0001 | t0034 | g0146 | AFR | YRI | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0067 | AFR | YRI | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | CHB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18747 | hp2 | a0001 | c0003 | t0028 | g0210 | EAS | CHB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18906 | hp1 | a0001 | c0002 | t0030 | g0100 | AFR | YRI | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0068 | AFR | YRI | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0258 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18946 | hp2 | a0001 | c0003 | t0061 | g0127 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18950 | hp1 | a0001 | c0001 | t0011 | g0219 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18953 | hp1 | a0001 | c0002 | t0006 | g0115 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18954 | hp2 | a0001 | c0001 | t0025 | g0239 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18956 | hp1 | a0001 | c0001 | t0022 | g0264 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18956 | hp2 | a0001 | c0002 | t0006 | g0116 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18959 | hp1 | a0001 | c0001 | t0067 | g0037 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18959 | hp2 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18960 | hp1 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18960 | hp2 | a0001 | c0001 | t0039 | g0266 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18962 | hp1 | a0001 | c0001 | t0033 | g0025 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18962 | hp2 | a0001 | c0001 | t0046 | g0290 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0275 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18968 | hp1 | a0001 | c0001 | t0022 | g0267 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18975 | hp2 | a0001 | c0001 | t0026 | g0237 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18981 | hp1 | a0001 | c0002 | t0006 | g0117 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0278 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18984 | hp1 | a0001 | c0001 | t0023 | g0273 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18984 | hp2 | a0001 | c0001 | t0043 | g0277 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18985 | hp2 | a0001 | c0001 | t0011 | g0205 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18988 | hp1 | a0001 | c0003 | t0003 | g0119 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18988 | hp2 | a0001 | c0005 | t0029 | g0230 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18993 | hp2 | a0001 | c0005 | t0029 | g0231 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18998 | hp2 | a0006 | c0007 | t0047 | g0226 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19003 | hp1 | a0001 | c0002 | t0006 | g0112 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0054 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19005 | hp1 | a0001 | c0001 | t0078 | g0058 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19005 | hp2 | a0001 | c0001 | t0009 | g0160 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19010 | hp1 | a0001 | c0001 | t0009 | g0176 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19010 | hp2 | a0001 | c0001 | t0028 | g0206 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0086 | AFR | LWK | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19030 | hp2 | a0001 | c0002 | t0013 | g0138 | AFR | LWK | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0085 | AFR | LWK | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0129 | AFR | LWK | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19055 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19055 | hp2 | a0001 | c0001 | t0018 | g0126 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19056 | hp1 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19056 | hp2 | a0001 | c0002 | t0006 | g0114 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19058 | hp2 | a0001 | c0001 | t0011 | g0158 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19060 | hp2 | a0001 | c0001 | t0022 | g0263 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19062 | hp2 | a0001 | c0001 | t0066 | g0125 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19064 | hp2 | a0001 | c0001 | t0033 | g0038 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19068 | hp2 | a0001 | c0001 | t0044 | g0261 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19077 | hp1 | a0001 | c0001 | t0008 | g0015 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19077 | hp2 | a0001 | c0001 | t0060 | g0022 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19083 | hp1 | a0001 | c0001 | t0027 | g0178 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19083 | hp2 | a0001 | c0001 | t0027 | g0276 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0271 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19086 | hp1 | a0001 | c0003 | t0003 | g0123 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19240 | hp1 | a0001 | c0001 | t0075 | g0029 | AFR | YRI | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA19240 | hp2 | a0001 | c0002 | t0013 | g0124 | AFR | YRI | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA20752 | hp1 | a0001 | c0001 | t0037 | g0064 | EUR | TSI | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA20752 | hp2 | a0001 | c0001 | t0015 | g0170 | EUR | TSI | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA20905 | hp1 | a0007 | c0012 | t0015 | g0223 | SAS | GIH | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA20905 | hp2 | a0001 | c0001 | t0051 | g0149 | SAS | GIH | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02109 | hp1 | a0001 | c0001 | t0032 | g0010 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02109 | hp2 | a0001 | c0001 | t0013 | g0069 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02486 | hp1 | a0001 | c0002 | t0013 | g0006 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02486 | hp2 | a0002 | c0004 | t0012 | g0145 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0142 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0077 | AFR | ACB | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18955 | hp1 | a0001 | c0002 | t0006 | g0113 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| NA18955 | hp2 | a0001 | c0001 | t0018 | g0024 | EAS | JPT | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0006 | g0065 | REF | REF | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0010 | g0103 | REF | REF | SPATS2L_chr2_200301693_200487264 | SPATS2L | chr2 | 200301693 | 200487264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200419349 | C | A | 1 | a0006 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.298C>A | p.Pro100Thr | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/13 | 600/6212 | 298/1677 | 100/558 | chr2 | 200419349 | |||
| chr2:200419455 | C | T | 1 | a0007 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.404C>T | p.Ser135Leu | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/13 | 706/6212 | 404/1677 | 135/558 | chr2 | 200419455 | |||
| chr2:200439281 | C | A | 1 | a0003 | 3 | HG01243.hp1 HG02145.hp2 HG02896.hp2 |
missense_variant | MODERATE | c.605C>A | p.Pro202His | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/13 | 907/6212 | 605/1677 | 202/558 | chr2 | 200439281 | |||
| chr2:200469992 | G | A | 2 | a0002 a0004 |
12 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(9): Show |
missense_variant | MODERATE | c.1036G>A | p.Ala346Thr | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/13 | 1338/6212 | 1036/1677 | 346/558 | chr2 | 200469992 | |||
| chr2:200473014 | G | A | 1 | a0004 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.1243G>A | p.Ala415Thr | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/13 | 1545/6212 | 1243/1677 | 415/558 | chr2 | 200473014 | |||
| chr2:200477931 | G | A | 1 | a0005 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1577G>A | p.Ser526Asn | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1879/6212 | 1577/1677 | 526/558 | chr2 | 200477931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200389268 | G | T | 1 | a0001c0013 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.24G>T | p.Val8Val | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/13 | 326/6212 | 24/1677 | 8/558 | chr2 | 200389268 | |||
| chr2:200419366 | C | T | 1 | a0001c0005 | 3 | HG00408.hp2 NA18988.hp2 NA18993.hp2 |
synonymous_variant | LOW | c.315C>T | p.Asn105Asn | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/13 | 617/6212 | 315/1677 | 105/558 | chr2 | 200419366 | |||
| chr2:200472944 | A | C | 2 | a0001c0002 a0003c0008 |
28 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(25): Show |
synonymous_variant | LOW | c.1173A>C | p.Ser391Ser | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/13 | 1475/6212 | 1173/1677 | 391/558 | chr2 | 200472944 | |||
| chr2:200477860 | G | A | 1 | a0001c0010 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.1506G>A | p.Pro502Pro | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1808/6212 | 1506/1677 | 502/558 | chr2 | 200477860 | |||
| chr2:200477893 | C | T | 1 | a0001c0003 | 18 | HG00423.hp1 HG00621.hp2 HG01070.hp2 others(15): Show |
synonymous_variant | LOW | c.1539C>T | p.His513His | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1841/6212 | 1539/1677 | 513/558 | chr2 | 200477893 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200306746 | CTG | C | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(38): Show |
152 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
5_prime_UTR_variant | MODIFIER | c.-248_-247delTG | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/13 | 82497 | chr2 | 200306746 | ||||||
| chr2:200306774 | T | C | 1 | a0001c0003t0038 | 1 | HG00423.hp1 | 5_prime_UTR_variant | MODIFIER | c.-221T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/13 | 82471 | chr2 | 200306774 | ||||||
| chr2:200306870 | C | T | 1 | a0001c0001t0057 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/13 | 82375 | chr2 | 200306870 | ||||||
| chr2:200389233 | A | G | 26 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0018 others(23): Show |
54 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-12A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/13 | 12 | chr2 | 200389233 | ||||||
| chr2:200478056 | C | A | 1 | a0001c0001t0022 | 3 | NA18956.hp1 NA18968.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*25C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 25 | chr2 | 200478056 | ||||||
| chr2:200478059 | T | G | 2 | a0001c0002t0030 a0003c0008t0058 |
3 | HG02145.hp2 HG02258.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*28T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 28 | chr2 | 200478059 | ||||||
| chr2:200478679 | AATAT | A | 4 | a0001c0001t0009 a0001c0001t0052 a0001c0001t0053 others(1): Show |
13 | HG00738.hp1 HG00741.hp2 HG01257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*655_*658delATAT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 655 | INFO_REALIGN_3_PRIME | chr2 | 200478679 | |||||
| chr2:200478785 | A | G | 1 | a0001c0001t0071 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*754A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 754 | chr2 | 200478785 | ||||||
| chr2:200479049 | T | C | 1 | a0002c0004t0019 | 4 | HG02723.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1018T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1018 | chr2 | 200479049 | ||||||
| chr2:200479319 | C | G | 12 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0051 others(9): Show |
32 | HG01517.hp2 HG01891.hp2 HG02109.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1288C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1288 | chr2 | 200479319 | ||||||
| chr2:200479337 | C | T | 1 | a0001c0001t0051 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1306C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1306 | chr2 | 200479337 | ||||||
| chr2:200479408 | A | G | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0022 others(4): Show |
33 | HG00438.hp1 HG00544.hp1 HG00639.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1377A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1377 | chr2 | 200479408 | ||||||
| chr2:200479436 | G | A | 1 | a0001c0001t0039 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1405G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1405 | chr2 | 200479436 | ||||||
| chr2:200479437 | G | A | 7 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0031 others(4): Show |
16 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1406G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1406 | chr2 | 200479437 | ||||||
| chr2:200479498 | G | T | 1 | a0001c0001t0066 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1467G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1467 | chr2 | 200479498 | ||||||
| chr2:200479711 | A | G | 68 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(65): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1680A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1680 | chr2 | 200479711 | ||||||
| chr2:200479768 | G | A | 59 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(56): Show |
191 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1737G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1737 | chr2 | 200479768 | ||||||
| chr2:200479823 | A | G | 1 | a0001c0001t0057 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1792A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1792 | chr2 | 200479823 | ||||||
| chr2:200479964 | G | A | 1 | a0001c0001t0043 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1933G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1933 | chr2 | 200479964 | ||||||
| chr2:200480009 | C | T | 66 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(63): Show |
199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1978C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 1978 | chr2 | 200480009 | ||||||
| chr2:200480072 | G | C | 1 | a0001c0001t0048 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2041G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2041 | chr2 | 200480072 | ||||||
| chr2:200480083 | G | T | 3 | a0001c0001t0031 a0001c0001t0072 a0001c0001t0073 |
4 | HG01975.hp1 HG03942.hp1 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2052G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2052 | chr2 | 200480083 | ||||||
| chr2:200480152 | G | A | 2 | a0001c0002t0030 a0003c0008t0058 |
3 | HG02145.hp2 HG02258.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2121G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2121 | chr2 | 200480152 | ||||||
| chr2:200480170 | T | C | 1 | a0002c0004t0068 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2139T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2139 | chr2 | 200480170 | ||||||
| chr2:200480252 | G | A | 1 | a0001c0001t0044 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2221G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2221 | chr2 | 200480252 | ||||||
| chr2:200480338 | C | CT | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
227 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2324dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2325 | INFO_REALIGN_3_PRIME | chr2 | 200480338 | |||||
| chr2:200480338 | C | CTT | 8 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0027 others(5): Show |
26 | HG00735.hp1 HG01192.hp1 HG01361.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2323_*2324dupTT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2325 | INFO_REALIGN_3_PRIME | chr2 | 200480338 | |||||
| chr2:200480351 | TTTTTGAG others(37): Show |
T | 6 | a0001c0001t0006 a0001c0001t0051 a0001c0002t0006 others(3): Show |
19 | HG01517.hp2 HG02258.hp2 HG02280.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2325_*2368delGAGA others(40): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2325 | INFO_REALIGN_3_PRIME | chr2 | 200480351 | |||||
| chr2:200480550 | T | G | 1 | a0001c0001t0071 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2519T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2519 | chr2 | 200480550 | ||||||
| chr2:200480597 | C | T | 1 | a0001c0001t0042 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2566C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2566 | chr2 | 200480597 | ||||||
| chr2:200480648 | G | A | 2 | a0001c0001t0046 a0001c0001t0060 |
2 | NA18962.hp2 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2617G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2617 | chr2 | 200480648 | ||||||
| chr2:200480684 | C | T | 1 | a0001c0001t0059 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2653C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2653 | chr2 | 200480684 | ||||||
| chr2:200480923 | T | C | 1 | a0001c0001t0040 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2892T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 2892 | chr2 | 200480923 | ||||||
| chr2:200481048 | A | C | 1 | a0001c0010t0065 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3017A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3017 | chr2 | 200481048 | ||||||
| chr2:200481063 | A | G | 1 | a0001c0001t0071 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3032A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3032 | chr2 | 200481063 | ||||||
| chr2:200481074 | G | T | 1 | a0006c0007t0047 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3043G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3043 | chr2 | 200481074 | ||||||
| chr2:200481449 | T | A | 2 | a0001c0003t0024 a0001c0003t0061 |
4 | HG02135.hp2 HG02155.hp1 HG02165.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3418T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3418 | chr2 | 200481449 | ||||||
| chr2:200481529 | A | T | 1 | a0001c0001t0076 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3498A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3498 | chr2 | 200481529 | ||||||
| chr2:200481677 | T | C | 1 | a0001c0001t0056 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3646T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3646 | chr2 | 200481677 | ||||||
| chr2:200481683 | G | C | 1 | a0001c0001t0052 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3652G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3652 | chr2 | 200481683 | ||||||
| chr2:200481703 | T | C | 2 | a0001c0002t0016 a0001c0002t0070 |
6 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3672T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3672 | chr2 | 200481703 | ||||||
| chr2:200481711 | C | T | 1 | a0001c0001t0053 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3680C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3680 | chr2 | 200481711 | ||||||
| chr2:200481825 | C | T | 1 | a0002c0004t0063 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3794C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3794 | chr2 | 200481825 | ||||||
| chr2:200481826 | A | G | 2 | a0001c0001t0033 a0002c0004t0063 |
3 | HG02895.hp2 NA18962.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3795A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3795 | chr2 | 200481826 | ||||||
| chr2:200481827 | C | G | 1 | a0002c0004t0063 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3796C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3796 | chr2 | 200481827 | ||||||
| chr2:200481827 | C | T | 1 | a0001c0001t0033 | 2 | NA18962.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3796C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3796 | chr2 | 200481827 | ||||||
| chr2:200481828 | C | G | 1 | a0001c0001t0033 | 2 | NA18962.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3797C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3797 | chr2 | 200481828 | ||||||
| chr2:200481830 | G | A | 1 | a0001c0001t0033 | 2 | NA18962.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3799G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3799 | chr2 | 200481830 | ||||||
| chr2:200481921 | C | T | 2 | a0001c0001t0036 a0001c0001t0077 |
3 | HG00099.hp1 HG01175.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3890C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3890 | chr2 | 200481921 | ||||||
| chr2:200481969 | T | C | 1 | a0001c0001t0026 | 2 | HG02015.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3938T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3938 | chr2 | 200481969 | ||||||
| chr2:200482012 | C | T | 2 | a0001c0001t0064 a0001c0002t0030 |
3 | HG02258.hp1 HG02717.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3981C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 3981 | chr2 | 200482012 | ||||||
| chr2:200482031 | CA | C | 84 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(81): Show |
275 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*4009delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 4009 | INFO_REALIGN_3_PRIME | chr2 | 200482031 | |||||
| chr2:200482136 | A | C | 70 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(67): Show |
209 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*4105A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 4105 | chr2 | 200482136 | ||||||
| chr2:200482159 | CTT | C | 4 | a0001c0001t0017 a0001c0001t0041 a0001c0001t0075 others(1): Show |
7 | HG01243.hp1 HG02055.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4129_*4130delTT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 4129 | chr2 | 200482159 | ||||||
| chr2:200482203 | C | A | 4 | a0001c0001t0017 a0001c0001t0041 a0001c0001t0075 others(1): Show |
7 | HG01243.hp1 HG02055.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4172C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 13/13 | 4172 | chr2 | 200482203 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200306928 | C | T | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
splice_region_variant&intron_variant | LOW | c.-73+6C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200306928 | |||||||
| chr2:200307002 | G | A | 2 | a0001c0001t0003g0003 a0002c0004t0068g0002 |
2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-73+80G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307002 | |||||||
| chr2:200307004 | C | T | 7 | a0001c0001t0003g0003 a0001c0001t0017g0142 a0001c0001t0017g0143 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-73+82C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307004 | |||||||
| chr2:200307098 | G | C | 1 | a0001c0001t0005g0148 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-73+176G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307098 | |||||||
| chr2:200307132 | C | T | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73+210C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307132 | |||||||
| chr2:200307175 | C | T | 11 | a0001c0001t0010g0140 a0001c0001t0014g0134 a0001c0001t0017g0136 others(8): Show |
11 | HG01891.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73+253C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307175 | |||||||
| chr2:200307198 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-73+276G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307198 | |||||||
| chr2:200307286 | G | A | 5 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-73+364G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307286 | |||||||
| chr2:200307305 | G | T | 1 | a0001c0001t0002g0292 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-73+383G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307305 | |||||||
| chr2:200307314 | C | G | 1 | a0001c0002t0045g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-73+392C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307314 | |||||||
| chr2:200307363 | C | T | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-73+441C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307363 | |||||||
| chr2:200307418 | G | A | 8 | a0001c0001t0014g0134 a0001c0001t0017g0136 a0001c0002t0006g0133 others(5): Show |
8 | HG01891.hp2 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73+496G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307418 | |||||||
| chr2:200307462 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-73+540C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307462 | |||||||
| chr2:200307463 | A | G | 1 | a0001c0001t0046g0290 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-73+541A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307463 | |||||||
| chr2:200307801 | C | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0007g0289 |
3 | HG01943.hp1 HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-73+879C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307801 | |||||||
| chr2:200307804 | A | G | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-73+882A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307804 | |||||||
| chr2:200307895 | C | T | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73+973C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307895 | |||||||
| chr2:200307905 | G | C | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-73+983G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307905 | |||||||
| chr2:200307957 | A | G | 2 | a0001c0001t0010g0129 a0003c0006t0017g0130 |
2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-73+1035A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200307957 | |||||||
| chr2:200308032 | G | C | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0051g0149 |
3 | HG01123.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-73+1110G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308032 | |||||||
| chr2:200308136 | G | T | 6 | a0001c0001t0041g0283 a0001c0002t0016g0279 a0001c0002t0016g0280 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73+1214G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308136 | |||||||
| chr2:200308239 | G | GA | 102 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0040 others(99): Show |
102 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.-73+1329dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200308239 | ||||||
| chr2:200308239 | G | GAA | 153 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(150): Show |
153 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-73+1328_-73+1329d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200308239 | ||||||
| chr2:200308276 | C | T | 108 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(105): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-73+1354C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308276 | |||||||
| chr2:200308325 | A | G | 108 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(105): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-73+1403A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308325 | |||||||
| chr2:200308377 | C | G | 108 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(105): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-73+1455C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308377 | |||||||
| chr2:200308447 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-73+1525A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308447 | |||||||
| chr2:200308501 | A | G | 1 | a0001c0001t0014g0128 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-73+1579A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308501 | |||||||
| chr2:200308624 | T | TAC | 6 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(3): Show |
6 | HG00621.hp1 HG00741.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.-73+1720_-73+1721d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200308624 | ||||||
| chr2:200308624 | T | TACAC | 3 | a0001c0001t0042g0189 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02056.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-73+1718_-73+1721d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200308624 | ||||||
| chr2:200308647 | A | G | 1 | a0001c0003t0061g0127 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-73+1725A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308647 | |||||||
| chr2:200308824 | T | C | 1 | a0001c0002t0013g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-73+1902T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308824 | |||||||
| chr2:200308897 | A | G | 37 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(34): Show |
37 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-73+1975A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200308897 | |||||||
| chr2:200309034 | C | T | 1 | a0001c0001t0015g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-73+2112C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200309034 | |||||||
| chr2:200309044 | T | G | 1 | a0001c0001t0002g0195 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-73+2122T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200309044 | |||||||
| chr2:200309168 | A | G | 1 | a0001c0001t0046g0290 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-73+2246A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200309168 | |||||||
| chr2:200309325 | A | G | 2 | a0001c0001t0010g0096 a0001c0001t0012g0095 |
2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-73+2403A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200309325 | |||||||
| chr2:200309573 | G | C | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-73+2651G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200309573 | |||||||
| chr2:200309584 | T | G | 2 | a0001c0001t0008g0013 a0001c0001t0021g0014 |
2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-73+2662T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200309584 | |||||||
| chr2:200309748 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-73+2826T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200309748 | |||||||
| chr2:200309775 | C | T | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-73+2853C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200309775 | |||||||
| chr2:200309812 | A | G | 1 | a0001c0002t0006g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-73+2890A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200309812 | |||||||
| chr2:200310384 | TCTGAGCC others(4): Show |
T | 1 | a0001c0002t0006g0093 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-73+3466_-73+3476d others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200310384 | ||||||
| chr2:200310431 | G | A | 4 | a0001c0001t0008g0015 a0001c0001t0008g0017 a0001c0001t0008g0018 others(1): Show |
4 | HG00438.hp1 NA18946.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73+3509G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200310431 | |||||||
| chr2:200310473 | A | G | 1 | a0001c0001t0002g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-73+3551A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200310473 | |||||||
| chr2:200310519 | C | T | 2 | a0001c0010t0065g0004 a0003c0006t0032g0012 |
2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-73+3597C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200310519 | |||||||
| chr2:200310521 | C | T | 100 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0040 others(97): Show |
100 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.-73+3599C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200310521 | |||||||
| chr2:200310540 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-73+3618C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200310540 | |||||||
| chr2:200310588 | A | G | 1 | a0001c0002t0013g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-73+3666A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200310588 | |||||||
| chr2:200311050 | G | A | 2 | a0002c0004t0012g0132 a0002c0004t0019g0131 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-73+4128G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200311050 | |||||||
| chr2:200311096 | G | A | 1 | a0001c0001t0040g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-73+4174G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200311096 | |||||||
| chr2:200311108 | T | A | 37 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(34): Show |
37 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-73+4186T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200311108 | |||||||
| chr2:200311121 | T | A | 2 | a0001c0002t0006g0019 a0002c0004t0012g0020 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+4199T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200311121 | |||||||
| chr2:200311174 | C | G | 2 | a0001c0002t0013g0138 a0001c0002t0081g0137 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-73+4252C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200311174 | |||||||
| chr2:200311348 | C | T | 37 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(34): Show |
37 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-73+4426C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200311348 | |||||||
| chr2:200311362 | G | C | 1 | a0001c0002t0006g0093 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-73+4440G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200311362 | |||||||
| chr2:200311488 | A | G | 1 | a0001c0001t0027g0276 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-73+4566A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200311488 | |||||||
| chr2:200311982 | G | T | 1 | a0001c0001t0003g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-73+5060G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200311982 | |||||||
| chr2:200312157 | A | T | 1 | a0001c0003t0003g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-73+5235A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312157 | |||||||
| chr2:200312178 | C | T | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-73+5256C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312178 | |||||||
| chr2:200312221 | C | T | 100 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0040 others(97): Show |
100 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.-73+5299C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312221 | |||||||
| chr2:200312257 | C | A | 3 | a0001c0001t0002g0192 a0001c0001t0007g0190 a0001c0001t0007g0191 |
3 | HG02132.hp2 HG02523.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-73+5335C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312257 | |||||||
| chr2:200312288 | C | A | 1 | a0001c0001t0009g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-73+5366C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312288 | |||||||
| chr2:200312404 | C | T | 3 | a0001c0003t0001g0274 a0001c0003t0001g0275 a0001c0003t0001g0278 |
3 | NA18966.hp2 NA18982.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-73+5482C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312404 | |||||||
| chr2:200312443 | G | A | 1 | a0001c0001t0005g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-73+5521G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312443 | |||||||
| chr2:200312470 | T | C | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-73+5548T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312470 | |||||||
| chr2:200312479 | A | C | 24 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(21): Show |
24 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-73+5557A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312479 | |||||||
| chr2:200312685 | G | A | 2 | a0001c0001t0017g0142 a0001c0001t0017g0143 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-73+5763G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312685 | |||||||
| chr2:200312721 | G | A | 3 | a0001c0002t0006g0019 a0001c0002t0006g0094 a0002c0004t0012g0020 |
3 | HG02572.hp1 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+5799G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312721 | |||||||
| chr2:200312734 | G | A | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-73+5812G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312734 | |||||||
| chr2:200312930 | G | A | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-73+6008G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200312930 | |||||||
| chr2:200313058 | A | G | 1 | a0001c0001t0023g0273 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-73+6136A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200313058 | |||||||
| chr2:200313213 | G | C | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-73+6291G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200313213 | |||||||
| chr2:200313434 | G | A | 1 | a0001c0002t0013g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-73+6512G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200313434 | |||||||
| chr2:200313511 | C | G | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-73+6589C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200313511 | |||||||
| chr2:200313818 | C | A | 2 | a0001c0001t0002g0199 a0001c0001t0002g0200 |
2 | NA18957.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-73+6896C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200313818 | |||||||
| chr2:200314077 | C | T | 1 | a0001c0001t0007g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-73+7155C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200314077 | |||||||
| chr2:200314288 | A | G | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-73+7366A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200314288 | |||||||
| chr2:200314415 | G | A | 1 | a0001c0001t0040g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-73+7493G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200314415 | |||||||
| chr2:200314495 | T | C | 3 | a0001c0002t0006g0019 a0001c0002t0006g0094 a0002c0004t0012g0020 |
3 | HG02572.hp1 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+7573T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200314495 | |||||||
| chr2:200314507 | ACTGCT | A | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-73+7586_-73+7590d others(7): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200314507 | |||||||
| chr2:200314711 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG00544.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.-73+7789C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200314711 | |||||||
| chr2:200314712 | G | A | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73+7790G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200314712 | |||||||
| chr2:200314729 | G | C | 1 | a0001c0001t0031g0021 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-73+7807G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200314729 | |||||||
| chr2:200314823 | G | A | 2 | a0001c0001t0055g0293 a0001c0001t0056g0294 |
2 | HG02165.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-73+7901G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200314823 | |||||||
| chr2:200314837 | TA | T | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73+7922delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200314837 | ||||||
| chr2:200315300 | T | C | 145 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(142): Show |
145 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.-73+8378T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200315300 | |||||||
| chr2:200315337 | C | T | 1 | a0001c0001t0005g0271 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-73+8415C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200315337 | |||||||
| chr2:200315362 | A | G | 26 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0260 others(23): Show |
26 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-73+8440A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200315362 | |||||||
| chr2:200315497 | C | G | 1 | a0001c0001t0076g0091 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-73+8575C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200315497 | |||||||
| chr2:200315607 | C | T | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73+8685C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200315607 | |||||||
| chr2:200315856 | C | CA | 45 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0157 others(42): Show |
45 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-73+8954dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200315856 | ||||||
| chr2:200315856 | C | CAA | 139 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(136): Show |
139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-73+8953_-73+8954d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200315856 | ||||||
| chr2:200316024 | C | CA | 17 | a0001c0001t0001g0202 a0001c0001t0002g0187 a0001c0001t0002g0249 others(14): Show |
17 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.-73+9123dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200316024 | ||||||
| chr2:200316024 | CA | C | 12 | a0001c0001t0001g0244 a0001c0001t0002g0183 a0001c0001t0003g0121 others(9): Show |
12 | HG01943.hp2 HG02109.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.-73+9123delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200316024 | ||||||
| chr2:200316131 | G | A | 8 | a0001c0001t0003g0003 a0001c0001t0017g0142 a0001c0001t0017g0143 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73+9209G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200316131 | |||||||
| chr2:200316148 | G | T | 3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 |
3 | NA18969.hp2 NA19004.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-73+9226G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200316148 | |||||||
| chr2:200316555 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-73+9633C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200316555 | |||||||
| chr2:200316705 | T | C | 152 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(149): Show |
152 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-73+9783T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200316705 | |||||||
| chr2:200316744 | T | C | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-73+9822T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200316744 | |||||||
| chr2:200316748 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-73+9826G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200316748 | |||||||
| chr2:200317200 | A | G | 4 | a0001c0001t0003g0120 a0001c0001t0020g0118 a0001c0003t0003g0119 others(1): Show |
4 | HG02129.hp1 NA18946.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73+10278A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200317200 | |||||||
| chr2:200317222 | C | T | 3 | a0001c0001t0008g0088 a0001c0001t0008g0089 a0001c0001t0073g0090 |
3 | HG01074.hp1 HG02055.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-73+10300C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200317222 | |||||||
| chr2:200317321 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-73+10399T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200317321 | |||||||
| chr2:200317342 | C | T | 37 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(34): Show |
37 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-73+10420C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200317342 | |||||||
| chr2:200317473 | A | G | 1 | a0001c0001t0031g0021 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-73+10551A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200317473 | |||||||
| chr2:200317938 | G | A | 2 | a0001c0001t0010g0129 a0003c0006t0017g0130 |
2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-73+11016G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200317938 | |||||||
| chr2:200317972 | A | G | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-73+11050A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200317972 | |||||||
| chr2:200318054 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0011g0248 |
2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-73+11132C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318054 | |||||||
| chr2:200318090 | C | A | 1 | a0001c0002t0013g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-73+11168C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318090 | |||||||
| chr2:200318126 | G | T | 1 | a0001c0001t0017g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-73+11204G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318126 | |||||||
| chr2:200318133 | C | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0007g0289 |
3 | HG01943.hp1 HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-73+11211C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318133 | |||||||
| chr2:200318407 | C | T | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-72-11024C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318407 | |||||||
| chr2:200318557 | T | C | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-72-10874T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318557 | |||||||
| chr2:200318714 | A | G | 3 | a0001c0001t0013g0085 a0001c0001t0013g0086 a0004c0009t0003g0084 |
3 | HG03139.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-72-10717A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318714 | |||||||
| chr2:200318736 | G | C | 287 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.-72-10695G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318736 | |||||||
| chr2:200318753 | G | A | 2 | a0001c0001t0008g0027 a0001c0001t0011g0205 |
2 | HG03834.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-72-10678G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318753 | |||||||
| chr2:200318771 | G | A | 2 | a0001c0001t0004g0028 a0002c0004t0068g0002 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-72-10660G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318771 | |||||||
| chr2:200318817 | G | T | 2 | a0001c0001t0001g0179 a0001c0001t0027g0178 |
2 | HG02132.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-72-10614G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318817 | |||||||
| chr2:200318945 | G | A | 1 | a0001c0001t0075g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-72-10486G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318945 | |||||||
| chr2:200318978 | A | G | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-72-10453A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200318978 | |||||||
| chr2:200319116 | G | A | 4 | a0001c0001t0002g0192 a0001c0001t0005g0198 a0001c0001t0007g0190 others(1): Show |
4 | HG02027.hp2 HG02132.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-10315G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319116 | |||||||
| chr2:200319165 | G | A | 145 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(142): Show |
145 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.-72-10266G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319165 | |||||||
| chr2:200319340 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-72-10091G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319340 | |||||||
| chr2:200319393 | C | T | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-72-10038C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319393 | |||||||
| chr2:200319415 | A | C | 1 | a0001c0003t0024g0242 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-72-10016A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319415 | |||||||
| chr2:200319564 | C | CA | 6 | a0001c0001t0014g0134 a0001c0002t0006g0133 a0001c0002t0081g0137 others(3): Show |
6 | HG01891.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-72-9843dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200319564 | ||||||
| chr2:200319564 | CA | C | 159 | a0001c0001t0001g0179 a0001c0001t0001g0251 a0001c0001t0002g0150 others(156): Show |
159 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.-72-9843delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200319564 | ||||||
| chr2:200319564 | CAA | C | 109 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(106): Show |
109 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-72-9844_-72-9843d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200319564 | ||||||
| chr2:200319625 | T | C | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-72-9806T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319625 | |||||||
| chr2:200319629 | G | C | 1 | a0001c0001t0011g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-72-9802G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319629 | |||||||
| chr2:200319952 | C | T | 6 | a0001c0002t0013g0124 a0001c0002t0030g0100 a0002c0004t0012g0098 others(3): Show |
6 | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-72-9479C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319952 | |||||||
| chr2:200319981 | T | G | 1 | a0001c0001t0007g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-72-9450T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319981 | |||||||
| chr2:200319990 | A | G | 100 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0040 others(97): Show |
100 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.-72-9441A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200319990 | |||||||
| chr2:200320116 | G | C | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-72-9315G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200320116 | |||||||
| chr2:200320235 | T | C | 287 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.-72-9196T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200320235 | |||||||
| chr2:200320417 | A | G | 1 | a0001c0001t0050g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-72-9014A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200320417 | |||||||
| chr2:200320515 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-72-8916T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200320515 | |||||||
| chr2:200320770 | A | G | 1 | a0001c0001t0003g0120 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-72-8661A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200320770 | |||||||
| chr2:200321132 | A | C | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-8299A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200321132 | |||||||
| chr2:200321136 | G | A | 1 | a0001c0001t0004g0033 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-72-8295G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200321136 | |||||||
| chr2:200321196 | C | A | 152 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(149): Show |
152 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-72-8235C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200321196 | |||||||
| chr2:200321298 | C | T | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-72-8133C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200321298 | |||||||
| chr2:200321642 | A | T | 2 | a0001c0010t0065g0004 a0003c0006t0032g0012 |
2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-72-7789A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200321642 | |||||||
| chr2:200321849 | C | T | 108 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(105): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-72-7582C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200321849 | |||||||
| chr2:200321861 | A | G | 1 | a0002c0004t0012g0132 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-72-7570A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200321861 | |||||||
| chr2:200322120 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-72-7311C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200322120 | |||||||
| chr2:200322500 | A | G | 1 | a0001c0001t0059g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-72-6931A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200322500 | |||||||
| chr2:200322593 | C | T | 11 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(8): Show |
11 | HG00642.hp1 HG01993.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.-72-6838C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200322593 | |||||||
| chr2:200322607 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-72-6824T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200322607 | |||||||
| chr2:200322935 | A | G | 12 | a0001c0001t0003g0122 a0001c0001t0004g0108 a0001c0001t0004g0111 others(9): Show |
12 | HG02723.hp2 HG02886.hp2 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.-72-6496A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200322935 | |||||||
| chr2:200323052 | A | G | 100 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0040 others(97): Show |
100 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.-72-6379A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200323052 | |||||||
| chr2:200323151 | G | T | 1 | a0001c0003t0024g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-72-6280G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200323151 | |||||||
| chr2:200323240 | C | G | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-72-6191C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200323240 | |||||||
| chr2:200323374 | T | A | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-72-6057T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200323374 | |||||||
| chr2:200323374 | T | C | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-72-6057T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200323374 | |||||||
| chr2:200323529 | C | T | 2 | a0001c0001t0010g0129 a0003c0006t0017g0130 |
2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-72-5902C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200323529 | |||||||
| chr2:200323829 | A | C | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-72-5602A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200323829 | |||||||
| chr2:200324060 | G | A | 2 | a0001c0001t0017g0087 a0001c0002t0006g0093 |
2 | HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-72-5371G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200324060 | |||||||
| chr2:200324204 | C | T | 1 | a0001c0001t0007g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-72-5227C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200324204 | |||||||
| chr2:200324239 | G | A | 2 | a0001c0001t0023g0207 a0001c0001t0023g0208 |
2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-72-5192G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200324239 | |||||||
| chr2:200324321 | A | C | 2 | a0001c0001t0013g0085 a0001c0001t0013g0086 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-72-5110A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200324321 | |||||||
| chr2:200324502 | G | C | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-72-4929G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200324502 | |||||||
| chr2:200324835 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-72-4596T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200324835 | |||||||
| chr2:200325452 | C | T | 1 | a0001c0001t0011g0299 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-72-3979C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200325452 | |||||||
| chr2:200325535 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-72-3896C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200325535 | |||||||
| chr2:200325644 | G | T | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-3787G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200325644 | |||||||
| chr2:200325824 | A | G | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-72-3607A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200325824 | |||||||
| chr2:200325905 | G | A | 58 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(55): Show |
58 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-72-3526G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200325905 | |||||||
| chr2:200325927 | TA | T | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-72-3502delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200325927 | ||||||
| chr2:200326009 | G | A | 26 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(23): Show |
26 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-72-3422G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200326009 | |||||||
| chr2:200326012 | A | G | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-3419A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200326012 | |||||||
| chr2:200326254 | G | A | 20 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0260 others(17): Show |
20 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-3177G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200326254 | |||||||
| chr2:200326311 | A | G | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-72-3120A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200326311 | |||||||
| chr2:200326457 | G | T | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-2974G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200326457 | |||||||
| chr2:200326799 | C | T | 37 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(34): Show |
37 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-72-2632C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200326799 | |||||||
| chr2:200326901 | A | AT | 136 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(133): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-72-2505dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200326901 | ||||||
| chr2:200326901 | A | ATT | 24 | a0001c0001t0001g0232 a0001c0001t0001g0251 a0001c0001t0002g0177 others(21): Show |
24 | HG00099.hp2 HG00423.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-72-2506_-72-2505d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200326901 | ||||||
| chr2:200326901 | ATT | A | 13 | a0001c0001t0010g0129 a0001c0001t0014g0105 a0001c0001t0014g0110 others(10): Show |
13 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.-72-2506_-72-2505d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200326901 | ||||||
| chr2:200326901 | ATTT | A | 16 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(13): Show |
16 | HG02129.hp1 HG02738.hp1 NA18946.hp2 others(13): Show |
intron_variant | MODIFIER | c.-72-2507_-72-2505d others(5): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200326901 | ||||||
| chr2:200326902 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-72-2529T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200326902 | |||||||
| chr2:200327398 | C | T | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-72-2033C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200327398 | |||||||
| chr2:200327403 | C | CA | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-72-2017dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200327403 | ||||||
| chr2:200327421 | A | G | 32 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(29): Show |
32 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.-72-2010A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200327421 | |||||||
| chr2:200327484 | A | G | 2 | a0001c0001t0012g0077 a0001c0001t0012g0078 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-72-1947A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200327484 | |||||||
| chr2:200327597 | T | C | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-72-1834T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200327597 | |||||||
| chr2:200327860 | G | GCA | 153 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0202 others(150): Show |
153 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-72-1552_-72-1551d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200327860 | ||||||
| chr2:200327860 | G | GCACA | 31 | a0001c0001t0001g0196 a0001c0001t0003g0120 a0001c0001t0003g0121 others(28): Show |
31 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-72-1554_-72-1551d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 200327860 | ||||||
| chr2:200327881 | T | C | 2 | a0001c0010t0065g0004 a0003c0006t0032g0012 |
2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-72-1550T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200327881 | |||||||
| chr2:200327944 | A | G | 26 | a0001c0001t0001g0196 a0001c0001t0001g0204 a0001c0001t0001g0220 others(23): Show |
26 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-72-1487A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200327944 | |||||||
| chr2:200328258 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG00544.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.-72-1173C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200328258 | |||||||
| chr2:200328343 | T | A | 1 | a0001c0001t0014g0128 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-72-1088T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200328343 | |||||||
| chr2:200328426 | G | T | 5 | a0001c0002t0030g0100 a0002c0004t0012g0098 a0002c0004t0012g0101 others(2): Show |
5 | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72-1005G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200328426 | |||||||
| chr2:200328441 | T | C | 32 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(29): Show |
32 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.-72-990T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200328441 | |||||||
| chr2:200328578 | G | A | 1 | a0001c0002t0013g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-72-853G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200328578 | |||||||
| chr2:200328605 | C | T | 1 | a0001c0003t0028g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-72-826C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200328605 | |||||||
| chr2:200328650 | G | A | 108 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(105): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-72-781G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200328650 | |||||||
| chr2:200328774 | A | C | 1 | a0001c0001t0011g0219 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-72-657A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200328774 | |||||||
| chr2:200329172 | C | T | 2 | a0001c0010t0065g0004 a0003c0006t0032g0012 |
2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-72-259C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200329172 | |||||||
| chr2:200329307 | G | A | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-72-124G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 1/12 | chr2 | 200329307 | |||||||
| chr2:200329514 | T | G | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+34T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200329514 | |||||||
| chr2:200329556 | C | A | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-23+76C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200329556 | |||||||
| chr2:200329572 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-23+92T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200329572 | |||||||
| chr2:200329623 | T | G | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+143T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200329623 | |||||||
| chr2:200329762 | A | G | 2 | a0001c0001t0012g0077 a0001c0001t0012g0078 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-23+282A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200329762 | |||||||
| chr2:200329781 | C | CA | 41 | a0001c0001t0001g0225 a0001c0001t0001g0228 a0001c0001t0002g0227 others(38): Show |
41 | HG01884.hp1 HG02109.hp1 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.-23+314dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200329781 | ||||||
| chr2:200329781 | C | CAA | 119 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(116): Show |
119 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.-23+313_-23+314dup others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200329781 | ||||||
| chr2:200329781 | C | CAAA | 19 | a0001c0001t0001g0233 a0001c0001t0002g0180 a0001c0001t0002g0181 others(16): Show |
19 | HG00738.hp1 HG00741.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-23+312_-23+314dup others(3): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200329781 | ||||||
| chr2:200329783 | A | G | 1 | a0001c0001t0036g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-23+303A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200329783 | |||||||
| chr2:200329969 | C | T | 1 | a0001c0001t0027g0178 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-23+489C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200329969 | |||||||
| chr2:200330104 | C | G | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+624C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330104 | |||||||
| chr2:200330213 | C | CTGTTATT others(175): Show |
186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-23+733_-23+734ins others(182): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330213 | |||||||
| chr2:200330213 | C | CTGTTATT others(170): Show |
1 | a0001c0001t0002g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-23+733_-23+734ins others(177): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330213 | |||||||
| chr2:200330214 | C | G | 187 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(184): Show |
187 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.-23+734C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330214 | |||||||
| chr2:200330222 | A | T | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+742A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330222 | |||||||
| chr2:200330425 | A | G | 8 | a0001c0001t0004g0108 a0001c0002t0006g0112 a0001c0002t0006g0113 others(5): Show |
8 | NA18953.hp1 NA18955.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+945A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330425 | |||||||
| chr2:200330524 | C | T | 1 | a0001c0001t0014g0050 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-23+1044C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330524 | |||||||
| chr2:200330680 | G | A | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-23+1200G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330680 | |||||||
| chr2:200330799 | C | T | 1 | a0001c0001t0011g0205 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-23+1319C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330799 | |||||||
| chr2:200330879 | C | T | 87 | a0001c0001t0003g0030 a0001c0001t0003g0040 a0001c0001t0003g0041 others(84): Show |
87 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.-23+1399C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330879 | |||||||
| chr2:200330973 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-23+1493C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200330973 | |||||||
| chr2:200331040 | G | C | 1 | a0001c0001t0046g0290 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-23+1560G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200331040 | |||||||
| chr2:200331138 | A | G | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-23+1658A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200331138 | |||||||
| chr2:200331155 | C | T | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-23+1675C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200331155 | |||||||
| chr2:200331161 | C | T | 1 | a0001c0001t0059g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-23+1681C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200331161 | |||||||
| chr2:200331170 | A | G | 5 | a0001c0002t0030g0100 a0002c0004t0012g0098 a0002c0004t0012g0101 others(2): Show |
5 | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+1690A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200331170 | |||||||
| chr2:200331196 | A | G | 3 | a0001c0001t0002g0252 a0001c0001t0002g0262 a0001c0001t0002g0268 |
3 | HG00423.hp2 HG00544.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-23+1716A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200331196 | |||||||
| chr2:200331611 | T | C | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+2131T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200331611 | |||||||
| chr2:200331834 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-23+2354C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200331834 | |||||||
| chr2:200331929 | A | G | 3 | a0001c0001t0021g0032 a0001c0001t0021g0074 a0001c0001t0021g0075 |
3 | HG02572.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-23+2449A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200331929 | |||||||
| chr2:200332161 | AGAGAGG | A | 288 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.-23+2699_-23+2704d others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332161 | ||||||
| chr2:200332485 | G | A | 1 | a0001c0001t0004g0035 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-23+3005G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200332485 | |||||||
| chr2:200332747 | G | GA | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-23+3278dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332747 | ||||||
| chr2:200332755 | A | T | 1 | a0001c0002t0013g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-23+3275A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200332755 | |||||||
| chr2:200332772 | C | CTG | 4 | a0001c0001t0010g0129 a0001c0001t0036g0076 a0001c0001t0077g0073 others(1): Show |
4 | HG00099.hp1 HG01243.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+3314_-23+3315d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332772 | ||||||
| chr2:200332772 | C | CTGTG | 10 | a0001c0001t0009g0152 a0001c0001t0009g0153 a0001c0001t0009g0155 others(7): Show |
10 | HG00738.hp1 HG00741.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23+3312_-23+3315d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332772 | ||||||
| chr2:200332772 | C | CTGTGTG | 47 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0213 others(44): Show |
47 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.-23+3310_-23+3315d others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332772 | ||||||
| chr2:200332772 | C | CTGTGTGT others(1): Show |
85 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(82): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-23+3308_-23+3315d others(10): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332772 | ||||||
| chr2:200332772 | C | CTGTGTGT others(3): Show |
8 | a0001c0001t0001g0224 a0001c0001t0001g0232 a0001c0001t0001g0265 others(5): Show |
8 | HG00408.hp1 HG01175.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+3306_-23+3315d others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332772 | ||||||
| chr2:200332772 | C | CTGTGTGT others(5): Show |
2 | a0001c0002t0016g0279 a0001c0002t0045g0291 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+3304_-23+3315d others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332772 | ||||||
| chr2:200332772 | C | CTGTGTGT others(7): Show |
5 | a0001c0001t0041g0283 a0001c0002t0016g0280 a0001c0002t0016g0281 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+3302_-23+3315d others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332772 | ||||||
| chr2:200332772 | CTG | C | 6 | a0001c0002t0013g0124 a0001c0002t0030g0100 a0002c0004t0012g0098 others(3): Show |
6 | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+3314_-23+3315d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332772 | ||||||
| chr2:200332772 | CTGTG | C | 3 | a0001c0001t0017g0136 a0001c0002t0013g0138 a0001c0002t0081g0137 |
3 | HG01891.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-23+3312_-23+3315d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200332772 | ||||||
| chr2:200332796 | A | G | 1 | a0001c0001t0025g0239 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-23+3316A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200332796 | |||||||
| chr2:200332820 | G | T | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+3340G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200332820 | |||||||
| chr2:200332946 | G | A | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+3466G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200332946 | |||||||
| chr2:200333093 | C | G | 101 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0040 others(98): Show |
101 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.-23+3613C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333093 | |||||||
| chr2:200333122 | C | CA | 8 | a0001c0001t0002g0246 a0001c0001t0004g0036 a0001c0001t0005g0198 others(5): Show |
8 | HG02027.hp2 HG02647.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+3652dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200333122 | ||||||
| chr2:200333335 | CT | C | 131 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(128): Show |
131 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.-23+3868delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200333335 | ||||||
| chr2:200333335 | CTTT | C | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+3866_-23+3868d others(5): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200333335 | ||||||
| chr2:200333428 | G | T | 1 | a0007c0012t0015g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-23+3948G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333428 | |||||||
| chr2:200333431 | T | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0220 a0001c0001t0001g0232 |
3 | HG00733.hp1 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-23+3951T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333431 | |||||||
| chr2:200333478 | T | A | 1 | a0001c0001t0004g0036 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-23+3998T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333478 | |||||||
| chr2:200333504 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-23+4024T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333504 | |||||||
| chr2:200333543 | G | A | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-23+4063G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333543 | |||||||
| chr2:200333567 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-23+4087A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333567 | |||||||
| chr2:200333619 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-23+4139A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333619 | |||||||
| chr2:200333748 | T | C | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-23+4268T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333748 | |||||||
| chr2:200333800 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-23+4320G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333800 | |||||||
| chr2:200333900 | CATT | C | 145 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(142): Show |
145 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.-23+4421_-23+4423d others(5): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200333900 | |||||||
| chr2:200334138 | A | T | 1 | a0001c0001t0002g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-23+4658A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334138 | |||||||
| chr2:200334199 | C | T | 1 | a0001c0001t0005g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-23+4719C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334199 | |||||||
| chr2:200334492 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-23+5012G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334492 | |||||||
| chr2:200334495 | CAGA | C | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+5021_-23+5023d others(5): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200334495 | ||||||
| chr2:200334508 | T | C | 1 | a0001c0001t0007g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-23+5028T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334508 | |||||||
| chr2:200334564 | G | A | 26 | a0001c0001t0001g0196 a0001c0001t0001g0204 a0001c0001t0001g0220 others(23): Show |
26 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-23+5084G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334564 | |||||||
| chr2:200334653 | A | G | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+5173A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334653 | |||||||
| chr2:200334860 | C | G | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-23+5380C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334860 | |||||||
| chr2:200334874 | A | C | 1 | a0001c0001t0044g0261 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-23+5394A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334874 | |||||||
| chr2:200334944 | C | T | 1 | a0001c0001t0075g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-23+5464C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334944 | |||||||
| chr2:200334945 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5465G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334945 | |||||||
| chr2:200334948 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5468A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334948 | |||||||
| chr2:200334950 | G | C | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5470G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334950 | |||||||
| chr2:200334952 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5472C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334952 | |||||||
| chr2:200334954 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5474C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334954 | |||||||
| chr2:200334955 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5475C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334955 | |||||||
| chr2:200334956 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5476A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334956 | |||||||
| chr2:200334957 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5477G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334957 | |||||||
| chr2:200334958 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5478C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334958 | |||||||
| chr2:200334962 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5482G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334962 | |||||||
| chr2:200334965 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5485C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334965 | |||||||
| chr2:200334970 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5490G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334970 | |||||||
| chr2:200334971 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5491G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334971 | |||||||
| chr2:200334972 | C | T | 31 | a0001c0001t0001g0216 a0001c0001t0003g0120 a0001c0001t0003g0121 others(28): Show |
31 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-23+5492C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334972 | |||||||
| chr2:200334975 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5495A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334975 | |||||||
| chr2:200334976 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5496G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334976 | |||||||
| chr2:200334977 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5497G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334977 | |||||||
| chr2:200334978 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5498A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334978 | |||||||
| chr2:200334999 | C | G | 6 | a0001c0002t0013g0124 a0001c0002t0030g0100 a0002c0004t0012g0098 others(3): Show |
6 | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+5519C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334999 | |||||||
| chr2:200334999 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-23+5519C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200334999 | |||||||
| chr2:200335108 | T | C | 37 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(34): Show |
37 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-23+5628T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200335108 | |||||||
| chr2:200335121 | G | A | 4 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(1): Show |
4 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+5641G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200335121 | |||||||
| chr2:200335381 | A | T | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-23+5901A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200335381 | |||||||
| chr2:200335393 | G | A | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-23+5913G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200335393 | |||||||
| chr2:200335393 | G | GA | 39 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0003g0066 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+5923dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200335393 | ||||||
| chr2:200335393 | GA | G | 108 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(105): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-23+5923delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200335393 | ||||||
| chr2:200335400 | A | G | 1 | a0002c0004t0019g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-23+5920A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200335400 | |||||||
| chr2:200335417 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-23+5937G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200335417 | |||||||
| chr2:200335723 | T | A | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-23+6243T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200335723 | |||||||
| chr2:200335971 | T | A | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+6491T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200335971 | |||||||
| chr2:200336069 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-23+6589T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336069 | |||||||
| chr2:200336095 | A | G | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-23+6615A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336095 | |||||||
| chr2:200336106 | A | G | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+6626A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336106 | |||||||
| chr2:200336170 | G | A | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+6690G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336170 | |||||||
| chr2:200336308 | G | T | 1 | a0001c0001t0018g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-23+6828G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336308 | |||||||
| chr2:200336322 | A | C | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+6842A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336322 | |||||||
| chr2:200336392 | A | G | 1 | a0001c0001t0044g0261 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-23+6912A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336392 | |||||||
| chr2:200336407 | T | A | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-23+6927T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336407 | |||||||
| chr2:200336408 | A | T | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-23+6928A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336408 | |||||||
| chr2:200336450 | G | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-23+6970G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336450 | |||||||
| chr2:200336467 | T | G | 218 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-23+6987T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336467 | |||||||
| chr2:200336930 | AT | A | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+7458delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200336930 | ||||||
| chr2:200336941 | A | G | 3 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
3 | HG03098.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-23+7461A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200336941 | |||||||
| chr2:200337126 | A | G | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-23+7646A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200337126 | |||||||
| chr2:200337136 | T | A | 1 | a0001c0002t0016g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-23+7656T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200337136 | |||||||
| chr2:200337338 | C | G | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+7858C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200337338 | |||||||
| chr2:200338023 | T | C | 1 | a0001c0001t0005g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-23+8543T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200338023 | |||||||
| chr2:200338256 | C | T | 1 | a0001c0001t0059g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-23+8776C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200338256 | |||||||
| chr2:200338342 | A | G | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-23+8862A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200338342 | |||||||
| chr2:200338385 | T | C | 3 | a0001c0001t0002g0252 a0001c0001t0002g0262 a0001c0001t0002g0268 |
3 | HG00423.hp2 HG00544.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-23+8905T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200338385 | |||||||
| chr2:200338387 | T | C | 26 | a0001c0001t0001g0196 a0001c0001t0001g0204 a0001c0001t0001g0220 others(23): Show |
26 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-23+8907T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200338387 | |||||||
| chr2:200338634 | T | A | 1 | a0002c0004t0019g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-23+9154T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200338634 | |||||||
| chr2:200339137 | A | G | 1 | a0001c0001t0003g0049 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-23+9657A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339137 | |||||||
| chr2:200339143 | A | T | 1 | a0001c0001t0079g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-23+9663A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339143 | |||||||
| chr2:200339369 | G | T | 1 | a0001c0001t0009g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+9889G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339369 | |||||||
| chr2:200339374 | C | T | 1 | a0001c0001t0076g0091 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-23+9894C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339374 | |||||||
| chr2:200339634 | G | A | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+10154G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339634 | |||||||
| chr2:200339658 | A | T | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-23+10178A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339658 | |||||||
| chr2:200339731 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-23+10251A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339731 | |||||||
| chr2:200339761 | T | A | 1 | a0001c0001t0025g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-23+10281T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339761 | |||||||
| chr2:200339806 | A | T | 186 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-23+10326A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339806 | |||||||
| chr2:200339852 | G | C | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-23+10372G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339852 | |||||||
| chr2:200339853 | G | T | 1 | a0001c0001t0002g0150 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-23+10373G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339853 | |||||||
| chr2:200339971 | C | T | 3 | a0001c0001t0004g0028 a0001c0001t0031g0021 a0002c0004t0068g0002 |
3 | HG02809.hp1 HG02886.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-23+10491C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200339971 | |||||||
| chr2:200340024 | G | A | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+10544G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200340024 | |||||||
| chr2:200340078 | G | A | 5 | a0001c0001t0017g0087 a0001c0002t0006g0019 a0001c0002t0006g0093 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+10598G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200340078 | |||||||
| chr2:200340101 | A | G | 2 | a0001c0010t0065g0004 a0003c0006t0032g0012 |
2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-23+10621A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200340101 | |||||||
| chr2:200340139 | G | A | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+10659G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200340139 | |||||||
| chr2:200340618 | C | T | 26 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0260 others(23): Show |
26 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-23+11138C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200340618 | |||||||
| chr2:200340659 | C | T | 2 | a0001c0001t0010g0129 a0003c0006t0017g0130 |
2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-23+11179C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200340659 | |||||||
| chr2:200340979 | A | G | 8 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0174 others(5): Show |
8 | HG00642.hp1 HG01993.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23+11499A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200340979 | |||||||
| chr2:200340992 | C | T | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-23+11512C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200340992 | |||||||
| chr2:200341089 | C | T | 4 | a0001c0001t0017g0087 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+11609C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200341089 | |||||||
| chr2:200341557 | G | A | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-23+12077G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200341557 | |||||||
| chr2:200341572 | CTG | C | 156 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(153): Show |
156 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-23+12096_-23+1209 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200341572 | ||||||
| chr2:200341653 | A | G | 2 | a0001c0001t0010g0071 a0001c0001t0064g0070 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-23+12173A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200341653 | |||||||
| chr2:200341691 | A | AT | 125 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(122): Show |
125 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-23+12228dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200341691 | ||||||
| chr2:200341691 | A | ATT | 41 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0251 others(38): Show |
41 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-23+12227_-23+1222 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200341691 | ||||||
| chr2:200341728 | C | T | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+12248C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200341728 | |||||||
| chr2:200341738 | G | GGAGT | 3 | a0001c0001t0003g0097 a0001c0001t0008g0067 a0001c0001t0018g0072 |
3 | HG03516.hp2 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-23+12260_-23+1226 others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200341738 | ||||||
| chr2:200341815 | G | A | 1 | a0001c0001t0031g0052 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-23+12335G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200341815 | |||||||
| chr2:200341962 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0043g0277 |
2 | HG00438.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-23+12482A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200341962 | |||||||
| chr2:200341980 | G | T | 5 | a0001c0001t0003g0003 a0001c0001t0017g0142 a0001c0001t0017g0143 others(2): Show |
5 | HG02559.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+12500G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200341980 | |||||||
| chr2:200341983 | C | T | 160 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(157): Show |
160 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.-23+12503C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200341983 | |||||||
| chr2:200342100 | T | C | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+12620T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200342100 | |||||||
| chr2:200342247 | G | A | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+12767G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200342247 | |||||||
| chr2:200342488 | T | C | 3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 |
3 | NA18969.hp2 NA19004.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-23+13008T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200342488 | |||||||
| chr2:200342538 | C | G | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-23+13058C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200342538 | |||||||
| chr2:200343063 | C | T | 1 | a0001c0002t0013g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-23+13583C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200343063 | |||||||
| chr2:200343085 | A | T | 222 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.-23+13605A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200343085 | |||||||
| chr2:200343153 | A | G | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+13673A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200343153 | |||||||
| chr2:200343510 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-23+14030A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200343510 | |||||||
| chr2:200343837 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-23+14357C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200343837 | |||||||
| chr2:200343886 | A | G | 2 | a0001c0010t0065g0004 a0003c0006t0032g0012 |
2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-23+14406A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200343886 | |||||||
| chr2:200343969 | A | C | 188 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.-23+14489A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200343969 | |||||||
| chr2:200344047 | T | A | 16 | a0001c0001t0002g0157 a0001c0001t0003g0040 a0001c0001t0003g0041 others(13): Show |
16 | HG02056.hp1 HG02109.hp1 HG04184.hp2 others(13): Show |
intron_variant | MODIFIER | c.-23+14567T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344047 | |||||||
| chr2:200344048 | A | T | 161 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-23+14568A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344048 | |||||||
| chr2:200344049 | A | T | 4 | a0001c0001t0003g0121 a0001c0001t0011g0248 a0001c0002t0016g0284 others(1): Show |
4 | HG02602.hp1 HG03516.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+14569A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344049 | |||||||
| chr2:200344055 | A | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-23+14575A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344055 | |||||||
| chr2:200344124 | G | A | 2 | a0001c0001t0034g0144 a0002c0004t0012g0145 |
2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-23+14644G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344124 | |||||||
| chr2:200344384 | C | T | 2 | a0001c0001t0002g0151 a0001c0001t0051g0149 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-23+14904C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344384 | |||||||
| chr2:200344496 | T | C | 30 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(27): Show |
30 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+15016T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344496 | |||||||
| chr2:200344520 | C | T | 2 | a0001c0001t0002g0151 a0001c0001t0051g0149 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-23+15040C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344520 | |||||||
| chr2:200344888 | A | G | 2 | a0001c0010t0065g0004 a0003c0006t0032g0012 |
2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-23+15408A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344888 | |||||||
| chr2:200344913 | G | T | 1 | a0001c0001t0025g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-23+15433G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344913 | |||||||
| chr2:200344981 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-23+15501C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200344981 | |||||||
| chr2:200345388 | A | G | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+15908A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200345388 | |||||||
| chr2:200346095 | T | C | 1 | a0001c0001t0009g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-23+16615T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200346095 | |||||||
| chr2:200346761 | A | G | 18 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(15): Show |
18 | HG01243.hp1 HG02129.hp1 HG02738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+17281A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200346761 | |||||||
| chr2:200346882 | C | T | 58 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(55): Show |
58 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-23+17402C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200346882 | |||||||
| chr2:200346993 | A | G | 99 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0040 others(96): Show |
99 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.-23+17513A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200346993 | |||||||
| chr2:200347805 | G | A | 12 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(9): Show |
12 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+18325G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200347805 | |||||||
| chr2:200348068 | A | G | 57 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0003g0120 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-23+18588A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348068 | |||||||
| chr2:200348187 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-23+18707G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348187 | |||||||
| chr2:200348316 | T | C | 2 | a0001c0001t0013g0085 a0001c0001t0013g0086 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-23+18836T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348316 | |||||||
| chr2:200348414 | A | G | 3 | a0001c0001t0008g0063 a0001c0001t0008g0080 a0001c0001t0074g0062 |
3 | HG00733.hp2 HG02602.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-23+18934A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348414 | |||||||
| chr2:200348429 | T | G | 1 | a0001c0003t0038g0168 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-23+18949T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348429 | |||||||
| chr2:200348509 | G | C | 1 | a0001c0001t0020g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-23+19029G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348509 | |||||||
| chr2:200348605 | G | A | 2 | a0001c0001t0001g0260 a0001c0001t0043g0277 |
2 | HG00438.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-23+19125G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348605 | |||||||
| chr2:200348784 | A | T | 206 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.-23+19304A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348784 | |||||||
| chr2:200348789 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-23+19309T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348789 | |||||||
| chr2:200348811 | C | T | 12 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(9): Show |
12 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+19331C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348811 | |||||||
| chr2:200348885 | GA | G | 7 | a0001c0001t0002g0151 a0001c0001t0004g0043 a0001c0001t0007g0272 others(4): Show |
7 | HG02976.hp2 HG03209.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+19421delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200348885 | ||||||
| chr2:200348902 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-23+19422T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200348902 | |||||||
| chr2:200349319 | G | C | 1 | a0001c0002t0006g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-23+19839G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200349319 | |||||||
| chr2:200349348 | C | A | 188 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(185): Show |
188 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.-23+19868C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200349348 | |||||||
| chr2:200349505 | G | C | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-23+20025G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200349505 | |||||||
| chr2:200349562 | C | T | 7 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(4): Show |
7 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+20082C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200349562 | |||||||
| chr2:200349605 | T | A | 1 | a0001c0001t0002g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-23+20125T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200349605 | |||||||
| chr2:200349665 | G | A | 18 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(15): Show |
18 | HG01243.hp1 HG02129.hp1 HG02738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+20185G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200349665 | |||||||
| chr2:200349871 | A | G | 220 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-23+20391A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200349871 | |||||||
| chr2:200350143 | G | A | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+20663G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200350143 | |||||||
| chr2:200350477 | T | G | 2 | a0001c0001t0008g0067 a0001c0001t0018g0072 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-23+20997T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200350477 | |||||||
| chr2:200350600 | T | C | 206 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.-23+21120T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200350600 | |||||||
| chr2:200350755 | C | T | 1 | a0001c0003t0003g0119 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-23+21275C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200350755 | |||||||
| chr2:200350851 | G | A | 7 | a0001c0001t0011g0295 a0001c0001t0011g0299 a0001c0001t0015g0297 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+21371G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200350851 | |||||||
| chr2:200350880 | G | A | 12 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(9): Show |
12 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+21400G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200350880 | |||||||
| chr2:200350956 | A | G | 1 | a0001c0001t0010g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-23+21476A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200350956 | |||||||
| chr2:200350990 | A | G | 2 | a0001c0001t0015g0170 a0001c0001t0015g0188 |
2 | HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-23+21510A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200350990 | |||||||
| chr2:200351151 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0005g0217 |
2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-23+21671A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200351151 | |||||||
| chr2:200351366 | A | G | 2 | a0001c0001t0032g0010 a0003c0006t0032g0012 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-23+21886A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200351366 | |||||||
| chr2:200351413 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-23+21933A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200351413 | |||||||
| chr2:200351557 | C | T | 26 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(23): Show |
26 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-23+22077C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200351557 | |||||||
| chr2:200351664 | A | T | 1 | a0001c0001t0014g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-23+22184A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200351664 | |||||||
| chr2:200351694 | G | A | 1 | a0001c0001t0059g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-23+22214G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200351694 | |||||||
| chr2:200351712 | A | AT | 39 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+22241dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200351712 | ||||||
| chr2:200352309 | GTTTTTAT others(5): Show |
G | 1 | a0001c0001t0008g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-23+22831_-23+2284 others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352309 | ||||||
| chr2:200352310 | TTTTTATA others(4): Show |
T | 1 | a0001c0001t0012g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-23+22832_-23+2284 others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352310 | ||||||
| chr2:200352311 | T | TTATATAT others(9): Show |
1 | a0001c0001t0010g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-23+22832_-23+2283 others(20): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTA | T | 6 | a0001c0001t0003g0003 a0001c0001t0004g0035 a0001c0001t0013g0086 others(3): Show |
6 | HG01070.hp1 HG02809.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2283 others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATA | T | 9 | a0001c0001t0004g0039 a0001c0001t0010g0007 a0001c0001t0013g0085 others(6): Show |
9 | HG01106.hp1 HG02280.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2283 others(10): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(1): Show |
T | 6 | a0001c0001t0008g0067 a0001c0001t0021g0075 a0001c0001t0033g0038 others(3): Show |
6 | HG02145.hp1 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2284 others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(3): Show |
T | 2 | a0001c0001t0004g0033 a0001c0001t0020g0051 |
2 | HG02056.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-23+22833_-23+2284 others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(5): Show |
T | 14 | a0001c0001t0003g0092 a0001c0001t0006g0046 a0001c0001t0012g0077 others(11): Show |
14 | HG01074.hp2 HG01099.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2284 others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(7): Show |
T | 14 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0004g0036 others(11): Show |
14 | HG00642.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2284 others(18): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(9): Show |
T | 16 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(13): Show |
16 | HG02717.hp1 HG02818.hp1 HG03540.hp2 others(13): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2284 others(20): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(11): Show |
T | 5 | a0001c0001t0004g0044 a0001c0001t0004g0047 a0001c0002t0013g0006 others(2): Show |
5 | HG00639.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2285 others(22): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(13): Show |
T | 2 | a0001c0001t0075g0029 a0001c0010t0065g0004 |
2 | HG02735.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-23+22833_-23+2285 others(24): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(17): Show |
T | 2 | a0001c0001t0010g0096 a0001c0001t0012g0095 |
2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-23+22833_-23+2285 others(28): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(23): Show |
T | 2 | a0001c0001t0059g0026 a0002c0004t0019g0135 |
2 | HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-23+22833_-23+2286 others(34): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(25): Show |
T | 3 | a0001c0001t0001g0204 a0001c0001t0032g0010 a0001c0003t0061g0127 |
3 | HG00733.hp1 HG02109.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-23+22833_-23+2286 others(36): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(27): Show |
T | 26 | a0001c0001t0001g0196 a0001c0001t0001g0220 a0001c0001t0001g0224 others(23): Show |
26 | HG00408.hp1 HG00735.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2286 others(38): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(29): Show |
T | 32 | a0001c0001t0002g0241 a0001c0001t0003g0120 a0001c0001t0003g0121 others(29): Show |
32 | HG00408.hp2 HG00621.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2286 others(40): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(31): Show |
T | 148 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0202 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-23+22833_-23+2287 others(42): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352311 | TTTTATAT others(37): Show |
T | 1 | a0001c0001t0010g0009 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-23+22833_-23+2287 others(48): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200352311 | ||||||
| chr2:200352313 | T | A | 4 | a0001c0001t0004g0023 a0001c0001t0010g0008 a0001c0002t0006g0093 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+22833T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200352313 | |||||||
| chr2:200352371 | A | G | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+22891A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200352371 | |||||||
| chr2:200352385 | C | T | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+22905C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200352385 | |||||||
| chr2:200353021 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-23+23541T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200353021 | |||||||
| chr2:200353102 | G | T | 222 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.-23+23622G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200353102 | |||||||
| chr2:200353192 | A | C | 1 | a0001c0001t0008g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-23+23712A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200353192 | |||||||
| chr2:200353525 | C | T | 2 | a0001c0001t0010g0096 a0001c0001t0012g0095 |
2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-23+24045C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200353525 | |||||||
| chr2:200353656 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-23+24176C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200353656 | |||||||
| chr2:200353714 | A | G | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-23+24234A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200353714 | |||||||
| chr2:200353717 | G | A | 2 | a0001c0010t0065g0004 a0003c0006t0032g0012 |
2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-23+24237G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200353717 | |||||||
| chr2:200354334 | C | T | 2 | a0001c0001t0003g0122 a0001c0001t0004g0111 |
2 | NA18971.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-23+24854C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200354334 | |||||||
| chr2:200354388 | T | C | 2 | a0001c0001t0010g0096 a0001c0001t0012g0095 |
2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-23+24908T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200354388 | |||||||
| chr2:200354507 | C | A | 39 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+25027C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200354507 | |||||||
| chr2:200354607 | C | CA | 56 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(53): Show |
56 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.-23+25136dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200354607 | ||||||
| chr2:200354617 | G | A | 288 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.-23+25137G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200354617 | |||||||
| chr2:200355001 | A | G | 1 | a0001c0002t0006g0117 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-23+25521A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200355001 | |||||||
| chr2:200355020 | G | A | 3 | a0001c0001t0021g0032 a0001c0001t0021g0074 a0001c0001t0021g0075 |
3 | HG02572.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-23+25540G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200355020 | |||||||
| chr2:200355315 | G | A | 1 | a0001c0001t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-23+25835G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200355315 | |||||||
| chr2:200355551 | T | C | 1 | a0001c0001t0042g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-23+26071T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200355551 | |||||||
| chr2:200355562 | G | A | 1 | a0001c0001t0010g0009 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-23+26082G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200355562 | |||||||
| chr2:200355766 | A | G | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+26286A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200355766 | |||||||
| chr2:200356422 | G | A | 1 | a0001c0001t0017g0142 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-23+26942G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200356422 | |||||||
| chr2:200356474 | G | T | 1 | a0001c0001t0004g0036 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-23+26994G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200356474 | |||||||
| chr2:200356495 | A | G | 5 | a0001c0001t0003g0003 a0001c0001t0017g0142 a0001c0001t0017g0143 others(2): Show |
5 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+27015A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200356495 | |||||||
| chr2:200356516 | C | A | 2 | a0001c0002t0013g0104 a0002c0004t0012g0101 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-23+27036C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200356516 | |||||||
| chr2:200356627 | A | T | 37 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(34): Show |
37 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-23+27147A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200356627 | |||||||
| chr2:200357210 | T | C | 5 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+27730T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357210 | |||||||
| chr2:200357215 | G | A | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+27735G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357215 | |||||||
| chr2:200357250 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-23+27770A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357250 | |||||||
| chr2:200357436 | C | T | 57 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(54): Show |
57 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-23+27956C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357436 | |||||||
| chr2:200357600 | C | G | 1 | a0001c0001t0007g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-23+28120C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357600 | |||||||
| chr2:200357680 | A | T | 113 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(110): Show |
113 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-23+28200A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357680 | |||||||
| chr2:200357743 | TC | T | 3 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0002t0006g0133 |
3 | HG02559.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-23+28264delC | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357743 | |||||||
| chr2:200357818 | A | G | 1 | a0001c0002t0030g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-23+28338A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357818 | |||||||
| chr2:200357935 | A | G | 27 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0260 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.-23+28455A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357935 | |||||||
| chr2:200357946 | G | C | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-23+28466G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200357946 | |||||||
| chr2:200358008 | T | G | 2 | a0002c0004t0019g0285 a0002c0004t0019g0286 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-23+28528T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200358008 | |||||||
| chr2:200358369 | G | A | 2 | a0001c0001t0003g0030 a0001c0002t0069g0053 |
2 | HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-23+28889G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200358369 | |||||||
| chr2:200358420 | T | C | 1 | a0001c0001t0027g0178 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-23+28940T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200358420 | |||||||
| chr2:200358473 | C | T | 286 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.-23+28993C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200358473 | |||||||
| chr2:200358489 | G | A | 4 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(1): Show |
4 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+29009G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200358489 | |||||||
| chr2:200358595 | C | CT | 166 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.-23+29127dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200358595 | ||||||
| chr2:200358595 | C | CTT | 40 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(37): Show |
40 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-23+29126_-23+2912 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200358595 | ||||||
| chr2:200358862 | C | G | 1 | a0001c0002t0016g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-23+29382C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200358862 | |||||||
| chr2:200358880 | C | T | 2 | a0001c0001t0002g0238 a0001c0001t0002g0292 |
2 | NA18966.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-23+29400C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200358880 | |||||||
| chr2:200358919 | C | T | 2 | a0001c0010t0065g0004 a0003c0006t0032g0012 |
2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-23+29439C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200358919 | |||||||
| chr2:200358993 | TA | T | 287 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.-23+29524delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200358993 | ||||||
| chr2:200359007 | C | T | 1 | a0001c0001t0059g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-23+29527C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200359007 | |||||||
| chr2:200359139 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-23+29659G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200359139 | |||||||
| chr2:200359274 | C | T | 1 | a0001c0013t0010g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-23+29794C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200359274 | |||||||
| chr2:200359413 | T | A | 1 | a0001c0001t0034g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-22-29810T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200359413 | |||||||
| chr2:200359823 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-29400C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200359823 | |||||||
| chr2:200359914 | G | T | 39 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(36): Show |
39 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.-22-29309G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200359914 | |||||||
| chr2:200360204 | A | G | 1 | a0001c0001t0020g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-22-29019A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200360204 | |||||||
| chr2:200360210 | C | T | 1 | a0001c0001t0025g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-22-29013C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200360210 | |||||||
| chr2:200360249 | A | T | 287 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.-22-28974A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200360249 | |||||||
| chr2:200360849 | G | A | 2 | a0001c0001t0013g0085 a0001c0001t0013g0086 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-22-28374G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200360849 | |||||||
| chr2:200360914 | TTCA | T | 71 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(68): Show |
71 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.-22-28303_-22-2830 others(7): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200360914 | ||||||
| chr2:200360967 | C | CTG | 3 | a0001c0001t0018g0072 a0001c0001t0075g0029 a0001c0002t0013g0124 |
3 | HG03516.hp2 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-22-28227_-22-2822 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200360967 | ||||||
| chr2:200360967 | C | CTGTG | 3 | a0001c0001t0001g0253 a0001c0001t0073g0090 a0001c0002t0016g0281 |
3 | HG03579.hp2 HG04228.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.-22-28229_-22-2822 others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200360967 | ||||||
| chr2:200360967 | C | CTGTGTG | 194 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.-22-28231_-22-2822 others(10): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200360967 | ||||||
| chr2:200360967 | C | CTGTGTGT others(1): Show |
13 | a0001c0001t0001g0265 a0001c0001t0002g0268 a0001c0001t0003g0120 others(10): Show |
13 | HG00423.hp2 HG01884.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.-22-28233_-22-2822 others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200360967 | ||||||
| chr2:200360967 | C | CTGTGTGT others(3): Show |
7 | a0001c0001t0005g0271 a0001c0001t0008g0015 a0001c0001t0008g0017 others(4): Show |
7 | HG00438.hp1 HG02280.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-28235_-22-2822 others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200360967 | ||||||
| chr2:200360967 | C | G | 1 | a0002c0004t0019g0131 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-22-28256C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200360967 | |||||||
| chr2:200360967 | CTG | C | 5 | a0001c0001t0010g0129 a0001c0001t0011g0248 a0001c0010t0065g0004 others(2): Show |
5 | HG01243.hp1 HG02602.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-28227_-22-2822 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200360967 | ||||||
| chr2:200361074 | A | C | 101 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(98): Show |
101 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.-22-28149A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361074 | |||||||
| chr2:200361079 | A | AC | 25 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0214 others(22): Show |
25 | HG00544.hp2 HG00621.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-22-28137dupC | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200361079 | ||||||
| chr2:200361079 | A | C | 3 | a0001c0001t0001g0265 a0001c0001t0002g0195 a0001c0001t0005g0198 |
3 | HG02027.hp2 HG03654.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-22-28144A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361079 | |||||||
| chr2:200361085 | CCA | C | 64 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(61): Show |
64 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.-22-28127_-22-2812 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200361085 | ||||||
| chr2:200361087 | A | C | 131 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(128): Show |
131 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-22-28136A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361087 | |||||||
| chr2:200361179 | A | C | 95 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(92): Show |
95 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.-22-28044A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361179 | |||||||
| chr2:200361184 | C | G | 1 | a0001c0001t0003g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-22-28039C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361184 | |||||||
| chr2:200361301 | A | C | 1 | a0001c0001t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-27922A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361301 | |||||||
| chr2:200361362 | G | A | 2 | a0001c0001t0010g0096 a0001c0001t0012g0095 |
2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-22-27861G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361362 | |||||||
| chr2:200361426 | T | C | 290 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.-22-27797T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361426 | |||||||
| chr2:200361525 | G | A | 185 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-22-27698G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361525 | |||||||
| chr2:200361593 | T | C | 15 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(12): Show |
15 | HG02738.hp1 NA18946.hp2 NA18953.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-27630T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200361593 | |||||||
| chr2:200362129 | C | A | 246 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-22-27094C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200362129 | |||||||
| chr2:200362139 | C | G | 16 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0194 others(13): Show |
16 | HG00621.hp1 HG01123.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-27084C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200362139 | |||||||
| chr2:200362220 | C | G | 1 | a0001c0001t0002g0209 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-22-27003C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200362220 | |||||||
| chr2:200362239 | C | A | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22-26984C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200362239 | |||||||
| chr2:200362337 | A | G | 126 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(123): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-22-26886A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200362337 | |||||||
| chr2:200362466 | A | G | 251 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(248): Show |
251 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-22-26757A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200362466 | |||||||
| chr2:200362605 | T | C | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22-26618T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200362605 | |||||||
| chr2:200362619 | G | A | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22-26604G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200362619 | |||||||
| chr2:200362661 | C | G | 1 | a0001c0001t0003g0049 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-22-26562C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200362661 | |||||||
| chr2:200362777 | G | GT | 126 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(123): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-22-26445dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200362777 | ||||||
| chr2:200363300 | TAGTGC | T | 246 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-22-25917_-22-2591 others(9): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200363300 | ||||||
| chr2:200363340 | C | T | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-22-25883C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200363340 | |||||||
| chr2:200363570 | A | G | 295 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(292): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.-22-25653A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200363570 | |||||||
| chr2:200364077 | C | T | 1 | a0001c0001t0007g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-22-25146C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364077 | |||||||
| chr2:200364167 | T | C | 251 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(248): Show |
251 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-22-25056T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364167 | |||||||
| chr2:200364218 | G | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-25005G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364218 | |||||||
| chr2:200364292 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-24931G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364292 | |||||||
| chr2:200364340 | G | A | 38 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(35): Show |
38 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-22-24883G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364340 | |||||||
| chr2:200364422 | C | T | 1 | a0001c0001t0005g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-22-24801C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364422 | |||||||
| chr2:200364554 | C | G | 1 | a0001c0002t0013g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-22-24669C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364554 | |||||||
| chr2:200364661 | A | C | 1 | a0001c0002t0030g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-22-24562A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364661 | |||||||
| chr2:200364683 | C | T | 1 | a0001c0001t0008g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-22-24540C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364683 | |||||||
| chr2:200364750 | G | A | 119 | a0001c0001t0003g0030 a0001c0001t0003g0040 a0001c0001t0003g0041 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-22-24473G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364750 | |||||||
| chr2:200364914 | G | C | 1 | a0002c0004t0019g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-22-24309G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200364914 | |||||||
| chr2:200365040 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-22-24183G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365040 | |||||||
| chr2:200365073 | G | A | 1 | a0001c0001t0018g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-22-24150G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365073 | |||||||
| chr2:200365261 | T | C | 250 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-22-23962T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365261 | |||||||
| chr2:200365353 | C | T | 126 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(123): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-22-23870C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365353 | |||||||
| chr2:200365413 | C | T | 1 | a0001c0001t0012g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-22-23810C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365413 | |||||||
| chr2:200365535 | G | A | 45 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22-23688G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365535 | |||||||
| chr2:200365551 | A | G | 249 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-22-23672A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365551 | |||||||
| chr2:200365558 | T | A | 1 | a0001c0002t0013g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-22-23665T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365558 | |||||||
| chr2:200365565 | A | G | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-23658A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365565 | |||||||
| chr2:200365881 | G | A | 1 | a0001c0001t0017g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-22-23342G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200365881 | |||||||
| chr2:200366125 | A | G | 15 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(12): Show |
15 | HG02738.hp1 NA18946.hp2 NA18953.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-23098A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200366125 | |||||||
| chr2:200366134 | C | G | 45 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22-23089C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200366134 | |||||||
| chr2:200366518 | G | C | 6 | a0001c0001t0004g0108 a0001c0002t0006g0112 a0001c0002t0006g0113 others(3): Show |
6 | NA18953.hp1 NA18955.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-22705G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200366518 | |||||||
| chr2:200366795 | G | A | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-22428G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200366795 | |||||||
| chr2:200366883 | T | A | 5 | a0001c0001t0008g0015 a0001c0001t0008g0017 a0001c0001t0008g0018 others(2): Show |
5 | HG00438.hp1 NA18747.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-22340T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200366883 | |||||||
| chr2:200366902 | A | G | 1 | a0001c0001t0003g0120 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-22-22321A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200366902 | |||||||
| chr2:200366988 | G | A | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22-22235G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200366988 | |||||||
| chr2:200366994 | G | A | 1 | a0001c0002t0081g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-22-22229G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200366994 | |||||||
| chr2:200367023 | A | G | 1 | a0001c0001t0053g0167 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-22-22200A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367023 | |||||||
| chr2:200367093 | A | G | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22-22130A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367093 | |||||||
| chr2:200367151 | C | T | 1 | a0001c0001t0014g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-22-22072C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367151 | |||||||
| chr2:200367306 | CATG | C | 15 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(12): Show |
15 | HG02738.hp1 NA18946.hp2 NA18953.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-21911_-22-2190 others(7): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200367306 | ||||||
| chr2:200367381 | C | T | 1 | a0001c0002t0006g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-22-21842C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367381 | |||||||
| chr2:200367386 | T | C | 1 | a0001c0001t0057g0298 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-22-21837T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367386 | |||||||
| chr2:200367423 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-22-21800A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367423 | |||||||
| chr2:200367427 | G | T | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-21796G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367427 | |||||||
| chr2:200367492 | C | G | 4 | a0001c0001t0035g0059 a0001c0001t0035g0061 a0001c0001t0037g0060 others(1): Show |
4 | HG01243.hp2 HG01517.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-21731C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367492 | |||||||
| chr2:200367545 | G | T | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22-21678G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367545 | |||||||
| chr2:200367708 | ATT | A | 246 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-22-21511_-22-2151 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200367708 | ||||||
| chr2:200367853 | A | G | 4 | a0001c0002t0030g0100 a0002c0004t0012g0098 a0002c0004t0063g0102 others(1): Show |
4 | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-21370A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367853 | |||||||
| chr2:200367899 | G | T | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22-21324G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367899 | |||||||
| chr2:200367926 | T | C | 2 | a0001c0001t0010g0096 a0001c0001t0012g0095 |
2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-22-21297T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367926 | |||||||
| chr2:200367999 | G | T | 246 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-22-21224G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200367999 | |||||||
| chr2:200368008 | C | A | 1 | a0001c0001t0005g0211 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-22-21215C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200368008 | |||||||
| chr2:200368139 | C | G | 119 | a0001c0001t0003g0030 a0001c0001t0003g0040 a0001c0001t0003g0041 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-22-21084C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200368139 | |||||||
| chr2:200368141 | G | A | 46 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(43): Show |
46 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.-22-21082G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200368141 | |||||||
| chr2:200368317 | T | C | 111 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(108): Show |
111 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-22-20906T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200368317 | |||||||
| chr2:200368741 | T | C | 1 | a0001c0002t0013g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-22-20482T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200368741 | |||||||
| chr2:200368779 | G | A | 119 | a0001c0001t0003g0030 a0001c0001t0003g0040 a0001c0001t0003g0041 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-22-20444G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200368779 | |||||||
| chr2:200368904 | A | G | 291 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.-22-20319A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200368904 | |||||||
| chr2:200368922 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-20301T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200368922 | |||||||
| chr2:200369078 | T | TA | 185 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(182): Show |
185 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.-22-20130dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200369078 | ||||||
| chr2:200369099 | G | GAGAT | 289 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.-22-20122_-22-2012 others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200369099 | ||||||
| chr2:200369099 | G | T | 2 | a0001c0001t0002g0182 a0001c0001t0009g0162 |
2 | HG01975.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.-22-20124G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200369099 | |||||||
| chr2:200369177 | G | C | 10 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(7): Show |
10 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-22-20046G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200369177 | |||||||
| chr2:200369449 | G | A | 1 | a0001c0001t0034g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-22-19774G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200369449 | |||||||
| chr2:200369493 | G | A | 126 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(123): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-22-19730G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200369493 | |||||||
| chr2:200369499 | A | C | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-19724A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200369499 | |||||||
| chr2:200369688 | G | A | 1 | a0002c0004t0012g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-22-19535G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200369688 | |||||||
| chr2:200369849 | T | G | 38 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0154 others(35): Show |
38 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-22-19374T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200369849 | |||||||
| chr2:200370064 | G | A | 1 | a0001c0001t0011g0158 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-22-19159G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200370064 | |||||||
| chr2:200370064 | G | C | 250 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-22-19159G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200370064 | |||||||
| chr2:200370065 | G | A | 4 | a0001c0002t0030g0100 a0002c0004t0012g0098 a0002c0004t0063g0102 others(1): Show |
4 | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-19158G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200370065 | |||||||
| chr2:200370145 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-22-19078C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200370145 | |||||||
| chr2:200370159 | T | C | 250 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-22-19064T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200370159 | |||||||
| chr2:200370289 | T | C | 1 | a0001c0003t0001g0278 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-22-18934T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200370289 | |||||||
| chr2:200370896 | G | A | 1 | a0001c0001t0014g0050 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-22-18327G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200370896 | |||||||
| chr2:200370916 | G | C | 1 | a0001c0001t0002g0292 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-22-18307G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200370916 | |||||||
| chr2:200371085 | A | G | 2 | a0001c0001t0055g0293 a0001c0001t0056g0294 |
2 | HG02165.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-22-18138A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371085 | |||||||
| chr2:200371094 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-18129C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371094 | |||||||
| chr2:200371164 | C | T | 250 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-22-18059C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371164 | |||||||
| chr2:200371253 | T | A | 1 | a0001c0001t0008g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-22-17970T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371253 | |||||||
| chr2:200371258 | T | C | 1 | a0001c0001t0007g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-22-17965T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371258 | |||||||
| chr2:200371294 | T | C | 249 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-22-17929T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371294 | |||||||
| chr2:200371331 | G | A | 1 | a0001c0001t0080g0016 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-22-17892G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371331 | |||||||
| chr2:200371458 | C | T | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-17765C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371458 | |||||||
| chr2:200371548 | G | A | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-17675G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371548 | |||||||
| chr2:200371794 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-17429T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371794 | |||||||
| chr2:200371830 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-17393G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371830 | |||||||
| chr2:200371916 | C | T | 2 | a0002c0004t0012g0132 a0002c0004t0019g0131 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-22-17307C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200371916 | |||||||
| chr2:200372094 | A | C | 1 | a0001c0002t0016g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-22-17129A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200372094 | |||||||
| chr2:200372101 | G | C | 1 | a0001c0001t0002g0200 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-17122G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200372101 | |||||||
| chr2:200372622 | G | T | 45 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22-16601G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200372622 | |||||||
| chr2:200372787 | T | C | 55 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(52): Show |
55 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.-22-16436T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200372787 | |||||||
| chr2:200373005 | C | T | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-22-16218C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200373005 | |||||||
| chr2:200373088 | A | T | 1 | a0001c0001t0002g0200 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-16135A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200373088 | |||||||
| chr2:200373262 | T | G | 1 | a0001c0001t0064g0070 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-22-15961T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200373262 | |||||||
| chr2:200373270 | CA | C | 51 | a0001c0001t0002g0200 a0001c0001t0003g0030 a0001c0001t0008g0013 others(48): Show |
51 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.-22-15931delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200373270 | ||||||
| chr2:200373270 | CAA | C | 75 | a0001c0001t0001g0251 a0001c0001t0002g0199 a0001c0001t0002g0246 others(72): Show |
75 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.-22-15932_-22-1593 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200373270 | ||||||
| chr2:200373270 | CAAA | C | 102 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(99): Show |
102 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-22-15933_-22-1593 others(7): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200373270 | ||||||
| chr2:200373270 | CAAAAAA | C | 37 | a0001c0001t0001g0179 a0001c0001t0002g0154 a0001c0001t0002g0157 others(34): Show |
37 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-22-15936_-22-1593 others(10): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200373270 | ||||||
| chr2:200373292 | AGAAC | A | 9 | a0001c0001t0003g0122 a0001c0001t0004g0108 a0001c0001t0004g0111 others(6): Show |
9 | NA18953.hp1 NA18955.hp1 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22-15930_-22-1592 others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200373292 | |||||||
| chr2:200373296 | C | A | 2 | a0001c0001t0003g0121 a0001c0002t0006g0112 |
2 | NA19003.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-22-15927C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200373296 | |||||||
| chr2:200373319 | A | G | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-15904A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200373319 | |||||||
| chr2:200373347 | A | G | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-15876A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200373347 | |||||||
| chr2:200373994 | G | A | 2 | a0001c0001t0002g0199 a0001c0001t0002g0200 |
2 | NA18957.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-22-15229G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200373994 | |||||||
| chr2:200374071 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-22-15152C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200374071 | |||||||
| chr2:200374256 | A | G | 3 | a0001c0001t0022g0263 a0001c0001t0022g0264 a0001c0001t0022g0267 |
3 | NA18956.hp1 NA18968.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-22-14967A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200374256 | |||||||
| chr2:200374279 | C | T | 126 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(123): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-22-14944C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200374279 | |||||||
| chr2:200374360 | G | A | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-14863G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200374360 | |||||||
| chr2:200374532 | C | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-14691C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200374532 | |||||||
| chr2:200374621 | G | A | 1 | a0001c0001t0008g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-22-14602G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200374621 | |||||||
| chr2:200374762 | A | G | 63 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(60): Show |
63 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.-22-14461A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200374762 | |||||||
| chr2:200374972 | A | T | 3 | a0001c0001t0004g0028 a0001c0001t0031g0021 a0002c0004t0068g0002 |
3 | HG02809.hp1 HG02886.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-22-14251A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200374972 | |||||||
| chr2:200375142 | T | C | 9 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(6): Show |
9 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-14081T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375142 | |||||||
| chr2:200375155 | G | A | 2 | a0001c0001t0032g0010 a0001c0010t0065g0004 |
2 | HG02109.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-22-14068G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375155 | |||||||
| chr2:200375200 | C | T | 63 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(60): Show |
63 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.-22-14023C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375200 | |||||||
| chr2:200375215 | G | A | 295 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(292): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.-22-14008G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375215 | |||||||
| chr2:200375234 | G | T | 45 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22-13989G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375234 | |||||||
| chr2:200375314 | T | C | 1 | a0001c0001t0054g0296 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-22-13909T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375314 | |||||||
| chr2:200375323 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-13900G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375323 | |||||||
| chr2:200375334 | A | G | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-13889A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375334 | |||||||
| chr2:200375363 | A | G | 74 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(71): Show |
74 | HG00408.hp1 HG00621.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.-22-13860A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375363 | |||||||
| chr2:200375582 | G | A | 126 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(123): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-22-13641G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375582 | |||||||
| chr2:200375656 | T | TA | 8 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0174 others(5): Show |
8 | HG00642.hp1 HG01993.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.-22-13566dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200375656 | ||||||
| chr2:200375952 | G | A | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-13271G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200375952 | |||||||
| chr2:200376159 | CTT | C | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-13060_-22-1305 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200376159 | ||||||
| chr2:200376319 | T | C | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22-12904T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200376319 | |||||||
| chr2:200376469 | G | T | 1 | a0001c0003t0061g0127 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-22-12754G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200376469 | |||||||
| chr2:200376657 | T | G | 291 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.-22-12566T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200376657 | |||||||
| chr2:200376692 | T | C | 10 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(7): Show |
10 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-22-12531T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200376692 | |||||||
| chr2:200376802 | A | T | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22-12421A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200376802 | |||||||
| chr2:200377040 | A | G | 1 | a0001c0001t0005g0211 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-22-12183A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377040 | |||||||
| chr2:200377077 | A | G | 1 | a0001c0001t0005g0211 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-22-12146A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377077 | |||||||
| chr2:200377212 | A | G | 250 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-22-12011A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377212 | |||||||
| chr2:200377244 | G | T | 63 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(60): Show |
63 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.-22-11979G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377244 | |||||||
| chr2:200377499 | A | G | 1 | a0001c0001t0007g0229 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-22-11724A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377499 | |||||||
| chr2:200377565 | T | A | 1 | a0001c0001t0017g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-22-11658T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377565 | |||||||
| chr2:200377570 | G | A | 125 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(122): Show |
125 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.-22-11653G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377570 | |||||||
| chr2:200377734 | C | A | 1 | a0001c0001t0008g0027 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-22-11489C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377734 | |||||||
| chr2:200377866 | C | T | 1 | a0002c0004t0019g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-22-11357C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377866 | |||||||
| chr2:200377875 | G | A | 27 | a0001c0001t0001g0196 a0001c0001t0001g0204 a0001c0001t0001g0220 others(24): Show |
27 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-22-11348G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377875 | |||||||
| chr2:200377961 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-22-11262T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377961 | |||||||
| chr2:200377965 | C | G | 1 | a0001c0001t0025g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-22-11258C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200377965 | |||||||
| chr2:200378129 | T | C | 2 | a0001c0001t0013g0085 a0001c0001t0013g0086 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-22-11094T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200378129 | |||||||
| chr2:200378263 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-10960T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200378263 | |||||||
| chr2:200378554 | G | A | 1 | a0001c0001t0004g0033 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-22-10669G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200378554 | |||||||
| chr2:200378875 | C | T | 1 | a0001c0002t0045g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-22-10348C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200378875 | |||||||
| chr2:200378949 | G | A | 1 | a0001c0001t0007g0184 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-22-10274G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200378949 | |||||||
| chr2:200378950 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-22-10273C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200378950 | |||||||
| chr2:200379185 | C | G | 1 | a0001c0001t0015g0297 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-22-10038C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200379185 | |||||||
| chr2:200379367 | A | G | 2 | a0001c0001t0023g0273 a0001c0001t0028g0206 |
2 | NA18984.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-22-9856A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200379367 | |||||||
| chr2:200379538 | A | C | 129 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(126): Show |
129 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-22-9685A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200379538 | |||||||
| chr2:200379661 | C | A | 1 | a0001c0001t0007g0218 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-22-9562C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200379661 | |||||||
| chr2:200379690 | G | A | 8 | a0001c0001t0002g0194 a0001c0001t0002g0235 a0001c0001t0002g0238 others(5): Show |
8 | HG00621.hp1 HG02015.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.-22-9533G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200379690 | |||||||
| chr2:200379691 | G | T | 7 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(4): Show |
7 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-9532G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200379691 | |||||||
| chr2:200379781 | C | T | 1 | a0001c0001t0007g0218 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-22-9442C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200379781 | |||||||
| chr2:200379910 | A | G | 3 | a0001c0001t0017g0136 a0001c0002t0013g0138 a0001c0002t0081g0137 |
3 | HG01891.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-22-9313A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200379910 | |||||||
| chr2:200380197 | T | A | 1 | a0001c0003t0001g0258 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-22-9026T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200380197 | |||||||
| chr2:200380383 | C | T | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-22-8840C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200380383 | |||||||
| chr2:200380549 | G | A | 32 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(29): Show |
32 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.-22-8674G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200380549 | |||||||
| chr2:200380681 | G | A | 6 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(3): Show |
6 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-8542G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200380681 | |||||||
| chr2:200380827 | C | G | 51 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(48): Show |
51 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.-22-8396C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200380827 | |||||||
| chr2:200381149 | A | G | 65 | a0001c0001t0001g0244 a0001c0001t0003g0040 a0001c0001t0003g0041 others(62): Show |
65 | HG00639.hp1 HG00642.hp2 HG01517.hp2 others(62): Show |
intron_variant | MODIFIER | c.-22-8074A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200381149 | |||||||
| chr2:200381153 | T | C | 1 | a0001c0002t0006g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-22-8070T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200381153 | |||||||
| chr2:200381295 | C | A | 1 | a0001c0001t0007g0229 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-22-7928C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200381295 | |||||||
| chr2:200381475 | A | G | 28 | a0001c0001t0001g0196 a0001c0001t0001g0204 a0001c0001t0001g0213 others(25): Show |
28 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22-7748A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200381475 | |||||||
| chr2:200381677 | G | A | 4 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(1): Show |
4 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-7546G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200381677 | |||||||
| chr2:200381686 | T | C | 1 | a0002c0004t0012g0132 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-22-7537T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200381686 | |||||||
| chr2:200381768 | T | C | 1 | a0001c0001t0008g0027 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-22-7455T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200381768 | |||||||
| chr2:200381790 | G | A | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-22-7433G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200381790 | |||||||
| chr2:200382114 | G | A | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-22-7109G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200382114 | |||||||
| chr2:200382145 | C | T | 61 | a0001c0001t0001g0244 a0001c0001t0003g0040 a0001c0001t0003g0041 others(58): Show |
61 | HG00639.hp1 HG00642.hp2 HG01517.hp2 others(58): Show |
intron_variant | MODIFIER | c.-22-7078C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200382145 | |||||||
| chr2:200382302 | T | C | 3 | a0001c0001t0001g0204 a0001c0001t0001g0220 a0001c0001t0001g0232 |
3 | HG00733.hp1 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-22-6921T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200382302 | |||||||
| chr2:200382389 | C | A | 1 | a0001c0001t0008g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-22-6834C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200382389 | |||||||
| chr2:200382420 | G | A | 1 | a0001c0002t0045g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-22-6803G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200382420 | |||||||
| chr2:200382756 | G | A | 138 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(135): Show |
138 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-22-6467G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200382756 | |||||||
| chr2:200382768 | C | T | 61 | a0001c0001t0001g0244 a0001c0001t0003g0040 a0001c0001t0003g0041 others(58): Show |
61 | HG00639.hp1 HG00642.hp2 HG01517.hp2 others(58): Show |
intron_variant | MODIFIER | c.-22-6455C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200382768 | |||||||
| chr2:200382774 | A | G | 32 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(29): Show |
32 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.-22-6449A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200382774 | |||||||
| chr2:200383040 | G | A | 2 | a0001c0002t0013g0104 a0002c0004t0012g0101 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-22-6183G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200383040 | |||||||
| chr2:200383057 | G | A | 138 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(135): Show |
138 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-22-6166G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200383057 | |||||||
| chr2:200383095 | C | T | 61 | a0001c0001t0001g0244 a0001c0001t0003g0040 a0001c0001t0003g0041 others(58): Show |
61 | HG00639.hp1 HG00642.hp2 HG01517.hp2 others(58): Show |
intron_variant | MODIFIER | c.-22-6128C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200383095 | |||||||
| chr2:200383194 | G | A | 2 | a0002c0004t0019g0131 a0002c0004t0019g0135 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-6029G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200383194 | |||||||
| chr2:200383252 | A | G | 1 | a0001c0001t0011g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-22-5971A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200383252 | |||||||
| chr2:200383288 | A | G | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-5935A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200383288 | |||||||
| chr2:200383316 | C | T | 294 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(291): Show |
294 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.-22-5907C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200383316 | |||||||
| chr2:200383589 | T | G | 1 | a0001c0002t0013g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-22-5634T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200383589 | |||||||
| chr2:200383620 | C | T | 1 | a0001c0002t0013g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-22-5603C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200383620 | |||||||
| chr2:200384022 | G | A | 4 | a0001c0001t0003g0003 a0001c0001t0010g0129 a0001c0001t0014g0134 others(1): Show |
4 | HG01243.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-5201G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200384022 | |||||||
| chr2:200384336 | T | TTTTATTT others(5): Show |
1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-4863_-22-4852d others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200384336 | ||||||
| chr2:200384336 | TTTTA | T | 248 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(245): Show |
248 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.-22-4855_-22-4852d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200384336 | ||||||
| chr2:200384392 | C | T | 1 | a0001c0001t0017g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-22-4831C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200384392 | |||||||
| chr2:200384513 | C | T | 52 | a0001c0001t0003g0030 a0001c0001t0003g0056 a0001c0001t0008g0015 others(49): Show |
52 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-22-4710C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200384513 | |||||||
| chr2:200384604 | G | A | 51 | a0001c0001t0003g0030 a0001c0001t0008g0015 a0001c0001t0008g0017 others(48): Show |
51 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.-22-4619G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200384604 | |||||||
| chr2:200384685 | A | G | 5 | a0001c0002t0030g0100 a0002c0004t0012g0098 a0002c0004t0012g0132 others(2): Show |
5 | HG02145.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-4538A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200384685 | |||||||
| chr2:200384770 | A | G | 1 | a0001c0001t0002g0195 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-22-4453A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200384770 | |||||||
| chr2:200384955 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0220 |
2 | HG00733.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-22-4268A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200384955 | |||||||
| chr2:200385102 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-22-4121G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385102 | |||||||
| chr2:200385262 | G | T | 2 | a0002c0004t0019g0131 a0002c0004t0019g0135 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-22-3961G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385262 | |||||||
| chr2:200385548 | C | G | 1 | a0001c0001t0007g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-22-3675C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385548 | |||||||
| chr2:200385697 | A | T | 1 | a0001c0001t0042g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-22-3526A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385697 | |||||||
| chr2:200385878 | G | A | 1 | a0001c0001t0048g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-22-3345G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385878 | |||||||
| chr2:200385884 | A | G | 1 | a0001c0001t0048g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-22-3339A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385884 | |||||||
| chr2:200385915 | G | A | 14 | a0001c0001t0008g0067 a0001c0001t0011g0001 a0001c0001t0011g0205 others(11): Show |
14 | HG00408.hp2 HG02155.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.-22-3308G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385915 | |||||||
| chr2:200385942 | C | T | 1 | a0001c0002t0030g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-22-3281C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385942 | |||||||
| chr2:200385964 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-22-3259C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385964 | |||||||
| chr2:200385965 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-22-3258C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200385965 | |||||||
| chr2:200386010 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-22-3213G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200386010 | |||||||
| chr2:200386043 | C | A | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-3180C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200386043 | |||||||
| chr2:200386126 | C | T | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-3097C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200386126 | |||||||
| chr2:200386132 | T | C | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-3091T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200386132 | |||||||
| chr2:200386165 | GGAGCCTG others(16): Show |
G | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-22-3034_-22-3012d others(25): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200386165 | ||||||
| chr2:200386205 | C | A | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-22-3018C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200386205 | |||||||
| chr2:200386309 | C | T | 14 | a0001c0001t0003g0121 a0001c0001t0003g0122 a0001c0001t0004g0111 others(11): Show |
14 | HG02738.hp1 NA18946.hp2 NA18953.hp1 others(11): Show |
intron_variant | MODIFIER | c.-22-2914C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200386309 | |||||||
| chr2:200386720 | G | C | 2 | a0001c0001t0010g0129 a0003c0006t0017g0130 |
2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-22-2503G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200386720 | |||||||
| chr2:200387140 | G | A | 3 | a0001c0001t0017g0136 a0001c0002t0013g0138 a0001c0002t0081g0137 |
3 | HG01891.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-22-2083G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200387140 | |||||||
| chr2:200387308 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-22-1915G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200387308 | |||||||
| chr2:200387603 | C | T | 3 | a0001c0001t0004g0028 a0001c0002t0013g0104 a0002c0004t0012g0101 |
3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-22-1620C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200387603 | |||||||
| chr2:200387612 | A | G | 62 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0204 others(59): Show |
62 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22-1611A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200387612 | |||||||
| chr2:200387632 | A | G | 106 | a0001c0001t0001g0159 a0001c0001t0001g0196 a0001c0001t0001g0202 others(103): Show |
106 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-22-1591A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200387632 | |||||||
| chr2:200388223 | G | A | 294 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(291): Show |
294 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.-22-1000G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388223 | |||||||
| chr2:200388288 | G | C | 1 | a0001c0002t0016g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-22-935G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388288 | |||||||
| chr2:200388295 | G | T | 1 | a0001c0002t0016g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-22-928G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388295 | |||||||
| chr2:200388396 | C | T | 3 | a0001c0001t0017g0136 a0001c0002t0013g0138 a0001c0002t0081g0137 |
3 | HG01891.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-22-827C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388396 | |||||||
| chr2:200388486 | C | T | 2 | a0001c0001t0013g0085 a0001c0001t0013g0086 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-22-737C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388486 | |||||||
| chr2:200388590 | T | C | 5 | a0001c0001t0003g0092 a0001c0001t0004g0036 a0001c0001t0033g0025 others(2): Show |
5 | HG04184.hp2 NA18962.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-633T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388590 | |||||||
| chr2:200388612 | GC | G | 292 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.-22-601delC | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200388612 | ||||||
| chr2:200388617 | C | G | 3 | a0001c0001t0008g0017 a0001c0001t0008g0018 a0001c0003t0028g0210 |
3 | NA18747.hp2 NA18946.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-22-606C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388617 | |||||||
| chr2:200388621 | C | G | 1 | a0001c0001t0018g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-22-602C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388621 | |||||||
| chr2:200388623 | A | G | 1 | a0001c0001t0025g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-22-600A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388623 | |||||||
| chr2:200388696 | GA | G | 11 | a0001c0001t0041g0283 a0001c0002t0006g0019 a0001c0002t0006g0115 others(8): Show |
11 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-22-515delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 200388696 | ||||||
| chr2:200388888 | A | G | 2 | a0001c0001t0031g0021 a0001c0001t0031g0052 |
2 | HG01975.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-22-335A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200388888 | |||||||
| chr2:200389046 | G | A | 43 | a0001c0001t0008g0015 a0001c0001t0008g0017 a0001c0001t0008g0018 others(40): Show |
43 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-22-177G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200389046 | |||||||
| chr2:200389186 | C | G | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-22-37C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 2/12 | chr2 | 200389186 | |||||||
| chr2:200389326 | G | C | 209 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.39+43G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200389326 | |||||||
| chr2:200389448 | A | G | 202 | a0001c0001t0001g0159 a0001c0001t0001g0196 a0001c0001t0001g0202 others(199): Show |
202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.39+165A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200389448 | |||||||
| chr2:200389554 | A | G | 281 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(278): Show |
281 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.39+271A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200389554 | |||||||
| chr2:200389790 | G | A | 1 | a0001c0001t0005g0211 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.39+507G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200389790 | |||||||
| chr2:200389954 | C | T | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.39+671C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200389954 | |||||||
| chr2:200390172 | C | G | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+889C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200390172 | |||||||
| chr2:200390184 | T | C | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+901T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200390184 | |||||||
| chr2:200390317 | G | T | 1 | a0001c0001t0067g0037 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.39+1034G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200390317 | |||||||
| chr2:200390355 | G | A | 1 | a0001c0001t0018g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.39+1072G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200390355 | |||||||
| chr2:200390411 | G | A | 54 | a0001c0001t0001g0244 a0001c0001t0003g0040 a0001c0001t0003g0041 others(51): Show |
54 | HG00639.hp1 HG00642.hp2 HG01192.hp2 others(51): Show |
intron_variant | MODIFIER | c.39+1128G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200390411 | |||||||
| chr2:200390709 | C | T | 1 | a0001c0001t0021g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.39+1426C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200390709 | |||||||
| chr2:200390743 | G | A | 1 | a0002c0004t0012g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.39+1460G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200390743 | |||||||
| chr2:200390788 | A | G | 1 | a0001c0001t0010g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.39+1505A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200390788 | |||||||
| chr2:200390854 | C | CA | 11 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0005g0201 others(8): Show |
11 | HG02129.hp2 HG02486.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.39+1585dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200390854 | ||||||
| chr2:200390868 | A | C | 2 | a0001c0001t0002g0151 a0001c0001t0051g0149 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.39+1585A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200390868 | |||||||
| chr2:200391084 | T | C | 13 | a0001c0001t0010g0071 a0001c0001t0014g0105 a0001c0001t0014g0110 others(10): Show |
13 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.39+1801T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200391084 | |||||||
| chr2:200391589 | G | A | 1 | a0001c0001t0003g0121 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.39+2306G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200391589 | |||||||
| chr2:200391825 | A | G | 1 | a0001c0003t0061g0127 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.39+2542A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200391825 | |||||||
| chr2:200391851 | A | C | 55 | a0001c0001t0001g0244 a0001c0001t0003g0040 a0001c0001t0003g0041 others(52): Show |
55 | HG00639.hp1 HG00642.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.39+2568A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200391851 | |||||||
| chr2:200391857 | AC | A | 5 | a0001c0002t0030g0100 a0002c0004t0012g0020 a0002c0004t0012g0098 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+2578delC | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200391857 | ||||||
| chr2:200392061 | G | A | 2 | a0001c0001t0031g0021 a0001c0001t0031g0052 |
2 | HG01975.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.39+2778G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200392061 | |||||||
| chr2:200392307 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.39+3024A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200392307 | |||||||
| chr2:200392480 | C | T | 137 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(134): Show |
137 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.39+3197C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200392480 | |||||||
| chr2:200392536 | C | G | 2 | a0001c0001t0003g0122 a0001c0001t0004g0111 |
2 | NA18971.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.39+3253C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200392536 | |||||||
| chr2:200392617 | T | G | 1 | a0001c0001t0004g0044 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.39+3334T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200392617 | |||||||
| chr2:200392830 | C | T | 2 | a0001c0001t0023g0207 a0001c0001t0023g0208 |
2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.39+3547C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200392830 | |||||||
| chr2:200392902 | G | T | 1 | a0001c0001t0043g0277 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.39+3619G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200392902 | |||||||
| chr2:200392956 | AG | A | 5 | a0001c0001t0059g0026 a0001c0002t0013g0138 a0001c0002t0081g0137 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+3674delG | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200392956 | |||||||
| chr2:200393124 | G | A | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.39+3841G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200393124 | |||||||
| chr2:200393296 | G | C | 1 | a0001c0002t0013g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.39+4013G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200393296 | |||||||
| chr2:200394194 | A | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.39+4911A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200394194 | |||||||
| chr2:200394369 | C | T | 1 | a0001c0003t0001g0257 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.39+5086C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200394369 | |||||||
| chr2:200395094 | A | C | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.39+5811A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395094 | |||||||
| chr2:200395138 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0039g0266 a0001c0001t0043g0277 |
3 | HG00438.hp2 NA18960.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.39+5855G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395138 | |||||||
| chr2:200395269 | C | G | 4 | a0001c0001t0010g0096 a0001c0001t0010g0140 a0001c0001t0071g0139 others(1): Show |
4 | HG02258.hp1 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+5986C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395269 | |||||||
| chr2:200395392 | A | G | 1 | a0001c0001t0002g0195 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.39+6109A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395392 | |||||||
| chr2:200395642 | A | G | 4 | a0001c0001t0003g0048 a0001c0001t0004g0047 a0001c0001t0005g0217 others(1): Show |
4 | HG00639.hp1 HG00642.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+6359A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395642 | |||||||
| chr2:200395662 | T | G | 1 | a0001c0001t0001g0253 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.39+6379T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395662 | |||||||
| chr2:200395757 | C | T | 1 | a0002c0004t0012g0132 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.39+6474C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395757 | |||||||
| chr2:200395874 | G | A | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.39+6591G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395874 | |||||||
| chr2:200395933 | C | T | 2 | a0001c0001t0008g0013 a0001c0001t0021g0014 |
2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.39+6650C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395933 | |||||||
| chr2:200395949 | T | A | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.39+6666T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200395949 | |||||||
| chr2:200396011 | G | GA | 27 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0121 others(24): Show |
27 | HG02145.hp1 HG02717.hp1 HG02738.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+6751dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396011 | ||||||
| chr2:200396011 | G | GAAAAAAA others(6): Show |
2 | a0001c0001t0001g0265 a0001c0001t0002g0234 |
2 | HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.39+6739_39+6751dup others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396011 | ||||||
| chr2:200396011 | G | GAAAAAAA others(8): Show |
1 | a0001c0001t0002g0252 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.39+6737_39+6751dup others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396011 | ||||||
| chr2:200396012 | A | G | 2 | a0001c0001t0023g0207 a0001c0001t0023g0208 |
2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.39+6729A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396012 | |||||||
| chr2:200396024 | A | T | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.39+6741A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396024 | |||||||
| chr2:200396028 | A | T | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.39+6745A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396028 | |||||||
| chr2:200396029 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.39+6747_39+6748ins others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396029 | ||||||
| chr2:200396029 | A | T | 2 | a0001c0001t0013g0085 a0001c0001t0013g0086 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+6746A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396029 | |||||||
| chr2:200396031 | A | AATATAAA others(7): Show |
1 | a0002c0004t0012g0132 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.39+6749_39+6750ins others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396031 | ||||||
| chr2:200396031 | A | T | 5 | a0001c0001t0001g0232 a0001c0001t0013g0085 a0001c0001t0013g0086 others(2): Show |
5 | HG01175.hp1 HG04204.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+6748A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396031 | |||||||
| chr2:200396031 | AAAATAT | A | 11 | a0001c0001t0001g0159 a0001c0001t0002g0180 a0001c0001t0008g0054 others(8): Show |
11 | HG00438.hp1 HG01074.hp1 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.39+6750_39+6755del others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396031 | ||||||
| chr2:200396031 | AAAATATA others(1): Show |
A | 8 | a0001c0001t0008g0015 a0001c0001t0008g0017 a0001c0001t0011g0299 others(5): Show |
8 | HG01243.hp2 HG01517.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+6750_39+6757del others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396031 | ||||||
| chr2:200396031 | AAAATATA others(7): Show |
A | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.39+6750_39+6763del others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396031 | ||||||
| chr2:200396032 | AAATATAT | A | 6 | a0001c0001t0002g0174 a0001c0001t0002g0177 a0001c0001t0002g0183 others(3): Show |
6 | HG00738.hp1 HG01993.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+6751_39+6757del others(7): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396032 | ||||||
| chr2:200396033 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(32): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(10): Show |
1 | a0001c0003t0001g0250 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(17): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0017g0142 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(25): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(22): Show |
1 | a0001c0002t0030g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(29): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(28): Show |
1 | a0001c0001t0002g0199 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(35): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(9): Show |
3 | a0001c0001t0002g0235 a0001c0003t0001g0256 a0001c0003t0001g0278 |
3 | HG02004.hp2 NA18982.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(19): Show |
1 | a0001c0002t0016g0279 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(26): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(29): Show |
1 | a0001c0001t0002g0200 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(36): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(8): Show |
1 | a0001c0003t0001g0269 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(17): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0055g0293 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(21): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0041g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(23): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0002g0262 a0001c0001t0002g0268 |
2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0031g0052 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0260 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(18): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(15): Show |
2 | a0001c0001t0005g0254 a0001c0002t0070g0147 |
2 | HG02615.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(22): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(28): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0005g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0027g0178 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(10): Show |
2 | a0001c0001t0014g0134 a0001c0002t0045g0291 |
2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(17): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0288 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(19): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0233 a0001c0002t0006g0019 |
2 | HG02572.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(21): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(18): Show |
2 | a0001c0001t0003g0003 a0001c0001t0043g0277 |
2 | HG03130.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(25): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(31): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(26): Show |
1 | a0001c0001t0010g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(33): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0007g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0002g0215 a0001c0003t0001g0274 |
2 | HG04184.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(11): Show |
4 | a0001c0001t0002g0194 a0001c0001t0003g0030 a0001c0001t0056g0294 others(1): Show |
4 | HG00621.hp1 HG00621.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(18): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0051g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(20): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(15): Show |
2 | a0001c0001t0002g0193 a0001c0001t0003g0082 |
2 | HG03710.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(22): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0010g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(24): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(6): Show |
1 | a0007c0012t0015g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(8): Show |
4 | a0001c0001t0002g0227 a0001c0001t0002g0238 a0001c0001t0002g0246 others(1): Show |
4 | HG01074.hp2 HG03704.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0002g0241 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(17): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0002g0151 a0001c0001t0003g0049 |
2 | HG01123.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(19): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(14): Show |
1 | a0005c0011t0001g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(21): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0023g0207 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(29): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(24): Show |
1 | a0001c0001t0002g0292 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(31): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(26): Show |
1 | a0001c0001t0023g0208 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(33): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(5): Show |
4 | a0001c0001t0002g0249 a0001c0001t0020g0118 a0001c0001t0022g0263 others(1): Show |
4 | HG02129.hp1 NA18956.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0005g0259 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(9): Show |
5 | a0001c0001t0001g0228 a0001c0001t0022g0267 a0001c0001t0026g0236 others(2): Show |
5 | HG02015.hp1 HG04204.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(11): Show |
3 | a0001c0001t0001g0204 a0001c0001t0002g0150 a0001c0001t0026g0237 |
3 | HG00733.hp1 HG01123.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(18): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(13): Show |
1 | a0001c0003t0024g0242 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(20): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0071g0139 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(22): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0220 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(24): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(27): Show |
1 | a0001c0001t0004g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(34): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0048g0221 a0001c0002t0013g0011 |
2 | HG01257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(11): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(6): Show |
2 | a0001c0001t0044g0261 a0002c0004t0012g0101 |
2 | HG03486.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(8): Show |
3 | a0001c0001t0005g0211 a0001c0001t0007g0218 a0001c0003t0024g0270 |
3 | HG02129.hp2 HG02165.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0011g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(19): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(14): Show |
3 | a0001c0001t0001g0216 a0001c0001t0007g0190 a0002c0004t0068g0002 |
3 | HG02886.hp1 NA19056.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(21): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0287 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(23): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0007g0289 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(25): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(20): Show |
1 | a0006c0007t0047g0226 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(27): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0225 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(29): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(30): Show |
1 | a0001c0001t0001g0224 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(37): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(5): Show |
4 | a0001c0001t0001g0251 a0001c0001t0015g0212 a0001c0001t0054g0296 others(1): Show |
4 | HG02895.hp1 HG03491.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0031g0021 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(11): Show |
1 | a0001c0003t0001g0257 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(18): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0209 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(20): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0007g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(22): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0005g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(26): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0005g0201 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(30): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAT others(6): Show |
2 | a0001c0001t0009g0153 a0003c0008t0058g0099 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAT others(8): Show |
2 | a0001c0001t0003g0120 a0001c0001t0023g0273 |
2 | NA18984.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAT others(10): Show |
1 | a0001c0001t0013g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(17): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAT others(12): Show |
2 | a0001c0001t0017g0143 a0003c0006t0032g0012 |
2 | HG02896.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(19): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAT others(14): Show |
1 | a0001c0001t0017g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(21): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAT others(16): Show |
1 | a0001c0001t0003g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(23): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAT others(18): Show |
1 | a0001c0001t0001g0253 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(25): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAAAT others(22): Show |
1 | a0001c0001t0015g0297 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(29): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAATA others(7): Show |
1 | a0001c0003t0024g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAAATA others(15): Show |
1 | a0001c0001t0002g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(22): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAATAT others(4): Show |
1 | a0001c0001t0003g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(11): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0027g0276 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAATAT others(12): Show |
3 | a0001c0001t0004g0045 a0001c0001t0007g0229 a0001c0001t0025g0239 |
3 | HG02071.hp1 NA18954.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.39+6751_39+6752ins others(19): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAAATAT others(18): Show |
1 | a0001c0003t0001g0275 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(25): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAAATATA others(5): Show |
1 | a0001c0001t0057g0298 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAATATAT others(6): Show |
1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AAATATAT others(8): Show |
1 | a0003c0006t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.39+6751_39+6752ins others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AATATAAA others(3): Show |
1 | a0001c0001t0017g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.39+6755_39+6756ins others(10): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AATATAAA others(5): Show |
3 | a0001c0001t0012g0078 a0001c0002t0006g0133 a0001c0002t0013g0104 |
3 | HG02622.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.39+6755_39+6756ins others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AATATAAA others(7): Show |
1 | a0001c0001t0012g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.39+6755_39+6756ins others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AATATAAA others(9): Show |
2 | a0001c0001t0012g0077 a0001c0002t0030g0100 |
2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.39+6755_39+6756ins others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | AATATATA others(11): Show |
1 | a0001c0002t0006g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.39+6767_39+6784dup others(18): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396033 | ||||||
| chr2:200396033 | A | ATATAAAT others(6): Show |
1 | a0002c0004t0012g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.39+6750_39+6751ins others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396033 | |||||||
| chr2:200396033 | A | ATATAAAT others(12): Show |
2 | a0002c0004t0019g0285 a0002c0004t0063g0102 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.39+6750_39+6751ins others(19): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396033 | |||||||
| chr2:200396033 | A | ATATAAAT others(14): Show |
1 | a0002c0004t0019g0286 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.39+6750_39+6751ins others(21): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396033 | |||||||
| chr2:200396033 | A | T | 15 | a0001c0001t0001g0232 a0001c0001t0002g0195 a0001c0001t0003g0092 others(12): Show |
15 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+6750A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396033 | |||||||
| chr2:200396034 | ATATATAT | A | 13 | a0001c0001t0002g0175 a0001c0001t0005g0186 a0001c0001t0007g0161 others(10): Show |
13 | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.39+6752_39+6758del others(7): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396034 | |||||||
| chr2:200396034 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0039g0266 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.39+6752_39+6762del others(11): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396034 | |||||||
| chr2:200396034 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0202 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.39+6752_39+6764del others(13): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396034 | |||||||
| chr2:200396034 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0005g0148 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.39+6752_39+6768del others(17): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396034 | |||||||
| chr2:200396035 | T | A | 35 | a0001c0001t0001g0265 a0001c0001t0003g0121 a0001c0001t0003g0122 others(32): Show |
35 | HG00544.hp1 HG01099.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.39+6752T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396035 | |||||||
| chr2:200396037 | T | A | 27 | a0001c0001t0001g0265 a0001c0001t0003g0121 a0001c0001t0003g0122 others(24): Show |
27 | HG00544.hp1 HG01106.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.39+6754T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396037 | |||||||
| chr2:200396039 | T | A | 6 | a0001c0001t0003g0121 a0001c0001t0005g0173 a0001c0001t0033g0038 others(3): Show |
6 | HG02280.hp2 HG03831.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+6756T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396039 | |||||||
| chr2:200396041 | T | A | 2 | a0001c0001t0033g0038 a0001c0001t0046g0290 |
2 | NA18962.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.39+6758T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396041 | |||||||
| chr2:200396043 | T | A | 2 | a0001c0001t0005g0186 a0001c0003t0038g0168 |
2 | HG00423.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.39+6760T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396043 | |||||||
| chr2:200396045 | T | A | 1 | a0001c0001t0005g0186 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.39+6762T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396045 | |||||||
| chr2:200396047 | T | A | 1 | a0001c0001t0039g0266 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.39+6764T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396047 | |||||||
| chr2:200396049 | T | A | 2 | a0001c0001t0001g0202 a0001c0001t0039g0266 |
2 | HG00738.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.39+6766T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396049 | |||||||
| chr2:200396051 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.39+6768T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396051 | |||||||
| chr2:200396053 | T | A | 1 | a0001c0001t0005g0148 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.39+6770T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396053 | |||||||
| chr2:200396055 | T | A | 1 | a0001c0001t0005g0148 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.39+6772T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396055 | |||||||
| chr2:200396056 | ATATATAT others(5): Show |
A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.39+6775_39+6786del others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396056 | ||||||
| chr2:200396060 | ATATATAT others(1): Show |
A | 7 | a0001c0001t0011g0001 a0001c0001t0011g0219 a0001c0001t0018g0055 others(4): Show |
7 | HG00408.hp2 HG02155.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+6779_39+6786del others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396060 | ||||||
| chr2:200396062 | ATATATT | A | 4 | a0001c0001t0005g0185 a0001c0001t0033g0038 a0001c0001t0034g0146 others(1): Show |
4 | HG00544.hp1 NA18522.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+6781_39+6786del others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396062 | ||||||
| chr2:200396064 | ATATT | A | 3 | a0001c0001t0059g0026 a0002c0004t0019g0131 a0002c0004t0019g0135 |
3 | HG01884.hp1 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.39+6783_39+6786del others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200396064 | ||||||
| chr2:200396068 | T | A | 228 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.39+6785T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396068 | |||||||
| chr2:200396168 | T | C | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+6885T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396168 | |||||||
| chr2:200396289 | A | G | 5 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(2): Show |
5 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+7006A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396289 | |||||||
| chr2:200396460 | C | T | 4 | a0001c0001t0003g0048 a0001c0001t0004g0047 a0001c0001t0005g0217 others(1): Show |
4 | HG00639.hp1 HG00642.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+7177C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396460 | |||||||
| chr2:200396694 | T | G | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.39+7411T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396694 | |||||||
| chr2:200396802 | T | C | 1 | a0001c0001t0007g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.39+7519T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200396802 | |||||||
| chr2:200397749 | G | T | 1 | a0001c0001t0010g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.39+8466G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200397749 | |||||||
| chr2:200397841 | A | C | 8 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0002t0013g0138 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+8558A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200397841 | |||||||
| chr2:200397844 | C | A | 1 | a0001c0002t0030g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.39+8561C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200397844 | |||||||
| chr2:200398063 | G | C | 5 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(2): Show |
5 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+8780G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200398063 | |||||||
| chr2:200398240 | G | A | 4 | a0001c0001t0001g0228 a0001c0001t0022g0263 a0001c0001t0022g0264 others(1): Show |
4 | NA18956.hp1 NA18968.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+8957G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200398240 | |||||||
| chr2:200398528 | T | C | 5 | a0001c0001t0059g0026 a0001c0002t0013g0138 a0001c0002t0081g0137 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+9245T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200398528 | |||||||
| chr2:200398742 | C | T | 2 | a0001c0001t0032g0010 a0001c0002t0013g0006 |
2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.39+9459C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200398742 | |||||||
| chr2:200398865 | T | C | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+9582T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200398865 | |||||||
| chr2:200398868 | C | CA | 4 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(1): Show |
4 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+9586dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200398868 | ||||||
| chr2:200399161 | C | G | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.39+9878C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200399161 | |||||||
| chr2:200399584 | CAAAT | C | 130 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(127): Show |
130 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.39+10305_39+10308d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200399584 | ||||||
| chr2:200399741 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.39+10458G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200399741 | |||||||
| chr2:200399944 | T | A | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.39+10661T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200399944 | |||||||
| chr2:200400122 | ACCAAAAA others(7): Show |
A | 3 | a0001c0001t0008g0088 a0001c0001t0008g0089 a0001c0001t0073g0090 |
3 | HG01074.hp1 HG02055.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.39+10856_39+10869d others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200400122 | ||||||
| chr2:200400168 | A | AT | 139 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.39+10892dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200400168 | ||||||
| chr2:200400313 | C | A | 19 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(16): Show |
19 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.39+11030C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200400313 | |||||||
| chr2:200400508 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.39+11225A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200400508 | |||||||
| chr2:200400908 | A | G | 1 | a0001c0001t0003g0121 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.40-11403A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200400908 | |||||||
| chr2:200400944 | T | C | 6 | a0001c0001t0001g0159 a0001c0001t0003g0056 a0001c0001t0008g0054 others(3): Show |
6 | NA18955.hp2 NA18981.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-11367T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200400944 | |||||||
| chr2:200400968 | G | A | 9 | a0001c0001t0008g0063 a0001c0001t0008g0080 a0001c0001t0008g0088 others(6): Show |
9 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.40-11343G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200400968 | |||||||
| chr2:200401005 | G | A | 5 | a0001c0001t0011g0001 a0001c0001t0011g0219 a0001c0005t0011g0001 others(2): Show |
5 | HG00408.hp2 HG02155.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-11306G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200401005 | |||||||
| chr2:200401200 | GGA | G | 130 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(127): Show |
130 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.40-11103_40-11102d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200401200 | ||||||
| chr2:200401279 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.40-11032G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200401279 | |||||||
| chr2:200401336 | AG | A | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.40-10974delG | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200401336 | |||||||
| chr2:200401384 | T | C | 1 | a0001c0003t0024g0242 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.40-10927T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200401384 | |||||||
| chr2:200401528 | C | T | 1 | a0001c0002t0030g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-10783C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200401528 | |||||||
| chr2:200401704 | AT | A | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.40-10597delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200401704 | ||||||
| chr2:200402325 | T | C | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.40-9986T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200402325 | |||||||
| chr2:200402449 | C | T | 1 | a0001c0001t0008g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.40-9862C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200402449 | |||||||
| chr2:200402796 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.40-9515T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200402796 | |||||||
| chr2:200402926 | C | A | 2 | a0001c0001t0015g0170 a0001c0001t0015g0188 |
2 | HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.40-9385C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200402926 | |||||||
| chr2:200402930 | A | G | 1 | a0001c0001t0008g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.40-9381A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200402930 | |||||||
| chr2:200402938 | T | G | 5 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(2): Show |
5 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-9373T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200402938 | |||||||
| chr2:200403014 | C | A | 1 | a0001c0001t0010g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.40-9297C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200403014 | |||||||
| chr2:200403053 | G | A | 1 | a0001c0001t0025g0239 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.40-9258G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200403053 | |||||||
| chr2:200403102 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.40-9209C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200403102 | |||||||
| chr2:200403245 | T | C | 1 | a0002c0004t0063g0102 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.40-9066T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200403245 | |||||||
| chr2:200403312 | CTT | C | 7 | a0001c0001t0010g0071 a0001c0001t0059g0026 a0001c0002t0013g0138 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-8998_40-8997del others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200403312 | |||||||
| chr2:200403355 | A | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.40-8956A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200403355 | |||||||
| chr2:200403828 | A | G | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.40-8483A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200403828 | |||||||
| chr2:200403836 | T | TCAAGGTC others(17): Show |
7 | a0001c0001t0010g0071 a0001c0001t0059g0026 a0001c0002t0013g0138 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-8472_40-8449dup others(24): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200403836 | ||||||
| chr2:200403933 | A | G | 1 | a0001c0001t0008g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.40-8378A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200403933 | |||||||
| chr2:200404288 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.40-8023T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200404288 | |||||||
| chr2:200404358 | C | G | 2 | a0001c0001t0009g0160 a0001c0001t0009g0176 |
2 | NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.40-7953C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200404358 | |||||||
| chr2:200404465 | A | G | 1 | a0001c0003t0001g0278 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.40-7846A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200404465 | |||||||
| chr2:200404805 | A | G | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.40-7506A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200404805 | |||||||
| chr2:200404891 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.40-7420T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200404891 | |||||||
| chr2:200404981 | G | A | 1 | a0001c0001t0008g0015 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.40-7330G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200404981 | |||||||
| chr2:200405381 | C | CA | 159 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.40-6917dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200405381 | ||||||
| chr2:200405381 | C | CAA | 6 | a0001c0001t0005g0148 a0001c0001t0005g0211 a0001c0001t0010g0096 others(3): Show |
6 | HG02258.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-6918_40-6917dup others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200405381 | ||||||
| chr2:200405388 | A | T | 1 | a0001c0001t0042g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.40-6923A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200405388 | |||||||
| chr2:200405533 | T | C | 106 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(103): Show |
106 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.40-6778T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200405533 | |||||||
| chr2:200405643 | A | G | 31 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(28): Show |
31 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.40-6668A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200405643 | |||||||
| chr2:200405815 | A | G | 106 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(103): Show |
106 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.40-6496A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200405815 | |||||||
| chr2:200406078 | T | C | 1 | a0002c0004t0019g0131 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.40-6233T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200406078 | |||||||
| chr2:200406408 | T | TAA | 5 | a0001c0001t0010g0071 a0001c0002t0013g0138 a0001c0002t0081g0137 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-5903_40-5902ins others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200406408 | |||||||
| chr2:200406409 | T | A | 8 | a0001c0001t0010g0071 a0001c0001t0034g0144 a0001c0001t0059g0026 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-5902T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200406409 | |||||||
| chr2:200406409 | T | TA | 13 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0004g0045 others(10): Show |
13 | HG00408.hp2 HG01243.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.40-5884dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200406409 | ||||||
| chr2:200406409 | TA | T | 22 | a0001c0001t0002g0174 a0001c0001t0002g0227 a0001c0001t0003g0056 others(19): Show |
22 | HG01099.hp1 HG01993.hp1 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.40-5884delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200406409 | ||||||
| chr2:200406456 | G | A | 2 | a0001c0001t0003g0030 a0001c0001t0011g0248 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.40-5855G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200406456 | |||||||
| chr2:200406700 | G | A | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.40-5611G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200406700 | |||||||
| chr2:200406708 | A | G | 5 | a0001c0002t0030g0100 a0002c0004t0012g0020 a0002c0004t0012g0098 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-5603A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200406708 | |||||||
| chr2:200406733 | C | T | 31 | a0001c0001t0001g0196 a0001c0001t0001g0204 a0001c0001t0001g0213 others(28): Show |
31 | HG00099.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.40-5578C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200406733 | |||||||
| chr2:200406734 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.40-5577G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200406734 | |||||||
| chr2:200407127 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.40-5184G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200407127 | |||||||
| chr2:200407293 | G | C | 240 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(237): Show |
240 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.40-5018G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200407293 | |||||||
| chr2:200407642 | A | G | 3 | a0001c0001t0008g0063 a0001c0001t0008g0080 a0001c0001t0074g0062 |
3 | HG00733.hp2 HG02602.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.40-4669A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200407642 | |||||||
| chr2:200407982 | A | G | 77 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(74): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.40-4329A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200407982 | |||||||
| chr2:200408238 | G | A | 10 | a0001c0001t0014g0105 a0001c0001t0014g0110 a0001c0001t0014g0128 others(7): Show |
10 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.40-4073G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408238 | |||||||
| chr2:200408247 | G | T | 7 | a0001c0001t0010g0071 a0001c0001t0059g0026 a0001c0002t0013g0138 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-4064G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408247 | |||||||
| chr2:200408308 | C | T | 1 | a0001c0003t0003g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.40-4003C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408308 | |||||||
| chr2:200408336 | C | T | 1 | a0001c0001t0018g0024 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.40-3975C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408336 | |||||||
| chr2:200408629 | G | A | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.40-3682G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408629 | |||||||
| chr2:200408708 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.40-3603C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408708 | |||||||
| chr2:200408768 | G | A | 2 | a0001c0001t0014g0110 a0001c0001t0014g0128 |
2 | HG01070.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.40-3543G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408768 | |||||||
| chr2:200408789 | A | G | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.40-3522A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408789 | |||||||
| chr2:200408840 | C | G | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.40-3471C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408840 | |||||||
| chr2:200408857 | G | T | 236 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.40-3454G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200408857 | |||||||
| chr2:200409059 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.40-3252G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200409059 | |||||||
| chr2:200409169 | G | A | 3 | a0001c0001t0003g0049 a0001c0001t0032g0010 a0001c0010t0065g0004 |
3 | HG01123.hp2 HG02109.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.40-3142G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200409169 | |||||||
| chr2:200409217 | T | G | 8 | a0001c0001t0002g0194 a0001c0001t0002g0235 a0001c0001t0002g0238 others(5): Show |
8 | HG00621.hp1 HG02015.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-3094T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200409217 | |||||||
| chr2:200409305 | T | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0031 a0001c0001t0066g0125 |
3 | NA18983.hp2 NA18994.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.40-3006T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200409305 | |||||||
| chr2:200409364 | C | CT | 7 | a0001c0001t0010g0071 a0001c0001t0059g0026 a0001c0002t0013g0138 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-2937dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200409364 | ||||||
| chr2:200409738 | T | C | 6 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-2573T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200409738 | |||||||
| chr2:200409754 | A | G | 1 | a0001c0001t0079g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.40-2557A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200409754 | |||||||
| chr2:200409810 | A | G | 2 | a0001c0001t0013g0085 a0001c0001t0013g0086 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40-2501A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200409810 | |||||||
| chr2:200409922 | G | A | 4 | a0001c0001t0010g0096 a0001c0001t0010g0140 a0001c0001t0071g0139 others(1): Show |
4 | HG02258.hp1 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-2389G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200409922 | |||||||
| chr2:200410313 | A | T | 1 | a0001c0001t0005g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.40-1998A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200410313 | |||||||
| chr2:200410412 | CA | C | 235 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(232): Show |
235 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.40-1890delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200410412 | ||||||
| chr2:200410421 | A | C | 1 | a0001c0001t0004g0031 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.40-1890A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200410421 | |||||||
| chr2:200410944 | C | G | 1 | a0001c0003t0024g0242 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.40-1367C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200410944 | |||||||
| chr2:200411014 | C | CAT | 4 | a0001c0001t0010g0008 a0001c0001t0010g0096 a0001c0002t0062g0107 others(1): Show |
4 | HG01884.hp2 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-1281_40-1280dup others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200411014 | ||||||
| chr2:200411014 | C | CATAT | 7 | a0001c0001t0010g0140 a0001c0001t0020g0118 a0001c0001t0071g0139 others(4): Show |
7 | HG02129.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.40-1283_40-1280dup others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200411014 | ||||||
| chr2:200411014 | CAT | C | 13 | a0001c0001t0006g0046 a0001c0001t0010g0071 a0001c0001t0017g0087 others(10): Show |
13 | HG01517.hp2 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.40-1281_40-1280del others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200411014 | ||||||
| chr2:200411076 | A | G | 1 | a0001c0001t0008g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.40-1235A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200411076 | |||||||
| chr2:200411341 | A | G | 7 | a0001c0001t0010g0071 a0001c0001t0059g0026 a0001c0002t0013g0138 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-970A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200411341 | |||||||
| chr2:200411483 | A | AT | 103 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(100): Show |
103 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.40-826dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200411483 | ||||||
| chr2:200411609 | T | G | 241 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.40-702T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200411609 | |||||||
| chr2:200411712 | A | ATTTACT | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.40-598_40-593dupTT others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200411712 | ||||||
| chr2:200411779 | T | A | 6 | a0001c0001t0002g0194 a0001c0001t0002g0235 a0001c0001t0002g0238 others(3): Show |
6 | HG00621.hp1 NA18950.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-532T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200411779 | |||||||
| chr2:200411798 | A | G | 4 | a0001c0001t0001g0251 a0001c0001t0005g0259 a0001c0001t0044g0261 others(1): Show |
4 | NA18941.hp2 NA18967.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-513A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200411798 | |||||||
| chr2:200411916 | G | A | 94 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(91): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.40-395G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200411916 | |||||||
| chr2:200412070 | A | G | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.40-241A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200412070 | |||||||
| chr2:200412190 | T | C | 1 | a0001c0001t0026g0237 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.40-121T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200412190 | |||||||
| chr2:200412248 | T | C | 9 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0005g0259 others(6): Show |
9 | HG00438.hp2 HG02523.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.40-63T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | chr2 | 200412248 | |||||||
| chr2:200412288 | C | CTT | 6 | a0001c0001t0010g0071 a0001c0001t0059g0026 a0001c0002t0013g0138 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-11_40-10dupTT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 200412288 | ||||||
| chr2:200412458 | T | C | 100 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(97): Show |
100 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.148+39T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200412458 | |||||||
| chr2:200412598 | C | T | 138 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.148+179C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200412598 | |||||||
| chr2:200412605 | C | CA | 43 | a0001c0001t0001g0179 a0001c0001t0002g0150 a0001c0001t0002g0194 others(40): Show |
43 | HG00099.hp1 HG00621.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.148+203dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 200412605 | ||||||
| chr2:200412605 | CA | C | 84 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(81): Show |
84 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.148+203delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 200412605 | ||||||
| chr2:200412633 | C | T | 1 | a0001c0013t0010g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.148+214C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200412633 | |||||||
| chr2:200412705 | A | T | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.148+286A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200412705 | |||||||
| chr2:200412784 | A | G | 1 | a0001c0001t0011g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.148+365A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200412784 | |||||||
| chr2:200412789 | C | T | 91 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(88): Show |
91 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.148+370C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200412789 | |||||||
| chr2:200412849 | C | T | 7 | a0001c0001t0010g0071 a0001c0001t0059g0026 a0001c0002t0013g0138 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+430C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200412849 | |||||||
| chr2:200412888 | T | TAA | 9 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(6): Show |
9 | HG02486.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.148+475_148+476dup others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 200412888 | ||||||
| chr2:200412896 | T | A | 1 | a0001c0001t0025g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.148+477T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200412896 | |||||||
| chr2:200412971 | G | C | 1 | a0003c0006t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.148+552G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200412971 | |||||||
| chr2:200413106 | G | A | 1 | a0001c0002t0013g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.148+687G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200413106 | |||||||
| chr2:200413279 | G | A | 1 | a0001c0001t0004g0031 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.148+860G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200413279 | |||||||
| chr2:200413294 | TTATC | T | 38 | a0001c0001t0001g0159 a0001c0001t0003g0056 a0001c0001t0008g0015 others(35): Show |
38 | HG00408.hp2 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.148+881_148+884del others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 200413294 | ||||||
| chr2:200413576 | T | G | 2 | a0001c0001t0036g0076 a0001c0001t0077g0073 |
2 | HG00099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.148+1157T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200413576 | |||||||
| chr2:200413652 | T | C | 1 | a0001c0001t0005g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.148+1233T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200413652 | |||||||
| chr2:200413851 | C | T | 1 | a0006c0007t0047g0226 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.148+1432C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200413851 | |||||||
| chr2:200413954 | C | T | 1 | a0001c0001t0009g0176 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.148+1535C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200413954 | |||||||
| chr2:200414043 | G | A | 1 | a0001c0001t0034g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.148+1624G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200414043 | |||||||
| chr2:200414448 | C | T | 1 | a0001c0001t0007g0218 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.149-1931C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200414448 | |||||||
| chr2:200414918 | A | G | 102 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(99): Show |
102 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.149-1461A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200414918 | |||||||
| chr2:200415012 | T | A | 1 | a0001c0001t0004g0043 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.149-1367T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415012 | |||||||
| chr2:200415016 | T | A | 242 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.149-1363T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415016 | |||||||
| chr2:200415140 | C | CTGAATTA others(10): Show |
1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.149-1239_149-1238i others(19): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415140 | |||||||
| chr2:200415141 | C | T | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.149-1238C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415141 | |||||||
| chr2:200415143 | G | T | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.149-1236G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415143 | |||||||
| chr2:200415144 | T | A | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.149-1235T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415144 | |||||||
| chr2:200415229 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.149-1150C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415229 | |||||||
| chr2:200415307 | A | G | 3 | a0001c0003t0001g0274 a0001c0003t0001g0275 a0001c0003t0001g0278 |
3 | NA18966.hp2 NA18982.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.149-1072A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415307 | |||||||
| chr2:200415322 | T | C | 9 | a0001c0001t0010g0071 a0001c0001t0032g0010 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-1057T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415322 | |||||||
| chr2:200415500 | T | C | 3 | a0001c0001t0017g0087 a0001c0002t0006g0093 a0001c0002t0006g0094 |
3 | HG02055.hp2 HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.149-879T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200415500 | |||||||
| chr2:200415999 | CCATATTT others(4): Show |
C | 1 | a0001c0001t0004g0043 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.149-377_149-367del others(11): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 200415999 | ||||||
| chr2:200416273 | C | CA | 23 | a0001c0001t0001g0244 a0001c0001t0001g0253 a0001c0001t0001g0287 others(20): Show |
23 | HG01099.hp2 HG01943.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-89dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 200416273 | ||||||
| chr2:200416273 | CA | C | 114 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0002g0150 others(111): Show |
114 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.149-89delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 200416273 | ||||||
| chr2:200416273 | CAA | C | 7 | a0001c0001t0007g0240 a0001c0001t0008g0067 a0001c0001t0014g0110 others(4): Show |
7 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-90_149-89delAA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 200416273 | ||||||
| chr2:200416324 | T | G | 1 | a0001c0001t0007g0218 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.149-55T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 4/12 | chr2 | 200416324 | |||||||
| chr2:200416613 | C | G | 1 | a0001c0001t0050g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.198+185C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200416613 | |||||||
| chr2:200416799 | T | C | 106 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(103): Show |
106 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.198+371T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200416799 | |||||||
| chr2:200416959 | G | A | 5 | a0001c0001t0003g0082 a0001c0001t0010g0096 a0001c0001t0010g0140 others(2): Show |
5 | HG02258.hp1 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+531G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200416959 | |||||||
| chr2:200417290 | A | T | 136 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(133): Show |
136 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.198+862A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417290 | |||||||
| chr2:200417307 | C | T | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198+879C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417307 | |||||||
| chr2:200417350 | GT | G | 7 | a0001c0001t0010g0071 a0001c0001t0059g0026 a0001c0002t0013g0138 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+932delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 200417350 | ||||||
| chr2:200417351 | T | G | 9 | a0001c0001t0010g0096 a0001c0001t0010g0140 a0001c0001t0071g0139 others(6): Show |
9 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+923T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417351 | |||||||
| chr2:200417615 | T | C | 73 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(70): Show |
73 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.198+1187T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417615 | |||||||
| chr2:200417678 | C | T | 1 | a0001c0001t0011g0205 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.198+1250C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417678 | |||||||
| chr2:200417916 | T | A | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1334T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417916 | |||||||
| chr2:200417920 | A | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1330A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417920 | |||||||
| chr2:200417924 | T | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1326T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417924 | |||||||
| chr2:200417925 | A | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1325A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417925 | |||||||
| chr2:200417927 | T | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1323T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417927 | |||||||
| chr2:200417928 | G | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1322G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417928 | |||||||
| chr2:200417930 | T | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1320T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417930 | |||||||
| chr2:200417931 | T | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1319T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417931 | |||||||
| chr2:200417932 | G | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1318G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417932 | |||||||
| chr2:200417933 | T | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1317T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417933 | |||||||
| chr2:200417934 | T | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1316T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417934 | |||||||
| chr2:200417935 | G | T | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1315G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417935 | |||||||
| chr2:200417937 | G | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1313G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417937 | |||||||
| chr2:200417938 | T | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1312T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417938 | |||||||
| chr2:200417939 | A | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1311A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417939 | |||||||
| chr2:200417941 | A | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1309A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417941 | |||||||
| chr2:200417943 | T | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1307T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417943 | |||||||
| chr2:200417944 | G | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1306G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417944 | |||||||
| chr2:200417945 | A | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1305A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417945 | |||||||
| chr2:200417946 | G | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1304G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417946 | |||||||
| chr2:200417949 | T | C | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1301T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200417949 | |||||||
| chr2:200417964 | G | GCAACTTC others(14): Show |
1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-1282_199-1281i others(23): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 200417964 | ||||||
| chr2:200418057 | G | A | 1 | a0001c0001t0026g0236 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.199-1193G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200418057 | |||||||
| chr2:200418074 | C | T | 6 | a0001c0001t0010g0071 a0001c0001t0059g0026 a0001c0002t0013g0138 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-1176C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200418074 | |||||||
| chr2:200418213 | C | T | 19 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(16): Show |
19 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.199-1037C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200418213 | |||||||
| chr2:200418217 | G | A | 91 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(88): Show |
91 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.199-1033G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200418217 | |||||||
| chr2:200418227 | G | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.199-1023G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200418227 | |||||||
| chr2:200418542 | C | A | 1 | a0001c0001t0002g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.199-708C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200418542 | |||||||
| chr2:200418581 | T | TAATA | 78 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(75): Show |
78 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.199-635_199-632dup others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 200418581 | ||||||
| chr2:200418581 | T | TAATAAAT others(1): Show |
24 | a0001c0001t0002g0174 a0001c0001t0003g0040 a0001c0001t0004g0111 others(21): Show |
24 | HG00738.hp1 HG01070.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-639_199-632dup others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 200418581 | ||||||
| chr2:200418581 | T | TAATAAAT others(5): Show |
5 | a0001c0001t0003g0122 a0001c0001t0009g0163 a0001c0002t0006g0117 others(2): Show |
5 | HG02258.hp1 HG02293.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-643_199-632dup others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 200418581 | ||||||
| chr2:200418581 | T | TAATTA | 3 | a0002c0004t0012g0145 a0002c0004t0019g0285 a0002c0004t0019g0286 |
3 | HG02486.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.199-666_199-665ins others(5): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 200418581 | ||||||
| chr2:200418581 | TAATA | T | 3 | a0001c0001t0011g0205 a0001c0001t0036g0076 a0001c0001t0077g0073 |
3 | HG00099.hp1 HG01496.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.199-635_199-632del others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 200418581 | ||||||
| chr2:200418581 | TAATAAAT others(1): Show |
T | 132 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(129): Show |
132 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.199-639_199-632del others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 200418581 | ||||||
| chr2:200418581 | TAATAAAT others(5): Show |
T | 1 | a0003c0008t0058g0099 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.199-643_199-632del others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 200418581 | ||||||
| chr2:200418626 | G | A | 1 | a0001c0001t0078g0058 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.199-624G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200418626 | |||||||
| chr2:200418960 | T | C | 4 | a0001c0001t0010g0096 a0001c0001t0010g0140 a0001c0001t0071g0139 others(1): Show |
4 | HG02258.hp1 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-290T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200418960 | |||||||
| chr2:200419213 | A | T | 3 | a0001c0001t0008g0067 a0001c0001t0018g0072 a0001c0001t0075g0029 |
3 | HG03516.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.199-37A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 5/12 | chr2 | 200419213 | |||||||
| chr2:200419616 | C | T | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.445+120C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200419616 | |||||||
| chr2:200419710 | A | AT | 81 | a0001c0001t0001g0159 a0001c0001t0001g0214 a0001c0001t0001g0216 others(78): Show |
81 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.445+233dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200419710 | ||||||
| chr2:200419710 | A | ATT | 17 | a0001c0001t0003g0121 a0001c0001t0005g0186 a0001c0001t0009g0160 others(14): Show |
17 | HG01243.hp2 HG01517.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.445+232_445+233dup others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200419710 | ||||||
| chr2:200419710 | A | ATTT | 8 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+231_445+233dup others(3): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200419710 | ||||||
| chr2:200419710 | AT | A | 12 | a0001c0001t0002g0182 a0001c0001t0002g0200 a0001c0001t0021g0075 others(9): Show |
12 | HG01070.hp2 HG02015.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+233delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200419710 | ||||||
| chr2:200419761 | G | A | 1 | a0001c0001t0034g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.445+265G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200419761 | |||||||
| chr2:200419815 | G | C | 14 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(11): Show |
14 | HG02486.hp2 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.445+319G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200419815 | |||||||
| chr2:200419839 | G | C | 9 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(6): Show |
9 | HG02486.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+343G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200419839 | |||||||
| chr2:200420024 | T | C | 15 | a0001c0001t0010g0071 a0001c0001t0010g0140 a0001c0001t0014g0105 others(12): Show |
15 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.445+528T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420024 | |||||||
| chr2:200420237 | A | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.445+741A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420237 | |||||||
| chr2:200420300 | C | CTCATGCA others(76): Show |
2 | a0001c0001t0032g0010 a0001c0010t0065g0004 |
2 | HG02109.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.445+841_445+842ins others(83): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200420300 | ||||||
| chr2:200420306 | C | A | 132 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(129): Show |
132 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.445+810C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420306 | |||||||
| chr2:200420416 | T | C | 1 | a0001c0003t0038g0168 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.445+920T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420416 | |||||||
| chr2:200420774 | A | T | 1 | a0001c0001t0010g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.445+1278A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420774 | |||||||
| chr2:200420780 | A | G | 1 | a0002c0004t0012g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445+1284A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420780 | |||||||
| chr2:200420785 | T | C | 1 | a0001c0001t0050g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.445+1289T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420785 | |||||||
| chr2:200420878 | C | G | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.445+1382C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420878 | |||||||
| chr2:200420904 | C | T | 1 | a0001c0003t0024g0242 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.445+1408C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420904 | |||||||
| chr2:200420955 | C | T | 33 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(30): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.445+1459C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200420955 | |||||||
| chr2:200421050 | G | T | 15 | a0001c0001t0010g0071 a0001c0001t0010g0140 a0001c0001t0014g0105 others(12): Show |
15 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.445+1554G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200421050 | |||||||
| chr2:200421053 | G | GT | 6 | a0001c0001t0002g0194 a0001c0001t0002g0235 a0001c0001t0002g0238 others(3): Show |
6 | HG00621.hp1 NA18950.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+1561dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200421053 | ||||||
| chr2:200421063 | C | T | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.445+1567C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200421063 | |||||||
| chr2:200421375 | C | T | 1 | a0001c0001t0048g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.445+1879C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200421375 | |||||||
| chr2:200421615 | T | G | 1 | a0001c0001t0012g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.445+2119T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200421615 | |||||||
| chr2:200421635 | C | T | 88 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(85): Show |
88 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.445+2139C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200421635 | |||||||
| chr2:200421830 | GCTTTCAC others(8): Show |
G | 3 | a0001c0001t0008g0067 a0001c0001t0018g0072 a0001c0001t0075g0029 |
3 | HG03516.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.445+2341_445+2355d others(17): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200421830 | ||||||
| chr2:200421857 | C | T | 16 | a0001c0001t0010g0071 a0001c0001t0010g0140 a0001c0001t0014g0105 others(13): Show |
16 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.445+2361C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200421857 | |||||||
| chr2:200422324 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.445+2828C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200422324 | |||||||
| chr2:200422330 | A | G | 9 | a0001c0001t0010g0071 a0001c0001t0010g0140 a0001c0001t0059g0026 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.445+2834A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200422330 | |||||||
| chr2:200422524 | GAGTA | G | 296 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.445+3031_445+3034d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200422524 | ||||||
| chr2:200422537 | C | CA | 121 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.445+3056dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200422537 | ||||||
| chr2:200422537 | CA | C | 96 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(93): Show |
96 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.445+3056delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200422537 | ||||||
| chr2:200422552 | A | AG | 14 | a0001c0001t0005g0156 a0001c0001t0014g0068 a0001c0001t0014g0134 others(11): Show |
14 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.445+3061dupG | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200422552 | ||||||
| chr2:200422570 | T | C | 5 | a0001c0002t0030g0100 a0002c0004t0012g0020 a0002c0004t0012g0098 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+3074T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200422570 | |||||||
| chr2:200422610 | A | G | 4 | a0001c0001t0009g0162 a0001c0001t0009g0165 a0001c0001t0009g0166 others(1): Show |
4 | HG01257.hp1 HG01975.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+3114A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200422610 | |||||||
| chr2:200422692 | A | C | 1 | a0001c0001t0009g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.445+3196A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200422692 | |||||||
| chr2:200422753 | C | T | 1 | a0001c0001t0010g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.445+3257C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200422753 | |||||||
| chr2:200422837 | C | T | 5 | a0001c0002t0030g0100 a0002c0004t0012g0020 a0002c0004t0012g0098 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+3341C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200422837 | |||||||
| chr2:200423200 | T | A | 14 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(11): Show |
14 | HG02486.hp2 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.445+3704T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200423200 | |||||||
| chr2:200423384 | T | C | 9 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(6): Show |
9 | HG02486.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+3888T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200423384 | |||||||
| chr2:200423921 | T | C | 23 | a0001c0001t0010g0071 a0001c0001t0010g0140 a0001c0001t0012g0077 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.445+4425T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200423921 | |||||||
| chr2:200424160 | C | G | 1 | a0003c0006t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.445+4664C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200424160 | |||||||
| chr2:200424323 | TA | T | 105 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(102): Show |
105 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.445+4837delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200424323 | ||||||
| chr2:200424496 | AAAAC | A | 3 | a0001c0001t0014g0105 a0001c0001t0014g0128 a0001c0001t0020g0106 |
3 | HG01099.hp1 HG01106.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.445+5012_445+5015d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200424496 | ||||||
| chr2:200424675 | A | G | 30 | a0001c0001t0010g0071 a0001c0001t0010g0140 a0001c0001t0012g0077 others(27): Show |
30 | HG01099.hp1 HG01106.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.445+5179A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200424675 | |||||||
| chr2:200424808 | T | C | 104 | a0001c0001t0001g0159 a0001c0001t0001g0233 a0001c0001t0002g0154 others(101): Show |
104 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.445+5312T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200424808 | |||||||
| chr2:200424925 | T | G | 7 | a0001c0001t0002g0249 a0001c0001t0020g0118 a0001c0001t0022g0263 others(4): Show |
7 | HG02129.hp1 HG02155.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.445+5429T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200424925 | |||||||
| chr2:200424997 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.445+5501C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200424997 | |||||||
| chr2:200425023 | T | C | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0007g0289 |
3 | HG01943.hp1 HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.445+5527T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425023 | |||||||
| chr2:200425033 | C | T | 74 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(71): Show |
74 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.445+5537C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425033 | |||||||
| chr2:200425070 | T | C | 1 | a0001c0003t0024g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.445+5574T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425070 | |||||||
| chr2:200425128 | G | C | 1 | a0001c0001t0011g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.445+5632G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425128 | |||||||
| chr2:200425128 | G | GC | 36 | a0001c0001t0001g0216 a0001c0001t0001g0232 a0001c0001t0001g0233 others(33): Show |
36 | HG00621.hp1 HG01099.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.445+5647dupC | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200425128 | ||||||
| chr2:200425128 | GC | G | 96 | a0001c0001t0001g0159 a0001c0001t0001g0204 a0001c0001t0001g0225 others(93): Show |
96 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.445+5647delC | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200425128 | ||||||
| chr2:200425128 | GCC | G | 76 | a0001c0001t0001g0196 a0001c0001t0001g0214 a0001c0001t0001g0220 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.445+5646_445+5647d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200425128 | ||||||
| chr2:200425129 | C | G | 1 | a0001c0001t0011g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.445+5633C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425129 | |||||||
| chr2:200425134 | C | G | 1 | a0001c0003t0001g0275 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.445+5638C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425134 | |||||||
| chr2:200425135 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.445+5639C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425135 | |||||||
| chr2:200425135 | C | G | 36 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(33): Show |
36 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.445+5639C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425135 | |||||||
| chr2:200425137 | C | A | 1 | a0001c0001t0076g0091 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.445+5641C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425137 | |||||||
| chr2:200425137 | C | G | 7 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.445+5641C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425137 | |||||||
| chr2:200425493 | C | T | 1 | a0001c0001t0010g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.445+5997C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425493 | |||||||
| chr2:200425658 | C | T | 1 | a0001c0001t0009g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.445+6162C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425658 | |||||||
| chr2:200425755 | G | A | 75 | a0001c0001t0001g0159 a0001c0001t0002g0154 a0001c0001t0002g0157 others(72): Show |
75 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.445+6259G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425755 | |||||||
| chr2:200425778 | G | A | 1 | a0001c0003t0001g0269 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.445+6282G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425778 | |||||||
| chr2:200425813 | A | G | 127 | a0001c0001t0001g0196 a0001c0001t0001g0204 a0001c0001t0001g0213 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.445+6317A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425813 | |||||||
| chr2:200425913 | A | C | 11 | a0001c0001t0003g0122 a0001c0001t0004g0111 a0001c0001t0005g0173 others(8): Show |
11 | NA18946.hp2 NA18953.hp1 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.445+6417A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425913 | |||||||
| chr2:200425927 | C | T | 1 | a0001c0001t0004g0083 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.445+6431C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200425927 | |||||||
| chr2:200426082 | CT | C | 139 | a0001c0001t0001g0159 a0001c0001t0001g0260 a0001c0001t0002g0157 others(136): Show |
139 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.445+6612delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200426082 | ||||||
| chr2:200426082 | CTT | C | 94 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0202 others(91): Show |
94 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.445+6611_445+6612d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200426082 | ||||||
| chr2:200426082 | CTTT | C | 6 | a0001c0001t0001g0287 a0001c0001t0003g0066 a0001c0001t0015g0212 others(3): Show |
6 | HG01099.hp2 HG01257.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+6610_445+6612d others(5): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200426082 | ||||||
| chr2:200426082 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.445+6600_445+6612d others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200426082 | ||||||
| chr2:200426286 | T | G | 6 | a0001c0001t0008g0013 a0001c0001t0013g0085 a0001c0001t0013g0086 others(3): Show |
6 | HG01070.hp1 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+6790T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200426286 | |||||||
| chr2:200426369 | A | C | 2 | a0001c0001t0010g0129 a0001c0001t0032g0010 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.445+6873A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200426369 | |||||||
| chr2:200426373 | A | G | 40 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(37): Show |
40 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.445+6877A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200426373 | |||||||
| chr2:200426387 | A | G | 154 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.445+6891A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200426387 | |||||||
| chr2:200426412 | A | G | 1 | a0002c0004t0068g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.445+6916A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200426412 | |||||||
| chr2:200426773 | C | G | 2 | a0001c0001t0010g0129 a0001c0001t0032g0010 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.445+7277C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200426773 | |||||||
| chr2:200426846 | G | A | 1 | a0001c0002t0013g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.445+7350G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200426846 | |||||||
| chr2:200426857 | C | G | 2 | a0001c0001t0031g0021 a0001c0001t0031g0052 |
2 | HG01975.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.445+7361C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200426857 | |||||||
| chr2:200427292 | T | G | 1 | a0001c0001t0010g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.445+7796T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200427292 | |||||||
| chr2:200427320 | A | C | 68 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(65): Show |
68 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.445+7824A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200427320 | |||||||
| chr2:200427378 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.445+7882C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200427378 | |||||||
| chr2:200427400 | G | A | 2 | a0001c0002t0013g0006 a0001c0002t0013g0124 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.445+7904G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200427400 | |||||||
| chr2:200427615 | A | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.445+8119A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200427615 | |||||||
| chr2:200427624 | A | C | 7 | a0001c0003t0001g0250 a0001c0003t0001g0256 a0001c0003t0001g0269 others(4): Show |
7 | HG01070.hp2 HG01978.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.445+8128A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200427624 | |||||||
| chr2:200427928 | T | G | 102 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.445+8432T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200427928 | |||||||
| chr2:200428002 | C | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0007g0289 |
3 | HG01943.hp1 HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.445+8506C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200428002 | |||||||
| chr2:200428030 | A | G | 64 | a0001c0001t0002g0154 a0001c0001t0002g0157 a0001c0001t0002g0174 others(61): Show |
64 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.445+8534A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200428030 | |||||||
| chr2:200428051 | C | CAG | 172 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.445+8556_445+8557d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200428051 | ||||||
| chr2:200428072 | AC | A | 116 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.445+8577delC | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200428072 | |||||||
| chr2:200428073 | C | A | 54 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(51): Show |
54 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.445+8577C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200428073 | |||||||
| chr2:200428698 | C | T | 1 | a0001c0001t0009g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.445+9202C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200428698 | |||||||
| chr2:200428926 | C | T | 97 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(94): Show |
97 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.445+9430C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200428926 | |||||||
| chr2:200428998 | G | A | 52 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.445+9502G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200428998 | |||||||
| chr2:200429120 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.445+9624G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200429120 | |||||||
| chr2:200430014 | C | T | 1 | a0001c0001t0009g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.446-9108C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200430014 | |||||||
| chr2:200430148 | G | A | 1 | a0001c0002t0006g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.446-8974G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200430148 | |||||||
| chr2:200430214 | A | G | 2 | a0001c0001t0054g0296 a0001c0001t0057g0298 |
2 | HG00099.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.446-8908A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200430214 | |||||||
| chr2:200430358 | T | C | 3 | a0001c0001t0008g0013 a0001c0001t0014g0110 a0001c0001t0021g0014 |
3 | HG01070.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.446-8764T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200430358 | |||||||
| chr2:200430479 | C | T | 51 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.446-8643C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200430479 | |||||||
| chr2:200430692 | C | A | 1 | a0001c0001t0002g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.446-8430C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200430692 | |||||||
| chr2:200430715 | C | CT | 28 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0004g0028 others(25): Show |
28 | HG01123.hp1 HG01361.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.446-8387dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200430715 | ||||||
| chr2:200430715 | CT | C | 14 | a0001c0001t0004g0083 a0001c0001t0014g0110 a0001c0001t0015g0170 others(11): Show |
14 | HG01070.hp1 HG01070.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.446-8387delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200430715 | ||||||
| chr2:200430774 | G | A | 2 | a0001c0001t0033g0025 a0001c0001t0060g0022 |
2 | NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.446-8348G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200430774 | |||||||
| chr2:200430778 | C | T | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.446-8344C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200430778 | |||||||
| chr2:200431308 | C | T | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.446-7814C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200431308 | |||||||
| chr2:200431741 | T | G | 1 | a0001c0003t0001g0255 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.446-7381T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200431741 | |||||||
| chr2:200431756 | A | G | 1 | a0001c0001t0003g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.446-7366A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200431756 | |||||||
| chr2:200431757 | C | T | 248 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.446-7365C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200431757 | |||||||
| chr2:200432038 | A | G | 16 | a0001c0001t0008g0067 a0001c0001t0012g0077 a0001c0001t0012g0078 others(13): Show |
16 | HG01975.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.446-7084A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200432038 | |||||||
| chr2:200432071 | G | A | 5 | a0001c0002t0030g0100 a0002c0004t0012g0020 a0002c0004t0012g0098 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-7051G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200432071 | |||||||
| chr2:200432081 | G | T | 1 | a0001c0001t0008g0054 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.446-7041G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200432081 | |||||||
| chr2:200432447 | CATTT | C | 94 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(91): Show |
94 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.446-6672_446-6669d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200432447 | ||||||
| chr2:200432805 | T | G | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.446-6317T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200432805 | |||||||
| chr2:200432937 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.446-6185T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200432937 | |||||||
| chr2:200433028 | T | C | 1 | a0001c0001t0003g0120 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.446-6094T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433028 | |||||||
| chr2:200433133 | T | C | 132 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(129): Show |
132 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.446-5989T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433133 | |||||||
| chr2:200433138 | C | T | 70 | a0001c0001t0002g0154 a0001c0001t0002g0157 a0001c0001t0002g0174 others(67): Show |
70 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.446-5984C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433138 | |||||||
| chr2:200433474 | T | C | 1 | a0001c0001t0020g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.446-5648T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433474 | |||||||
| chr2:200433573 | A | G | 3 | a0001c0001t0010g0140 a0001c0001t0071g0139 a0001c0002t0030g0141 |
3 | HG02258.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.446-5549A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433573 | |||||||
| chr2:200433643 | A | G | 134 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.446-5479A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433643 | |||||||
| chr2:200433797 | A | G | 3 | a0001c0001t0008g0054 a0001c0001t0023g0207 a0001c0001t0023g0208 |
3 | HG00735.hp2 HG01106.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.446-5325A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433797 | |||||||
| chr2:200433804 | C | T | 293 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.446-5318C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433804 | |||||||
| chr2:200433914 | G | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.446-5208G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433914 | |||||||
| chr2:200433924 | A | G | 3 | a0001c0002t0013g0138 a0001c0002t0081g0137 a0002c0004t0019g0135 |
3 | HG01891.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.446-5198A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433924 | |||||||
| chr2:200433932 | T | C | 243 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.446-5190T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200433932 | |||||||
| chr2:200434018 | A | G | 96 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.446-5104A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200434018 | |||||||
| chr2:200434184 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.446-4938G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200434184 | |||||||
| chr2:200434224 | T | C | 10 | a0001c0001t0059g0026 a0001c0002t0013g0138 a0001c0002t0030g0100 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.446-4898T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200434224 | |||||||
| chr2:200434312 | C | G | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.446-4810C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200434312 | |||||||
| chr2:200434739 | A | G | 40 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(37): Show |
40 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.446-4383A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200434739 | |||||||
| chr2:200435170 | C | T | 1 | a0001c0001t0004g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.446-3952C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435170 | |||||||
| chr2:200435409 | T | G | 171 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.446-3713T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435409 | |||||||
| chr2:200435431 | C | A | 126 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(123): Show |
126 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.446-3691C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435431 | |||||||
| chr2:200435496 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0220 |
2 | HG00733.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.446-3626G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435496 | |||||||
| chr2:200435509 | C | T | 11 | a0001c0001t0001g0202 a0001c0001t0059g0026 a0001c0002t0013g0138 others(8): Show |
11 | HG00738.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.446-3613C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435509 | |||||||
| chr2:200435510 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.446-3612G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435510 | |||||||
| chr2:200435596 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.446-3526C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435596 | |||||||
| chr2:200435622 | A | T | 1 | a0001c0001t0001g0251 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.446-3500A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435622 | |||||||
| chr2:200435688 | G | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.446-3434G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435688 | |||||||
| chr2:200435805 | A | C | 40 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(37): Show |
40 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.446-3317A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435805 | |||||||
| chr2:200435880 | A | G | 1 | a0001c0001t0003g0121 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.446-3242A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435880 | |||||||
| chr2:200435928 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.446-3194G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200435928 | |||||||
| chr2:200436245 | C | T | 1 | a0001c0002t0013g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.446-2877C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200436245 | |||||||
| chr2:200436477 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.446-2645C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200436477 | |||||||
| chr2:200436486 | AG | A | 5 | a0001c0001t0001g0204 a0001c0001t0001g0220 a0001c0001t0001g0232 others(2): Show |
5 | HG00733.hp1 HG01175.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.446-2634delG | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200436486 | ||||||
| chr2:200436513 | T | C | 98 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(95): Show |
98 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.446-2609T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200436513 | |||||||
| chr2:200436757 | G | A | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.446-2365G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200436757 | |||||||
| chr2:200437148 | T | C | 172 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(169): Show |
172 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.446-1974T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200437148 | |||||||
| chr2:200437468 | C | T | 2 | a0001c0001t0015g0212 a0007c0012t0015g0223 |
2 | HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.446-1654C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200437468 | |||||||
| chr2:200437827 | A | G | 3 | a0003c0006t0017g0130 a0003c0006t0032g0012 a0003c0008t0058g0099 |
3 | HG01243.hp1 HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.446-1295A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200437827 | |||||||
| chr2:200437925 | T | C | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.446-1197T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200437925 | |||||||
| chr2:200438038 | G | A | 1 | a0001c0001t0014g0134 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.446-1084G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438038 | |||||||
| chr2:200438043 | G | A | 3 | a0001c0001t0004g0044 a0001c0001t0004g0045 a0001c0001t0004g0083 |
3 | NA18954.hp1 NA18975.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.446-1079G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438043 | |||||||
| chr2:200438076 | T | C | 1 | a0002c0004t0019g0286 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.446-1046T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438076 | |||||||
| chr2:200438083 | G | C | 1 | a0001c0001t0021g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.446-1039G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438083 | |||||||
| chr2:200438116 | A | G | 134 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.446-1006A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438116 | |||||||
| chr2:200438149 | A | G | 1 | a0001c0001t0028g0206 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.446-973A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438149 | |||||||
| chr2:200438287 | G | T | 96 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.446-835G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438287 | |||||||
| chr2:200438318 | C | CT | 134 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.446-802dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200438318 | ||||||
| chr2:200438400 | TCAGGCCA others(4): Show |
T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.446-719_446-709del others(11): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 200438400 | ||||||
| chr2:200438504 | A | C | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.446-618A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438504 | |||||||
| chr2:200438628 | A | T | 39 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(36): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.446-494A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438628 | |||||||
| chr2:200438650 | C | T | 2 | a0001c0001t0004g0028 a0002c0004t0068g0002 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.446-472C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438650 | |||||||
| chr2:200438679 | A | C | 1 | a0001c0002t0030g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-443A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438679 | |||||||
| chr2:200438734 | C | T | 39 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(36): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.446-388C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438734 | |||||||
| chr2:200438931 | A | G | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.446-191A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 6/12 | chr2 | 200438931 | |||||||
| chr2:200439468 | A | G | 1 | a0001c0001t0005g0211 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.652+140A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200439468 | |||||||
| chr2:200439635 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.652+307A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200439635 | |||||||
| chr2:200439898 | A | C | 3 | a0001c0001t0010g0140 a0001c0001t0071g0139 a0001c0002t0030g0141 |
3 | HG02258.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.652+570A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200439898 | |||||||
| chr2:200439973 | G | A | 1 | a0002c0004t0012g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.652+645G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200439973 | |||||||
| chr2:200440129 | T | G | 1 | a0001c0003t0038g0168 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.653-520T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200440129 | |||||||
| chr2:200440346 | G | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.653-303G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200440346 | |||||||
| chr2:200440363 | A | G | 172 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.653-286A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200440363 | |||||||
| chr2:200440420 | C | G | 1 | a0001c0001t0032g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.653-229C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200440420 | |||||||
| chr2:200440426 | T | G | 12 | a0001c0001t0010g0071 a0001c0001t0010g0096 a0001c0001t0059g0026 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.653-223T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200440426 | |||||||
| chr2:200440503 | G | C | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.653-146G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200440503 | |||||||
| chr2:200440541 | A | G | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.653-108A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 7/12 | chr2 | 200440541 | |||||||
| chr2:200440828 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.788+44C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200440828 | |||||||
| chr2:200440892 | A | T | 1 | a0001c0001t0020g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.788+108A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200440892 | |||||||
| chr2:200441259 | G | A | 2 | a0001c0001t0013g0085 a0001c0001t0013g0086 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.788+475G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200441259 | |||||||
| chr2:200441411 | G | A | 5 | a0001c0002t0030g0100 a0002c0004t0012g0020 a0002c0004t0012g0098 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.788+627G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200441411 | |||||||
| chr2:200441416 | A | G | 169 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.788+632A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200441416 | |||||||
| chr2:200441468 | G | A | 2 | a0001c0001t0004g0039 a0001c0001t0005g0271 |
2 | NA19068.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.788+684G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200441468 | |||||||
| chr2:200441609 | G | C | 1 | a0001c0001t0005g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.788+825G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200441609 | |||||||
| chr2:200441800 | T | A | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.788+1016T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200441800 | |||||||
| chr2:200441814 | T | C | 6 | a0001c0001t0008g0013 a0001c0001t0013g0085 a0001c0001t0013g0086 others(3): Show |
6 | HG01070.hp1 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.788+1030T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200441814 | |||||||
| chr2:200442277 | C | A | 2 | a0001c0001t0014g0105 a0001c0001t0020g0106 |
2 | HG01106.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.788+1493C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200442277 | |||||||
| chr2:200442510 | CTAGAGGC others(5): Show |
C | 6 | a0001c0001t0003g0092 a0001c0001t0004g0036 a0001c0001t0033g0025 others(3): Show |
6 | HG04184.hp2 NA18962.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.788+1728_788+1739d others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200442510 | ||||||
| chr2:200443015 | A | C | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.788+2231A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443015 | |||||||
| chr2:200443050 | A | G | 6 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0246 others(3): Show |
6 | HG01074.hp2 HG01123.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.788+2266A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443050 | |||||||
| chr2:200443130 | A | C | 1 | a0001c0001t0014g0105 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.788+2346A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443130 | |||||||
| chr2:200443133 | C | T | 1 | a0001c0001t0064g0070 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.788+2349C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443133 | |||||||
| chr2:200443161 | T | G | 1 | a0001c0001t0004g0036 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.788+2377T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443161 | |||||||
| chr2:200443225 | G | C | 1 | a0002c0004t0019g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.788+2441G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443225 | |||||||
| chr2:200443258 | T | C | 1 | a0001c0001t0004g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.788+2474T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443258 | |||||||
| chr2:200443394 | T | C | 75 | a0001c0001t0002g0154 a0001c0001t0002g0157 a0001c0001t0002g0174 others(72): Show |
75 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.788+2610T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443394 | |||||||
| chr2:200443577 | T | C | 12 | a0001c0001t0010g0071 a0001c0001t0010g0096 a0001c0001t0059g0026 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.788+2793T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443577 | |||||||
| chr2:200443670 | A | C | 98 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(95): Show |
98 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.788+2886A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443670 | |||||||
| chr2:200443675 | T | C | 8 | a0001c0002t0006g0019 a0001c0002t0016g0279 a0001c0002t0016g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+2891T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443675 | |||||||
| chr2:200443763 | C | T | 243 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.788+2979C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443763 | |||||||
| chr2:200443817 | T | A | 126 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(123): Show |
126 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.788+3033T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200443817 | |||||||
| chr2:200444584 | GAA | G | 39 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(36): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.788+3802_788+3803d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200444584 | ||||||
| chr2:200444589 | C | T | 1 | a0001c0003t0001g0255 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.788+3805C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200444589 | |||||||
| chr2:200444629 | T | G | 1 | a0001c0001t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.788+3845T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200444629 | |||||||
| chr2:200444716 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.788+3932C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200444716 | |||||||
| chr2:200444802 | C | T | 39 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(36): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.788+4018C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200444802 | |||||||
| chr2:200444824 | T | C | 129 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(126): Show |
129 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.788+4040T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200444824 | |||||||
| chr2:200444871 | A | G | 4 | a0001c0001t0003g0048 a0001c0001t0014g0105 a0001c0001t0014g0128 others(1): Show |
4 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+4087A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200444871 | |||||||
| chr2:200444873 | A | C | 3 | a0003c0006t0017g0130 a0003c0006t0032g0012 a0003c0008t0058g0099 |
3 | HG01243.hp1 HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.788+4089A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200444873 | |||||||
| chr2:200444884 | C | CT | 9 | a0001c0001t0014g0068 a0001c0002t0006g0019 a0001c0002t0016g0279 others(6): Show |
9 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.788+4109dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200444884 | ||||||
| chr2:200445153 | GA | G | 13 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(10): Show |
13 | HG01975.hp1 HG02055.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.788+4379delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200445153 | ||||||
| chr2:200445318 | A | G | 5 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 others(2): Show |
5 | HG02486.hp1 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.788+4534A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200445318 | |||||||
| chr2:200445424 | G | A | 5 | a0001c0002t0006g0112 a0001c0002t0006g0113 a0001c0002t0006g0114 others(2): Show |
5 | NA18953.hp1 NA18955.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.788+4640G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200445424 | |||||||
| chr2:200445487 | A | G | 1 | a0001c0002t0030g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.788+4703A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200445487 | |||||||
| chr2:200445601 | C | T | 25 | a0001c0001t0010g0071 a0001c0001t0010g0096 a0001c0001t0012g0077 others(22): Show |
25 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.788+4817C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200445601 | |||||||
| chr2:200445764 | GT | G | 146 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(143): Show |
146 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.788+4990delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200445764 | ||||||
| chr2:200445764 | GTT | G | 96 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(93): Show |
96 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.788+4989_788+4990d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200445764 | ||||||
| chr2:200446059 | C | T | 1 | a0001c0001t0005g0148 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.788+5275C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200446059 | |||||||
| chr2:200446591 | C | T | 39 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(36): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.788+5807C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200446591 | |||||||
| chr2:200447049 | G | C | 133 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.788+6265G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447049 | |||||||
| chr2:200447303 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.788+6519T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447303 | |||||||
| chr2:200447382 | C | T | 1 | a0001c0002t0006g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.788+6598C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447382 | |||||||
| chr2:200447388 | C | T | 39 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(36): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.788+6604C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447388 | |||||||
| chr2:200447468 | A | G | 2 | a0001c0001t0036g0076 a0001c0001t0077g0073 |
2 | HG00099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.788+6684A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447468 | |||||||
| chr2:200447479 | G | A | 1 | a0001c0001t0009g0165 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.788+6695G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447479 | |||||||
| chr2:200447606 | A | C | 160 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.788+6822A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447606 | |||||||
| chr2:200447631 | A | G | 1 | a0001c0003t0003g0119 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.788+6847A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447631 | |||||||
| chr2:200447691 | T | A | 3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 |
3 | NA18969.hp2 NA19004.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.788+6907T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447691 | |||||||
| chr2:200447940 | A | G | 235 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(232): Show |
235 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.788+7156A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200447940 | |||||||
| chr2:200448016 | A | G | 5 | a0001c0002t0030g0100 a0002c0004t0012g0020 a0002c0004t0012g0098 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.788+7232A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448016 | |||||||
| chr2:200448074 | G | C | 45 | a0001c0001t0001g0233 a0001c0001t0003g0092 a0001c0001t0008g0015 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.788+7290G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448074 | |||||||
| chr2:200448152 | A | G | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.788+7368A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448152 | |||||||
| chr2:200448195 | A | G | 1 | a0001c0001t0015g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.788+7411A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448195 | |||||||
| chr2:200448207 | T | A | 2 | a0001c0001t0004g0033 a0001c0001t0073g0090 |
2 | HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.788+7423T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448207 | |||||||
| chr2:200448212 | T | C | 1 | a0001c0001t0003g0049 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.788+7428T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448212 | |||||||
| chr2:200448217 | A | G | 8 | a0001c0001t0010g0140 a0001c0001t0071g0139 a0001c0002t0030g0141 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.788+7433A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448217 | |||||||
| chr2:200448244 | C | A | 2 | a0001c0002t0030g0141 a0002c0004t0012g0101 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.788+7460C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448244 | |||||||
| chr2:200448322 | A | G | 1 | a0001c0002t0016g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.788+7538A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448322 | |||||||
| chr2:200448510 | T | G | 1 | a0001c0001t0037g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.788+7726T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448510 | |||||||
| chr2:200448545 | A | G | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.788+7761A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448545 | |||||||
| chr2:200448582 | A | C | 237 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.788+7798A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448582 | |||||||
| chr2:200448639 | C | T | 4 | a0001c0001t0037g0060 a0001c0001t0049g0245 a0001c0001t0050g0203 others(1): Show |
4 | HG01243.hp2 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+7855C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448639 | |||||||
| chr2:200448721 | A | G | 1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.788+7937A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448721 | |||||||
| chr2:200448976 | G | A | 5 | a0001c0001t0059g0026 a0001c0002t0013g0138 a0001c0002t0081g0137 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.788+8192G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200448976 | |||||||
| chr2:200449065 | C | G | 3 | a0001c0001t0008g0013 a0001c0001t0014g0110 a0001c0001t0021g0014 |
3 | HG01070.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.788+8281C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200449065 | |||||||
| chr2:200449169 | T | G | 3 | a0003c0006t0017g0130 a0003c0006t0032g0012 a0003c0008t0058g0099 |
3 | HG01243.hp1 HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.788+8385T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200449169 | |||||||
| chr2:200449265 | T | C | 107 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(104): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.788+8481T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200449265 | |||||||
| chr2:200449341 | A | G | 2 | a0001c0001t0017g0087 a0001c0002t0006g0093 |
2 | HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.788+8557A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200449341 | |||||||
| chr2:200449465 | A | C | 36 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(33): Show |
36 | HG00438.hp2 HG00621.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.788+8681A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200449465 | |||||||
| chr2:200449551 | A | G | 68 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(65): Show |
68 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.788+8767A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200449551 | |||||||
| chr2:200449603 | T | C | 117 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(114): Show |
117 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.788+8819T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200449603 | |||||||
| chr2:200450012 | G | A | 46 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(43): Show |
46 | HG00438.hp2 HG00621.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.788+9228G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200450012 | |||||||
| chr2:200450045 | G | A | 60 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(57): Show |
60 | HG00438.hp2 HG00621.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.788+9261G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200450045 | |||||||
| chr2:200450051 | C | T | 57 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(54): Show |
57 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.788+9267C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200450051 | |||||||
| chr2:200450132 | C | G | 2 | a0001c0001t0010g0129 a0001c0001t0032g0010 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.788+9348C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200450132 | |||||||
| chr2:200450241 | C | G | 18 | a0001c0001t0001g0214 a0001c0001t0001g0233 a0001c0001t0001g0253 others(15): Show |
18 | HG00438.hp1 HG01099.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.788+9457C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200450241 | |||||||
| chr2:200450308 | T | A | 1 | a0001c0001t0010g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.789-9461T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200450308 | |||||||
| chr2:200450384 | A | T | 47 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(44): Show |
47 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.789-9385A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200450384 | |||||||
| chr2:200450833 | G | A | 10 | a0001c0001t0010g0096 a0001c0001t0012g0077 a0001c0001t0012g0078 others(7): Show |
10 | HG02486.hp2 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.789-8936G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200450833 | |||||||
| chr2:200451046 | C | T | 6 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.789-8723C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451046 | |||||||
| chr2:200451094 | G | A | 6 | a0001c0001t0059g0026 a0001c0002t0013g0138 a0001c0002t0062g0107 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.789-8675G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451094 | |||||||
| chr2:200451101 | T | G | 34 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(31): Show |
34 | HG00438.hp2 HG00621.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-8668T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451101 | |||||||
| chr2:200451286 | C | T | 2 | a0001c0001t0004g0028 a0002c0004t0068g0002 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.789-8483C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451286 | |||||||
| chr2:200451491 | G | A | 34 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(31): Show |
34 | HG00438.hp2 HG00621.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-8278G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451491 | |||||||
| chr2:200451516 | C | G | 248 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.789-8253C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451516 | |||||||
| chr2:200451547 | C | T | 1 | a0001c0002t0006g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.789-8222C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451547 | |||||||
| chr2:200451653 | G | A | 33 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(30): Show |
33 | HG00438.hp2 HG00621.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-8116G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451653 | |||||||
| chr2:200451722 | T | A | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.789-8047T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451722 | |||||||
| chr2:200451832 | C | CT | 89 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0180 others(86): Show |
89 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.789-7933dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200451832 | ||||||
| chr2:200451837 | C | T | 217 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(214): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.789-7932C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200451837 | |||||||
| chr2:200452045 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0220 a0001c0001t0001g0232 |
3 | HG00733.hp1 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.789-7724G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200452045 | |||||||
| chr2:200452094 | G | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.789-7675G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200452094 | |||||||
| chr2:200452417 | G | T | 2 | a0001c0002t0030g0141 a0003c0008t0058g0099 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.789-7352G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200452417 | |||||||
| chr2:200452684 | G | T | 1 | a0001c0001t0002g0195 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.789-7085G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200452684 | |||||||
| chr2:200452727 | C | G | 247 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.789-7042C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200452727 | |||||||
| chr2:200452892 | TA | T | 124 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.789-6864delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200452892 | ||||||
| chr2:200452892 | TAA | T | 125 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(122): Show |
125 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.789-6865_789-6864d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200452892 | ||||||
| chr2:200452920 | T | C | 251 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(248): Show |
251 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.789-6849T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200452920 | |||||||
| chr2:200453229 | G | A | 130 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.789-6540G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453229 | |||||||
| chr2:200453251 | C | T | 14 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0005g0259 others(11): Show |
14 | HG00544.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.789-6518C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453251 | |||||||
| chr2:200453298 | C | A | 1 | a0001c0001t0009g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.789-6471C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453298 | |||||||
| chr2:200453303 | A | G | 1 | a0001c0001t0037g0060 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.789-6466A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453303 | |||||||
| chr2:200453402 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.789-6367T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453402 | |||||||
| chr2:200453464 | A | G | 10 | a0001c0001t0010g0096 a0001c0001t0018g0072 a0001c0001t0075g0029 others(7): Show |
10 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.789-6305A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453464 | |||||||
| chr2:200453511 | G | A | 5 | a0001c0002t0030g0141 a0002c0004t0012g0145 a0002c0004t0019g0285 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.789-6258G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453511 | |||||||
| chr2:200453650 | G | A | 29 | a0001c0001t0003g0048 a0001c0001t0005g0185 a0001c0001t0005g0186 others(26): Show |
29 | HG00544.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.789-6119G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453650 | |||||||
| chr2:200453797 | C | G | 1 | a0001c0001t0004g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.789-5972C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453797 | |||||||
| chr2:200453836 | G | C | 2 | a0001c0001t0010g0096 a0001c0010t0065g0004 |
2 | HG02735.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.789-5933G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453836 | |||||||
| chr2:200453927 | C | T | 1 | a0001c0001t0010g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.789-5842C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453927 | |||||||
| chr2:200453967 | T | G | 1 | a0001c0001t0005g0201 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.789-5802T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200453967 | |||||||
| chr2:200454072 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.789-5697G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454072 | |||||||
| chr2:200454212 | T | G | 1 | a0001c0001t0002g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.789-5557T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454212 | |||||||
| chr2:200454254 | G | A | 150 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.789-5515G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454254 | |||||||
| chr2:200454298 | G | A | 125 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.789-5471G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454298 | |||||||
| chr2:200454570 | TTAAC | T | 14 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0005g0259 others(11): Show |
14 | HG00544.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.789-5196_789-5193d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200454570 | ||||||
| chr2:200454577 | T | C | 14 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0005g0259 others(11): Show |
14 | HG00544.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.789-5192T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454577 | |||||||
| chr2:200454749 | C | G | 1 | a0001c0001t0052g0164 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.789-5020C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454749 | |||||||
| chr2:200454751 | G | A | 1 | a0001c0002t0016g0279 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.789-5018G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454751 | |||||||
| chr2:200454768 | A | G | 249 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.789-5001A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454768 | |||||||
| chr2:200454794 | C | T | 243 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.789-4975C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454794 | |||||||
| chr2:200454798 | C | T | 66 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(63): Show |
66 | HG00408.hp2 HG00544.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.789-4971C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454798 | |||||||
| chr2:200454893 | T | G | 2 | a0001c0005t0029g0230 a0001c0005t0029g0231 |
2 | NA18988.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.789-4876T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454893 | |||||||
| chr2:200454997 | G | A | 129 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.789-4772G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200454997 | |||||||
| chr2:200455070 | C | A | 249 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.789-4699C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200455070 | |||||||
| chr2:200455097 | A | C | 2 | a0001c0001t0003g0048 a0001c0001t0015g0170 |
2 | HG00642.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.789-4672A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200455097 | |||||||
| chr2:200455336 | G | A | 1 | a0001c0001t0005g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.789-4433G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200455336 | |||||||
| chr2:200455456 | G | C | 1 | a0001c0001t0004g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.789-4313G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200455456 | |||||||
| chr2:200455617 | C | T | 5 | a0001c0001t0017g0087 a0001c0001t0032g0010 a0001c0002t0006g0093 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-4152C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200455617 | |||||||
| chr2:200455808 | G | A | 98 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(95): Show |
98 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.789-3961G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200455808 | |||||||
| chr2:200455928 | A | G | 5 | a0001c0001t0017g0087 a0001c0001t0032g0010 a0001c0002t0006g0093 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-3841A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200455928 | |||||||
| chr2:200456058 | A | G | 1 | a0001c0002t0013g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.789-3711A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456058 | |||||||
| chr2:200456478 | A | G | 1 | a0001c0001t0010g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.789-3291A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456478 | |||||||
| chr2:200456481 | G | A | 130 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.789-3288G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456481 | |||||||
| chr2:200456520 | C | T | 99 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(96): Show |
99 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.789-3249C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456520 | |||||||
| chr2:200456534 | G | A | 4 | a0001c0002t0013g0006 a0001c0002t0013g0124 a0001c0002t0013g0138 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-3235G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456534 | |||||||
| chr2:200456598 | A | C | 1 | a0001c0001t0071g0139 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.789-3171A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456598 | |||||||
| chr2:200456609 | G | A | 1 | a0001c0001t0067g0037 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.789-3160G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456609 | |||||||
| chr2:200456612 | G | A | 1 | a0001c0001t0005g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.789-3157G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456612 | |||||||
| chr2:200456828 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.789-2941A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456828 | |||||||
| chr2:200456896 | C | A | 4 | a0001c0001t0017g0087 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-2873C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200456896 | |||||||
| chr2:200457070 | G | C | 1 | a0001c0002t0030g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.789-2699G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200457070 | |||||||
| chr2:200457223 | T | TAC | 8 | a0001c0001t0010g0140 a0001c0002t0006g0112 a0001c0002t0006g0113 others(5): Show |
8 | HG02145.hp1 HG03209.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.789-2510_789-2509d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200457223 | ||||||
| chr2:200457223 | T | TACAC | 5 | a0001c0001t0004g0044 a0001c0001t0004g0045 a0001c0001t0004g0083 others(2): Show |
5 | HG02572.hp1 NA18946.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-2512_789-2509d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200457223 | ||||||
| chr2:200457223 | TAC | T | 10 | a0001c0001t0004g0028 a0001c0001t0008g0013 a0001c0001t0012g0077 others(7): Show |
10 | HG02559.hp2 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.789-2510_789-2509d others(4): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200457223 | ||||||
| chr2:200457223 | TACAC | T | 30 | a0001c0001t0001g0214 a0001c0001t0001g0224 a0001c0001t0001g0253 others(27): Show |
30 | HG00408.hp1 HG01257.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.789-2512_789-2509d others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200457223 | ||||||
| chr2:200457223 | TACACAC | T | 149 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.789-2514_789-2509d others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200457223 | ||||||
| chr2:200457223 | TACACACA others(1): Show |
T | 67 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0001g0251 others(64): Show |
67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.789-2516_789-2509d others(10): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200457223 | ||||||
| chr2:200457223 | TACACACA others(3): Show |
T | 1 | a0001c0002t0062g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.789-2518_789-2509d others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200457223 | ||||||
| chr2:200457305 | C | T | 98 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(95): Show |
98 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.789-2464C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200457305 | |||||||
| chr2:200457561 | C | G | 1 | a0001c0001t0004g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.789-2208C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200457561 | |||||||
| chr2:200457812 | T | C | 291 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.789-1957T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200457812 | |||||||
| chr2:200457850 | T | A | 3 | a0001c0001t0008g0013 a0001c0001t0021g0014 a0001c0001t0048g0221 |
3 | HG01257.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.789-1919T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200457850 | |||||||
| chr2:200457973 | A | G | 1 | a0001c0001t0006g0046 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.789-1796A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200457973 | |||||||
| chr2:200458135 | T | C | 125 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.789-1634T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200458135 | |||||||
| chr2:200458617 | T | A | 66 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(63): Show |
66 | HG00408.hp2 HG00544.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.789-1152T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200458617 | |||||||
| chr2:200458733 | TA | T | 132 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.789-1024delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 200458733 | ||||||
| chr2:200458764 | G | A | 66 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(63): Show |
66 | HG00408.hp2 HG00544.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.789-1005G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200458764 | |||||||
| chr2:200458823 | A | G | 242 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.789-946A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200458823 | |||||||
| chr2:200458925 | G | A | 1 | a0002c0004t0019g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.789-844G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200458925 | |||||||
| chr2:200459038 | T | C | 144 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.789-731T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200459038 | |||||||
| chr2:200459150 | G | A | 1 | a0001c0001t0004g0036 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.789-619G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200459150 | |||||||
| chr2:200459162 | C | T | 126 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.789-607C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200459162 | |||||||
| chr2:200459255 | T | G | 9 | a0001c0001t0018g0072 a0001c0001t0075g0029 a0001c0002t0030g0141 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.789-514T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200459255 | |||||||
| chr2:200459355 | C | G | 66 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(63): Show |
66 | HG00408.hp2 HG00544.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.789-414C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200459355 | |||||||
| chr2:200459443 | G | C | 14 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0005g0259 others(11): Show |
14 | HG00544.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.789-326G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200459443 | |||||||
| chr2:200459454 | T | C | 2 | a0001c0001t0003g0003 a0001c0002t0045g0291 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.789-315T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200459454 | |||||||
| chr2:200459514 | G | T | 5 | a0001c0001t0017g0087 a0001c0001t0032g0010 a0001c0002t0006g0093 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-255G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 8/12 | chr2 | 200459514 | |||||||
| chr2:200459910 | T | C | 9 | a0001c0001t0018g0072 a0001c0001t0075g0029 a0001c0002t0030g0141 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+83T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200459910 | |||||||
| chr2:200460310 | C | T | 15 | a0001c0001t0003g0048 a0001c0001t0014g0105 a0001c0001t0014g0110 others(12): Show |
15 | HG00639.hp2 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.847+483C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200460310 | |||||||
| chr2:200460612 | G | A | 1 | a0002c0004t0063g0102 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.847+785G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200460612 | |||||||
| chr2:200460676 | G | A | 7 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(4): Show |
7 | HG03688.hp2 HG03927.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+849G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200460676 | |||||||
| chr2:200460855 | C | G | 1 | a0001c0001t0079g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.847+1028C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200460855 | |||||||
| chr2:200461103 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.847+1276C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200461103 | |||||||
| chr2:200461290 | G | C | 1 | a0001c0001t0010g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.847+1463G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200461290 | |||||||
| chr2:200461441 | G | A | 3 | a0001c0001t0008g0013 a0001c0001t0021g0014 a0001c0001t0048g0221 |
3 | HG01257.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.847+1614G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200461441 | |||||||
| chr2:200461601 | A | G | 3 | a0001c0001t0008g0013 a0001c0001t0021g0014 a0001c0001t0048g0221 |
3 | HG01257.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.847+1774A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200461601 | |||||||
| chr2:200461667 | C | G | 1 | a0001c0001t0071g0139 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.847+1840C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200461667 | |||||||
| chr2:200461724 | T | C | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.847+1897T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200461724 | |||||||
| chr2:200461743 | A | G | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.847+1916A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200461743 | |||||||
| chr2:200462025 | AT | A | 129 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.847+2200delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 200462025 | ||||||
| chr2:200462029 | T | A | 1 | a0001c0001t0049g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.847+2202T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462029 | |||||||
| chr2:200462051 | C | T | 14 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0005g0259 others(11): Show |
14 | HG00544.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.847+2224C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462051 | |||||||
| chr2:200462121 | T | C | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.847+2294T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462121 | |||||||
| chr2:200462241 | T | A | 1 | a0001c0001t0007g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.847+2414T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462241 | |||||||
| chr2:200462314 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.847+2487G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462314 | |||||||
| chr2:200462437 | C | T | 5 | a0001c0002t0030g0141 a0002c0004t0012g0145 a0002c0004t0019g0285 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+2610C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462437 | |||||||
| chr2:200462547 | A | G | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.847+2720A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462547 | |||||||
| chr2:200462582 | G | A | 2 | a0001c0002t0030g0141 a0003c0008t0058g0099 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.847+2755G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462582 | |||||||
| chr2:200462756 | A | C | 1 | a0001c0001t0008g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.847+2929A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462756 | |||||||
| chr2:200462782 | C | A | 5 | a0001c0002t0030g0141 a0002c0004t0012g0145 a0002c0004t0019g0285 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+2955C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462782 | |||||||
| chr2:200462785 | G | A | 2 | a0001c0001t0003g0041 a0001c0001t0003g0092 |
2 | HG04184.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.847+2958G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462785 | |||||||
| chr2:200462908 | G | A | 249 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.847+3081G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200462908 | |||||||
| chr2:200462940 | CAAT | C | 6 | a0001c0002t0016g0279 a0001c0002t0016g0280 a0001c0002t0016g0281 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.847+3130_847+3132d others(5): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 200462940 | ||||||
| chr2:200463004 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.847+3177G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200463004 | |||||||
| chr2:200463011 | A | G | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.847+3184A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200463011 | |||||||
| chr2:200463042 | C | CA | 30 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(27): Show |
30 | HG00408.hp2 HG00733.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.847+3220dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 200463042 | ||||||
| chr2:200463042 | C | CG | 5 | a0001c0001t0037g0060 a0001c0001t0037g0064 a0001c0001t0049g0245 others(2): Show |
5 | HG01243.hp2 HG02735.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+3215_847+3216i others(3): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200463042 | |||||||
| chr2:200463199 | C | T | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.847+3372C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200463199 | |||||||
| chr2:200463544 | C | T | 1 | a0001c0003t0003g0119 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.847+3717C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200463544 | |||||||
| chr2:200463682 | A | G | 290 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.848-3608A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200463682 | |||||||
| chr2:200464037 | T | A | 9 | a0001c0001t0017g0087 a0001c0001t0018g0072 a0001c0001t0032g0010 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.848-3253T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464037 | |||||||
| chr2:200464040 | A | C | 1 | a0001c0001t0004g0033 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.848-3250A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464040 | |||||||
| chr2:200464145 | C | A | 13 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0005g0259 others(10): Show |
13 | HG00544.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.848-3145C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464145 | |||||||
| chr2:200464210 | A | G | 1 | a0001c0001t0012g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.848-3080A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464210 | |||||||
| chr2:200464221 | G | A | 1 | a0001c0001t0006g0046 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.848-3069G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464221 | |||||||
| chr2:200464347 | G | A | 1 | a0001c0001t0010g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.848-2943G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464347 | |||||||
| chr2:200464401 | T | C | 131 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.848-2889T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464401 | |||||||
| chr2:200464448 | A | G | 32 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0238 others(29): Show |
32 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.848-2842A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464448 | |||||||
| chr2:200464490 | G | A | 198 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.848-2800G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464490 | |||||||
| chr2:200464638 | T | A | 9 | a0001c0001t0017g0087 a0001c0001t0018g0072 a0001c0001t0032g0010 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.848-2652T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464638 | |||||||
| chr2:200464777 | CA | C | 198 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.848-2511delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 200464777 | ||||||
| chr2:200464989 | T | A | 1 | a0002c0004t0063g0102 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.848-2301T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200464989 | |||||||
| chr2:200465186 | G | A | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.848-2104G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465186 | |||||||
| chr2:200465248 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.848-2042C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465248 | |||||||
| chr2:200465486 | C | A | 242 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.848-1804C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465486 | |||||||
| chr2:200465529 | C | T | 1 | a0001c0001t0007g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.848-1761C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465529 | |||||||
| chr2:200465608 | G | A | 94 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(91): Show |
94 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.848-1682G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465608 | |||||||
| chr2:200465860 | G | A | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.848-1430G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465860 | |||||||
| chr2:200465925 | A | G | 96 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(93): Show |
96 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.848-1365A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465925 | |||||||
| chr2:200465968 | C | T | 6 | a0001c0002t0006g0112 a0001c0002t0006g0113 a0001c0002t0006g0114 others(3): Show |
6 | NA18953.hp1 NA18955.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.848-1322C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465968 | |||||||
| chr2:200465981 | G | A | 1 | a0001c0001t0036g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.848-1309G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465981 | |||||||
| chr2:200465986 | C | T | 1 | a0001c0001t0036g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.848-1304C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465986 | |||||||
| chr2:200465987 | A | G | 1 | a0001c0001t0036g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.848-1303A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465987 | |||||||
| chr2:200465988 | T | C | 1 | a0001c0001t0036g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.848-1302T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465988 | |||||||
| chr2:200465989 | G | A | 1 | a0001c0001t0036g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.848-1301G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465989 | |||||||
| chr2:200465994 | G | T | 1 | a0001c0001t0036g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.848-1296G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200465994 | |||||||
| chr2:200466000 | C | G | 1 | a0001c0001t0009g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.848-1290C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466000 | |||||||
| chr2:200466010 | C | T | 3 | a0001c0001t0017g0142 a0001c0001t0017g0143 a0001c0001t0041g0283 |
3 | HG02559.hp1 HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.848-1280C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466010 | |||||||
| chr2:200466081 | A | G | 1 | a0001c0001t0008g0027 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.848-1209A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466081 | |||||||
| chr2:200466088 | G | C | 1 | a0001c0001t0005g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.848-1202G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466088 | |||||||
| chr2:200466206 | C | T | 102 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(99): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.848-1084C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466206 | |||||||
| chr2:200466300 | CTTTTTTC others(1): Show |
C | 6 | a0001c0001t0005g0156 a0001c0001t0007g0161 a0001c0001t0007g0171 others(3): Show |
6 | HG00735.hp1 HG01192.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-988_848-981del others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 200466300 | ||||||
| chr2:200466309 | T | C | 6 | a0001c0001t0005g0156 a0001c0001t0007g0161 a0001c0001t0007g0171 others(3): Show |
6 | HG00735.hp1 HG01192.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-981T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466309 | |||||||
| chr2:200466359 | G | T | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.848-931G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466359 | |||||||
| chr2:200466566 | A | G | 9 | a0001c0001t0018g0072 a0001c0001t0075g0029 a0001c0002t0030g0141 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.848-724A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466566 | |||||||
| chr2:200466707 | T | G | 112 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(109): Show |
112 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.848-583T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466707 | |||||||
| chr2:200466937 | G | A | 1 | a0002c0004t0068g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.848-353G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466937 | |||||||
| chr2:200466942 | G | A | 2 | a0001c0002t0030g0141 a0003c0008t0058g0099 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.848-348G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466942 | |||||||
| chr2:200466972 | G | A | 2 | a0001c0002t0016g0280 a0001c0002t0070g0147 |
2 | HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.848-318G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466972 | |||||||
| chr2:200466978 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0021g0014 a0001c0001t0048g0221 |
3 | HG01257.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.848-312C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200466978 | |||||||
| chr2:200467124 | G | A | 6 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.848-166G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 9/12 | chr2 | 200467124 | |||||||
| chr2:200467652 | C | T | 1 | a0001c0002t0069g0053 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.957+253C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200467652 | |||||||
| chr2:200467716 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0021g0014 a0001c0001t0048g0221 |
3 | HG01257.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.957+317C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200467716 | |||||||
| chr2:200467750 | C | A | 108 | a0001c0001t0001g0228 a0001c0001t0001g0251 a0001c0001t0001g0260 others(105): Show |
108 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.957+351C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200467750 | |||||||
| chr2:200467768 | C | T | 1 | a0001c0001t0014g0128 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.957+369C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200467768 | |||||||
| chr2:200467811 | G | A | 5 | a0001c0002t0030g0141 a0002c0004t0012g0145 a0002c0004t0019g0285 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+412G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200467811 | |||||||
| chr2:200468110 | T | C | 1 | a0001c0001t0048g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.957+711T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468110 | |||||||
| chr2:200468278 | T | C | 113 | a0001c0001t0001g0228 a0001c0001t0001g0251 a0001c0001t0001g0260 others(110): Show |
113 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.957+879T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468278 | |||||||
| chr2:200468347 | T | TACACAC | 9 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0003g0056 others(6): Show |
9 | HG01257.hp2 HG02132.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.957+975_957+980dup others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(1): Show |
7 | a0001c0001t0032g0010 a0001c0002t0016g0279 a0001c0002t0016g0280 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.957+973_957+980dup others(8): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(3): Show |
1 | a0001c0005t0029g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.957+971_957+980dup others(10): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(5): Show |
9 | a0001c0001t0001g0228 a0001c0001t0003g0042 a0001c0001t0004g0028 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.957+969_957+980dup others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(7): Show |
39 | a0001c0001t0005g0186 a0001c0001t0005g0259 a0001c0001t0007g0190 others(36): Show |
39 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.957+967_957+980dup others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(9): Show |
15 | a0001c0001t0001g0202 a0001c0001t0005g0185 a0001c0001t0007g0191 others(12): Show |
15 | HG00544.hp1 HG00738.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.957+965_957+980dup others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(11): Show |
5 | a0001c0001t0005g0271 a0001c0001t0017g0142 a0001c0001t0017g0143 others(2): Show |
5 | HG02165.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+963_957+980dup others(18): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(13): Show |
13 | a0001c0001t0002g0241 a0001c0001t0004g0039 a0001c0001t0008g0013 others(10): Show |
13 | HG01070.hp2 HG01175.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+961_957+980dup others(20): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(15): Show |
20 | a0001c0001t0001g0265 a0001c0001t0002g0180 a0001c0001t0002g0181 others(17): Show |
20 | HG00639.hp1 HG01978.hp1 HG03654.hp1 others(17): Show |
intron_variant | MODIFIER | c.957+959_957+980dup others(22): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(17): Show |
28 | a0001c0001t0001g0251 a0001c0001t0001g0288 a0001c0001t0002g0157 others(25): Show |
28 | HG00423.hp1 HG00423.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.957+957_957+980dup others(24): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(19): Show |
26 | a0001c0001t0001g0220 a0001c0001t0001g0224 a0001c0001t0001g0244 others(23): Show |
26 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.957+955_957+980dup others(26): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(21): Show |
29 | a0001c0001t0001g0214 a0001c0001t0001g0232 a0001c0001t0001g0233 others(26): Show |
29 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.957+953_957+980dup others(28): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(23): Show |
31 | a0001c0001t0001g0196 a0001c0001t0001g0204 a0001c0001t0001g0213 others(28): Show |
31 | HG00621.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.957+951_957+980dup others(30): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(25): Show |
16 | a0001c0001t0001g0216 a0001c0001t0002g0175 a0001c0001t0002g0177 others(13): Show |
16 | HG00642.hp1 HG02015.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.957+949_957+980dup others(32): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(27): Show |
9 | a0001c0001t0002g0154 a0001c0001t0002g0238 a0001c0001t0005g0211 others(6): Show |
9 | HG02015.hp1 HG03516.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.957+980_957+981ins others(34): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(29): Show |
4 | a0001c0001t0003g0003 a0001c0001t0013g0085 a0001c0001t0020g0051 others(1): Show |
4 | HG00099.hp2 HG02056.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.957+980_957+981ins others(36): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(31): Show |
3 | a0001c0001t0014g0050 a0001c0001t0059g0026 a0001c0002t0045g0291 |
3 | HG01074.hp2 HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.957+980_957+981ins others(38): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(33): Show |
3 | a0001c0001t0002g0150 a0001c0001t0002g0174 a0002c0004t0019g0135 |
3 | HG01123.hp1 HG01993.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.957+980_957+981ins others(40): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | T | TACACACA others(26): Show |
1 | a0001c0001t0002g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.957+976_957+977ins others(33): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468347 | TACACACA others(3): Show |
T | 1 | a0001c0001t0008g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.957+971_957+980del others(10): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468347 | ||||||
| chr2:200468378 | A | ACACACAC others(15): Show |
1 | a0001c0001t0008g0054 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.957+980_957+981ins others(22): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200468378 | ||||||
| chr2:200468379 | C | CACACACA others(18): Show |
1 | a0001c0001t0005g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.957+980_957+981ins others(25): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468379 | |||||||
| chr2:200468442 | G | A | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957+1043G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468442 | |||||||
| chr2:200468464 | T | C | 7 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0002c0004t0012g0020 others(4): Show |
7 | HG01943.hp1 HG01993.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.957+1065T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468464 | |||||||
| chr2:200468492 | T | A | 74 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0002g0180 others(71): Show |
74 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.957+1093T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468492 | |||||||
| chr2:200468507 | A | T | 1 | a0001c0001t0037g0060 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.957+1108A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468507 | |||||||
| chr2:200468589 | T | C | 260 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(257): Show |
260 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.957+1190T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468589 | |||||||
| chr2:200468731 | C | G | 6 | a0001c0002t0016g0279 a0001c0002t0016g0280 a0001c0002t0016g0281 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.958-1183C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468731 | |||||||
| chr2:200468816 | A | T | 1 | a0001c0001t0034g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.958-1098A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468816 | |||||||
| chr2:200468904 | C | T | 38 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0003g0048 others(35): Show |
38 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.958-1010C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468904 | |||||||
| chr2:200468944 | A | G | 1 | a0001c0001t0008g0027 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.958-970A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468944 | |||||||
| chr2:200468946 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-968A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468946 | |||||||
| chr2:200468947 | A | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-967A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468947 | |||||||
| chr2:200468948 | A | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-966A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468948 | |||||||
| chr2:200468949 | A | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-965A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468949 | |||||||
| chr2:200468950 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-964T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468950 | |||||||
| chr2:200468951 | A | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-963A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468951 | |||||||
| chr2:200468958 | A | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-956A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468958 | |||||||
| chr2:200468959 | G | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-955G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468959 | |||||||
| chr2:200468961 | A | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-953A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468961 | |||||||
| chr2:200468962 | C | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-952C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468962 | |||||||
| chr2:200468963 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-951A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468963 | |||||||
| chr2:200468965 | G | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-949G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468965 | |||||||
| chr2:200468966 | C | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-948C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468966 | |||||||
| chr2:200468970 | G | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-944G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468970 | |||||||
| chr2:200468971 | G | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-943G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468971 | |||||||
| chr2:200468973 | G | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-941G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468973 | |||||||
| chr2:200468974 | T | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-940T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468974 | |||||||
| chr2:200468979 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-935C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468979 | |||||||
| chr2:200468980 | A | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-934A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468980 | |||||||
| chr2:200468984 | C | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-930C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468984 | |||||||
| chr2:200468988 | T | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-926T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468988 | |||||||
| chr2:200468989 | G | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-925G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468989 | |||||||
| chr2:200468991 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-923A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468991 | |||||||
| chr2:200468992 | A | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-922A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468992 | |||||||
| chr2:200468994 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-920A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468994 | |||||||
| chr2:200468996 | T | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-918T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200468996 | |||||||
| chr2:200469000 | T | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-914T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469000 | |||||||
| chr2:200469002 | C | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-912C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469002 | |||||||
| chr2:200469003 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-911T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469003 | |||||||
| chr2:200469008 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-906T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469008 | |||||||
| chr2:200469009 | G | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-905G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469009 | |||||||
| chr2:200469011 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-903C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469011 | |||||||
| chr2:200469019 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-895A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469019 | |||||||
| chr2:200469020 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-894A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469020 | |||||||
| chr2:200469023 | T | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-891T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469023 | |||||||
| chr2:200469024 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-890A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469024 | |||||||
| chr2:200469026 | A | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-888A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469026 | |||||||
| chr2:200469027 | C | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-887C>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469027 | |||||||
| chr2:200469028 | A | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-886A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469028 | |||||||
| chr2:200469035 | T | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-879T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469035 | |||||||
| chr2:200469037 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-877G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469037 | |||||||
| chr2:200469044 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-870A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469044 | |||||||
| chr2:200469045 | G | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-869G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469045 | |||||||
| chr2:200469047 | A | C | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-867A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469047 | |||||||
| chr2:200469048 | C | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-866C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469048 | |||||||
| chr2:200469049 | C | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-865C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469049 | |||||||
| chr2:200469050 | C | A | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-864C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469050 | |||||||
| chr2:200469053 | A | G | 1 | a0001c0001t0004g0035 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.958-861A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469053 | |||||||
| chr2:200469092 | C | A | 1 | a0002c0004t0019g0131 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.958-822C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469092 | |||||||
| chr2:200469122 | A | G | 1 | a0001c0001t0009g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.958-792A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469122 | |||||||
| chr2:200469419 | C | T | 1 | a0004c0009t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.958-495C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469419 | |||||||
| chr2:200469519 | G | C | 1 | a0001c0001t0020g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.958-395G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469519 | |||||||
| chr2:200469542 | TTTCTC | T | 6 | a0001c0002t0016g0279 a0001c0002t0016g0280 a0001c0002t0016g0281 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.958-369_958-365del others(5): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 200469542 | ||||||
| chr2:200469681 | C | A | 38 | a0001c0001t0001g0228 a0001c0001t0003g0048 a0001c0001t0005g0185 others(35): Show |
38 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.958-233C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469681 | |||||||
| chr2:200469707 | C | A | 1 | a0001c0001t0007g0218 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.958-207C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 10/12 | chr2 | 200469707 | |||||||
| chr2:200470129 | A | G | 60 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0003g0048 others(57): Show |
60 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1060+113A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200470129 | |||||||
| chr2:200470186 | A | G | 2 | a0002c0004t0019g0131 a0002c0004t0019g0135 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1060+170A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200470186 | |||||||
| chr2:200470293 | T | G | 2 | a0001c0001t0011g0295 a0001c0001t0048g0221 |
2 | HG01257.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1060+277T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200470293 | |||||||
| chr2:200470492 | A | G | 2 | a0001c0001t0011g0295 a0001c0001t0048g0221 |
2 | HG01257.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1060+476A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200470492 | |||||||
| chr2:200470712 | A | G | 2 | a0001c0002t0030g0100 a0001c0002t0030g0141 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1060+696A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200470712 | |||||||
| chr2:200470869 | T | C | 2 | a0002c0004t0019g0131 a0002c0004t0019g0135 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1060+853T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200470869 | |||||||
| chr2:200470945 | G | A | 4 | a0002c0004t0019g0131 a0002c0004t0019g0135 a0002c0004t0068g0002 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060+929G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200470945 | |||||||
| chr2:200471004 | G | A | 271 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(268): Show |
271 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.1060+988G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200471004 | |||||||
| chr2:200471090 | C | T | 2 | a0002c0004t0019g0131 a0002c0004t0019g0135 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1060+1074C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200471090 | |||||||
| chr2:200471205 | A | G | 2 | a0002c0004t0019g0131 a0002c0004t0019g0135 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1060+1189A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200471205 | |||||||
| chr2:200471316 | C | T | 1 | a0001c0002t0006g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1060+1300C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200471316 | |||||||
| chr2:200471460 | C | CTT | 8 | a0001c0001t0017g0136 a0001c0001t0017g0142 a0001c0001t0017g0143 others(5): Show |
8 | HG01243.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061-1370_1061-136 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 200471460 | ||||||
| chr2:200471547 | G | A | 1 | a0001c0002t0030g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1061-1285G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200471547 | |||||||
| chr2:200471615 | C | T | 1 | a0001c0002t0006g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1061-1217C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200471615 | |||||||
| chr2:200471677 | T | G | 4 | a0001c0001t0031g0021 a0001c0001t0031g0052 a0001c0001t0072g0057 others(1): Show |
4 | HG01975.hp1 HG03942.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1061-1155T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200471677 | |||||||
| chr2:200471789 | T | C | 7 | a0001c0002t0016g0279 a0001c0002t0016g0280 a0001c0002t0016g0281 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1061-1043T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200471789 | |||||||
| chr2:200471906 | A | G | 6 | a0001c0002t0016g0279 a0001c0002t0016g0280 a0001c0002t0016g0281 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1061-926A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200471906 | |||||||
| chr2:200472138 | G | C | 1 | a0001c0001t0079g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1061-694G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200472138 | |||||||
| chr2:200472294 | A | G | 1 | a0001c0001t0010g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1061-538A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200472294 | |||||||
| chr2:200472361 | G | A | 1 | a0001c0001t0004g0033 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1061-471G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200472361 | |||||||
| chr2:200472457 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1061-375G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200472457 | |||||||
| chr2:200472546 | C | T | 1 | a0001c0001t0027g0276 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1061-286C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200472546 | |||||||
| chr2:200472636 | G | C | 35 | a0001c0001t0001g0228 a0001c0001t0001g0251 a0001c0001t0001g0260 others(32): Show |
35 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1061-196G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200472636 | |||||||
| chr2:200472667 | T | A | 4 | a0002c0004t0019g0131 a0002c0004t0019g0135 a0002c0004t0019g0285 others(1): Show |
4 | HG02723.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-165T>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200472667 | |||||||
| chr2:200472755 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1061-77C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 11/12 | chr2 | 200472755 | |||||||
| chr2:200473083 | G | GA | 50 | a0001c0001t0001g0225 a0001c0001t0001g0228 a0001c0001t0001g0251 others(47): Show |
50 | HG00621.hp2 HG01361.hp1 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.1281+46dupA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200473083 | ||||||
| chr2:200473236 | G | A | 2 | a0001c0001t0003g0121 a0002c0004t0068g0002 |
2 | HG02886.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1281+184G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473236 | |||||||
| chr2:200473329 | A | G | 284 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(281): Show |
284 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.1281+277A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473329 | |||||||
| chr2:200473367 | C | T | 3 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0095 |
3 | HG02559.hp2 HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1281+315C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473367 | |||||||
| chr2:200473432 | A | G | 1 | a0001c0003t0001g0256 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1281+380A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473432 | |||||||
| chr2:200473481 | T | G | 1 | a0002c0004t0012g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1281+429T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473481 | |||||||
| chr2:200473488 | T | G | 8 | a0001c0001t0017g0087 a0001c0001t0017g0136 a0001c0001t0017g0142 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+436T>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473488 | |||||||
| chr2:200473516 | A | C | 1 | a0001c0001t0007g0184 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1281+464A>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473516 | |||||||
| chr2:200473525 | C | T | 6 | a0001c0002t0013g0006 a0001c0002t0013g0011 a0001c0002t0013g0104 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281+473C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473525 | |||||||
| chr2:200473714 | G | A | 6 | a0001c0002t0006g0112 a0001c0002t0006g0113 a0001c0002t0006g0114 others(3): Show |
6 | NA18953.hp1 NA18955.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281+662G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473714 | |||||||
| chr2:200473829 | G | T | 1 | a0001c0001t0010g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1281+777G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473829 | |||||||
| chr2:200473890 | CT | C | 80 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0154 others(77): Show |
80 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1281+839delT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473890 | |||||||
| chr2:200473914 | T | C | 119 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0004g0023 others(116): Show |
119 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1281+862T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473914 | |||||||
| chr2:200473955 | G | A | 14 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(11): Show |
14 | HG00408.hp2 HG02155.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+903G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473955 | |||||||
| chr2:200473985 | G | A | 1 | a0001c0001t0009g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1281+933G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200473985 | |||||||
| chr2:200474021 | T | C | 14 | a0001c0001t0017g0087 a0001c0001t0017g0136 a0001c0001t0017g0142 others(11): Show |
14 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1281+969T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474021 | |||||||
| chr2:200474103 | C | CT | 42 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0009g0152 others(39): Show |
42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1281+1063dupT | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200474103 | ||||||
| chr2:200474103 | C | CTT | 6 | a0002c0004t0012g0020 a0002c0004t0012g0098 a0002c0004t0012g0101 others(3): Show |
6 | HG02486.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281+1062_1281+106 others(6): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200474103 | ||||||
| chr2:200474103 | C | CTTT | 8 | a0001c0001t0017g0087 a0001c0001t0017g0136 a0001c0001t0017g0142 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+1061_1281+106 others(7): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200474103 | ||||||
| chr2:200474121 | A | T | 80 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0009g0152 others(77): Show |
80 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.1281+1069A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474121 | |||||||
| chr2:200474224 | G | A | 1 | a0002c0004t0012g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1281+1172G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474224 | |||||||
| chr2:200474365 | G | A | 1 | a0001c0001t0003g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1281+1313G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474365 | |||||||
| chr2:200474431 | A | G | 23 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0039g0266 others(20): Show |
23 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1281+1379A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474431 | |||||||
| chr2:200474547 | C | A | 6 | a0001c0002t0006g0112 a0001c0002t0006g0113 a0001c0002t0006g0114 others(3): Show |
6 | NA18953.hp1 NA18955.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281+1495C>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474547 | |||||||
| chr2:200474594 | T | C | 1 | a0001c0001t0015g0297 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1281+1542T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474594 | |||||||
| chr2:200474655 | A | G | 1 | a0001c0001t0022g0264 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1281+1603A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474655 | |||||||
| chr2:200474751 | TAGGTAAT others(5): Show |
T | 1 | a0001c0001t0004g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1281+1701_1281+171 others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200474751 | ||||||
| chr2:200474834 | C | T | 46 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(43): Show |
46 | HG00099.hp1 HG00408.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1281+1782C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474834 | |||||||
| chr2:200474839 | C | T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1281+1787C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474839 | |||||||
| chr2:200474877 | A | G | 23 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0039g0266 others(20): Show |
23 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1281+1825A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474877 | |||||||
| chr2:200474938 | C | T | 1 | a0001c0001t0005g0211 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1281+1886C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200474938 | |||||||
| chr2:200475416 | C | T | 1 | a0001c0001t0048g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1282-2220C>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200475416 | |||||||
| chr2:200475602 | G | C | 28 | a0001c0001t0004g0023 a0001c0001t0004g0031 a0001c0001t0004g0033 others(25): Show |
28 | HG00438.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1282-2034G>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200475602 | |||||||
| chr2:200475750 | G | T | 16 | a0001c0002t0006g0019 a0001c0002t0006g0093 a0001c0002t0006g0094 others(13): Show |
16 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-1886G>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200475750 | |||||||
| chr2:200475761 | A | G | 121 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1282-1875A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200475761 | |||||||
| chr2:200475847 | CA | C | 29 | a0001c0001t0004g0023 a0001c0001t0004g0028 a0001c0001t0004g0031 others(26): Show |
29 | HG00438.hp1 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1282-1783delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200475847 | ||||||
| chr2:200475908 | G | A | 5 | a0001c0001t0037g0060 a0001c0001t0037g0064 a0001c0001t0049g0245 others(2): Show |
5 | HG01243.hp2 HG02735.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-1728G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200475908 | |||||||
| chr2:200476011 | A | G | 51 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0009g0152 others(48): Show |
51 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1282-1625A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200476011 | |||||||
| chr2:200476266 | T | C | 46 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0154 others(43): Show |
46 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1282-1370T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200476266 | |||||||
| chr2:200476470 | T | C | 5 | a0001c0002t0016g0280 a0001c0002t0016g0281 a0001c0002t0016g0282 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-1166T>C | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200476470 | |||||||
| chr2:200476893 | G | A | 8 | a0001c0001t0017g0087 a0001c0001t0017g0136 a0001c0001t0017g0142 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-743G>A | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200476893 | |||||||
| chr2:200476909 | A | G | 125 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0196 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1282-727A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200476909 | |||||||
| chr2:200477014 | A | T | 1 | a0005c0011t0001g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1282-622A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200477014 | |||||||
| chr2:200477213 | TTTTCTGT others(6): Show |
T | 1 | a0001c0010t0065g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1282-414_1282-402d others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477213 | ||||||
| chr2:200477250 | A | G | 30 | a0001c0001t0032g0010 a0001c0002t0006g0019 a0001c0002t0006g0093 others(27): Show |
30 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1282-386A>G | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200477250 | |||||||
| chr2:200477515 | T | TAAAAAAA others(2): Show |
6 | a0001c0001t0041g0283 a0001c0001t0075g0029 a0001c0002t0013g0006 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282-106_1282-98du others(10): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(3): Show |
4 | a0001c0001t0017g0143 a0001c0002t0013g0124 a0001c0002t0013g0138 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-107_1282-98du others(11): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(4): Show |
2 | a0001c0001t0017g0142 a0001c0001t0032g0010 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1282-108_1282-98du others(12): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(6): Show |
6 | a0001c0002t0016g0280 a0001c0002t0016g0282 a0001c0002t0016g0284 others(3): Show |
6 | HG02258.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282-110_1282-98du others(14): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(7): Show |
5 | a0001c0002t0006g0112 a0001c0002t0006g0115 a0001c0002t0016g0279 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1282-111_1282-98du others(15): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(8): Show |
6 | a0001c0001t0048g0221 a0001c0002t0006g0113 a0001c0002t0006g0114 others(3): Show |
6 | HG01257.hp2 HG03579.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282-112_1282-98du others(16): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(10): Show |
3 | a0002c0004t0012g0101 a0002c0004t0012g0145 a0002c0004t0063g0102 |
3 | HG02486.hp2 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1282-114_1282-98du others(18): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(11): Show |
1 | a0002c0004t0012g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1282-115_1282-98du others(19): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(12): Show |
1 | a0002c0004t0012g0132 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1282-116_1282-98du others(20): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(13): Show |
2 | a0001c0001t0017g0087 a0002c0004t0012g0020 |
2 | HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1282-117_1282-98du others(21): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(14): Show |
1 | a0003c0006t0017g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1282-118_1282-98du others(22): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(19): Show |
1 | a0003c0006t0032g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1282-98_1282-97ins others(26): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | T | TAAAAAAA others(30): Show |
1 | a0001c0001t0017g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1282-98_1282-97ins others(37): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | TA | T | 97 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0001g0202 others(94): Show |
97 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1282-98delA | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | TAA | T | 8 | a0001c0001t0001g0196 a0001c0001t0001g0287 a0001c0001t0007g0184 others(5): Show |
8 | HG01943.hp1 HG01943.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1282-99_1282-98del others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477515 | TAAAAAA | T | 44 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0009g0152 others(41): Show |
44 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1282-103_1282-98de others(7): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477515 | ||||||
| chr2:200477517 | A | T | 4 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0003g0056 others(1): Show |
4 | HG02132.hp1 NA18955.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-119A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200477517 | |||||||
| chr2:200477518 | A | T | 1 | a0001c0001t0018g0126 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1282-118A>T | SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | chr2 | 200477518 | |||||||
| chr2:200477615 | ATC | A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0001t0003g0056 others(2): Show |
5 | HG02132.hp1 NA18955.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-17_1282-16del others(2): Show |
SPATS2L | ENSG00000196141.14 | transcript | ENST00000409140.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 200477615 |