Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11075 |
| ensemblid | ENSG00000104435.14 |
| hgncid | 10577 |
| symbol | STMN2 |
| name | stathmin 2 |
| refseq_nuc | NM_007029.4 |
| refseq_prot | NP_008960.2 |
| ensembl_nuc | ENST00000220876.12 |
| ensembl_prot | ENSP00000220876.7 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 79611117 |
| end | 79666158 |
| strand | + |
| ver | v1.2 |
| region | chr8:79611117-79666158 |
| region5000 | chr8:79606117-79671158 |
| regionname0 | STMN2_chr8_79611117_79666158 |
| regionname5000 | STMN2_chr8_79606117_79671158 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 179 | 401 | 86 | 74 | 176 | 16 | 47 | 134 | STMN2_chr8_79606117_79671158 | STMN2 | MAKTA others(174): Show |
chr8 | 79606117 | 79671158 |
| a0002 | 0/0 | 179 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | MAKTA others(174): Show |
chr8 | 79606117 | 79671158 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 537 | 396 | 82 | 73 | 176 | 16 | 47 | STMN2_chr8_79606117_79671158 | STMN2 | ATGGC others(532): Show |
chr8 | 79606117 | 79671158 | ||
| a0001c0002 | 0/0 | 537 | 5 | 4 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | ATGGC others(532): Show |
chr8 | 79606117 | 79671158 | ||
| a0002c0003 | 0/0 | 537 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | ATGGC others(532): Show |
chr8 | 79606117 | 79671158 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1903 | 380 | 77 | 70 | 169 | 16 | 46 | STMN2_chr8_79606117_79671158 | STMN2 | AGTCT others(1898): Show |
chr8 | 79606117 | 79671158 |
| a0001c0001t0002 | 0/0 | 1904 | 10 | 0 | 3 | 6 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | AGTCT others(1899): Show |
chr8 | 79606117 | 79671158 |
| a0001c0001t0003 | 0/0 | 1903 | 2 | 2 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | AGTCT others(1898): Show |
chr8 | 79606117 | 79671158 |
| a0001c0001t0004 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | AGTCC others(1898): Show |
chr8 | 79606117 | 79671158 |
| a0001c0001t0005 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | AGTCT others(1899): Show |
chr8 | 79606117 | 79671158 |
| a0001c0001t0006 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | AGTCT others(1898): Show |
chr8 | 79606117 | 79671158 |
| a0001c0001t0007 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | AGTCT others(1898): Show |
chr8 | 79606117 | 79671158 |
| a0001c0002t0001 | 0/0 | 1903 | 5 | 4 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | AGTCT others(1898): Show |
chr8 | 79606117 | 79671158 |
| a0002c0003t0001 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | AGTCT others(1898): Show |
chr8 | 79606117 | 79671158 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0008 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0033 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0002t0001g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | GBR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CDX | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CDX | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0280 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | MSL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0111 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | STU | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | YRI | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | LWK | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0224 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | YRI | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ASW | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ASW | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | GIH | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | GIH | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | USA | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | USA | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | USA | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | USA | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0097 | REF | REF | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0033 | REF | REF | STMN2_chr8_79606117_79671158 | STMN2 | chr8 | 79606117 | 79671158 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:79636871 | G | C | 1 | a0002 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.89G>C | p.Arg30Pro | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/5 | 168/1903 | 89/540 | 30/179 | chr8 | 79636871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:79641505 | G | A | 1 | a0001c0002 | 5 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.243G>A | p.Leu81Leu | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/5 | 322/1903 | 243/540 | 81/179 | chr8 | 79641505 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:79611121 | T | C | 1 | a0001c0001t0004 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/5 | 75 | chr8 | 79611121 | ||||||
| chr8:79664989 | T | TA | 2 | a0001c0001t0002 a0001c0001t0005 |
11 | HG01256.hp2 HG01943.hp2 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*128dupA | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 5/5 | 129 | INFO_REALIGN_3_PRIME | chr8 | 79664989 | |||||
| chr8:79665002 | AC | A | 2 | a0001c0001t0001 a0001c0002t0001 |
10 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*129delC | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 5/5 | 129 | chr8 | 79665002 | ||||||
| chr8:79665003 | C | A | 1 | a0001c0001t0001 | 6 | HG02129.hp2 HG04184.hp1 NA18612.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*129C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 5/5 | 129 | chr8 | 79665003 | ||||||
| chr8:79665283 | T | C | 1 | a0001c0001t0003 | 2 | HG03225.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 5/5 | 409 | chr8 | 79665283 | ||||||
| chr8:79665506 | T | C | 1 | a0001c0001t0005 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*632T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 5/5 | 632 | chr8 | 79665506 | ||||||
| chr8:79665618 | G | T | 1 | a0001c0001t0007 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*744G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 5/5 | 744 | chr8 | 79665618 | ||||||
| chr8:79665843 | C | A | 1 | a0001c0001t0006 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*969C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 5/5 | 969 | chr8 | 79665843 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:79611301 | A | G | 41 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
53 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.19+87A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79611301 | |||||||
| chr8:79611432 | G | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+218G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79611432 | |||||||
| chr8:79611574 | C | CT | 40 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
52 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.19+372dupT | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79611574 | ||||||
| chr8:79611574 | CT | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.19+372delT | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79611574 | ||||||
| chr8:79611757 | A | G | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02723.hp1 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+543A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79611757 | |||||||
| chr8:79611814 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.19+600G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79611814 | |||||||
| chr8:79611950 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.19+736G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79611950 | |||||||
| chr8:79611961 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.19+747G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79611961 | |||||||
| chr8:79612058 | C | A | 4 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0002g0132 others(1): Show |
4 | HG01256.hp2 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+844C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79612058 | |||||||
| chr8:79612070 | GC | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.19+863delC | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79612070 | ||||||
| chr8:79612125 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | HG00423.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.19+911G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79612125 | |||||||
| chr8:79612286 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.19+1072G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79612286 | |||||||
| chr8:79612367 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.19+1153G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79612367 | |||||||
| chr8:79612384 | G | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0283 others(6): Show |
14 | HG00558.hp2 NA18939.hp2 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.19+1170G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79612384 | |||||||
| chr8:79612462 | CTTAAG | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(33): Show |
41 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.19+1254_19+1258del others(5): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79612462 | ||||||
| chr8:79612876 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19+1662C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79612876 | |||||||
| chr8:79612946 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0326 a0001c0001t0001g0327 others(4): Show |
9 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+1732C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79612946 | |||||||
| chr8:79613218 | C | G | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0006g0280 others(2): Show |
8 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+2004C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79613218 | |||||||
| chr8:79613384 | C | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.19+2170C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79613384 | |||||||
| chr8:79613412 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.19+2198C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79613412 | |||||||
| chr8:79613531 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.19+2317C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79613531 | |||||||
| chr8:79613557 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(101): Show |
133 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.19+2343C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79613557 | |||||||
| chr8:79613714 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.19+2500G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79613714 | |||||||
| chr8:79613821 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19+2607A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79613821 | |||||||
| chr8:79613974 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.19+2760C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79613974 | |||||||
| chr8:79613996 | TATAA | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(44): Show |
62 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.19+2786_19+2789del others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79613996 | ||||||
| chr8:79614106 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.19+2892T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79614106 | |||||||
| chr8:79614215 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0276 |
3 | NA18612.hp1 NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.19+3001G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79614215 | |||||||
| chr8:79614228 | A | T | 1 | a0001c0001t0001g0324 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.19+3014A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79614228 | |||||||
| chr8:79614276 | G | A | 93 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.19+3062G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79614276 | |||||||
| chr8:79614321 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.19+3107T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79614321 | |||||||
| chr8:79614519 | A | G | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 |
3 | HG02040.hp2 NA18939.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.19+3305A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79614519 | |||||||
| chr8:79614727 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.19+3513T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79614727 | |||||||
| chr8:79614997 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.19+3783T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79614997 | |||||||
| chr8:79615151 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.19+3937A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79615151 | |||||||
| chr8:79615176 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19+3962G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79615176 | |||||||
| chr8:79615358 | C | T | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG01070.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+4144C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79615358 | |||||||
| chr8:79615706 | A | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+4492A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79615706 | |||||||
| chr8:79615748 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.19+4534A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79615748 | |||||||
| chr8:79615824 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.19+4610G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79615824 | |||||||
| chr8:79615889 | T | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.19+4675T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79615889 | |||||||
| chr8:79616206 | A | G | 93 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.19+4992A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79616206 | |||||||
| chr8:79616242 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.19+5028G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79616242 | |||||||
| chr8:79616437 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.19+5223G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79616437 | |||||||
| chr8:79616599 | A | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+5385A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79616599 | |||||||
| chr8:79616723 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0122 others(2): Show |
9 | HG02027.hp1 HG02071.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+5509C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79616723 | |||||||
| chr8:79616738 | G | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.19+5524G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79616738 | |||||||
| chr8:79617069 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.19+5855T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79617069 | |||||||
| chr8:79617133 | TTGAG | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(101): Show |
133 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.19+5921_19+5924del others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79617133 | ||||||
| chr8:79617652 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.19+6438G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79617652 | |||||||
| chr8:79617985 | T | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+6771T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79617985 | |||||||
| chr8:79618041 | T | A | 93 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.19+6827T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79618041 | |||||||
| chr8:79618150 | G | T | 1 | a0001c0001t0001g0037 | 2 | NA18942.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.19+6936G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79618150 | |||||||
| chr8:79618373 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.19+7159T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79618373 | |||||||
| chr8:79618404 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18961.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.19+7190G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79618404 | |||||||
| chr8:79618559 | T | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+7345T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79618559 | |||||||
| chr8:79618628 | A | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.19+7414A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79618628 | |||||||
| chr8:79618706 | A | C | 1 | a0001c0001t0001g0267 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.19+7492A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79618706 | |||||||
| chr8:79618737 | T | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.19+7523T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79618737 | |||||||
| chr8:79618748 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.19+7534G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79618748 | |||||||
| chr8:79619084 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.19+7870A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619084 | |||||||
| chr8:79619177 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.19+7963A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619177 | |||||||
| chr8:79619238 | G | C | 1 | a0001c0001t0001g0300 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.19+8024G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619238 | |||||||
| chr8:79619302 | A | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+8088A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619302 | |||||||
| chr8:79619440 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.19+8226A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619440 | |||||||
| chr8:79619530 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG00544.hp2 HG02080.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+8316A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619530 | |||||||
| chr8:79619662 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.19+8448C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619662 | |||||||
| chr8:79619683 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19+8469A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619683 | |||||||
| chr8:79619730 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.19+8516G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619730 | |||||||
| chr8:79619982 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.19+8768A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79619982 | |||||||
| chr8:79620107 | A | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(38): Show |
50 | HG00423.hp1 HG00639.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.19+8893A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79620107 | |||||||
| chr8:79620144 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.19+8930G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79620144 | |||||||
| chr8:79620262 | G | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0087 others(9): Show |
14 | HG00558.hp1 HG01192.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.19+9048G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79620262 | |||||||
| chr8:79620438 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(42): Show |
59 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.19+9224T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79620438 | |||||||
| chr8:79620722 | G | T | 1 | a0001c0001t0001g0219 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.19+9508G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79620722 | |||||||
| chr8:79620856 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.19+9642T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79620856 | |||||||
| chr8:79620951 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19+9737C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79620951 | |||||||
| chr8:79620958 | C | A | 1 | a0001c0001t0001g0037 | 2 | NA18942.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.19+9744C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79620958 | |||||||
| chr8:79621011 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19+9797C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621011 | |||||||
| chr8:79621038 | C | T | 35 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(32): Show |
39 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.19+9824C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621038 | |||||||
| chr8:79621134 | G | GCT | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02723.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.19+9920_19+9921ins others(2): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621134 | |||||||
| chr8:79621135 | T | C | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02723.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.19+9921T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621135 | |||||||
| chr8:79621183 | G | C | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02723.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.19+9969G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621183 | |||||||
| chr8:79621213 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.19+9999T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621213 | |||||||
| chr8:79621273 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(101): Show |
133 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.19+10059G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621273 | |||||||
| chr8:79621408 | C | A | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02723.hp1 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+10194C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621408 | |||||||
| chr8:79621410 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.19+10196T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621410 | |||||||
| chr8:79621422 | T | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.19+10208T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621422 | |||||||
| chr8:79621610 | T | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+10396T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621610 | |||||||
| chr8:79621662 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.19+10448G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621662 | |||||||
| chr8:79621876 | A | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+10662A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621876 | |||||||
| chr8:79621909 | G | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.19+10695G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621909 | |||||||
| chr8:79621921 | C | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(9): Show |
13 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.19+10707C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79621921 | |||||||
| chr8:79622100 | C | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+10886C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79622100 | |||||||
| chr8:79622101 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.19+10887A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79622101 | |||||||
| chr8:79622118 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.19+10904G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79622118 | |||||||
| chr8:79622452 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.19+11238C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79622452 | |||||||
| chr8:79622507 | C | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(37): Show |
54 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.19+11293C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79622507 | |||||||
| chr8:79622688 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.19+11474C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79622688 | |||||||
| chr8:79622932 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0323 |
3 | HG01167.hp2 HG01169.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19+11718C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79622932 | |||||||
| chr8:79622933 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.19+11719G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79622933 | |||||||
| chr8:79622999 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.19+11785T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79622999 | |||||||
| chr8:79623172 | G | T | 93 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.19+11958G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623172 | |||||||
| chr8:79623183 | T | C | 17 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
18 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.19+11969T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623183 | |||||||
| chr8:79623316 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.19+12102C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623316 | |||||||
| chr8:79623405 | G | T | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+12191G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623405 | |||||||
| chr8:79623417 | T | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
12 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.19+12203T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623417 | |||||||
| chr8:79623421 | A | G | 1 | a0001c0001t0001g0289 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.19+12207A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623421 | |||||||
| chr8:79623476 | G | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
57 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.19+12262G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623476 | |||||||
| chr8:79623508 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0049 |
4 | HG00140.hp1 HG01433.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+12294A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623508 | |||||||
| chr8:79623782 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.19+12568T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623782 | |||||||
| chr8:79623852 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19+12638T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79623852 | |||||||
| chr8:79624002 | T | C | 1 | a0001c0002t0001g0279 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.19+12788T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624002 | |||||||
| chr8:79624108 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.20-12694A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624108 | |||||||
| chr8:79624137 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(39): Show |
54 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.20-12665G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624137 | |||||||
| chr8:79624166 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.20-12636A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624166 | |||||||
| chr8:79624180 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.20-12622C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624180 | |||||||
| chr8:79624200 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.20-12602A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624200 | |||||||
| chr8:79624318 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.20-12484G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624318 | |||||||
| chr8:79624441 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.20-12361G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624441 | |||||||
| chr8:79624453 | C | CA | 30 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0050 others(27): Show |
34 | HG00280.hp1 HG00733.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.20-12324dupA | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79624453 | ||||||
| chr8:79624453 | CA | C | 20 | a0001c0001t0001g0051 a0001c0001t0001g0083 a0001c0001t0001g0084 others(17): Show |
23 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.20-12324delA | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79624453 | ||||||
| chr8:79624453 | CAAAA | C | 30 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(27): Show |
35 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.20-12327_20-12324d others(6): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79624453 | ||||||
| chr8:79624453 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | NA18950.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.20-12333_20-12324d others(12): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79624453 | ||||||
| chr8:79624470 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
6 | HG00140.hp1 HG01433.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-12332A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624470 | |||||||
| chr8:79624474 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0045 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.20-12324_20-12323i others(16): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79624474 | ||||||
| chr8:79624474 | A | AAAAAAAA others(5): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | HG01258.hp2 HG01515.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.20-12324_20-12323i others(14): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79624474 | ||||||
| chr8:79624475 | AAAAG | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
6 | HG00140.hp1 HG01433.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-12312_20-12309d others(6): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79624475 | ||||||
| chr8:79624479 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(3): Show |
6 | HG01258.hp2 HG01515.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-12323G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624479 | |||||||
| chr8:79624541 | A | G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(16): Show |
20 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.20-12261A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624541 | |||||||
| chr8:79624577 | C | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-12225C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624577 | |||||||
| chr8:79624642 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.20-12160A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624642 | |||||||
| chr8:79624643 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.20-12159G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624643 | |||||||
| chr8:79624645 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.20-12157A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624645 | |||||||
| chr8:79624656 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.20-12146C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624656 | |||||||
| chr8:79624819 | T | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(15): Show |
20 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.20-11983T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79624819 | |||||||
| chr8:79624990 | AT | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(15): Show |
20 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.20-11806delT | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79624990 | ||||||
| chr8:79625117 | A | C | 20 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(17): Show |
25 | HG00140.hp1 HG01167.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.20-11685A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79625117 | |||||||
| chr8:79625337 | A | T | 1 | a0001c0001t0001g0081 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.20-11465A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79625337 | |||||||
| chr8:79625756 | G | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(30): Show |
37 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.20-11046G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79625756 | |||||||
| chr8:79625761 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.20-11041C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79625761 | |||||||
| chr8:79625784 | C | T | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-11018C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79625784 | |||||||
| chr8:79626021 | TAATA | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(117): Show |
151 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.20-10779_20-10776d others(6): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79626021 | ||||||
| chr8:79626122 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.20-10680T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626122 | |||||||
| chr8:79626153 | T | TG | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.20-10649_20-10648i others(3): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626153 | |||||||
| chr8:79626191 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.20-10611A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626191 | |||||||
| chr8:79626195 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.20-10607T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626195 | |||||||
| chr8:79626215 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.20-10587G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626215 | |||||||
| chr8:79626238 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.20-10564T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626238 | |||||||
| chr8:79626289 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(115): Show |
146 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.20-10513T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626289 | |||||||
| chr8:79626446 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.20-10356C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626446 | |||||||
| chr8:79626487 | G | A | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-10315G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626487 | |||||||
| chr8:79626818 | G | C | 1 | a0001c0001t0001g0257 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.20-9984G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626818 | |||||||
| chr8:79626916 | A | C | 1 | a0001c0001t0001g0329 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.20-9886A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626916 | |||||||
| chr8:79626920 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.20-9882A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626920 | |||||||
| chr8:79626989 | G | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.20-9813G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79626989 | |||||||
| chr8:79627152 | T | C | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.20-9650T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79627152 | |||||||
| chr8:79627388 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(37): Show |
50 | HG00639.hp1 HG01069.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.20-9414T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79627388 | |||||||
| chr8:79627396 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.20-9406A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79627396 | |||||||
| chr8:79627738 | T | TCTAA | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(116): Show |
147 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.20-9063_20-9060dup others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79627738 | ||||||
| chr8:79628107 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.20-8695G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628107 | |||||||
| chr8:79628126 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0038 others(15): Show |
24 | HG00558.hp2 HG02056.hp1 HG02523.hp2 others(21): Show |
intron_variant | MODIFIER | c.20-8676G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628126 | |||||||
| chr8:79628209 | G | C | 8 | a0001c0001t0001g0130 a0001c0001t0001g0262 a0001c0001t0001g0263 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-8593G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628209 | |||||||
| chr8:79628306 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(98): Show |
127 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.20-8496G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628306 | |||||||
| chr8:79628310 | C | T | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-8492C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628310 | |||||||
| chr8:79628312 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.20-8490C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628312 | |||||||
| chr8:79628325 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.20-8477G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628325 | |||||||
| chr8:79628649 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.20-8153A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628649 | |||||||
| chr8:79628722 | A | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.20-8080A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628722 | |||||||
| chr8:79628770 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(110): Show |
141 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.20-8032C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79628770 | |||||||
| chr8:79628773 | G | GA | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-8022dupA | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79628773 | ||||||
| chr8:79629049 | T | A | 1 | a0001c0001t0001g0041 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.20-7753T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79629049 | |||||||
| chr8:79629532 | C | T | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-7270C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79629532 | |||||||
| chr8:79629570 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.20-7232G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79629570 | |||||||
| chr8:79629572 | A | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(116): Show |
147 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.20-7230A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79629572 | |||||||
| chr8:79629792 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(116): Show |
147 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.20-7010C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79629792 | |||||||
| chr8:79630140 | C | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(98): Show |
127 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.20-6662C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79630140 | |||||||
| chr8:79630164 | A | G | 2 | a0001c0002t0001g0005 a0001c0002t0001g0279 |
5 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-6638A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79630164 | |||||||
| chr8:79630362 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02922.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.20-6440T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79630362 | |||||||
| chr8:79630366 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(116): Show |
147 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.20-6436A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79630366 | |||||||
| chr8:79630552 | C | T | 2 | a0001c0002t0001g0005 a0001c0002t0001g0279 |
5 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-6250C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79630552 | |||||||
| chr8:79630690 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.20-6112T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79630690 | |||||||
| chr8:79630843 | C | T | 8 | a0001c0001t0001g0130 a0001c0001t0001g0262 a0001c0001t0001g0263 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-5959C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79630843 | |||||||
| chr8:79630901 | TA | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(118): Show |
152 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.20-5894delA | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79630901 | ||||||
| chr8:79630980 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0034 others(37): Show |
51 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.20-5822C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79630980 | |||||||
| chr8:79631132 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.20-5670G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79631132 | |||||||
| chr8:79631368 | G | C | 1 | a0001c0001t0003g0026 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.20-5434G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79631368 | |||||||
| chr8:79631563 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.20-5239C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79631563 | |||||||
| chr8:79631685 | G | A | 1 | a0001c0001t0003g0026 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.20-5117G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79631685 | |||||||
| chr8:79631753 | T | C | 2 | a0001c0002t0001g0005 a0001c0002t0001g0279 |
5 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-5049T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79631753 | |||||||
| chr8:79631755 | A | T | 1 | a0001c0001t0003g0026 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.20-5047A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79631755 | |||||||
| chr8:79631759 | A | G | 2 | a0001c0002t0001g0005 a0001c0002t0001g0279 |
5 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-5043A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79631759 | |||||||
| chr8:79631845 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.20-4957C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79631845 | |||||||
| chr8:79631919 | T | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(98): Show |
127 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.20-4883T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79631919 | |||||||
| chr8:79632074 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(42): Show |
59 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.20-4728A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79632074 | |||||||
| chr8:79632156 | C | T | 7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG02145.hp1 HG02723.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-4646C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79632156 | |||||||
| chr8:79632189 | T | C | 2 | a0001c0002t0001g0005 a0001c0002t0001g0279 |
5 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-4613T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79632189 | |||||||
| chr8:79632201 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.20-4601G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79632201 | |||||||
| chr8:79632215 | GTATA | G | 7 | a0001c0001t0001g0130 a0001c0001t0001g0262 a0001c0001t0001g0263 others(4): Show |
7 | HG01884.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-4582_20-4579del others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79632215 | ||||||
| chr8:79632255 | C | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
51 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.20-4547C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79632255 | |||||||
| chr8:79632510 | C | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(42): Show |
59 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.20-4292C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79632510 | |||||||
| chr8:79632556 | C | T | 2 | a0001c0002t0001g0005 a0001c0002t0001g0279 |
5 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-4246C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79632556 | |||||||
| chr8:79632760 | A | C | 1 | a0001c0001t0001g0292 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.20-4042A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79632760 | |||||||
| chr8:79632956 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0002t0001g0005 others(1): Show |
7 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-3846C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79632956 | |||||||
| chr8:79633009 | C | CT | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-3785dupT | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79633009 | ||||||
| chr8:79633332 | A | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.20-3470A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633332 | |||||||
| chr8:79633431 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20-3371T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633431 | |||||||
| chr8:79633472 | T | C | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-3330T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633472 | |||||||
| chr8:79633695 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.20-3107C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633695 | |||||||
| chr8:79633821 | T | A | 1 | a0001c0001t0003g0026 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.20-2981T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633821 | |||||||
| chr8:79633867 | C | T | 1 | a0001c0001t0003g0026 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.20-2935C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633867 | |||||||
| chr8:79633877 | T | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0245 a0001c0001t0002g0246 |
11 | NA18941.hp1 NA18942.hp1 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-2925T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633877 | |||||||
| chr8:79633900 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(42): Show |
59 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.20-2902G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633900 | |||||||
| chr8:79633922 | T | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.20-2880T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633922 | |||||||
| chr8:79633949 | T | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-2853T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633949 | |||||||
| chr8:79633984 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.20-2818C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79633984 | |||||||
| chr8:79634094 | T | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.20-2708T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634094 | |||||||
| chr8:79634159 | G | T | 1 | a0001c0001t0001g0329 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.20-2643G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634159 | |||||||
| chr8:79634217 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.20-2585T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634217 | |||||||
| chr8:79634225 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(113): Show |
147 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.20-2577G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634225 | |||||||
| chr8:79634226 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0245 a0001c0001t0002g0246 |
11 | NA18941.hp1 NA18942.hp1 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-2576T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634226 | |||||||
| chr8:79634311 | A | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-2491A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634311 | |||||||
| chr8:79634312 | T | TTA | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-2489_20-2488dup others(2): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 79634312 | ||||||
| chr8:79634370 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.20-2432G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634370 | |||||||
| chr8:79634371 | C | T | 1 | a0001c0001t0006g0280 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.20-2431C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634371 | |||||||
| chr8:79634614 | A | G | 1 | a0001c0001t0006g0280 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.20-2188A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634614 | |||||||
| chr8:79634782 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.20-2020A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634782 | |||||||
| chr8:79634974 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(100): Show |
129 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.20-1828C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634974 | |||||||
| chr8:79634985 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(100): Show |
129 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.20-1817G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79634985 | |||||||
| chr8:79635058 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.20-1744G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79635058 | |||||||
| chr8:79635091 | T | C | 34 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(31): Show |
38 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.20-1711T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79635091 | |||||||
| chr8:79635451 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.20-1351T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79635451 | |||||||
| chr8:79635542 | G | T | 84 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.20-1260G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79635542 | |||||||
| chr8:79635762 | G | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.20-1040G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79635762 | |||||||
| chr8:79636176 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.20-626C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79636176 | |||||||
| chr8:79636197 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.20-605A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79636197 | |||||||
| chr8:79636208 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.20-594C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79636208 | |||||||
| chr8:79636470 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.20-332C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79636470 | |||||||
| chr8:79636590 | A | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-212A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79636590 | |||||||
| chr8:79636689 | T | C | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0002t0001g0005 others(1): Show |
7 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-113T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 1/4 | chr8 | 79636689 | |||||||
| chr8:79637023 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0127 a0001c0001t0001g0210 |
3 | HG00738.hp2 NA18985.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.115+126G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79637023 | |||||||
| chr8:79637085 | TAAC | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0080 |
3 | HG01081.hp2 HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.115+193_115+195del others(3): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 79637085 | ||||||
| chr8:79637252 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0105 a0001c0001t0001g0106 |
4 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+355G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79637252 | |||||||
| chr8:79637336 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.115+439T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79637336 | |||||||
| chr8:79637388 | C | T | 1 | a0001c0001t0003g0026 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.115+491C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79637388 | |||||||
| chr8:79637896 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.115+999A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79637896 | |||||||
| chr8:79637927 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
186 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.115+1030G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79637927 | |||||||
| chr8:79638078 | G | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(34): Show |
42 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.115+1181G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638078 | |||||||
| chr8:79638381 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.115+1484C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638381 | |||||||
| chr8:79638382 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.115+1485G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638382 | |||||||
| chr8:79638540 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.115+1643T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638540 | |||||||
| chr8:79638554 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.115+1657G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638554 | |||||||
| chr8:79638588 | T | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.115+1691T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638588 | |||||||
| chr8:79638676 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.115+1779C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638676 | |||||||
| chr8:79638832 | T | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.115+1935T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638832 | |||||||
| chr8:79638872 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(105): Show |
138 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.115+1975G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638872 | |||||||
| chr8:79638897 | T | C | 3 | a0001c0001t0001g0183 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG00738.hp1 HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.115+2000T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79638897 | |||||||
| chr8:79639146 | A | G | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.116-2232A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79639146 | |||||||
| chr8:79639156 | T | C | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0002t0001g0005 others(1): Show |
7 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-2222T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79639156 | |||||||
| chr8:79639207 | A | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.116-2171A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79639207 | |||||||
| chr8:79639714 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.116-1664A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79639714 | |||||||
| chr8:79639984 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0247 |
3 | HG01515.hp2 HG01517.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.116-1394G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79639984 | |||||||
| chr8:79640003 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.116-1375C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640003 | |||||||
| chr8:79640227 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.116-1151C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640227 | |||||||
| chr8:79640319 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.116-1059G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640319 | |||||||
| chr8:79640377 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0326 a0001c0001t0001g0327 others(4): Show |
9 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-1001G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640377 | |||||||
| chr8:79640379 | C | T | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-999C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640379 | |||||||
| chr8:79640451 | C | CT | 93 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.116-921dupT | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 79640451 | ||||||
| chr8:79640562 | G | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.116-816G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640562 | |||||||
| chr8:79640824 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.116-554G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640824 | |||||||
| chr8:79640833 | T | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.116-545T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640833 | |||||||
| chr8:79640845 | A | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.116-533A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640845 | |||||||
| chr8:79640909 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02145.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.116-469G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640909 | |||||||
| chr8:79640914 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.116-464T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640914 | |||||||
| chr8:79640970 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0276 |
3 | NA18612.hp1 NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.116-408G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640970 | |||||||
| chr8:79640972 | C | T | 41 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
53 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.116-406C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640972 | |||||||
| chr8:79640986 | C | A | 1 | a0001c0001t0001g0311 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.116-392C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640986 | |||||||
| chr8:79640997 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.116-381G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79640997 | |||||||
| chr8:79641002 | T | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.116-376T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79641002 | |||||||
| chr8:79641119 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0002t0001g0005 others(1): Show |
7 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-259C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79641119 | |||||||
| chr8:79641132 | C | A | 1 | a0001c0001t0001g0327 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.116-246C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79641132 | |||||||
| chr8:79641277 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-101G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 2/4 | chr8 | 79641277 | |||||||
| chr8:79641580 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.288+30C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79641580 | |||||||
| chr8:79641594 | C | T | 1 | a0001c0001t0006g0280 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.288+44C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79641594 | |||||||
| chr8:79641614 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.288+64G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79641614 | |||||||
| chr8:79641628 | G | GCA | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(61): Show |
78 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.288+121_288+122dup others(2): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | G | GCACA | 63 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0019 others(60): Show |
73 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.288+119_288+122dup others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | G | GCACACA | 18 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0066 others(15): Show |
19 | HG01168.hp1 HG01169.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.288+117_288+122dup others(6): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0186 others(1): Show |
4 | HG01106.hp2 HG02735.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+115_288+122dup others(8): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | G | GCACACAC others(3): Show |
1 | a0001c0001t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.288+113_288+122dup others(10): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | GCA | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
53 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.288+121_288+122del others(2): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | GCACA | G | 19 | a0001c0001t0001g0035 a0001c0001t0001g0079 a0001c0001t0001g0161 others(16): Show |
20 | HG01361.hp1 HG01934.hp2 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.288+119_288+122del others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | GCACACA | G | 2 | a0001c0001t0001g0095 a0001c0001t0003g0026 |
3 | HG03225.hp1 HG03516.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.288+117_288+122del others(6): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | GCACACAC others(1): Show |
G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(41): Show |
57 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.288+115_288+122del others(8): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | GCACACAC others(3): Show |
G | 3 | a0001c0001t0001g0162 a0001c0001t0001g0209 a0001c0001t0001g0322 |
3 | HG02132.hp2 NA19085.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.288+113_288+122del others(10): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641628 | GCACACAC others(5): Show |
G | 15 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
19 | HG00140.hp1 HG00741.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.288+111_288+122del others(12): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79641628 | ||||||
| chr8:79641632 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0002g0244 |
2 | HG02055.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.288+82A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79641632 | |||||||
| chr8:79641634 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0281 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.288+84A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79641634 | |||||||
| chr8:79641638 | A | G | 2 | a0001c0001t0001g0305 a0001c0001t0003g0026 |
3 | HG02155.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.288+88A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79641638 | |||||||
| chr8:79641643 | C | T | 1 | a0001c0001t0003g0026 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.288+93C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79641643 | |||||||
| chr8:79641681 | G | A | 71 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
88 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.288+131G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79641681 | |||||||
| chr8:79641779 | T | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(41): Show |
57 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.288+229T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79641779 | |||||||
| chr8:79642153 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.288+603T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642153 | |||||||
| chr8:79642206 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.288+656G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642206 | |||||||
| chr8:79642297 | T | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+747T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642297 | |||||||
| chr8:79642364 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.288+814A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642364 | |||||||
| chr8:79642589 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.288+1039A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642589 | |||||||
| chr8:79642718 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.288+1168T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642718 | |||||||
| chr8:79642726 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0002t0001g0005 others(1): Show |
7 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.288+1176C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642726 | |||||||
| chr8:79642769 | A | T | 56 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(53): Show |
70 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.288+1219A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642769 | |||||||
| chr8:79642810 | T | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.288+1260T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642810 | |||||||
| chr8:79642822 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.288+1272A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642822 | |||||||
| chr8:79642861 | C | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0282 a0001c0001t0006g0280 |
3 | HG01109.hp2 HG02965.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.288+1311C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642861 | |||||||
| chr8:79642871 | G | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
360 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.288+1321G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642871 | |||||||
| chr8:79642873 | C | CAT | 48 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(45): Show |
60 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.288+1336_288+1337d others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79642873 | ||||||
| chr8:79642873 | CAT | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0166 |
4 | HG00609.hp2 NA18975.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+1336_288+1337d others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79642873 | ||||||
| chr8:79642993 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.288+1443A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79642993 | |||||||
| chr8:79643106 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.288+1556A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643106 | |||||||
| chr8:79643139 | A | ATG | 4 | a0001c0001t0001g0130 a0001c0001t0001g0185 a0001c0001t0001g0214 others(1): Show |
4 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+1599_288+1600d others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643139 | ||||||
| chr8:79643149 | G | GTA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(82): Show |
104 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.288+1618_288+1619d others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643149 | ||||||
| chr8:79643149 | G | GTATA | 46 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(43): Show |
56 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.288+1616_288+1619d others(6): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643149 | ||||||
| chr8:79643149 | G | GTATATA | 31 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0024 others(28): Show |
37 | HG00639.hp1 HG01515.hp2 HG01516.hp2 others(34): Show |
intron_variant | MODIFIER | c.288+1614_288+1619d others(8): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643149 | ||||||
| chr8:79643149 | G | GTATATAT others(1): Show |
20 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0042 others(17): Show |
24 | HG00140.hp1 HG00140.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.288+1612_288+1619d others(10): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643149 | ||||||
| chr8:79643149 | G | GTATATAT others(3): Show |
6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+1610_288+1619d others(12): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643149 | ||||||
| chr8:79643149 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.288+1608_288+1619d others(14): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643149 | ||||||
| chr8:79643149 | GTA | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0034 others(37): Show |
51 | HG00323.hp1 HG00621.hp2 HG02040.hp2 others(48): Show |
intron_variant | MODIFIER | c.288+1618_288+1619d others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643149 | ||||||
| chr8:79643151 | A | G | 52 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(49): Show |
66 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.288+1601A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643151 | |||||||
| chr8:79643197 | T | TA | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+1653dupA | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643197 | ||||||
| chr8:79643228 | C | CTA | 4 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0192 others(1): Show |
4 | HG00639.hp2 HG02559.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+1697_288+1698d others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643228 | ||||||
| chr8:79643228 | C | CTATATA | 5 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(2): Show |
5 | HG02257.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.288+1693_288+1698d others(8): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643228 | ||||||
| chr8:79643228 | CTATA | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0034 others(35): Show |
49 | HG00323.hp1 HG00621.hp2 HG02040.hp2 others(46): Show |
intron_variant | MODIFIER | c.288+1695_288+1698d others(6): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643228 | ||||||
| chr8:79643228 | CTATATA | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(10): Show |
17 | HG00140.hp1 HG01167.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.288+1693_288+1698d others(8): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643228 | ||||||
| chr8:79643375 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0032 |
4 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+1825C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643375 | |||||||
| chr8:79643507 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.288+1957T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643507 | |||||||
| chr8:79643533 | T | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+1983T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643533 | |||||||
| chr8:79643664 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.288+2114A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643664 | |||||||
| chr8:79643751 | A | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+2201A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643751 | |||||||
| chr8:79643805 | A | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0079 others(6): Show |
12 | HG00609.hp2 HG02523.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.288+2255A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643805 | |||||||
| chr8:79643862 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.288+2312C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643862 | |||||||
| chr8:79643965 | G | GT | 46 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(43): Show |
58 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.288+2424dupT | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79643965 | ||||||
| chr8:79643988 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.288+2438T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79643988 | |||||||
| chr8:79644265 | G | A | 8 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG01346.hp2 HG01433.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.288+2715G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79644265 | |||||||
| chr8:79644357 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.288+2807T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79644357 | |||||||
| chr8:79644502 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+2952G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79644502 | |||||||
| chr8:79644562 | C | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0034 others(34): Show |
48 | HG00323.hp1 HG00621.hp2 HG02040.hp2 others(45): Show |
intron_variant | MODIFIER | c.288+3012C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79644562 | |||||||
| chr8:79644626 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0002t0001g0005 others(1): Show |
7 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.288+3076C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79644626 | |||||||
| chr8:79644769 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0034 others(39): Show |
56 | HG00323.hp1 HG00621.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.288+3219C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79644769 | |||||||
| chr8:79644789 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.288+3239G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79644789 | |||||||
| chr8:79644921 | G | A | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0002t0001g0005 others(1): Show |
7 | HG01167.hp1 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.288+3371G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79644921 | |||||||
| chr8:79645007 | T | A | 1 | a0001c0001t0001g0249 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.288+3457T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79645007 | |||||||
| chr8:79645008 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.288+3458C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79645008 | |||||||
| chr8:79645127 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.288+3577C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79645127 | |||||||
| chr8:79645154 | C | CA | 59 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(56): Show |
73 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.288+3616dupA | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79645154 | ||||||
| chr8:79645331 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0034 others(32): Show |
46 | HG00323.hp1 HG00621.hp2 HG02040.hp2 others(43): Show |
intron_variant | MODIFIER | c.288+3781C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79645331 | |||||||
| chr8:79645385 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0034 others(32): Show |
46 | HG00323.hp1 HG00621.hp2 HG02040.hp2 others(43): Show |
intron_variant | MODIFIER | c.288+3835C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79645385 | |||||||
| chr8:79645445 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.288+3895G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79645445 | |||||||
| chr8:79645508 | G | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
71 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.288+3958G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79645508 | |||||||
| chr8:79645679 | T | TTAGGATG others(12): Show |
9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+4136_288+4154d others(21): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79645679 | ||||||
| chr8:79645993 | A | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+4443A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79645993 | |||||||
| chr8:79646179 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.288+4629C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646179 | |||||||
| chr8:79646278 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.288+4728C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646278 | |||||||
| chr8:79646313 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.288+4763G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646313 | |||||||
| chr8:79646508 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.288+4958G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646508 | |||||||
| chr8:79646568 | G | A | 6 | a0001c0001t0001g0266 a0001c0001t0001g0274 a0001c0001t0001g0293 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+5018G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646568 | |||||||
| chr8:79646799 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.288+5249T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646799 | |||||||
| chr8:79646803 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0139 a0001c0001t0001g0295 |
3 | HG01243.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.288+5253T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646803 | |||||||
| chr8:79646811 | T | A | 17 | a0001c0001t0001g0015 a0001c0001t0001g0138 a0001c0001t0001g0144 others(14): Show |
19 | HG00673.hp1 HG00741.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.288+5261T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646811 | |||||||
| chr8:79646978 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0240 a0001c0001t0001g0247 others(5): Show |
9 | HG02056.hp1 NA18943.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.288+5428G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646978 | |||||||
| chr8:79646984 | G | A | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(322): Show |
394 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.288+5434G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79646984 | |||||||
| chr8:79647200 | A | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0127 |
3 | HG00735.hp2 HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.288+5650A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79647200 | |||||||
| chr8:79647241 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0060 a0001c0001t0001g0077 |
4 | HG02074.hp1 HG02129.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+5691T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79647241 | |||||||
| chr8:79647258 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00423.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.288+5708T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79647258 | |||||||
| chr8:79647443 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0281 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.288+5893C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79647443 | |||||||
| chr8:79647601 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.288+6051G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79647601 | |||||||
| chr8:79647774 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0117 |
3 | HG02258.hp1 HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.288+6224C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79647774 | |||||||
| chr8:79647775 | T | C | 7 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0196 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.288+6225T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79647775 | |||||||
| chr8:79647874 | T | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(21): Show |
30 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.288+6324T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79647874 | |||||||
| chr8:79647976 | C | A | 6 | a0001c0001t0001g0035 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
7 | NA18961.hp1 NA18975.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.288+6426C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79647976 | |||||||
| chr8:79648073 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.288+6523C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79648073 | |||||||
| chr8:79648226 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.289-6645A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79648226 | |||||||
| chr8:79648416 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.289-6455C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79648416 | |||||||
| chr8:79648449 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.289-6422G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79648449 | |||||||
| chr8:79648453 | C | CT | 102 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(99): Show |
125 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(122): Show |
intron_variant | MODIFIER | c.289-6397dupT | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79648453 | ||||||
| chr8:79648453 | C | CTT | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(117): Show |
142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.289-6398_289-6397d others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79648453 | ||||||
| chr8:79648453 | C | CTTT | 11 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0059 others(8): Show |
12 | HG00423.hp1 HG00741.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.289-6399_289-6397d others(5): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79648453 | ||||||
| chr8:79648453 | CT | C | 7 | a0001c0001t0001g0147 a0001c0001t0001g0240 a0001c0001t0001g0248 others(4): Show |
7 | HG01070.hp1 HG01496.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-6397delT | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79648453 | ||||||
| chr8:79648722 | C | T | 16 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(13): Show |
21 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.289-6149C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79648722 | |||||||
| chr8:79648749 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.289-6122C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79648749 | |||||||
| chr8:79648807 | A | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
20 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.289-6064A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79648807 | |||||||
| chr8:79648967 | T | C | 3 | a0001c0001t0001g0266 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02896.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.289-5904T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79648967 | |||||||
| chr8:79649286 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0170 |
3 | HG01891.hp1 HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.289-5585G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79649286 | |||||||
| chr8:79649321 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.289-5550A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79649321 | |||||||
| chr8:79649467 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.289-5404G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79649467 | |||||||
| chr8:79649602 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.289-5269G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79649602 | |||||||
| chr8:79649795 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.289-5076T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79649795 | |||||||
| chr8:79649830 | A | C | 1 | a0001c0001t0001g0287 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.289-5041A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79649830 | |||||||
| chr8:79649873 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.289-4998C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79649873 | |||||||
| chr8:79649926 | T | C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.289-4945T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79649926 | |||||||
| chr8:79649948 | T | G | 1 | a0001c0001t0001g0330 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.289-4923T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79649948 | |||||||
| chr8:79650024 | C | T | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(220): Show |
266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.289-4847C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79650024 | |||||||
| chr8:79650052 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.289-4819C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79650052 | |||||||
| chr8:79650430 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0157 a0001c0001t0001g0159 others(1): Show |
4 | HG00673.hp1 HG02083.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-4441G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79650430 | |||||||
| chr8:79650462 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.289-4409C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79650462 | |||||||
| chr8:79650635 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.289-4236G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79650635 | |||||||
| chr8:79650814 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.289-4057C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79650814 | |||||||
| chr8:79650977 | A | G | 40 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0042 others(37): Show |
42 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.289-3894A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79650977 | |||||||
| chr8:79651019 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.289-3852T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79651019 | |||||||
| chr8:79651069 | A | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(3): Show |
7 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.289-3802A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79651069 | |||||||
| chr8:79651495 | C | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.289-3376C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79651495 | |||||||
| chr8:79651526 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.289-3345T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79651526 | |||||||
| chr8:79652067 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.289-2804T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79652067 | |||||||
| chr8:79652140 | T | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02723.hp1 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.289-2731T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79652140 | |||||||
| chr8:79652218 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.289-2653T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79652218 | |||||||
| chr8:79652343 | T | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.289-2528T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79652343 | |||||||
| chr8:79652419 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0274 a0001c0001t0001g0295 |
3 | HG01243.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.289-2452T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79652419 | |||||||
| chr8:79652470 | G | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02723.hp1 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.289-2401G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79652470 | |||||||
| chr8:79652718 | C | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.289-2153C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79652718 | |||||||
| chr8:79652783 | T | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
104 | HG00544.hp2 HG00558.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.289-2088T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79652783 | |||||||
| chr8:79653148 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0049 |
4 | HG00140.hp1 HG01433.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-1723C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79653148 | |||||||
| chr8:79653292 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.289-1579G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79653292 | |||||||
| chr8:79653324 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.289-1547C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79653324 | |||||||
| chr8:79653363 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(3): Show |
7 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.289-1508C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79653363 | |||||||
| chr8:79653803 | A | G | 49 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(46): Show |
56 | HG00544.hp2 HG00558.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.289-1068A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79653803 | |||||||
| chr8:79653820 | T | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0038 others(14): Show |
23 | HG00558.hp2 HG02056.hp1 NA18939.hp2 others(20): Show |
intron_variant | MODIFIER | c.289-1051T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79653820 | |||||||
| chr8:79654239 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | NA18953.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.289-632C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79654239 | |||||||
| chr8:79654311 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(46): Show |
63 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.289-560C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79654311 | |||||||
| chr8:79654356 | A | AG | 32 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0055 others(29): Show |
33 | HG00621.hp2 HG00735.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.289-509dupG | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79654356 | ||||||
| chr8:79654386 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.289-485A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79654386 | |||||||
| chr8:79654471 | GGAA | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0025 others(8): Show |
17 | HG01891.hp1 HG02027.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.289-394_289-392del others(3): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 79654471 | ||||||
| chr8:79654510 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.289-361C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79654510 | |||||||
| chr8:79654585 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.289-286A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79654585 | |||||||
| chr8:79654662 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.289-209C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 3/4 | chr8 | 79654662 | |||||||
| chr8:79655268 | G | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
19 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.480+206G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655268 | |||||||
| chr8:79655294 | G | A | 1 | a0002c0003t0001g0111 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.480+232G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655294 | |||||||
| chr8:79655459 | G | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0073 a0001c0001t0001g0074 |
3 | HG02698.hp1 HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.480+397G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655459 | |||||||
| chr8:79655571 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.480+509A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655571 | |||||||
| chr8:79655572 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.480+510T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655572 | |||||||
| chr8:79655597 | T | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
19 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.480+535T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655597 | |||||||
| chr8:79655727 | A | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.480+665A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655727 | |||||||
| chr8:79655845 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.480+783T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655845 | |||||||
| chr8:79655891 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0062 others(5): Show |
11 | HG00323.hp1 HG01192.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+829C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655891 | |||||||
| chr8:79655994 | G | A | 27 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0105 others(24): Show |
32 | HG00673.hp1 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.480+932G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79655994 | |||||||
| chr8:79656065 | A | G | 26 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0039 others(23): Show |
34 | HG00609.hp1 HG00733.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.480+1003A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656065 | |||||||
| chr8:79656130 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(21): Show |
29 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.480+1068A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656130 | |||||||
| chr8:79656150 | G | A | 22 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(19): Show |
27 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.480+1088G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656150 | |||||||
| chr8:79656201 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.480+1139G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656201 | |||||||
| chr8:79656315 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.480+1253G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656315 | |||||||
| chr8:79656388 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.480+1326A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656388 | |||||||
| chr8:79656411 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.480+1349C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656411 | |||||||
| chr8:79656433 | T | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
19 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.480+1371T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656433 | |||||||
| chr8:79656623 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.480+1561C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656623 | |||||||
| chr8:79656699 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0213 a0001c0001t0001g0323 |
4 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1637C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656699 | |||||||
| chr8:79656700 | T | A | 201 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
239 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.480+1638T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656700 | |||||||
| chr8:79656737 | T | G | 31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0045 others(28): Show |
33 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.480+1675T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656737 | |||||||
| chr8:79656816 | T | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
8 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+1754T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656816 | |||||||
| chr8:79656861 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.480+1799A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656861 | |||||||
| chr8:79656884 | G | GTTTTTTT others(6): Show |
7 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
8 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+1829_480+1830i others(15): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 79656884 | ||||||
| chr8:79656885 | T | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0039 others(24): Show |
35 | HG00609.hp1 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.480+1823T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656885 | |||||||
| chr8:79656896 | T | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
8 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+1834T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656896 | |||||||
| chr8:79656897 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
8 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+1835A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656897 | |||||||
| chr8:79656908 | G | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
8 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+1846G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79656908 | |||||||
| chr8:79657030 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.480+1968C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79657030 | |||||||
| chr8:79657134 | G | A | 24 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(21): Show |
29 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.480+2072G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79657134 | |||||||
| chr8:79657217 | T | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(24): Show |
32 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.480+2155T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79657217 | |||||||
| chr8:79657219 | T | G | 4 | a0001c0001t0001g0282 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG01109.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2157T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79657219 | |||||||
| chr8:79657639 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(21): Show |
33 | HG00639.hp1 HG01515.hp2 HG01517.hp2 others(30): Show |
intron_variant | MODIFIER | c.480+2577T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79657639 | |||||||
| chr8:79657731 | C | A | 1 | a0001c0001t0001g0306 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.480+2669C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79657731 | |||||||
| chr8:79657857 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG01109.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2795G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79657857 | |||||||
| chr8:79657964 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG00140.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.480+2902G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79657964 | |||||||
| chr8:79658557 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0006g0280 |
2 | HG01109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.480+3495C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79658557 | |||||||
| chr8:79658596 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.480+3534G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79658596 | |||||||
| chr8:79658703 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.480+3641T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79658703 | |||||||
| chr8:79658773 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.480+3711A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79658773 | |||||||
| chr8:79658902 | C | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.480+3840C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79658902 | |||||||
| chr8:79658965 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.480+3903C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79658965 | |||||||
| chr8:79658990 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.480+3928G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79658990 | |||||||
| chr8:79659001 | C | G | 1 | a0001c0001t0001g0302 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.480+3939C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659001 | |||||||
| chr8:79659101 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.480+4039A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659101 | |||||||
| chr8:79659286 | G | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(11): Show |
18 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.480+4224G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659286 | |||||||
| chr8:79659312 | C | A | 78 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(75): Show |
93 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.480+4250C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659312 | |||||||
| chr8:79659320 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.480+4258T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659320 | |||||||
| chr8:79659395 | T | G | 62 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
70 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.480+4333T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659395 | |||||||
| chr8:79659493 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0039 others(26): Show |
37 | HG00609.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.480+4431C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659493 | |||||||
| chr8:79659528 | T | C | 3 | a0001c0001t0001g0022 a0001c0002t0001g0005 a0001c0002t0001g0279 |
7 | HG01167.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+4466T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659528 | |||||||
| chr8:79659687 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG01109.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.480+4625G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659687 | |||||||
| chr8:79659711 | C | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(20): Show |
29 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.480+4649C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659711 | |||||||
| chr8:79659773 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.480+4711T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659773 | |||||||
| chr8:79659865 | C | G | 25 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(22): Show |
31 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.480+4803C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659865 | |||||||
| chr8:79659870 | A | AT | 25 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(22): Show |
31 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.480+4808_480+4809i others(3): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659870 | |||||||
| chr8:79659872 | G | A | 25 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(22): Show |
31 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.480+4810G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659872 | |||||||
| chr8:79659873 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.480+4811C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659873 | |||||||
| chr8:79659877 | G | C | 25 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(22): Show |
31 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.480+4815G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659877 | |||||||
| chr8:79659929 | A | G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(13): Show |
21 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.480+4867A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659929 | |||||||
| chr8:79659996 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0270 |
2 | HG01070.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.481-4819A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79659996 | |||||||
| chr8:79660038 | T | C | 25 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0027 others(22): Show |
31 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.481-4777T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79660038 | |||||||
| chr8:79660183 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.481-4632C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79660183 | |||||||
| chr8:79660190 | G | A | 202 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
239 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.481-4625G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79660190 | |||||||
| chr8:79660392 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.481-4423A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79660392 | |||||||
| chr8:79660801 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481-4014C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79660801 | |||||||
| chr8:79660932 | GA | G | 40 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(37): Show |
44 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-3881delA | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 79660932 | ||||||
| chr8:79660993 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.481-3822G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79660993 | |||||||
| chr8:79661014 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.481-3801G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661014 | |||||||
| chr8:79661166 | A | G | 40 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(37): Show |
44 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-3649A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661166 | |||||||
| chr8:79661167 | G | A | 1 | a0001c0001t0007g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.481-3648G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661167 | |||||||
| chr8:79661167 | G | C | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.481-3648G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661167 | |||||||
| chr8:79661181 | G | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
10 | HG01167.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.481-3634G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661181 | |||||||
| chr8:79661246 | C | T | 1 | a0001c0001t0007g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.481-3569C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661246 | |||||||
| chr8:79661381 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0213 others(1): Show |
6 | HG01167.hp2 HG01169.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-3434G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661381 | |||||||
| chr8:79661514 | T | C | 11 | a0001c0001t0001g0064 a0001c0001t0001g0096 a0001c0001t0001g0105 others(8): Show |
11 | HG01070.hp1 HG01243.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.481-3301T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661514 | |||||||
| chr8:79661585 | G | A | 25 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0096 others(22): Show |
27 | HG00673.hp1 HG01070.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.481-3230G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661585 | |||||||
| chr8:79661668 | C | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0041 others(19): Show |
27 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.481-3147C>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661668 | |||||||
| chr8:79661798 | A | C | 25 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0096 others(22): Show |
27 | HG00673.hp1 HG01070.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.481-3017A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79661798 | |||||||
| chr8:79662019 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0293 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.481-2796G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662019 | |||||||
| chr8:79662035 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.481-2780T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662035 | |||||||
| chr8:79662079 | T | C | 61 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(58): Show |
74 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.481-2736T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662079 | |||||||
| chr8:79662219 | G | A | 1 | a0001c0001t0001g0011 | 3 | NA18948.hp2 NA18951.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.481-2596G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662219 | |||||||
| chr8:79662455 | A | T | 1 | a0001c0001t0007g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.481-2360A>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662455 | |||||||
| chr8:79662460 | A | G | 40 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(37): Show |
44 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-2355A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662460 | |||||||
| chr8:79662502 | C | A | 31 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0032 others(28): Show |
34 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.481-2313C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662502 | |||||||
| chr8:79662550 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.481-2265A>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662550 | |||||||
| chr8:79662561 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.481-2254G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662561 | |||||||
| chr8:79662874 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01081.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.481-1941A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79662874 | |||||||
| chr8:79663031 | C | A | 1 | a0001c0001t0001g0007 | 3 | HG01884.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.481-1784C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663031 | |||||||
| chr8:79663033 | C | T | 39 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(36): Show |
43 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.481-1782C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663033 | |||||||
| chr8:79663120 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.481-1695T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663120 | |||||||
| chr8:79663202 | T | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
19 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.481-1613T>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663202 | |||||||
| chr8:79663243 | T | C | 1 | a0001c0001t0007g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.481-1572T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663243 | |||||||
| chr8:79663251 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.481-1564C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663251 | |||||||
| chr8:79663303 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.481-1512C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663303 | |||||||
| chr8:79663315 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.481-1500C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663315 | |||||||
| chr8:79663488 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.481-1327C>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663488 | |||||||
| chr8:79663488 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.481-1327C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663488 | |||||||
| chr8:79663510 | G | A | 39 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(36): Show |
43 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.481-1305G>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663510 | |||||||
| chr8:79663529 | G | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01081.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.481-1286G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663529 | |||||||
| chr8:79663672 | T | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0144 a0001c0001t0001g0150 others(10): Show |
15 | HG00673.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.481-1143T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663672 | |||||||
| chr8:79663719 | T | A | 40 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(37): Show |
44 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-1096T>A | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663719 | |||||||
| chr8:79663728 | A | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0245 others(6): Show |
14 | HG00558.hp2 NA18939.hp2 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.481-1087A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663728 | |||||||
| chr8:79663893 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
379 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.481-922T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663893 | |||||||
| chr8:79663981 | GA | G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(13): Show |
21 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.481-825delA | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 79663981 | ||||||
| chr8:79663990 | A | G | 6 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0108 others(3): Show |
6 | HG02630.hp1 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-825A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79663990 | |||||||
| chr8:79664000 | A | G | 1 | a0001c0001t0007g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.481-815A>G | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664000 | |||||||
| chr8:79664006 | C | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0041 others(17): Show |
25 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.481-809C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664006 | |||||||
| chr8:79664119 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
10 | HG01167.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.481-696T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664119 | |||||||
| chr8:79664173 | T | C | 3 | a0001c0001t0001g0183 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG00738.hp1 HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.481-642T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664173 | |||||||
| chr8:79664321 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.481-494G>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664321 | |||||||
| chr8:79664335 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.481-480C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664335 | |||||||
| chr8:79664382 | G | C | 40 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(37): Show |
44 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-433G>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664382 | |||||||
| chr8:79664469 | C | T | 16 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(13): Show |
21 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.481-346C>T | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664469 | |||||||
| chr8:79664538 | T | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.481-277T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664538 | |||||||
| chr8:79664569 | T | C | 40 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(37): Show |
44 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-246T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664569 | |||||||
| chr8:79664596 | T | C | 40 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(37): Show |
44 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-219T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664596 | |||||||
| chr8:79664688 | C | CCTCT | 39 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(36): Show |
43 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.481-125_481-124ins others(4): Show |
STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 79664688 | ||||||
| chr8:79664707 | T | C | 40 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0029 others(37): Show |
44 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-108T>C | STMN2 | ENSG00000104435.14 | transcript | ENST00000220876.12 | protein_coding | 4/4 | chr8 | 79664707 |